Substitution of the Side-Chain-Constrained Amino Acids β-Methyl-2‘,6‘-Dimethyl-4‘-Methoxytyrosine in Position 2 of a Bicyclic Oxytocin Analogue Provides Unique Insights into the Bioactive Topography of Oxytocin Antagonists-Reference-Cited by-同舟云学术

Substitution of the Side-Chain-Constrained Amino Acids β-Methyl-2‘,6‘-Dimethyl-4‘-Methoxytyrosine in Position 2 of a Bicyclic Oxytocin Analogue Provides Unique Insights into the Bioactive Topography of Oxytocin Antagonists

Published:1998-07-01 Issue:29 Volume:120 Page:7393-7394
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liao Subo¹,Shenderovich Mark D.¹,Zhang Zhigang¹,Maletinska Lenka¹,Slaninova Jirina¹,Hruby Victor J.¹

Affiliation:

1. Department of Chemistry, the University of Arizona Tucson, Arizona 85721 Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences, Prague, Czech Republic

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja980848b

Reference31 articles.

1. Conformational restrictions of biologically active peptides via amino acid side chain groups

2. Medicinal Chemistry in the Golden Age of Biology: Lessons from Steroid and Peptide Research

3. Conformational and topographical considerations in the design of biologically active peptides

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