Alkaloids from Marine Ascidians

About 300 alkaloid structures isolated from marine ascidians are discussed in term of their occurrence, structural type and reported pharmacological activity. Some major groups (e.g., the lamellarins and the ecteinascidins) are discussed in detail, highlighting their potential as therapeutic agents for the treatment of cancer or viral infections.


Introduction
Ascidians belong to the phylum Chordata, which encompasses all vertebrate animals, including mammals and, therefore, they represent the most highly evolved group of animals commonly investigated by marine natural products chemists. Together with the other classes (Thaliacea, Appendicularia, and Sorberacea) included in the subphylum Urochordata (=Tunicata), members of the class Ascidiacea are commonly referred to as tunicates, because their body is covered by a saclike case or tunic, or as sea squirts, because many species expel streams of water through a siphon when disturbed. There are roughly 3,000 living species of tunicates, of which ascidians are the most abundant and, thus, the mostly chemically investigated. An interest in ascidians' chemistry was kindled as early as 1847, when a German physiologist discovered the presence in the blood cells of these invertebrates of large amounts of vanadium and sulfuric acid, along with an uncharacterized nitrogenous metabolite. The conquest to understand the role of vanadium in ascidians' blood has led to a huge amount of chemical and biological studies and led to the isolation very unstable hydroquinoid compounds, called tunichromes [1,2], whose biological function as well as functional role in the OPEN ACCESS vanadium complexation remains still unclear [3,4]. Then, attention has focused on ascidians because of their biologically active metabolites and the chemistry of ascidians has become one of the most active fields of marine natural products; it has been amply demonstrated that these sea creatures are prolific producers of unusual structures with significant bioactivities [5,6].
Ascidians' chemistry is dominated by the presence of nitrogenous metabolites which could be basically divided into two structural type-based groups, peptides and polycyclic aromatic alkaloids. This review describes the chemistry of ascidians' alkaloids; its overall goal is to display the huge chemical diversity in this group of marine secondary metabolites. Ascidians' alkaloids class indeed includes a large variety of structures, ranging from complex pyridoacridines and tyrosine-derived alkaloids to simple protoalkaloids. About 300 alkaloid structures isolated from marine ascidians will be discussed in term of their occurrence, structural type and reported pharmacological activity. They will be presented in an order based on their general structural type or on a plausible biosynthetic origin (amino acid origin). Some major groups (e.g., the lamellarins and the ecteinascidins) will be discussed in detail, highlighting their potential as therapeutic agents for the treatment of cancer or viral infections.

Pyridoacridine Alkaloids
Pyridoacridine alkaloids isolated from ascidians are typically tetra-or penta-cyclic aromatic alkaloids based on the pyrido[k,l]acridine skeleton, usually possessing a functionalized alkylamine side chain. Many of these compounds have generated interest both as challenging problems for structure elucidation and synthesis as well as for their bioactivities. In general, pyridoacridines are cytotoxic and some of them possess potent anti-viral, anti-fungal, anti-bacterial, anti-tumor and anti-parasitic activity [7]. For the majority of this class, cytotoxicity has been shown to be due to DNA-binding properties, topoisomerase (TOPO) inhibition or the production of reactive oxygen species (ROS) [7]. In fact, the main structural feature of these alkaloids is the core of a planar iminoquinone moiety which can intercalate into DNA and cleave the DNA double helix or inhibit the action of TOPO II. Thus, there has been considerable interest on the potential of these compounds as antitumor agents [8,9]; the great chemical diversity in this family of alkaloids provided a large set of tools to manipulate the TOPO II activity, either stimulating cleavage of DNA through stabilization of covalent TOPO II-DNA complexes or promoting the catenation of DNA [10]. During the past 25 years, both natural pyridoacridines and their analogues have constituted excellent targets for synthetic works [9], confirming that this family of alkaloids as a whole is of interest as a source of new lead structures for drug development.
