Next Article in Journal
Preparation, Characterization, and In Vivo Evaluation of Amorphous Icaritin Nanoparticles Prepared by a Reactive Precipitation Technique
Next Article in Special Issue
Zinc (II) and AIEgens: The “Clip Approach” for a Novel Fluorophore Family. A Review
Previous Article in Journal
A Multimethodological Characterization of Cannabis sativa L. Inflorescences from Seven Dioecious Cultivars Grown in Italy: The Effect of Different Harvesting Stages
Previous Article in Special Issue
Sulfanyl Porphyrazines with Morpholinylethyl Periphery—Synthesis, Electrochemistry, and Photocatalytic Studies after Deposition on Titanium(IV) Oxide P25 Nanoparticles
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 26
Issue 10
10.3390/molecules26102909
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Concise Synthesis of a BODIPY-Labeled Tetrasaccharide Related to the Antitumor PI-88

by
Juan Ventura
1,
Clara Uriel
1,
Ana M. Gomez
1,*,
Edurne Avellanal-Zaballa
2,
Jorge Bañuelos
2,*,
Inmaculada García-Moreno
3 and
Jose Cristobal Lopez
1,*
1
Instituto de Química Orgánica General, IQOG-CSIC, Juan de la Cierva 3, 28006 Madrid, Spain
2
Departamento de Química Física, Universidad del Pais Vasco-EHU, Apartado 644, 48080 Bilbao, Spain
3
Instituto de Química-Física “Rocasolano”, IQFR-CSIC, Serrano 119, 28006 Madrid, Spain
*
Authors to whom correspondence should be addressed.
Molecules 2021, 26(10), 2909; https://doi.org/10.3390/molecules26102909
Submission received: 14 April 2021 / Revised: 6 May 2021 / Accepted: 12 May 2021 / Published: 14 May 2021
(This article belongs to the Special Issue Exclusive Feature Papers in Colorants)
Browse Figures
Versions Notes

Abstract

:
A convergent synthetic route to a tetrasaccharide related to PI-88, which allows the incorporation of a fluorescent BODIPY-label at the reducing-end, has been developed. The strategy, which features the use of 1,2-methyl orthoesters (MeOEs) as glycosyl donors, illustrates the usefulness of suitably-designed BODIPY dyes as glycosyl labels in synthetic strategies towards fluorescently-tagged oligosaccharides.

Graphical Abstract

1. Introduction

The recognition of the crucial role of heparanase enzyme, an endo-β-D-glucuronidase able to degrade heparan sulfate (HS) in the extracellular matrix and basement membranes, in a number of pathological processes, such as metastasis and angiogenesis, has triggered the development of heparanase inhibitors [1,2,3,4,5,6]. Among these inhibitors PI-88, a mixture of functionalized mannose oligosaccharides, i.e., 1, 2, (Figure 1), that potently inhibited heparanase and in vitro angiogenesis, has been considered as a promising candidate and has received considerable attention [7]. On the other hand, fluorescent labeling of biomolecules has been recognized as a research topic of great significance, since such labeling facilitates the investigation of glycoconjugates and their interaction in biological systems at high sensitivity [8,9,10,11,12]. Among the types of fluorescent dyes commonly employed as tags, borondipyrromethene (BODIPY, 4, 4-difluoro-4-bora-3a, 4a-diaza-s-indacene) dyes, e.g., 3 (Figure 1) have excelled. Several reasons can be cited for this preference: their high fluorescent quantum yields (∅), excellent photochemical and chemical stabilities, and, arguably, the relatively facile modulation of their photophysical and/or chemical properties by means of synthetic postfunctionalization of their indacene core [13,14,15,16,17,18].
Based on these precedents, we thought it would be of interest to investigate the feasibility of a synthetic approach to BODIPY-labeled PI-88 saccharide components, where the fluorescent dye is incorporated from the beginning of the synthetic sequence. Additionally, we envisioned that the incorporation of the lipophilic BODIPY moiety at the reducing end of a PI-88 saccharide analogue would bring one additional advantage by facilitating the visualization and detection of the synthetic intermediates along the saccharide synthesis [19]. Additionally, in light of some reported literature precedents [20], the incorporation of the lipophilic BODIPY core to the saccharidic ensemble could lead to ameliorated biological activity in the ensuing saccharides. Thus, in this Article, we report a synthetic approach to a PI-88 tetrasaccharide analogue [21] featuring the use of 1,2-methyl orthoester (MeOE) glycosyl donors, i.e., 4 (Figure 1), in which a BODIPY-type fluorescent probe could be attached at the reducing end of the saccharides from the beginning of the synthesis.

