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Substrate Report for: Methyl-L-lactate

General
Type Alkyl ester, Propionate
Chemical_Nomenclature methyl (2S)-2-hydroxypropanoate
Canonical SMILES CC(C(=O)OC)O
InChI InChI=1S/C4H8O3/c1-3(5)4(6)7-2/h3,5H,1-2H3/t3-/m0/s1
InChIKey LPEKGGXMPWTOCB-VKHMYHEASA-N
Other name(s) Methyl (S)-(-)-lactate ; Methyl L-lactate ; (-)-Methyl L-lactate ; (S)-Methyl lactate ; (S)-Lactic acid methyl ester
________________________________________________________________________________________________
MW|104.10
Formula|C4H8O3
CAS_number|27871-49-4
PubChem|94386
UniChem|LPEKGGXMPWTOCB-VKHMYHEASA-N
IUPHAR|
Wikipedia|

Target
Families | Methyl-L-lactate ligand of proteins in family: Hormone-sensitive_lipase_like, LYsophospholipase_carboxylesterase
Protein | 9actn-a0a2d1pk72

References:
Search PubMed for references concerning: Methyl-L-lactate

3 more
    Title: Determinants and prediction of esterase substrate promiscuity patterns
    Martinez-Martinez M, Coscolin C, Santiago G, Chow J, Stogios PJ, Bargiela R, Gertler C, Navarro-Fernandez J, Bollinger A and Ferrer M <32 more author(s)>
    Ref: ACS Chemical Biology, 13:225, 2018 : PubMed

            

    Title: Lipase-catalyzed enantioselective synthesis of (R,R)-lactide from alkyl lactate to produce PDLA (poly D-lactic acid) and stereocomplex PLA (poly lactic acid)
    Jeon BW, Lee J, Kim HS, Cho DH, Lee H, Chang R, Kim YH
    Ref: J Biotechnol, 168:201, 2013 : PubMed

            

    Title: Lipase-catalyzed oligomerization and hydrolysis of alkyl lactates: direct evidence in the catalysis mechanism that enantioselection is governed by a deacylation step
    Ohara H, Onogi A, Yamamoto M, Kobayashi S
    Ref: Biomacromolecules, 11:2008, 2010 : PubMed