Peptides and peptidomimetics having anti-proliferative...

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

Reexamination Certificate

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Details

C930S020000

Reexamination Certificate

active

06995135

ABSTRACT:
This invention provides compounds including peptides and peptidomimetics that can be used to treat cell proliferative disorders, such as those associated with benign and malignant tumor cells. While the invention is not limited to any particular mechanism, the compounds of the invention appear to function at least in part by inhibiting G2 cell cycle checkpoint. Thus, invention compounds can be used to inhibit cell growth alone or be used in combination with a nucleic acid damaging treatment to inhibit cell growth.

REFERENCES:
patent: 01/21771 (2001-03-01), None
patent: 01/94411 (2001-12-01), None
Suganuma et al., “Sensitization of Cancer Cells to DNA Damage-induced Cell Death by Specific Cell Cycle G2Checkpoint Abrogation”,Cancer Research, Dec. 1, 1999; 59:5887-5891; XP002181645.
Kobayashi et al., “Selective Cancer Cell Killing by a Novel G2 Checkpoint Abrogating Peptide”, Proceedings of the Annual Meeting of the American Assocation for Cancer Research, Mar. 2001; #4892 p. 911, XP-001173131.
Ito et al., “Phylogenetic Relationships of Amaryllidaceae Based on matK Sequence Data”,J. Plant Res., Jun. 1999; 112(1106):207-216, XP008027543.
Hayakawa et al., “Sequence Analysis of theXestia c-nigrumGranulovirus Genome”,Virology, Sep. 30, 1999; 262(2):277-297, XP004439794.
Nestor et al., “Luteinizing Hormone-Releasing Hormone Antagonists Containing Very Hydrophobic Amino Acids”,J. Med. Chem.,1984; 27:1170-1174, XP002288202.
Maryanoff et al., “Protease-Activated Receptor-2 (PAR-2): Structure-Function Study of Receptor Activation by Diverse Peptides Related to Tethered-Ligand Epitopes”,Archives of Biochemistry and Biophysics, Feb. 15, 2001; 386(2):195-204, XP002971306.

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