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50 publications found

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Group #1

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Triterpene glycosides ofHedera canariensis II. Determination of the structures of glycosides L-E2 and L-H3 from the leaves of Algerian ivy[1]A. S. Shashkov, [2]V. I. Grishkovets, [3]L. A. Yakovishin, [4]I. N. Shchipanova, [5]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF02336095 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; 30-norhederagenin [missing]2006-03-15
Triterpene Glycosides from Cussonia paniculata. II. Acetylated Glycosides from Leaves[1]V. I. Grishkovets, [2]I. I. Dovgii, [3]V. V. Kachala, [4]A. S. Shashkov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/S10600-005-0172-1 [ORCID]
beta-sitosterol [missing]; Cussonia paniculata [missing]; hederagenin 3-O-arabinoside [missing]; Saponin PE [missing]; Scheffursoside C [missing]2005-07-01
Triterpene glycosies of Hedera taurica VIII. Taurosides F1, F2, and F3 and a triterpenoid sulfate[1]V. I. Grishkovets, [2]N. V. Tolkacheva, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00629952 [ORCID]
Hedera taurica [missing]; Hederoside F [missing]2004-12-10
Triterpene glycosides of Hedera taurica VII. Structures of taurosides A and D from the leaves of Crimean ivy[1]V. I. Grishkovets, [2]N. V. Tolkacheva, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630363 [ORCID]
sitogluside [missing]; Hedera taurica [missing]; stigmasterol 3-O-beta-D-glucoside [missing]; Tauroside D [missing]2004-12-10
Triterpene glycosides ofHedera helix II. Determination of the structure of glycoside L-6d from common ivy leaves[1]A. S. Shashkov, [2]V. I. Grishkovets, [3]A. E. Kondratenko, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630605 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; CWYUSFMWQKCWDK-UHFFFAOYSA-N [missing]; 10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; Glycoside L-F2 [missing]2004-11-26
Triterpene glycosides fromHedera canariensis VI. Structure of L-G1 and L-G1b glycosides from leaves of canary ivy[1]L. A. Yakovishin, [2]V. I. Grishkovets, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF02323291 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; 30-norhederagenin [missing]; OEEIXDVEDJTQPJ-CNPWXMHRSA-N [missing]; ZWYKDDVVXUXZHA-VRVJSPLRSA-N [missing]1999-09-01
Triterpene glycosides ofHedera canariensis IV. Structures of glycosides L-F3, L-G0, and L-Gla from the leaves of Algerian ivy[1]L. A. Yakovishin, [2]V. I. Grishkovets, [3]I. N. Shchipanova, [4]A. S. Shashkov, [5]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF02238212 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; RHHSFOQSESHVRS-ZJSHWQRDSA-N [missing]; YYMHTAGTVKFQOP-KPFPMFHISA-N [missing]; ZCCWQTVZGNRCJQ-XZRDZOFRSA-N [missing]1999-01-01
