4.5 Review

The discovery and development of IP3 receptor modulators: an update

期刊

EXPERT OPINION ON DRUG DISCOVERY
卷 16, 期 6, 页码 709-718

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/17460441.2021.1858792

关键词

Adenophostin; IP3; IP3R; ITPR; xestospongin; 2-APB; drug design; structure

资金

  1. National Institutes of Health (NIH): National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) [R01-DK123259, R01-DK033823, R00-DK107895]
  2. National Institutes of Health (NIH): National Heart, Lung, and Blood Institute (NHLBI) [R01-HL146691, T32-HL144456]
  3. American Heart Association [AHA-20POST35211151]
  4. National Institutes of Health (NIH): National Institute on Aging (NIA) [R56-AG066431]

向作者/读者索取更多资源

Significant progress has been made in the research of IP3R modulators, but challenges still exist, especially in the need for specific antagonists targeting different subtypes of IP3R.
Introduction: Inositol 1,4,5-trisphosphate receptors (IP3Rs) are intracellular calcium (Ca2+) release channels located on the endoplasmic/sarcoplasmic reticulum. The availability of the structure of the ligand-binding domain of IP3Rs has enabled the design of compatible ligands, but the limiting step remains their actual effectiveness in a biological context. Areas covered: This article summarizes the compelling literature on both agonists and antagonists targeting IP3Rs, emphasizing their strengths and limitations. The main challenges toward the discovery and development of IP3 receptor modulators are also described. Expert opinion: Despite significant progress in recent years, the pharmacology of IP3R still has major drawbacks, especially concerning the availability of specific antag onists. Moreover, drugs specifically targeting the three different subtypes of IP3R are especially needed.

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