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The Journal of Pharmacology and Experimental Therapeutics|July 1, 1995
Functional characterization of the nonpeptide neurokinin3 (NK3) receptor antagonist, SR142801 on the human NK3 receptor expressed in Chinese hamster ovary cellsF Oury-Donat, P Carayon, O Thurneyssen, et al.
Biochemical Pharmacology|September 15, 1994
Malformin-A1 inhibits the binding of interleukin-1 beta (IL1 beta) and suppresses the expression of tissue factor in human endothelial cells and monocytesJ M Herbert, P Savi, A Lalé, et al.
FEBS Letters|December 16, 1996
Effect of substance P on cytokine production by human astrocytic cells and blood mononuclear cells: characterization of novel tachykinin receptor antagonistsJ M Derocq, M Ségui, C Blazy, et al.
Journal De Pharmacologie|January 1, 1985
[Adrenergic and purinergic receptors and bronchial motoricity]C Advenier
British Journal of Pharmacology|August 28, 1998
In vitro characterization of tachykinin NK2-receptors modulating motor responses of human colonic muscle stripsT Croci, G Aureggi, L Manara, et al.
Canadian Journal of Physiology and Pharmacology|July 1, 1995
Tachykinin NK2 receptors further characterized in the lung with nonpeptide receptor antagonistsC Advenier
Pharmacology|May 1, 1996
Pharmacological characterization of SR 142801: a new non-peptide antagonist of the neurokinin NK-3 receptorX K Nguyen-Le, Q T Nguyen, F Gobeil, et al.
Neuropeptides|December 31, 1997
Biochemical and pharmacological activities of SR 144190, a new potent non-peptide tachykinin NK2 receptor antagonistX Emonds-Alt, C Advenier, C Cognon, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1993
Two nonpeptide tachykinin antagonists act through epitopes on corresponding segments of the NK1 and NK2 receptorsU Gether, Y Yokota, X Emonds-Alt, et al.
Journal of Neurochemistry|April 1, 1994
SR 140333, a novel, selective, and potent nonpeptide antagonist of the NK1 tachykinin receptor: characterization on the U373MG cell lineF Oury-Donat, I A Lefevre, O Thurneyssen, et al.
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