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用于先导化合物鉴定的生物活性天然产物与超强酸化学:以用于降压药物发现的选择性hCA III和L型钙电流抑制剂为例

Bioactive Natural Product and Superacid Chemistry for Lead Compound Identification: A Case Study of Selective hCA III and L-Type Ca Current Inhibitors for Hypotensive Agent Discovery.

作者信息

Carreyre Hélène, Carré Grégoire, Ouedraogo Maurice, Vandebrouck Clarisse, Bescond Jocelyn, Supuran Claudiu T, Thibaudeau Sébastien

机构信息

Superacid Group/Organic Synthesis Team, Université de Poitiers, IC2MP-UMR CNRS 7285, 86073 Poitiers CEDEX 09, France.

STIM-ERL CNRS 7368 Université de Poitiers, 86073 Poitiers Cedex 9, France.

出版信息

Molecules. 2017 May 31;22(6):915. doi: 10.3390/molecules22060915.

Abstract

Dodoneine (Ddn) is one of the active compounds identified from , which is a medicinal plant used in African pharmacopeia and traditional medicine for the treatment of hypertension. In the context of a scientific program aiming at discovering new hypotensive agents through the original combination of natural product discovery and superacid chemistry diversification, and after evidencing dodoneine's vasorelaxant effect on rat aorta, superacid modifications allowed us to generate original analogues which showed selective human carbonic anhydrase III (hCA III) and L-type Ca current inhibition. These derivatives can now be considered as new lead compounds for vasorelaxant therapeutics targeting these two proteins.

摘要

多东宁(Ddn)是从一种药用植物中鉴定出的活性化合物之一,该植物在非洲药典和传统医学中用于治疗高血压。在一项旨在通过天然产物发现与超强酸化学多样化的原始组合来发现新型降压药的科学计划中,在证实多东宁对大鼠主动脉的血管舒张作用后,超强酸修饰使我们能够生成具有选择性抑制人碳酸酐酶III(hCA III)和L型钙电流的原始类似物。这些衍生物现在可被视为针对这两种蛋白质的血管舒张疗法的新型先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a348/6152723/601333dc3e77/molecules-22-00915-g001.jpg

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