Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Carl D. Perchonock"'
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 23:625-636
Two 14C-labelled leukotriene receptor antagonists were prepared from two aryl bromides and potassium [14C]cyanide. Potassium cyanide was converted to copper(I) [14C]cyanide and was subsequently used to displace the bromine atom from two aryl bromides
Autor:
John G. Gleason, Joseph Alan Finkelstein, Carl D. Perchonock, Lenora B. Cieslinski, Henry M. Sarau, Irene Nijole Uzinskas
Publikováno v:
Tetrahedron Letters. 24:2457-2460
Syntheses of 7,7- and 10,10-dimethyleicosa-5(Z),8(Z),11(Z)-trienoic acids ( 5 and 6 , which possess 5-lipoxygenase inhibitory activity, are described.
Publikováno v:
The Journal of Organic Chemistry. 45:1950-1953
Publikováno v:
Tetrahedron Letters. 19:1629-1632
Autor:
L. M. Vickery, R. M. Muccitelli, M A Wasserman, S. S. Tucker, Erhard Kf, J. F. Devan, Irene N. Uzinskas, John G. Gleason, M. E. Mccarthy, Carl D. Perchonock
Publikováno v:
Journal of Medicinal Chemistry. 29:1442-1452
A series of 5-alkynyl- and 5-aryl-4,6-dithianonanedioic acids and related compounds has been prepared for evaluation of leukotriene antagonist activity. The alkynyl compounds were prepared by thioacetal exchange from the corresponding acetylenic acet
Publikováno v:
Tetrahedron Letters. 18:1855-1858
Autor:
S. Mong, Carl D. Perchonock, John G. Gleason, Karl F. Erhard, S. T. Crooke, Ralph F. Hall, M. E. Mccarthy, K. Kondrad, J. S. Frazee, Thomas W. Ku
Publikováno v:
Journal of Medicinal Chemistry. 30:959-961
Autor:
L. M. Vickery, S. Mong, R. M. Muccitelli, John G. Gleason, M. O. Scott, M A Wasserman, S. S. Tucker, Karl F. Erhard, G. Chi-Rosso, B M Weichman, Irene N. Uzinskas, J. F. Newton, J. F. Devan, M. E. Mccarthy, Carl D. Perchonock, Stanley T. Crooke, T. Kirchner, H.-L. Wu
Publikováno v:
ChemInform. 18
Autor:
S. S. Tucker, J. F. Devan, R. M. Muccitelli, M A Wasserman, T. Kirchner, Carl D. Perchonock, Erhard Kf, L. M. Vickery, John G. Gleason, McCarthy Me
Publikováno v:
Journal of medicinal chemistry. 28(9)
Autor:
Barry M. Weichman, Jeris F. DeVan, Thomas W. Ku, R. M. Muccitelli, Carl D. Perchonock, Stephanie S. Tucker, Beth W. Volpe, Mary E. McCarthy, M A Wasserman, Irene Nijole Uzinskas, William E. Bondinell, Lynne M. Vickery, John G. Gleason
Publikováno v:
Prostaglandins. 29(1)
A series of desamino-2-nor-leukotriene analogs has been prepared by the reaction of various thiols with several methyl trans-4,5-epoxy-6Z-alkenoates, followed by deprotection. The products were assessed for their ability to antagonize the LTD4-induce