共查询到20条相似文献,搜索用时 437 毫秒
1.
L. A. Yakovishin V. I. Grishkovets A. S. Shashkov V. Ya. Chirva 《Chemistry of Natural Compounds》1999,35(5):543-546
Two new minor triterpene glycosides L-G1, and L-G2b, the 3-O-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-gentiobiosyl and 3-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl-(1→4)-O-(6-O-acetyl-β-D-glucopyranosyl)-(1→6)-O-β-D
glucopyranosyl esters of 30-norhederagenin, respectively, are isolated from the leaves of canary ivy (Hedera canariensis Willd.). The structures of the glycosides are found by chemical methods and1H and13C NMR spectroscopy.
Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 623–626, September–October, 1999. 相似文献
2.
A. A. Shashkov V. I. Grishkovets O. Ya. Tsvetkov V. Ya. Chirva 《Chemistry of Natural Compounds》1993,29(4):502-508
The previously known glycosides 3-O-α-L-arabinopyranosyl-28-O-[α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl]hederagenin
and 3-O-[α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranosyl]-28-O-[α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl]hederagenin
and the new triterpene glycoside tauroside St-H1 — 3-O-β-D-glucopyransyl-28-O-[α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl]hederagenin — have
been isolated from the stems ofHedera taurica Carr.
M. V. Frunze Simferopol' State University. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 571–579, July–August,
1993. 相似文献
3.
V. I. Grishkovets L. A. Yakovishin I. N. Shchipanova A. S. Shashkov V. Ya. Chirva 《Chemistry of Natural Compounds》1998,34(6):694-698
The leaves of Algerian ivyHedera canariensis Willd. (Araliaceae) have yielded two new triterpene glycosides — caulophyllogenin 3-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside (L-F2) and its 28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-gentiobiosyl ester (L-I2) - and also the previously known hederagenin 3-O-α-L-rhamnopyranosyl-(1→2)-O-β-D-glucopyranoside (L-F1). The structures of the glycosides were established on the basis of chemical transformations and1H and13C NMR spectroscopy.
Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 777–781, November–December, 1998. 相似文献
4.
V. I. Grishkovets A. A. Loloiko A. S. Shashkov V. Ya. Chirva 《Chemistry of Natural Compounds》1990,26(6):663-666
We have isolated from Crimean ivy berries in addition previously known triterpene glycosides — 3-O-α-L-arabinopyranosyl-28-O-[O-α-L-rhamnopyranosyl-(1
→ 4)-O-β-D-glycopyranosyl-(1 → 6)-β-D-glucopyranosyl]hederagenin, 3-O-[O-α-L-rhamnopyranosyl-(1 → 2)-α-L-arabinopyranosyl]-28-O-[O-α-L-rhamnopyranosyl-(1
→ 4)-O-β-D-glucopyranosyl-(1 → 6)-β-D-glycopyranosyl]hederagenin, the new triterpene glycosides hederoside H2-3-O-[O-β-D-glycopyranosyl-(1 → 2)-β-D-glycopyranosyl-(1 → 2)-β-D-glucopyranosyl]-28-O-[O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl]oleanolic
acid- and hederoside I-3-O-[O-β-D-glucopyranosyl-(1 → 2)-β-D-glucopyranosyl]-28-O-[O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranosyl]hederagenin.
Details of their13C NMR spectra are given.
M. V. Frunze Simferopol' State University. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 779–783, November–December,
1990. 相似文献
5.
V. I. Grishkovets A. E. Kondratenko N. V. Tolkacheva A. S. Shashkov V. Ya. Chirva 《Chemistry of Natural Compounds》1994,30(6):689-692
The leaves of common ivy have yielded 11 triterpene glycosides: the 3-O-α-L-pyranosides of oleanolic acid (1), of echinocystic
acid (2), and of hederagenin; the 3-O-[O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranoside]s of oleanolic acid (4), of echinocystic
acid (5), and of hederagenin (6); the O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester of
hederagenin 3-O-α-L-pyranoside (7); the O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester of hederagenin 3-O-[O-α-L-pyranosyl-(1→2)-α-L-arabinopyranoside]
(9); and the O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl esters of oleanolic acid, echinocystic
acid, and hederagenin 3-O-[O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside]s (8), (10), and (11), respectively. This is the
first time that compounds (1), (2), (5), (7), (9), and (10) have been found in this plant.
