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Design, Synthesis, and Pharmacological Evaluation of Second-Generation Soluble Adenylyl Cyclase (sAC, ADCY10) Inhibitors with Slow Dissociation Rates

Authors :
Michael Miller
Thomas Rossetti
Jacob Ferreira
Lubna Ghanem
Melanie Balbach
Navpreet Kaur
Lonny R. Levin
Jochen Buck
Maria Kehr
Sandrine Coquille
Joop van den Heuvel
Clemens Steegborn
Makoto Fushimi
Efrat Finkin-Groner
Robert W. Myers
Stacia Kargman
Nigel J. Liverton
David J. Huggins
Peter T. Meinke
Source :
J Med Chem
Publication Year :
2022
Publisher :
American Chemical Society (ACS), 2022.

Abstract

Soluble adenylyl cyclase (sAC: ADCY10) is an enzyme involved in intracellular signaling. Inhibition of sAC has potential therapeutic utility in a number of areas. For example, sAC is integral to successful male fertility: sAC activation is required for sperm motility and ability to undergo the acrosome reaction, two processes central to oocyte fertilization. Pharmacologic evaluation of existing sAC inhibitors for utility as on-demand, nonhormonal male contraceptives suggested that both high intrinsic potency, fast on and slow dissociation rates are essential design elements for successful male contraceptive applications. During the course of the medicinal chemistry campaign described here, we identified sAC inhibitors that fulfill these criteria and are suitable for in vivo evaluation of diverse sAC pharmacology.

Details

ISSN :
15204804 and 00222623
Volume :
65
Database :
OpenAIRE
Journal :
Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....1c1b764b03322568b2d6bccba1a32f50
Full Text :
https://doi.org/10.1021/acs.jmedchem.2c01133