Myrsinane-Type Diterpenes: A Comprehensive Review on Structural Diversity, Chemistry and Biological Activities

Euphorbia species are important sources of polycyclic and macrocyclic diterpenes, which have been the focus of natural-product-based drug research due to their relevant biological properties, including anticancer, multidrug resistance reversal, antiviral, and anti-inflammatory activities. Premyrsinane, cyclomyrsinane, and myrsinane diterpenes are generally and collectively designated as myrsinane-type diterpenes. These compounds are derived from the macrocyclic lathyrane structure and are characterized by having highly oxygenated rearranged polycyclic systems. This review aims to describe and summarize the distribution and diversity of 220 myrsinane-type diterpenes isolated in the last four decades from about 20 Euphorbia species. Some myrsinane diterpenes obtained from Jatropha curcas are also described. Discussion on their plausible biosynthetic pathways is presented, as well as isolation procedures and structural elucidation using nuclear magnetic resonance spectroscopy. Furthermore, the most important biological activities are highlighted, which include cytotoxic and immunomodulatory activities, the modulation of efflux pumps, the neuroprotective effects, and the inhibition of enzymes such as urease, HIV-1 reverse transcriptase, and prolyl endopeptidase, among other biological effects.


Introduction
Natural products (NPs) have been crucial in drug discovery and development, with more than half of the current clinically used drugs based on natural compound pharmacophore [1].In fact, over the last four decades, nearly two-thirds of medications containing novel chemical entities have come from NPs or chemically created analogues of NPs [2], highlighting their role in the treatment of cancer and infective diseases but also cardiovascular diseases and even diabetes and multiple sclerosis [3].Some relevant examples include the antidiabetic drugs liraglutide and semaglutide, which result from the optimization of the exendin-4 peptide obtained from Heloderma lizard venom [4]; fingolimod, a derivative of the natural metabolite myriocin isolated from Isaria sinclairii used as a sphingosine-1phosphate (S1P) receptor modulator to treat multiple sclerosis [5,6]; and even, paclitaxel (Taxol) isolated first from the Pacific yew Taxus brevifolia and currently used to treat a high variety of cancers [7,8].These molecules can be used directly in therapy as they are isolated from natural sources or obtained through chemical processes, creating derivatives or even fully synthetic compounds, which use the natural scaffold as a structural model to create more effective analogues [9].
The importance of using natural compounds as medicines is related to their wide range of recognized biological activities and unique structural features, which can be extremely useful to overcome drug-target and protein-protein interaction issues [10].In fact, when compared to traditional synthetic medicines, natural compounds have unique properties, such as higher molecular weights, more sp 3 carbon and oxygen atoms, less nitrogen and halogen atoms, and more H-bond acceptors and donors, among other features [3].Although pharmaceutical companies' efforts to discover new natural products have significantly decreased over recent decades, the values presented by Newman and Crag (2020) demonstrated that the "influence of natural product structures" has not significantly decreased in that time, at least with regard to drug approvals that are based on such structures [2,3,11].
The Euphorbia genus comprises more than 2000 recognized species, being the largest genus of the Euphorbiaceae family and the third largest genus of angiosperm plants.Euphorbia species have a worldwide distribution, exhibiting an extraordinary variety in morphology, from small ephemeral, annual, or perennial herbaceous plants to big shrubs, small trees, lianas, and even cactus-like succulents [12,13].Many Euphorbia species have been historically used to cure digestive and respiratory problems, inflammation, intestinal parasites, and tumors, among other conditions [12].These therapeutic properties are attributable to the presence of different secondary metabolites, namely, polycyclic and macrocyclic diterpenes (lathyranes, jatrophanes, and their rearranged derivatives), among others.Diterpenoids have been the focus of natural-product-based drug development among Euphorbia species due to their broad spectrum of therapeutically relevant bioactivities, including anticancer, multidrug resistance reversal, antiviral, and anti-inflammatory activities [12].For example, an ingenane ester from E. peplus, ingenol 3-angelate (ingenol mebutate, PEP005, Picato ® , LEO Pharma, Ballerup, Denmark), was authorized by the FDA in 2012 and the EMA in 2013 to treat actinic keratoses.However, due to negative side effects, this medication has sadly been discontinued [14].On the other hand, resiniferatoxin, a daphnane orthoester derived from E. resinifera, is a strong capsaicin receptor agonist that is now being tested in a phase III clinical study for the treatment of overactive bladders and chronic pain [12].
To the best of our knowledge, to date, there are no reviews exclusively addressing myrsinane-type diterpenes.Therefore, this comprehensive review will focus on premyrsinane-, cyclomyrsinane-, and myrsinane-type diterpenes, covering the period from 1995 to 2023, with emphasis on their biosynthesis, isolation, structural identification, and biological activities.
The literature search was carried out from January to April 2023 on Web of Science, ScienceDirect, and PubMed, using several combinations of keywords and truncation (e.g., combinations of myrsinane, premyrsinane, and cyclomyrsinane with Euphorbia, Jatropha, and biological activity).The timespan from 1995 to 2023 was considered.Only peer-reviewed research articles or reviews were considered; no restrictions on language or the geographical origin of authors were applied.The literature was individually screened by the authors, applying as exclusion criteria, poor quality, inaccurate data, and articles or reviews that were not considered relevant to the aim of the review.Mendeley Reference Manager Software (version 1. 19.8, 2020) was used to manage the references and eliminate duplicates.

Biosynthetic Considerations
Terpenes, also known as isoprenoids, are, by far, the most diverse group of secondary metabolites, comprising over 80,000 identified natural compounds.They have a wide distri-bution in plants, microorganisms, insects, and marine invertebrates, playing a crucial role in the metabolism and gathering of an important source of bioactive compounds [28,29].The terpenic scaffold results from the assembly of the C5 units of isopentenyl diphosphate (IPP) and its isomer dimethylally pyrophosphate (DMAPP) from two major biosynthetic routes, the mevalonate and the 2-C-methyl-d-erythritol-4-phosphate pathways.The variation in the number of repeats, rearrangements, and cyclization reactions catalyzed by prenyltransferases and terpene synthases gives rise to the chemical and structural diversity.Accordingly, they are classified as hemiterpenes (C 5 ), monoterpenes (C 10 ), diterpenes (C 20 ), triterpenes (C 30 ), and tetraterpenes (C 40 ) based on the number of the five carbon units.
Diterpenes arise from geranylgeranyl diphosphate (GGPP, C 20 ) via electrophilic cyclization reactions mediated by carbocation formation and catalyzed by diterpene cyclases and further Wagner-Meerwein rearrangements, which generate their vast chemical diversity [30][31][32].One of the most important cyclization reactions of GGPP is the formation of copalyl diphosphate (copalyl-PP), which plays a central role in the biosynthesis of polycyclic diterpenes, such as abietanes, pimaranes, kauranes, and atisanes (Figure 1) [32].The second mode of GGPP cyclization leads to macrocyclic structures, namely, the monocyclic cembrane, the bicyclic casbane, and its unsaturated derivative, casbene.Even though the biogenetic routes are poorly understood and many mechanistic details remain uncertain, these diterpenes have been considered the precursors of lathyrane and jatrophane frameworks [23,[32][33][34].These structurally unique polyoxygenated macrocyclic diterpenes and their polycyclic derivatives have a very limited distribution in nature, being restricted to the Euphorbiaceae and Thymelaceae families, which increases their biogenetic and chemotaxonomic significance [12,15,27,35].Over the last two decades, macrocyclic diterpenes and their derivatives have been the subject of academic attention due to their biogenetic relevance, structural complexity, and biological properties [12,15,20,23].

