Zobrazeno 1 - 10
of 791
pro vyhledávání: '"T M Brennan"'
Autor:
Daniel Schirlin, Debra L. Taylor, C. G. Bridges, P. S. Ahmed, J.-M. Hornsperger, Celine Tarnus, A. S. Tyms, V. Van Dorsselaer, T M Brennan
Publikováno v:
Antiviral Chemistry and Chemotherapy. 8:205-214
MDL 74,695, a novel dipeptide-like compound containing the ‘difluorostatone type’ transition state mimic and a potent inhibitor of the human immunodeficiency virus (HIV) proteinase, was investigated for anti-HIV activity in vitro. The compound sh
Autor:
H. C. Chui, R. M. Biefeld, B. E. Hammons, W. G. Breiland, T. M. Brennan, E. D. Jones, H. K. Moffat, M. H. Kim, P. Grodzinski, K. H. Chang, H. C. Lee
Publikováno v:
Journal of Electronic Materials. 26:37-42
We have performed an extensive study of GaAs, Al0.22Ga0.78As, and In0.16Ga0.84As grown using tertiarybutylarsine (TBA) in an ultra-high purity metalorganic chemical vapor deposition multi-wafer reactor. Key results include: high purity TBA AlGaAs lay
Publikováno v:
Antiviral Chemistry and Chemotherapy. 7:253-260
MDL 74968 (9-[2-methylidene-3-(phosphonomethoxy)-propyl]guanine), a novel acyclonucleotide derivative of guanine, inhibited human immunodeficiency virus type 1 (HIV-1) replication in vitro with activity comparable to that of adefovir (PMEA; 9-(2-phos
Autor:
J M Hornsperger, A. S. Tyms, J F Navé, C G Bridges, Debra Taylor, P Casara, P S Ahmed, T. M. Brennan
Publikováno v:
Antimicrobial Agents and Chemotherapy. 40:1072-1077
The novel acyclonucleotide derivative of guanine, 9-[2-methylidene-3-(phosphonomethoxy)propyl] guanine (MDL 74,968), had antiviral activity comparable to those of 9-(2-phosphonomethoxyethyl) adenine (PMEA) and 2',3'-dideoxyinosine against laboratory
Publikováno v:
Antiviral Chemistry and Chemotherapy. 6:307-311
The basis of azidothymidine (AZT) insensitivity in the human JM T-cell line has been investigated. It was shown that uptake of radiolabelled thymidine or AZT into cellular acid-soluble pools of JM cells was about 10-fold lower than that seen in AZT-s
Publikováno v:
Antiviral Chemistry and Chemotherapy. 6:143-152
The anti-human immunodeficiency virus type 1 (HIV-1) activity of the α-glucosidase 1 inhibitor 6-0-butanoylcastanospermine (MDL 28574) was assessed in combination with the 2′,3′-dideoxynucleoside analogues zidovudine (AZT), didanosine (ddl) and
Publikováno v:
Journal of Applied Physics. 76:7907-7914
The effects of built‐in biaxial strain on Γ‐X transport in n‐GaAs/i‐InxAl1−xAs/n‐GaAs pseudomorphic single‐barrier structures (x=0, 0.03, and 0.06) are studied by measuring temperature‐dependent I‐V characteristics. For the accurat
Publikováno v:
Antiviral Research. 25:169-175
The intercellular adhesion molecule (ICAM-1, CD54) and its counter receptor, the integrin leukocyte function associated antigen 1 (LFA-1, CD11a/CD18), have important roles in the immune response. These include guiding leukocytes to sites of inflammat
Autor:
S. R. Kurtz, T.J. Drummond, J. A. Olsen, B. E. Hammons, A. J. Howard, I. J. Fritz, T. M. Brennan
Publikováno v:
Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films. 12:1003-1008
Using atomic force microscopy (AFM), we have investigated the effects of growth temperature and dopant incorporation on the surface morphology of molecular beam epitaxy grown graded buffer layers and strained layer superlattices (SLSs) in the InGaAlA
Autor:
T M Brennan, Celine Tarnus, D. Janowick, A. S. Tyms, S. Baltzer, F. Weber, V. Van Dorsselaer, D.L. Taylor, J.M. Remy, Daniel Schirlin
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1213-1218
Replacement of the benzylamine carboxy terminus with a (R)-valinol ether carboxy terminus confers high inhibitory activity to derivatives of the difluorostatone and even difluorostatine types against HIV-1 protease. In HIV infected cells, the difluor