Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Larry S. Eichmeier"'
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 15:513-521
A direct chiral HPLC method has been developed and validated to quantitate the enantiomers of MDL 74 156, the primary metabolite of dolasetron mesylate, in human plasma over the concentration range 1.70–340 ng ml−1. Dolasetron mesylate is a 5-HT3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::355becc3aef4d0490900f318d162feb2
https://doi.org/10.1016/s0731-7085(96)01827-4
https://doi.org/10.1016/s0731-7085(96)01827-4
Publikováno v:
Biomedical Chromatography. 6:295-299
A sensitive and selective liquid chromatographic method to quantitate MDL 201,012 in human plasma was developed and validated. MDL 201,012 (I), diethyl-MDL 201,012 (internal standard, II) and desmethyldiol-MDL 201,012 (masking agent, III) were isolat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4af726c066eba91f53051aa87631037
https://doi.org/10.1002/bmc.1130060610
https://doi.org/10.1002/bmc.1130060610
Autor:
Robert C. Lanman, Bruce Morrill, Dennis H. Giesing, Michael B Lanman, Dale K Yu, Larry S Eichmeier, Alfred T Elvin
Publikováno v:
Clinical Pharmacology and Therapeutics. 48:26-33
Single doses of 1 gm 5-aminosalicylic acid (5-ASA) suspension was administered to 24 healthy volunteers during both fasting and fed conditions. For subjects in a fasting state, plasma 5-ASA and acetyl 5-ASA concentrations peaked rapidly 1 hour after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a27a7fab66e6254cf318a2af25ccaddb
https://doi.org/10.1038/clpt.1990.113
https://doi.org/10.1038/clpt.1990.113
Publikováno v:
Biomedical chromatography : BMC. 8(5)
A sensitive and selective liquid chromatographic procedure to quantitate the deflazacort metabolite 21-hydroxy-deflazacort (DF-21OH) in human plasma was developed and validated. DF-21OH and fludrocortisone acetate (internal standard, IS) were isolate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4a18ab5604c4cc826a71a63f1dbbc99
https://pubmed.ncbi.nlm.nih.gov/7841767
https://pubmed.ncbi.nlm.nih.gov/7841767
Autor:
Michael E. Caplis, Larry S. Eichmeier
Publikováno v:
Analytical Chemistry. 47:841A-844a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43b526d9f6e9e9335ec4336cf4f66ba8
https://doi.org/10.1021/ac60359a050
https://doi.org/10.1021/ac60359a050
Publikováno v:
Organic Mass Spectrometry. 20:247-252
The origin of the [M–69]+ and [M–111]+ signals in the mass spectrum of taraxasterol was studied through the use of C(18), (19), (21), (22) and/or (30) deuteriated derivatives. The generality of these signals for ring systems with an exocyclic met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::750e670392c387e215c2ee9e4b1f16b4
https://doi.org/10.1002/oms.1210200315
https://doi.org/10.1002/oms.1210200315
Publikováno v:
Journal of Analytical Toxicology. 4:58-62
High pressure liquid chromatography procedures are reported for the determination of amitriptyline and its metabolite, nortriptyline, and for imipramine and its metabolite, desipramine. Separations and quantitations were carried out at ambient temper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d808d47cca7f0478ffc0f3835daedb
https://doi.org/10.1093/jat/4.2.58
https://doi.org/10.1093/jat/4.2.58
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 20:1395-1405
Taraxasterols specifically labelled at various ring E sites were synthesized as were cyclohexanes and decalins substituted by a methyl group and an exocyclic methylene moiety similar to the ring Esystem of this terpene. Preparation of deuterated anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e70918632ce39a57e9a58101ca33b1f
https://doi.org/10.1002/jlcr.2580201211
https://doi.org/10.1002/jlcr.2580201211
Autor:
David M. Piatak, Larry S. Eichmeier
Publikováno v:
Phytochemistry. 11:436-438
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fda850495719377d1a5d0b45b6ea3231
https://doi.org/10.1016/s0031-9422(00)90040-2
https://doi.org/10.1016/s0031-9422(00)90040-2