Biosynthetic Considerations
Terpenes, also known as isoprenoids, are, by far, the most diverse group of secondary metabolites, comprising over 80,000 identified natural compounds.They have a wide distribution in plants, microorganisms, insects, and marine invertebrates, playing a crucial role in the metabolism and gathering of an important source of bioactive compounds [28,29].The terpenic scaffold results from the assembly of the C5 units of isopentenyl diphosphate (IPP) and its isomer dimethylally pyrophosphate (DMAPP) from two major biosynthetic routes, the mevalonate and the 2-C-methyl-d-erythritol-4-phosphate pathways.The variation in the number of repeats, rearrangements, and cyclization reactions catalyzed by prenyltransferases and terpene synthases gives rise to the chemical and structural diversity.Accordingly, they are classified as hemiterpenes (C5), monoterpenes (C10), diterpenes (C20), triterpenes (C30), and tetraterpenes (C40) based on the number of the five carbon units.
Diterpenes arise from geranylgeranyl diphosphate (GGPP, C20) via electrophilic cyclization reactions mediated by carbocation formation and catalyzed by diterpene cyclases and further Wagner-Meerwein rearrangements, which generate their vast chemical diversity [30][31][32].One of the most important cyclization reactions of GGPP is the formation of copalyl diphosphate (copalyl-PP), which plays a central role in the biosynthesis of polycyclic diterpenes, such as abietanes, pimaranes, kauranes, and atisanes (Figure 1) [32].The second mode of GGPP cyclization leads to macrocyclic structures, namely, the monocyclic cembrane, the bicyclic casbane, and its unsaturated derivative, casbene.Even though the biogenetic routes are poorly understood and many mechanistic details remain uncertain, these diterpenes have been considered the precursors of lathyrane and jatrophane frameworks [23,[32][33][34].These structurally unique polyoxygenated macrocyclic diterpenes and their polycyclic derivatives have a very limited distribution in nature, being restricted to the Euphorbiaceae and Thymelaceae families, which increases their biogenetic and chemotaxonomic significance [12,15,27,35].Over the last two decades, macrocyclic diterpenes and their derivatives have been the subject of academic attention due to their biogenetic relevance, structural complexity, and biological properties [12,15,20,23].From GGPP to polycyclic and macrocyclic diterpenes-a biosynthetic proposal (adapted from [18]).
Lathyrane diterpenes are characterized by a flexible twenty carbon skeleton, with a 5:11:3 fused ring system derived from the intramolecular cyclization of casbene [31,33].Further intramolecular reactions and rearrangements on the lathyrane framework create several polycyclic derivatives, including the jatropholane-, tigliane-, ingol-, and premyrsinane-type diterpenes (Figure 2).Premyrsinanes, myrsinanes, and cyclomyrsinanes are generally and collectively designated as myrsinane-type diterpenes.Only a few explanations concerning the biosynthesis of this kind of diterpenes have been reported, and the subject is still controversial From GGPP to polycyclic and macrocyclic diterpenes-a biosynthetic proposal (adapted from [18]).
Lathyrane diterpenes are characterized by a flexible twenty carbon skeleton, with a 5:11:3 fused ring system derived from the intramolecular cyclization of casbene [31,33].Further intramolecular reactions and rearrangements on the lathyrane framework create several polycyclic derivatives, including the jatropholane-, tigliane-, ingol-, and premyrsinanetype diterpenes (Figure 2).Premyrsinanes, myrsinanes, and cyclomyrsinanes are generally and collectively designated as myrsinane-type diterpenes.Only a few explanations concerning the biosynthesis of this kind of diterpenes have been reported, and the subject is still controversial [18,[36][37][38].Accordingly, it is suggested that premyrsinanes derive from the cyclization at C-12 and C-6 of lathyranes, giving rise to the 5/7/6/3-fused tetracyclic skeleton.Myrsinane structures derive from the cleavage between C-9 and C-10, forming a 5/7/6-fused tricyclic structure.On the other hand, cyclomyrsinane-type diterpenes result from a C-C bond migration to create the cyclobutane ring characteristic of these compounds.Similar to the lathyranes, myrsinane-type diterpenes also possess a high variety of oxygenated functions (hydroxyl, keto, epoxy) and acyl groups, such as acetyl, propionyl, butanoyl, isobutanoyl, 2-methylbutanoyl, angeloyl, tigloyl, benzoyl, and nicotinoyl.Due to biogenetic reasons, Rings A and B and Rings B and C have a trans configuration, while the cyclopropane ring has a cis configuration with H-9α and H-11α.Structural variants also include different stereochemistry on some chiral centers, the number and position of the double bonds, and the frequent presence of a hemiacetal or a 13/17-epoxy ring.[18,[36][37][38].Accordingly, it is suggested that premyrsinanes derive from the cyclization at C-12 and C-6 of lathyranes, giving rise to the 5/7/6/3-fused tetracyclic skeleton.Myrsinane structures derive from the cleavage between C-9 and C-10, forming a 5/7/6-fused tricyclic structure.On the other hand, cyclomyrsinane-type diterpenes result from a C-C bond migration to create the cyclobutane ring characteristic of these compounds.Similar to the lathyranes, myrsinane-type diterpenes also possess a high variety of oxygenated functions (hydroxyl, keto, epoxy) and acyl groups, such as acetyl, propionyl, butanoyl, isobutanoyl, 2methylbutanoyl, angeloyl, tigloyl, benzoyl, and nicotinoyl.Due to biogenetic reasons, Rings A and B and Rings B and C have a trans configuration, while the cyclopropane ring has a cis configuration with H-9α and H-11α.Structural variants also include different stereochemistry on some chiral centers, the number and position of the double bonds, and the frequent presence of a hemiacetal or a 13/17-epoxy ring.The first myrsinane diterpenes were isolated from E. myrsinitis as polyester mixtures and reported in 1982 by Rentzea et al. [39].In this work, the ester M1 was reduced with LiAlH4, yielding the parent polyalcohol as a mixture of epimers (14β:α, 2:1, Figure 3), for which the name myrsinol was proposed, thus giving the name of the entire series [39].The first myrsinane diterpenes were isolated from E. myrsinitis as polyester mixtures and reported in 1982 by Rentzea et al. [39].In this work, the ester M1 was reduced with LiAlH 4 , yielding the parent polyalcohol as a mixture of epimers (14β:α, 2:1, Figure 3), for which the name myrsinol was proposed, thus giving the name of the entire series [39].[18,[36][37][38].Accordingly, it is suggested that premyrsinanes derive from the cyclization at C-12 and C-6 of lathyranes, giving rise to the 5/7/6/3-fused tetracyclic skeleton.Myrsinane structures derive from the cleavage between C-9 and C-10, forming a 5/7/6-fused tricyclic structure.On the other hand, cyclomyrsinane-type diterpenes result from a C-C bond migration to create the cyclobutane ring characteristic of these compounds.Similar to the lathyranes, myrsinane-type diterpenes also possess a high variety of oxygenated functions (hydroxyl, keto, epoxy) and acyl groups, such as acetyl, propionyl, butanoyl, isobutanoyl, 2methylbutanoyl, angeloyl, tigloyl, benzoyl, and nicotinoyl.Due to biogenetic reasons, Rings A and B and Rings B and C have a trans configuration, while the cyclopropane ring has a cis configuration with H-9α and H-11α.Structural variants also include different stereochemistry on some chiral centers, the number and position of the double bonds, and the frequent presence of a hemiacetal or a 13/17-epoxy ring.The first myrsinane diterpenes were isolated from E. myrsinitis as polyester mixtures and reported in 1982 by Rentzea et al. [39].In this work, the ester M1 was reduced with LiAlH4, yielding the parent polyalcohol as a mixture of epimers (14β:α, 2:1, Figure 3), for which the name myrsinol was proposed, thus giving the name of the entire series [39].From a biogenetic point of view, the authors postulated that 13,17-epoxymyrsinol would be derived from 6,17-epoxy-18-hydroxylathyrol, as depicted in Figure 4 [36].More than ten years later, the first premyrsinane-type diterpenes (154-159) were isolated from E. allepica [40,41], and cyclomyrsinol diterpenes (52,53,208) were isolated from E. prolifera [42] and E. seguieriana [37].Jeske et al. corrected the stereochemistry at C-5 that had been wrongly assigned as H-5α [37,39].Therefore, based on the NOE correlations and the existence of a large J 4,5 coupling constant value (11.5 Hz) that was indicative of the trans orientation of H-4 and H-5, the ester substituent at C-5 was assigned to have an α-orientation [37].
From a biogenetic point of view, the authors postulated that 13,17-epoxymyrsinol would be derived from 6,17-epoxy-18-hydroxylathyrol, as depicted in Figure 4 [36].More than ten years later, the first premyrsinane-type diterpenes (154-159) were isolated from E. allepica [40,41], and cyclomyrsinol diterpenes (52,53,208) were isolated from E. prolifera [42] and E. seguieriana [37].Jeske et al. corrected the stereochemistry at C-5 that had been wrongly assigned as H-5α [37,39].Therefore, based on the NOE correlations and the existence of a large J4,5 coupling constant value (11.5 Hz) that was indicative of the trans orientation of H-4 and H-5, the ester substituent at C-5 was assigned to have an αorientation [37].A different biogenetic pathway was also suggested, taking 5,6-epoxylathyranes as a precursor (Figure 5) [37].In this way, the premyrsinane ring system seems to be derived from the opening of the 5,6-epoxy, followed by the formation of the C-6/C-12 bridge.Further protonation of the C-18 hydroxyl group leads to the dehydration and opening of the cyclopropane ring, creating the myrsinane structure (Figure 5-pathway A).On the other hand, the cyclomyrsinane scaffold was suggested to be formed by the nucleophilic attack of a water molecule on C-10, dehydration of the C-18 hydroxyl group, and C-9/C-18 bond migration, giving rise to the cyclobutane ring (Figure 5-pathway B).Nowadays, the scientific research regarding the biogenetic relationships on lathyrane-and myrsinane-type diterpenes is still very scarce, and only a few studies have been carried out aiming at mimetizing those transformations under laboratory conditions [43][44][45][46].Recently, Wang et al. proposed a chemical conversion method to obtain two new diterpenes with the myrsinane and euphoractane skeletons from a lathyrane diterpene (Euphorbia factor L1), together with an unnatural diterpene with a 5/7/7/4 fused-scaffold A different biogenetic pathway was also suggested, taking 5,6-epoxylathyranes as a precursor (Figure 5) [37].In this way, the premyrsinane ring system seems to be derived from the opening of the 5,6-epoxy, followed by the formation of the C-6/C-12 bridge.Further protonation of the C-18 hydroxyl group leads to the dehydration and opening of the cyclopropane ring, creating the myrsinane structure (Figure 5-pathway A).On the other hand, the cyclomyrsinane scaffold was suggested to be formed by the nucleophilic attack of a water molecule on C-10, dehydration of the C-18 hydroxyl group, and C-9/C-18 bond migration, giving rise to the cyclobutane ring (Figure 5-pathway B).
From a biogenetic point of view, the authors postulated that 13,17-epoxymyrsinol would be derived from 6,17-epoxy-18-hydroxylathyrol, as depicted in Figure 4 [36].More than ten years later, the first premyrsinane-type diterpenes (154-159) were isolated from E. allepica [40,41], and cyclomyrsinol diterpenes (52,53,208) were isolated from E. prolifera [42] and E. seguieriana [37].Jeske et al. corrected the stereochemistry at C-5 that had been wrongly assigned as H-5α [37,39].Therefore, based on the NOE correlations and the existence of a large J4,5 coupling constant value (11.5 Hz) that was indicative of the trans orientation of H-4 and H-5, the ester substituent at C-5 was assigned to have an αorientation [37].A different biogenetic pathway was also suggested, taking 5,6-epoxylathyranes as a precursor (Figure 5) [37].In this way, the premyrsinane ring system seems to be derived from the opening of the 5,6-epoxy, followed by the formation of the C-6/C-12 bridge.Further protonation of the C-18 hydroxyl group leads to the dehydration and opening of the cyclopropane ring, creating the myrsinane structure (Figure 5-pathway A).On the other hand, the cyclomyrsinane scaffold was suggested to be formed by the nucleophilic attack of a water molecule on C-10, dehydration of the C-18 hydroxyl group, and C-9/C-18 bond migration, giving rise to the cyclobutane ring (Figure 5-pathway B).Nowadays, the scientific research regarding the biogenetic relationships on lathyrane-and myrsinane-type diterpenes is still very scarce, and only a few studies have been carried out aiming at mimetizing those transformations under laboratory conditions [43][44][45][46].Recently, Wang et al. proposed a chemical conversion method to obtain two new diterpenes with the myrsinane and euphoractane skeletons from a lathyrane diterpene (Euphorbia factor L1), together with an unnatural diterpene with a 5/7/7/4 fused-scaffold Nowadays, the scientific research regarding the biogenetic relationships on lathyraneand myrsinane-type diterpenes is still very scarce, and only a few studies have been carried out aiming at mimetizing those transformations under laboratory conditions [43][44][45][46].Recently, Wang et al. proposed a chemical conversion method to obtain two new diterpenes with the myrsinane and euphoractane skeletons from a lathyrane diterpene (Euphorbia factor L1), together with an unnatural diterpene with a 5/7/7/4 fused-scaffold [45].Starting from the lathyrane-type compound, the postulated mechanism involved a Lewis acidmediated reaction in which the cyclopropane opening/intramolecular Michael additions are involved to build the various diterpene skeletons, including the myrsinane, as depicted in Figure 6, confirming the biosynthetic connection between these compounds [45].Another chemical transformation process from lathyranes to premyrsinanes was achieved in a study conducted by Xiao et al. (Figure 6a) [46].Two new premyrsinane-type diterpenes (PM1 and PM2, Figure 6b), as diastereomers, were synthesized from the Euphorbia factor L3 under the catalysis of iron, involving intramolecular Michael addition reactions with free radicals [46].[45].Starting from the lathyrane-type compound, the postulated mechanism involved a Lewis acid-mediated reaction in which the cyclopropane opening/intramolecular Michael additions are involved to build the various diterpene skeletons, including the myrsinane, as depicted in Figure 6, confirming the biosynthetic connection between these compounds [45].Another chemical transformation process from lathyranes to premyrsinanes was achieved in a study conducted by Xiao et al. (Figure 6a) [46].Two new premyrsinane-type diterpenes (PM1 and PM2, Figure 6b), as diastereomers, were synthesized from the Euphorbia factor L3 under the catalysis of iron, involving intramolecular Michael addition reactions with free radicals [46].