Simferopol' State University. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 742–746, November–December, 1994. 相似文献
6.
E. A. Khamidullina A. S. Gromova V. I. Litskii A. L. Vereshchagin A. A. Semenov M. F. Larin 《Chemistry of Natural Compounds》1989,25(4):441-447
Four new cycloartane glycosides have been isolated from a methanolic extract ofThalictrum squarrosum Stephan ex Willd.: squarroside A1 (I) — (21R, 22S, 23R)-3β-(β-D-glucopyranosyloxy)-21α-methoxy-21,23-epoxycycloart-24-ene-22β,30-diol,
C30H60O10; squarroside A2 (II) — the (21S)-epimer of compound (I); squarroside B1 (III) (21R, 22S, 23R)-3gb-[O-α-L-rhamnopyranosyl-(1
→ 6)-β-D-glucopyranosyloxy]-21α-methoxy-21,23-epoxycycloart-24-ene-22β,30-diol, C43H70O14; and squarroside B2 (IV) — the (21S)-epimer of compound (III). The proposed structures were determined on the basis of1H and13C NMR spectroscopy, FAB mass spectrometry, and chemical transformations.
Irkutsk Institute of Organic Chemistry, Siberian Branch, USSR Academy of Sciences. Translated from Khimiya Prirodnykh Soedinenii,
No. 4, pp. 516–523, July–August, 1989. 相似文献
7.
A. S. Shashkov V. I. Grishkovets L. A. Yakovishin I. N. Shchipanova V. Ya. Chirva 《Chemistry of Natural Compounds》1998,34(6):690-693
The structures of two new triterpene glycosides, L-E2 and L-H3 from the leaves of Algerian ivyHedera canariensis Willd. (fam. Araliaceae), have been established on the basis of chemical and spectral characteristics: they are 30-norhederagenin
3-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside and the 28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-gentiobiosyl ester of 30-norhederagenin 3-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside, respectively.
Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 772–776, November–December, 1998. 相似文献
8.
D. A. Panov V. I. Grishkovets V. V. Kachala A. S. Shashkov 《Chemistry of Natural Compounds》2006,42(1):49-54
Thirteen known glycosides of hederagenin and oleanolic acid and the three new triterpene glycosides of oleanolic acid-28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester 3-O-β-D-glucopyranosyl-(1→4)-O-β-D-xylopyranosyl-(1→ 3)-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside of oleanolic acid and the 28-O-α-L-rhamnopyranosyl-(1→4)-O-6-O-acetyl-β-D-glucopyranosyl-(1→ 6)-O-β-D-glucopyranosyl esters 3-O-β-D-xylopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside of oleanolic acid and 3-O-β-D-glucopyranosyl-(1→4)-O-β-Dxylopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→ 2)-O-α-L-arabinopyranoside of oleanolic acid were isolated from leaves of Kalopanax septemlobum var. typicum introduced to Crimea.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 40–43, January–February, 2006. 相似文献
9.
G. V. Khodakov 《Chemistry of Natural Compounds》2010,46(4):572-575
Three new triterpene oleanane glycosides, melilotosides A1, B1, and C1, and non-glycosylated soyasapogenol B were isolated from Melilotus officinalis (L.) Pall. (Fabaceae) roots. The structures
of the glycosides were proved using chemical transformations and spectral data. Melilotoside A1 is soyasapogenol B 3-O-β-Dxylopyranoside; melilotoside B1, soyasapogenol B 3-O-[β-D-galactopyranosyl-(1-2)-f-D-xylopyranoside]; melilotoside C1, soyasapogenol B 3-O-[α-L-rhamnopyranosyl-(1-2)-β-D-galactopyranosyl(1-2)-β-Dxylopyranoside]. 相似文献
10.
