New clicked thiirane derivatives as gelatinase inhibitors: the relevance of the P1′ segment
B. Fabre,a
K. Filipiak,ab
C. Coderch,a
J. M. Zapico,a
Rodrigo J. Carbajo,c
Anne K. Schott,c
Antonio Pineda-Lucena,c
B. de Pascual-Teresa*a and
A. Ramos*a
Abstract
Gelatinases (MMP-2 and MMP-9),
a subfamily of Matrix Metalloproteinases (MMPs), are involved in
several pathologies and especially in cancer. Thiirane is a latent-zinc
binding group used for the design of potent inhibitors of gelatinases.
Here we report a new family of thiirane inhibitors, obtained by click
chemistry. Thus, an azide fragment containing the thiirane group was
connected to several lipophilic alkynes, which were designed to interact
with the S1′ pocket of the two gelatinases. Our hit compound (2f) displayed submicromolar inhibition of MMP-2 (IC50 = 0.62 μM). Computational studies have been used to compare the binding mode of compound 2f in MMP-2 with the reference thiirane inhibitor (SB-3CT), allowing us to discuss the relevance of the P1′ segment in order to maximize potency.
Supplementary files
Publication details
The article was received on 04 Nov 2013, accepted on 01 Apr 2014 and first published on 03 Apr 2014
Article type:
Paper
DOI:
10.1039/C3RA46402D
Citation:
RSC Adv., 2014,4, 17726-17735
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