Isolation and Structural Identification
The majority of myrsinane-type diterpenes have been isolated from Euphorbia species; however, some compounds have also been isolated from Jatropha species, in particular Jatropha curcas [47][48][49].
These compounds are usually obtained from the dried or fresh whole plant, but other specific parts, such as the seeds, roots, and latex, have also been used [50,51].The isolation of diterpene polyesters is challenging as they are frequently present in plants only in trace amounts and as complex mixtures of compounds with the same core scaffold.Therefore, a multistep procedure is always necessary.After grinding, the extraction of the vegetable sample is usually carried out via maceration at room temperature using organic solvents, which are critical to ensure the efficient extraction of the target compounds.Commonly used solvents include methanol, ethanol, acetone, chloroform, petroleum ether, and mixtures of these solvents.Due to the ester nature of the compounds, acidic or basic reagents should not be used to avoid hydrolysis or transesterification reactions.Evaporation of the solvent under vacuum at low temperature (35-45 °C) results in a crude extract that needs to be further fractionated.The next step is generally a liquid-liquid partition process, where n-hexane or petroleum ether are usually used to defat the extract, followed by a partition with ethyl acetate (EtOAc) and water or mixtures with acetonitrile in order to concentrate the diterpenic compounds in the organic phase.Depending on the extraction solvents and the amount of the crude extract, other techniques could also be used, including vacuum liquid chromatography over RP-18 silica gel or poliamide to remove fats, hydrophilic compounds, and chlorophylls [52][53][54][55].The EtOAc or acetonitrile crude fraction previously obtained is further fractionated through a combination of

