4.7 Article

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

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 65, 期 22, 页码 15208-15226

出版社

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

关键词

-

资金

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

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据