2. Academic Validation
  3. Fragment-based discovery of indole inhibitors of matrix metalloproteinase-13

Fragment-based discovery of indole inhibitors of matrix metalloproteinase-13

  • J Med Chem. 2011 Dec 8;54(23):8174-87. doi: 10.1021/jm201129m.
Steven J Taylor 1,  Asitha Abeywardane,  Shuang Liang,  Ingo Muegge,  Anil K Padyana,  Zhaoming Xiong,  Melissa Hill-Drzewi,  Bennett Farmer,  Xiang Li,  Brandon Collins,  John Xiang Li,  Alexander Heim-Riether,  John Proudfoot,  Qiang Zhang,  Daniel Goldberg,  Ljiljana Zuvela-Jelaska,  Hani Zaher,  Jun Li,  Neil A Farrow
Affiliations

Affiliation

  • 1 Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut 06877-0368, United States. steven.taylor@boehringeringelheim.com
PMID: 22017539 DOI: 10.1021/jm201129m
Abstract

Matrix metalloproteases (MMPs) play an important role in cartilage homeostasis under both normal and inflamed disease states and, thus, have become attractive targets for the treatment of arthritic diseases. Herein, we describe the identification of a potent, selective MMP-13 Inhibitor, developed using fragment-based structure-guided lead identification and optimization techniques. Virtual screening methods identified a novel, indole-based MMP-13 Inhibitor that bound into the S1' pocket of the protein exhibiting a novel interaction pattern hitherto not observed in MMP-13 inhibitors. X-ray crystallographic structures were used to guide the elaboration of the fragment, ultimately leading to a potent inhibitor that was >100-fold selective over nine other MMP isoforms tested.

Figures
Products
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z