Transmembrane nfat inhibitory peptide

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

Reexamination Certificate

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Details

C514S002600, C514S012200, C530S300000, C530S324000, C530S326000

Reexamination Certificate

active

10504333

ABSTRACT:
The present invention aims to solve the conventional problems by providing a peptide compound, in which when administered to a patient of immunologic disease, cardiac hypertrophy or a disease caused by NFAT activation, the period from administration to actual exhibition of effectiveness is short and there are no side effects or antigenicity. Specifically, the present invention relates to a membrane permeable NFAT inhibitory peptide comprising several consecutive arginines and a NFAT-activity inhibitory peptide sequence; a NFAT activation inhibitory agent comprising the peptide; and a immunosuppressive agent and cardiac hypertrophy suppressive agent, comprising the peptide compound as the active ingredient.

REFERENCES:
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patent: 6982082 (2006-01-01), Schreiber et al.
patent: 2002-153288 (2002-05-01), None
patent: WO 01/43694 (2001-06-01), None
patent: WO 03/006619 (2003-01-01), None
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Aramburu J. et al., “Affinity-Driven Peptide Selection of an NFAT Inhibitor More Selective Than Cyclosporin A”, Science, American Association for the Advancement of Science, US, vol. 285, Sep. 24, 1999, pp. 2129-2133, XP 002939935.
Lindgren M. et al., “Cell-Penetrating Peptides”, Trends in Pharmacological Sciences, Elsevier, Haywarth, GB, vol. 21, No. 3, Mar. 2000, pp. 99-103, XP002290884.
Noguchi H. et al., “A New Cell-Permeable Peptide Allows Successful Allogeneic Islet Transplantation in Mice”, Nature Medicine, vol. 10, No. 3, Mar. 2004, pp. 305-309, XP002351236.
Supplementary European Search Report dated Nov. 9, 2005.

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