The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 14, 2008

Filed:

Oct. 18, 2004
Applicants:

John S. Wai, Harleysville, PA (US);

Thorsten E. Fisher, Hatfield, PA (US);

Linghang Zhuang, Chalfont, PA (US);

Donnette D. Staas, Harleysville, PA (US);

Terry A. Lyle, Lederach, PA (US);

Boyoung Kim, Lansdale, PA (US);

Mark W. Embrey, North Wales, PA (US);

Catherine M. Wiscount, Allentown, PA (US);

Lekhanh O. Tran, Norristown, PA (US);

Melissa Egbertson, Ambler, PA (US);

Kelly L. Savage, Schwenksville, PA (US);

Inventors:

John S. Wai, Harleysville, PA (US);

Thorsten E. Fisher, Hatfield, PA (US);

Linghang Zhuang, Chalfont, PA (US);

Donnette D. Staas, Harleysville, PA (US);

Terry A. Lyle, Lederach, PA (US);

Boyoung Kim, Lansdale, PA (US);

Mark W. Embrey, North Wales, PA (US);

Catherine M. Wiscount, Allentown, PA (US);

Lekhanh O. Tran, Norristown, PA (US);

Melissa Egbertson, Ambler, PA (US);

Kelly L. Savage, Schwenksville, PA (US);

Assignee:

Merck & Co., Inc., Rahway, NJ (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A01N 43/58 (2006.01); A01N 43/60 (2006.01); A61K 31/50 (2006.01); A61K 31/495 (2006.01); C07D 471/00 (2006.01); C07D 487/00 (2006.01); C07D 241/36 (2006.01);
U.S. Cl.
CPC ...
Abstract

Hydroxy-substituted pyridopyrrolopyrazine dione compounds are inhibitors of HIV integrase and inhibitors of HIV replication. In one embodiment, the dione compounds are of Formula (I): (I) wherein a, b, A, B, R, R, R, R, R, R, Rand Rare defined herein. The compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines.


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