Isolation and Structural Identification
The majority of myrsinane-type diterpenes have been isolated from Euphorbia species; however, some compounds have also been isolated from Jatropha species, in particular Jatropha curcas [47][48][49].
These compounds are usually obtained from the dried or fresh whole plant, but other specific parts, such as the seeds, roots, and latex, have also been used [50,51].The isolation of diterpene polyesters is challenging as they are frequently present in plants only in trace amounts and as complex mixtures of compounds with the same core scaffold.Therefore, a multistep procedure is always necessary.After grinding, the extraction of the vegetable sample is usually carried out via maceration at room temperature using organic solvents, which are critical to ensure the efficient extraction of the target compounds.Commonly used solvents include methanol, ethanol, acetone, chloroform, petroleum ether, and mixtures of these solvents.Due to the ester nature of the compounds, acidic or basic reagents should not be used to avoid hydrolysis or transesterification reactions.Evaporation of the solvent under vacuum at low temperature (35-45 • C) results in a crude extract that needs to be further fractionated.The next step is generally a liquid-liquid partition process, where n-hexane or petroleum ether are usually used to defat the extract, followed by a partition with ethyl acetate (EtOAc) and water or mixtures with acetonitrile in order to concentrate the diterpenic compounds in the organic phase.Depending on the extraction solvents and the amount of the crude extract, other techniques could also be used, including vacuum liquid chromatography over RP-18 silica gel or poliamide to remove fats, hydrophilic compounds, and chlorophylls [52][53][54][55].The EtOAc or acetonitrile crude fraction previously obtained is further fractionated through a combination of different chromatographic techniques, with column chromatography over silica-gel being the first to be carried out.Normally, this first column is eluted with mixtures of n-hexane-EtOAc or n-hexane-CH 2 Cl 2 of increasing polarities.NMR or even LC-MS/MS analysis has been frequently used to identify the fractions rich in diterpenes, aimed at conducting a directed and less time-consuming isolation [50,56,57].The chromatographic fractions are monitored using thin layer chromatography (TLC) and associated based on their similar profile.Not all diterpenes exhibit UV absorption at 254 nm, and there is no specific visualization reagent for their identification.Therefore, the spots must be identified by spraying with suitable visualization reagents, such as mixtures of H 2 SO 4 /acetic acid/H 2 O or H 2 SO 4 /H 2 O (1:1), followed by heating at 105 • C until the development of a black or dark brown color.Further fractionations can be achieved using normal silica gel and other different adsorbents, including reversed-phase silica gel and Sephadex LH-20 gel.In addition, vacuum liquid chromatography (VLC) and centrifugal planar chromatography (CPC) have also been used.Preparative high-performance chromatography, supercritical fluid chromatography (SFC), recrystallization, and preparative thin-layer chromatography are also employed to obtain pure compounds [50,56,57].
A combination of extensive spectroscopic techniques including 1D ( 1 H-and 13 C-NMR and DEPT) and 2D nuclear magnetic resonance ( 1 H-1 H-COSY, HSQC, HMBC, and NOESY), mass spectrometry (MS), and infrared (IR) spectroscopy has to be employed for the structural elucidation and identification of the isolated compounds.
For practical reasons, in this review, it would not be possible to present and discuss the NMR data of all the structural variations of myrsinane-type diterpenes isolated to date.Notwithstanding, the 1 H-and 13 C-NMR spectroscopic data of some representative premyrsinane, myrsinane, and cyclomyrsinane diterpenes, and the most important features are summarized and discussed below.Myrsinane-type diterpenes rarely occur as free alcohols but rather in the esterified form.
The 1 H-NMR spectra of premyrsinane diterpenes generally exhibit signals attributed to four methyls (one secondary and three tertiary), four diastereotopic methylene groups, including one oxygenated at C-17, and three oxymethyne protons (H-3, H5, and H-7) (e.g., Compound 25, Figure 7).Importantly, the presence of a gem-dimethyl-substituted cyclopropane ring, characteristic of these compounds but also of lathyrane diterpenes, is indicated by a pair of high-field methine signals at δ H 0.72 (dd, H-11) and δ H 0.82 (m, H-9), associated with the unusual up-field chemical shift of the quaternary carbon C-10 at δ C 17.8.In addition to the acyl groups present in polyester diterpenes, the 13 C spectra show twenty carbon resonances discriminated by the DEPT experiment as four methyl groups, three methylenes (one oxygenated at δ C 69.9), nine methynes (three oxygenated at δ C 81.5-65.8),and four quaternary carbons (two oxygenated at δ C 86.6 and 90.2) [58].
different chromatographic techniques, with column chromatography over silica-gel being the first to be carried out.Normally, this first column is eluted with mixtures of n-hexane-EtOAc or n-hexane-CH2Cl2 of increasing polarities.NMR or even LC-MS/MS analysis has been frequently used to identify the fractions rich in diterpenes, aimed at conducting a directed and less time-consuming isolation [50,56,57].The chromatographic fractions are monitored using thin layer chromatography (TLC) and associated based on their similar profile.Not all diterpenes exhibit UV absorption at 254 nm, and there is no specific visualization reagent for their identification.Therefore, the spots must be identified by spraying with suitable visualization reagents, such as mixtures of H2SO4/acetic acid/H2O or H2SO4/H2O (1:1), followed by heating at 105 °C until the development of a black or dark brown color.Further fractionations can be achieved using normal silica gel and other different adsorbents, including reversed-phase silica gel and Sephadex LH-20 gel.In addition, vacuum liquid chromatography (VLC) and centrifugal planar chromatography (CPC) have also been used.Preparative high-performance chromatography, supercritical fluid chromatography (SFC), recrystallization, and preparative thin-layer chromatography are also employed to obtain pure compounds [50,56,57].
A combination of extensive spectroscopic techniques including 1D ( 1 H-and 13 C-NMR and DEPT) and 2D nuclear magnetic resonance ( 1 H-1 H-COSY, HSQC, HMBC, and NOESY), mass spectrometry (MS), and infrared (IR) spectroscopy has to be employed for the structural elucidation and identification of the isolated compounds.
For practical reasons, in this review, it would not be possible to present and discuss the NMR data of all the structural variations of myrsinane-type diterpenes isolated to date.Notwithstanding, the 1 H-and 13 C-NMR spectroscopic data of some representative premyrsinane, myrsinane, and cyclomyrsinane diterpenes , and the most important features are summarized and discussed below.Myrsinane-type diterpenes rarely occur as free alcohols but rather in the esterified form.
The 1 H-NMR spectra of premyrsinane diterpenes generally exhibit signals attributed to four methyls (one secondary and three tertiary), four diastereotopic methylene groups, including one oxygenated at C-17, and three oxymethyne protons (H-3, H5, and H-7) (e.g., Compound 25, Figure 7).Importantly, the presence of a gem-dimethyl-substituted cyclopropane ring, characteristic of these compounds but also of lathyrane diterpenes, is indicated by a pair of high-field methine signals at δH 0.72 (dd, H-11) and δH 0.82 (m, H-9), associated with the unusual up-field chemical shift of the quaternary carbon C-10 at δC 17.8.In addition to the acyl groups present in polyester diterpenes, the 13 C spectra show twenty carbon resonances discriminated by the DEPT experiment as four methyl groups, three methylenes (one oxygenated at δC 69.9), nine methynes (three oxygenated at δC 81.5-65.8),and four quaternary carbons (two oxygenated at δC 86.6 and 90.2) [58].The NMR data of cyclomyrsinane diterpenes are very similar to premyrsinanes (Figures 7 and 8).When comparing Compounds 25 and 8 [51,58], the most remarkable differences in the 1 H-NMR spectra are the downfield shift of the H-9 and H-10 methine signals (δH The NMR data of cyclomyrsinane diterpenes are very similar to premyrsinanes (Figures 7 and 8).When comparing Compounds 25 and 8 [51,58], the most remarkable differences in the 1 H-NMR spectra are the downfield shift of the H-9 and H-10 methine signals (δ H 2.41 and 2.75) and the absence of one tertiary methyl signal (C-19) that is replaced by an additional diastereotopic methylene signal corresponding to H-19 in the cyclobutane ring.These data are corroborated by the 13 C-NMR data, where the absence of the quaternary carbon at δ C 17.8 and the presence of an additional methylene carbon (δ C ~35.0) are very suggestive of a different D-ring on the molecule (a cyclobutane ring instead of a cyclopropane).In addition, the 13 C-NMR data of Compound 8 (Figure 8) point to a carbonyl signal at δ C 204.4 that, together with the downfield shift of C-6 (δ C 62.6), indicate the presence of a ketone group at C-7 [51].
These data are corroborated by the 13 C-NMR data, where the absence of the quaternary carbon at δC 17.8 and the presence of an additional methylene carbon (δC ~ 35.0) are very suggestive of a different D-ring on the molecule (a cyclobutane ring instead of a cyclopropane).In addition, the 13 C-NMR data of Compound 8 (Figure 8) point to a carbonyl signal at δC 204.4 that, together with the downfield shift of C-6 (δC 62.6), indicate the presence of a ketone group at C-7 [51].By comparing the NMR data of premyrsinane and myrsinane diterpenes, it is evident that, except for the rings C and D, the 1 H and 13 C chemical shifts are almost identical (Figures 7  and 9).Therefore, the most significant differences are, as expected, the absence of the cyclopropane signals and the additional existence of several NMR signals that are indicative of the myrsinane scaffold.In this way, the presence of the olefinic signals at δH 5.89 (δC 133.5) and δH 6.29 (δC 123.6) confirms the existence of the vic-disubstituted double bond (Δ 8,9 ).The double bond Δ 10,18 is deduced from the presence of two broad singlets assigned to the exocyclic methylene protons at δH 4.64 and δH 4.71 and corroborated by the vinylic methyl signal at δH 1.85, characteristic of the isopropenyl group (Compound 205, Figure 9).The 13 C NMR data support the presence of the two double bonds, revealing the additional resonances of the olefinic carbons (δC ~ 123.6, 133.5, 146.9, and 112.3).In some myrsinane diterpenes, the existence of a keto group at C-14 is common (Compound 176, Figure 9) and deduced in the 13 C NMR by the presence of the signal at δC 202.9 and the absence of one oxygenated methyne carbon.The location of the ketone at C-14 can be further supported by the down-field shift of H-1α (δH 3.52) and of the neighboring CH3-20 methyl group that appeared at δH 1.58 due to the anisotropic effect of the carbonyl group at C-14 when compared to the 14-acyl diterpene NMR data (Compound 205, Figure 9) [37,59].By comparing the NMR data of premyrsinane and myrsinane diterpenes, it is evident that, except for the rings C and D, the 1 H and 13 C chemical shifts are almost identical (Figures 7 and 9).Therefore, the most significant differences are, as expected, the absence of the cyclopropane signals and the additional existence of several NMR signals that are indicative of the myrsinane scaffold.In this way, the presence of the olefinic signals at δ H 5.89 (δ C 133.5) and δ H 6.29 (δ C 123.6) confirms the existence of the vic-disubstituted double bond (∆ 8,9 ).The double bond ∆ 10,18 is deduced from the presence of two broad singlets assigned to the exocyclic methylene protons at δ H 4.64 and δ H 4.71 and corroborated by the vinylic methyl signal at δ H 1.85, characteristic of the isopropenyl group (Compound 205, Figure 9).The 13 C NMR data support the presence of the two double bonds, revealing the additional resonances of the olefinic carbons (δ C ~123.6, 133.5, 146.9, and 112.3).In some myrsinane diterpenes, the existence of a keto group at C-14 is common (Compound 176, Figure 9) and deduced in the 13 C NMR by the presence of the signal at δ C 202.9 and the absence of one oxygenated methyne carbon.The location of the ketone at C-14 can be further supported by the down-field shift of H-1α (δ H 3.52) and of the neighboring CH 3 -20 methyl group that appeared at δ H 1.58 due to the anisotropic effect of the carbonyl group at C-14 when compared to the 14-acyl diterpene NMR data (Compound 205, Figure 9) [37,59].  1C-NMR spectroscopic data of myrsinane diterpenes 205 [37] and 176 [59].
Some rearranged myrsinane derivatives have also been isolated, possessing a tetrahydrofuran moiety between C-10 and C-13 (Figure 10).These compounds have a close resemblance to myrsinane diterpenes in most of their NMR features.Nevertheless, some differences are evident, namely, the replacement of the olefinic protons at C-18 by   13 C-NMR spectroscopic data of myrsinane diterpenes 205 [37] and 176 [59].
Some rearranged myrsinane derivatives have also been isolated, possessing a tetrahydrofuran moiety between C-10 and C-13 (Figure 10).These compounds have a close resemblance to myrsinane diterpenes in most of their NMR features.Nevertheless, some differences are evident, namely, the replacement of the olefinic protons at C-18 by one tertiary methyl signal at δ 1.04 (s, H-18), the absence of the olefinic carbon signals at   13 C-NMR spectroscopic data of myrsinane diterpenes 205 [37] and 176 [59].
Some rearranged myrsinane derivatives have also been isolated, possessin tetrahydrofuran moiety between C-10 and C-13 (Figure 10).These compounds ha close resemblance to myrsinane diterpenes in most of their NMR features.Neverth some differences are evident, namely, the replacement of the olefinic protons at C-1 one tertiary methyl signal at δ 1.04 (s, H-18), the absence of the olefinic carbon sign δC 146.3 (C-10) and δC 112.3 (C-18), and the appearance of a signal at δC 79.3, correspon to the resonance of C-10 (Compound 4, Figure 10) [51].The analysis of HMQC/HSQC and 1 H-1 H-COSY spectra allows the assignment of a protons and carbon resonances and reveals the existence of three sequences of corre protons, as depicted in Figure 11.The connectivities of these fragments are assigne the heteronuclear 2 JC-H and 3 JC-H couplings displayed in the HMBC spectra betwee quaternary carbons and the protons of the three spin systems, allowing the linkage o referred fragments, the confirmation of the myrsinane-type scaffolds, and the locati the acyl moieties (Figure 11).Importantly, the HMBC correlations between the quater carbon C-13 and the protons H-17 and H-12 and between C-5 and H-12 and H-17 a the assignment of the C-13/C-17 saturated furan ring, a very common featu premyrsinane, myrsinane, and cyclomyrsinane diterpenes.The analysis of HMQC/HSQC and 1 H-1 H-COSY spectra allows the assignment of all the protons and carbon resonances and reveals the existence of three sequences of correlated protons, as depicted in Figure 11.The connectivities of these fragments are assigned by the heteronuclear 2 J C-H and 3 J C-H couplings displayed in the HMBC spectra between the quaternary carbons and the protons of the three spin systems, allowing the linkage of the referred fragments, the confirmation of the myrsinane-type scaffolds, and the location of the acyl moieties (Figure 11).Importantly, the HMBC correlations between the quaternary carbon C-13 and the protons H-17 and H-12 and between C-5 and H-12 and H-17 allow the assignment of the C-13/C-17 saturated furan ring, a very common feature in premyrsinane, myrsinane, and cyclomyrsinane diterpenes.The relative configuration of the compounds is deduced from coupling constants analyses together with NOESY experiments, which establish the connectivities of the correlated protons through space.Based on biosynthetic reasons, the trans A-B ring fusion (Figure 2) and the α-oriented H-4, characteristic of macrocyclic diterpenes, are always taken as a reference point.In addition, for all the reported myrsinol-type diterpenes, Rings B and C (as well as Rings C and D in premyrsinanes and cyclomyrsinanes) are also trans- The relative configuration of the compounds is deduced from coupling constants analyses together with NOESY experiments, which establish the connectivities of the correlated protons through space.Based on biosynthetic reasons, the trans A-B ring fusion (Figure 2) and the α-oriented H-4, characteristic of macrocyclic diterpenes, are always taken as a reference point.In addition, for all the reported myrsinol-type diterpenes, Rings B and C (as well as Rings C and D in premyrsinanes and cyclomyrsinanes) are also trans-fused, and the diastereotopic methylene protons H-17 are α-oriented.In this way, the existence or absence of NOESY cross peaks between these key protons and the remaining protons or acyl groups allows the establishment of the stereochemistry of all the tetrahedral stereocenters of the molecule.

