Zobrazeno 1 - 4
of 4
pro vyhledávání: '"J J, Oleynek"'
Autor:
R J, Hill, J J, Oleynek, C F, Hoth, M A, Kiron, W, Weng, R T, Wester, W R, Tracey, D R, Knight, R A, Buchholz, S P, Kennedy
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 280(1)
The role of adenosine A1 and A3 receptors in mediating cardioprotection has been studied predominantly in rabbits, yet the pharmacological characteristics of rabbit adenosine A1 and A3 receptor subtypes are unknown. Thus, the rabbit adenosine A3 rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ad8fc091cc2d72ead40cc17f7ec1352
https://pubmed.ncbi.nlm.nih.gov/8996189
https://pubmed.ncbi.nlm.nih.gov/8996189
Autor:
J J, Oleynek, D M, Sedlock, C J, Barrow, K C, Appell, F, Casiano, D, Haycock, S J, Ward, P, Kaplita, A M, Gillum
Publikováno v:
The Journal of antibiotics. 47(4)
WIN 64821, a secondary metabolite produced by Aspergillus sp. (ATCC 74177) was found to inhibit radiolabeled substance P (SP) binding in a variety of tissues, including those of human origin. This compound inhibited, in a competitive manner, the bind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0049dc71d0ea025648a7c23ce4648ec
https://pubmed.ncbi.nlm.nih.gov/7515038
https://pubmed.ncbi.nlm.nih.gov/7515038
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 258(3)
Evidence from contractile, radioisotope ion flux and electrophysiological studies suggest that minoxidil sulfate (MNXS) acts as a K+ channel opener in vascular smooth muscle. This study was designed to examine possible biochemical mechanisms by which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e9eacb86e928abd60d7ed510cd1c009
https://pubmed.ncbi.nlm.nih.gov/1890613
https://pubmed.ncbi.nlm.nih.gov/1890613
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 256(2)
The mechanisms of pinacidil-induced direct vasodilation were studied in vitro in RMA and RAO. In RMA, pinacidil produced dose-dependent relaxations of norepinephrine (5 microM)-induced contractions with an IC50 of 0.2 microM. This component of pinaci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da8f730f87a6fdb0ae6ba8542579fd34
https://pubmed.ncbi.nlm.nih.gov/1993992
https://pubmed.ncbi.nlm.nih.gov/1993992