2. Results

Several synthetic approaches to analogues of tetra- and pentasaccharides 1 have already been reported [22,23,24,25,26,27,28]. In those approaches, different types glycosyl donors have been employed. We have been interested in the use of 1,2-methyl orthoesters (MeOEs) [29,30,31,32,33] as an inexpensive alternative to Fraser–Reid’s n-pentenyl orthoester glycosyl donors (NPOEs) [34,35,36]. The former derivatives were shown to display good regioselectivity, similar to that of NPOEs [31]. Accordingly, our convergent 1 + 1 + 2 approach to BODIPY-tagged tetramannan, 10 (Scheme 1) was based on our previous studies on the selective mono-glycosylation at position O-3 in mannopyranose substrates possessing a 2,3,4 triol moiety, i.e., 6, 7 (Scheme 1), with MeOE glycosyl donors, 4a, 4b, and 9 [31]. Thus, our strategy involved two glycosidic disconnections A and B (Scheme 1). Disconnection A (Scheme 1), leading to BODIPY-disaccharide 6, was envisioned by glycosylation of a benzylated mannopyranoside 5, exposing only one hydroxyl group (O-2) for the glycosyl coupling, with MeOE donor 4a. On the other hand, disconnection B (Scheme 1) was imagined by regioselective mono-glycosylation of triol 6, at position O-3’, according to precedents from our research group [31], by a disaccharide MeOE donor, 9.
The synthetic route started with the glycosylation of BODIPY 11 [37], readily available through a one-pot transformation using phthalide and pyrrole as the starting materials, followed by in situ coordination with BF3.OEt2 [38], with methyl orthoester 4c, to yield BODIPY glycoside 12 (80% yield, Scheme 2a). However, attempted saponification of the 2-O-Bz substituent in 12, by treatment with Et3N or NaOMe in methanol, resulted in the production of the undesired B(OMe)2-BODIPY derivatives 13 and 14, where the fluorine atoms were replaced by methoxy groups (Scheme 2a). These derivatives, although also fluorescent [39], proved to be labile under the acidic conditions required in the next glycosylation events. We then turned our attention to borondiphenyl BODIPY 15, a more chemically robust yet fluorescent BODIPY analogue [40]. Access to 15 was also affected by slightly modifying our one-pot procedure [38], from phthalide and pyrrole, by simply replacing BF3.OEt2 by B(Ph)3 in the borondipyrromethene ring closing reaction (Scheme 2b) [41].
The synthetic routes to the two fragments in the convergent approach to PI-88 tetrasaccharide analogue 10, glycosyl acceptor 6 and glycosyl donor 9, are depicted in Scheme 3a,b. Thus, glycosylation of hydroxymethyl BODIPY 15 with benzylated MeOE 4c, followed by saponification (NaOMe/MeOH), led to BODIPY-mannopyranoside 5 (Scheme 3a). The latter was then glycosylated with tri-O-benzoyl MeOE 4a, to yield BODIPY disaccharide 16a in moderate yield (52%). Next, protecting group manipulations in compound 16a, including de-O-benzoylation leading to tetraol 16b, and selective monosilylation at the primary hydroxyl group at O-6’ in the latter [terbutyldiphenylsilyl chloride, 4-dimethylaminopyridine (DMAP), in dimethyl formamide (DMF)] produced 2’,3’,4’-triol 6, (Scheme 3a).
On the other hand, the route to MeOE-disaccharide donor 9 started from phenyl thiomannopyranoside 7 (Scheme 3b). Accordingly, regioselective mono-glycosylation at O-3 of 2,3,4-triol 7 with MeOE 4b, based on precedents from our research group [31,42], yielded phenyl 1-thiomannopyranoside 8 in good yield (Scheme 3b). To conclude, a three-step sequence from 8, including perbenzoylation, anomeric bromination, and orthoester formation from an intermediate glycosyl bromide according to Wei et al. [43], allowed its conversion to MeOE disaccharide donor 9 (Scheme 3b).
Finally, glycosyl acceptor 6, containing a mannopyranoside triol unit, was regioselectively mono-glycosylated at O-3’with MeOE disaccharide 9 [44], to yield PI-88 tetrasaccharide precursor analogue 10, in 53% yield (Scheme 4). An alternative glycosylation of 6 with a MeOE monosaccharide, e.g., 4a or 4b, rather than with a disaccharide, i.e., 9, in our hands consistently led to low yields of the trisaccharide analogue.
To impel the advanced applications of the new glycoprobes, we analyzed the photonic behavior of BODIPY 15 and its saccharide derivatives 16a and 10, under low (photophysical properties) and high (laser properties) irradiation regimes. The replacement of the fluorine atoms at the boron bridge, as in 11 [38], by phenyl groups, as in 15 [45], had low impact on the spectral properties of BODIPY (Figure 2) but induced both a decrease of the emission efficiency (Table 1) and a biexponential character of the fluorescent lifetime (Table S1), regardless of the environmental properties. The free motion of these phenyl rings chelating the boron atom reduced the planarity of the dipyrrin core (computed bending angles in the dipyrrin core up to 16° in the excited state, Figure 2), increasing the internal conversion processes with a deleterious effect on the fluorescence signal. The labelling of a disaccharide or tetrasaccharide with BODIPY 15, as in compound 16a and 10, respectively, widened the absorption spectrum, while the spectral profile of fluorescence matched that of its precursor (Figure 2). It is noteworthy that BODIPYs 10 and 16a displayed a brighter fluorescence with longer lifetimes than their non-glycosylated counterpart 15 in all tested media and regardless of the number of saccharide units appended (Table 1 and Table S1). Thus, glycosylation of the ortho-hydroxymethyl group of the C-8-aryl residue led to a more rigid and compact molecular structure, e.g., 16a and 10, owing to the higher steric hindrance imposed by the bulky disaccharide. In fact, the structural arrangement of the C-8-benzyl residue in 16a was nearly orthogonal (twisting dihedral angle computed in the ground state of 75° in 15 vs. 85° in 16a), reducing the internal conversion pathways associated to conformational freedom. Consequently, BODIPY-saccharides 16a and 10 behaved as efficient and stable fluorescent glycoprobes even under laser irradiation conditions, exhibiting a lasing efficiency up to 38% in the green spectral region (540 nm, Table 1) with high photostability, since their laser emission remained at the initial level even after 70,000 pump pulses. This good tolerance to intense and prolonged irradiation is a highly desirable property for fluorescent labels to provide long-lasting bioimages. Therefore, from a photonic point of view, the ortho- position of 8-phenyl BODIPYs is highlighted as a suitable grafting position to tag (oligo)saccharides, even resulting in an amelioration of the photonic performance of the original labeling dye.

3. Conclusions

In summary, we developed a convergent, efficient, synthetic strategy to BODIPY-labeled PI-88 tetrasaccharide components (10) [46], which serves to illustrate the scope and usefulness of MeOEs as glycosyl donors. The inclusion of the BODIPY-tag from the beginning of the synthesis facilitates the visual recognition (thin-layer chromatography, TLC) of the labeled-saccharide acceptor and the glycosylated products therefrom, among the rest of the non-fluorescent side-products arising from side-reactions of the MeOE glycosyl donor [36]. This feature becomes particularly appealing when excess amounts of glycosyl donors are required to lead the glycosylation to completion. On the other hand, the chemically stable 4, 4’-diphenyl BODIPY derivative (15), used as a tag, displayed good fluorescent properties and photostability under strong and prolonged irradiation, and was also able to withstand all reaction conditions employed in the synthetic sequence leading to 10 [20]. Our results also indicate that the incorporation of carbohydrate subunits at the ortho-hydroxymethyl group of the C-8-aryl substituent has a beneficial effect on the, already, good photophysical features of the BODIPY dye.

4. Materials and Methods

4.1. General Information

The solvents and reagents used in the transformations included in the manuscript were obtained from commercial sources. In the glycosylation experiments, the adventitious water content was removed by repeated evaporation of the sample with toluene. The temperature at which the reactions were carried out will be mentioned unless room temperature was used. The glycosylation reactions were carried out in dried flasks fitted with rubber septa under an argon atmosphere.
A 5.0 M stock solution of triethyloxonium tetrafluoroborate, employed in the preparation of the BODIPYs, was prepared by dissolving 25 g (0.131 mmol) of the salt in 26.3 mL of anhydrous methylene chloride.
Anhydrous MgSO4 was used to dry organic solutions during workup. Evaporation of the solvents was performed using a rotary evaporator (Buchi, Flawil, Switzerland). Flash column chromatography was used to purify or separate the samples. Thin-layer chromatography (TLC) was conducted on Kieselgel 60 F254. Spots corresponding to BODIPY-containing molecules were spotted under visible light. TLCs were then inspected under UV irradiation (254 nm) followed by charring with a solution of 20% aqueous H2SO4 (200 mL) in AcOH (800 mL). 1H and 13C-NMR spectra were recorded in CDCl3 at 300, 400, or 500 MHz and 75, 101, or 126 MHz, respectively. Chemical shifts are expressed in parts per million (δ scale) downfield from tetramethylsilane and are referenced to residual protium in the NMR solvent (CHCl3: δ 7.25 ppm, CD3OD: δ 4.870 ppm). Coupling constants (J) are given in Hz. All presented 13C-NMR spectra are proton decoupled. Mass spectra were recorded by direct injection with an Accurate Mass Q-TOF LC/MS spectrometer (Agilent Technologies, Santa Clara, CA, USA) equipped with an electrospray ion source in positive mode.

4.2. General Procedures

4.2.1. General Procedure for Glycosylation. Procedure A

A previously dried mixture of a glycosyl donor and glycosyl acceptor was dissolved in anhydrous dichloromethane (≈3 mL/0.1 mmol). Previously dried (200 °C, one night) 4Å molecular sieves were added to the mixture. The reaction was cooled to −30 °C, and then BF3.OEt2 (3.0 equiv) was added. After 5–10 min, the reaction mixture was diluted with dichloromethane and the ensuing solution washed with saturated aqueous NaHCO3 solution. The organic layer was dried over Na2SO4, filtered, and evaporated under vacuum. The resulting crude mixture was purified by chromatography on silica gel (eluent: hexane-ethyl acetate mixtures).

4.2.2. General Procedure for Debenzoylation. Procedure B

The corresponding compound was dissolved in methanol (25 mL/ mmol) and triethylamine (6 mL/ mmol) was added to the resulting solution. The reaction mixture was refluxed overnight, the solvents evaporated, and the ensuing residue concentrated. Purification by flash chromatography was carried out using hexane-ethyl acetate mixtures, as eluent.

