L-arabinosyl-ferulate
General
Chemical_Nomenclature : [(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
Canonical SMILES : COC1=C(C=CC(=C1)\/C=C\/C(=O)OC2[C@@H]([C@H]([C@@H](CO2)O)O)O)O
InChI : InChI=1S\/C15H18O8\/c1-21-11-6-8(2-4-9(11)16)3-5-12(18)23-15-14(20)13(19)10(17)7-22-15\/h2-6,10,13-17,19-20H,7H2,1H3\/b5-3+\/t10-,13+,14-,15?\/m1\/s1
InChIKey : VPLBTCXDRTZZKU-MPMSGYSISA-N
Other name(s) : (3,4,5-trihydroxyoxan-2-yl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
MW : 326.30
Formula : C15H18O8
CAS_number :
PubChem : 154674615, 141240095
UniChem : VPLBTCXDRTZZKU-MPMSGYSISA-N
Target
Structures : No structure
Families : FaeC, Esterase_phb
References (1)
| Title : Optimization of enzymatic synthesis of l-arabinose ferulate catalyzed by feruloyl esterases from Myceliophthora thermophila in detergentless microemulsions and assessment of its antioxidant and cytotoxicity activities - Antonopoulou_2018_Process.Biochem_65_100 |
| Author(s) : Antonopoulou I , Papadopoulou A , Iancu L , Cerullo G , Ralli M , Jutten P , Piechot A , Faraco V , Kletsas D , Rova U , ,Christakopoulos P |
| Ref : Process Biochemistry , 48 :100 , 2018 |
| Abstract : |
| PubMedSearch : Antonopoulou_2018_Process.Biochem_65_100 |
| PubMedID: |