Small-molecule inhibitor: TAPI-1

Summary Literature

Name

Common name
TAPI-1
Other names
tumor necrosis factor-alpha protease inhibitor-1

Inhibition

History
TAPI-1 was first described by Mohler et al. (1994) (their compound 1).
Peptidases inhibited
Inhibits adam 17 peptidase.

Chemistry

CID at PubChem
9827273
Structure
[TAPI-1 (M12.217 inhibitor) structure ]
Chemical/biochemical name
N-{D,L-[2-(hydroxyaminocarbonyl)-methyl]-4-methylpentanoyl}L-3-(2' naphthyl)-alanyl-L-alanine 2-aminoethyl amide
Formula weight
500

General

Inhibitor class
This compound contains functionality of the hydroxamate class of metallopeptidase inhibitors. The first full report of hydroxamates as metallopeptidase inhibitors was that of Nishino & Powers (1978). These are reversible inhibitors in which the hydroxamic acid group forms a bidentate complex with the active site zinc. A structure (Holmes & Matthews, 1981) showed both the carbonyl oxygen and the hydroxyl oxygen close to the zinc. Specificity is achieved by fitting of other parts of the molecules to prime-side substrate-binding sites. An excellent early review of the hydroxamates as metallopeptidase inhibitors was that of Powers & Harper (1986) (pp. 244-253).