Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Lloyd Frick"'
Autor:
Lloyd Frick, John C. Drach, Joseph H. Chan, Dean W. Selleseth, Stanley D. Chamberlain, George W. Koszalka, Ernest H. Dark, Robert J. Harvey, Karen K. Biron, Leroy B. Townsend, R E Dornsife, Michelle G. Davis
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 19:101-123
A series of 2'-deoxy analogues of the antiviral agent 5,6-dichloro-2-isopropylamino-1-(beta-L-ribofuranosyl)-1H-benzimidazole (1263W94) were synthesized and evaluated for activity against human cytomegalovirus (HCMV) and for cytotoxicity. The 2-subst
Publikováno v:
American Journal of Infection Control. 43:S43-S44
Publikováno v:
Pharmaceutical Science & Technology Today. 1:12-18
Cassette dosing, combining many test chemicals into one dose solution, is an attractive method for increasing the throughput of in vivo pharmacokinetic experiments. This dosing technique depends on the sensitivity and selectivity of modern analytical
Autor:
Barry G. Shearer, Edward P. Garvey, Jeffrey Alan Oplinger, Lloyd Frick, Furfine Eric Steven, Shuliang Lee
Publikováno v:
Journal of Medicinal Chemistry. 40:1901-1905
S-Ethyl N-phenylisothiourea (4) has been found to be a potent inhibitor of both the human constitutive and inducible isoforms of nitric oxide synthase. A series of substituted N-phenylisothiourea analogues was synthesized to investigate the structure
Publikováno v:
American Journal of Infection Control. 44:S87
Autor:
T. J. Holmes, Marty St. Clair, George W. Koszalka, Thomas A. Krenitsky, C. L. Burns, Devron Averett, M. L. English, Lloyd Frick, Thomas Spector
Publikováno v:
ChemInform. 25
Autor:
Donald J. Nelson, P A Furman, R E Dornsife, Lloyd Frick, D C Liotta, M T Paff, J A Wurster, James A. Fyfe, L J Wilson, Michelle G. Davis
Publikováno v:
Antimicrobial Agents and Chemotherapy. 36:2686-2692
The anti-hepatitis B (anti-HBV) activities of the (-) and (+) enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine (2'-deoxy-3'-thia-5-fluorocytosine [FTC]) were studied by using an HBV-transfected cell line (HepG2 derivative
Autor:
Sab A. Randhawa, Lloyd Frick, Vicente Samano, David Lee Musso, John A. Ray, Wendy Y. Mills, Stanley D. Chamberlain, Terrence L. Smalley
Publikováno v:
ChemInform. 39
A novel series of potent substituted anilinoquinolines were discovered as c-fms inhibitors. The potency could be manipulated upon modification of the C4 aniline and C7 aryl functionality. Pharmacokinetic analysis identified a metabolically stable ana
Autor:
David Lee Musso, Wendy Y. Mills, Vicente Samano, John A. Ray, Sab A. Randhawa, Lloyd Frick, Stanley D. Chamberlain, Terrence L. Smalley
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(22)
A novel series of potent substituted anilinoquinolines were discovered as c-fms inhibitors. The potency could be manipulated upon modification of the C4 aniline and C7 aryl functionality. Pharmacokinetic analysis identified a metabolically stable ana
Autor:
Renae M. Crosby, David W. Rusnak, Jeff T. Hutchins, Alan Payne, Scott Depee, Peiyuan Lin, Stanley D. Chamberlain, Ian James, Jennifer H. Johnson, Marilyn Jansen, Min-Hwa Jasmine Lin, Lloyd Frick, Eva Shaw, K. Fuller, James G. Conway, Timothy J. Chambers, Janet H. Parham, Frederick C. Kull, Sarva M. Tadepalli, Bart J. Votta, Barry R. Keith, Brad McDonald
Colony-stimulating-factor-1 (CSF-1) signaling through cFMS receptor kinase is increased in several diseases. To help investigate the role of cFMS kinase in disease, we identified GW2580, an orally bioavailable inhibitor of cFMS kinase. GW2580 complet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e29eabb628cf54b5f8efe6bf8539a2
https://europepmc.org/articles/PMC1276040/
https://europepmc.org/articles/PMC1276040/