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1.
M. M. Benidze O. D. Dzhikiya T. A. Pkheidze É. P. Kemertelidze A. S. Shashkov 《Chemistry of Natural Compounds》1988,23(4):448-452
Two new steroid glycosides have been isolated from the leaves of aloe yucca and their structures have been established. Glycosides B and C are tigogenin penta-and hexaosides. Glycoside B, which we have called yuccaloeside B is (25R)-5-spirostan-3-ol 3-{[O--D-glucopyranosyl-(12)]-[O--L-rhamnopyranosyl-(14)-O--D-glucopyranosyl-(13)]-O--D-glucopyranosyl-(14)--D-galactopyranoside}, and glycoside C, which we have called yuccaloeside C is (25R)-5-spirostan-3-ol 3-{[(O--D-glucopyranosyl-(13)-O--D-glucopyranosyl-(12)]-[O--L-rhamnopyranosyl-(14)-O--D-glucopyranosyl-(13)]-O--D-glucopyranosyl-(14)--D-galactopyranoside}.N. G. Kutateladze Institute of Pharmacochemistry of the Georgian SSR Academy of Sciences, Tbilisi. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 537–542, July–August, 1987. 相似文献
2.
I. P. Dragalin A. P. Gulya V. V. Krokhmalyuk P. K. Kintya 《Chemistry of Natural Compounds》1976,11(6):772-774
Summary From the roots ofYucca filamentosa L. we have isolated a new sarsasapogenin glycoside, yuccoside E, which is 3-O-{[O--D-galactopyranosyl(1 2)]-[-O--D-galactopyranosyl(1 6)]-O--D-glucopyranosyl-(1 4)--D-glucopyranosyl}-(25S), 5 -spirostan-3-ol.Institute of Chemistry, Academy of Sciences of the Moldavian SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 747–750, November–December, 1975. 相似文献
3.
Summary FromAllium narcissiflorum Wells have been isolated for the first time trillin and a glycoside B, which proved to be 3-O-[-O-D-glucopyranosyl-(1 3)-O--D-glucopyranosyl-(1 6)-O--D-glucopyranosyl-(1 ]-26-O-[-D-glucopyranosyl-(1 ]-25R-furost-5-ene-3,22 , 26-triol.Institute of Chemistry, Academy of Sciences of the Moldavian SSR, Kishinev. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 55–58, January–February, 1976. 相似文献
4.
V. Ya. Chirva P. K. Kintya V. A. Sosnovskii P. E. Krivenchuk N. Ya. Zykova 《Chemistry of Natural Compounds》1970,6(2):213-215
Conclusions The structure of two triterpone glycosides fromSapindus mukorossi Gaertn. has been established. It has been shown that sapindoside A is hederagenin 3-O--L-arabinosyl-(2 1)--L-rhamnopyranoside and sapindoside B is the 3-O--L-arabopyranosyl-(2 1)-O--L-rhamnopyranosyl-(3 1)--D-xylopyranoside. 相似文献
5.
Sh. Sh. Afiyatullov A. I. Kalinovskii V. A. Stonik 《Chemistry of Natural Compounds》1988,23(6):691-696
Two new triterpene glycosides — cucmariosides C1 and C2 — have been isolated from the Far Eastern holothurianEupentacta (=Cucumaria)fraudatrix Djakonov et Baranova. Their structures have been established with the aid of13C NMR and PMR spectroscopy, partial acid hydrolysis, periodate oxidation, and methylation as 16-acetoxy-3-{[3-O-methyl--D-xylopyranosyl-(13)--D-glucopyranosyl-(14)] [-D-xylopyranosyl-(12)]--D-quinovopyranosyl-(12)--D-xylopyranosyloxy}holosta-7,23,24(cis)-triene and 16-acetoxy-3-{[3-O-methyl--D-xylopyranosyl-(13)--D-glucopyranosyl-(14)] [-D-xylopyranosyl-(12)]--D-quinovopyranosyl-(12)--D-xylopyranosyloxy}holosta-7,22,24(trans)-triene, respectively.Pacific Ocean Institute of Bioorganic Chemistry of the Far-Eastern Scientific Center of the USSR Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 831–837, November–December, 1987. 相似文献
6.
