Human ADAM-10 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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Details

C514S252110, C514S252140, C514S253020, C514S253110, C544S121000, C544S336000, C544S357000

Reexamination Certificate

active

07629341

ABSTRACT:
The present invention provides compounds useful for inhibiting the ADAM-10 protein, with selectivity versus MMP-1. Such compounds are useful in the in vitro study of the role of ADAM-10 (and its inhibition) in biological processes. The present invention also comprises pharmaceutical compositions comprising one or more ADAM-10 inhibitors according to the invention in combination with a pharmaceutically acceptable carrier. Such compositions are useful for the treatment of cancer, arthritis, and diseases related to angiogenesis. Correspondingly, the invention also comprises methods of treating forms of cancer, arthritis, and diseases related to angiogenesis in which ADAM-10 plays a critical role.

REFERENCES:
patent: 5215549 (1993-06-01), Hsu
patent: 5380525 (1995-01-01), Leedle et al.
patent: 5739300 (1998-04-01), Toepfer et al.
patent: 5753653 (1998-05-01), Bender et al.
patent: 5861510 (1999-01-01), Piscopio et al.
patent: 6153757 (2000-11-01), Zook et al.
patent: 6166005 (2000-12-01), De et al.
patent: 6225311 (2001-05-01), Levin et al.
patent: 6333324 (2001-12-01), Neya et al.
patent: 6387901 (2002-05-01), Chupak
patent: 6489324 (2002-12-01), Neya et al.
patent: 6500948 (2002-12-01), Zook et al.
patent: 6509337 (2003-01-01), Piscopio et al.
patent: 6545038 (2003-04-01), De et al.
patent: 6599890 (2003-07-01), McClure et al.
patent: 6716833 (2004-04-01), Levin et al.
patent: 6812227 (2004-11-01), Levin et al.
patent: 6849732 (2005-02-01), Zook et al.
patent: 7030242 (2006-04-01), Noe et al.
patent: 7132424 (2006-11-01), Picard et al.
patent: 7223751 (2007-05-01), Chung et al.
patent: 7282496 (2007-10-01), Sandanayaka et al.
patent: 2003/0008849 (2003-01-01), Levin et al.
patent: 2003/0060473 (2003-03-01), Neya et al.
patent: 2003/0181441 (2003-09-01), McClure et al.
patent: 2003/0186958 (2003-10-01), De et al.
patent: 2004/0063672 (2004-04-01), Frost et al.
patent: 2004/0106631 (2004-06-01), Bernardelli et al.
patent: 2004/0229817 (2004-11-01), Duggal et al.
patent: 2005/0113346 (2005-05-01), Levin et al.
patent: 2005/0130958 (2005-06-01), Li et al.
patent: 2005/0215549 (2005-09-01), McClure et al.
patent: 2005/0282905 (2005-12-01), Horiuchi
patent: 2006/0199820 (2006-09-01), Bannen et al.
patent: 2007/0015207 (2007-01-01), Ludovici et al.
patent: 2007/0142391 (2007-06-01), Page et al.
patent: 2007/0155730 (2007-07-01), Leit et al.
patent: 43 27 026 (1995-02-01), None
patent: 1 016 245 (1966-01-01), None
patent: 2000247975 (2000-09-01), None
patent: WO 96/33172 (1996-10-01), None
patent: WO9633172 (1996-10-01), None
patent: 97/20824 (1997-06-01), None
patent: WO 97/20824 (1997-06-01), None
patent: WO9720824 (1997-06-01), None
patent: WO 98/08825 (1998-03-01), None
patent: WO9808825 (1998-03-01), None
patent: WO 98/27069 (1998-06-01), None
patent: 98/32748 (1998-07-01), None
patent: WO 98/34918 (1998-08-01), None
patent: WO9834918 (1998-08-01), None
patent: 98/43963 (1998-10-01), None
patent: WO 99/58531 (1999-11-01), None
patent: WO9958531 (1999-11-01), None
patent: WO 00/09492 (2000-02-01), None
patent: WO0009492 (2000-02-01), None
patent: WO 00/44709 (2000-08-01), None
patent: 01/55112 (2001-08-01), None
patent: WO 02/067866 (2002-09-01), None
patent: WO 02/083112 (2002-10-01), None
patent: WO 02/088115 (2002-11-01), None
patent: WO 03/037852 (2003-05-01), None
patent: 03/051825 (2003-06-01), None
patent: WO 03/048142 (2003-06-01), None
patent: WO 03/055851 (2003-07-01), None
patent: WO 03/057214 (2003-07-01), None
patent: WO 03/106381 (2003-12-01), None
patent: WO 2004/014892 (2004-02-01), None
patent: WO 2004/026818 (2004-04-01), None
patent: WO 2004/071390 (2004-08-01), None
patent: WO 2004/073599 (2004-09-01), None
patent: WO 2006/076442 (2006-07-01), None
patent: WO 2007/022638 (2007-03-01), None
patent: WO 2007/039736 (2007-04-01), None
Letavic et al, Synthesis and biological activity of piperazine-based dual MMP-13 and TNF-alpha converting enzyme inhibitors. Bioorg Med Chem Lett. Oct. 6, 2003;13(19):3243-6.
Feit et al., “Structure-activity studies on sulfamyl diuretics”, Journal of Medicinal Chemistry, 15(4), 1972, 437-440.
Shahripour, A. B. et al., “Structure-based design of caspase—1 inhibitor containing a diphenyl ether sulfonamide”, Biorganic & Medicinal Chemistry Letters, 11(20), 2001, 2779-2782.
Neale, A. J. et al., “Internuclear cyclizations of aromatic sulfonyl chlorides. Tribenz [b,d,f] oxepin and tribenzo [b,d,f] thiepin”, Tetrahedron, 21(6), 1299-313., 1965.

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