Distribution, Diversity, and Biological Activities of Myrsinane-Type Diterpenes from Euphorbia Species
Over recent decades, approximately 225 diterpenes have been isolated from several Euphorbia species.Herein, the distribution and the broad structural diversity of these diterpenes are summarized, also focusing on the reported biological activities.

E. falcata
Several new myrsinane-(1-6), cyclomyrsinane-(7-15), and premyrsinane-type diterpenes (16-19) (Figure 12), named falcatins A-S, and a known cyclomyrsinane (51), named euphorprolitherin [60], were isolated from E. falcata methanolic extract [51,60].These compounds, together with the known premyrsinane 20 and the cyclomyrsinanes 21-23 previously isolated from E. prolifera and E. falcata (Figure 12) [42,58,61], were studied for their GIRK and hERG channel-inhibitory activities, using an automated patch-clamp method [51].The GIRK channels (G protein-activated inwardly rectifying potassium ion channels) are targets for the treatment of arrhythmias, as it was found that the selective inhibition of these channels reduces the number and the duration of atrial fibrillation episodes.On the other hand, hERG channels, also known as Kv11.1, are K + -selective voltage-gated ion channels, which mediate the rapid delayed rectifier K + current (IKr) in ventricular myocytes.The hERG channels can be inhibited by different compounds, modifying the action potential of the heart muscle, increasing the risk of ventricular fibrillation and sudden cardiac death [51].The possible potassium channel-blocking ability of Compounds 1-19, 20, and 21-23 has been evaluated.The GIRK channel inhibitory assay was performed on HEK-293 (human embryonic kidney) at two concentrations (1 and 10 µM).Twelve compounds (1-3, 8, 9, 12, 14-15, and 20-23) were able to block the GIRK channel activity, with values ranging from 61 to 83% at 10 µM.In order to evaluate the selectivity of their GIRK blocking effect, further studies were performed on the HEK-hERG (human embryonic kidney cells) cell line at three concentrations (3, 10, and 30 µM).Among the tested compounds, falcatins A-C (1-3), H (8), and I (9) showed low inhibitory effects on the hERG channel and were, therefore, considered selective inhibitors of GIRK channels and potential lead compounds for the treatment of atrial fibrillation.Even though a detailed structure-activity relationship could not be established, the most promising compounds 1-3 have a myrsinane scaffold, with a carbonyl function at C-7, an ether bridge between C-17 and C-13, and no epoxy functionality between C-10 and C-13 [51].
Compounds 21-23, together with premyrsinanes 20 and 24-26 previously isolated from this plant (Figure 12) [58], were evaluated for their antiproliferative activity against cervix adenocarcinoma (HeLa), endometrial adenocarcinoma (Ishikawa), and breast epithelial adenocarcinoma (MCF7) cell lines, using cisplatin as a positive control [61].The tested diterpenes exhibited weak-to-moderate antiproliferative activity, with 25 being the most active, exhibiting a significant activity in all three cell lines (83.9% (HeLa), 93.6% (A431), and 59.2% (MCF7)), when tested at 30 µg/mL.The compounds were also evaluated for their ability to inhibit rhodamine 123 efflux in L5178 mouse lymphoma cells and the corresponding MDR sublines overexpressing MDR1 efflux pumps.On these sublines, where MDR1 is highly expressed, compounds with fluorescence activity ratio (FAR) values higher than 10 are regarded as strong modulators.Diterpenes 21, 22, and 24-26 were the most active, showing FAR values ranging from 52.6 to 74.5, when tested at 20 µM.Moreover, when tested at 2 µM, the compounds were also very active, exhibiting FAR values between 12.6 (26) and 46.1 (21) when compared with the positive control verapamil (FAR 8.7 at 22 µM).The type of in vitro interactions between the diterpenes and doxorubicin was also studied through combination assays on MDR mouse T-lymphoma cells.All compounds showed a synergistic effect with the anticancer drug.Compound 21 was considered of special interest for further studies since it was a strong modulator of the MDR pump and showed a strong synergism when tested in combination with doxorubicin [61].
Int. J. Mol.Sci.2024, 25, x FOR PEER REVIEW 11 of 33 able to block the GIRK channel activity, with values ranging from 61 to 83% at 10 µM.In order to evaluate the selectivity of their GIRK blocking effect, further studies were performed on the HEK-hERG (human embryonic kidney cells) cell line at three concentrations (3, 10, and 30 µM).Among the tested compounds, falcatins A-C (1-3), H (8), and I ( 9) showed low inhibitory effects on the hERG channel and were, therefore, considered selective inhibitors of GIRK channels and potential lead compounds for the treatment of atrial fibrillation.Even though a detailed structure-activity relationship could not be established, the most promising compounds 1-3 have a myrsinane scaffold, with a carbonyl function at C-7, an ether bridge between C-17 and C-13, and no epoxy functionality between C-10 and C-13 [51].Compounds 21-23, together with premyrsinanes 20 and 24-26 previously isolated from this plant (Figure 12) [58], were evaluated for their antiproliferative activity against cervix adenocarcinoma (HeLa), endometrial adenocarcinoma (Ishikawa), and breast epithelial adenocarcinoma (MCF7) cell lines, using cisplatin as a positive control [61].The tested diterpenes exhibited weak-to-moderate antiproliferative activity, with 25 being the most active, exhibiting a significant activity in all three cell lines (83.9% (HeLa), 93.6% (A431), and 59.2% (MCF7)), when tested at 30 µg/mL.The compounds were also evaluated for their ability to inhibit rhodamine 123 efflux in L5178 mouse lymphoma cells and the  27) and J196-9-4 (28) (Figure 13) were isolated from the methanol extract and studied as possible modulators of Pgp in the human breast adenocarcinoma (MCF-7) cell line and its multidrug resistant subline (MCF-7/Adr) [62,63].The structure of the compounds was very similar, only differing in the type of substituent at C-5 and C-14.It was found that both compounds were noncytotoxic to the tested cells at concentrations below 50 µM.When tested on the MCF-7/Adr cell line with daunorubicin, vincristine, and topotecan, the IC 50 values of MCF-7/Adr to the anticancer drugs declined significantly.The best results were obtained for Compound 27 in combination with vincristine (IC 50 = 0.063 ± 0.017 µM, reversal ratio value of 219.6, when coapplied with 10 µM of 27).In the same experimental conditions, Compound 28 exhibited an IC 50 value of 1.41 ± 0.054 µM.Further assays showed that both diterpenes inhibited the efflux of rhodamine-123 mediated by P-gp without changing the transcription level of ABCB1 gene, which suggested a direct inhibition of the drug efflux.Moreover, they were also able to stimulate ATPase activity at a low concentration, and it was suggested that they act as a competitive inhibitor of the enzyme.In this way, they might compete with cytotoxic drugs for Pgp binding sites, preventing the drug efflux [62,63].

E. kopetdaghi (Prokh.) Prokh
Riahi et al. reported two undescribed cyclomyrsinol diterpenes, 68 and 69, named kopetdaghinane A and B (Figure 14), with an unusual 13/17 hemiacetal group in the tetrahydrofuran ring, isolated from the dichlorometane/acetone (2:1) extract of E kopetdaghi (Prokh.)Prokh.aerial parts [70].The cytotoxicity of 68 against MCF-7 and OVCAR-3 cancer cells was evaluated, and the compound showed dose-dependent activity, with IC50 values of 38.10 ± 2.05 µM and 51.23 ± 2.67 µM against MCF-7 and OCVAR-3 cancer cells, respectively.Moreover, this compound presents selectivity indexes against both cell lines of 18.36 ± 0.39 and 13.65 ± 0.29 against MCF-7 and OVCAR-3 cancer cells.Kopetdaghinane A (68) inhibits the growth of MCF-7 breast cancer cells through the activation of the mitochondrial apoptotic pathway.The results of Western blot analysis showed that the expression of Bcl-2 (an antiapoptotic protein) was remarkably decreased in response to treatment with 68, whereas the expression of Bax protein (a proapoptotic protein) was increased.Regarding caspase-6 activity, the treatment of MCF-7 cells with an increasing concentration of 68 (1 to 100 µM) induced a marked increase in the activity of caspase-6 in a concentration-and time-dependent manner, with a depletion in mitochondria membrane potential (ΔΨm) [70].Several diterpenes were also isolated from the roots of E. prolifera (29-35) (Figure 13) [64,65].Compounds 29 and 30 were tested for their neuroprotective activity against MPP + -induced neuronal cell death in human dopaminergic neuroblastoma cells, using bakkenolide H as a positive control.Both compounds showed neuroprotective effects without exhibiting significant cytotoxicity [64].