The Hückel approximation in MO LCAO is used to show that the anion system of cyclopent-4-ene-1,3-dione should have two * transitions: a weak one at long wavelengths, NV1, and a strong one at short wavelengths, C=C(1,3)V1. An ethylene, phenyl, or acyl group at position 2 gives rise to a new strong band, NC=C(2), Nbenz, or NC=O (2). A p-nitrophenyl group at position 2 gives rise to a strong NNO2 band, which overlaps the weak NV1 band, while the Nbenz band becomes weak and is virtually lost from the spectrum. 相似文献
7.
A. É. Timbekova A. L. Vereschagin A. A. Semenov N. K. Abubakirov 《Chemistry of Natural Compounds》1990,26(2):178-183
A new triterpene pentaglycoside — medicoside L — has been isolated from the roots ofMedicago sativa L. (Leguminosae). It has the structure of medicagenic acid 28-O--D-glucopyranoside 3-O-{[O--D-glucopyranosyl-(1 2)][O--L-rhamnopyranosyl-(1 3)]-O--D-glucopyranosyl-(1 2)}--D-glucopyranoside.Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 221–228, March–April, 1990. 相似文献
8.
A. B. Makhmatkulov Z. A. Kuliev A. D. Bdovin M. R. Yagudaev V. M. Malikov 《Chemistry of Natural Compounds》1992,28(1):48-54
Six proanthocyanidins have been isolated from the roots ofPolygonium coriarium. The structures of three oligomeric proanthocyanidins have been established: taranin, consisting of [epigallocatechin gallate]-(48)-[epigallocatechin gallate]-(48)-[epigallocatechin-(48)-epigallocatechin2-(48)-epigallocatechin; taranoside A - [epigallocatechin gallate]-7-0-[-(16)--D-Glcp]3-(48)-[epigallocatechin-(48)-epigallocatechin]2-(48)-gallocatechin; and taranoside B - [epigallocatechin gallate]-7-O-[-(16)--D-Glcp]4-(48)-[epigallocatechin-(48)-epigallocatechin]2-(48)-epigallocatechin-(48)-[epigallocatechin gallate).Institute of the Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 59–67, January–February, 1992 相似文献
9.
N. P. Elinov G. A. Vitovskaya E. P. Anan'eva Yu. B. Maryukhta 《Chemistry of Natural Compounds》1986,21(6):704-708
The structure of an extracellular mannan formed by the yeastBullera tsugae has been studied. It has been shown that the repeating unit of this polysaccharide contains -(13)- and -(14)-bound D-mannopyranose residues in equimolar ratio. A comparison has been made of the polymer under investigation with the extracellular mannan from a yeast of the genusRhodotorula.
Leningrad Institute of Pharmaceutical Chemistry. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 746–750, November–December, 1985. 相似文献
10.
Summary Two triterpene glycosides — caulosides b and c — have been isolated from a methanolic extract of the leaves ofCaulophyllum robustum maxim. Cauloside b has been identified as hederagenin 3--L-rhamnopyranosyl-(12)--L-arabinopyranoside, while cauloside c has the structure of hederagenin 3-0--L-arabinopyranosyl(13)--L-pyranosyl-(12)--L-arabinopyranoside.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Scientific Center of the Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 174–176, March–April, 1979. 相似文献
11.
Conclusions The triterpene glycosides scabiosides D, E, F, and G have been isolated from the roots ofPatrinia scabiosofolia Fisch. et Link. It has been established that scabioside D is O--D-glucopyranosyl-(1 4)-O--L-arabopyranosyl-(1 3)-O-oleanoloyl-(28 1)--D-xylopyranose, and scabioside E is O--D-glucopyranosyl-(1 4)-O--L-arabopyranosyl-(1 3)-O-oleanoloyl-(28 1)-O--D-xylopyranosyl-(4 1)--L-rhamnopyranose. 相似文献
12.