Glycosides of the bulbs ofLilium regale[1]A. S. Gur'eva, [2]P. K. Kintya, [3]N. E. Mashchenko, [4]A. S. Shashkov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF01372346 [ORCID]
Lilium regale [missing]; disogluside [missing]; Prosapogenin A [missing]; KNZSXKKCTOYLSV-LQVCIKEXSA-N [missing]; LHHAGBJPCRSFHH-HHBSHQIMSA-N [missing]; Lilioglycoside [missing]; QUMAKTXJGFOROP-VJIQELDSSA-N [missing]1996-05-01
Triterpene and steroid glycosides of the genusMelilotus and their genins III. Funkioside B and protodioscin from the seeds ofMelilotus tauricus[1]G. V. Khodakov, [2]A. S. Shashkov, [3]P. K. Kintya, [4]Yu. A. Akimov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630609 [ORCID]
Lotus corniculatus [missing]; protodioscin [missing]; Melilotus tauricus [missing]; Funlioside B [missing]1994-11-01
Triterpene and steroid glycosides of the genusMelilotus and their genins II. Melilotoside D from the roots ofMelilotus albus[1]A. S. Shashkov, [2]G. V. Khodakov, [3]Yu. A. Akimov, [4]P. K. Kintya, [5]V. I. Grishkovets [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630608 [ORCID]
Melilotus albus [missing]; Melilotus officinalis [missing]; Lotus strictus [missing]; MKFBJAPUHISATM-QJSANWBGSA-N [missing]; Melilotoside D [missing]1994-11-01
Glycosides of (+)-syringaresinol and 2-methylbut-3-en-2-yl β-D-glucopyranoside from the leaves ofNolina microcarpa[1]G. V. Shevchuk, [2]A. S. Shashkov, [3]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630606 [ORCID]
Nolina microcarpa [missing]; (+)-syringaresinol beta-D-glucoside [missing]; liriodendrin [missing]; 3-Buten-1-ol, 2-methyl- [missing]; Crenulatin [missing]1994-11-01
Triterpene glycosides of Hedera taurica VI. Structures of hederosides G, H1, H2, and I from the berries of Crimean ivy[1]V. I. Grishkovets, [2]A. A. Loloiko, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630077 [ORCID]
Hedera taurica [missing]; hederacoside D [missing]; RYHDIBJJJRNDSX-ADAPURKRSA-N [missing]; hederacoside C [missing]; UEHILKCNLIKLEV-COMCTQTGSA-N [missing]; Hederoside I [missing]; VKICMPRVQHZPRV-UHFFFAOYSA-N [missing]; VKICMPRVQHZPRV-ULTYXNRESA-N [missing]; YPIHCZNMLNJVSW-DTYYCHTMSA-N [missing]; YPIHCZNMLNJVSW-UHFFFAOYSA-N [missing]1990-11-01
A sulfated glycoside from the preparation “tribestan”[1]N. E. Mashchenko, [2]R. Gyulemetova, [3]P. K. Kintya, [4]A. S. Shashkov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00601288 [ORCID]
Tribulus terrestris [missing]; gracillin [missing]; dioscin [missing]; protodioscin [missing]; Kallstroemia maxima [missing]; Protogracillin [missing]; disogluside [missing]; GMCGZPQYTRHQRU-ZFPKZURZSA-N [missing]; YQEMAEKYNNOCBY-MYGKTZIBSA-N [missing]; (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(9S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol [missing]1990-09-01