E. kopetdaghi (Prokh.) Prokh
Riahi et al. reported two undescribed cyclomyrsinol diterpenes, 68 and 69, named kopetdaghinane A and B (Figure 14), with an unusual 13/17 hemiacetal group in the tetrahydrofuran ring, isolated from the dichlorometane/acetone (2:1) extract of E. kopetdaghi (Prokh.)Prokh.aerial parts [70].The cytotoxicity of 68 against MCF-7 and OVCAR-3 cancer cells was evaluated, and the compound showed dose-dependent activity, with IC 50 values of 38.10 ± 2.05 µM and 51.23 ± 2.67 µM against MCF-7 and OCVAR-3 cancer cells, respectively.Moreover, this compound presents selectivity indexes against both cell lines of 18.36 ± 0.39 and 13.65 ± 0.29 against MCF-7 and OVCAR-3 cancer cells.Kopetdaghinane A (68) inhibits the growth of MCF-7 breast cancer cells through the activation of the mitochondrial apoptotic pathway.The results of Western blot analysis showed that the expression of Bcl-2 (an antiapoptotic protein) was remarkably decreased in response to treatment with 68, whereas the expression of Bax protein (a proapoptotic protein) was increased.Regarding caspase-6 activity, the treatment of MCF-7 cells with an increasing concentration of 68 (1 to 100 µM) induced a marked increase in the activity of caspase-6 in a concentration-and time-dependent manner, with a depletion in mitochondria membrane potential (∆Ψm) [70].From the acetone/chloroform (1:2) extract of the aerial parts of this species, three new cyclomyrsinol diterpenes were isolated [71].Compound 70 (Figure 14) was noncytotoxic against the mouse embryo fibroblast cell line (3T3-L1) and rat Wistar hepatocyte cell lines (CC-1).Several assays were also carried out to study the immunomodulating activity of 70, including a lymphocyte proliferation assay, the effect on interleukin-2 (IL-2) From the acetone/chloroform (1:2) extract of the aerial parts of this species, three new cyclomyrsinol diterpenes were isolated [71].Compound 70 (Figure 14) was noncytotoxic against the mouse embryo fibroblast cell line (3T3-L1) and rat Wistar hepatocyte cell lines (CC-1).Several assays were also carried out to study the immunomodulating activity of 70, including a lymphocyte proliferation assay, the effect on interleukin-2 (IL-2) production, a phagocyte oxidative burst, and ROS production effects.It was found that 70 potently suppresses phytohemagglutinin-activated T-cell proliferation in a dose-dependent manner, with an IC 50 value of 1.83 ± 0.15 µg/mL (Prednisolone was used as positive control, with an IC 50 1.45 ± 0.2 µg/mL).It also suppressed the IL-2 production, with an IC 50 of 19.0 ± 0.7 µg/mL.The authors postulated that the simultaneous inhibition of T-cell proliferation and suppression of IL-2 production could suggest the possibility of interfering not only by downregulating IL-2 production but also directly with IL-2 function or even by the IL-2 deprivation-mediated apoptosis in vitro [71].Compound 70 was also able to inhibit the production of reactive oxygen species (IC 50 1.54 ± 0.1 µg/mL), an effect that was suggested to be possible through ROS scavenging or by the inhibition of the enzymes (NADPH oxidase, catalase, and myeloperoxidase) involved in the signal transduction pathway of ROS generation process.The bioactivity of Compounds 71 and 72 (Figure 14) was not evaluated.
In a recent study, Rabbani et al. tested the cytotoxicity of six diterpenes, 72-74, 76, 78, and 151, previously isolated from E. sodgiana, E. kopetdaghi, and E. aellenii [52,71,72] on two breast cancer cells (4T1 and MCF-7) [73].The results showed that 151 has the most cytotoxic effects against both cells, with IC 50 values of 8 and 12 µg/mL for the MCF 7 and 4T1 cell lines, respectively.Furthermore, the cells treated with 5 and 10 µg/mL of Compound 151 for 24 h showed 37 and 55% of apoptotic cells.However, these cytotoxicity assays raise some doubts as a positive control was not used in this research, and, in addition, the results in µg/mL make it difficult to compare with data from other studies regarding cytotoxicity tests as normally these are given in µM.
A cyclomyrsinol named as TAMEC (82, Figure 14) [74] was evaluated on anxiety and depression-like behaviors as there is a significant prevalence of these disorders in people with multiple sclerosis (MS) [74].The effects of TAMEC treatment on the progression of these clinical symptoms were studied in mice with experimental autoimmune encephalomyelitis (EAE) because it is the most widely used animal model to study multiple sclerosis (MS) at the research bench.This compound reduced anxiety and depression and reduced proinflammatory cytokines in the hippocampus of EAE-induced mice.More studies should be conducted to determine the involved histopathology and molecular mechanisms of TAMEC in modulating behavior in EAE-induced mice.

E. gedrosiaca Rech.f., Aellen & Esfand
In a study on the composition of E. gedrosiaca Rech.f., Aellen & Esfand., Yazdiniapour et al. isolated and identified from a dichloromethane/acetone extract of the whole plant two new myrsinanes, 83 and 84 [54] (Figure 15), and two known cyclomyrsinanes, 53 and 85 (Figures 13 and 15, respectively), previously reported from E. prolifera and E. aellenii [42,75].The evaluation of their cytotoxicity against B16F10 and A375 melanoma cells indicated that, on both cell lines, these compounds showed cytotoxicity effects.According to the results, IC 50 values for the treatment of melanoma cells by the new myrsinanes 83 and 84 were 58.45 [54].
The evaluation of their cytotoxicity against B16F10 and A375 melanoma cells indic on both cell lines, these compounds showed cytotoxicity effects.According to th IC50 values for the treatment of melanoma cells by the new myrsinanes 83 and 84 w and 55.43 µM on B16F10 and 20.66 and 21.88 µM on A375 cells, respectiv cyclomyrsinanes 53 and 85 showed IC50 values of 86.52 and 82.27 µM on B16F10 a and 39.87 µM on A375 cells, respectively.These findings demonstrated that Myrs and 84 clearly induce more cell death than Cyclomyrsinanes 53 and 85 [54].A very recent study led to the isolation of four premyrsinane diterpenes myrsinane diterpene [76].Premyrsinanes 120, 131, 132, and 136 had previou isolated from E. sanctae-catharinae [77] and E. pithyusa [69].Myrsinane 49 has a isolated from E. prolifera [60].MDA-MB-231 and MCF-7, two cell lines associa breast cancer, were used to assess the cytotoxic activity of these compounds, u MTT viability assay.Compound 120, with an IC50 value of 10.8 µM, was the most against both cell lines, particularly the MDA-MB-231 cell line.Premyrsinanes and 136 presented IC50 values of 24.5, 27.3, and 22.2 µM, respectively, against th MB-231 cell line.When tested for cytotoxicity against these two cell lines, Comp showed less potency than the other four diterpenes.However, the IC50 value of can be considered modest on the MDA-MB-231 cell line [76].A very recent study led to the isolation of four premyrsinane diterpenes and one myrsinane diterpene [76].Premyrsinanes 120, 131, 132, and 136 had previously been isolated from E. sanctae-catharinae [77] and E. pithyusa [69].Myrsinane 49 has also been isolated from E. prolifera [60].MDA-MB-231 and MCF-7, two cell lines associated with breast cancer, were used to assess the cytotoxic activity of these compounds, using the MTT viability assay.Compound 120, with an IC 50 value of 10.8 µM, was the most effective against both cell lines, particularly the MDA-MB-231 cell line.Premyrsinanes 131, 132, and 136 presented IC 50 values of 24.5, 27.3, and 22.2 µM, respectively, against the MDA-MB-231 cell line.When tested for cytotoxicity against these two cell lines, Compound 49 showed less potency than the other four diterpenes.However, the IC 50 value of 33.7 µM can be considered modest on the MDA-MB-231 cell line [76].
A recent study [89] aimed to explore the inhibitory effects of Compound 112 (named TPEM) on the growth of two human ovarian cancer cell lines, OVCAR-3 and Caov-4.The results obtained demonstrated that TPEM exerted inhibitory effects on these cells, dependent on the dose.The IC 50 values found against OVCAR-3 and Caov-4 cells were 41.27 ± 1.52 and 36.44 ± 2.41 µM, respectively.In order to identify the molecular mechanism responsible for the observed cytotoxicity, the activity of caspase-3 was investigated, as this enzyme plays an essential role in the apoptotic signaling pathway.The results indicated that caspase-3 activity was notably increased by TPEM compared to the control group.In addition, 112 also exerts its cytotoxic activity by raising the level of ROS in cells [89].
TPEM) on the growth of two human ovarian cancer cell lines, OVCAR-3 and Caov-4.The results obtained demonstrated that TPEM exerted inhibitory effects on these cells, dependent on the dose.The IC50 values found against OVCAR-3 and Caov-4 cells were 41.27 ± 1.52 and 36.44 ± 2.41 µM, respectively.In order to identify the molecular mechanism responsible for the observed cytotoxicity, the activity of caspase-3 was investigated, as this enzyme plays an essential role in the apoptotic signaling pathway.The results indicated that caspase-3 activity was notably increased by TPEM compared to the control group.In addition, 112 also exerts its cytotoxic activity by raising the level of ROS in cells [89].

E. sanctae-catharinae Fayed
From the aerial parts of Euphorbia sanctae-catharinae Fayed, an endemic species in Egypt, three new premyrsinane diterpenoids, namely, euphosantianane E-G (114-116), (Figure 17) were isolated [90].Elshamy and collaborators performed an interesting correlation with the chemical composition of this endemic species of Egypt with other Euphorbia species through an agglomerative hierarchical clustering (AHC) analysis.E. sanctae-catharinae was grouped with E. bupleuroides, E. fidjiana, E. fischeriana, E. pithyusa subsp.cupanii, E. prolifera, and E. seguieriana.However, the Pearson correlation coefficient analysis revealed that E. sanctaecatharinae showed a close correlation to E. bupleuroides (0.888), followed by E. prolifera (0.880), and then E. pithyusa subsp.cupanii (0.870) based on the composition of the terpenoid composition.Myrsinol diterpenoids were the main constituents of these Euphorbia species, while other diterpenoid compounds such as abietane, lathyrane types, and others, as well as cycloartane triterpene, were also identified in these plants.In previous studies, these authors had already isolated from Euphorbia sanctae-catharinae nine premyrsinanes, (117-123) (Figure 17) four of which (117-120) were isolated for the first time, as well as previously reported metabolites that included three flavonoids [77].Compounds 117-120 exhibited moderate antiproliferative activity against human cancer cell lines of colon (Caco-2) and lung (A549).Compounds 119 and 120 exhibited an IC 50 value of 31.0 µM and 33.2 µM against Caco-2 cells and an IC 50 value of 21.5 µM and 32.8 µM against A549 cells, respectively [90].

