3b92
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(New page: 200px<br /><applet load="3b92" size="350" color="white" frame="true" align="right" spinBox="true" caption="3b92, resolution 2.00Å" /> '''Novel thio-based TAC...)
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Revision as of 09:37, 23 January 2008
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Novel thio-based TACE inhibitors Part 2: Rational design, synthesis and SAR of thiol-contaning aryl sufones
Overview
A series of potent thiol-containing aryl sulfone TACE inhibitors were, designed and synthesized. The SAR and MMP selectivity of the series were, investigated. In particular, compound 8b showed excellent in vitro potency, against the isolated enzyme and good selectivity over MMP-2, -7, -8, -9, and -13. The X-ray structure of 8b in complex with TACE was also obtained.
About this Structure
3B92 is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as ADAM 17 endopeptidase, with EC number 3.4.24.86 Full crystallographic information is available from OCA.
Reference
Novel thiol-based TACE inhibitors. Part 2: Rational design, synthesis, and SAR of thiol-containing aryl sulfones., Bandarage UK, Wang T, Come JH, Perola E, Wei Y, Rao BG, Bioorg Med Chem Lett. 2007 Nov 13;. PMID:18054488
Page seeded by OCA on Wed Jan 23 11:37:08 2008
Categories: ADAM 17 endopeptidase | Homo sapiens | Single protein | Wei, Y. | 440 | ZN | Alternative splicing | Aryl-sulfonamide | Cleavage on pair of basic residues | Glycoprotein | Hydrolase | Membrane | Metal-binding | Metalloprotease | Notch signaling pathway | Phosphorylation | Protease | Sh3-binding | Tace inhibitors | Tnf-alpha converting enzyme | Transmembrane | Zinc | Zymogen