Group #2

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Steroids of the spirostan and furostan series from Nolina microcarpa IV. Structures of nolinogenin, nolinospiroside B, and nolinofuroside B[1]G. V. Shevchuk, [2]Yu. S. Vollerner, [3]A. S. Shashkov, [4]M. B. Gorovits, [5]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630172 [ORCID]
Nolina microcarpa [missing]; Nolinospiroside B [missing]; Nolinofuroside B [missing]2004-12-10
Tripenoid glycosides of alfalfa. VII. Medicosides E and F[1]A. É. Timbekova, [2]A. S. Shashkov, [3]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630211 [ORCID]
Medicago sativa [missing]; Medicoside F [missing]; Medicoside E [missing]2004-11-26
Triterpene glycosides of alfalfa VIII. Medinoside E from the leaves[1]A. É. Timbekova, [2]A. S. Shashkov, [3]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630212 [ORCID]
Medicago sativa [missing]; Medinoside E [missing]2004-11-26
Phytoecdysteroids of plants of the genus Serratula. Ajugasterone C 20,22-monoacetonide from Serratura wolffii[1]K. Miladera, [2]Z. Saatov, [3]Yu. D. Kholodova, [4]M. B. Gorovits, [5]A. S. Shashkov, [6]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00629794 [ORCID]
2004-11-26
Steroids of the spirostan and furostan series from plants of the genus Allium. XXVII. Alliosterol and allosides A and B from Allium suvorovii and Allium stipitatum ? Structural analogs of furostanols[1]Yu. S. Vollerner, [2]S. D. Kravets, [3]A. S. Shashkov, [4]B. Tashkhodzhaev, [5]M. B. Gorovits, [6]M. R. Yagudaev, [7]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00629759 [ORCID]
Allium stipitatum [missing]; Allium suworowii [missing]; Alloside B [missing]; Alloside A [missing]2004-11-26
Steroids of the spirostan and furostan series from plants of the genus Allium. Structure of anzurogenin A from Allium suvorovii and A. stipitatum[1]Yu. S. Vollerner, [2]S. D. Kravits, [3]A. S. Shashkov, [4]M. B. Gorovits, [5]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00597575 [ORCID]
diosgenin [missing]; Allium stipitatum [missing]; Allium suworowii [missing]; Yuccagenin [missing]; Alliogenin [missing]; Anzurogenin A [missing]2004-11-24
Triterpene glycosides ofScheffleropsis angkae. II. Structure of glycosides L-E1, L-E2, L-K1, and L-K2[1]A. S. Stolyarenko, [2]V. I. Grishkovets, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF02238340 [ORCID]
Schefflera subintegra [missing]; (1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-6a-(hydroxymethyl)-1,2,6b,9,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid [missing]; GJYZUWYMGVAEKB-XSZAPIORSA-N [missing]; IOOZDEIXPWWSBT-RDJDRYPDSA-N [missing]; Guaianin N [missing]; OTPKBELVFIMVQF-ZWRWPXEASA-N [missing]; 3beta-[(3-O-beta-D-Glucopyranosyl-alpha-L-arabinopyranosyl)oxy]urs-12-en-28-oic acid [missing]; ZFMQTIIBFLOBCK-YMVZIHOTSA-N [missing]2000-05-01
Triterpene glycosides ofHedera helix III. Structure of the triterpene sulfates and their glycosides[1]V. I. Grishkovets, [2]A. E. Kondratenko, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF02238213 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; Hedera taurica [missing]; 10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; ILKZUGRHLIZRQK-UHFFFAOYSA-N [missing]; hederacoside D [missing]; 9-(Hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; Methyl 9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate [missing]; Hederagenin base + O-Hex [missing]; CMTHKQBIQCNSHW-UHFFFAOYSA-N [missing]; 6-[[8a-Carboxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid [missing]; FYBHGBVHRPQYQC-GWIVOYSISA-N [missing]; Glycoside L-G3;Tauroside G3 [missing]; CID 15127236 [missing]; 2,2,6a,6b,9,9,12a-Heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; 10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; 2-[2-[[8a-(Hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol [missing]; Momordin Ib [missing]; Sapindoside A [missing]; 10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; Methyl 10-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate [missing]; MYVNIRXXBZQJLZ-UHFFFAOYSA-N [missing]; chikusetsusaponin 5 [missing]; NHWXLQPHNIUEFJ-UHFFFAOYSA-N [missing]; eleutheroside M [missing]; OEEIXDVEDJTQPJ-UHFFFAOYSA-N [missing]; OVJNJRGKGRKYIY-UHFFFAOYSA-N [missing]; (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; PVNXMFDNBHBTQH-UHFFFAOYSA-N [missing]; RGTOZRZIOJHHFA-UHFFFAOYSA-N [missing]; RHHSFOQSESHVRS-UHFFFAOYSA-N [missing]; RJWVNQDEFVAPCR-UHFFFAOYSA-N [missing]; 10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; 10-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; hederacoside C [missing]; 5-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; VKICMPRVQHZPRV-UHFFFAOYSA-N [missing]; VPMAVMNCCCVJSK-CXGCXQJASA-N [missing]; 6-[[8a-[6-[[6-(Acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid [missing]; 10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; 6-[(8a-Carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-3,4-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid [missing]; 10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; XQHVCDKAFHCPPN-UHFFFAOYSA-N [missing]; 10-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; Hederasaponin F [missing]; YPIHCZNMLNJVSW-UHFFFAOYSA-N [missing]; YYMHTAGTVKFQOP-UHFFFAOYSA-N [missing]; ZCCWQTVZGNRCJQ-UHFFFAOYSA-N [missing]; ZGMSGGSISLPGEC-UHFFFAOYSA-N [missing]; 2,2,6a,6b,9,9,12a-Heptamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; ZWYKDDVVXUXZHA-UHFFFAOYSA-N [missing]1999-01-01
Triterpene glycosides ofHedera canariensis. I. Structures of glycosides L-A, L-B1, L-B2, L-C, L-D, L-E1 1, L-G1, L-G2, L-G3, L-G4, L-H1, L-H2, AND L-I1 from the leaves ofHedera canariensis[1]V. I. Grishkovets, [2]D. Yu Sidorov, [3]L. A. Yakovishin, [4]N. N. Arnautov, [5]A. S. Shashkov, [6]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF01372340 [ORCID]
Hedera helix [missing]; Hedera canariensis [missing]; α-hederin [missing]; hederagenin 3-O-arabinoside [missing]; beta-Hederin [missing]; kalopanaxsaponin b [missing]; cauloside D [missing]; dipsacoside b [missing]; Hederasaponin B [missing]; (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; MYVNIRXXBZQJLZ-ZHEUBHLBSA-N [missing]; NHWXLQPHNIUEFJ-XSFOBXPPSA-N [missing]; PVNXMFDNBHBTQH-WZJLZQBYSA-N [missing]; 3-O-alpha-L-Arabinopyranosylechinocystic acid [missing]; WQVNDHHTUJYLTJ-XDNDNJDCSA-N [missing]1996-05-01
Triterpene glycosides ofHedera helix I. The structures of glycosides L-1, L-2a, L-2b, L-3, L-4a, L-4b, L-6a, L-6b, L-6c, L-7a, and L7-b from the leaves of common ivy[1]V. I. Grishkovets, [2]A. E. Kondratenko, [3]N. V. Tolkacheva, [4]A. S. Shashkov, [5]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630604 [ORCID]
Hedera helix [missing]; α-hederin [missing]; hederagenin 3-O-arabinoside [missing]; beta-Hederin [missing]; kalopanaxsaponin b [missing]; cauloside D [missing]; dipsacoside b [missing]; Hederasaponin B [missing]; (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid [missing]; Tauroside D [missing]; PVNXMFDNBHBTQH-WZJLZQBYSA-N [missing]; 3-O-alpha-L-Arabinopyranosylechinocystic acid [missing]; WQVNDHHTUJYLTJ-XDNDNJDCSA-N [missing]1994-11-01
Triterpene glycosides of Hedera taurica X. Structures of compounds F4, I, and J from the leaves of Crimean ivy[1]V. I. Grishkovets, [2]N. V. Tolkacheva, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630436 [ORCID]
