Zobrazeno 1 - 10
of 32
pro vyhledávání: '"J F, Kachur"'
Autor:
T. Kita, C. E. Smith, K. F. Fok, K. L. Duffin, W. M. Moore, P. J. Karabatsos, J. F. Kachur, F. K. Hamra, N. V. Pidhorodeckyj, L. R. Forte, al. et
Publikováno v:
American Journal of Physiology-Renal Physiology. 266:F342-F348
Guanylin, a peptide homologue of the bacterial heat-stable enterotoxins (ST), is an endogenous activator of guanylate cyclase C (GC-C). We have initiated a search for other members of the guanylin peptide family and in the current study describe a "g
Autor:
Lalita Noronha-Blob, W. J. Rzeszotarski, S. G. Farmer, J. F. Kachur, J. P. Carter, T. C. Adams, Carl Kaiser, M. E. Guzewska, Andrea C. Dupont
Publikováno v:
ChemInform. 22
Several dithiane derivatives, prepared as intermediates for compounds structurally related to the therapeutically useful antimuscarinic agent oxybutynin, were effective inhibitors of calcium ion induced contraction of guinea pig ileal strips and of K
Autor:
T. C. Adams, M. E. Guzewska, Carl Kaiser, S. G. Farmer, J. P. Carter, Lalita Noronha-Blob, W. J. Rzeszotarski, J. F. Kachur, Andrea C. Dupont
Publikováno v:
Journal of Medicinal Chemistry. 34:1585-1593
Several dithiane derivatives, prepared as intermediates for compounds structurally related to the therapeutically useful antimuscarinic agent oxybutynin, were effective inhibitors of calcium ion induced contraction of guinea pig ileal strips and of K
Autor:
Carl Kaiser, D. W. Mcpherson, W. J. Rzeszotarski, Bonnie Sturm, V. H. Audia, M. Abreu, M. Weitzberg, J. F. Kachur
Publikováno v:
Journal of Medicinal Chemistry. 33:307-310
A series of 3-quinuclidinyl atrolactate [3-(1-azabicyclo[2.2.2]octyl) 2-hydroxy-2-phenylpropionate, QNA] derivatives in which the methyl group of the parent is substituted with a tertiary amino substituent was prepared and tested for antimuscarinic a
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 268(3)
Previously, we reported that SC-41930 is a potent leukotriene B4 (LTB4) receptor antagonist. An analog of SC-41930, SC-51146, was evaluated as an antagonist of LTB4 receptors. SC-51146 was shown to bind to LTB4 high affinity binding sites on human ne
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 262(1)
Endothelin-like immunoreactivity has been detected in all regions of the rat gastrointestinal tract. In the present study, we studied the effect of endothelin-1 (ET-1) on muscle contraction and ion transport in the rat colon. Isometric tension was re
Autor:
D, Villani-Price, D C, Yang, R E, Walsh, D J, Fretland, R H, Keith, G, Kocan, J F, Kachur, T S, Gaginella, B S, Tsai
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 260(1)
7-[3-(4-acetyl-3-methoxy-2-propylphenoxy)-propoxy]-3,4-dihydro-8- propyl-2H-1-benzopyran-2-carboxylic acid (SC-41930), a leukotriene B4 (LTB4) receptor antagonist with anti-inflammatory activity in animal models of colitis, was evaluated for effects
Publikováno v:
Gastroenterology. 101(5)
Cholecystokinin (CCK) receptors are currently divided into at least two subtypes: a CCK-A subtype, responsive to the sulfated form of cholecystokinin octapeptide (CCK-8) and selectively antagonized by L-364,718, and a CCK-B subtype, which shares equa
1. Neurokinin A (NKA) is a mammalian tachykinin distributed principally in the nervous system, including the myenteric innervation of the gut. 2. NKA may be involved in neurogenic inflammation and as a modulatory factor in the diarrhoea associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e7eb0fa26190be4d3ba8cefeca27ba
https://europepmc.org/articles/PMC1180051/
https://europepmc.org/articles/PMC1180051/
Publikováno v:
Biochemical pharmacology. 41(6-7)
Inflammatory phagocytic leukocytes produce superoxide and hydrogen peroxide and secrete myeloperoxidase (MPO) into the extracellular medium. MPO catalyzes the oxidation of Cl- by H2O2 to yield chlorinated oxidants (e.g. HOCl and NH2Cl), which have be