Optimal pH 8.5 to 9 for the Hydrolysis of Vixotrigine and Other Basic Substrates of Carboxylesterase-1 in Human Liver Microsomes
Author:
Affiliation:
1. Drug Metabolism and Pharmacokinetics
2. Current affiliation of JLJ: Drug Metabolism and Pharmacokinetics, Takeda, San Diego, CA, USA
3. Clinical Pharmacology and Pharmacometrics, Biogen, Cambridge, MA, USA
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00498254.2021.2018629
Reference24 articles.
1. Bergmann, F., Rimon, S., 1958. The Effect of pH Variations on the Activities of C-Esterase. Biochemical Journal, 70, 339-344.
2. Gleason, N.J., Vostrikov, V.V., Greathouse, D.V., Koeppe, R.E., 2013. Buried Lysine, but Not Arginine, Titrates and Alters Transmembrane Helix Tilt. Proceedings of the National Academy of Sciences of the United States of America, 110, 1692 − 1695.
3. Friedman, J.R., Voeltz, G.K., 2011. The ER in 3D: a multifunctional dynamic membrane network. Trends in Cell Biology, 21, 709-717.
4. Hinckley, C.A., Kuryshev, Y., Sers, A., Barre, A., Buisson, B., Naik, H., and Hajos, M., 2021. Characterization of Vixotrigine, a Broad-Spectrum Voltage-Gated Sodium Channel Blocker. Molecular Pharmacology, 99, 49–59.
5. IMAI, T., 2006. Human Carboxylesterase Isozymes: Catalytic Properties and Rational Drug Design. Drug Metabolism and Pharmacokinetics, 21, 173–185.
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