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1.
Two new polyhydroxysteroids and five new glycosides were isolated from the starfishCeramaster patagonicus and their structures were elucidated: 5α-cholestane-3β,6α,15β,16β,26-pentol, (22E)-5α-cholest-22-ene-3β,6α,8,15α,24-pentol, (22E)-28-O-[O-(2-O-methyl-β-d-xylopyranosyl)-(1→2)-β-d-galactofuranosyl]-24-hydroxymethyl-5α-cholest-22-ene-3β,4β, 6α,8,15β,16β,28-heptol (ceramasteroside C1), (22E)-28-O-[O-(2,4-di-O-methyl-β-d-xylopyranosyl)-(1→2)-β-d-galactofuranosyl]-24-hydroxymethyl-5α-cholest-22-ene-3β, 6α,8,15β,16β,28-hexol (ceramasteroside C2), (22E)-28-O-[O-methyl-β-d-xylopyranosyl)-(1→2)-β-d-galactofuranosyl]-24-hydroxymethyl-5α-cholest-22-ene-3β,6α,8,15β,16β 28-hexol (eramasteroside C3), (22E)-28-O-[O-(2-O-methyl-β-d-xylopyranosyl)-(1→2)-β-d-galactofuranosyl]-24-methyl-5α-cholest-22-ene-3β,4β,6α,8, 15β, 26-hexol (ceramasteroside C4), and (22E)-28-O-[O-(2-O-methyl-β-d-xylopyranosyl)-(1→2)-β-d-xylopyranosyl]-5α-cholest-22-ene-3β,6α,8,15β,24-pentol (ceramasteroside C5)). Three known polyhydroxysteroids (24-methylene-5α-cholestane-3β,6α,8,15β,16β,26-hexol, 5α-cholestane-3β,6α,8,15β,16β,26-hexol,
and 5α-cholestane-3β,6β,15α,16β,26-pentol) were also isolated.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 190–195, January, 1997. 相似文献
2.
N. V. Ivanchina T. V. Malyarenko A. A. Kicha A. I. Kalinovskii P. S. Dmitrenok 《Russian Chemical Bulletin》2008,57(1):204-208
Nine steroidal compounds including three new steroidal glycosides, viz., sodium (24S)-3,24-di-O-(β-D-xylopyranosyl)-5α-cholestane-3β,6β,8,15α,24-pentol 15-sulfate (fuscaside A), (24S)-3,24-di-O-(β-D-xylopyranosyl)-5α-cholestane-3β,6β,8,15α,24-pentol (fuscaside B), and (22E,24R)-24-O-(β-D-xylopyranosyl)-5α-cholest-22-ene-3β,6α,8,15β,24-pentol (desulfated minutoside A); three previously known glycosides, viz., distolasterosides D1 and D2 and pycno-podioside A; two previously known polyhydroxysteroids, viz., 5α-cholestane-3β,6α,8,15β,16β,26-hexaol and 5α-cholestan-3β,4β,6α,7⇇8,15β,16β,26-octol; and the known sodium 24,25-dihydro-marthasterone
3-sulfate were isolated from the Far-Eastern starfish Lethasterias fusca. The structures of these compounds were elucidated by NMR spectroscopy and mass spectrometry.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 196–200, January, 2008. 相似文献
3.
A. A. Kicha N. V. Ivanchina A. I. Kalinovsky P. S. Dmitrenok V. A. Stonik 《Russian Chemical Bulletin》2005,54(5):1266-1271
A fraction of sulfated polyhydroxylated steroids from the Far-Eastern starfish Ctenodiscus crispatus was investigated. The main component of this fraction was identified as (22E,24R,25R)-24-methyl-5α -cholest-22-en-3β,5,6β,15α,25,26-hexol 26-O-sulfate. For the compound stereoisomeric with respect to the side chain, the (24R,25S) or (24S,25R) relative configurations were assigned to the C(24) and C(25) chiral centers. The structures of two other compounds isolated
from the fraction were identified as (22E, 24ξ)-26,27-bisnor-24-methyl-5α-cholest-22-en-3β,5,6β,15α,25-pentol 25-O-sulfate and (22E, 24ξ,25ξ)-24-methyl-5α-cholest-22-en-3β,5,6β,8,15α,25,26-heptol 26-O-sulfate.
