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US 8,242,115 B2Granted
Materials and methods to potentiate cancer treatment
AssigneeLuitpold Pharmaceuticals, Inc.
InventorsJames Halbrook, Edward A. Kesicki, Laurence E. Burgess, Stephen T. Schlachter, Charles T. Eary, Justin G. Schiro, Hongmei Huang, Michael Evans, Yongxin Han
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Abstract
Compounds that inhibit DNA-dependent protein kinase, compositions comprising the compounds, methods to inhibit the DNA-PK biological activity, methods to sensitize cells the agents that cause DNA lesions, and methods to potentiate cancer treatment are disclosed.
Claims13
A compound having the formula,
- wherein:
- A is
- B is aryl or a nitrogen-containing heteroaryl;
- R9 is H or OH;
- R10 is H, O-alkyl or CN;
- and
- R3 is hydrogen or ORh;
- wherein Rb is hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, or substituted heteroaryl, and Rh, independently, is hydrogen, alkyl, substituted alkyl, cycloalkyl, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;
- wherein said substituted alkyl is an alkyl group with one substituent or more than one substituent bound to the same carbon or different carbons,
- wherein each substituent is independently selected from the group consisting of cycloalkyl, aryl, heteroaryl, heterocyclic, substituted aryl, substituted heteroaryl, substituted heterocyclic, N(Rh′)2, ORh′, SRh′, sulfoxide, sulfonyl, halo, carboxyl, acyl, carboxy, hydrazino, hydrazono, and hydroxyamino, wherein each Rh′, independently, is hydrogen, alkyl, cycloalkyl, aryl, or heteroaryl,
- or a pharmaceutically acceptable salt thereof.
8 more elements
Dependencies are inferred from the claim text.