Glycosides Of Polyhydroxysteroids Research Articles

Structural Characterization of Polar Steroid Compounds of the Far Eastern Starfish Lethasterias fusca by Nanoflow Liquid Chromatography Coupled to Quadrupole Time-of-Flight Tandem Mass Spectrometry.

Nanoflow liquid chromatography coupled with a captive spray ionization time-of-flight tandem mass spectrometer (nLC/CSI-QTOF-MS/MS) was used in the structural determination of polar steroid compounds of starfish Lethasterias fusca. A total of 207 compounds including 106 asterosaponins, 81 glycosides of polyhydroxysteroids, and 14 polyhydroxylated steroids were detected and characterized by MS and MS/MS. Twenty compounds among them were unambiguously identified using authentic standard compounds, isolated earlier from this and other starfish species. The other compounds were tentatively characterized by accurate mass measurement and comparing retention times and characteristic MS/MS fragmentation patterns with reference standards. Moreover, fragmentation behaviors of a series of pure standards of starfish polar steroids and polyhydroxysteroid compounds detected in L. fusca have been extensively investigated and characteristic fragmentation pathways were described and used for the characterization of unknown compounds.

Two New Steroidal Monoglycosides, Anthenosides A₁ and A₂, and Revision of the Structure of Known Anthenoside A with Unusual Monosaccharide Residue from the Starfish Anthenea aspera.

Two new polyhydroxysteroidal glycosides, anthenosides A1 (1) and A2 (2), and one previously known steroidal glycoside anthenoside A (3) were isolated from extract of the tropical starfish Anthenea aspera. Structures of 1–3 were determined by analysis of the spectroscopic data as well as chemical transformations. As a result, the structure of anthenoside A has been revised and the structures of 1 and 2 were established. Glycosides 1–3 contain a 2-acetamido-2-deoxy-4-O-methyl-β-d-glucopyranosyl residue, found in the starfish steroidal glycosides for the first time. All the isolated compounds slightly inhibited cell viability of human cancer T-47D cells and did not show cytotoxic effects against RPMI-7951 cells. Glycoside 1 slightly inhibited colony formation of human cancer RPMI-7951 cells by 16% while compound 2 decreased the number of colonies of T-47D cells by 40%.

Granulatosides D, E and other polar steroid compounds from the starfish Choriaster granulatus. Their immunomodulatory activity and cytotoxicity

Two new steroid glycosides, granulatosides D (1) and E (2), belonging to the group of bi- and monoglycosides of polyhydroxysteroids, respectively, were isolated from the ethanolic extract of the starfish Choriaster granulatus along with thirteen previously known glycosides of polyhydroxysteroids (3–15) and one steroid heptaol (16). The structures of the new compounds were elucidated by extensive NMR and ESIMS techniques. Cytotoxic and immunomodulatory activities of compounds 1, 3–8, and 10–16 using murine splenocytes and peritoneal macrophages were studied. At a dose of 0.1 μM new glycoside 1 showed immunomodulatory properties, increasing the intracellular ROS (reactive oxygen species) level in peritoneal murine macrophages by 20% and decreasing intracellular ROS level by 21% in pre-treated with endotoxic lipopolysaccharide from E. coli (LPS) peritoneal macrophages.

Cytotoxic Polyhydroxysteroidal Glycosides from Starfish Culcita novaeguineae.

Four new polyhydroxysteroidal glycosides—culcinosides A–D (1, 2, 4, and 7)—along with three known compounds—echinasteroside C (3), linckoside F (5), and linckoside L3 (6)—were isolated from the ethanol extract of starfish Culcita novaeguineae collected from the Xisha Islands of the South China Sea. The structures of new compounds were elucidated through extensive spectroscopic studies and chemical evidence, especially two-dimensional (2D) NMR techniques. The cytotoxicity of the new compounds against human glioblastoma cell lines U87, U251, and SHG44 were evaluated.

Six New Polyhydroxysteroidal Glycosides, Anthenosides S1-S6, from the Starfish Anthenea sibogae.

Six new polyhydroxysteroidal glycosides, anthenosides S1 -S6 (1-6), along with a mixture of two previously known related glycosides, 7 and 8, were isolated from the methanolic extract of the starfish Anthenea sibogae. The structures of 1-6 were established by NMR and HR-ESI-MS techniques as well as by chemical transformations. All new compounds have a 5α-cholest-8(14)-ene-3α,6β,7β,16α-tetrahydroxysteroidal nucleus and differ from majority of starfish glycosides in positions of carbohydrate moieties at C(7) and C(16) (1-4, 6) or only at C(16) (5). The 4-O-methyl-β-d-glucopyranose residue (2) and Δ24 -cholestane side chain (3) have not been found earlier in the starfish steroidal glycosides. The mixture of 7 and 8 slightly inhibited the proliferation of human breast cancer T-47D cells and decreased the colony size in the colony formation assay.

