Substituted 1-benzoyl-3-cyano-pyrrolo [1,2-a] quinolines and...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C546S094000, C544S126000, C544S361000, C514S233200, C514S253030

Reexamination Certificate

active

07135480

ABSTRACT:
The present invention is directed to substituted 1-benzoyl-3-cyano-pyrrolo[1,2-α]quinolines and analogs thereof, represented by the general Formula I:wherein R1–R8, L, Q, dash line and Ar are defined herein. The present invention also relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention can be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

REFERENCES:
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Georgescu, E.I. et al.: N-bridged heterocyclic compounds. Revue Roumaine de Chimie, vol. 46, pp. 357-362, 2001.
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Matusiak, G., “1,3-Dipolar Cycloaddition Reactions of the Ylide Derived from 6-Phenacyl-benzo[f][1,7]naphthyridinium Bromide,”Aust. J. Chem.52:149-151, Commonwealth Scientific and Industrial Research Organization (1999).
Wei, X., et al., “A Facile One-step Synthesis of Aromatic Indolizines by 1,3-Dipolar Cycloaddition of Pyridinium and Related Heteroaromatic Ylides with Alkenes in the Presence of TPCD [Copy4(HCrO4)2],”J. Chem. Soc. Perkin Trans. l1:2487-2489, The Royal Society of Chemistry (1993).
International Search Report for International Application No. PCT/US03/39550, U.S. Patent and Trademark Office, mailed on Jun. 22, 2004.

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