(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
IUPHAR :
Wikipedia :
-3-[1]naphthyloxy-propane-1,2-diol.gif)
Target
Families : (R)-3-[1]naphthyloxy-propane-1,2-diol ligand of proteins in family: Epoxide_hydrolase
Stucture : 4IO0 Crystal structure of F128A mutant of an epoxide hydrolase from Bacillus megaterium complexed with its product (R)-3-[1]naphthyloxy-propane-1,2-diol
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 : Kong_2014_Proc.Natl.Acad.Sci.U.S.A_111_15717 |
| ESTHER : Kong_2014_Proc.Natl.Acad.Sci.U.S.A_111_15717 |
| PubMedSearch : Kong_2014_Proc.Natl.Acad.Sci.U.S.A_111_15717 |
| PubMedID: 25331869 |
| Gene_locus related to this paper: bacme-g9bex6 |