Hedera taurica [missing]; methyl (4aR,5R,6aR,6aS,6bR,8aS,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate [missing]; YAWJHQZYFGHLSY-KDEOLCFCSA-N [missing]1992-11-01
Steroids of the spirostan and furostan series from nolina microcarpa III. Structure of nolinofurosides G and H[1]G. V. Shevchuk, [2]Yu. S. Vollerner, [3]A. S. Shashkov, [4]M. B. Gorovits, [5]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00629931 [ORCID]
Nolina microcarpa [missing]; [(1S,2S,4S,8S,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-14-yl] hydrogen sulfate [missing]; UOVPNRYUBZGFNE-GQOTVEFXSA-N [missing]1991-11-01
Steroids of the furostan and spirostan series from Nolina microcarpa II. structures of nolinospiroside D and nolinofurosides D, E, and F[1]G. V. Shevchuk, [2]Yu. S. Vollerner, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630362 [ORCID]
Nolina microcarpa [missing]; DREADZZMWCBWPA-NGGLJIRASA-N [missing]; Nolinospiroside D [missing]; NSNUSRJUPCLYHS-HYBPNVACSA-N [missing]; NXYMADNBCYMQOQ-HDZRGBNQSA-N [missing]1991-09-01
Triterpene glycosides of Hedera taurica. V. Structure of hederosides C and E1 from Crimean ivy berries[1]V. I. Grishkovets, [2]A. A. Loloiko, [3]A. S. Shashkov, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00607540 [ORCID]
Hedera taurica [missing]; α-hederin [missing]; IKBJJBUMCSZLLR-POQUFAKPSA-N [missing]; XRAOSDJJKHKKPY-ATMJNGMXSA-N [missing]1990-01-01
Steroids of the spirostan and furostan series from plants of the genus Allium. XXV. Structure of anzurogenin B from Allium suvorovii and Allium Stipitatum[1]Yu. S. Vollerner, [2]S. D. Kravets, [3]A. S. Shashkov, [4]M. B. Gorovits, [5]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00596746 [ORCID]
Allium stipitatum [missing]; diosgenin [missing]; Anzurogenin B [missing]; 5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,18,19-tetrol [missing]; Spirost-5-en-2,3-diol [missing]; 15,16,18-Trihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one [missing]1988-01-01
Triterpene glycosides ofHedera taurica I. Structure of tauroside E from the leaves ofHedera taurica[1]A. S. Shashkov, [2]V. I. Grishkovets, [3]A. A. Loloiko, [4]V. Ya. Chirva [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00600827 [ORCID]
Hedera taurica [missing]; α-hederin [missing]; KEOITPILCOILGM-NUJXUPTKSA-N [missing]; Sapindoside A [missing]1987-01-01
Steroids of the spirostand and furostan series from plants of the genusAllium. II. The structure of alliospiroside B fromAllium cepa[1]C. D. Kravets, [2]Yu. S. Vollerner, [3]M. B. Gorovits, [4]A. S. Shashkov, [5]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00599259 [ORCID]
Allium cepa [missing]; Alliospiroside B [missing]; HWYCRLFVQVFKPD-HYWUOLERSA-N [missing]; (25S)-1beta-(2-O-alpha-L-Rhamnopyranosyl-beta-D-xylopyranosyloxy)spirost-5-en-3beta-ol [missing]1986-09-01
Steroids of the spirostan and furostan series from plants of the genus Allium. XXI. Structure of alliospiroside a and alliofuroside a from Allium cepa[1]S. D. Kravets, [2]Yu. S. Vollerner, [3]M. B. Gorovits, [4]A. S. Shashkov, [5]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00574733 [ORCID]
Allium cepa [missing]; 25(S)-Ruscogenin 1-O-I<<-L-rhamnopyranosyl-(1 L2)-EC-D-xylopyranoside [missing]1986-03-01
Triterpene glycosides ofSilphium perfoliatum. IV. Structure of siliphioside C[1]É. S. Davidyants, [2]Zh. M. Putieva, [3]A. S. Shashkov, [4]V. A. Bandyukova, [5]N. K. Abubakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00579143 [ORCID]
Silphium perfoliatum [missing]; Silphioside C [missing]1985-07-01