4.2.3. General Procedure for Silylation. Procedure C

The corresponding compound was dissolved in dry DMF (20 mL/mmol), and to this solution imidazole (4 equiv.) was added. After stirring for 5–10 min in an ice bath, under argon, terbutyldiphenylsilyl chloride (1.2 equiv.) and a small amount of dimethylaminopiridine DMAP were added. The ice bath was removed, and the reaction mixture was left with stirring at room temperature for 24 h. The reaction mixture was then diluted with ethyl acetate and extracted with a saturated aqueous NaHCO3 solution and brine. The combined organic solutions were dried over anhydrous MgSO4 and evaporated under vacuum. The resulting crude mixture was purified by chromatography on silica gel (eluent: hexane-ethyl acetate mixtures).

4.2.4. General Procedure for Characterization of Polyol Derivatives as Peracetates. Procedure D

The corresponding polyol was dissolved in pyridine (1 mL/0.1 mmol substrate) and acetic anhydride (0.5 mL/mmol substrate) was then added. The reaction mixture was stirred at room temperature (normally 24 h). After completion of the reaction (t.l.c.), the solvent was evaporated, and the resulting crude mixture was purified by chromatography on silica gel (eluent: hexane-ethyl acetate mixtures).

4.3. Synthesis

4.3.1. BF2-Bodipy 11

This compound was prepared according to our previously described method [38], from phthalide and pyrrole.

4.3.2. Mannopyranosyl BODIPY 12

This compound was prepared by glycosylation of BODIPY 11 (26 mg, 0.088 mmol) with orthoester 4c (100 mg, 0.178 mmol), according to the general procedure for glycosylation, procedure A. Flash chromatography (hexane- ethyl acetate; 85:15) yielded BODIPY-mannoside 12 (64 mg, 80%). 1H-NMR (500 MHz, CDCl3) δ 8.05–7.16 (m, 24H), 6.68 (dd, J = 12.4, 4.2 Hz, 2H), 6.47 (dd, J = 4.2, 1.8 Hz, 1H), 6.33 (dd, J = 4.3, 1.8 Hz, 1H), 5.40 (dd, J = 3.1, 1.9 Hz, 1H), 4.86 (d, J = 1.9 Hz, 1H), 4.79 (d, J = 10.7 Hz, 1H), 4.72–4.65 (m, 3H), 4.52–4.42 (m, 4H), 4.37 (d, J = 11.8 Hz, 1H), 4.01 (t, J = 9.6 Hz, 1H), 3.88–3.75 (m, 3H), 3.58 (dd, J = 10.9, 1.9 Hz, 1H), 3.50–3.44 (m, 1H) 13C-NMR (125 MHz, CDCl3) δ 165.7, 145.3, 145.2, 144.8, 138.7, 138.6, 138.2, 135.7, 135.4, 133.2, 132.9, 132.6, 131.2, 131.0 (×2), 130.2, 130.1 (×2), 130.0, 128.9, 128.5, 128.4 (×5), 128.2 (×2), 127.9, 127.7 (×2), 127.6 (×2), 119.2, 118.8, 97.5, 78.1, 75.3, 74.1, 73.5, 72.0, 71.6, 68.8 (×3), 68.3, 67.3, 51.1, 29.8; 19F-NMR (376 MHz, CDCl3) δ −145.4 (q, JB–F = 28.9 Hz), −145.4 (q, JB–F = 28.9 Hz); HRMS (ESI-TOF): calc for C50H49BF2N3O7 [M + NH4]+; 852.37407 found 852.36969.

4.3.3. Mannopyranosyl BODIPY 13

This compound was obtained when applying the general procedure for debenzoylation, procedure B, to BODIPY-mannoside 12 (60 mg, 0.087 mmol) followed by flash chromatography (hexane- ethyl acetate; 6:4). Compound 13 (56 mg, 78%): 1H-NMR (300 MHz, CDCl3) δ 8.04–7.12 (m, 24H), 6.66 (ddd, J = 10.4, 4.2, 1.1 Hz, 2H), 6.48 (ddd, J = 4.2, 1.8, 0.7 Hz, 1H), 6.43 (ddd, J = 4.2, 1.8, 0.7 Hz, 1H), 5.42 (dd, J = 3.1, 2.0 Hz, 1H), 4.87–4.77 (m, 2H), 4.74–4.60 (m, 3H), 4.51–4.36 (m, 4H), 4.04 (t, J = 9.5 Hz, 1H), 3.98–3.88 (m, 1H), 3.78 (dd, J = 10.6, 3.5 Hz, 1H), 3.66–3.53 (m, 2H) 3.12 (s, 3H), 3.03 (s, 3H); 19F-NMR (376 MHz, CDCl3): showed not peaks at all; HRMS (ESI-TOF): calc for C52H51BN2NaO9 [M + Na]+; 881.35682 found 881.35690.

4.3.4. Mannopyranosyl BODIPY 14

Treatment of compound 12 (80 mg, 0.096 mmoles) with sodium methoxide in MeOH, at 65 °C for 1 h resulted in the consumption of the starting material. Then, addition of solid NH4Cl and stirring for 15 min followed by filtration and solvent evaporation provided a residue that was purified by chromatography on silica gel (hexane-ethyl acetate; 3:7) to give dimethoxyboron-derivative 14 (56 mg, 78%). 1H-NMR (300 MHz, CDCl3) δ 7.88–7.03 (19H), 6.68 (dd, J = 4.2, 1.3 Hz, 1H), 6.60 (dd, J = 4.2, 1.3 Hz, 1H), 6.42 (dt, J = 4.3, 1.8 Hz, 1H), 4.74 (d, J = 10.8 Hz, 1H), 4.59–4.35 (m, 9H), 3.78–3.50 (m, 6H), 3.38–3.33 (m, 1H), 3.20 (s, 3H), 3.06 (s, 3H); 13C-NMR (125 MHz, CDCl3) δ 152.8, 144.9, 144.5, 136.7, 136.6, 135.7, 133.7, 133.6, 130.4, 130.0, 129.8, 129.7, 129.4, 128.5 (×2), 128.4 (×2), 128.3 (×2), 128.1 (×2), 128.0 (×2), 127.8 (×2), 127.7 (×2), 118.5, 118.1, 100.6, 79.9, 75.2, 74.1, 73.6, 71.7, 71.4, 69.1, 68.5, 68.3, 67.3, 50.3, 49.8 HRMS (ESI-TOF): calc for C45H47BN2NaO8 [M + Na]+; 777.33254 found 777.33546.

4.3.5. B(Ph)2-BODIPY 15

This compound was prepared by treatment of a toluene solution of a dipyrromethane intermediate (obtained by reaction of phthalide with pyrrole) (44 mg, 0.198 mmol), with triphenylborane (48 mg, 0.198 mmol). The mixture, under argon, was refluxed for 24 h. Then, the solvent was evaporated, and the residue dissolved in dichloromethane (10 mL), to which 10 mL of a 1M solution of NaOH were added. The ensuing mixture was kept with stirring for one night. The organic layer was separated and dried over MgSO4, filtered, and evaporated. The residue was purified by for chromatography on silica gel (hexane-ethyl acetate; 8:2) to afford compound 15 (38 mg, 46%). 1H-NMR (400 MHz, CDCl3) δ 7.64–6.97 (m, 14H), 6.75 (d, J = 4.2 Hz, 2H), 6.55–6.39 (m, 2H), 4.35 (s, 2H) 13C-NMR (100 MHz, CDCl3) δ 145.5 (×2), 145.1, 139.7, 135.5, 133.8 (×2), 132.5, 131.7 (×2), 129.8, 129.7, 128.7 (×2), 128.2, 127.6 (×3), 127.1, 126.7, 126.2, 118.0 (×2), 62.9 HRMS (ESI-TOF): calc for C28H24BN2O8 [M + H]+; 415.19812 found 415.19815.

