Edward J. Kusner

THE INHIBITION BY DISODIUM CROMOGLYCATE IN VITRO OF ANAPHYLACTICALLY INDUCED HISTAMINE RELEASE FROM RAT PERITONEAL MAST CELLS

Edward J. Kusner, Bernard Dubnick, David Herzig · Journal of Pharmacology and Experimental Therapeutics · 1973 · 82 citations

Determination of SRS-A release from guinea-pig lungs by a radioimmunoassay

David Aharony, Paul Dobson, Peter R Bernstein et al. · Biochemical and Biophysical Research Communications · 1983 · 47 citations

Physiology, Immunology, Pulmonary Physiology +3

Synthesis, Structure-Activity Relationships, and Pharmacological Evaluation of a Series of Fluorinated 3-Benzyl-5-Indolecarboxamides: Identification of 4-[[5-[((2R)-2-Methyl-4,4,4-trifluorobutyl)carbamoyl]-1-methylindol-3-yl]methyl]-3methoxy-N-[(2-methylphenyl)sulfonyl]benzamide, a Potent, Orally Active Antagonist of Leukotrienes D4 and E4

Robert T. Jacobs, Peter R Bernstein, Laura A. Cronk et al. · Journal of Medicinal Chemistry · 1994 · 41 citations · Full text

Biochemical and pharmacological characterization of ICI 198,615: a peptide leukotriene receptor antagonist

Robert D. Krell, Edward J. Kusner, David Aharony et al. · European Journal of Pharmacology · 1989 · 28 citations

Inflammation, Molecular Pharmacology, Cytokine +8

Substituted 3-(phenylmethyl)-1H-indole-5-carboxamides and 1-(phenylmethyl)indole-6-carboxamides as potent, selective, orally active antagonists of the peptidoleukotrienes

Robert T. Jacobs, Frederick J. Brown, Laura A. Cronk et al. · Journal of Medicinal Chemistry · 1993 · 22 citations · Full text

Corresponding Indole Amides, Medicinal Chemistry, Pharmaceutical Science +15