About: 1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one

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About: 1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one Goto Sponge NotDistinct Permalink

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group of stereoisomers with the chemical formula C₄₀H₃₈O₁₀

Attributes	Values
rdf:type	Item
description	groep van stereo-isomeren (nl) group of stereoisomers with the chemical formula C₄₀H₃₈O₁₀ (en) група стереоізомерів з хімічною формулою C₄₀H₃₈O₁₀ (uk)
rdfs:label	1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one (en)
skos:prefLabel	1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one (en)
name	1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one (en)
instance of	wds:Q105138076-807E3B72-9BCD-4755-BDDF-D304270BC942
instance of	group of stereoisomers
subclass of	wds:Q105138076-ABDA1D54-CBD0-4FAC-9E28-DB08C7B0DCD9
subclass of	3'C-substituted chalcone
found in taxon	wds:Q105138076-068ABE77-48F7-40CF-832D-2F7181C45DE4 wds:Q105138076-5197260B-B50B-4B28-B3EC-EF9D7ACB823A wds:Q105138076-BA2BFD71-6D0E-4857-994A-455158296545
found in taxon	Morus mongolica Morus alba Morus macroura
UniChem compound ID	wds:Q105138076-1238680E-57F3-48EE-B74D-1EEE91E9753C
canonical SMILES	wds:Q105138076-B3590235-F1CF-46F8-8385-04B019CA7DA3
InChI	wds:Q105138076-BE982173-D9C4-4ED6-89DE-AFD4FB306E23
InChIKey	wds:Q105138076-2DDE7ED6-8C99-45F2-9364-D2847D0353A7
chemical formula	wds:Q105138076-26D18E44-38BC-49B4-96CA-D909675E8D5C
PubChem CID	wds:Q105138076-1AB8AEB1-F02B-4979-B3AD-0AB80E6E86D3
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID73167443
UniChem compound ID	70536650
canonical SMILES	O=C(C=CC1=CC=C(O)C=C1O)C2=CC=C(O)C(=C2O)C3C=C(C)CC(C4=CC=C(O)C=C4O)C3C(=O)C5=CC=C(O)C(=C5O)CC=C(C)C
InChI	InChI=1S/C40H38O10/c1-20(2)4-9-26-32(44)14-12-28(38(26)48)40(50)36-29(25-10-8-24(42)19-35(25)47)16-21(3)17-30(36)37-33(45)15-11-27(39(37)49)31(43)13-6-22-5-7-23(41)18-34(22)46/h4-8,10-15,17-19,29-30,36,41-42,44-49H,9,16H2,1-3H3
InChIKey	KBAPHKOHTBBCTO-UHFFFAOYSA-N
chemical formula	C₄₀H₃₈O₁₀
PubChem CID	73167443
mass	wds:Q105138076-12617AE0-99D9-4EA6-94F8-4AB1F1C501E5
mass	678.246497416 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q105138076
is subclass of of	(E)-1-[3-[(1R,5R,6S)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one (2E)-1-[3-[(1S,5S,6R)-6-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methyl-2-cyclohexen-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)-2-propen-1-one (E)-1-[3-[(1R,5S,6R)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 2-Propen-1-one, 1-(3-((1S,5R,6S)-6-(2,4-dihydroxy-3-(3-methyl-2-butenyl)benzoyl)-5-(2,4-dihydroxyphenyl)-3-methyl-2-cyclohexen-1-yl)-2,4-dihydroxyphenyl)-3-(2,4-dihydroxyphenyl)-, (2E)-
is subclass of of	wds:Q104400269-0D575FD3-A400-4F92-9F84-83901C45F4B4 wds:Q105138072-3C9A0791-FB0E-4A31-A831-827108DE6B44 wds:Q105138075-D4153311-237F-4E71-AEFE-FBDF136DA4D7 wds:Q105138077-ACC26019-52C4-4A54-BD49-0789ABFEBB20
is main subject of	Hypoxia-inducible factor-1 inhibitory benzofurans and chalcone-derived diels-alder adducts from Morus species. Guangsangons F-J, anti-oxidant and anti-inflammatory Diels-Alder type adducts, from Morus macroura Miq. Kuwanon J, a new Diels-Alder adduct and chalcomoracin from callus culture of Morus alba L. Absolute Configuration of Natural Diels-Alder Type Adducts from the Morus Root Bark Direct NMR evidence for the equivalent participation of L-phenylalanine and L-tyrosine in the biosynthesis of the intermolecular Diels–Alder type adducts of prenylchalcone and prenylated 2-arylbenzofuran in Morus alba cell cultures A chimeric hemiterpene biosynthesis inMorus alba cell cultures
is main subject of	wds:Q104912256-AC529230-6B9E-4072-9120-13AA09086FF3 wds:Q105108704-633BD1BD-6826-43EC-B738-284FD23070A3 wds:Q39906785-A64D048C-4C0A-47CA-BFBD-B4C0B038449F wds:Q45149261-8F1181DA-CAFB-4852-A6A9-A7BB58B5DFC2 wds:Q115951233-49FDCDEE-2A58-4484-A743-E1660C5FD598 wds:Q105138074-2E5AFE56-DC36-43A4-A96F-D64AB1C4BB52

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