E. pithyusa L.
In a previous study, nearly all EtOAc and MeOH extracts of eleven Euphorbiaceae species showed significant anti-chikungunya virus (CHIKV) activity, including E. pithyusa L. extracts [91].Encouraged by these results, Esposito et al. isolated six new premyrsinanes (124-129) and one new myrsinane (130), together with a known compound (136) (Figure 18) and two known dideoxyphorbol esters from the aerial parts of E. pithyusa [92].These compounds were evaluated against CHIKV replication, and from the tested compounds, the one that stands out in terms of anti CHIKV activity is the diterpene 129, with an EC 50 value of 11 ± 1.4 µM and a selectivity index of 5.8.The other premyrsinol esters (124-128 and 236) and the myrsinol ester 130 were not active (EC 50 ≥ 50 µM and SI < 5).Interestingly, in the premyrsinol series, all compounds except Compound 130 have an ester group at C-7, suggesting that the acetate group at this location may be detrimental to antiviral activity [92].Previously, Appendino et al. had already isolated seven new premyrsinane diterpenoids (131-137) (Figure 18) from the whole plant acetone extract of E. pithyusa subsp.Cupanii [69].Among them, 136 was also isolated and identified by Xu et

E. cupanii
The very close taxonomic relationship between E. cupanii and E. pithyusa led Esposito and collaborators to investigate the diterpene ester content of E. cupanii using LC-MS/MS [57].Molecular networking coupled with unsupervised substructure annotation (MS2LDA) indicated the presence of new premyrsinane/myrsinane diterpene esters in E. cupanii extract fractions, which was confirmed by the isolation of six new myrsinanes (138-143) and six new premyrsinanes (144-149) (Figure 18), along with other known diterpenes, namely, phorbol esters.In conclusion, the profile of E. cupanii is marked by myrsinol and 13,17-oxy-premyrsinol esters.As several phorboids isolated from Euphorbia spp.were shown to inhibit chikungunya virus (CHIKV) replication, the authors in this research only evaluated these compounds for their ability to inhibit CHIKV replication and did not evaluate myrsinanes and premyrsinanes [57].

E. aellenii Rech
The immune system is an important target for the development of treatment strategies to improve the management of infections.Moreover, it has been known for many years that the modulation of the immune response is possible using compounds

E. cupanii
The very close taxonomic relationship between E. cupanii and E. pithyusa led Esposito and collaborators to investigate the diterpene ester content of E. cupanii using LC-MS/MS [57].Molecular networking coupled with unsupervised substructure annotation (MS2LDA) indicated the presence of new premyrsinane/myrsinane diterpene esters in E. cupanii extract fractions, which was confirmed by the isolation of six new myrsinanes (138-143) and six new premyrsinanes (144-149) (Figure 18), along with other known diterpenes, namely, phorbol esters.In conclusion, the profile of E. cupanii is marked by myrsinol and 13,17-oxy-premyrsinol esters.As several phorboids isolated from Euphorbia spp.were shown to inhibit chikungunya virus (CHIKV) replication, the authors in this research only evaluated these compounds for their ability to inhibit CHIKV replication and did not evaluate myrsinanes and premyrsinanes [57].

E. aellenii Rech
The immune system is an important target for the development of treatment strategies to improve the management of infections.Moreover, it has been known for many years that the modulation of the immune response is possible using compounds isolated from plants.Two new (150 and 85 Figures 15 and 19, respectively)) and one known (200) cyclomyrsinane-type diterpenes were isolated from E. aellenii Rech.f. [75,93].In vitro immunomodulatory activity was assessed by measuring the phytohemagglutinin (PHA)-induced T-cell proliferation.All compounds showed low inhibitory activity (0-23%) when tested at 0.5 µg/mL; however, the effect increased when tested at higher concentrations, with inhibition values ranging from 15% to 29% (at 5 µg/mL) and 38% to 53% (at 50 µg/mL).The most active compound was 200, which exhibited an IC 50  (PHA)-induced T-cell proliferation.All compounds showed low inhibitory activity (0-23%) when tested at 0.5 µg/mL; however, the effect increased when tested at higher concentrations, with inhibition values ranging from 15% to 29% (at 5 µg/mL) and 38% to 53% (at 50 µg/mL).The most active compound was 200, which exhibited an IC50 value of 40.4 ± 9.35 µg/mL.A previous phytochemical investigation of the chloroform fraction of the methanol extract of the aerial parts afforded two 14-desoxo-10, 18-dihydromyrsinane diterpenoids (151 and 152, Figure 19), which were tested for their immunomodulatory effect.Compound 151 showed an antiproliferative effect on lymphocytes but also the capacity to inhibit the zymosan-induced oxidative burst in whole blood phagocytes (up to 50%) at a concentration of less than 0.5 µg/mL [72].

E. aleppica L.
A study of new cytotoxic diterpenes of the premysinane type from E. aleppica L. was conducted by Zolfaghari et al. [53].A new compound 153 and a previously isolated compound 154 [94] (Figure 19) were tested against MCF-7 and MDA-MB 231 breast cancer cells.Compound 153 showed moderate cytotoxicity, but Compound 154 exhibited an higher dose-dependent cytotoxic effect, with IC50 values of 17.6 ± 1.2 and 16.7 ± 1.5 µM against MCF-7 and MDA-MB 231, respectively.The authors suggested that the cytotoxic activity is probably due to the presence of 14-O-acetyl instead of the ketone group at C-14 and 17-O-acetylated hemiacetal instead of the 13(17)-epoxy ring in Compound 153.In addition to 154, several diterpenoids of the premyrsinane type with different substituted patterns had already been found when extracts of acetone and petroleum ether/Et2O/MeOH (1:1:1) were studied (155-163) [38,40,41,94].

E. lathyris L.
From the seeds of E. lathyris L., Qian Wang et al. found, for the first time, a new diterpenoid of the premysinane type, called premylanin (164) (Figure 20), along with A previous phytochemical investigation of the chloroform fraction of the methanol extract of the aerial parts afforded two 14-desoxo-10, 18-dihydromyrsinane diterpenoids (151 and 152, Figure 19), which were tested for their immunomodulatory effect.Compound 151 showed an antiproliferative effect on lymphocytes but also the capacity to inhibit the zymosan-induced oxidative burst in whole blood phagocytes (up to 50%) at a concentration of less than 0.5 µg/mL [72].

E. aleppica L.
A study of new cytotoxic diterpenes of the premysinane type from E. aleppica L. was conducted by Zolfaghari et al. [53].A new compound 153 and a previously isolated compound 154 [94] (Figure 19) were tested against MCF-7 and MDA-MB 231 breast cancer cells.Compound 153 showed moderate cytotoxicity, but Compound 154 exhibited an higher dose-dependent cytotoxic effect, with IC 50 values of 17.6 ± 1.2 and 16.7 ± 1.5 µM against MCF-7 and MDA-MB 231, respectively.The authors suggested that the cytotoxic activity is probably due to the presence of 14-O-acetyl instead of the ketone group at C-14 and 17-O-acetylated hemiacetal instead of the 13(17)-epoxy ring in Compound 153.In addition to 154, several diterpenoids of the premyrsinane type with different substituted patterns had already been found when extracts of acetone and petroleum ether/Et 2 O/MeOH (1:1:1) were studied (155-163) [38,40,41,94].

E. lathyris L.
From the seeds of E. lathyris L., Qian Wang et al. found, for the first time, a new diterpenoid of the premysinane type, called premylanin (164) (Figure 20), along with thirteen known compounds and four new diterpenoids of the latyrane type.The cytotoxicity of the isolated compounds against the cancer cell lines HCT116, MCF-7, 786-0, and HepG2 was evaluated, but 164 exhibited little inhibitory activity at 50 µM for 24 h [95].thirteen known compounds and four new diterpenoids of the latyrane type.The cytotoxicity of the isolated compounds against the cancer cell lines HCT116, MCF-7, 786-0, and HepG2 was evaluated, but 164 exhibited little inhibitory activity at 50 µM for 24 h [95].In a more recent study, Compound 165 (Figure 20), a novel premyrsinane diterpenoid, and other diterpenes with various skeleton types were also isolated from the seeds [96].