Actually, all of the -carboline metabolites isolated thus far are related biosynthetically; the production of these metabolites is generally believed to involve the coupling of tryptophan with a second amino acid, whose nature clearly affects C1 substitution. For example, eudistomins A (54), M (55), G (50), and P (52) may be considered to be derived from tryptophan and glutamine [39], while the 2-fenylacetyl--carbolines, eudistomines R (56) and T (57), are, in addition to tryptophan, made up of phenylalanine or phenylpyruvic acid. Similarly, the unusual aminoacids, p-methylphenyl-L-alanine and S-methyl-D-cysteine have been supposed to be involved in the production of eudistomidins B (83) and C (64) [46], respectively. A proline-derived precursor is evident in eudistomins G, I, P (50-52), A (54), and M (55), eudistomidin A (63), and woodinine (85). In vivo studies with E. olivaceum confirmed that tryptophan and proline are the primary precursors of eudistomin I (51) [65]. Some of the most intriguing members of these alkaloids are those bearing an oxathiazepine ring (eudistomins C, E, F, K, and L, 91-95) which apparently originate from condensation of tryptophan with cysteine [44]. Eudistalbins A (65) and B (66) likely derive from leucine.
The -carboline alkaloids display a variety of biological activities, including a broad spectrum of antibiotic activity, cytotoxicity, calmodulin antagonistic properties. However, the most notable pharmacological feature is the strong antiviral properties displayed by some members of the family [66,67]. The tetrahydro--carbolines generally exhibited higher levels of biological activity than their fully aromatic relatives; the oxathiazepino-eudistomins 88-94, for example, exhibit the highest level of antiviral activity and were also endowed with antimicrobial activity. Eudistomin K (91) is significantly active against Herpes simplex Type I (HSV-1) and Polio virus, while the sulfoxide (94) and debromo (90) derivatives are active against both virus but less potent. Enhancement of antiviral activity correlates to bromination at C7 ( Figure 12). There are only few examples of reported dihydro--carbolines from ascidians. The first was isoeudistomin U (99) which was initially reported to be a 4-substituted dihydro--carboline derivative [64], but whose structure was revised to 3,4-dihydroeudistomin U after total synthesis [68]; the bioactivity of isoeudistomin U was reported to be similar to that of the related eudistomin U (59). A 1,2-dehydro analogue of trypargine, named trypargimine (100), has been reported from a previously undescribed Eudistoma sp. [52]. Also -carbolines are not common ascidians' metabolites. The grossularines (101)(102)(103) from Dendrodoa grossularia are the sole representatives of this structural class and are the first -carbolines to be isolated from a natural source ( Figure 12). The initial structure reported for grossularine (=grossularine-1) [69] was incorrect and it was revised when data for both grossularine-1 (101) and -2 (103) were reported [70]. Both grossularines are cytotoxic and cause accumulation of cells in the G1-phase; grossularine-2 appears to act on DNA as a mono-intercalating agent. N,N-didesmethylgrossularine-1 (102) has been reported from Polycarpa aurata but no activity data were presented [71].

Indole-Based Alkaloids
The structures of indole based alkaloids isolated from ascidians span a wide range of complexity, spreading from the simple 6-bromoindole-3-carbaldehyde, isolated from Pyura sacciformis [72] and previously found in a marine pseudomonad [73], to the complex indolocarbazoles of the staurosporine type 104-112 isolated from ascidians belonging to the family Polycitoridae ( Figure 13) [74][75][76][77][78][79]. Staurosporine and its derivatives have been isolated from various actinomycete strains as well as from some marine organisms, including ascidians [80]. These alkaloids were shown to be strong inhibitors of several kinases, in particular protein kinase C (PKC); other activities include inhibition of platelet aggregation and smooth muscle contraction, induction of cell cycle arrest and apoptosis, and the reversal of multidrug resistance in some cancer cell lines. The potential of these derivatives as anticancer agents is supported by the example of 7-hydroxystaurosporine which is in clinical phase I trials at the NCI [77]. 