4.3.6. Mannopyranosyl BODIPY 5

This compound was prepared by glycosylation of BODIPY 15 (73 mg, 0.176 mmol) with MeOE 4c (150 mg, 0.264 mmol), according to the general procedure for glycosylation, procedure A. After standard work-up, purification by flash chromatography (hexane- ethyl acetate; 9:1) furnished a mixture of the 2-O-benzoyl derivative of compound 5 (102 mg, 72%) and “rearranged” methyl mannopyranoside (1HNMR). This mixture was dissolved in MeOH, under argon, and treated with NaOMe/MeOH at room temperature for 24 h. When t.l.c. showed disappearance of the fluorescent starting material, solid NH4Cl was added. The resulting solution was kept with stirring for 15 min, filtered, and the solvent was evaporated. Purification by flash chromatography (hexane-ethyl acetate; 7:3) allowed the isolation of BODIPY-mannoside 5 (92 mg, 87%). 1H-NMR (500 MHz, CDCl3) δ 7.61 (s, 1H), 7.52 (s, 1H) 7.47–7.09 (m, 29H), 6.70 (dd, J = 26.9, 4.3 Hz, 2H), 6.43–6.34 (m, 2H), 4.74 (d, J = 10.7 Hz, 1H), 4.60 (d, J = 12.2 Hz, 1H), 4.53–4.39 (m, 4H), 4.37 (bs, 2H), 4.28 (d, J = 11.6 Hz, 1H), 3.73 (t, J = 9.5 Hz, 1H), 3.64–3.46 (m, 4H), 3.39–3.35 (m, 1H); 13C-NMR (125 MHz, CDCl3) δ 145.3 (×2), 145.2, 138.4, 138.1, 136.0, 135.6, 134.9, 133.8, 133.5 (×2), 132.2 (×3), 130.2, 129.6, 129.5, 129.2, 129.1, 128.6 (×2), 128.5 (×2), 128.4 (×3), 128.1 (×2), 128.0 (×2), 127.9, 127.8 (×2), 127.7 (×2), 127.6 (×2), 126.6, 126.3, 117.8, 117.6, 98.6, 80.2, 75.3, 74.1, 73.5 (×2), 71.7, 71.3, 68.8, 67.7, 67.3 HRMS (ESI-TOF): calc for C55H55BN3O6 [M + NH4]+; 846.41876 found 846.41891.

4.3.7. BODIPY Disaccharide 16a

This compound was prepared by glycosylation of 5 (70 mg, 0.083 mmol) with MeOE 4a (57 mg, 0.100 mmol), according to the general procedure for glycosylation, procedure A. Purification by flash chromatography (hexane-ethyl acetate; 7:3) afforded compound 16a (62 mg, 52%). 1H-NMR (400 MHz, CDCl3) δ 8.08–7.05 (m, 49 H), 6.69 (ddd, J = 12.0, 4.3, 1.2 Hz, 2H), 6.39 (ddd, J = 19.1, 4.3, 1.8 Hz, 2H), 6.11 (t, J = 10.1 Hz, 1H), 5.93 (dd, J = 10.1, 3.2 Hz, 1H), 5.87 (dd, J = 3.2, 1.9 Hz, 1H), 5.17 (d, J = 2.0 Hz, 1H), 4.84 (d, J = 10.9 Hz, 1H), 4.80 (d, J = 1.9 Hz, 1H), 4.66 (d, J = 12.3 Hz, 1H), 4.60–4.39 (m, 7H), 4.42 (d, J = 12.1 Hz, 1H), 4.33 (dd, J = 12.3, 3.6 Hz, 1H), 4.24 (d, J = 12.0 Hz, 1H), 4.00 (t, J = 9.6 Hz, 1H), 3.79 (d, J = 2.4 Hz, 1H), 3.75–3.63 (m, 2H), 3.61–3.52 (m, 2H); 13C-NMR (125 MHz, CDCl3) δ 166.2, 165.6, 165.3, 165.1, 145.5, 145.4, 144.9, 138.5, 138.5, 138.3, 136.0, 135.2 (×2), 133.5 (×2), 133.2 (×3), 133.1 (×2), 132.5 (×2), 132.4, 130.3, 130.2, 130.0 (×6),129.9 (×2), 129.6 (×2), 129.4 (×2), 129.1, 128.9, 128.7 (×2), 128.6 (×2), 128.5 (×4), 128.4 (×5), 128.3 (×2), 127.9 (×3), 127.8, 127.7 (×2), 127.6 (×2), 127.5 (×3), 126.4 (×2) (65 signals for aromatic carbons) 117.8, 117.7, 99.4, 97.8, 79.5, 75.9, 75.2, 74.4, 73.3 (×2), 72.2, 72.0, 70.2, 70.0, 69.1, 68.7, 66.8, 66.7, 62.6 HRMS (ESI-TOF): calc for C89H77BKN2O15 [M + K]+; 1447.51131 found 1447.51484 (M + K)+.

4.3.8. BODIPY-Disaccharide Tetraol 16b

This compound was prepared according to the general procedure for debenzoylation, procedure B, from compound 16a (60 mg, 0.087 mmol). Purification by flash chromatography (hexane-ethyl acetate; 2:8) afforded fluorescent disaccharide 16b (40 mg, quantitative yield). 1H-NMR (500 MHz, CDCl3) δ 7.56–7.11 (m, 29H), 6.69–6.66 (m,2H), 6.37 (ddd, J = 12.6, 4.3, 1.8 Hz, 2H), 4.93 (bs, 1H), 4.74 (d, J = 10.8 Hz, 1H), 4.67 (bs, 1H) 4.56–4.51 (m, 2H), 4.42–4.36 (m, 4H), 4.25 (d, J = 12.3 Hz, 1H), 3.98 (bs, 1H), 3.87–3.77 (m, 5H), 3.69–3.64 (m,3H), 3.59–3.52 (m, 4H), 3.44–3.37 (m, 4H) 13C-NMR (125 MHz, CDCl3) δ 145.5, 145.3, 145.0, 138.5 (×2), 138.4, 136.0, 135.2, 135.1, 133.7, 133.4, 133.2 (×2), 133.1, 132.9, 132.5 (×2), 130.3, 130.2, 129.6, 129.1, 128.8 (22), 128.5 (×5), 128.4 (×2), 128.0 (×2), 127.8 (×3), 127.7 (×3), 127.6 (×4), 126.5, 126.4, 117.9 (×2), 101.5, 97.6, 79.5, 75.3, 75.2, 74.4, 73.4, 72.5, 72.1, 72.0, 71.6, 70.9, 68.8, 66.6, 61.6; API-ES positive mode: [M + Na]+ = 1031.3.

