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Substrate Report for: 3-O-Acetylpapaveroxine

General
Type Isoquinoline, Benzodioxo, Acetate
Chemical_Nomenclature [(S)-(2-formyl-3,4-dimethoxyphenyl)-[(5R)-4-methoxy-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl] acetate
Canonical SMILES CC(=O)OC(C1C2=C(C3=C(C=C2CCN1C)OCO3)OC)C4=C(C(=C(C=C4)OC)OC)C=O
InChI InChI=1S/C24H27NO8/c1-13(27)33-22(15-6-7-17(28-3)21(29-4)16(15)11-26)20-19-14(8-9-25(20)2)10-18-23(24(19)30-5)32-12-31-18/h6-7,10-11,20,22H,8-9,12H2,1-5H3/t20-,22+/m1/s1
InChIKey JUUOWVIBIPDOSQ-IRLDBZIGSA-N
Other name(s) C21591
________________________________________________________________________________________________
MW|457.47
Formula|C24H27NO8
CAS_number|
PubChem|14106961
UniChem|JUUOWVIBIPDOSQ-IRLDBZIGSA-N
IUPHAR|
Wikipedia|

Target
Families | 3-O-Acetylpapaveroxine ligand of proteins in family: Plant_carboxylesterase

References:
Search PubMed for references concerning: 3-O-Acetylpapaveroxine
    Title: Family portraits: the enzymes behind benzylisoquinoline alkaloid diversity
    Dastmalchi M, Park MR, Morris JS, Facchini P
    Ref: Phytochemistry Review, 17:249, 2018 : PubMed

            

    Title: Acetylation serves as a protective group in noscapine biosynthesis in opium poppy
    Dang TT, Chen X, Facchini PJ
    Ref: Nat Chemical Biology, 11:104, 2015 : PubMed