Efficient Synthesis of New Peptidyl Chloromethyl Ketones for the Application of Proteinase K Inhibitors-Reference-Cited by-同舟云学术

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Efficient Synthesis of New Peptidyl Chloromethyl Ketones for the Application of Proteinase K Inhibitors

Published:2011-09-14 Issue:1 Volume:42 Page:40-45
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Kore Anilkumar R.¹,Shanmugasundaram Muthian¹

Affiliation:

1. a Life Technologies Inc., Bioorganic Chemistry Division , Austin , Texas , USA

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2010.521290

Reference13 articles.

1. Irreversible Inhibitors of Serine, Cysteine, and Threonine Proteases

2. Proteases Universally Recognize Beta Strands In Their Active Sites

3. Haloenol lactones: enzyme-activated irreversible inactivators for serine proteases. Inactivation of alpha-chymotrypsin.

4. Novel inactivators of serine proteases based on 6-chloro-2-pyrone

Cited by 2 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. Current Synthetic Routes to Peptidyl Mono-Fluoromethyl Ketones (FMKs) and Their Applications;Molecules;2020-11-28

2. protease inhibitors;Catalysis from A to Z;2020-04-18

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