3b92

Revision as of 12:37, 23 January 2008 by OCA (talk | contribs) (New page: left|200px<br /><applet load="3b92" size="350" color="white" frame="true" align="right" spinBox="true" caption="3b92, resolution 2.00Å" /> '''Novel thio-based TAC...)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Novel thio-based TACE inhibitors Part 2: Rational design, synthesis and SAR of thiol-contaning aryl sufones

File:3b92.jpg


3b92, resolution 2.00Å

Drag the structure with the mouse to rotate

OverviewOverview

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 StructureAbout 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.

ReferenceReference

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

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA