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Substrate Report for: Menthylbenzoate

General
Type Aryl ester, Benzoate
Chemical_Nomenclature (5-methyl-2-propan-2-ylcyclohexyl) benzoate
Canonical SMILES CC1CCC(C(C1)OC(=O)C2=CC=CC=C2)C(C)C
InChI InChI=1S/C17H24O2/c1-12(2)15-10-9-13(3)11-16(15)19-17(18)14-7-5-4-6-8-14/h4-8,12-13,15-16H,9-11H2,1-3H3
InChIKey TTYVYRHNIVBWCB-UHFFFAOYSA-N
Other name(s) Menthyl benzoate ; 2-(Isopropyl)-5-methylcyclohexyl benzoate ; (5-methyl-2-propan-2-ylcyclohexyl) benzoate ; (-)-Menthyl benzoate
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MW|260.37
Formula|C17H24O2
CAS_number|71617-14-6
PubChem|93868
UniChem|TTYVYRHNIVBWCB-UHFFFAOYSA-N
IUPHAR|
Wikipedia|

Target
Families | Menthylbenzoate ligand of proteins in family: Hormone-sensitive_lipase_like
Protein | 9gamm-a0a0a7dhw7

References:
Search PubMed for references concerning: Menthylbenzoate
    Title: Cloning and Characterization of an Enantioselective l-Menthyl Benzoate Hydrolase from Acinetobacter sp. ECU2040
    Yin JG, Xu GC, Zheng GW, Xu JH
    Ref: Appl Biochem Biotechnol, 176:1102, 2015 : PubMed

            

    Title: Enantioselective Hydrolysis of d,l-Menthyl Benzoate to L-(-)-Menthol by Recombinant Candida rugosa Lipase LIP1
    Vorlova S, Bornscheuer UT, Gatfield I, Hilmer JM, Bertram HJ, Schmid RD
    Ref: Adv Synth Catal, 344:1152, 2002 : PubMed