About: [6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

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About: [6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 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 C₃₀H₃₈O₁₅

Attributes	Values
rdf:type	Item
description	groep van stereo-isomeren (nl) group of stereoisomers with the chemical formula C₃₀H₃₈O₁₅ (en) група стереоізомерів з хімічною формулою C₃₀H₃₈O₁₅ (uk)
rdfs:label	[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (en)
skos:prefLabel	[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (en)
name	[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (en)
instance of	wds:Q104396798-01929B5D-1AAA-4EF3-8396-C0F009AF51FD
instance of	group of stereoisomers
subclass of	wds:Q104396798-81829BB5-7F59-43A0-B7D0-F9E0299DF656
subclass of	alkyl caffeate ester
found in taxon	wds:Q104396798-449EE822-2935-478B-A7D2-0B83BEF4E7CA wds:Q104396798-625432D5-2FEC-42C0-84A7-94BB1C3F6898 wds:Q104396798-6F4F6E5D-CFBA-46E9-9A74-9F90FA917EF8 wds:Q104396798-F42A68AE-A058-4C4D-A83C-22835B4AABFB wds:Q104396798-FD50649B-A1E7-413F-912C-57DAC178EFEA
found in taxon	Solanum dulcamara Euphrasia pectinata Solanum pseudopersicum Euphrasia nemorosa Betonica orientalis
UniChem compound ID	wds:Q104396798-9F9666AE-8AF2-433A-AF1B-978D2C63E481
canonical SMILES	wds:Q104396798-0C33B539-58D2-4AA2-BD04-1886559B6FBA
InChI	wds:Q104396798-0A273E7B-0B13-41D5-BBC4-6795ADC593A7
InChIKey	wds:Q104396798-83B0B0A7-2C0F-4055-83B8-EAFCCF959028
chemical formula	wds:Q104396798-7D8DEAB9-68E4-4452-B3C1-5B5E2A65E1CD
PubChem CID	wds:Q104396798-576EC521-C63C-4DC0-AFA6-6CC436AD6136
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID74027662
UniChem compound ID	76995331
canonical SMILES	O=C(OC1C(OC(OCCC2=CC=C(O)C(O)=C2)C(O)C1OC3OC(C)C(O)C(O)C3O)CO)C=CC4=CC=C(O)C(OC)=C4
InChI	InChI=1S/C30H38O15/c1-14-23(36)24(37)25(38)30(42-14)45-28-26(39)29(41-10-9-16-3-6-17(32)19(34)11-16)43-21(13-31)27(28)44-22(35)8-5-15-4-7-18(33)20(12-15)40-2/h3-8,11-12,14,21,23-34,36-39H,9-10,13H2,1-2H3
InChIKey	ZMYQRHSOVRDQDL-UHFFFAOYSA-N
chemical formula	C₃₀H₃₈O₁₅
PubChem CID	74027662
mass	wds:Q104396798-D2D403D7-B78F-4576-B6A2-240B707E6D83
mass	638.221070516 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104396798
is subclass of of	Leucosceptoside A cis-Leucosceptoside A [(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate [(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate [(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate [(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
is subclass of of	wds:Q105379836-B526659E-690A-4661-A5DB-BF3C79318DEC wds:Q105379843-6BF318EB-CCF6-4580-AE63-91219A45D8D3 wds:Q105379837-8D6C2376-8CCA-465A-896F-CB59F0855249 wds:Q105379839-3050E782-5739-4CD5-AF8B-2F207DD38E22 wds:Q105379838-B668D98C-9A2E-4BC6-8F78-B252D3E0D8AF wds:Q105379840-F2A2030D-FEB0-4BD4-A19B-2E010134B0B6
is main subject of	Steroidal glycosides from the underground parts of Solanum sodomaeum An iridoid glucoside from dipsacus asperoides Iridoid and phenylpropanoid glycosides fromStachys macrantha Iridoid and phenylethanoid glycosides from Phlomis tuberosa L. Antioxidant and antiinflammatory activities of Sideritis perfoliata subsp. perfoliata (Lamiaceae). Lignan and phenylpropanoid glycosides from Fernandoa adenophylla Three acylated flavone glycosides from Sideritis ozturkii Aytac & Aksoy
is main subject of	wds:Q28295986-175BF8C9-5AED-43C2-BAB9-8159E58134E2 wds:Q104388391-B0D14F12-DC4A-4F77-B5A7-E81E0471EC5D wds:Q43674912-650D363F-53B2-48C4-88CE-BF51A5881B33 wds:Q44997310-017B1161-533C-4978-80FA-2BA939D47982 wds:Q43809765-15F847C0-032F-4595-93B0-EFBE0D84F40F wds:Q46666357-CF6F0E5F-DEC3-4249-9ACD-7C0E2095A774 wds:Q71316258-5862BA07-F19D-4FDA-983C-4EAAEE54CCF5

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