Literature DB >> 18288992

Advances in matrix metalloproteinase inhibitors based on pyrrolidine scaffold.

Xian-Chao Cheng1, Qiang Wang, Hao Fang, Wen-Fang Xu.   

Abstract

Matrix metalloproteinases (MMPs) play an important role in many physiological and pathological processes. MMP inhibitors have been considered as potential therapeutics for neoplasitc, rheumatic and cardiovascular diseases. Our group and others have been developing pyrrolidine scaffold-based MMP inhibitors for a number of years, and numerous compounds have been reported in the literature. These compounds can be classified as sulfonamide pyrrolidine derivatives, proline-containing peptidomimetics and acyl pyrrolidine derivatives. These synthetic MMP inhibitors show low nanomolar activity for some MMP subclasses, thus confirming pyrrolidine ring an excellent scaffold from which to design MMP inhibitors. This review will focus primarily on the structure, activity and selectivity profiles of pyrrolidine scaffold-based MMP inhibitors.

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Year:  2008        PMID: 18288992

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  5 in total

1.  Use of a new spirophosphine to achieve catalytic enantioselective [4 + 1] annulations of amines with allenes to generate dihydropyrroles.

Authors:  Søren Kramer; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2015-03-17       Impact factor: 15.419

2.  Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine.

Authors:  Christopher J Cordier; Rylan J Lundgren; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2013-07-19       Impact factor: 15.419

3.  Matrix metalloproteinase inhibitors based on the 3-mercaptopyrrolidine core.

Authors:  Yonghao Jin; Mark D Roycik; Dale B Bosco; Qiang Cao; Manuel H Constantino; Martin A Schwartz; Qing-Xiang Amy Sang
Journal:  J Med Chem       Date:  2013-05-16       Impact factor: 7.446

4.  Phosphine-catalyzed [3 + 2] annulation of β-sulfonamido-substituted enones with trans-α-cyano-α,β-unsaturated ketones for the synthesis of highly substituted pyrrolidines.

Authors:  Zhenzhen Gao; Lei Xie; Lusha Ji; Xin Ma; Xiaojing Li; Honglei Liu; Hongchao Guo
Journal:  RSC Adv       Date:  2021-12-17       Impact factor: 3.361

5.  Prediction on the inhibition ratio of pyrrolidine derivatives on matrix metalloproteinase based on gene expression programming.

Authors:  Yuqin Li; Guirong You; Baoxiu Jia; Hongzong Si; Xiaojun Yao
Journal:  Biomed Res Int       Date:  2014-05-22       Impact factor: 3.411

  5 in total

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