11-Hydroxystaurosporine (105), from Eudistoma sp., is a PKC inhibitor about 30% more potent than staurosporine [74] whereas 3-hydroxystaurosporine (104), from E. toealensis, is one of the most active staurosporine-type inhibitors of cell proliferation described so far [77]. Derivatives 111 and 112, from Cystodites solitus, displayed cytotoxic activity in the submicromolar range against three human tumour cell lines [79]. A number of 3-substituted indoles have been isolated from ascidians. Examples are 6-bromotryptamine (113) and its derivatives 114-116, isolated from Didemnum candidum [81], conicamin (117), from Aplidium conicum, with histamine-antagonistic activity [82], citorellamine (118), from Polycitorella mariae, the first indole disulfide dihydrochloride from a marine organism [83,84], and the indolyl-3glyoxylic acid derivatives polyandrocarpamides A-C (119-121) [85]. Dendrodoa grossularia was the source of several indole alkaloids with different heterocyclic moieties linked at the 3-position (compounds 122-125) [86][87][88][89]. Among them, alboinon (125) contained an oxadiazinone system, found in nature for the first time ( Figure 14) [88].  Meridianins A-G (126-132), from Aplidium meridianum [90,91], are brominated and/or hydroxylated 3-(2-aminopyrimidine)-indoles differing in the bromine and /or hydroxyl substitution ( Figure 15). They constitute a new family of protein kinase inhibitors, inhibiting various protein kinases such as cyclin-dependent kinases, glycogen synthase kinase-3, cyclic nucleotide-dependent kinases and casein kinase 1; they also prevent proliferation and induce apoptosis probably due to their ability to enter cells and to interfere with the activity of kinases important for cell division and death [92]. Structurally related to meridianins are aplicyanins A-F (133-138), from A. cyaneum, containing a 6-tetrahydropyrimidine substituent at C-3; these alkaloids can be considered reduced forms of the relevant meridianins and, thus, their biogenetic precursors ( Figure 15) [93].  Kottamides A-D (139)(140)(141)(142), from Pycnoclavella kottae [94], are imidazol-4-one containing alkaloids; their biogenesis could involve stereospecific imidazolone ring formation from modified Trp-Val-Ile and Trp-Ile-Ala tripeptide precursors ( Figure 16) [96]. Kottamide E (143) represent the first report of a natural product bearing a 4-amino-1,2-dithiolane-4-carboxylic acid residue [95]. Wakayin (144), from Clavelina sp., contains an uncommon pyrroloiminoquinone moiety; it is one of the first camptothecin (CPT)-like TOPO I inhibitors isolated from a marine organism, the indole ring linked to the bispyrroleiminoquinone core playing a significant role in this activity ( Figure 16) [96]. Four predator-deterrent alkaloids possessing a novel indole-maleimide-imidazole carbon skeleton, didemnimides A-D (145)(146)(147)(148), were isolated from a Caribbean collection of Didemnum conchyliatum [97]. They were the first examples of a new alkaloid structural class and add to a relatively small group of naturally occurring maleimides. Successively, didemnimide E (149) was isolated from Didemnum granulatum collected in Brazil together with a less polar and deep purple cyclized didemnimide alkaloid, isogranulatimide (150) [98]. Almost at the same time, Fenical's group independently obtained this compound from D. conchyliatum [99]. Compound 150 is the cyclization product of didemnimide A (145) formed via a C-2 indole condensation with the imidazole nitrogen and represented the first alkaloid to be isolated with this cyclized indole-maleimide-imidazole structure. Isogranulatimide (150) and its isomer granulatimide (151) could be biomimetically synthesized involving the photocyclization of 145. Subsequently, 151 and its 6-bromo derivative 152 were obtained as naturally occurring compounds from a new collection of Brazilian D. granulatum [100]. Isogranulatimide (150) was reported as the first non-cytotoxic, specific G2 cell cycle checkpoint inhibitor, and the mechanism of this antitumor action was elucidated at molecular level ( Figure 17) [98,101].

Tyrosine-and Phenylalanine-Derived Alkaloids
Tyrosine is the precursor of a wide number of alkaloids whose structures are characterized by possessing the Ar-C 2 -N subunit derived from Tyr, commonly via dopamine; often, additional Ar-C 1 and Ar-C 2 moieties are present, derived from a partial degradation of the amino acids Phe or Tyr. The aromatic ring of all these subunits is usually oxygenated at 4-, 3,4-, or 3,4,5-positions. The amino acid DOPA [2-amino,3-(3′,4′-dihydroxyphenyl) propionic acid], in particular, appears to play an important role in the ascidians' metabolism, serving as the apparent precursor not only of peptide products, but also of unique alkaloid structures, such as those of lamellarins and ecteinascidins (see below).
