About: 4-Prenylresveratrol

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About: 4-Prenylresveratrol Goto Sponge NotDistinct Permalink

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

chemical compound

Attributes	Values
rdf:type	Item
description	composto chimico (it) химическое соединение (ru) chemical compound (en) composé chimique (fr) תרכובת (he) kemisk forbindelse (da) compositum chemicum (la) chemische Verbindung (de) քիմիական միացություն (hy) chemická sloučenina (cs) chemická zlúčenina (sk) chemische verbinding (nl) kemia kombinaĵo (eo) związek chemiczny (pl) cheemesch Verbindung (lb) chemical compound (en-ca) chemical compound (en-gb) chemiese verbinding (af) chemische Verbindung (de-ch) component quimic (oc) compost químic (ca) composto químico (gl) composto químico (pt) composto químico (pt-br) compuesto quimico (an) compuestu químicu (ast) compus chimic (ro) kemiallinen yhdiste (fi) kjemisk forbindelse (nb) kjemisk sambinding (nn) komponim kimik (sq) konposatu kimiko (eu) senyawa kimia (id) ķīmisks savienojums (lv) хімічна сполука (uk) مركب كيميائي (ar) کیٖمیٲیی مُرَکَب (ks) রাসায়নিক যৌগ (bn) രാസസം‌യുക്തം (ml) compuesto químico (es)
rdfs:label	4-Prenylresveratrol (en)
skos:prefLabel	4-Prenylresveratrol (en)
name	4-Prenylresveratrol (en)
isomeric SMILES	wds:Q27105529-7B306943-3D18-449C-B9D0-1E36A5F7FB8A
isomeric SMILES	CC(=CCC1=C(C=C(C=C1O)/C=C/C2=CC=C(C=C2)O)O)C
instance of	wds:Q27105529-1370A3DB-36F6-401D-BD73-70B418CE6E24
instance of	type of chemical entity
subclass of	wds:Q27105529-3BA56B58-A7F2-4814-B75D-3CE82D2C3714 wds:Q27105529-C16BCEA9-609A-4F38-98A0-E36B7CCD6CFC
subclass of	stilbenoid aromatic polyketide
found in taxon	wds:Q27105529-20275D02-80D8-4776-9062-B6A4CB2FA0D5 wds:Q27105529-280CDD2A-D7CC-4CED-9866-2E77D0887799 wds:Q27105529-A87AC256-5836-41C1-85B8-37E412EF379B
found in taxon	peanut Bagassa breadfruit
UniChem compound ID	wds:Q27105529-664FC93D-F312-4F51-8D7D-BADAF7A4B4EE
CAS Registry Number	wds:Q27105529-FCFFF899-4FFC-4320-A462-C0D3EE560759
canonical SMILES	wds:Q27105529-061954A2-E552-4420-9A1E-FD6B55CDA9AD
InChI	wds:Q27105529-D3CAC493-22B6-4585-98FE-89D75522F017
InChIKey	wds:Q27105529-10C777DC-712C-4E8D-BE8C-D0D49B20CCF0
chemical formula	wds:Q27105529-D43113AB-1681-4F51-A949-65AC48D4D36A
DSSTox substance ID	wds:Q27105529-81BA4D3E-DE10-4154-B0EC-2CC7321FF58D
ChemSpider ID	wds:Q27105529-76FCAAA4-4660-4524-A810-8E333563769D
PubChem CID	wds:Q27105529-62C7B574-007F-48D6-AD01-A393FF443DE2
KEGG ID	wds:Q27105529-597C576E-080F-4905-92CD-0D38EBCF45A0
ChEBI ID	wds:Q27105529-F2B89208-112D-484D-BF88-54165690C68F
DSSTOX compound identifier	wds:Q27105529-DD240468-71A0-486C-A7B0-E9E708B25970
ChemSpider ID	http://rdf.chemspider.com/4445040
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5281725
KEGG ID	http://www.kegg.jp/entry/C10285
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_1927
UniChem compound ID	1073978
CAS Registry Number	61517-87-1
canonical SMILES	CC(=CCC1=C(C=C(C=C1O)C=CC2=CC=C(C=C2)O)O)C
InChI	InChI=1S/C19H20O3/c1-13(2)3-10-17-18(21)11-15(12-19(17)22)5-4-14-6-8-16(20)9-7-14/h3-9,11-12,20-22H,10H2,1-2H3/b5-4+
InChIKey	WWFOQQIWOKJBSJ-SNAWJCMRSA-N
chemical formula	C₁₉H₂₀O₃
DSSTox substance ID	DTXSID50415185
ChemSpider ID	4445040
PubChem CID	5281725
KEGG ID	C10285
ChEBI ID	1927
DSSTOX compound identifier	DTXCID40366036
ChEMBL ID	wds:Q27105529-DDD4F1A6-8C9D-4EF3-8536-EC9BB9CB8D63
ChEMBL ID	http://rdf.ebi.ac.uk/resource/chembl/molecule/CHEMBL2230263
ChEMBL ID	CHEMBL2230263
LIPID MAPS ID	wds:Q27105529-49A3E062-09A8-41E3-8A87-630442DB2119
KNApSAcK ID	wds:Q27105529-48A52448-6897-4E7E-BE23-6B9FC20A3C69
LIPID MAPS ID	LMPK13090014
KNApSAcK ID	C00002901
mass	wds:Q27105529-D5BD8D40-FC45-4085-84AE-BA13B96F429F
mass	296.141245 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q27105529
is main subject of	Secondary metabolites of Bagassa guianensis Aubl. wood: a study of the chemotaxonomy of the Moraceae family New stilbene phytoalexins from American cultivars of Arachis hypogaea Two novel stilbene phytoalexins from Arachis hypogaea The 5 alpha-reductase inhibitory components from heartwood of Artocarpus incisus: structure-activity investigations

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