Aryl Acetylenes as Mechanism-Based Inhibitors of Cytochrome P450-Dependent Monooxygenase Enzymes-Reference-Cited by-同舟云学术

Aryl Acetylenes as Mechanism-Based Inhibitors of Cytochrome P450-Dependent Monooxygenase Enzymes

Published:1997-01-01 Issue:1 Volume:10 Page:91-102
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Foroozesh Maryam¹,Primrose Ginny¹,Guo Zuyu¹,Bell L. Chastine¹,Alworth William L.¹,Guengerich F. Peter¹

Affiliation:

1. Department of Chemistry, Tulane University, New Orleans, Louisiana 70118-5645, and Department of Biochemistry and Center in Molecular Toxicology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/tx960064g

Reference47 articles.

1. The P450 Superfamily: Update on New Sequences, Gene Mapping, Accession Numbers, Early Trivial Names of Enzymes, and Nomenclature

2. Cytochrome P450

3. Prough, R. A., and Spearman, M. E. (1987) Endogenous and dietary chemicals: metabolism and interaction with cytochrome P-450. In: Mammalian Cytochromes P-450(Guengerich, F. P., Ed.) Vol. II, pp 153−172, CRC Press, Boca Raton, FL.

Cited by 89 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ethyl 2-[(2-oxo-2H-chromen-6-yl)oxy]acetate;Acta Crystallographica Section E Crystallographic Communications;2024-05-31

2. Bromopyrene Symphony: Synthesis and Characterisation of Isomeric Derivatives at Non-K Region and Nodal Positions for Diverse Functionalisation Strategies;Molecules;2024-03-03

3. Design, Synthesis, and Biological Studies of Flavone-Based Esters and Acids as Potential P450 2A6 Inhibitors;Chemical Research in Toxicology;2023-11-14

4. CYP1A inhibitors: Recent progress, current challenges, and future perspectives;Medicinal Research Reviews;2023-06-19

5. Discovery of a Novel Potent and Selective HSD17B13 Inhibitor, BI-3231, a Well-Characterized Chemical Probe Available for Open Science;Journal of Medicinal Chemistry;2023-02-02