Zobrazeno 1 - 10
of 31
pro vyhledávání: '"F R Mangan"'
Synthesis and anti-arthritic activity of a series of 1-aryl-3-dimethylamino-1,4-dihydroisoquinolines
Autor:
Jose Bermudez, F. R. Mangan, P. A. Wyman, Thomson Michael John, Roger Edward Markwell, Ian Hughes, Eric H. Karran, Stephen A. Smith
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:2571-2576
1-Aryl-3-dimethylamino-1,4-dihydroisoquinoline ( 1 ) were synthesised from 1-aryl-1,4-dihydroisoquinol-3-ones ( 2 ) by heating in dimethylcarbamyl chloride. Compounds bearing electron withdrawing substituents on the 1-aryl ring were active in inhibit
Autor:
Thomson Michael John, Jose Bermudez, Roger Edward Markwell, Stephen A. Smith, F. R. Mangan, P. A. Wyman, Ian Hughes, Eric H. Karran
Publikováno v:
ChemInform. 25
1-Aryl-3-dimethylamino-1,4-dihydroisoquinoline ( 1 ) were synthesised from 1-aryl-1,4-dihydroisoquinol-3-ones ( 2 ) by heating in dimethylcarbamyl chloride. Compounds bearing electron withdrawing substituents on the 1-aryl ring were active in inhibit
Autor:
B. Dewald, J. G. R. Elferink, D. Gemsa, M. Kazatchkine, E. Jellum, M. Cremer, J. Winkelmann, Jozef Vermylen, F. Maillet, D. G. Wickens, C. M. Willis, A. G. Herman, S. Leyck, H. Bult, M. Baggiolini, W. Paul, E. Alesse, K. Brune, E. L. Mehler, T. Appelboom, T. L. Dormandy, G. M. Laekeman, R. Görtz, K. Joop, G. Doekes, A. Timmermans, M. Fagerhol, H. P. Hartwig, L. Drummond, H. U. Gubler, D. K. Gemmell, J. E. Vincent, E. H. Karran, E. Etschenberg, M. Pierart, R. J. T. Ouwendijk, A. Sturk, A. Herchuelz, E. Fischer, M. J. Parnham, M. H. Jouvin, J. Reuse, A. J. M. Schreurs, F. R. Mangan, J. C. Riemersma, F. P. Nijkamp, Ch. Gillebert, P. Henricks, E. Stolz, C. Lakatos, C. F. Moldow, F. Nijkamp, F. Bussolino, L. L. M. Thomas, M. Pelletier, P. U. Angeletti, G. Deby-Dupont, J. Morley, K. Willard, M. Delronche, T. Payne, C. Tetta, J. W. ten Cate, M. Guillaume, D. Bitter-Suermann, J. L. Junien, C. Deby, H. ten Cate, G. Emanuelli, F. J. Zijlstra, I. L. Bonta, G. R. Elliott, J. H. P. Wilson, J. P. Giroud, H. R. Büller, P. A. Henricks, E. S. Kalter, J. Verhoef, G. Montrocchio, C. Antro, L. A. van Es, R. Verwilghen, M. J. P. Adolfs, C. P. Page, G. Ianni, A. P. Green, U. Hadding, H. P. Hartung, J. Habicht, G. Camussi, H. Deckmyn, A. Weyns, H. Siegl, B. N. Bouma, A. Van Gossum, C. Lambré, E. Schrauwen, P. G. Robins, E. Munthe, M. A. Continenza, M. R. Daha, A. Houvenaghel, J. Fontaine, M. G. Cifone, W. C. van Dijk, K. D. Rainsford, M. A. Boogaerts, H. Ott, Jean Pierre Famaey, M. Rampart, P. Conti
Publikováno v:
Clinical Rheumatology. 1:140-152
Autor:
A. P. Green, F. R. Mangan
Publikováno v:
Agents and Actions. 13:368-372
Nitrocellulose discs were implanted subcutaneously into mice and cell accumulation measured 96 hours later. Cell accumulation was inhibited by the anti-inflammatory steroids hydrocortisone, dexamethasone and triamcinolone acetonide, but higher doses
Autor:
Elizabeth A. Boyle, F. R. Mangan, Thomson Michael John, P. A. Wyman, Roger Edward Markwell, Robert William Ward, Stephen A. Smith
Publikováno v:
Journal of Medicinal Chemistry. 29:894-898
The synthesis of a series of 7-aroyl-2,3-dihydrobenzo[b]furan-3-carboxylic acids and 7-benzoyl-2,3-dihydrobenzo[b]thiophene-3-carboxylic acids is described. The isomeric 4-benzoyl-1,3-dihydrobenzo[c]furan-1-carboxylic acid was also prepared. Compound
Publikováno v:
Biochemical Journal. 144:413-426
1. Aldolase was selected as a suitable marker for following the androgenic regulation of mRNA synthesis in the prostate gland. 2. Antibodies raised in rabbits against crystalline prostate aldolase were used to monitor the synthesis of this androgen-i
Publikováno v:
Journal of Pharmacy and Pharmacology. 36:314-317
BRL 20459 is a novel compound which displays anti-inflammatory activity when applied topically in the croton oil and cantharadin rat ear inflammation models. The compound does not inhibit uv-induced erythema in the guinea-pig or granuloma formation i
Autor:
Elizabeth A. Boyle, F. R. Mangan
Publikováno v:
Journal of Pharmacy and Pharmacology. 34:570-575
The time-course of cell migration into saline-soaked sponge implants over 5 days showed peak polymorphonuclear leucocyte (PMNL) infiltration at 24 h. In common with the corticosteroids dexamethasone and hydrocortisone, and the non-steroidal anti-infl
Publikováno v:
Journal of Pharmacy and Pharmacology. 34:562-569
Nabumetone is a compound of novel structure which displays acute anti-inflammatory activity in the carrageenan-induced oedema model in rats and the ultraviolet-induced erythema model in guinea-pigs. Its activity in these tests is greater than that of
Publikováno v:
Journal of Pharmacy and Pharmacology. 35:358-362
The penetration of radioactivity into inflamed sites induced by subcutaneously implanted cotton pellets was studied in the rat after oral administration of [14C]nabumetone. Equilibration between inflamed site and plasma concentrations was slow, maxim