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Development of Novel Anti-HIV Pyrimidobenzothiazine Derivatives (Hardcover, 2013 ed.)
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Development of Novel Anti-HIV Pyrimidobenzothiazine Derivatives (Hardcover, 2013 ed.)
Series: Springer Theses
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The author successfully developed novel anti-HIV PD 404182
derivatives that exhibited submicromolar inhibitory activity
against both HIV-1 and HIV-2. His thesis is in three parts. The
first part expounds efficient methods for the synthesis of
tricyclic heterocycles related to PD 404182 based on the sp2-carbon
heteroatom bond formations. Starting from arene or haloarene, C O,
C N, or C S bonds were formed by simply changing the reactants.
These synthetic methods provide powerful approaches for the
divergent preparation of pyrimido-benzoxazine, -quinazoline, or
-benzothiazine derivatives. The second part explains SAR studies of
PD 404182 for the development of anti-HIV agents. Through
optimization studies of the central 1,3-thiazin-2-imine core, the
benzene and cyclic amidine ring parts, 3-fold more potent
inhibitors were obtained compared with the lead compound. The
author also reveals by a time-of-drug-addition experiment that PD
404182 derivatives impaired HIV replication at the binding or
fusion stage. The third part of the thesis elucidates the
development of photoaffinity probes for the target identification
of PD 404182. By the photolabeling experiment of HIV-1-infected H9
cells using these probes, the author detected proteins specifically
bound to PD 404182. These new anti-HIV agents may be promising
agents for anti-HIV therapy because their mechanisms of action
differ from those of the currently approved anti-HIV agents.
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