Zobrazeno 1 - 10
of 127
pro vyhledávání: '"A.T. Mcknight"'
Autor:
Kneen Clare O, Michael J. Gilbert, David F. Tattersall, A.T. McKnight, Mark Duchnowski, Colin T. Dourish, Nigel R. Newberry, Margaret S. Beer, Nikki Mudunkotuwa, Michael Rigby, Christopher John Swain, Janet J. Maguire
Publikováno v:
Drug Development Research. 25:17-28
The 5-HT3 receptor antagonist properties of the novel compound L-683,877 (−) (2′-(1-methyl-1H-indol-3-yl)-)spiro(1-azabicyclo[2.2.2]octane-3,5′(4′H)-oxazole) have been characterised in vitro and in vivo. In radioligand binding studies, L-683,
Publikováno v:
Neuropharmacology. 33(6)
The effect of sulphated cholecystokinin octapeptide (CCK-8S) on immediate early gene expression in the rat CNS was investigated using the technique of in situ hybridization. A rapid and transient induction of c-fos, NGFI-A and NGFI-B (nerve growth fa
Autor:
Kate Scholey, J.E. Semark, A.T. McKnight, Shil Patel, E.A. Harley, Nigel R. Newberry, Peter H. Hutson, Richard Hargreaves, Leslie J. Street, Stephen B. Freedman
Publikováno v:
British journal of pharmacology. 107(2)
1. L-689,660, 1-azabicyclo[2.2.2]octane, 3-(6-chloropyrazinyl)maleate, a novel cholinomimetic, demonstrated high affinity binding (pKD (apparent) 7.42) at rat cerebral cortex muscarinic receptors. L-689,660 had a low ratio (34) of pKD (apparent) valu
Autor:
Janet J. Maguire, Leslie L. Iversen, Brian John Williams, Alan C. Foster, A.T. McKnight, A.E. Fletcher, Jenny Longmore, N.J. Elliott, R. Tridgett
Publikováno v:
British journal of pharmacology. 104(2)
1. The interaction at tachykinin receptors of a series of novel cyclic hexapeptides has been examined by use of radioligand binding assays (NK1 and NK3 sites in rat cortex, NK2 sites in hamster urinary bladder) and functional pharmacological assays (
Autor:
Leslie L. Iversen, Nigel R. Newberry, Janet J. Maguire, R. Baker, A.T. McKnight, Michael J. Gilbert, N.T. Mudunkotuwa, Shil Patel, Leslie J. Street, Stephen B. Freedman, J.K. Tang, Angus Murray Macleod, E.A. Harley, John Saunders
Publikováno v:
Scopus-Elsevier
1 A novel series of non-quaternary oxadiazole-based muscarinic agonists demonstrated high affinity for muscarinic receptors. 2. These agonists possessed high efficacy in the nanomolar range at muscarinic receptors in the superior cervical ganglion, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4578b6d195a713546d7503725df9c4ac
https://europepmc.org/articles/PMC1917727/
https://europepmc.org/articles/PMC1917727/
Autor:
P. Hitchcott, A.T. McKnight
Publikováno v:
Trends in Neurosciences. 17:44-45
Autor:
Leslie L. Iversen, Raymond Baker, A.T. McKnight, John Saunders, Kate Scholey, Richard Hargreaves, Nigel R. Newberry, Stephen B. Freedman, Graham Andrew Showell, Shil Patel, E.A. Harley
Publikováno v:
European Journal of Pharmacology. 215:135-136
The oxadiazole L-687,306 is a high affinity muscarinic agonist with a N-methylscopolamine/ oxotremorine-M binding profile predictive of a partial agonist. L-687,306 showed marked selectivity in functional pharmacological assays. L-687,306 was a parti
Publikováno v:
Journal of Neurochemistry. 45:1034-1042
Following incubation of [3H]dynorphin A (1-8) and [3H]dynorphin A (1-9) with suspensions of guinea pig brain membranes, analysis of the supernatants by HPLC has shown that both peptides are degraded at 25 degrees C and at 0 degrees C. Bestatin and ca
Publikováno v:
Proceedings of the Royal Society of London. Series B. Biological Sciences. 213:171-182
The effects of electrical field stimulation on the contents of[Met]enkephalin and [Leu]enkephalin were determined in myenteric plexus-longitudinal muscle preparations of the guinea-pig small intestine. Cycloheximide (0.1 mM) was present in all experi