Stereoselective Metabolism of Halothane Enantiomers to Trifluoroacetylated Liver Proteins-Reference-Cited by-同舟云学术

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Stereoselective Metabolism of Halothane Enantiomers to Trifluoroacetylated Liver Proteins

Published:1995-01 Issue:1-2 Volume:27 Page:179-189
ISSN:0360-2532
Container-title:Drug Metabolism Reviews
language:en
Short-container-title:Drug Metabolism Reviews

Author:

Martin Jackie L.,Meinwald Jerrold,Radford Peter,Liu Zhi,Graf Mary Louise M.,Pohl Lance R.

Publisher

Informa UK Limited

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

Link

http://www.tandfonline.com/doi/pdf/10.3109/03602539509029822

Reference61 articles.

1. Pharmacodynamic and pharmacokinetic differences between drug enantiomers in humans: An overview

2. Enantiomer specific pharmacokinetics

3. RACEMATES OR ENANTIOMERS: REGULATORY APPROACHES

4. Chirality in bioactive agents and its pitfalls

5. Stereoisomers in clinical oncology: Why it is important to know what the right and left hands are doing

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1. Antibody-based detection of lysine modification of hepatic protein in mice treated with retrorsine;Journal of Environmental Science and Health, Part C;2020-10-01

2. Molecular Bases for Anesthetic Agents: Halothane as a Halogen‐ and Hydrogen‐Bond Donor;Angewandte Chemie International Edition;2019-09-02

3. Molecular Bases for Anesthetic Agents: Halothane as a Halogen‐ and Hydrogen‐Bond Donor;Angewandte Chemie;2019-07-30

4. Drug Metabolism;The Organic Chemistry of Drug Design and Drug Action;2014

5. The highly stereoselective decarboxylation of (+)-1-bromo-1-chloro-2,2,2-trifluoropropanoic acid to give (+)-1-bromo-1-chloro-2,2,2-trifluoroethane [(+)-halothane] with retention of configuration;Tetrahedron: Asymmetry;2012-02

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