A New Steroidal Glycoside Granulatoside C from the Starfish Choriaster granulatus, Unexpectedly Combining Structural Features of Polar Steroids from Several Different Marine Invertebrate Phyla

A new unique steroidal glycoside, granulatoside C (1), was isolated from the ethanol extract of the starfish Choriaster granulatus. The structure of 1 was elucidated by extensive NMR and ESI-MS techniques as (20 R)-16,21- O-di-(P-D-fucopyranosyl)-24-methyl-cholesta-5,24(28)-diene-3p,7a,16a,21-tetraol (1). This glycoside is unusual one, because combines some characteristic structural peculiarities of steroids from several different phyla of marine invertebrates, it has a range of structural features that not previously found in starfish polyhydroxysteroidal glycosides, such as Δ5-3β,7α,16α-trihydroxysteroidal nucleus, Δ24(28)-21-hydroxy-24-methyl-cholestane side chain and 16,21-diglycosylation by D-fucopyranosyl residues, but also characteristic of sponges, ophiuroids and soft corals, respectively.

Anthenosides L-U, Steroidal Glycosides with Unusual Structural Features from the Starfish Anthenea aspera.

Ten new polyhydroxysteroidal glycosides, anthenosides L-U (1-10), with rare positions of carbohydrate fragment attachments, were isolated from the starfish Anthenea aspera. The structures of 1-10 were established by NMR and ESIMS techniques as well as by chemical transformations. The unoxidized Δ22-24-nor-cholestane (1), (24S)-Δ22-24-methylcholestane (2-5), and Δ22-cholestane (7) side chains of the steroidal aglycons, 3-O-methyl-β-d-galactofuranosyl residue (2, 8), and 5α-cholest-8(14)-ene-3α,7β,16α-trihydroxysteroidal nucleus (9, 10) have not been found previously in starfish polar steroidal compounds. The mixture of glycosides 9 and 10 showed hemolytic activity with an EC50 = 8 μM. Compound 4 at a dose of 10 μM exhibited a potential immunomodulatory action, decreasing by 24% the intracellular ROS content in RAW 264.7 murine macrophages, induced by pro-inflammatory endotoxic lipopolysaccharide from E. coli.

Three New Cytotoxic Polyhydroxysteroidal Glycosides from Starfish Craspidaster hesperus.

Three new polyhydroxysteroidal glycosides, hesperuside A (1), B (2), and C (3), as well as a known novaeguinoside A (4), were isolated from the ethanol extract of starfish Craspidaster hesperus collected from the South China Sea. Their structures were elucidated by extensive spectroscopic methods and chemical evidence. The compounds 1–3 present unprecedented carbohydrate chain 3-O-methyl-β-d-galactopyranose, which differ from each other in the side chains. These compounds exhibited cytotoxicity against human tumor cells BEL-7402, MOLT-4, and A-549 in vitro.

LC-ESI MS/MS profiling of polar steroid metabolites of the Far Eastern starfish Patiria (=Asterina) pectinifera

Profiling of asterosaponins, polyhydroxysteroids and glycosides of polyhydroxysteroids of the common in the Far Eastern sea waters starfish Patiria (=Asterina) pectinifera was performed by LC-ESI MS and LC-APPI MS. The 72 polar steroid metabolites, including 35 asterosaponins, 22 polyhydroxysteroids and 15 sulfated glycosides of polyhydroxysteroids, were detected and identified using the LC–MS and LC–MS/MS spectra. The steroid metabolome of P. pectinifera is characterized by large number of sulfated and non-sulfated highly oxidized compounds with cholestane, ergostane and stigmastane skeleton systems of aglycones. Some peculiarities of biosynthesis of the starfish polar steroids were discussed. It was suggested that biosynthesis of asterosaponins from diet sterols is executed in a mosaic type manner with transformations in aglycone moieties and elongation of carbohydrate chains proceeding independently from each other and simultaneously.

Six new polyhydroxy steroidal glycosides from Dregea sinensis Hemsl

Absract The phytochemical investigation of the roots of Dregea sinensis Hemsl yielded six new polyhydroxy steroidal glycosides (1–6). The chemical structures have been elucidated on the basis of extensive one- and two-dimensional NMR spectroscopy, as well as by mass spectrometry. The cytotoxic activity of these compounds were evaluated in vitro while compounds 3 and 4 showed weak activity against human leukemia cells (HL-60) with IC 50 values of 14.10 μM and 19.16 μM, respectively.

Polyhydroxysteroidal Glycosides from the Starfish Anthenea chinensis

Ten new polyhydroxysteroidal glycosides, anthenosides B-K (2-11), were isolated from the ethanol extract of the starfish Anthenea chinensis. Their structures were elucidated by extensive spectroscopic studies and chemical evidence. The unprecedented carbohydrate chain 6-O-methyl-beta-d-galactofuranosyl-(1-->3)-(6-O-methyl-beta-d-galactofuranose) was present in all the compounds except compounds 10 and 11. Compounds 5, 7, a mixture of 8 and 9, and a mixture of 10 and 11 showed inhibitory activity against human tumor K-562 and BEL-7402 cells. Furthermore, the mixture of 10 and 11 also exhibited cytotoxicity against human tumor U87MG cells and promoted tubulin polymerization.