Dedicated to Academician N. K. Kochetkov on the occasion of his 90th birthday.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1229–1234, May, 2005. 相似文献
4.
A. A. Kicha N. V. Ivanchina A. I. Kalinovskii P. S. Dmitrenok E. V. Sokolova I. G. Agafonova 《Chemistry of Natural Compounds》2007,43(1):76-80
Five sulfated steriodal compounds including one new glycoside called linckoside L7 (1) and four previously known glycosides
2–5 were isolated from the starfish Linckia laevigata. The structure sodium (22E, 24R)-3-O-(2-O-methyl-β-D-xylopyranosyl)-29-O-(β-D-xylopyranosyl)-24-ethylcholest-4,22-dien-3β,6β,8,15α,16β,29-hexaol 15-O-sulfate was proposed for L7. Linckoside L7 inhibited fertilization and egg-cell development in the sea urchin Strongylocentrotus intermedius.
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Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 64–67, January–February, 2007. 相似文献
5.
N. N. Trofimova A. S. Gromova V. I. Lutsky A. A. Semenov S. A. Avilov A. I. Kalinovsky D. Li N. L. Owen 《Russian Chemical Bulletin》1998,47(7):1395-1398
Two triterpenoid diglycosides of the cycloartane series were isolated from the terrestrial part ofThalictrum minus L. (Ranunculaceae). Genins of these glycosides are side-chain structural isomers—3-O-β-d-galactopyranosyl-29-O-β-d-glucopyranosyl-9β, 19-cyclo-20(S)-lanost-24(Z)-ene-3β, 16β, 22(S), 26, 29-pentaol and 3-O-β-d-galactopyranosyl-29-O-β-d-glucopyranosyl-9β, 19-cyclo-20(S)-lanost-25-ene-3β, 16β,22(S), 24ζ, 29-pentaol. The structures of these glycosides were established using 1D and 2D NMR spectroscopy and FAB mass spectrometry.
For Part 9, see Ref. 1.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1434–1437, July, 1998. 相似文献
6.
V. N. Odinokov I. V. Galyautdinov A. A. Fatykhov L. M. Khalilov 《Russian Chemical Bulletin》2000,49(11):1923-1924
A new phytoecdysteroid,viz, 2-deoxy-3-epi-4β, 20-dihydroxycedysone ((20R,22R)-3α,4β 14α,20,22,25-hexahydroxy-5β-cholest-7-en-6-one), named coronatasteronc, was isolated fromSerratula coronata and identified by NMR spectroscopy.
Published inIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1954–1955, November, 2000. 相似文献
7.
A. A. Kicha N. V. Ivanchina T. T. T. Huong A. I. Kalinovsky P. S. Dmitrenok P. Q. Long 《Russian Chemical Bulletin》2010,59(11):2133-2136
A new minor asterosaponin (20S)-6-O-{β-d-fucopyranosyl-(1→2)-[β-d-fucopyranosyl-(1→4)-β-d-quinovopyranosyl-(1→2)]-β-d-quinovopyranosyl-(1→3)-β-d-quinovopyranosyl}-3β,6α,20-trihydroxycholest-9(11)-en-23-one 3-sulfate (archasteroside C) was isolated from the starfish
Archaster typicus collected in shallow coastal waters of Vietnam. The structure of archasteroside C was determined by 2D NMR spectroscopy and
electrospray ionization (ESI) tandem mass spectrometry. 相似文献
8.
Hua Tang Zeng-lei Wang Hong-jun Zhang Ping Cheng Shu-juan Piao Wan-sheng Chen Hou-wen Lin Hai-feng Tang 《Chemistry of Natural Compounds》2010,46(3):390-392
One new compound, 3β-hydroxy-25-methoxy-(23E)-cholesta-5,23-diene (1), together with five known steroids, cholesteryl myristate (2), cholest-4-en-3-one (3), cholesterol (4), 3β,5α,9α-trihydroxy-(22E,24R)-ergosta7,22-dien-6-one (5), and 3β,5α,6β-trihydroxy-(22E,24R)-ergosta-7,22-diene (6), were isolated and identified from the marine bryozoan Bugula neritina. 相似文献
9.
