WAY 170523
目录号 : GC13707WAY 170523 是一种有效的选择性 MMP-13(基质金属蛋白酶 13)抑制剂,IC50 为 17 nM。 WAY 170523 可以直接减弱 ERK1/2 磷酸化。 WAY 170523抑制PC-3细胞的侵袭,可用于前列腺癌研究。
Cas No.:307002-73-9
Sample solution is provided at 25 µL, 10mM.
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Description:IC50: 17 nm (MMP-13)
Collagenase 3 is an enzyme that in humans is encoded by the MMP13 gene. Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis .
In vitro: The combination of NMR spectroscopy with molecular modeling techniques and HTS data resulted in the design of a novel, potent, and selective MMP-13 inhibitor (WAY-170523) which has an IC50 of 17 nM for MMP-13 and showed >5800-, 56-, and >500-fold selectivity against MMP-1, MMP-9, and TACE, respectively. To the best of our knowledge, this represents the first example of a potent MMP-13 inhibitor that has been shown to be selective against MMP-9 [1].
In vivo: In order to investigate a putative role of MMP-13 in ISO-dependent cardiac dysfunction, the authors infused WT mice with ISO for 7 days and concurrently delivered the specific MMP-13 inhibitor WAY170523 daily by i.p injection. Remarkably, they found that WAY170523 completely abolished ISO-dependent increase of the left ventricular systolic diameter and preserved cardiac function in ISO-infused animals without modifying the hypertrophic response similar to the PAR1 KO animals. [2].
Clinical trial: WAY-170523 is currently in the preclinical development and no clinical trial is ongoing.
References:
[1] James M. Chen, Frances C. Nelson, Jeremy I. Levin, Dominick Mobilio, Franklin J. Moy, Ramaswamy Nilakantan, Arie Zask, and Robert Powers. Structure-Based Design of a Novel, Potent, and Selective Inhibitor for MMP-13 Utilizing NMR Spectroscopy and Computer-Aided Molecular Design. J. Am. Chem. Soc. 2000, 122, 9648-9654
[2] Jaffré F, Friedman AE, Hu Z, Mackman N, Blaxall BC. β-adrenergic receptor stimulation transactivates protease-activated receptor 1 via matrix metalloproteinase 13 in cardiac cells. Circulation. 2012;125(24):2993-3003.
Cas No. | 307002-73-9 | SDF | |
化学名 | N-(2-(4-(N-benzyl-N-(2-(hydroxycarbamoyl)-4,6-dimethylphenyl)sulfamoyl)phenoxy)ethyl)benzofuran-2-carboxamide | ||
Canonical SMILES | O=C(C1=CC2=CC=CC=C2O1)NCCOC3=CC=C(S(=O)(N(C4=C(C)C=C(C)C=C4C(NO)=O)CC5=CC=CC=C5)=O)C=C3 | ||
分子式 | C33H31N3O7S | 分子量 | 613.68 |
溶解度 | <61.37mg/ml in DMSO; <61.37mg/ml in ethanol | 储存条件 | Desiccate at RT |
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1 mg | 5 mg | 10 mg | |
1 mM | 1.6295 mL | 8.1476 mL | 16.2951 mL |
5 mM | 0.3259 mL | 1.6295 mL | 3.259 mL |
10 mM | 0.163 mL | 0.8148 mL | 1.6295 mL |
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