Urotensin-II agonists and antagonists

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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Details

C514S016700, C530S311000, C530S328000

Reexamination Certificate

active

10399542

ABSTRACT:
The present invention is directed to a novel class of cyclic polypeptides of the formula: (R1)a-AA1-cyclo[AA2-AA3-AA4-AA5-AA6-Cys]-AA7-R2, pharmaceutically acceptable salts thereof, wherein the variables are as defined in the specification, which inhibit the effects of urotensin-II and are useful for treating a variety of diseases and/or conditions characterized by an excess of urotensin-II including ischaemic heart disease, congestive heart failure, portal hypertension, variceal bleeding, hypotension, angina pectoris, myocardial infarction, ulcers, anxiety, schizophrenia, manic depression, delirium, dementia, mental retardation and/or dyskinesias.

REFERENCES:
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patent: 2004/0171530 (2004-09-01), Coy et al.
patent: 2004/0181032 (2004-09-01), Coy et al.
patent: 2 786 489 (2000-06-01), None
patent: WO 01/37780 (2001-05-01), None
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Hocart, S. J. et al, “Highly Potent Cyclic Disulfide Antagonists of Somatostatin,” J. Medicinal Chem., 1999, 42(11) :1863-1871, XP002189091.
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Waugh, D. et al., “Purification and characterization of urotensin II from the brain of a teleost (trout,Oncorhynchus mykiss) and an elasmobranch (skate,Raja rhina),” Gen. and Comp. Endo., 1993, 92:419-427.
Coulouarn, Y. et al., “Cloning of the cDNA encoding urotensin II precursor in frog and human reveals intense expression of the urotensin II gene in motoneruons of the spinal cord,” PNAS, 1998, 95:15803-15808.

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