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Inhibitor Report for: (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
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MW|218.25
Formula|C13H14O3
CAS_number|61248-78-0
PubChem|6604764
UniChem|BYNNMWGWFIGTIC-LLVKDONJSA-N
IUPHAR|
Wikipedia|

Target
Families | (R)-3-[1]naphthyloxy-propane-1,2-diol ligand of proteins in family: Epoxide_hydrolase
Stucture | 1 structure: 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:
Search PubMed for references concerning: (R)-3-[1]naphthyloxy-propane-1,2-diol
    Title: Engineering of an epoxide hydrolase for efficient bioresolution of bulky pharmaco substrates
    Kong XD, Yuan S, Li L, Chen S, Xu JH, Zhou J
    Ref: Proc Natl Acad Sci U S A, 111:15717, 2014 : PubMed