Penning_2000_J.Med.Chem_43_721

Reference

Title : Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase - Penning_2000_J.Med.Chem_43_721
Author(s) : Penning TD , Chandrakumar NS , Chen BB , Chen HY , Desai BN , Djuric SW , Docter SH , Gasiecki AF , Haack RA , Miyashiro JM , Russell MA , Yu SS , Corley DG , Durley RC , Kilpatrick BF , Parnas BL , Askonas LJ , Gierse JK , Harding EI , Highkin MK , Kachur JF , Kim SH , Krivi GG , Villani-Price D , Pyla EY , Smith WG
Ref : Journal of Medicinal Chemistry , 43 :721 , 2000
Abstract :

Leukotriene B(4) (LTB(4)) is a pro-inflammatory mediator that has been implicated in the pathogenesis of a number of diseases including inflammatory bowel disease (IBD) and psoriasis. Since the action of LTA(4) hydrolase is the rate-limiting step for LTB(4) production, this enzyme represents an attractive pharmacological target for the suppression of LTB(4) production. From an in-house screening program, SC-22716 (1, 1-[2-(4-phenylphenoxy)ethyl]pyrrolidine) was identified as a potent inhibitor of LTA(4) hydrolase. Structure-activity relationship (SAR) studies around this structural class resulted in the identification of a number of novel, potent inhibitors of LTA(4) hydrolase, several of which demonstrated good oral activity in a mouse ex vivo whole blood assay.

PubMedSearch : Penning_2000_J.Med.Chem_43_721
PubMedID: 10691697

Related information

Citations formats

Penning TD, Chandrakumar NS, Chen BB, Chen HY, Desai BN, Djuric SW, Docter SH, Gasiecki AF, Haack RA, Miyashiro JM, Russell MA, Yu SS, Corley DG, Durley RC, Kilpatrick BF, Parnas BL, Askonas LJ, Gierse JK, Harding EI, Highkin MK, Kachur JF, Kim SH, Krivi GG, Villani-Price D, Pyla EY, Smith WG (2000)
Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase
Journal of Medicinal Chemistry 43 :721

Penning TD, Chandrakumar NS, Chen BB, Chen HY, Desai BN, Djuric SW, Docter SH, Gasiecki AF, Haack RA, Miyashiro JM, Russell MA, Yu SS, Corley DG, Durley RC, Kilpatrick BF, Parnas BL, Askonas LJ, Gierse JK, Harding EI, Highkin MK, Kachur JF, Kim SH, Krivi GG, Villani-Price D, Pyla EY, Smith WG (2000)
Journal of Medicinal Chemistry 43 :721