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Journal of Medicinal Chemistry|September 1, 1980
Evaluation of rotenone and related compounds as antagonists of slow-reacting substance of anaphylaxisR J Ashack, L P McCarty, R S Malek, et al.
Bioorganic & Medicinal Chemistry|September 1, 1996
Inhibition of steroid C17(20) lyase with C-17-heteroaryl steroidsJ P Burkhart, C A Gates, M E Laughlin, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Preparation of alpha-keto ester enol acetates as potential prodrugs of human neutrophil elastase inhibitorsJ P Burkhart, S Mehdi, J R Koehl, et al.
Biochemical and Biophysical Research Communications|January 30, 1990
The inhibition of human neutrophil elastase and cathepsin G by peptidyl 1,2-dicarbonyl derivativesS Mehdi, M R Angelastro, J P Burkhart, et al.
Journal of Medicinal Chemistry|December 10, 1993
Xanthines with C8 chiral substituents as potent and selective adenosine A1 antagonistsN P Peet, N L Lentz, M W Dudley, et al.
Bioorganic & Medicinal Chemistry Letters|February 18, 1999
The synthesis of ketomethylene pseudopeptide analogues of dipeptide aldehyde inhibitors of calpainM R Angelastro, A L Marquart, S Mehdi, et al.
Journal of Medicinal Chemistry|November 1, 1986
3-(1H-tetrazol-5-yl)-4(3H)-quinazolinone sodium salt (MDL 427): a new antiallergic agentN P Peet, L E Baugh, S Sunder, et al.
Nucleosides & Nucleotides|January 5, 2000
The synthesis and biological activity of a highly selective adenosine A2a receptor agonistD R Borcherding, N L Lentz, P M Weintraub, et al.
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