共查询到20条相似文献,搜索用时 30 毫秒
1.
Formononetin, prunetin, genistein, genistin, and a new genistein glycoside genistein-7-O-β-D-galactopyranoside were isolated from the aerial part of Trifolium pratense L. The structures of the isolated compounds were established based on chemical transformations and UV, 1H, and 13C NMR spectra.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 141–143, March–April, 2008. 相似文献
2.
E. A. Krasnov V. A. Raldugin I. V. Shilova E. Yu. Avdeeva 《Chemistry of Natural Compounds》2006,42(2):148-151
A chromatographically inseparable crystalline mixture of the previously undescribed quercetin-4′-O-β-galactopyranoside and the known quercetin-3-O-β-glucopyranoside (isoquercitrin) in a 7:5 ratio was isolated from the extract of the aerial part of Filipendula ulmaria (L.) Maxim.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 122–124, March–April, 2006. 相似文献
3.
Xiaodong Jia Xingzeng Zhao Ming Wang Yu Chen Yunfa Dong Xu Feng 《Chemistry of Natural Compounds》2008,44(6):692-695
Two new coumarin biosides, tert-O-β-D-apiofuranosyl-(1→6)-O-β-D-glucopyranosyl-byakangelicin (1) and 2′-O-β-D-apiofuranosyl-(1→6)-β-D-glucopyranosyl-peucedanol (2), were isolated from the fresh roots of Angelica dahurica. The structures of the new compounds were elucidated on the basis of spectral analysis.
Published in Khimiya Prirodnykh Soedinenii, No. 6, pp. 561–563, November–December, 2008. 相似文献
4.
D. A. Panov V. I. Grishkovets V. V. Kachala A. S. Shashkov 《Chemistry of Natural Compounds》2006,42(1):61-66
Sixteen triterpene glycosides, three of which were new, hederagenin 28-O-β-D-glucuronopyranosyl ester and 28-O-β-D-gentiobiosyl ester and oleanolic acid 3-O-α-L-arabinopyranoside, were isolated from stem bark of Kalopanax septemlobum. The glycoside contents in stem bark of two varieties, maximowiczii and typicum, were compared.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 49–53, January–February, 2006. 相似文献
5.
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
6.
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
7.
The new cycloartane glycoside cyclogaleginoside D, which has the structure 25-O-β-D-glucopyranoside-20S, 25R-epoxycycloartan-3β, 6α, 16β, 25-tetraol 3-O-β-D-(2-O-acetyl)xylopyranoside was isolated from Astragalus galagiformis stems. The structure of the glycoside was established using chemical transformations and IR, PMR, and 13C NMR spectral data.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 255–256, May–June, 2006. 相似文献
8.
Huang Yun Cui Lijian Zhan Wenhong Dou Yuhong Wang Yongli Wang Qiang Zhao Ding 《Chemistry of Natural Compounds》2007,43(6):672-677
A novel steroidal saponin, along with 12 known steroidal compounds, was isolated from the rhizomes of Paris polyphylla var. chinensis. Spectral data, including two-dimensional NMR, showed that the structure of the novel saponin was 3β,21-dihydroxypregnane-5-en-20S-(22,16)-lactone-1-O-α-L-rhamnopyranosyl(1→2)-[β-D-xylopyranosyl(1→3)]-β-D-glucopyranoside. The isolated steroidal compounds were evaluated for their cytotoxic activity on human gastric cancer cell
line HepG2, SGC7901, BxPC3. Diosgenin-3-O-α-L-rhamnopyranosyl(1→2)[α-L-rabinofuranosyl(1→4)]-β-D-glucopyranoside exhibited the most potent cytotoxic activity among the isolated steroids.
Published in Khimiya Prirodnykh Soedinenii, No. 6, pp. 556–560, November–December, 2007. 相似文献
9.
Bing Luo Kun Zou Zhiyong Guo Feijun Dan Juizhi Wang Hui Wang 《Chemistry of Natural Compounds》2009,45(3):371-373
A new compound, β-sitosterylglucoside-3′-O-linoleate, named balanoinvolin, and three known compounds coniferin, methylconiferin, and 4-O-β-D-glucopyranosylconiferyl aldehyde, were isolated from Balanophora involucrate Hook. f. and their structures were determined by MS and 1D/2D NMR spectra.
Published in Khimiya Prirodnykh Soedinenii, No. 3, pp. 315–317, May–June, 2009. 相似文献
10.
