About: Urs-12-ene-3,28-diol, (3beta)-

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About: Urs-12-ene-3,28-diol, (3beta)- Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

group of stereoisomers with the chemical formula C₃₀H₅₀O₂

Attributes	Values
rdf:type	Item
description	groep van stereo-isomeren (nl) група стереоізомерів з хімічною формулою C₃₀H₅₀O₂ (uk) group of stereoisomers with the chemical formula C₃₀H₅₀O₂ (en)
rdfs:label	Urs-12-ene-3,28-diol, (3beta)- (en)
skos:prefLabel	Urs-12-ene-3,28-diol, (3beta)- (en)
name	Urs-12-ene-3,28-diol, (3beta)- (en)
instance of	wds:Q104201352-8E449472-F2AC-4A6D-AB65-D51EE57A111D
instance of	group of stereoisomers
subclass of	wds:Q104201352-604A3374-3291-4406-BEAA-08AAC5D740D1
subclass of	taraxastane / ursane triterpenoid
found in taxon	wds:Q104201352-1318E611-2447-4055-A388-BB16058E75C9 wds:Q104201352-17CB814C-C7EC-42D4-AEAF-6844A9CB7488 wds:Q104201352-1DFECA59-F7CD-4A3F-8D21-00377ABA59CF wds:Q104201352-379DB0D2-00C7-45DA-8FA9-85B4DEA85BA7 wds:Q104201352-4099527C-C6C0-4F8C-B843-8F0CC3231346 wds:Q104201352-432110F5-1C3C-415D-A1AC-89C269057F8B wds:Q104201352-63678854-08F5-4164-98C5-0CB47ED91FBF wds:Q104201352-756F64E8-55E7-4F35-9C7E-60B6E0224012 wds:Q104201352-9BC672F0-C701-45AC-9527-B89A130F053D wds:Q104201352-ACD5DDD7-0F23-4816-A393-DC13357DE85C wds:Q104201352-B5C1CDD6-AB75-468B-BA0E-C98B1112F3C4 wds:Q104201352-C8E189D5-D84B-49E7-A3CB-B4CED042FF6E wds:Q104201352-FB396EC3-7A26-4F6A-8F9A-4BEF85B1D161
found in taxon	Diospyros kaki Diospyros Euphorbia paralias Olea europaea Olea Prunus Cydonia oblonga Diospyros maingayi Diospyros lotus Ilex affinis Euphorbia micractina Ilex buxifolia Nardophyllum bryoides
UniChem compound ID	wds:Q104201352-4E155C96-9B60-4970-97EB-57E2D4A12E9F
canonical SMILES	wds:Q104201352-DF16C6D5-4806-4A84-AD08-9ED4871043FD
InChI	wds:Q104201352-F94EE0E1-4911-44D9-A3F7-593AA367C703
InChIKey	wds:Q104201352-2D5E61E4-B635-43D3-B6FA-4BBD6F643219
chemical formula	wds:Q104201352-B4DD2DEF-094C-436C-8DEA-2DF153129145
PubChem CID	wds:Q104201352-8B2F7C02-E693-4E79-9FD8-828FE6483C8A
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3266408
UniChem compound ID	23610145
canonical SMILES	OCC12CCC(C)C(C)C2C3=CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC1
InChI	InChI=1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3
InChIKey	XUARCIYIVXVTAE-UHFFFAOYSA-N
chemical formula	C₃₀H₅₀O₂
PubChem CID	3266408
mass	wds:Q104201352-F9E24182-B494-4BD3-9061-43A23C3757F7
mass	442.38108084 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104201352
is subclass of of	urs-12-ene-3β,28-diol (3R,4aS,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol (3S,4aR,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol (3S,4aS,6aR,6bS,8aS,11S,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol (3S,4aS,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol
is subclass of of	wds:Q104201353-66CF52D8-9ECB-4BB7-A727-FC4DA5B0FD14 wds:Q105342061-313473A5-01E8-4B5B-9D6B-2AA2F726FC27 wds:Q105342058-912C2753-6E87-4CDE-AF36-A09C6B9F1688 wds:Q105342059-7165E6E6-3FBA-425D-B935-1460E138E538 wds:Q105342062-7AB39E89-D160-4095-9633-8D3626A29873
is main subject of	Three new triterpenes from Nerium oleander and biological activity of the isolated compounds Chemical Constituents of the Roots of Euphorbia micractina Pharmacology and chemotaxonomy of Diospyros Phytochemical study of Euphorbia paralias Studies on the Constituents of Leaves of Rhododendron degronianum CAHR. Role of Nitric Oxide and Hydrogen Sulfide in the Vasodilator Effect of Ursolic Acid and Uvaol from Black Cherry Prunus serotina Fruits Two new lupane-type triterpenes from diospyros maritima Sterols and triterpenes of Diospyros montana Triterpenoids from Brazilian Ilex species and their in vitro antitrypanosomal activity. Cytotoxic terpenoids from Nardophyllum bryoides Verbesinosides A-F, 15,27-cyclooleanane saponins from the American native plant Verbesina virginica Sterols and triterpenoids from the fruit of Cydonia oblonga miller. Bioassay-guided isolation of the antidiabetic principle from Sorbus decora (Rosaceae) used traditionally by the Eeyou Istchee Cree First Nations
is main subject of	wds:Q39701291-C11B5A23-7D6C-4F1A-BFCB-B539192FDEF3 wds:Q39130649-0BC9DEFF-BF2C-4239-999A-5B726884361B wds:Q45281983-93927C04-53FB-470C-9882-2DE915B0A9F7 wds:Q45118232-8375DEFC-8C71-424A-98CD-98BE2E198B10 wds:Q43287209-BF97DA6E-6DAE-4738-A24B-3FD388AEA830 wds:Q105000752-AABA7867-2060-41E0-A633-6F349FE457F7 wds:Q105342057-65C8E3A7-7BA3-4CB6-BD5C-5F52854B4297 wds:Q42926316-A1B7D2C9-E9E3-4325-88F6-1C80ABBA47FA wds:Q74602629-12559E1C-0716-4291-A08B-E3BD17A7F2A3 wds:Q77462786-B5AB3DA8-D6ED-43DB-A33B-136F46A62F20 wds:Q118256215-09B83010-D123-4AB3-86BC-0B0CBA6C2B14 wds:Q37305428-D26CFD64-C21C-4B54-94DC-DABCDFED2A18 wds:Q87088527-2BE68FD4-902D-4004-A450-A07C3787ADE0

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