Group #3

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Components of Haplophyllum pedicellatum[1]V. I. Akhmedjanova, [2]A. S. Shashkov, [3]L. Angenot, [4]R. Shakirov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/S10600-008-9166-0 [ORCID]
2008-12-19
Folipidine, a New Type Quinoline Alkaloid from Plants of the Haplophyllum Genus[1]V. I. Akhmedzhanova, [2]Kh. A. Rasulova, [3]I. A. Bessonova, [4]A. S. Shashkov, [5]N. D. Abdullaev, [6]L. Angenot [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/S10600-005-0075-1 [ORCID]
Haplophyllum griffithianum [missing]; skimmianine [missing]; Lopac-D-7814 [missing]; (1S,2S,3R)-1-(4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl)butane-1,2,3,4-tetrol [missing]2005-01-01

Group #4

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Structures of two new diterpenoids from Teucrium polium[1]A. M. Galstyan, [2]A. S. Shashkov, [3]G. B. Oganesyan, [4]V. A. Mnatsakanyan, [5]É. P. Serebryakov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630646 [ORCID]
Teucrium polium [missing]; (1R,8S,9S,10S,11R,12R)-9-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-11-hydroxy-12-(hydroxymethyl)-10-methyl-2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9-carboxylic acid [missing]; (1S,8S,9R,10R,12R)-9-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-12-(hydroxymethyl)-10-methyl-2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9-carboxylic acid [missing]1992-09-01
Phenylpropanoid glycosides of Teucrium polium[1]G. B. Oganesyan, [2]A. M. Galstyan, [3]V. A. Mnatsakanyan, [4]A. S. Shashkov, [5]P. V. Agababyan [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00630353 [ORCID]
verbascoside [missing]; Teucrium polium [missing]; teupolioside [missing]; [(2R,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate [missing]; CID 10373017 [missing]1991-09-01

Group #5

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Triterpene saponins of Caltha polypetala. Glycosides G and I[1]M. M. Vugalter, [2]G. E. Dekanosidze, [3]O. D. Dzhikiya, [4]A. S. Shashkov, [5]�. P. Kemertelidze [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00596749 [ORCID]
Caltha polypetala [missing]2004-12-10
Steroid glycosides of the leaves of Yucca aloifolia[1]M. M. Benidze, [2]O. D. Dzhikiya, [3]T. A. Pkheidze, [4]É. P. Kemertelidze, [5]A. S. Shashkov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/BF00597803 [ORCID]
Yucca aloifolia [missing]; KDCJQGJICKTTAC-WFOZKSPSSA-N [missing]; RQVBTHASPDINHQ-PPMCLAIVSA-N [missing]1987-07-01

Group #6

TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Alkaloids of Arundo donax L. Part 15. A New Dimeric Indole Alkaloid Arundarine from the Roots of Arundo donax L[1]V. U. Khuzhaev, [2]I. Zh. Zhalolov, [3]M. G. Levkovich, [4]S. F. Aripova, [5]A. S. Shashkov [Full author list]ChemInform [missing]DOI: 10.1002/CHIN.200518178 [ORCID]
Arundo donax [missing]; Arundarine [missing]2005-04-06
Alkaloids of Arundo donax L.[1]V. U. Khuzhaev, [2]I. Zh. Zhalolov, [3]M. G. Levkovich, [4]S. F. Aripova, [5]A. S. Shashkov [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-005-0033-X [ORCID]
Arundo donax [missing]; gramine [missing]; 3,3'-diindolylmethane [missing]; N-phenyl-1-naphthylamine [missing]; N-phenyl-2-naphthylamine [missing]; Deoxyvasicinone [missing]; 3-[2-(methylamino)ethyl]indole-2,3-diol [missing]; Bis(4-ethoxycarbonylphenylamino)methane [missing]; 1'-Methylspiro[1,2-dihydro-3,1-benzoxazine-4,3'-pyrrolidine]-2'-one [missing]; Donaxarine [missing]; Arundarine [missing]2004-08-01

