4.7 Article

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

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 65, Issue 22, Pages 15208-15226

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.2c01133

Keywords

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Funding

  1. NIH
  2. Male Contraceptive Initiative (MCI)
  3. [P50 HD100549]
  4. [R01 HD088571]
  5. [F31 AG069501]
  6. [F31 HD105363]

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Soluble adenylyl cyclase is an enzyme involved in intracellular signaling, and it plays a crucial role in male fertility. Evaluation of sAC inhibitors provides essential information for the development of male contraceptives.
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.

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