Li-Min Dai Jian Tang Hui-Liang Li Yun-Heng Shen Cai-Yun Peng Wei-Dong Zhang 《Chemistry of Natural Compounds》2009,45(3):325-329
A new stilbene glycoside, 5-methylresveratrol-3,4′-O-β-D-diglucopyranoside (1), was isolated from the n-butanol fraction of the rhizomes of Veratrum dahuricum, together with five known stilbenoids: resveratrol-3-O-β-D-glycoside (2), 4′-methylresveratrol-3-O-β-D-glycoside (3), oxyresveratrol-4′-O-β-D-glycoside (4), oxyresveratrol-3-O-β-D-glycoside (5), and oxyresveratrol-3,4′-O-β-D-diglycoside (6), and found for the first time in the investigated plant. The structures of six isolates were identified on the basis of
1D and 2D NMR data. Compounds 1–6 showed platelet aggregation inhibition, and compound 1 had an IC50 value of 383.6 μM against platelet aggregation induced by AA.
Published in Khimiya Prirodnykh Soedinenii, No. 3, pp. 279–282, May–June, 2009. 相似文献
11.
M. P. Yuldashev B. A. Muminova A. A. Drenin E. Kh. Botirov 《Chemistry of Natural Compounds》2007,43(1):34-36
The new flavone glucoside viscioside, luteolin-4′-O-β-D-galactopyranoside, in addition to the known flavonoids apigenin, luteolin, quercetin, cinaroside, luteolin-4′-O-β-D-glucoside, and isoquercitrin were isolated from the aerial part of Vicia subvillosa.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 30–31, January–February, 2007. 相似文献
12.
From the branch tissue of Cephalotaxus mannii, the endophytic fungal strain CMM was isolated and determined to belong to the genus Aspergillus according to its internal
transcribed spacer (ITS) sequence of rDNA (ITS1-5.8S-ITS2). From the extracts of the fermentation broth of CMM, a new compound,
namely 5-O-α-D-glucopyranosyl-5-hydroxymellein (1), was isolated, together with a known compound 4-hydroxymellein (2). Their structures were elucidated on the basis of 1D and 2D NMR data.
Published in Khimiya Prirodnykh Soedinenii, No. 5, pp. 461–462, September-October, 2008. 相似文献
13.
Hyun-Jung Lee Oh-Kyu Lee Yeong-Han Kwon Don-Ha Choi Ha-Young Kang Hyeon-Yong Lee Ki-Hyon Paik Hak-Ju Lee 《Chemistry of Natural Compounds》2006,42(4):415-418
Four known isoflavone glucosides have been isolated from the bark of Amorpha fruticosa, which is a traditional remedy plant,
for the first time. They were elucidated as 3′-hydroxy-4′-methoxyisoflavone-7-O-β-D-glucopyranoside (1), 4′,6-dimethoxyisoflavone-7-O-β-D-glucopyranoside (2), 4′-methoxyisoflavone-7-O-β-D-glucopyranoside (3), and 3′,5-dihydroxy-4′-methoxyisoflavone-7-O-β-D-glucopyranoside (4), based on the UV, FT-IR, EIMS, FABMS, HREIMS, and NMR (1H and 13C, DEPT, COSY, NOESY, HMQC, and HMBC) data.
Published in Khimiya Prirodnykh Soedinenii, No. 4, pp. 336–338, July–August, 2006. 相似文献
14.
A method for preparative production of 3β,20S-dihydroxydammar-24-en-12-one 3,20-di-O-β-D-glucopyranoside (1), a glycoside from Panax japonicus, chikusetsusaponin-LT8 was developed. Chemical transformation of betulafolientriol, a component of Betula leaves extract, produced the 12-keto-20S-protopanaxadiol (3β,20S-dihydroxydammar-24-en-12-one) (2), exhaustive glycosylation of which by 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosylbromide (3) under Koenigs—Knorr reaction conditions with subsequent removal of protecting groups formed 3β,20S-dihydroxydammar-24-en-12-one
3,20-di-O-β-D-glucopyranoside (1). The principal glycosylation product was 3β,20S-dihydroxydammar-24-en-12-one 3-O-β-D-glucopyranoside if equimolar amounts of (2) and (3) were used.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 44–48, January–February, 2006. 相似文献
15.
T. V. Tyumkina I. F. Nuriev L. M. Khalilov V. R. Akhmetova U. M. Dzhemilev 《Chemistry of Natural Compounds》2009,45(1):61-65
The structure of a new compound was determined using PMR and 13C NMR spectroscopy (HHCOSY, HSBC, HMBC, ROESY) as 2-[3′-methoxy,4-O-β-D-galactopyranos-1-yl)benzyl]-3-(3″,4″-dimethoxybenzyl)-4hydroxybutyric acid, which was isolated for the first time from
seeds of Scotch thistle Onopordum acanthium L.
