Acythiols and component thiol compositions as anti-HIV and...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai

Reexamination Certificate

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C514S354000, C514S355000, C514S448000, C514S461000

Reexamination Certificate

active

08076372

ABSTRACT:
Certain thiol and acylthiol compounds inhibit retrovirus growth by attacking the highly conserved zinc finger regions of essential viral proteins. These compounds, compositions containing them, and methods of using them to treat retroviral infections such as HIV are described. These compounds are also useful for preparation of vaccines comprised of inactivated retroviruses such as HIV, prevention of the transmission of such retroviruses, and detection of retroviral proteins.

REFERENCES:
patent: 2850491 (1958-09-01), Brenner
patent: 4560506 (1985-12-01), Weller, III et al.
patent: 2007/0293478 (2007-12-01), Zimmermann et al.
patent: WO 99/65871 (1999-12-01), None
patent: WO 03/060098 (2003-07-01), None
Goel, A., et al., “Benzamide-Based Thiolcarbamates: A New Class of HIV-1 NCp7 Inhibitors,” Bioorganic & Medicinal Chemistry Letters, 2002, vol. 12, pp. 767-770.
Song, Y., et al., “Synthesis and Biological Properties of Amino Acid Amide Ligand-Based Pyridinioalkanoyl Thioesters as Anti-HIV Agents,” Bioorganic & Medicinal Chemistry, 2002, vol. 10, pp. 1263-1273.
Turpin, et al., “Synthesis and Biological Properties of Novel Pyridinioalkanoyl Thiolesters (PATE) as Anti-HIV-1 Agents That Target the Viral Nucleocapsid Protein Zinc Fingers”,J. Med. Chem. (1999) 42:67-86.

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