Biological activities of steroid glycosides from starfish

Glycosides of polyhydroxysteroids from starfish were compared with regard to hemolytic activities on mouse red blood cells and cytotoxicity on developing eggs of sea urchin Strongylocentrotus intermedius. Mediasteroside M 1 from Mediaster murrayi with a 2- O-methyl group at a xylose residue exerted lower activity than mediasteroside M 2 without this group. Ceramasteroside C 2 from Ceramaster patagonicus having a 2,4-di- O-Me-Xyl p residue had more activity in comparison with ceramasteroside C 3 with 2- O-Me-Xyl p. Activities of rathbuniosides R 1 (four OH-groups) and R 2 (five OH-groups) from Asterias rathbuni, and culcitosides C 2 (six OH-groups) and C 3 (five OH-groups) from Culcita novaeguineae were inversely proportional to the number of hydroxyl groups of the aglycon. There was a correlation between cytotoxic and hemolytic activities. The results indicated that salt concentration, temperature and pH values are important for the hemolytic activity of steroid glycosides.

Investigation of the polar steroids from an Antarctic Starfish of the family Echinasteridae: isolation of twenty seven polyhydroxysteroids and steroidal oligoglycosides, structures and biological activities

An investigation of the extracts from a starfish collected in the Antarctic Sea, Echinasteridae family, has led to the isolation of thirteen glycosides of polyhydroxysteroids (1–13), fourteen polyhydroxysteroids (14–27), which are the subject of this report, and seven asterosaponins (penta-and hexa-saccharides), described in a previous paper. Glycosides 1–13 are composed of the same 3β,4β,6α,8,15β,26-hexahydroxysteroidal aglycone with small variations in the side chains, and a carbohydrate portion made up of one or two monosaccharide units attached at C-26, except 11, which has a steroidal aglycone with a 24,28-dihydroxylated side chain and the monosaccharide unit attached at C-24. The structures of the polyhydroxysteroids (14–27) have the hydroxyl groups typically disposed on one side of the steroid nucleus, i.e. 3β,4β,6β (or α),8,15α (or β) and 16β and the majority of them possess a 26-hydroxyl function. A selection of fifteen compounds were tested against human non-small-cell lung carcinoma cells and found to be moderately cytotoxic.

Starfish saponins, 52. Chemical constituents from the starfish Echinaster brasiliensis.

This paper reports an analysis of the chemical constituents from the Caribbean starfish Echinaster brasiliensis collected at Grand Bahama Island. This species is completely devoid of cyclic steroidal glycosides, previously isolated from two species of the genus Echinaster in place of the more common penta- and hexa-glycoside steroidal sulfates ("asterosaponins"). Two typical "asterosaponins" and ten glycosides of polyhydroxysteroids were instead isolated in relatively large amounts from E. brasiliensis. The asterosaponins include the known marthasteroside A1 [1] and the new brasiliensoside [2], while the glycosides of polyhydroxysteroids include seven new compounds (six monoglycosides and one diglycoside). The known echinasteroside A, previously found in Echinaster sepositus and in the related Henricia laeviuscula (both belonging to the family Echinasteridae), and laeviusculosides C and I from H. laeviuscula were also isolated. Most of the glycosides from E. brasiliensis are 3-O-beta-xylopyranosides of delta 4-3 beta,6 beta,8,15 alpha,16 beta pentahydroxysteroid aglycones, having different side chains and sometimes a sulfate group at C-15, structural features which are typical of steroidal glycosides from starfishes of the family Echinasteridae. Continuing the analysis of the constituents of E. brasiliensis, we have also isolated a series of anthraquinones, known animal pigments found only in echinoderms and particularly in Crinoidea and in the Echinasteridae family of Asteroidea.

Starfish saponins, Part 51. Steroidal oligoglycosides from the starfish Distolasterias nipon.

A reinvestigation of the extracts from the starfish Distolasterias nipon, collected at Mutsu Bay, Japan, has led to the isolation of six glycosides of polyhydroxysteroids and six asterosaponins. Four steroidal glycosides have been identified as distolasterosides D1 [1] and D2 [2] (previously isolated from the same organism), and pycnopodioside C [5] and pisasteroside A [6], previously found in the related species Pycnopodia helianthoides and Pisaster ochraceus (family Asteridae), respectively. Two asterosaponins have been identified as the common versicoside A [7] and thornasteroside A [7a]. The two remaining glycosides of polyhydroxysteroids, named distolasterosides D4 [3] and D5 [4], and four asterosaponins designated nipoglycosides A [8], B [9], C [10], and D [11] are new compounds, and their structures have been elucidated mainly by interpretation of spectral data and comparison with known compounds.