Design, Synthesis, Pharmacological Evaluation, and Structure−Activity Study of Novel Endomorphin Analogues with Multiple Structural Modifications-Reference-Cited by-同舟云学术

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Design, Synthesis, Pharmacological Evaluation, and Structure−Activity Study of Novel Endomorphin Analogues with Multiple Structural Modifications

Published:2011-02-02 Issue:5 Volume:54 Page:1462-1472
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mallareddy Jayapal Reddy¹,Borics Attila¹,Keresztes Attila¹,Kövér Katalin E.²,Tourwé Dirk³,Tóth Géza¹

Affiliation:

1. Institute of Biochemistry, Biological Research Center, Hungarian Academy of Sciences, P.O. Box 521, H-6701 Szeged, Hungary

2. Department of Chemistry, University of Debrecen, P.O. Box 21, H-4010 Debrecen, Hungary

3. Department of Organic Chemistry, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm101515v

Reference61 articles.

1. Endogenous opiates: 1998☆

2. Endogenous opiates: 1997

3. A potent and selective endogenous agonist for the µ-opiate receptor

4. Endomorphin synthesis in rat brain from intracerebroventricularly injected [3H]-Tyr-Pro: A possible biosynthetic route for endomorphins

5. Dipeptidyl-peptidase IV (CD26)-role in the inactivation of regulatory peptides

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