4.3.9. BODIPY-Disaccharide Silylated Triol 6

The general procedure for silylation, procedure C, was applied to tetraol 16b (56 mg, 0.056 mmol), although this time pyridine, rather than DMF, was used as solvent. Purification by flash chromatography (hexane-ethyl acetate; 6:4) yielded triol 6 (48 mg, 69%). 1H-NMR (400 MHz, CDCl3) δ 7.72–7.10 (m, 39H), 6.64 (ddd, J = 5.6, 4.3, 1.2 Hz, 2H), 6.34 (ddd, J = 12.6, 4.3, 1.8 Hz, 2H), 4.97 (d, J = 1.7 Hz, 1H), 4.76 (d, J = 10.8 Hz, 1H), 4.65–4.59 (m, 2H), 4.54–4.38 (m, 4H), 4.36 (bs 2H), 4.18 (d, J = 12.2 Hz, 1H), 3.99 (bs, 1H), 3.87–3.57 (m, 13H), 3.45–3.40 (m, 2H),1.04 (s, 9H) 13C-NMR (100 MHz, CDCl3) δ 145.5, 145.4, 145.1, 138.8, 138.7, 138.5, 136.1, 135.8, 135.2, 133.4, 133.2, 133.1, 133.0, 132.7, 130.2, 129.5, 129.3, 128.6, 128.5, 128.1, 128.0, 127.8, 127.7, 127.6, 127.5, 126.5 (48 aromatic carbons), 118.0, 117.9, 101.2, 98.1, 79.9, 75.3, 74.6, 73.5 (×2), 72.3, 72.1 (×2), 71.5 (×2), 71.4, 70.5 (×2), 70.1, 69.1, 66.6, 65.1, 53.7, 27.1 (×3), 19.5; API-ES, positive mode: [M + Na]+ = 1269.30; HRMS (ESI-TOF): calc for C156H155BN2O26Si3 [M + Na]+; 2591.02041 found 2591.01683.

4.3.10. Thioglycosyl Disaccharide 8

According to the general procedure for glycosylation, procedure A, thioglycoside 7 (50 mg, 0.098 mmol) was glycosylated with orthoester 4b (146 mg, 0.196 mmol) in CH2Cl2 (3 mL). After 5 min, the reaction was quenched, the organic extract concentrated, and the resulting residue chromatographed over silica gel flash column (hexane-ethyl acetate; 9:1) to give diol 8 (65 mg, 58%). For the sake of characterization, and according to the general procedure for acetylation, procedure D, the corresponding peracetyl derivative 8-Acet was prepared (68 mg, quantitative yield). [α]D21: −39.3°, (c 0.8, CHCl3) 1H-NMR (400 MHz, CDCl3) δ 8.18–7.10 (m, 40H), 6.35 (t, J = 10.2 Hz, 1H), 5.71 (dd, J = 10.3, 3.3 Hz, 1H), 5.53–5.45 (m, 4H), 5.32 (d, J = 1.8 Hz, 1H), 4.38–4.34 (m, 1H), 4.25–4.20 (m, 2H), 3.92–3.80 (m, 2H), 3.78–3.61 (m, 2H), 2.20 (s, 3H), 2.12 (s, 3H), 1.07 (s, 9H), 1.06 (s, 9H) 13C-NMR (100 MHz, CDCl3) δ 170.5, 170.1, 165.8, 165.6, 165.5, 136.0 (×4), 135.9 (×2), 135.7 (×2), 133.9, 133.7, 133.5, 133.4, 133.3, 133.2, 133.0, 131.9 (×2), 130.2 (×2), 130.0 (×4), 129.9 (×2), 129.8, 129.7 (×2), 129.5 (×2), 129.3 (×2), 128.8 (×2), 128.6 (×2), 128.5 (×2), 127.9 (×4), 127.8 (×2), 99.4, 86.3, 75.6, 73.3, 72.9, 72.2, 71.2, 70.3, 68.2, 66.2, 63.2, 61.9, 26.95 (×3), 26.86 (×3), 21.7, 21.0, 19.5 (×2); API-ES, positive mode:1324.5 [M + NH4]+.

4.3.11. 1,2-Methyl Orthoester Disaccharide 9

Benzoylation (BzCl, pyridine) of compound 8 (498 mg, 0.41 mmol), followed by purification by flash chromatography (hexane-ethyl acetate; 85:15) provided the corresponding benzoylated disaccharide intermediate 8-Bzl (450 mg, 88%). A portion of this compound (298 mg, 0.208 mmol) was dissolved in CH2Cl2 (3 mL), and cooled to 0 ºC, in the darkness, then bromine (15 μL, 0.314 mmol) was added. When the starting material had disappeared (t.l.c.) the reaction mixture was washed with 10% aqueous sodium thiosulfate solution containing sodium bicarbonate saturated aqueous solution, and water. The organic extract was dried over Na2SO4, filtered, and concentrated. Without further purification, the residue was dissolved in acetonitrile (1 mL) to which solution, methanol (84 μL), tetrabutylammonium bromide (Bu4NBr) (47 mg), sodium bicarbonate (35 mg), and molecular sieves 4Å (previously dried) were added. The resulting reaction mixture was stirred for one night, the molecular sieves were then filtered, and the solvent concentrated. The ensuing residue was purified by flash chromatography (hexane-ethyl acetate; 9:1, containing 1% of triethylamine ) to afford the 1,2-methyl orthoester disaccharide 9 (182.6 mg, 65% (two steps)) [α]D21: −89.2 (c 1.2, CHCl3) 1H-NMR (400 MHz, CDCl3) δ 8.05–7.09 (m, 45H), 6.20 (t, J = 10.1 Hz, 1H), 5.84 (dd, J = 10.2, 3.3 Hz, 1H), 5.62 (dd, J = 9.8, 8.7 Hz, 1H), 5.50 (d, J = 3.0 Hz, 1H), 5.44 (dd, J = 3.4, 1.8 Hz, 1H), 5.27 (d, J = 1.8 Hz, 1H), 4.84 (dd, J = 4.1, 3.0 Hz, 1H), 4.50 (d, J = 10.1 Hz, 1H), 4.23 (d, J = 9.8 Hz, 1H), 3.95–3.88 (m, 2H), 3.77–3.62 (m, 3H), 2.96 (s, 3H), 1.06 (s, 9H), 0.91 (s, 9H).13C-NMR (100 MHz, CDCl3) δ 165.5, 165.3 (×2), 165.2, 136.2, 136.0 (×2), 135.8 (×6), 133.5, 133.4, 133.3, 133.2, 133.1, 130.1 (×4), 130.0 (×2), 129.9 (×3), 129.8 (×2), 129.7 (×3), 129.6, 129.5, 129.4, 128.7 (×2), 128.6 (×2), 128.5 (×2), 128.4 (×4), 127.8 (×3), 127.7 (×4), 126.9 (×2), 122.9, 100.1, 98.1, 78.6, 77.9, 75.5, 72.2, 71.0, 70.5, 68.2, 66.6, 63.7, 62.4, 51.5, 26.9 (×3), 26.9 (×3), 19.5, 19.3 HRMS (ESI-TOF): calc for C80H84NO16Si2 [M + NH4]+ 1370.5323; found 1370.5323 [M + NH4]+.

