ENSIKLOPEDIA Cari Tekan Enter untuk memulai pencarian cepat. Kembali ke Ensiklopedia Arsip Wikipedia Indonesia Genkwanin Genkwanin Genkwanin Names IUPAC name 4′,5-Dihydroxy-7-methoxyflavone Systematic IUPAC name 5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one Other names GengkwaninApigenin 7-methyl ether4′,5-dihydroxy-7-methoxy flavone5,4′-Dihydroxy-7-methoxyflavone5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one Identifiers CAS Number 437-64-9 Y 3D model (JSmol) Interactive imageInteractive image ChEMBL ChEMBL210635 N ChemSpider 4444936 N ECHA InfoCard 100.195.986 PubChem CID 5281617 UNII 5K3I5D6B2B Y CompTox Dashboard (EPA) DTXSID80195908 InChI InChI=1S/C16H12O5/c1-20-11-6-12(18)16-13(19)8-14(21-15(16)7-11)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3 NKey: JPMYFOBNRRGFNO-UHFFFAOYSA-N NInChI=1/C16H12O5/c1-20-11-6-12(18)16-13(19)8-14(21-15(16)7-11)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3Key: JPMYFOBNRRGFNO-UHFFFAOYAO SMILES COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)OCOc1cc(c2c(=O)cc(oc2c1)c3ccc(cc3)O)O Properties Chemical formula C16H12O5 Molar mass 284.267 g·mol−1 Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references Chemical compound Genkwanin is an O-methylated flavone, a type of flavonoid. It can be found in the seeds of Alnus glutinosa,[1] in the leaves of the ferns Notholaena bryopoda and Asplenium normale,[2] and in the leaves of trees in the genus Aquilaria.[3] References ↑ O'Rourke, Ciara; Byres, Maureen; Delazar, Abbas; Kumarasamy, Yashodharan; Nahar, Lutfun; Stewart, Fiona; Sarker, Satyajit D. (2005). "Hirsutanonol, oregonin and genkwanin from the seeds of Alnus glutinosa (Betulaceae)". Biochemical Systematics and Ecology. 33 (7): 749–752. Bibcode:2005BioSE..33..749O. doi:10.1016/j.bse.2004.10.005. Archived from the original on 2012-08-23. Retrieved 2010-02-23. ↑ UmiKalsom, Yusuf; Harborne, Jeffrey B. (1991). "Flavonoid distribution in asplenioid ferns". Pertanika. 14 (3): 297–300. ↑ Kakino, Mamoru; Hara, Hideaki (2016). "Pharmacological Effects of Aquilaria SPP. Leaves and Their Chemical Constituents". Agarwood. Tropical Forestry. pp. 125–136. doi:10.1007/978-981-10-0833-7_8. ISBN 978-981-10-0832-0. vteFlavones and their conjugatesAglyconesMonohydroxyflavone 3-Hydroxyflavone 6-Hydroxyflavone Dihydroxyflavones Chrysin 4',7-Dihydroxyflavone 7,8-Dihydroxyflavone Trihydroxyflavones Apigenin Baicalein Galangin Norwogonin 7,8,3'-Trihydroxyflavone 6,7,4'-Trihydroxyflavone Tetrahydroxyflavones Fisetin Kaempferol Isoscutellarein Luteolin Norartocarpetin Scutellarein Pentahydroxyflavones Herbacetin Morin Quercetin Nortangeretin 6-Hydroxyluteolin Norwightin Hypolaetin Tricetin O-methylated flavones 4',7-Dihydroxy-6-methoxyflavone Acacetin Alnetin Artocarpetin Chrysoeriol Cirsilineol Cirsiliol Cirsimaritin Diosmetin Eupatilin Genkwanin Hispidulin Nepetin Nobiletin Oroxylin A Pratol Salvigenin Sinensetin Tangeretin Techtochrysin Tricin Wogonin Zapotin Glycosidesof apigenin Apiin Apigetrin Isovitexin Rhoifolin Saponarin Schaftoside Vicenin-2 Vitexin of baicalein Baicalin Tetuin of hypolaetin Hypolaetin 8-glucoside Hypolaetin 8-glucuronide of luteolin Cynaroside Isoorientin Orientin Veronicastroside Luteolin-7-O-glucuronide Giraldiin A and B Nepitrin Oroxindin ScutellarinAcetylated Artocarpetin A Artoindonesianin P Sulfated glycosidesTheograndin I and IIPolymers Amentoflavone Ochnaflavone Drugs Diosmin Hidrosmin Category This article about an aromatic compound is a stub. You can help Wikipedia by adding missing information.vte