Botryllazines A and B (199 and 200) have been isolated from Botryllus leachii ( Figure 22); the structure of botryllazine A is unprecedented since three tyrosine precursors are involved in the formation of a pyrazine nucleus. It has been proposed that the biogenetic pathway leading to botryllazyne B from two tyrosine units involves amide formation and, subsequently cyclization via imine formation [126]. Haouamines A and B (201 and 202), from Aplidium haouarianum [127], demonstrates intriguing stereochemical features; in solution, each haouamine exists as an inseparable mixture of two interconverting isomers derived by the presence of a highly strained 3-aza- [7]paracyclophane moiety in their structures ( Figure 22). Even if one Ar-C 2 -N and three Ar-C 2 subunits can be readily identified in the structures of haouamines, the oxygenation pattern of all these units, hydroxylated at the meta position with respect to the C2 chain, does not allow establishing a relationship between these alkaloids and the amino acid tyrosine. Thus, the biosynthesis of these alkaloids should imply either an unusual loss of the C4 hydroxyl group of tyrosine along the biosynthetic pathway or the involvement of an undescribed natural amino acid precursor exclusively meta hydroxylated [127].  (199)(200) and haouamines (201)(202).
The lamellarins form a group of more than 50 highly condensed DOPA-and TOPA-derived pyrrole cytotoxic alkaloids which have attracted researchers' interest due to both their structural originality and complex mechanism of action. Lamellarins were first isolated from the prosobranch mollusk Lamellaria sp. in 1985 [128]. They were later extracted from and identified in various species of Didemnum ascidians [129][130][131][132][133][134] and sponges [135,136] collected from very diverse areas, which suggests a potential microbial link to their biosynthesis [137,138].
The lamellarins fall into two structural groups, depending on whether the central pyrrole ring is fused (Group I) or unfused (Group II) to adjacent aromatic rings ( Figure 23). Group I could be further divided into two subgroups, Ia, including compounds with an olefin at C5/C6, and Ib, with compounds in which this olefin is saturated. Each group includes derivatives in which phenolic hydroxyl groups are substituted by methoxy, sulphate or acetate functions.The lamellarins isolated from ascidians possess the hexacyclic skeleton of Group I; selected structures of ascidians' lamellarins are reported in Figure 24.   A wide range of different biological properties are reported for this family of alkaloids, including antibiotic activity, immunomodulation, antioxidant activity [137][138][139]. A few members of the family revealed HIV-1 integrase inhibition activity, although this pharmacological activity has not been so far thoroughly explored. The HIV-1 integrase, providing the integration of the proviral DNA into host cell chromosomal DNA, constitutes an attractive target because no human cellular homologue of this enzyme exists. Lamellarin α 20-sulfate (223) exhibited a potent in vitro inhibition against the HIV-1 integrase [134]; it is able to act at two different steps of the catalytic cycle, the terminal cleavage and the strand transfer. Moreover, this compound inhibits the viral replication in cultured cells at non-toxic doses. Its sulphate group plays a critical role because the desulphated analogue lamellarin  (213) is inactive. However, the most common and remarkable property of the lamellarins is their capacity to inhibit the proliferation of cancer cells. The majority of lamellarins are considerably cytotoxic, with IC 50 (or LD 50 ) values in the nanomolar to micromolar range, depending on the experimental conditions and the nature of the compounds. A noticeable exception is that of the sulphated lamellarins, which are not cytotoxic presumably due to reduced cell uptake. Lamellarin D (206) is one of the most cytotoxic compounds of the family and, in the series of its derivatives, precise structure-activity relationships have been delineated [140]. Analogues with hydroxyl groups at both the C8 and C20 positions are the most cytotoxic, whereas the OH at C14 and methoxy groups at C13 and C21 seem to be less important to maintain the cytotoxic potential [141].
