Type : Naphthalen
Chemical_Nomenclature : (2R)-3-naphthalen-1-yloxypropane-1,2-diol
Canonical SMILES : C1=CC=C2C(=C1)C=CC=C2OCC(CO)O
InChI : InChI=1S\/C13H14O3\/c14-8-11(15)9-16-13-7-3-5-10-4-1-2-6-12(10)13\/h1-7,11,14-15H,8-9H2\/t11-\/m1\/s1
InChIKey : BYNNMWGWFIGTIC-LLVKDONJSA-N
Other name(s) : UNII-1438YC8097 || (2R)-3-(1-Naphthalenyloxy)-1,2-propanediol || 1,2-Propanediol, 3-(1-naphthalenyloxy)-, (2R)- || 1438YC8097\; (-)-Propranolol glycol || 3-naphthalen-1-yloxypropane-1,2-diol || UNII-57WL5996AW || 1,2-Propanediol, 3-(1-naphthalenyloxy)-, (2S)- || Propranolol glycol || Propanolol glycol || 36112-95-5
MW : 218.25
Formula : C13H14O3
CAS_number : 61248-78-0
PubChem : 6604764
UniChem : BYNNMWGWFIGTIC-LLVKDONJSA-N
Families : (R)-3-[1]naphthyloxy-propane-1,2-diol ligand of proteins in family
Epoxide_hydrolase
Structure :
4IO0
Protein :
bacme-g9bex6
Title : Engineering of an epoxide hydrolase for efficient bioresolution of bulky pharmaco substrates - Kong_2014_Proc.Natl.Acad.Sci.U.S.A_111_15717 |
Author(s) : Kong XD , Yuan S , Li L , Chen S , Xu JH , Zhou J |
Ref : Proc Natl Acad Sci U S A , 111 :15717 , 2014 |
Abstract : |
PubMedSearch : Kong_2014_Proc.Natl.Acad.Sci.U.S.A_111_15717 |
PubMedID: 25331869 |
Gene_locus related to this paper: bacme-g9bex6 |