Zobrazeno 1 - 10
of 35
pro vyhledávání: '"D. T. Walz"'
Publikováno v:
International Archives of Allergy and Immunology. 69:93-97
The subcutaneous administration of 0.01–10 mg/kg of the antiallergic agent disodium cromoglycate on day 0 30 min prior to sensitization of C57B1/6 male mice with 5% 2-phenyl-4-ethoxy-methylene oxazolone proved to cause a significant stimulation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54da6ac062713695ecae138cbe10371e
https://doi.org/10.1159/000233154
https://doi.org/10.1159/000233154
Autor:
D. E. Griswold, D. T. Walz, Blaine M. Sutton, Ivan Lantos, Paul Elliot Bender, K. A. Razgaitis, M. J. Dimartino
Publikováno v:
Journal of Medicinal Chemistry. 27:72-75
Isomeric 5(6)-(4-pyridyl)- and 6(5)-(4-substituted-phenyl)-2,3-dihydroimidazo[2,1-b]thiazoles were prepared by a mixed benzoin-imidazothione route, and their structures were assigned by spectral comparison to compounds of established substitution pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cab33a902eeffc59159f09643594ed5
https://doi.org/10.1021/jm00367a014
https://doi.org/10.1021/jm00367a014
Publikováno v:
Annals of the Rheumatic Diseases. 30:303-306
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24c03da35fd8b68afab92c8591888626
https://doi.org/10.1136/ard.30.3.303
https://doi.org/10.1136/ard.30.3.303
Publikováno v:
Experimental Biology and Medicine. 137:1466-1469
SummaryTopical application of aspirin (6%) or hydrocortisone (2%) in hydroalcoholic solutions significantly reduced edema formation and local hyperpyrexia associated with the primary lesion of adjuvant arthritis in rats. Topical application of aspiri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9d1b7fa80e60c0032fd360ba8d39427
https://doi.org/10.3181/00379727-137-35811
https://doi.org/10.3181/00379727-137-35811
Publikováno v:
Journal of medicinal chemistry. 17(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d37a50cbfd7d6dd0043fa610c497d02
https://pubmed.ncbi.nlm.nih.gov/4808463
https://pubmed.ncbi.nlm.nih.gov/4808463
Autor:
A E, Finkelstein, F R, Roisman, V, Batista, F G, de Nudelman, E H, de Titto, M, Mizraji, D T, Walz
Publikováno v:
The Journal of rheumatology. 7(2)
We studied the dose-response to a new oral gold compound in 28 patients with definite rheumatoid arthritis, divided in 4 groups of 7 patients, each treated with different doses of auranofin for 3 months. Clinical and laboratory parameters were record
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05d45357d2581e0d148f26e330dca9ff
https://pubmed.ncbi.nlm.nih.gov/6768887
https://pubmed.ncbi.nlm.nih.gov/6768887
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccc24acc9132e31fa8a94045779e9045
https://doi.org/10.1002/chin.197420428
https://doi.org/10.1002/chin.197420428
Publikováno v:
The Journal of rheumatology. 10(1)
Serum, blood and cell-associated gold were determined at various time periods after intravenous administration of 1 mg Au/kg of auranofin (AF), gold sodium thiomalate (GSTM) and aurothioglucose (GTG). AF gold exhibited an early phase of decay with hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::647133a6000ab18a997bc341565b0877
https://pubmed.ncbi.nlm.nih.gov/6405031
https://pubmed.ncbi.nlm.nih.gov/6405031
Publikováno v:
The Journal of rheumatology. Supplement. 8
Auranofin's (AF) physical, chemical, pharmacological, and pharmacokinetic properties differ from those of gold sodium thiomalate (GSTM). AF is lipid soluble, monomeric, nonconductive and is not a potent sulfhydryl reagent. In further contrast to GSTM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a7add4d5fcc464d1f021678c68e64dc
https://pubmed.ncbi.nlm.nih.gov/6813492
https://pubmed.ncbi.nlm.nih.gov/6813492
Pharmacokinetics of gold following administration of auranofin (SK+FD-39162) and myochrysine to rats
Publikováno v:
The Journal of rheumatology. 7(6)
Auranofin orally administered to rats resulted in delayed and protracted peak blood and serum gold levels occurring 24 to 48 h post administration. During this period, the gold concentration in blood was higher than in serum indicating that a major p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::164e4d6ba347be4767a0b3ba5e1a25d6
https://pubmed.ncbi.nlm.nih.gov/6782245
https://pubmed.ncbi.nlm.nih.gov/6782245