Lamellarins thus represent an important source of structures to develop anticancer drugs, although few aspects of their mechanism of actions are known, in particular their capacities to interfere with topoisomerase I and mitochondria, both contributing to their potent cytotoxicity. In particular, TOPO I has been found to be the major (but not the unique) target for lamellarin D (206) [142,143]; this key discovery has opened the doors to the determination of structure-function relationships and the rational design of lamellarin analogues of pharmaceutical interest. For example, the double bond between carbons 5 and 6 in the quinoline B-ring is a crucial element for topoisomerase I inhibition [142]. In addition, some lamellarins, have been reported to act as nontoxic inhibitors of acquired multidrug resistance (MDR) in various cancer cell lines. Lamellarin I (207) is a MDR modulator, inhibiting directly P-glycoprotein mediated drug efflux at non-lethal doses [144]. In light of their fascinating unique structures and intriguing biological properties, lamellarins still are a particularly important subject for synthetic as well as pharmacological studies [137][138][139].
Pyrrole-derived alkaloids related to lamellarin include lukianols (224-225), isolated from an unidentified Pacific tunicate [145], polycitones (226-227) and polycitrins (228-229), from Polycitor species [146,147], and ningalins (230-233), from Didemnum sp. (Figure 25) [148]. The structures of the lukianols A and B contained a pyrrolooxazinone moiety; they appear to arise by the same biogenetic pathways leading to lamellarin O and P isolated from the marine sponge Dendrilla cactos [135]. Lukianol A (224) inhibited DNA synthesis in L1210 lymphocytic leukemia cell lines with less effect on RNA and protein synthesis, demonstrating a therapeutic profile very similar to current clinically used anticancer agents [145]. Ningalins A-D (230-233) are condensed aromatic systems with the unifying theme that all appear derived from the condensation of two, three, four, and five DOPA precursors, respectively. Although a potential role for these alkaloids in metal sequestration has not been demonstrated they are structurally related to other metal binding ascidian-derived o-catechols; it is thus conceivable that they too participate in the metal chelating phenomena characteristic of this class of marine invertebrates [137,145].
Tetrahydroisoquinoline alkaloids are uncommon in ascidians, but the sole representatives of this class, ecteinascidins, isolated mainly from the Caribbean ascidian Ecteinascidia turbinata, are probably the most useful anticancer agents found to date in a marine source. The lead compound, Yondelis® (trabectedin, ET-743, 235), is the first representative of a marine natural product to receive marketing authorization for the treatment of patients with soft tissue sarcomas (STS) [149]. Apart from the biological activity, ET-743 exhibits an extraordinary three-dimensional molecular architecture, which has made a fascinating target for the synthetic organic chemists allowing a number of original synthetic and semi-synthetic methodologies for the preparation of a wide variety of ecteinascidins to be discovered [150]. The first description and structural characterization of six new chemical entities called ecteinascidins, ET 729 (234), ET 743 (235), ET 745 (236), ET 759A (237), ET 759B (238), and ET 770 (239), was reported by the Rinehart group in 1990 of which ET-743 was the most abundant representative [151]. Simultaneously, Wright and coworkers described compounds 234 and 235 [152], but the unequivocal assignment of the absolute stereochemistry was achieved only when the X-ray crystal structures of the natural N 12 -oxide of ET-743 (240) and a synthetic O-methyl analogue of N 12 -formyl ET-729 (241) were solved [153]. Successively, a number of additional new members of this class of molecules have been isolated, such as compounds 242 and 243 [154], 244-247 [155], 248 [156], 249-252 [157] (Figure 26). The unique structure of ecteinascidins consists of a monobridged pentacyclic skeleton composed of two fused tetrahydroisoquinoline rings (subunits A and B) linked to a 10-membered lactone bridge through a benzylic sulfide linkage. Most ecteinascidins have an additional tetrahydroisoquinoline or tetrahydro--carboline ring (subunit C) attached to the rest of the structure through a spiro-ring. As for the biogenesis of the ecteinascidins, it has been proposed that A-B units could be formed by condensation of two DOPA-derived building blocks, and the tetrahydroisoquinoline ring in unit B is closed by condensation with a serine-(or glycine-) derived aldehyde as in the case of the related saframycins. S-Adenosylmethionine is the likely source of methyl groups at C-6, O-7, C-16, O-17, and N-12 [157]. Initially, ecteinascidins were found to be cytotoxic against L1210 leukaemia cells (IC 50 value of 0.5 ng/mL) [151] and were later shown to possess strong in vivo antitumour effects in various mice models bearing P388 lymphoma, B16 melanoma, M5076 ovarian sarcoma, lewis and lX-1 human lung carcinoma, and MX-1 human mammary carcinoma xenografts [154]. ET-743 (235) was selected for further development; studies on its mechanism of action revealed it as the first of a new class of DNA binding agents with a complex, transcription-targeted mechanism of action. Trabectedin binds to the minor groove of DNA with preference for GC-rich triplets and subsequently forms covalent adducts with the N2-position through its carbinolamine moiety [158][159][160]. ET-743, under the trade name Yondelis, was approved for the treatment of refractory soft-tissue sarcomas by the European Commission in July 2007; the currently ongoing Phase III trials along with the already existing clinical evidence may provide enough data for the Food and Drug Administration for an approval in the US [161]. Based on the preclinical results, trabectedin is also being developed for ovarian, prostate, lung, breast and pediatric cancers [149,162,163].   Figure 26. Structures of ecteinascidins.

