Coniferyl-p-coumarate

General

Type : Hydroxycinnamic-ester

Chemical_Nomenclature : [(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate

Canonical SMILES : COC1=C(C=CC(=C1)\/C=C\/COC(=O)\/C=C\/C2=CC=C(C=C2)O)O

InChI : InChI=1S\/C19H18O5\/c1-23-18-13-15(6-10-17(18)21)3-2-12-24-19(22)11-7-14-4-8-16(20)9-5-14\/h2-11,13,20-21H,12H2,1H3\/b3-2+,11-7+

InChIKey : UPNLRNQUIJXYPN-LFWRRJNUSA-N

Other name(s) : coniferyl p-coumarate  ||  coniferyl coumarate  ||  bmse010291  ||  SCHEMBL13499768  ||  CHEBI:86599  ||  Q27159279  ||  3-(4-Hydroxyphenyl) acrylic acid 3-(4-hydroxy-3-methoxyphenyl) llyl ester  ||  (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate


MW : 326.3

Formula : C19H18O5

CAS_number :

PubChem : 10892754

UniChem : UPNLRNQUIJXYPN-LFWRRJNUSA-N

Target

Structures : No structure

Families : Tannase, Lipase_3

References (1)

Title : Feruloyl esterases as a tool for the release of phenolic compounds from agro-industrial by-products - Benoit_2006_Carbohydr.Res_341_1820
Author(s) : Benoit I , Navarro D , Marnet N , Rakotomanomana N , Lesage-Meessen L , Sigoillot JC , Asther M
Ref : Carbohydr Res , 341 :1820 , 2006
Abstract :
PubMedSearch : Benoit_2006_Carbohydr.Res_341_1820
PubMedID: 16697997
Gene_locus related to this paper: aspng-faeb , aspni-FAEA