E. macrorrhiza C.A. Mey
From the acetone extract of the whole plant of E. macrorrhiza C.A. Mey., several macrocyclic and rearranged macrocyclic diterpenes were isolated, including a new premyrsinane, macroripremyrsinone A (166), and jatrophodione A (167), previously isolated from Jatropha curcas [47] (Figure 20).Compound 166 was shown to be noncytotoxic against the human oral epidermoid carcinoma (KB) cell line and its navelbine-selected ABCB1 overexpressing (KBv200) cell line (IC50 > 50 µM), whereas 167 exhibited IC50 values of 22.46 ± 2.72 µM and 47.87 ± 0.30 µM for the KB and KBv200 cell lines, respectively.Compound 167 was also tested in combination with the anticancer drug navelbine for its ability to modulate multidrug resistance on the KBv200 cell line which overexpresses P-gp and exhibited MDR reversal activity (IC50 0.37 ± 0.013 µM) [97].In a more recent study, Compound 165 (Figure 20), a novel premyrsinane diterpenoid, and other diterpenes with various skeleton types were also isolated from the seeds [96].
Ghanadian et al. isolated two new cyclomyrsinol esters (199 and 200) (Figure 22) from the methanol extract of E. microsciadia Boiss.aerial parts [93].Compound 199 was tested for its in vitro antiangiogenic activity on vascular endothelium growth factor in cultured human umbilical vein endothelial cells, showing 23.9 ± 2.6% inhibition at the lower concentration of 0.5 µg/mL.In addition, the antiangiogenic effect was correlated with the concentration, increasing at 5 µg/mL to 34.6 ± 2.7% and further increasing at 50 µg /mL to 42.1 ± 0.8%.
Jeske et al. isolated from the whole E. seguieriana var.seguieriana Neck.plant seven myrsinane-type diterpenes (201-207) (Figure 22) and a cyclomyrsinane derivative, 208 [37].Another cyclomyrsinol diterpene derivative (209) was identified by Öksüz et al. from In 2000, Abbas et al. isolated from the acetone extract of aerial parts of E. cheiradenia Boiss.& Hohen.three myrsinane derivatives with an unusual tetrahydrofuran moiety due to the epoxy bridge between C -10 and C-13, namely, cheiradone (180), cheiradone A (181), and cheiradone B (182) (Figure 21).Among them, cheiradone (180) showed inhibitory   22), two novel diterpenes with an unusual 10,11-seco-premyrsinane skeleton, from Jatropha curcas L. twigs [49].These compounds are the first example of the cleavage of C10/C11 bond of the cyclopropane ring in the premyrsinanes.Their biogenetic pathway is summarized in Figure 5. Compound 220 was tested as an inhibitor of thioredoxin reductase, a major regulator of the intracellular redox homeostasis, whose deactivation is believed to be implicated in the inhibition of the proliferation and induction of necrosis or apoptosis.The diterpene exhibited potent inhibitory activity, with an IC50 value at 10.0 µM, was more active than the positive control curcumin (IC50 25.0 µM) [49].
The phytochemical study of the air-dried roots of Jatropha curcas cv.nigroviensrugosus extract resulted in the isolation of four premyrsinane diterpenes, named jatrophodiones B-E (223-226) [48] (Figure 22), which were structurally similar to jatrophodione A (222), Ghanadian et al. isolated two new cyclomyrsinol esters (199 and 200) (Figure 22) from the methanol extract of E. microsciadia Boiss.aerial parts [93].Compound 199 was tested for its in vitro antiangiogenic activity on vascular endothelium growth factor in cultured human umbilical vein endothelial cells, showing 23.9 ± 2.6% inhibition at the lower concentration of 0.5 µg/mL.In addition, the antiangiogenic effect was correlated with the concentration, increasing at 5 µg/mL to 34.6 ± 2.7% and further increasing at 50 µg /mL to 42.1 ± 0.8%.
Bao et al. isolated jatrocurcadiones A (220) and B (221) (Figure 22), two novel diterpenes with an unusual 10,11-seco-premyrsinane skeleton, from Jatropha curcas L. twigs [49].These compounds are the first example of the cleavage of C10/C11 bond of the cyclopropane ring in the premyrsinanes.Their biogenetic pathway is summarized in Figure 5. Compound 220 was tested as an inhibitor of thioredoxin reductase, a major regulator of the intracellular redox homeostasis, whose deactivation is believed to be implicated in the inhibition of the proliferation and induction of necrosis or apoptosis.The diterpene exhibited potent inhibitory activity, with an IC 50 value at 10.0 µM, was more active than the positive control curcumin (IC 50 25.0µM) [49].
The phytochemical study of the air-dried roots of Jatropha curcas cv.nigroviensrugosus extract resulted in the isolation of four premyrsinane diterpenes, named jatrophodiones B-E (223-226) [48] (Figure 22), which were structurally similar to jatrophodione A (222), previously isolated from the same species by Xu et al. [47].Jatrophodiones D (225) and E (226) were isolated as an inseparable mixture of isomers, only differing in the stereochemical centre at C-3.These compounds were evaluated for cytotoxicity against HL-60, SMMC-772, A-549, MCF-7, and SW480 human tumor cell lines but were inactive in this test (IC 50 > 40 µM) [48].

Conclusions
Over the past four decades, more than 200 myrsinane-type diterpenes have been isolated from Euphorbia species.It is interesting to note that the presence of these type of compounds are restricted to only around 20 species, of which E. falcata, E. prolifera, E. kopetdaghi, and E. decipiens stand out.In this way, they can be regarded as potential chemotaxonomic markers of some Euphorbia species due to of their delimited distribution and structural diversity.
The biosynthesis of myrsinane diterpenes is still not fully understood, particularly the mechanistic details on the conversion of the lathyrane skeleton to premyrsinane and its derivative counterparts.Herein, we discussed the possible biosynthetic pathways and chemical conversion of premyrsinanes to cyclomyrsinanes and myrsinanes.Furthermore, some relevant information about the isolation procedures and structural identification of representative myrsinane-type diterpenes, using NMR spectroscopy, is also presented for the first time in a schematic and comprehensive manner.It is our hope that the summarized key spectroscopic features will help researchers to identify myrsinane-type diterpenes in a faster and more straightforward manner.
Most of the research data published in the literature have described the isolation and structural identification of new myrsinane polyesters and reported some biological activities that are summarized in Table 1.The most frequently performed experiments were aimed at exploring the cytotoxic potential against several cancer cell lines, the modulation of multidrug resistance, immunomodulatory and neuroprotective effects, and the inhibition of enzymes such as urease, HIV-1 reverse transcriptase, and prolyl endopeptidase.However, when compared to other Euphorbia diterpenes, such as lathyranes and jatrophanes, that have been extensively investigated, the biological activity of myrsinane-type diterpenes is still much less studied, and these compounds were, in general, less bioactive.In addition, in the majority of the studies, the mechanisms of action have not been explored nor has the structure-activity relationships been established, probably due to the reduced amount of the isolated compounds, which is always an important drawback in these studies.For the same reason, there are currently no reported in vivo or toxicological studies.• Exhibited a more effective neuroprotective effect against MPP + -induced neuronal cell death in SH-SY5Y cells than guanosine used as positive control. [68] EtOH 95% (roots) 54 • Compound 54 showed cytotoxicity against human ovarian cancer cell line (A2780), with an IC 50 value of 7.7 µM. [67] E. santae catharinae DCM:MeOH (1:1) (aerial parts) 117-120 Nevertheless, the data gathered in this review encompass the academic works and efforts of several research teams across the globe, and, in our opinion, it is quite pertinent.Through a chemotaxonomic approach, it can be used to identify other promising species to investigate, as plants belonging to the same genus or family should produce similar specific secondary metabolites.Moreover, these outcomes would provide researchers with new insights to more easily identify these types of structures and compare biological activities with previously identified myrsinane-type diterpenoids, which can help to find possible therapeutic application for these compounds.

Figure 6 .
Figure 6.(a) Chemical transformation of Euphorbia factor L1 as proposed by Wang and collaborators in 2019 [45].(b) Structure of PM1 and PM2 obtained under the catalysis of iron [46].

Figure 6 .
Figure 6.(a) Chemical transformation of Euphorbia factor L1 as proposed by Wang and collaborators in 2019 [45].(b) Structure of PM1 and PM2 obtained under the catalysis of iron [46].

Figure 12 .
Figure 12.Chemical structures of myrsinane-type diterpenes isolated from E. falcata.3.2.E. prolifera Buch.-HamE. prolifera Buch.-Ham.dried roots, known in China as Langdu, are a herbal medicine traditionally used to treat cancer and inflammation.The myrsinane diterpenes J196-10-1 (27) and J196-9-4 (28) (Figure13) were isolated from the methanol extract and studied as possible modulators of Pgp in the human breast adenocarcinoma (MCF-7) cell line and its multidrug resistant subline (MCF-7/Adr)[62,63].The structure of the compounds was very similar, only differing in the type of substituent at C-5 and C-14.It was found that both compounds were noncytotoxic to the tested cells at concentrations below 50 µM.When tested on the

Table 1 .
Summary of the main biological activities reported in the literature for myrsinane-type diterpenes isolated from Euphorbia species.Compound 200 showed in vitro immunomodulatory activity (IC 50 40.4± 9.35 µg/mL) and a significant inhibition of lymphocyte proliferation at 50 µg/mL.Compound 154 exhibited cytotoxic activity against two breast cancer cell lines (IC 50 17.6 ± 1.2 and 16.7 ± 1.5 µM, MCF-7 and MDA-MB231, respectively).Moderate cytotoxicity against several cancer cell lines (IC 50 between 24.5 and 37.7 µM).The mechanism responsible for the observed cytotoxic effect was related to an increase in caspase-3 activity; Compound 112 also raised the ROS levels in cancer cells.

•
Significant analgesic activity when administered to mice at dose of 5-20 mg/kg i.p. (This activity is comparable to that of 100 mg/kg of aspirin or ibuprofen.)Compounds 21, 22, and 24-26 were strong modulators of MDR1 efflux pump on MDR mouse T-lymphoma cells (FAR values between 52.6 and 74.5 when tested at 20 µM).Compound 21 was also very active when tested at 2 µM (FAR 46.1) and displayed a synergistic effect with doxorubicine.

Table 1 .
Cont.Compounds 27 and 28 were strong modulators of P-gp expressed in MCF-7 cell line, with IC 50 values of 0.063 and 1.41 µM, respectively; 27 exhibited a reverse ratio value of 219.6 when in combination with vincristine and inhibited the efflux of rhodamine-123 mediated by P-gp, without changing the transcription level of ABCB1 gene as Compound 28.•Compounds 27 and 28 stimulated ATPase activity at low concentrations, and it was suggested they act as competitive inhibitors.