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Serving 500+ biopharmaceutical companies globally:

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Generated: July 25, 2017

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Title:Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
Abstract: Compounds that inhibit P13K.delta. activity, including compounds that selectively inhibit P13K.delta. activity, are disclosed. Methods of inhibiting phosphatidylinositol 3-kinase delta isoform (P13K.delta.) activity, and methods of treating diseases, such as disorders of immunity and inflammation in which P13K.delta. plays a role in leukocyte function, using the compounds also are disclosed.
Inventor(s): Fowler; Kerry W. (Seattle, WA), Huang; Danwen (Sammamish, WA), Kesicki; Edward A. (Bothell, WA), Ooi; Hua Chee (Kirkland, WA), Oliver; Amy (Bothell, WA), Ruan; Fuqiang (Bellevue, WA), Treiberg; Jennifer (Redmond, WA), Puri; Kamal Deep (Lynnwood, WA)
Assignee: ICOS Corporation (Indianapolis, IN)
Application Number:13/730,276
Patent Claims: 1. A method of inhibiting a growth or a proliferation of cancer cells of hematopoietic origin comprising contacting the cancer cells with an effective amount of a compound, wherein said compound is ##STR00183## or a pharmaceutically acceptable salt thereof.

2. The method of claim 1, wherein the cancer .[.of hematopoietic origin is.]. .Iadd.cells are .Iaddend.lymphoma, leukemia, or multiple myeloma .Iadd.cells.Iaddend..

3. The method of claim 2, wherein the compound or the pharmaceutically acceptable salt thereof is the S-enantiomer.

4. A method of treating a condition in a subject, wherein the condition is lymphoma, leukemia or multiple myeloma, comprising administering to the subject an effective amount of a compound, wherein the compound is .[.5-fluoro-3-phenyl-2-[1-(9H-purin-6 -ylamino)-propyl]-3H-quinazolin-4-one.]. ##STR00184## or a pharmaceutically acceptable salt thereof.

5. The method of claim 4, wherein the condition is selected from the group consisting of Burkitt's lymphoma, Hodgkins' lymphoma, non-Hodgkins lymphoma, lymphocytic lymphoma, lymphocytic leukemia, multiple myeloma and chronic myeloid leukemia.

6. The method of claim 4, wherein the compound or the pharmaceutically acceptable salt thereof is the S-enantiomer.
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