Vitronectin receptor antagonist pharmaceuticals
AssigneeBristol-Myers Squibb Pharma Company
InventorsThomas D. Harris, John A. Barrett, Alan P. Carpenter, JR., Milind Rajopadhye
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AssigneeBristol-Myers Squibb Pharma Company
InventorsThomas D. Harris, John A. Barrett, Alan P. Carpenter, JR., Milind Rajopadhye
Estimating the term…
The present invention describes novel compounds of the formula: (Q)d-Ln-Ch, useful for the diagnosis and treatment of cancer, methods of imaging tumors in a patient, and methods of treating cancer in a patient. The present invention also provides novel compounds useful for monitoring therapeutic angiogenesis treatment and destruction of new angiogenic vasculature. The present invention further provides novel compounds useful for imaging atherosclerosis, restenosis, cardiac ischemia, and myocardial reperfusion injury. The present invention still further provides novel compounds useful for the treatment of rheumatoid arthritis. The pharmaceuticals are comprised of a targeting moiety that binds to a receptor that is upregulated during angiogenesis, an optional linking group, and a therapeutically effective radioisotope or diagnostically effective imageable moiety. The imageable moiety is a gamma ray or positron emitting radioisotope, a magnetic resonance imaging contrast agent, an X-ray contrast agent, or an ultrasound contrast agent.
A compound, comprising:
A diagnostic or therapeutic metallopharmaceutical composition, comprising:
A compound, comprising:
A process for the preparation of diagnostic or therapeutic metallopharmaceutical composition, said process comprising generating a macrostructure from a plurality of molecular components wherein the plurality of components includes a targeting moiety and a chelator, wherein the targeting moiety is a quinolone nonpeptide, which is bound to the chelator, and binds to a receptor that is upregulated during angiogenesis and the compound has 0-1 linking groups between the targeting moiety and chelator.
Dependencies are inferred from the claim text.