*For No. XII, see [1].
Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 53–55, January–February, 2009. 相似文献
16.
Twelve cardiac glycosides and aglycons were isolated from Strophanthus kombe seeds. Of these, eight were identified as cymarin, K-strophanthin-β, K-strophanthoside, periplocymarin, 17α-strophadogenin, erysimin (= helveticoside), erysimoside, and neoglucoerysimoside.
Four glycosides, preliminarily designated Sk-x, Sk-y, Sk-z, and Sk-20, were new. Their chemical structures were established
as 3β-O-β-D-glucopyranosyl-5β,14β,16β-trihydroxy-19-oxo-17α-card-20(22)enolide (17α-strophadogenin-3-O-β-D-glucoside), 3β-O-β-D-cymaropyranosyl-5β,14β,16β-trihydroxy-19-oxo-17α-card-20(22)enolide (17α-strophadogenin-3-O-β-D-cymaroside), 3β-O-β-D-cymaropyranosyl-4′-O-β-D-glucopyranosyl-6″-O-β-D-glucopyranosyl-5β, 14β,16β-trihydroxy-19-oxo-17α-card-20(22)enolide (17α-strophadogenin-3-O-strophanthotrioside), and 3-O-β-D-digitoxopyranosyl-4′-O-β-D-glucopyranosyl-6″-O-β-D-glucopyranosyl-5β,14β, 19-trihydroxy-card-20(22)enolide (strophanthidol-3-O-gentiobiosyldigitoxoside), respectively.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 156–159, March–April, 2006. 相似文献
17.
I. M. Chung H. Y. Park S. C. Chun J. J. Kim A. Ahmad 《Chemistry of Natural Compounds》2007,43(4):417-421
Three new compounds, 4-hydroxymethylene-7-(9,9,13-trimethylcyclohexyl)-heptanyl-3′,7′,7′-trimethylcyclohexa-2′,4′-dien-1′-oate
(1), 1-(n-hexadec-7-enoxy)-6-(n-octadecanoxy)-β-D-glucopyranoside (2), and (Z)-12-hydroxy-9-octadecenoic acid-12-β-D-glucopyranoside (3), along with the known compound hexacosanoic acid (4), were isolated and identified from the rice hulls of Oryza sativa. Their structures were elucidated by 1D and 2D NMR spectroscopic techniques (1H-1H COSY, 1H-13C HETCOR, DEPT) aided by EIMS, FABMS, HRFABMS, and IR spectra.
Published in Khimiya Prirodnykh Soedinenii, No. 4, pp. 344–347, July–August, 2007. 相似文献
18.
The new natural compound lavandoside with the structure ferulic acid 4-O-β-D-glucopyranoside was isolated by column chromatography over silica gel and polyamide from the extract of Lavandula spica flowers. The chemical structure of lavandoside was established using UV, NMR, and mass spectra and chemical transformations.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 133–134, March–April, 2008. 相似文献
19.
A. K. Umbetova M. I. Choudhary N. A. Sultanova G. Sh. Burasheva Zh. A. Abilov 《Chemistry of Natural Compounds》2006,42(3):332-335
The taraxeran-14-ene-type triterpenoids methyl 3-β-al-D-fridoolean-14-en-28-oate (1), 3-α-[3″,4′-dihydroxytrans-cinnamoyl]-oxy-D-fridoolean-14-en-28-oic acid (2), and β-sitosterol (3) were isolated from the aerial part of plants from the genus Tamarix (T. laxa, T. elongata) (Tamaricaceae). The structures of the triterpenoids were proved using spectral data (IR, UV, PMR, 13C NMR, 2D NMR 1H-1H COSY, HMQC, HMBC, mass). Compound 1 is new and not previously described in the literature.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 271–273, May–June, 2006. 相似文献
20.
Ting Han Huiliang Li Qiaoyan Zhang Hanchen Zheng Luping Qin 《Chemistry of Natural Compounds》2006,42(5):567-570
Two new thiazinediones along with five known compounds were isolated from the fruits of Xanthium strumarium L. The structures of the two new compounds were determined to be 7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol[1,4]thiazine-3,5-dione-11-O-β-D-glucopyranoside (1) and 2-hydroxy-7-hydroxymethyl-8,8-dimethyl-4,8-dihydrobenzol[1,4]thiazine-3,5-dione-11-O-β-D-glucopyranoside (2). The five known compounds were identified as xanthiazone (3), chlorogenic acid (4), ferulic acid (5), formononetin (6), and ononin (7), respectively.
Published in Khimiya Prirodnykh Soedinenii, No. 5, pp. 456–458, September–October, 2006. 相似文献