3-p-Coumaroylquinic-acid
General
Type : Glycoside
Chemical_Nomenclature : (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid
Canonical SMILES : C1[C@H]([C@@H]([C@@H](C[C@]1(C(=O)O)O)OC(=O)\/C=C\/C2=CC=C(C=C2)O)O)O
InChI : InChI=1S\/C16H18O8\/c17-10-4-1-9(2-5-10)3-6-13(19)24-12-8-16(23,15(21)22)7-11(18)14(12)20\/h1-6,11-12,14,17-18,20,23H,7-8H2,(H,21,22)\/b6-3+\/t11-,12-,14+,16-\/m1\/s1
InChIKey : BMRSEYFENKXDIS-QHAYPTCMSA-N
Other name(s) : 3-p-coumaroylquinic acid || 3-O-Coumaroylquinic acid || 5-O-Coumaroylquinic acid || 3-p-Coqa || 5-O-p-coumaroylquinic acid || SCHEMBL21240786 || CHEBI:75499 || CHEBI:167530 || CQ
MW : 338.31
Formula : C16H18O8
CAS_number : 87099-71-6
PubChem : 9945785
UniChem : BMRSEYFENKXDIS-QHAYPTCMSA-N
Target
Structures : No structure
Families : Tannase
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 |