Lysine-Derived Alkaloids
Alkaloids based on a 2-amino-3-hydroxyoctadecane moiety, generally referred to as lysine-derived metabolites, have been found in several genera of ascidians. Monocyclic examples are the piperidine alkaloids, which are among the most abundant metabolites of terrestrial plants, but there are relatively few examples isolated from marine organisms.
Pseudodistomins A (253) and B (254), from Pseudodistoma kanoko, represent the first piperidine alkaloids obtained from marine sources [164]. The structure of the side chains of 253 and 254 has been revised after the first disclosure of the molecules [165,166], while the stereostructure of the piperidine nucleus has been established by synthesis of their tetrahydroacetyl derivatives [167,168]. Other members of the group have been successively isolated, from other Pseudodistoma species, including pseudodistomin C (255), with the absolute configuration at C-4 and C-5 opposite to those found in 253 and 254 [169], and pseudodistomins D-F (256-258) (Figure 27) [170]. Pseudodistomins A and B exhibited cytotoxic activity with calmodulin antagonistic activity; pseudodistomins B-F were found to be active in a cell-based assay for DNA damage induction. Uoamines A (259) and B (260) also are monocyclic piperidine alkaloids isolated form Aplidium uouo; in these compounds, the 3-hydroxyl group present on the piperidine nucleus is esterified by (E)-or (Z)-3-thiomethylacrylic acid, respectively ( Figure 27) [171].  Bi-and tricyclic members of the lysine-derived alkaloids group have been most often found in Clavelina species and include quinolizidines and indolizidines derivatives. Clavepictines A (261) and B (262) and pictamine (263) are homologous quinolizidine alkaloids isolated from Bermudan and Venezuelan collections of the tunicate C. picta, respectively [172,173]. With the use of NOE experiments, 261 was determined to have a cis ring junction in the quinolizidine moiety, with the decadienyl side chain in the equatorial orientation, and the methyl and acetoxy substituents oriented trans-diaxial. An X-ray analysis of clavepictine B (262) confirmed the proposed relative stereochemistry and conformation. Both clavepictines inhibited the growth of murine leukemia and human solid tumor cell lines at concentrations less than 9 g/mL. Pictamine (263) is a bis-nor analogue of clavapictine A, bearing two less carbons on the side-chain. C. picta has also been the source of a series of indolizidine metabo1ites, piclavines A-C (264-266) ( Figure 28) [174]. They consist of three series of isomeric compounds, differing in the number of double bonds on the side chain. Each group is composed of an inseparable mixture of stereoisomers, which differ at the C2 chiral center, as well as at each of the double bonds. The piclavines are the first indolizidines isolated from a marine source; they exhibited antifungal and antimicrobial activity against Gram-positive bacteria. Tasmanian collections of C. cylindrica yielded the tricyclic alkaloids cylindricines A-K (267-277) [175][176][177]; cylindricine B (268) represented the first example of the new perhydropyrido[2,1-j]quinoline ring system, while cylindricine A (269) is the first perhydropyrrolo-[2,1-j]quinoline known from nature ( Figure 29). The skeleton of cylindricines A (267), C-I (269-275), and K (277) is closely related to the indolizidine system of piclavines by having an extra 6-membered carbocyclic fused ring. In the same way, structures of cylindricines B (268) and J (276) are related to the quinolizidine system of the clavepictines and pictamines. Cylindricines F (272) and G (273) are the first thiocyanates from an ascidian. Closely related to cylindricines A and B, are polycitorols A (278) and B (279), isolated from a marine ascidian of the family Polycitoridae [178]; they lack C-4 oxygenation found in cylindricines and have a OH group instead of a chlorine atom at C-13 and a butyl instead of a hexyl appendage at C-2 ( Figure 29). Other analogous metabolites are lepadiformines A-C (280-282) isolated from C. lepadiformis and C. moluccensis [179,180] and fasicularin (283) from Nephteis fasicularis [181]. The initially reported structure of lepadiformine A was revised through its total synthesis; in the same study fasicularin (283) was also synthesized, allowing its absolute configuration to be assigned ( Figure 29) [182]. Early biological experiments on fasicularin suggested that its cytotoxic properties may stem from its ability to damage cellular DNA [181]. Successive studies revealed fasicularin as the first natural product found to generate a DNA-alkylating aziridinium ion via a mechanism analogous to the clinically used anticancer drugs mechlorethamine, melphalan, and chlorambucil [183]. Biological studies on lepadiformines showed that they have marked effects on the cardiovascular system when tested on frog atrial myocytes, the potency varying with the alkaloid structure [180].
The ritterazines and cephalostatines share many common structural features. Both consist of two highly oxygenated C27 steroid units fused via a pyrazine ring at C-2 and C-3; both chains of the steroid units usually form either 5/5 or 5/6 spiroketals. While cephalostatins in general are more oxygenated on the right side, the ritterazines have the more oxygenated left side. Hydroxyl groups are seen at C-12, C-17, C-23, C-26, C-12′, and C-23′ in the cephalostatins, whereas C-12, C-7′, C-12′, C-17′, and C-25′ are hydroxylated in the ritterazines (Figure 33) [206].   Although less potent than cephalostatins, ritterazines also possess high inhibitory activity against a series of human cancer cell lines. Not surprisingly, the most active constituent of R. tokioka (ritterazine B, 323) contains nearly the same right-hand side steroidal unit (323: no 17R-hydroxy moiety) as the most active cephalostatins. A COMPARE pattern-recognition analysis gave correlation coefficients of ~0.9 between cephalostatins and ritterazines in NCI-10 cell lines, suggesting they share the same mechanism. However, the antineoplastic mechanism of the cephalostatins is presently largely unknown. The fingerprint of cephalostatin activity in the NCI 60-tumor panel is quite different from other known anticancer agents, likely indicating a new mechanism of action. Recent studies revealed that cephalostatin 1 affects cells by disrupting the mitochondrial transmembrane potential and, thus, inducing apoptosis [207]. Pro-apoptotic properties have also been demonstrated for ritterazine B (323) although apoptosis induced by this compound appeared to be independent of the caspase pathway. Neither cleavage nor degradation of caspase targets was indeed observed, indicating that ritterazine B might be a potent inducer of apoptosis acting via a novel antimitotic mechanism [208]. The relative simplicity of ritterazines promises greater synthetic accessibility with probable retention of significant bioactivity. Isolation of closely related cephalostatins and ritterazines from different phyla raises questions as to the true origin of bissteroidal pyrazines; a shared symbiontic microorganism could be responsible for the biosynthesis of these compounds [207].

Conclusions
An intensive research effort during the last 25 years has generated an impressive number of alkaloids isolated from marine ascidians, which remain unique among marine invertebrates in that they overwhelmingly produce this kind of metabolites. Many of these compounds exhibited biomedically important activities; among them, cytotoxicity is the most frequently listed activity. Unfortunately, the chemical ecology of these organisms has not received significant attention and several intriguing aspects of their chemistry still remain unsettled. These include whether symbionts, which are commonly associated with ascidians, play a role in their secondary metabolism, and what purpose these compounds serve for the producing organism in nature.