Evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase
摘要:
Syntheses and evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase (NOS) are discussed. An extensive SAR was established for pyrrolidin-2-imines class of compounds. The amidines came out as the most potent inhibitors in addition to displaying selectivity. (C) 2004 Elsevier Ltd. All rights reserved.
MAXWELL R. J.; MOORE G. G.; SILBERT L. S., J. ORG. CHEM. <JOCE-AH>, 1977, 42, NO 9, 1517-1520
作者:MAXWELL R. J.、 MOORE G. G.、 SILBERT L. S.
DOI:——
日期:——
Evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase
作者:K Shankaran、Karla L Donnelly、Shrenik K Shah、Ravindra N Guthikonda、Malcolm MacCoss、John L Humes、Stephen G Pacholok、Stephan K Grant、T.M Kelly、K.K Wong
DOI:10.1016/j.bmcl.2004.06.033
日期:2004.9
Syntheses and evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase (NOS) are discussed. An extensive SAR was established for pyrrolidin-2-imines class of compounds. The amidines came out as the most potent inhibitors in addition to displaying selectivity. (C) 2004 Elsevier Ltd. All rights reserved.
Thiocyanations. 4. Cyclization of 1-isothiocyanato-2-thiocyanates. A stereospecific route to the preparation of 4,5-thiazolidine-2-thiones
作者:Robert J. Maxwell、Gordon G. Moore、Leonard S. Silbert