4.3.12. BODIPY-Tetrasaccharide 10

BODIP disaccharide 6 (21 mg, 0.017 mmol) was glycosylated with glycosyl donor 9 (vide infra) (45 mg, 0.034 mmol), according to the general procedure for glycosylation, procedure A. Purification by flash chromatography (hexane-ethyl acetate; 8:2) yielded tetrasaccharide 10 (23 mg, 53%). 1H-NMR (500 MHz, CDCl3) δ 8.05–6.98 (m, 84H), 6.62 (td, J = 4.3, 1.3 Hz, 2H), 6.31 (dd, J = 4.3, 1.8 Hz, 1H), 6.28 (dd, J = 4.3, 1.8 Hz, 1H), 6.21 (t, J = 10.1 Hz, 1H), 5.66 (d, J = 8.7 Hz, 1H), 5.59–5.52 (m, 2H), 5.40 (bs, 1H) 5.37 (m, 1H), 5.31 (bs, 1H), 5.20 (bs, 1H), 4.71–4.69 (m, 2H), 4.62–4.45 (m, 6H), 4.39–4.28 (m, 5H), 4.21–4.03 (m, 4H), 3.99–3.68 (m, 12H), 3.64–3.56 (m, 2H), 3.49–3.35 (m, 4H), 1.02 (s, 9H), 0.99 (s, 9H), 0.95 (s, 9H) 13C-NMR (125 MHz, CDCl3) δ 165.7, 165.5, 165.2, 165.0 (×2), 145.4, 145.3, 144.9, 138.6, 138.6, 138.4, 138.0, 136.2, 135.9 (×4), 135.8 (×3), 135.7 (×3), 135.6 (×4), 135.1, 133.6, 133.5, 133.4, 133.3, 133.2, 133.1(×3), 133.0, 132.9, 132.7 (×2), 132.6 (×2), 132.3, 130.2 (×2), 130.1 (×2), 130.0 (×2), 129.9, 129.8 (×6), 129.7 (×2), 129.5 (×2), 129.4 (×2), 129.2 (×3), 128.8, 128.7, 128.5 (×4), 128.4 (×11), 128.2, 128.0, 127.9, 127.8, 127.7 (×5), 127.6, 127.4 (×4), 127.2, 126.5, 126.4, 125.4, 117.9 (×2), 101.1, 99.1, 98.2, 98.0, 81.5, 80.1, 76.2, 75.1, 74.6, 73.4 (×2), 72.9, 72.3 (×2), 72.2, 72.0, 71.9 (×2), 71.8, 70.6, 70.4, 69.5, 69.1, 68.3, 66.6, 66.2, 65.8, 64.4, 63.8, 61.5, 53.6, 27.0 (×3), 26.8 (×3), 26.7 (×3), 19.5, 19.3, 19.0; HRMS (ESI-TOF): calc for C156H155BN2O26Si3 [M + Na]+; 2591.02041 found 2591.01683.

Supplementary Materials

The following are available online, Phtophysical data (Table S1). Experimental conditions for photophysical properties, and quantum mechanical calculations. 1H- and 13C-NMR of all compounds.

Author Contributions

Development of the synthetic scheme, structural analysis of the saccharide derivatives, conceptualization of the results, J.V.; Design of the saccharide synthesis, conceptualization of the results, C.U.; Design of the saccharide and BODIPY syntheses, preparation of the manuscript, A.M.G.; Photophysical experiments, E.A.-Z.; Photophysical experiments, conceptualization of the results, preparation of the manuscript, J.B.; Laser experiments, supervision, I.G.-M.; Conceptualization of the results, supervision, manuscript preparation, J.C.L.; Funding acquisition, A.M.G., J.B., I.G.-M., J.C.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Spanish MINISTERIO DE ECONOMIA Y COMPETITIVIDAD, GOBIERNO DE ESPAÑA (projects MAT2017–83856-C3-1-P and 3-P, PiD2020-1147555GB-C33), the MINISTERIO DE CIENCIA INNOVACION Y UNIVERSIDADES (project RTI2018-094862-B-I00), and the GOBIERNO VASCO (project IT912-16).

Data Availability Statement

Data sharing is not applicable to this article.

Acknowledgments

E.A.-Z. Thanks the MINISTERIO DE ECONOMIA Y COMPETITIVIDAD for a postdoctoral contract. The authors thank SGIker of UPV/EHU for technical support with the computational calculations, which were carried out in the “arina” informatic cluster.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Sample Availability

No samples of the compounds are available from the authors.

