Vanilloid fatty hydroxamates as therapeutic anti-inflammatory pharmaceuticals
申请人:Laskin Jeffrey D.
公开号:US09422233B2
公开(公告)日:2016-08-23
Three unique subtypes of N-hydroxyamides and N-hydroxycarbamates containing both the vanilloid moiety (4-hydroxy-3-methoxybenzyl) and a lipophilic aliphatic moiety. Also disclosed are direct syntheses of these vanilloid fatty hydroxamates. The compounds possess inhibitory activity against the enzymes fatty acid amide hydrolase (FAAH) and matrix metallo-proteinase 9 (MMP-9). In addition, these substances bind to the calcium channel protein TRPV1 and inhibit vesicant-induced inflammation in skin and cornea. The compounds have utility in treating topical or systemic inflammatory processes in the skin and/or eye.
SULSKY, RICHARD;DERNERS, JAMES P., TETRAHEDRON LETT., 30,(1989) N 1, C. 31-34
作者:SULSKY, RICHARD、DERNERS, JAMES P.
DOI:——
日期:——
US9422233B2
申请人:——
公开号:US9422233B2
公开(公告)日:2016-08-23
Alkylation of n-benzyloxyureas and carbamates
作者:Richard Sulsky、James P. Demers
DOI:10.1016/s0040-4039(01)80314-2
日期:——
Vanilloid Fatty Hydroxamates as Therapeutic Anti-inflammatory Pharmaceuticals
申请人:Laskin Jeffrey D.
公开号:US20120252891A1
公开(公告)日:2012-10-04
Three unique subtypes of N-hydroxyamides and N-hydroxycarbamates containing both the vanilloid moiety (4-hydroxy-3-methoxybenzyl) and a lipophilic aliphatic moiety. Also disclosed are direct syntheses of these vanilloid fatty hydroxamates. The compounds possess inhibitory activity against the enzymes fatty acid amide hydrolase (FAAH) and matrix metallo-proteinase 9 (MMP-9). In addition, these substances bind to the calcium channel protein TRPV1 and inhibit vesicant-induced inflammation in skin and cornea. The compounds have utility in treating topical or systemic inflammatory processes in the skin and/or eye.