Macrocyclic Inhibitors of Penicillopepsin. 3. Design, Synthesis, and Evaluation of an Inhibitor Bridged between P2 and P1‘-Reference-Cited by-同舟云学术

Macrocyclic Inhibitors of Penicillopepsin. 3. Design, Synthesis, and Evaluation of an Inhibitor Bridged between P2 and P1‘

Published:1998-04-30 Issue:19 Volume:120 Page:4622-4628
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Smith Whitney W.¹,Bartlett Paul A.¹

Affiliation:

1. Contribution from the Department of Chemistry, University of California, Berkeley, California 94720-1460

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja973713z

Reference27 articles.

1. Macrocyclic Inhibitors of Penicillopepsin. 1. Design, Synthesis, and Evaluation of an Inhibitor Bridged between P1 and P3

2. Macrocyclic Inhibitors of Penicillopepsin. 2. X-ray Crystallographic Analyses of Penicillopepsin Complexed with a P3−P1 Macrocyclic Peptidyl Inhibitor and with Its Two Acyclic Analogues

3. Blundell, T. L.; Sibanda, B. L.; Hemmings, A.; Foundling, S. F.; Tickle, I. J.; Pearl, L. H.; Wood, S. P. InMolecular Graphics and DrugDesign; Burgen, A. S. V., Roberts, G. C. K., Tute, M. S., Eds.; Elsevier Science Publishers BV: Amsterdam, 1986; pp 321−334.

4. Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogs

5. CAVEAT: A program to facilitate the design of organic molecules

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