About: [6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate

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About: [6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 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 C₃₂H₄₄O₈

Attributes	Values
rdf:type	Item
description	groep van stereo-isomeren (nl) group of stereoisomers with the chemical formula C₃₂H₄₄O₈ (en) група стереоізомерів з хімічною формулою C₃₂H₄₄O₈ (uk)
rdfs:label	[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate (en)
skos:prefLabel	[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate (en)
name	[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate (en)
instance of	wds:Q105177791-DD29770F-2675-4407-8B10-66C6F3446A11
instance of	group of stereoisomers
subclass of	wds:Q105177791-A99D337D-68E9-4F49-8338-BACA8FC0A790
subclass of	cucurbitane triterpenoid
found in taxon	wds:Q105177791-06F0FA94-4ECF-42B1-BD37-6DF6226EB0E2 wds:Q105177791-504494E9-EDD5-4C28-9883-5E488D78D47A wds:Q105177791-53605431-398E-4F78-8870-387FF71DAAFA wds:Q105177791-E780BF77-FEC4-421D-A9E9-86B243C8A073 wds:Q105177791-FA197908-1686-4A75-9E9F-CB71C00485FD
found in taxon	Bryonia dioica Bryonia alba Bacopa Cucurbita andreana Ecballium elaterium
UniChem compound ID	wds:Q105177791-3A3A3FED-CD9D-4350-82FB-2D065554B0DD
Probes And Drugs ID	wds:Q105177791-498FF2F9-B737-4D5B-AB50-C31FC056E910
Human Metabolome Database ID	wds:Q105177791-FF0EC047-966E-4F76-BBDB-342B856F219C
canonical SMILES	wds:Q105177791-2918B9CD-220B-4EAE-B7F3-C2B996B1E80B
InChI	wds:Q105177791-C72FF9BE-AADD-4B43-A9E0-50EBB5E4E330
InChIKey	wds:Q105177791-62B29B1B-CF5F-472A-A204-79022D496972
chemical formula	wds:Q105177791-9855D2E2-E714-4078-8A94-629B6A1F5FD2
PubChem CID	wds:Q105177791-D0E309B2-B2EA-4EA8-AAC4-29C2ABFD8437
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2887
UniChem compound ID	68367792
Probes And Drugs ID	PD045381
Human Metabolome Database ID	HMDB0250581
canonical SMILES	O=C(OC(C=CC(=O)C(O)(C)C1C(O)CC2(C)C3CC=C4C(C=C(O)C(=O)C4(C)C)C3(C(=O)CC12C)C)(C)C)C
InChI	InChI=1S/C32H44O8/c1-17(33)40-27(2,3)13-12-23(36)32(9,39)25-21(35)15-29(6)22-11-10-18-19(14-20(34)26(38)28(18,4)5)31(22,8)24(37)16-30(25,29)7/h10,12-14,19,21-22,25,34-35,39H,11,15-16H2,1-9H3
InChIKey	NDYMQXYDSVBNLL-UHFFFAOYSA-N
chemical formula	C₃₂H₄₄O₈
PubChem CID	2887
mass	wds:Q105177791-F0D9B83B-783A-4815-93DC-22A5C0E59C13
mass	556.303618368 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q105177791
is subclass of of	[(E,6R)-6-[(8S,9R,10S,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate [(E,6S)-6-[(8S,9R,10S,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate [(E,6S)-6-[(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate
is subclass of of	wds:Q105177785-392B3FFF-A2AC-4BAA-8373-98129FE5AB2D wds:Q105177787-41DB8C5F-BE6F-42EA-BC4D-806ACB22B96D wds:Q105177792-A139BF63-FDFB-4B83-A9BA-B726D0DFE8E4
is main subject of	Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis Immunomodulatory activity of cucurbitacin E isolated from Ecballium elaterium Anticancer and antiinflammatory activities of cucurbitacins from Cucurbita andreana Isoleirung und struktur der cucurbitacine aus Bryonia dioica Die cucurbitacine in Bryonia alba und Bryonia dioica Cucurbitacin S, a new cucurbitacin from Bryonia dioica Cucurbitacins from Bacopa monnieri.
is main subject of	wds:Q44225281-14356CE6-015E-4300-9915-483A298A9256 wds:Q104978716-25E469E5-496B-49A3-94F1-33F1429FFFBB wds:Q34420420-8B63C07F-414A-4F37-96AA-C05DFE1F78F4 wds:Q55043756-D6B20809-35F8-493B-9A91-1D4A2423BF24 wds:Q44782393-F01F781D-817A-4709-80AE-3FAF029E75F1 wds:Q104936265-50F713FC-BCC7-418C-A7C8-FEB0F88A235E wds:Q110014616-2BCCD764-3CF0-44E4-977E-620FDC354B4D

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