Newer aminopyrimidinimino isatin analogues as non-nucleoside HIV-1 reverse transcriptase inhibitors for HIV and other opportunistic infections of AIDS: Design, synthesis and biological evaluation
ACQUIRED IMMUNE DEFICIENCY SYNDROME;
ANIMAL CELL;
ARTICLE;
BACTERIAL INFECTION;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SYNTHESIS;
HEPATITIS C VIRUS;
MYCOBACTERIUM TUBERCULOSIS;
NONHUMAN;
OPPORTUNISTIC INFECTION;
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Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1-specific nucleoside analogue [2',5'-bis-O-(tert-butyldimethylsilyl)-beta-d-ribofuranosyl]-3'-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide)thymine (TSAO-T)
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Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors
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Synthesis, antibacterial, antifungal and anti-HIV activities of norfloxacin Mannich bases
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