(R)-3-[1]naphthyloxy-propane-1,2-diol

General

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

Target

Families : (R)-3-[1]naphthyloxy-propane-1,2-diol ligand of proteins in family
Epoxide_hydrolase

Structure :
4IO0

Protein :
bacme-g9bex6

References (1)

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