V. I. Grishkovets I. I. Dovgii V. V. Kachala A. S. Shashkov 《Chemistry of Natural Compounds》2005,41(4):436-441
Structures of 13 new acetylated triterpene glycosides from leaves of Cussonia paniculata (Araliaceae) were established as
28-O-(2-O-acetyl- and 3-O-acetyl-α-L-rhamnopyranosyl)-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β -D-glucopyranosides of 23-hydroxybetulinic
acid (1a and 1b) and hederagenin (2a and 2b), 3-O-α-L-arabinopyranosyl-28-O-(2-O-acetyl- and 3-O-acetyl-a-L-rhamnopyranosyl)-(1→ 4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glycopyranosides
of oleanic (3a and 3b) and ursolic (3c and 3d) acids, 3-O-α-L-arabinopyranosyl-28-O-(4-O-acetyl-, 2-O-acetyl-, and 3-O-acetyl-α-L-rhamnopyranosyl)-(1→4)-O-β-D-glucopyranosyl-(1→
6)-O-β-D-glucopyranosides of hederagenin (4, d5a and 5b), and 3-O-β-D-glucopyranosyl-(1→2)-O-α-L-arabinopyranosyl-28-O-(2-O-acetyl- and 3-O-acetyl-α-L-rhamnopyranosyl)-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-
glucopyranosides of oleanic acid (6a and 6b). The structures of the compounds were established using chemical methods and NMR spectroscopy.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 351–356, July–August, 2005. 相似文献
11.
I. I. Dovgii V. I. Grishkovets V. V. Kachala A. S. Shashkov 《Chemistry of Natural Compounds》2006,42(2):182-185
Structures of eight triterpene glycosides, of which the 28-O-(2-O-acetyl-and 3-O-acetyl-α-L-rhamnopyranosyl)-(1→4)-O-β-D-glucopyranosyl-(1→ 6)-O-β-D-glucopyranosyl esters of hederagenin 3-O-β-D-glucopyranosyl-(1→ 2)-O-α-L-arabinopyranoside (J1a and J1b) were new, from Cussonia paniculata (Araliaceae) leaves were established using chemical and NMR spectroscopic methods.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 149–152, March–April, 2006. 相似文献
12.
Yu Chen Xu Feng Xiaodong Jia Ming Wang Jinyu Liang Yunfa Dong 《Chemistry of Natural Compounds》2008,44(1):39-43
The structures of seven triterpene glycosides (1–7), of which the 23-O-acetyl, 28-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester of hederagenin 3-O-β-D-glucopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside (2) was new, from the flower buds of Lonicera macranthoides were established using chemical and NMR spectroscopic methods.
Published in Khimiya Prirodnykh Soedinenii, No. 1, pp. 32–34, January–February, 2008. 相似文献
13.
G. B. Oganesyan A. M. Galstyan V. A. Mnatsakanyan A. S. Shashkov P. V. Agababyan 《Chemistry of Natural Compounds》1991,27(5):556-559
Together with poliumoside we have isolated for the first time from golden germander verbascoside and a new phenylpropanoid
glycoside (teupolioside) for which the structure of 2-(3,4-dihydroxyphenyl)ethyl O-β-D-galactopyranosyl-(1→2)-O-α-L-rhamnopyranosyl-(1→3)-4-O-caffeoyl-β-D-glucopyranoside
is proposed. A mixture of poliumoside and teupolioside revealed a moderate antibacterial activity.
A. L. Mnadzhoyan Institute of Fine Organic Chemistry, Armenian Academy of Sciences, Erevan. Translated from Khimiya Prirodnykh
Soedinenii, No. 5, pp. 630–634, September–October, 1991. 相似文献
14.
L. A. Yakovishin N. I. Borisenko M. I. Rudnev E. V. Vetrova V. I. Grishkovets 《Chemistry of Natural Compounds》2010,46(1):49-52
Self-association of hederagenin 3-O-α-L-rhamnopyranosyl-(1→2)-O-α-L-arabinopyranoside (α-hederin) and its 28-O-α-L-rhamnopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ether (hederacoside C) with cholesterol was studied using mass spectrometry (ESI MS). Possible complexation
of the glycosides with cholesterol was examined. The ichtyotoxic activity of the glycosides and their mixtures with cholesterol
to Barbus fefrozona was studied. 相似文献
15.