A. A. Kicha N. V. Ivanchina A. I. Kalinovsky P. S. Dmitrenok V. A. Stonik 《Russian Chemical Bulletin》2000,49(10):1794-1795
A new polyhydroxylated steroidal glycoside, asterosaponin P2, was isolated from the Far-Eastern starfishPatiria (Asterina) pectinifera. The glycoside was identified as the 24R)-29-O-[2-O-sulfo-α-L-arabinofuranosyl]-24-ethyl-5α-cholestane-3β, 6α,8β,15α,16β,29-hexol Na salt.
Published inIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1818–1820, October. 2000 相似文献
10.
E. V. Levina A. I. Kalinovskii V. A. Stonik P. S. Dmitrenok 《Russian Chemical Bulletin》2003,52(7):1623-1628
Two new compounds were isolated from two Far-Eastern starfish species, Henricia sanguinolenta and H. leviuscula leviuscula, collected in the Sea of Okhotsk, viz., the glycoside sanguinoside C, (20R,22E,24R,25S)-3-O-(2,3,4-tri-O-methyl--xylopyranosyl)-24-methyl-5-cholest-22-ene-3,4,6,8,15,26-hexol, and a steroidal ketone, (20R,24S)-3,6,24-trihydroxy-5-cholestan-15-one. They exhibit moderate cytostatic activity with respect to the eggs of sea urchin Strongylocentrotus intermedius. 相似文献
11.
Levina E. V. Andriyashchenko P. V. Kalinovskii A. I. Stonik V. A. 《Russian Chemical Bulletin》2001,50(2):313-315
Two new steroid compounds, 3,6-dihydroxy-5-cholesta-9(11),24-dien-23-one 3-sulfate and 3,6-dihydroxy-5-cholest-9(11)-en-23-one 3-sulfate, were isolated from the Pacific starfish Lysastrosoma anthosticta as the corresponding sodium salts and identified. Two previously known glycosides of 24(S)-5-cholestane-3,6,8,15,24-pentol were also isolated and identified as sodium 24-O--d-glucopyranoside 6"-sulfate (pycnopodioside C) and sodium 24-O--d-xylopyranoside 4"-sulfate (luridoside A). 相似文献
12.
A. A. Kicha A. I. Kalinovskii N. V. Ivanchina V. A. Stonik 《Russian Chemical Bulletin》1998,47(10):2032-2033
A new polyhydroxysteroid was isolated from the starfishLuidiaster dawsoni; the structure of the product was established as (24S,25R)-24-methylcholestane-3β, 5α, 6β, 15α, 16β, 26-hexaol. A mixture of methyl-α- and β-d-glucopyranosides was also isolated from the extract of this starfish.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2088–2090, October, 1998. 相似文献
13.
Xiao Guang Ma Hai Feng Tang Chang Hai Zhao Ning Ma Min Na Yao Ai Dong Wen 《中国化学快报》2009,20(10):1227-1230
Two new 24-hydroxylated asterosaponins,sodium(20R,24S)-6α-O-(4-O-sodiumsulfato-β-D-quinovopyranosyl)-5α-cholest-9(11)-en-3β,24-diol 3-sulfate(1) and sodium(20R,24S)-6α-O-[3-O-methyl-β-D-quinovopyranosyl-(1→2)-β-D-xylopyranosyl-(1→3)-β-D-glucopyranosyl]-5α-cholest-9(11)-en-3β,24-diol 3-sulfate(2),were isolated from the starfish Culcita novaeguineae.Their structures were elucidated by extensive spectral analysis and chemical evidences. 相似文献
14.
The structure of a new cycloartane-type triterpene glycoside, cyclomacroside E, which was isolated from roots of Astragalus macropus Bunge (Leguminosae), was established as 3-O-α-L-rhamnopyranoside,24-O[(β-D-xylopyranosyl)(1→2)-β-D-xylopyranoside]-24R-cycloartan-1α,3β,7β,24,25-pentaol. 相似文献
15.
