Inhibitors of HIV-1 capsid formation: substituted aryl...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S377000, C514S461000, C548S125000, C548S196000, C549S473000

Reexamination Certificate

active

11271437

ABSTRACT:
Substituted aryl aminomethyl thiazole ureas and analogues thereof that act as inhibitors of viral capsid formation, including HIV capsid formation, are provided here. Generally the virus capsid formation inhibitors described herein are compounds of Formula Iwherein the variables A, R1, R2, R3, R4, X, Y, Z, A5, A6, A7, R8, R9, R12, and R13are defined herein. Pharmaceutical compositions comprising such compounds and methods of treating animals infected with a virus having a capsid protein are provided herein. Methods of using such compounds to treat human patients infected with an HIV virus and reducing the mortality of AIDS are also provided herein.

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Chaimbault, et al. “Synthesis, Antitumour and Anti-HIV Screening of Oxazolidines and Oxazolidinones Derivatives” Pharm. Pharmacol. Commun. 1999, vol. 5, pp. 211-215.
Chun Tang, et al., “Antiviral Inhibition of the HIV-1 Capsid Protein,” J. Mol. Biol. 32: 1013-1020 (2003).
Chaimbault, C. et al., “Synthesis, Antitumour and Anti-HIV Screening of Oxazolidines and Oxazolidinones Derivatives,”Pharm. Pharmacol. Commun. (1999) 5: 211-215.
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International Search Report for International Application No. PCT/US2005/041358, mailed Jul. 6, 2006.

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