Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M L Constanzer"'
Autor:
M. L. Constanzer, B. K. Matuszewski
Publikováno v:
Chirality. 4:515-519
The indirect chiral separation of the four stereoisomers (1)-(4) of a novel carbonic anhydrase inhibitor with two chiral centers in the molecule is reported. The method is based on chemical derivatization of the secondary amino group of the inhibitor
Publikováno v:
Analytical chemistry. 70(5)
Contrary to common perceptions, the reliability of quantitative assays for the determination of drugs in biological fluids using high-performance liquid chromatography with tandem mass spectrometric (LC/MS/MS) detection methods and the integrity of r
Autor:
E C Shamblen, S J Justice, Gregory A. Winchell, C M Chavez, Daniel Z. Wang, K. C. Lasseter, David L. Ebel, A. Van Hecken, I De Lepeleire, M L Constanzer, Jules I. Schwartz, Barry J. Gertz, P. J. De Schepper
Publikováno v:
The Journal of clinical endocrinology and metabolism. 81(8)
Two isozymes (types 1 and 2) of 5 alpha-reductase (5 alpha R; EC 1.3.99.5), with differential tissue distribution, have been identified in humans. These enzymes catalyze the reduction of testosterone (T) to dihydrotestosterone (DHT). The contribution
Publikováno v:
Pharmaceutical research. 11(3)
Several approaches to the separation of four stereoisomers, 1-4, of a novel, topically active, carbonic anhydrase inhibitor, 1, with two chiral centers in the molecule and four isomers, 5-8, of its chiral metabolite, 5, were evaluated. These methods
Autor:
Daniel Z. Wang, David L. Ebel, Wesley Tanaka, Jules I. Schwartz, Mary Flynn, S. Adcock, M L Constanzer, Barry J. Gertz, Gregory A. Winchell
Publikováno v:
Clinical Pharmacology & Therapeutics. 59:166-166
Autor:
A. N. Chremos, R. L. Williams, J. Antonello, J. R. Ryan, M. L. Constanzer, K. C. Yeh, J. H. Lin, H. B. Hucker, S. M. Kanovsky, P. Vlasses
Publikováno v:
Biopharmaceutics & Drug Disposition. 8:549-560
Pharmacokinetics and bioavailability of famotidine, a new H2-receptor antagonist, were investigated in healthy subjects in five clinical studies. Linear pharmacokinetics were observed following either intravenous or oral administration. Plasma cleara