R. Zh. Karimov R. U. Umarova Z. Saatov M. G. Levkovich N. D. Abdullaev 《Chemistry of Natural Compounds》1998,34(5):609-612
Two new triterpene glycosides of the cycloartane series, which have been called cyclostipulosides A and B, have been isolated
in the individual form from the roots ofTragacantha stipulosa Boviss. Their structures have been established by physicochemical methods. Cyclostipuloside A is 24R-cycloartane-3β,6α,16β,24,25-pentaol
16-O-β-D-glucopyranoside 3-O-β-D-xylopyranoside, and cyclostipuloside B is 24R-cycloartane-3β,6α,16β,24,25-pentaol 6-O-α-L-arabinopyranoside 16-O-β-D-glucopyranoside 3-O-β-D-xylopyranoside. By the acid hydrolysis of cyclostipulosides A and B we have obtained the new glycoside
24R-cycloartane-3β,6α,16β,24,25-pentaol 16-O-β-D-glucopyranoside.
Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, fax (371) 120
64 75. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 670–674, September–October, 1998. 相似文献
16.
Jian Zhang Zhi-Qi Yin Peng Cao You-Bin Li Jin-Ao Duan 《Chemistry of Natural Compounds》2008,44(6):701-703
A new flavonol derivative 3, 8-dihydroxy-10-methoxy-5-H-isochromeno[4, 3-b]chromen-7-one (1) together with four known compounds, glutinone (2), luteolin (3), acacetin 7-O-α-L-rhamnopyranosyl- (1→6)-β-D-glucopyranoside (4), and rutin (5) were isolated from the dried roots of Fagopyrum dibotrys. Their structures were determined by UV, IR, MS, 1H, and 13C NMR spectroscopic analysis, including 2D NMR.
Published in Khimiya Prirodnykh Soedinenii, No. 6, pp. 567–568, November–December, 2008. 相似文献
17.
New Oligomeric Proanthocyanidins from Bark of <Emphasis Type="Italic">Platanus orientalis</Emphasis>
S. Z. Nishanbaev Z. A. Kuliev N. K. Khidyrova A. D. Vdovin N. D. Abdullaev Kh. M. Shakhidoyatov 《Chemistry of Natural Compounds》2005,41(4):404-409
Two oligomeric proanthocyanidinglycosides were isolated from bark of Platanus orientalis. Their structures and relative configurations were established as 7-O-β-D-Glcp-(−)-epicatechingallate-(4β-8)-(−)-epicatechin-(4β-8)-(−)-epicatechin-(4β-8)-5-O-β-D-Glcp-epicatechingallate
(Pl-1) and 7-O-β-D-Glc→6-O-β-D-Glcp-(−)-epigallocatechingallate-(4β-8)-(+)-catechingallate-(4β-8)-(+)-catechingallate-(4β-8)-(−)-epigallocatechingallate-(4α-8)-(−)-epicatechin-(4β-8)-[5-O-β-D-Glcp-→6-O-β-D-Glc→6-galloyl(−)-epigallocatechingallate
(Pl-7).
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 325–330, July–August, 2005. 相似文献
18.
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
19.
A. S. Gromova A. A. Semenov V. I. Lutskii S. V. Zinchenko N. N. Trofimova Ya. V. Rashkes 《Chemistry of Natural Compounds》1994,30(3):363-367
Thalicoside D — a new triterpene glycoside isolated fromThalictrum minus L. (Ranunculaceae) — has the structure of oleanolic acid 3-O-[O-α-L-rhamnopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→4)-α-L-arabinopyranoside
28-O-[O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside]. This structure was established by the use of the results of acid and
alkaline hydrolyses, SIMS spectra, and one- and two-dimensional NMR spectroscopy.
Deceased. 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