Zobrazeno 1 - 5
of 5
pro vyhledávání: '"K F, Wright"'
Autor:
H J, Showell, M J, Conklyn, R, Alpert, G P, Hingorani, K F, Wright, M A, Smith, E, Stam, E D, Salter, D N, Scampoli, S, Meltzer, L A, Reiter, K, Koch, A D, Piscopio, S R, Cortina, A, Lopez-Anaya, E R, Pettipher, A J, Milici, R J, Griffiths
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 285(3)
CP-195543 [(+)-2-(3-benzyl-4-hydroxy-chroman-7-yl)-4-trifluoromethyl-benzoic acid] is a structurally novel, selective and potent leukotriene B4 (LTB4) receptor antagonist. In vitro CP-195543 inhibited [3H]LTB4 binding to high-affinity LTB4 receptors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8820a50f6b81802f34218a6f301f753
https://pubmed.ncbi.nlm.nih.gov/9618393
https://pubmed.ncbi.nlm.nih.gov/9618393
Publikováno v:
Canadian journal of physiology and pharmacology. 75(8)
CP-80,633, a selective phosphodiesterase (PDE) 4 inhibitor, potently reverses histamine bronchoconstriction in anesthetized guinea pigs (ED50 10 micrograms/kg) but only weakly relaxes histamine-constricted guinea pig trachea (EC50 137 microM). Using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::944ca50289b7f5684c63bc65c9fe0610
https://pubmed.ncbi.nlm.nih.gov/9360015
https://pubmed.ncbi.nlm.nih.gov/9360015
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 268(3)
Previous attempts to discern and quantify the selectivity of agonists for A1 versus A2 adenosine receptors in vivo have been confounded by the activation of baroreceptor reflexes and/or simultaneous expression of responses to both A1 and A2 receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::172f65e8f5012eb41ea76e54f1611ddd
https://pubmed.ncbi.nlm.nih.gov/8138929
https://pubmed.ncbi.nlm.nih.gov/8138929
Publikováno v:
Advances in prostaglandin and thromboxane research. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e000cd84ff6709c350b48a0924a7cb66
https://pubmed.ncbi.nlm.nih.gov/6770601
https://pubmed.ncbi.nlm.nih.gov/6770601
Publikováno v:
Artery. 10(6)
Tranylcypromine (TCP), which can inhibit prostacyclin (PGI2) synthesis in vitro, has been shown to facilitate platelet aggregation in damaged cerebral arterioles of the mouse when given intraperitoneally (50 mg/kg) one hour before inducing aggregatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3c28271533e5c7949b7d1c5b6c6f9fa
https://pubmed.ncbi.nlm.nih.gov/6961890
https://pubmed.ncbi.nlm.nih.gov/6961890