Apoptosis inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S253110, C514S235500, C514S357000, C514S343000, C514S253060, C514S314000, C514S311000, C514S307000, C514S253050, C544S128000, C544S363000, C544S360000, C544S124000, C546S276400, C546S159000, C546S201000, C546S145000, C546S338000

Reexamination Certificate

active

07816352

ABSTRACT:
The present invention provides compounds that act as selective agents to protect against unintentional cell death or tissue damage and can relieve side effects of cancer treatment such as, for example, oral mucositis, hair loss, diarrhea due to damage to the gastrointestinal epithelium, and myelosuppression. In addition, these compounds can be used to prevent premature cell death when the cell death is caused by signals from damaged cells, for example, signals generated as the result of a traumatic incident or an ischemic episode.

REFERENCES:
patent: WO-2006/099301 (2006-09-01), None
patent: WO-2006/099301 (2006-09-01), None
patent: WO-2006099301 (2006-09-01), None
Gupta, et. al., Synthesis and reactions of pyridinium iodides of substituted acetophenones. Journal of the Indian Chemical Society, 1971, vol. 48, No. 9.
Hcaplus 1972:46046 abstract, “Synthesis and reactions of pyridinium iodides of substituted acetophenones”, Gupta et. al., 1971.
Karljikovic et. al., “Determination of Acidic Constants of some Phenyl-hydroxyiminoethyl Quinolinium Compounds”, Monatshefte fur Chemie 117, 661-670 (1986).
Hcaplus 1988:33102 Abstract, “Silver electrode in direct potentiometric determination of 4′- and 6′-methyl derivatives of 1-(2-phenyl-2-hydroxyiminoethyl)-1-quinolinium chloride”, Karljikovic-Rajic et. al., (1987).
Patani et. al., “Bioisosterism: A Rational Approach in Drug Design” Chem. Rev. 1996, 96, 3147-3176.
Hcaplus 2005:244454, “Quinolinium salt as a potent inhibitor of lymphocyte apoptosis”, Barchechath et. al., Bioorganic & Medicinal Chemistry Letters article accepted Feb. 16, 2005.
Barchechath et. al., “Quinolinium salt as a potent inhibitor of lymphocyte apoptosis”, Bioorganic & Medicinal Chemistry Letters 15 (2005), pp. 1785-1788.
Patani et. al., “Bioisosterism: A Rational Approach in Drug Design”, Chem. Rev. 1996, 96, pp. 3147-3176.
Artyomov, V. A., et al., “Synthesis of Imidazo [1,2-a} pyridines from Pyridines and p-Bromophenacyl Bromide O-Methyloxime”,Synthesis; 8, (1996),927-929.
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Gupta, D. , et al., “Synthesis and Reactions of pyridinium iodides of substituted acetophenones”,Journal of the Indian Chemical Society; 48(9), (1971).
Karljikovic-Rajic, K. , et al., “Silver Electrode in Direct Potentiometric Determination of 4′- and 6-methyl derivatives of 1-(2-phenyl-2-hydroxyiminoethyl)-1-quinolinium chloride”,Journale de Pharmacie de Belgique.
Artyomov, V. A., et al., “Synthesis of Imidazo[1,2-alpha]pyridines from Pyridines andpBromophenacyl BromideO-Methyloxime”,Synthesis, 8, (1996), 927-929.
Fico, G. , et al., “RAPD analysis and flavonoid composition of Aconitum as an aid for Taxonomic discrimination”,Biochemical Systematics and Ecology, 31(3), (2003), Abstract Only, Chemical Abstracts Doc. No. 140:90496, 3 p.
Gupta, D. , et al., “Synthesis and Reactions of pyridinium iodides of substituted acetophenones”,Journal of the Indian Chemical Society; 48(9), (1971), Abstract Only, Chemical Abstracts Doc. No. 76:46046, 2 p.
Karljikovic-Rajic, K. , et al., “Silver Electrode in Direct Potentiometric Determination of 4′- and 6′-methyl derivatives of 1-(2-phenyl-2-hydroxyiminoethyl)-1-quinolinium chloride”,Journale de Pharmacie de Beligique, 42(4), (1987), Abstract Only, Chemical Abstracts Doc. No. 108:33102, 2 p.

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