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Chemical Compound Review:

SureCN10698031 (1-methylindol-3-yl) ethanoate

Synonyms: IFLab1_005801, AC1L2RKR, KB-90763, BBL013014, STK020416, ...

Masson, P. et al., Hrabovská, A. et al., Sadar, M.H. et al.

Masson, Froment, Fort, Ribes, Bec, Balny, Schopfer, Hrabovská, Debouzy, Froment, Devínsky, Pauliková, Masson,

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High impact information on ZINC00143037

The presence of a long lag phase, with no oscillations, in substrate hydrolysis by rat butyrylcholinesterase was also observed with N-methylindoxyl acetate as substrate [1].
Hydrolysis of the neutral substrate N-methylindoxyl acetate (NMIA) by wild-type human butyrylcholinesterase (BuChE) and peripheral site mutants (D70G, Y332A, D70G/Y332A) was found to follow the Michaelis-Menten kinetics [2].
Butyrylcholinesterase-catalyzed hydrolysis of N-methylindoxyl acetate: analysis of volume changes upon reaction and hysteretic behavior [2].

Biological context of ZINC00143037

Transient kinetics of the acetylcholinesterase catalyzed hydrolysis of N-methylindoxyl acetate [3].

References

Rat butyrylcholinesterase-catalysed hydrolysis of N-alkyl homologues of benzoylcholine. Hrabovská, A., Debouzy, J.C., Froment, M.T., Devínsky, F., Pauliková, I., Masson, P. FEBS J. (2006) [Pubmed]
Butyrylcholinesterase-catalyzed hydrolysis of N-methylindoxyl acetate: analysis of volume changes upon reaction and hysteretic behavior. Masson, P., Froment, M.T., Fort, S., Ribes, F., Bec, N., Balny, C., Schopfer, L.M. Biochim. Biophys. Acta (2002) [Pubmed]
Transient kinetics of the acetylcholinesterase catalyzed hydrolysis of N-methylindoxyl acetate. Sadar, M.H., Laidler, K.J. Can. J. Biochem. (1975) [Pubmed]

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