A. Fargašová A. Bumbálová E. Havránek 《Journal of Radioanalytical and Nuclear Chemistry》1997,218(1):107-110
Bioaccumulation of six metals (Cu2+, Cu+, Mo6+, Mn2+, V5+, Ni2+) and their combinations by algaScenedesmus quadricauda was determined by using radio nuclide X-ray fluorescence (RXFA). The metals were added into the cultivation medium in concentrations corresponding with EC50 value for each metal. The obtained results indicate that Ni2+, Cu2+ and Cu+ were accumulated in high amounts (20%, 17.5% and 15.19%) the Mo6+ ion (<0.2%) was accumulated in the lowest amount. For metal-metal interactions in accumulation of metal ions by algaS. quadricauda three types of answers were determined: inhibition (MoCu2+, Ni, Mn, V; VNi, Mn; MnNi, Cu2+, Cu+; Cu+Ni; Cu2+Ni; NiMn, V), enhancement (VCu+; Cu2+Mn;Cu+V, Mn; MnV; NiCu2+, Cu+) and neutral effect (VMo; Cu2+Mo; Cu+Mo; MuMo; NiMo). 相似文献
13.
S. D. Kravets Yu. S. Vollerner A. S. Shashkov M. B. Gorovits N. K. Abubakirov 《Chemistry of Natural Compounds》1988,23(6):700-706
Two new steroid glycosides of the spirostan series have been isolated from the fruit ofAllium cepa L. (family Liliaceae): alliospirosides C and D. On the basis of chemical transformations and spectral characteristics it has been established that the aglycon of both glycosides is a new steroid sapogenin — cepagenin — having the structure of (24S,25R)-spirost-5-ene-1,3,24-triol. Alliospirosides C and D are cepagenin 1-O-[O--L-rhamnopyranosyl-(12)-L-arabinopyranoside] and 1-O-[O--L-rhamnopyranosyl-(12)-O--D-galactopyranoside], respectively.Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 843–849, November–December, 1987. 相似文献
14.
V. G. Strigunov N. I. Grishkovets N. V. Tolkacheva A. S. Shashkov 《Chemistry of Natural Compounds》2001,37(2):173-176
Stem bark ofTetrapanaxpapyriferum yielded the new triterpene glycosides 3-O-[-D-glucopyranosyl-(13)]--D-galactopyranosyl-(12)-O--L-arabinopyranosides of oleanolic and echinocystic acids and their 28-O--L-rhamnopyranosyl-(14)-O--D-glucopyranosyl-(16)-O--D-glucopyranosyl esters. Their structures were established using chemical and physicochemical methods 相似文献
15.
P. K. Kintya A. I. Stamova L. B. Bakinovskii V. V. Krokhmalyuk 《Chemistry of Natural Compounds》1978,14(3):290-294
Summary The chemical structures of two new steroid glycosides from the leaves ofPolygonatum latifolium have been shown. Polygonatoside E is 3-[0--D-glucopyranosyl-(1 3)-0--D-glucopyranosyl-(1 4)-0--d-galactopyranosyl-(1 3)--D-glucopyranosyloxy]-(25R)-spirost-5-ene, and protopolygonatoside E is 26--D-galactopyranosyl-(1 3)--D-glucopyranosyloxy]-(25R)-furost-5-en-22-ol.Institute of Chemistry, Academy of Sciences of the Moldavian SSR, Kishenev. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 350–354, May–June, 1978. 相似文献
16.
