Design and Synthesis of Potent Hexapeptide and Heptapeptide Gonadotropin-Releasing Hormone Antagonists by Truncation of a Decapeptide Analogue Sequence-Reference-Cited by-同舟云学术

Design and Synthesis of Potent Hexapeptide and Heptapeptide Gonadotropin-Releasing Hormone Antagonists by Truncation of a Decapeptide Analogue Sequence

Published:2000-06-30 Issue:15 Volume:43 Page:2831-2836
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Yahalom Dror¹,Rahimipour Shai¹,Koch Yitzhak¹,Ben-Aroya Nurit¹,Fridkin Mati¹

Affiliation:

1. Departments of Organic Chemistry and Neurobiology, Weizmann Institute of Science, Rehovot 76100, Israel

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm990433g

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4. STUDIES WITH FRAGMENTS OF A HIGHLY ACTIVE ANALOGUE OF LUTEINIZING HORMONE RELEASING HORMONE

5. Active reduced-size hexapeptide analogs of luteinizing hormone-releasing hormone

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