PDK-1/Akt signaling inhibitors
OwnerChing-Shih Cheninventor
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OwnerChing-Shih Cheninventor
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A new class of phosphoinositide-dependent kinase-1 (PDK-1) inhibitors of formula I: wherein X is selected from the group consisting of alkyl and haloalkyl; Ar is an aryl radical selected from the group consisting of phenyl, biphenyl, naphthyl, anthryl, phenanthryl, and fluorenyl; and wherein Ar is optionally substituted with one or more radicals selected from the group consisting of halo, C1-C4 alkyl, C1-C4 haloalkyl, azido, C1-C4 azidoalkyl, aryl, akylaryl, haloaryl, haloalkylaryl, and combinations thereof; and R is selected from the group consisting of nitrile, acetonitrile, ethylnitrile, propylnitrile, carboxamide, amidine, tetrazole, oxime, hydrazone, acetamidine, aminoacetamide, guanidine, and urea. Also provided are methods of using the compounds for the treatment and prevention of cancer in humans.
A compound of formula I
A compound of formula 2
A compound of formula III:
A compound of formula IV:
A compound of formula V
A method of inducing apoptosis in unwanted rapidly proliferating cells, the method comprising the step of contacting a therapeutically effective amount of a compound of formula I
A method for treating, inhibiting, or delaying the onset of cancer, wherein the cancer is selected from the group consisting of leukemia, non-small cell lung cancer, colon cancer, central nervous system cancer, melanoma, ovarian cancer, renal cancer, prostate cancer, and breast cancer, in a subject in need of such treatment, the method comprising administering a therapeutically effective amount of a compound of formula I:
A method for preventing restenosis in a subject that has undergone an angioplasty or stent procedure, the method comprising administering a therapeutically effective amount of a compound of formula I:
Dependencies are inferred from the claim text.