Group #7

Matched potential author: Alexander S. Shashkov - author of 776 items
TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Structure of the O-polysaccharide of Escherichia coli O60[1]A. V. Perepelov, [2]O. I. Naumenko, [3]S. N. Senchenkova, [4]A. S. Shashkov, [5]A. O. Chizhov, [6]Yu. A. Knirel [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-018-2340-Z [ORCID]
Escherichia coli [missing]2018-11-01Alexander S. Shashkov (Q96034980; 776 items)
Structure of О-polysaccharide of Escherichia coli O95: a disaccharide repeating unit containing d-fucose and d-threo-pent-2-ulose (xylulose)[1]A. V. Perepelov, [2]S. N. Senchenkova, [3]N. A. Kalinchuk, [4]A. S. Shashkov, [5]Yu. A. Knirel [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-018-2310-5 [ORCID]
Escherichia coli [missing]2018-10-01Alexander S. Shashkov (Q96034980; 776 items)
Escherichia coli O106, a new member of a group of enteric bacteria sharing an O-polysaccharide backbone structure[1]A. S. Shashkov, [2]S. N. Senchenkova, [3]O. I. Naumenko, [4]N. A. Kalinchuk, [5]A. V. Perepelov, [6]Yu. A. Knirel [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-018-2253-X [ORCID]
Escherichia coli [missing]2018-08-01Alexander S. Shashkov (Q96034980; 776 items)
New fructan — the O-specific polysaccharide from Escherichia coli O92[1]S. N. Senchenkova, [2]Guangnan Xu, [3]Yanfen Qi, [4]A. V. Perepelov, [5]A. S. Shashkov, [6]Bin Liu, [7]Yu. A. Knirel [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-017-1889-2 [ORCID]
Escherichia coli [missing]2017-07-01Alexander S. Shashkov (Q96034980; 776 items)
Structure of the O-polysaccharides of Escherichia coli O162 containing 4-deoxy-D-arabino-hexose and structurally related O-polysaccharides of E. coli O101[1]A. S. Shashkov, [2]S. N. Senchenkova, [3]A. V. Perepelov, [4]Yu. A. Knirel [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-017-1802-Z [ORCID]
Escherichia coli [missing]2017-04-01Alexander S. Shashkov (Q96034980; 776 items)
Structure of the O-polysaccharide of Erwinia carotovora ssp. atroseptica GSPB 9205 containing a new higher branched monosaccharide[1]S. N. Senchenkova, [2]A. S. Shashkov, [3]Yu. A. Knirel, [4]M. Ahmed, [5]A. Mavridis, [6]K. Rudolph [Full author list]Russian Chemical Bulletin [missing]DOI: 10.1007/S11172-005-0394-1 [ORCID]
Erwinia carotovora [missing]2005-05-01Alexander S. Shashkov (Q96034980; 776 items)

Misc

Matched potential author: Alexander S. Shashkov - author of 776 items
TitleAuthors (identified)Published InIdentifier(s)TopicPublished DateMatch?
Cell Wall Glycopolymers as a Diagnostic Trait of Arthrobacter crystallopoietes[1]N. V. Potekhina, [2]E. V. Ariskina, [3]A. S. Shashkov, [4]T. M. Tul’skaya, [5]L. I. Evtushenko [Full author list]Mikrobiologija [missing]DOI: 10.1134/S0026261722300051 [ORCID]
2022-06-01Alexander S. Shashkov (Q96034980; 776 items)
The isolation, preliminary structural studies, and physiological activity of water-soluble polysaccharides from the squeezed berries of the snowball treeViburnum opulus[1]R. G. Ovodova, [2]V. V. Golovchenko, [3]S. V. Popov, [4]A. S. Shashkov, [5]Yu. S. Ovodov [Full author list]Russian journal of bioorganic chemistry [missing]DOI: 10.1007/BF02758861 [ORCID]
Viburnum opulus [missing]; Maltotriose [missing]2008-06-04
Cycloartanes from Astragalus flexus[1]T. Kh. Naubeev, [2]K. K. Uteniyazov, [3]V. V. Kachala, [4]A. S. Shashkov [Full author list]Chemistry of Natural Compounds [missing]DOI: 10.1007/S10600-007-0135-9 [ORCID]
Astragalus flexus [missing]; Astrasieversianin XVI [missing]; astragaloside IV [missing]; Astragaloside VII [missing]; Astrasieversianin15(RG) [missing]; Astraverrucin I [missing]; Astrasieversianin X [missing]2007-05-01
A novel approach to the synthesis of regular monocyclopentanoids of the sesquiterpene series[1]V. V. Veselovskii, [2]B. T. Zhuzbaev, [3]S. M. Adekenov, [4]A. S. Shashkov, [5]A. M. Moiseenkov [Full author list]Bulletin of the Russian Academy of Sciences Division of Chemical Science [missing]DOI: 10.1007/BF00863075 [ORCID]
1992-03-01

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NameDescriptionAuthored itemsIdentifiersEmployer(s)
Alexander S. Shashkovbiochemist776N.D. Zelinsky Institute of Organic Chemistry [missing]
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