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Substrate Report for: Glycidyl-phenyl-ether

General
Type Epoxide
Chemical_Nomenclature 2-(phenoxymethyl)oxirane
Canonical SMILES C1C(O1)COC2=CC=CC=C2
InChI InChI=1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2
InChIKey FQYUMYWMJTYZTK-UHFFFAOYSA-N
Other name(s) glycidyl phenyl ether ; 2-(Phenoxymethyl)oxirane ; Phenyl glycidyl ether ; 1,2-Epoxy-3-phenoxypropane ; Oxirane, (phenoxymethyl)-
________________________________________________________________________________________________
MW|150.17
Formula|C9H10O2
CAS_number|122-60-1
PubChem|31217
UniChem|FQYUMYWMJTYZTK-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | Glycidyl-phenyl-ether ligand of proteins in family: Epoxide_hydrolase
Protein | aspni-hyl1, 9sphn-q3vax0

References:
Search PubMed for references concerning: Glycidyl-phenyl-ether

6 more
    Title: Effect of fungal mycelia on the HPLC-UV and UV-vis spectrophotometric assessment of mycelium-bound epoxide hydrolase using glycidyl phenyl ether
    Dolcet MM, Torres M, Canela R
    Ref: N Biotechnol, 33:449, 2016 : PubMed

            

    Title: Directed evolution of an enantioselective epoxide hydrolase: uncovering the source of enantioselectivity at each evolutionary stage
    Reetz MT, Bocola M, Wang LW, Sanchis J, Cronin A, Arand M, Zou J, Archelas A, Bottalla AL and Mowbray SL <1 more author(s)>
    Ref: Journal of the American Chemical Society, 131:7334, 2009 : PubMed

            

    Title: Enhancing the enantioselectivity of an epoxide hydrolase by directed evolution
    Reetz MT, Torre C, Eipper A, Lohmer R, Hermes M, Brunner B, Maichele A, Bocola M, Arand M and Furstoss R <3 more author(s)>
    Ref: Org Lett, 6:177, 2004 : PubMed