Structure of codonoside B 总被引:4,自引:0,他引:4
On the basis of chemical transformations and physicochemical characteristics of the compounds obtained it has been established that codonoside B — the main triterpene glycoside ofCodonopsis lanceolata (Sieb. et Zucc.) Benth. et Hook., has the structure of echinocystic acid 3-O--D-glucopyranuronoside 28-O-[O--D-xylopyranosyl-(1 4)-O--L-rhamnopyranosyl-(1 4)-O--D-glucopyranosyl-(1 2)--L-arabinopyranoside].Far Eastern State University, Vladivostok. Pacific Ocean Institute of Organic Chemistry, Far Eastern Branch, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 368–372, May–June, 1989. 相似文献
17.
V. I. Kalinin A. I. Kalinovskii Sh. Sh. Afiyatullov 《Chemistry of Natural Compounds》1988,24(2):187-189
The holothurianEupentacta pseudoquinquisemita Deichmann collected in Kraternaya Bay, Ushishir Islands has yielded two triterpene pentaosides — the previously known cucumarioside C2, and cucumarioside H, which is a new glycoside. With the aid of13C NMR spectroscopy and solvolytic desulfation its structure has been determined as 6-acetoxy-3-([3-O-methyl--D-xylopyranosyl-(1 3)--D-glucopyranosyl-(1 4)] [-D-xylopyranosyl-(1 4)] [-D-xylopyranosyl-(1 2)]--D-quinovopy-ranosyl-(1 2)-(4-O-sulfato--D-xylopyranosyloxy)holosta-7,22,24(trans)-triene. Cucumarioside H was also identified inEupentacta (=Cucumaria)fraudatrix from Posyet Bay, Sea of Japan.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, USSR Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 221–225, March–April, 1988. 相似文献
18.
4-O--D-Manopyranosyl-D-mannose, O--D-mannopyranosyl-(l4)-O--D-mannopyranosyl-(14)-D-mannose, and 0--D-mannopyranosyl-(14)-O--D-mannopyranosyl-(l4)-O--D-mannopyranosyl-(l4)-D-mannose have been isolated fron the products of the partial hydrolysis of ungeromannan-V, obtained fron the bulbs ofUngernia vvedneskyi, and have been identified. This set of oligosaccharides confirms the regular structure of the carbohydrate chain of ungeromannan-V, which consists of a linear sequence of -14-bound D-mannose residues.DeceasedTranslated from Khimiya Prirodnykh Soedineii, No. 4, pp. 434–436, July–August, 1981. 相似文献
19.
Conclusions It has been found that the roots ofSaponaria officinalis L. contain three oligosaccharides.Two of them have been isolated: gentiobiose and the pentasaccharide saponarose. It has been shown that the latter is O--D-galactopyranosyl-(1 3)-O--D-galactopyranosyl-(1 3)-O--D-galactopyranosyl-(1 3)-O--D-galactopyranosyl-(1 1)--D-glucopyranoside.Khimiya Prirodnykh Soedinenii, Vol. 5, No. 6, pp. 469–473, 1969 相似文献
20.
S. A. Zinova V. V. Isakov A. I. Kalinovskii Zh. I. Ul'kova K. P. Ulanova L. I. Glebko 《Chemistry of Natural Compounds》1992,28(3-4):305-311
The isolation of four triterpene glycosides from the roots of the dahurian anemonePulsatilla dahurica (Fisch. ex DC) Spreng, is described together with their identification, on the basis of chemical transformations, spectral characteristics, and literature analogies, as hederagenin 3-O--L-arabinoside, hederagenin 3-O-[O--D-glucopyranosyl-(12)--L-arabinopyranoside], hederagenin 3-O--L-arabinopyranoside 28-O-[O--L-rhamnopyranosyl-(14)--D-glucopyranosyl-(16)--D-glucopyranoside], and hederagenin 3-O-[O--D-glucopyranosyl-(14)--L-arabinopyranoside] 28-O-[O--L-rhamnopyranosyl-(14)--D-glucopyranosyl-(16)--D-glucopyranoside].Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, Russian Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, Nos. 3,4, pp. 349–356, May–August, 1992. 相似文献