E. V. Levina A. I. Kalinovskii P. V. Andriyashchenko P. S. Dmitrenok E. V. Evtushenko V. A. Stonik 《Russian Chemical Bulletin》2004,53(11):2634-2638
Three polyhydroxylated steroids were isolated from the Far-Eastern starfish Hippasteria phrygiana collected from the Sea of Okhotsk and were characterized as a new glycoside phrygioside A, viz., sodium (20R, 24S)-3,4,7,8,15,24-hexahydroxy-24-O-[3-O-methyl--D-xylopyranosyl-(12)--L-arabinofuranosyl]-5-cholestan-6-yl sulfate, its aglycone, and the already known marthasterone sulfate.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2526–2529, November, 2004. 相似文献
16.
A furostanol saponin mixture and a known phytoecdysteroid were isolated from the roots of Helleborus orientalis Lam. Their structures were established as 26-[(β-D-glucopyranosyl)oxy]-22α-hidroxyfurosta-5,25(27)-dien-1β,3β,11α-triol (1a), 26-[(β-D-glucopyranosyl)oxy]-22α-methoxyfurosta-5,25(27)-dien-1β,3β,11α-triol (1b), and 20-hydroxy-β-ecdyson-3-O-β-D-glycoside (2). Acid hydrolysis of 1a,b gave (1β,3β,11α,22α)-22,26-dimethoxyfurosta-5,25(27)-dien-1,3,11-triol (aglycone 1) and of 2 gave 20-hydroxy-β-ecdyson (aglycone 2). Their structures were elucidated by spectral analysis.
Published in Khimiya Prirodnykh Soedinenii, No. 1, pp. 75–77, January–February, 2007. 相似文献
17.
Two new ceramides were isolated from the 95% EtOH extract of traditional Chinese medicinal plant Isatis indigotica. Their structures were elucidated as 1-O-β-D-glucopyranosyl-(2S, 3R)-N-(2′-hydroxype-ntacosanoyl)-octadeca-11E-sphingenine (1) and 1-O-β-D-glucopyranosyl-(2S,3R)-N-(2′-hydroxyhe xacosanoyl)-octadeca-11E-sphingenine (2) on the basis of spectroscopic data. Their cytotoxic effects were evaluated by using MTT method. 相似文献
18.
A new triterpene cycloartane glycoside called askendoside K was isolated from roots of Astragalus taschkendicus Bunge (Leguminosae). The structure of this glycoside was established using chemical and biochemical transformations and spectral
data. Askendoside K was a bisdesmoside of cycloorbigenin C and had the structure 23R,24R-cycloartan-3β,6α,16β,23,24,25-hexaol 3-O-[(α-L-arabinopyranosyl)(1 → 2)-β-D-xylopyranoside],23-O-[(β-D-glucuronopyranosyl)(1 → 2)-β-D-glucopyranoside]. 相似文献
19.
The structure of the new cycloartane glycoside cyclomacroside B that was isolated from Astragalus macropus Bunge (Leguminosae) was shown to be 1,7-di-O-acetyl-24R-cycloartan-1α,3β,7β,24,25-pentaol 3-O-α-Lrhamnopyranoside-24-O-β-D-xylopyranoside. 相似文献
20.
M. R. Maisashvili Dzh. K. Kuchukhidze V. S. Kikoladze L. N. Gvazava 《Chemistry of Natural Compounds》2012,48(1):86-90
Two new steroidal glycosides were isolated by fractionation of total extracted substances from inflorescences and flower stalks
of Allium rotundum (Alliaceae). The structures were determined on the basis of chemical transformations, physical constants,
and spectral data as 26-O-β-D-glucopyranosyl-(25R)-5α-furostan2α,3β,22α,26-tetraol 3-O-β-D-glucopyranosyl-(1 → 2)[β-D-xylopyranosyl-(1 → 3)]-β-D-glucopyranosyl(1 → 4)-β-D-galactopyranoside (2) and (25R)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1 → 3)-βD-glucopyranosyl-(1 → 2)-[β-D-xylopyranosyl-(1 → 3)]-β-D-glucopyranosyl-(1 → 4)-β-D-galactopyranoside (3). 相似文献