2a8h
Crystal structure of catalytic domain of TACE with Thiomorpholine Sulfonamide Hydroxamate inhibitor
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OverviewOverview
A series of thiomorpholine sulfonamide hydroxamate TACE inhibitors, all, bearing propargylic ether P1' groups, was explored. In particular, compound 5h has excellent in vitro potency against isolated TACE enzyme, and in cells, oral activity in a model of TNF-alpha production and a, collagen-induced arthritis model, was selected as a clinical candidate for, the treatment of RA.
About this StructureAbout this Structure
2A8H is a Single protein structure of sequence from Homo sapiens with ZN and 4NH as ligands. Active as ADAM 17 endopeptidase, with EC number 3.4.24.86 Full crystallographic information is available from OCA.
ReferenceReference
Acetylenic TACE inhibitors. Part 3: Thiomorpholine sulfonamide hydroxamates., Levin JI, Chen JM, Laakso LM, Du M, Schmid J, Xu W, Cummons T, Xu J, Jin G, Barone D, Skotnicki JS, Bioorg Med Chem Lett. 2006 Mar 15;16(6):1605-9. Epub 2006 Jan 19. PMID:16426848
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