References

  1. Ferro, V.; Hammond, E.; Fairweather, J.K. The development of inhibitors of heparanase, a key enzyme involved in tumour metastasis, angiogenesis and inflammation. Rev. Med. Chem. 2004, 4, 693–702. [Google Scholar] [CrossRef] [PubMed]
  2. Hammond, E.; Bytheway, I.; Ferro, V. Heparanase as a target for anticancer therapeutics: New developments and future prospects. In New Developments in Therapeutic Glycomics; Delehedde, M., Lortat-Jacob, H., Eds.; Research Signpost: Trivandrum, India, 2006; pp. 251–282. [Google Scholar]
  3. Miao, H.Q.; Liu, H.; Navarro, E.; Kussie, P.; Zhu, Z. Development of heparanase inhibitors for anti-cancer therapy. Curr. Med. Chem. 2006, 13, 2101–2111. [Google Scholar]
  4. McKenzie, E.A. Heparanase: A target for drug discovery in cancer and inflammation. Br. J. Pharmacol. 2007, 151, 1–14. [Google Scholar] [CrossRef] [Green Version]
  5. Jia, L.; Ma, S. Recent advances in the discovery of heparanase inhibitors as anticancer agents. Eur. J. Med. Chem. 2016, 121, 209–220. [Google Scholar] [CrossRef]
  6. Chhabra, M.; Ferro, V. The development of assays for heparanase enzymatic activity: Towards a gold standard. Molecules 2018, 23, 2971. [Google Scholar] [CrossRef] [Green Version]
  7. Chhabra, M.; Ferro, V. PI-88 and related heparan sulfate mimetics. In Heparanase: From Basic Research to Clinical Applications, 1st ed.; Vlodavsky, I., Sanderson, R.D., Ilan, N., Eds.; Springer-Nature: Cham, Switzerland, 2020; Chapter 19; pp. 473–492. [Google Scholar]
  8. Mechref, Y.; Novotny, M.V. Structural investigations of glycoconjugates at high sensitivity. Chem. Rev. 2002, 102, 321–369. [Google Scholar] [CrossRef]
  9. Xia, B.; Kawar, Z.S.; Ju, T.; Alvarez, R.A.; Sachdev, G.P.; Cummings, R.D. Versatile fluorescent derivatization of glycans for glycomic analysis. Nat. Methods 2005, 2, 845–850. [Google Scholar] [CrossRef] [PubMed]
  10. Kobayashi, H.; Ogawa, M.; Alford, R.; Choyke, P.L.; Urano, Y. New strategies for fluorescent probe design in medical diagnostic imaging. Chem. Rev. 2010, 110, 2620–2640. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Ueno, T.; Nagano, T. Fluorescent probes for sensing and imaging. Nat. Methods 2011, 8, 642–645. [Google Scholar] [CrossRef] [PubMed]
  12. Keithley, R.B.; Rosenthal, A.S.; Essaka, D.C.; Tanaka, H.; Yoshimura, Y.; Palcic, M.M.; Hindsgaul, O.; Dovichi, N.J. Capillary electrophoresis with three-color fluorescence detection for the analysis of glycosphingolipid metabolism. Analyst 2013, 138, 164–170. [Google Scholar] [CrossRef] [Green Version]
  13. Louret, A.; Burgess, K. BODIPY Dyes and their derivatives: Syntheses and spectroscopic properties. Chem. Rev. 2007, 107, 4891–4932. [Google Scholar]
  14. Ziessel, R.; Ulrich, G.; Harriman, A. The chemistry of BODIPY: A new El Dorado for fluorescence tools. New. J. Chem. 2007, 31, 496–501. [Google Scholar] [CrossRef]
  15. Ulrich, G.; Ziessel, R.; Harriman, A. The chemistry of fluorescent BODIPY dyes: Versatility unsurpassed. Angew. Chem. Int. Ed. 2008, 47, 1184–1201. [Google Scholar] [CrossRef] [PubMed]
  16. Boens, N.; Verbelen, B.; Dehaen, W. Postfunctionalization of the BODIPY core: Synthesis and spectroscopy. Eur. J. Org. Chem. 2015, 30, 6577–6595. [Google Scholar] [CrossRef] [Green Version]
  17. Bañuelos, J. BODIPY Dye, the most versatile fluorophore ever? Chem. Rec. 2016, 16, 335–348. [Google Scholar] [CrossRef]
  18. Boens, N.; Verbelen, B.; Ortiz, M.J.; Jiao, L.; Dehaen, W. Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core. Coord. Chem. Rev. 2019, 399, 213024. [Google Scholar] [CrossRef]
  19. Uriel, C.; Permingeat, C.; Ventura, J.; Avellanal-Zaballa, E.; Bañuelos, J.; Garcia-Moreno, I.; Gómez, A.M.; López, J.C. BODIPYs as chemically stable fluorescent tags for synthetic glycosylation strategies towards fluorescently labeled saccharides. Chem. Eur. J. 2020, 26, 5388–5399. [Google Scholar] [CrossRef]
  20. Ekblad, M.; Adamiak, B.; Bergstrom, T.; Johnstone, K.D.; Karoli, T.; Liu, L.; Ferro, V.; Trybala, E. A highly lipophilic sulfated tetrasaccharide glycoside related to muparfostat (PI-88) exhibits virucidal activity against herpes simplex virus. Antivir. Res. 2010, 86, 196–203. [Google Scholar] [CrossRef]
  21. Handley, P.N.; Carroll, A.; Ferro, V. New structural insights into the oligosaccharide phosphate fraction of Pichia (Hansenula) holstii NRRL Y2448 phosphomannan. Carbohydr. Res. 2017, 446–447, 68–75. [Google Scholar] [CrossRef]
  22. Gu, G.; Wei, G.; Du, Y. Synthesis of a 6V-sulfated mannopentasaccharide analogue related to PI-88. Carbohydr. Res. 2004, 339, 1155–1162. [Google Scholar] [CrossRef]
  23. Namme, R.; Mitsugi, T.; Takahashi, H.; Ikegami, S. Synthesis of PI-88 analogue using novel O-glycosidation of exo-methylenesugars. Tetrahedron Lett. 2005, 46, 3033–3036. [Google Scholar] [CrossRef]
  24. Fairweather, J.K.; Hammond, E.; Johnstone, K.D.; Ferro, V. Synthesis and heparanase inhibitory activity of sulfated mannooligosaccharides related to the antiangiogenic agent PI-88. Bioorg. Med. Chem. 2008, 16, 699–709. [Google Scholar] [CrossRef]
  25. Valerio, S.; Pastore, A.; Adinolfi, M.; Iadonisi, A. Sequential one-pot glycosidations catalytically promoted: Unprecedented strategy in oligosaccharide synthesis for the straightforward assemblage of the antitumor PI-88 pentasaccharide. J. Org. Chem. 2008, 73, 4496–4503. [Google Scholar] [CrossRef] [PubMed]
  26. Liu, L.; Johnstone, K.D.; Fairweather, J.K.; Dredge, K.; Ferro, V. An improved synthetic route to the potent angiogenesis inhibitor benzyl Manα(1→3)-Manα(1→3)-Manα(1→3)-Manα(1→2)-Man hexadecasulfate. Aust. J. Chem. 2009, 62, 546–552. [Google Scholar] [CrossRef] [Green Version]
  27. Pastore, A.; Adinolfi, M.; Iadonisi, A.; Valerio, S. One-pot catalytic glycosidation/Fmoc removal−An iterable sequence for straightforward assembly of oligosaccharides related to HIC gp120. Eur. J. Org. Chem. 2010, 4, 711–718. [Google Scholar] [CrossRef]
  28. Mong, K.-K.T.; Shiau, K.-S.; Lin, Y.H.; Cheng, K.-C.; Lin, C.-H. A concise synthesis of single components of partially sulfated oligomannans. Org. Biomol. Chem. 2015, 13, 11550–11560. [Google Scholar] [CrossRef]
  29. Kochetkov, N.K.; Khorlin, A.J.; Bochkov, A.F. New synthesis of glycosides. Tetrahedron Lett. 1964, 5, 289–293. [Google Scholar] [CrossRef]
  30. Kochetkov, N.K.; Khorlin, A.J.; Bochkov, A.F. A new method of glycosylation. Tetrahedron 1967, 23, 693–707. [Google Scholar] [CrossRef]
  31. Uriel, C.; Ventura, J.; Gómez, A.M.; López, J.C.; Fraser-Reid, B. Methyl 1,2-orthoesters as useful glycosyl donors in glycosylation reactions: A comparison with n-pent-4-enyl 1,2 orthoesters. Eur. J. Org. Chem. 2012, 16, 3122–3131. [Google Scholar] [CrossRef]
  32. Uriel, C.; Ventura, J.; Gómez, A.M.; López, J.C.; Fraser-Reid, B. Unexpected stereocontrolled access to 1α,1’β-disaccharides from methyl 1,2-ortho esters. J. Org. Chem. 2012, 77, 795–800. [Google Scholar] [CrossRef] [PubMed]
  33. Uriel, C.; Rijo, P.; Fernandes, A.S.; Gómez, A.M.; Fraser-Reid, B.; López, J.C. Methyl 1,2-orthoesters in acid-washed molecular sieves mediated glycosylations. Chem. Select 2016, 1, 6011–6015. [Google Scholar] [CrossRef]
  34. Lu, J.; Fraser-Reid, B. The antituberculosis, antitumor, multibranched dodecafuranoarabinan of Mycobacterium species has been assembled from a single n-pentenylfuranoside source. Chem. Commun. 2005, 7, 862–864. [Google Scholar] [CrossRef] [PubMed]
  35. Jayaprakash, K.N.; Lu, J.; Fraser-Reid, B. Synthesis of a lipomannan component of the cell-wall complex of Mycobacterium tuberculosis is based on Paulsen’s concept of donor/acceptor “match”. Angew. Chem. Int. Ed. 2005, 44, 5894–5898. [Google Scholar] [CrossRef]
  36. Fraser-Reid, B.; Loópez, J.C. Orthoesters and Related Derivatives. In Handbook of Chemical Glycosylation: Advances in Stereoselectivity and Therapeutic Relevance; Demchenko, A.V., Ed.; Wiley-VCH: New York, NY, USA, 2008; Chapter 5.1. [Google Scholar]
  37. Roacho, R.I.; Metta-Magaña, A.J.; Peña-Cabrera, E.; Pannell, K.H. Synthesis, structural characterization, and spectroscopic properties of the ortho, meta and para isomers of 8-(HOCH2-C6H4)-BODIPY and 8-(MeOC6H4)-BODIPY. J. Phys. Org. Chem. 2013, 26, 345–351. [Google Scholar] [CrossRef]
  38. Del Rio, M.; Lobo, F.; Lopez, J.C.; Oliden, A.; Bañuelos, J.; Lopez-Arbeloa, I.; Garcia-Moreno, I.; Gomez, A.M. One-pot synthesis of rotationally restricted, conjugatable, BODIPY derivatives from phthalides. J. Org. Chem. 2017, 82, 1240–1247. [Google Scholar] [CrossRef]
  39. Bodio, E.; Goze, C. Investigation of B-F substitution of BODIPY and aza-BODIPY dyes: Development of B-O and B-C BODIPYs. Dyes Pigment. 2019, 160, 700–710. [Google Scholar] [CrossRef]
  40. Yang, L.; Simionescu, R.; Lough, A.; Yan, H. Some observations relating to the stability of the BODIPY fluorophore under acidic and basic conditions. Dyes Pigment. 2011, 91, 264–267. [Google Scholar] [CrossRef]
  41. Nguyen, A.L.; Fronczek, F.R.; Smith, K.M.; Vicente, M.G.H. Synthesis of 4,4’-functionalized BODIPYs from dipyrrins. Tetrahedron Lett. 2015, 56, 6348–6351. [Google Scholar] [CrossRef] [Green Version]
  42. Lopez, J.C.; Agocs, A.; Uriel, C.; Gomez, A.M.; Fraser-Reid, B. Iterative, orthogonal strategy for oligosaccharide synthesis based on the regioselective glycosylation of polyol acceptors with partially unprotected n-pentenyl-orthoesters: Further evidence for reciprocal donor acceptor selectivity. Chem. Commun. 2005, 40, 5088–5090. [Google Scholar] [CrossRef] [PubMed]
  43. Wei, S.; Zhao, J.; Shao, H. A facile method for the preparation of sugar orthoesters promoted by anhydrous sodium bicarbonate. Can. J. Chem. 2009, 87, 1733–1737. [Google Scholar] [CrossRef] [Green Version]
  44. Vidadala, S.R.; Thadke, S.A.; Hotha, S. Orthogonal activation of propargyl and n-pentenyl glycosides and 1,2-orthoesters. J. Org. Chem. 2009, 74, 9233–9236. [Google Scholar] [CrossRef] [PubMed]
  45. Duran-Sampedro, G.; Esnal, I.; Agarrabeitia, A.R.; Bañuelos-Prieto, J.; Cerdan, L.; Garcia-Moreno, I.; Costela, A.; Lopez-Arbeloa, I.; Ortiz, M.-J. First highly efficient and photostable E and C derivatives of 4,4,-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) as dye lasers in the liquid phase, thin films, and solid-state rods. Chem. Eur. J. 2014, 20, 2646–2653. [Google Scholar] [CrossRef] [PubMed]
  46. Patel, I.; Woodcock, J.; Beams, R.; Stranick, S.J.; Niewendaal, R.; Gilman, J.W.; Mulenos, M.R.; Sayes, C.M.; Salari, M.; DeLoid, G.; et al. Fluorescently labeled cellulose nanofibers for environmental health and safety studies. Nanomaterials 2021, 11, 1015. [Google Scholar] [CrossRef] [PubMed]
Molecules 26 02909 g001 550
Figure 1. PI-88 (1,2), BODIPY (3), IUPAC numbering) and 1,2-methyl orthoester glycosyl donors (4) used in this study.
Figure 1. PI-88 (1,2), BODIPY (3), IUPAC numbering) and 1,2-methyl orthoester glycosyl donors (4) used in this study.
Molecules 26 02909 g001
Molecules 26 02909 sch001 550
Scheme 1. Retrosynthesis of PI-88 tetrasaccharide analogue 10, involving the sole use of 1,2-methyl orthoester glycosyl donors, 4 and 9.
Scheme 1. Retrosynthesis of PI-88 tetrasaccharide analogue 10, involving the sole use of 1,2-methyl orthoester glycosyl donors, 4 and 9.
Molecules 26 02909 sch001
Molecules 26 02909 sch002 550
Scheme 2. (a) Glycosylation of BODIPY 11 with MeOE 4c and saponification attempts; (b) one-pot synthesis of 4,4-diphenyl BODIPY 15.
Scheme 2. (a) Glycosylation of BODIPY 11 with MeOE 4c and saponification attempts; (b) one-pot synthesis of 4,4-diphenyl BODIPY 15.
Molecules 26 02909 sch002
Molecules 26 02909 sch003 550
Scheme 3. (a) Synthesis of BODIPY disaccharide acceptor 6; (b) access to MeOE-disaccharide donor 9, from thioglycoside 7, by regioselective glycosylation with MeOE 4b and subsequent orthoester formation on the ensuing disaccharidic thioglycoside intermediate 8.
Scheme 3. (a) Synthesis of BODIPY disaccharide acceptor 6; (b) access to MeOE-disaccharide donor 9, from thioglycoside 7, by regioselective glycosylation with MeOE 4b and subsequent orthoester formation on the ensuing disaccharidic thioglycoside intermediate 8.
Molecules 26 02909 sch003
Molecules 26 02909 sch004 550
Scheme 4. Regioselective glycosylation of triol 6 with MeOE-disaccharide 9 leading to tetrasaccharide 10.
Scheme 4. Regioselective glycosylation of triol 6 with MeOE-disaccharide 9 leading to tetrasaccharide 10.
Molecules 26 02909 sch004
Molecules 26 02909 g002 550
Figure 2. Absorption (in blue) and normalized fluorescence (in red) spectra of BODIPY 15 and its glycosylated derivative 16a in diluted solution of ethyl acetate. The spectral profiles of 10 fully resemble those of 16a. The excited state optimized geometry of 15 in two different views is also enclosed with key dihedral angles to show the bending of the chromophore.
Figure 2. Absorption (in blue) and normalized fluorescence (in red) spectra of BODIPY 15 and its glycosylated derivative 16a in diluted solution of ethyl acetate. The spectral profiles of 10 fully resemble those of 16a. The excited state optimized geometry of 15 in two different views is also enclosed with key dihedral angles to show the bending of the chromophore.
Molecules 26 02909 g002
Table
Table 1. Photophysical 1 and laser 2 properties of BODIPY 15, and glycosylated derivatives 16a and 10, in ethyl acetate. For the sake of comparison, the corresponding photophysical data of the F-BODIPY counterpart (in ethanol) have been added. For additional photophysical data, see Table S1.
Table 1. Photophysical 1 and laser 2 properties of BODIPY 15, and glycosylated derivatives 16a and 10, in ethyl acetate. For the sake of comparison, the corresponding photophysical data of the F-BODIPY counterpart (in ethanol) have been added. For additional photophysical data, see Table S1.
Compoundλab (nm)εmaxλfl (nm)∅<τ> (ns)λla (nm)Eff (%)
11499.56.4513.00.746.4554060
15497.04.8511.50.222.8353318
16a500.04.5516.00.313.1954538
10500.54.1515.00.313.5754736
1 Registered under a soft irradiation regime; dye concentration: 2 μM. Absorption (λab) and fluorescence (λfl) wavelength, molar absorption (εmax) (104 M−1 cm−1), fluorescence quantum yield (∅), and amplitude-average lifetime (<τ>). 2 Recorded under a hard irradiation regime; dye concentration 2 mM. Peak wavelength for the laser emission (λla) and efficiency (Eff (%)) defined as the ratio between the energy of the laser output and the pump energy incident on the cell surface.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ventura, J.; Uriel, C.; Gomez, A.M.; Avellanal-Zaballa, E.; Bañuelos, J.; García-Moreno, I.; Lopez, J.C. A Concise Synthesis of a BODIPY-Labeled Tetrasaccharide Related to the Antitumor PI-88. Molecules 2021, 26, 2909. https://doi.org/10.3390/molecules26102909

AMA Style

Ventura J, Uriel C, Gomez AM, Avellanal-Zaballa E, Bañuelos J, García-Moreno I, Lopez JC. A Concise Synthesis of a BODIPY-Labeled Tetrasaccharide Related to the Antitumor PI-88. Molecules. 2021; 26(10):2909. https://doi.org/10.3390/molecules26102909

Chicago/Turabian Style

Ventura, Juan, Clara Uriel, Ana M. Gomez, Edurne Avellanal-Zaballa, Jorge Bañuelos, Inmaculada García-Moreno, and Jose Cristobal Lopez. 2021. "A Concise Synthesis of a BODIPY-Labeled Tetrasaccharide Related to the Antitumor PI-88" Molecules 26, no. 10: 2909. https://doi.org/10.3390/molecules26102909

Article Metrics

Back to TopTop