Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2006-03-15
2009-10-13
Wilson, James O (Department: 1624)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C514S388000, C514S395000, C548S163000, C548S222000, C548S304700, C548S306100
Reexamination Certificate
active
07601745
ABSTRACT:
The present invention relates to compounds of the general formula (III) or pharmaceutically acceptable salts thereof with an acid or a base, or pharmaceutically acceptable prodrugs or a stereoisomer thereof,whereinR3is H, —C(O)NRaRb, halogen, alkyl, haloalkyl, aryl, heteroaryl, OH, SH, NR4′OR5′, NH2, amine, alkylamine, alkoxy, cycloalkyl, heterocycloalkyl, hydroxyalkyl, or haloalkyloxy;R4is H, halogen, alkyl, —C(NR7)NR7R8, —(CH2)paryl, —(CH2)pNR7R8, —C(O)NR7R8, —N═CR7R8, —NR7C(O)R8, cycloalkyl, heterocycloalkyl, haloalkyl, hydroxyalkyl, hyodroxyalkylamino, alkylamino, heteroaryl, or aryl;R5is halogen, alkyl, —C(NR7)NR7R8, —(CH2)paryl, —(CH2)pNR7R8, —C(O)NR7R8, —N═CR7R8, —NR7C(O)R8, cycloalkyl, heterocycloalkyl, haloalkyl, hydroxyalkyl, hydroxyalkylamino, alkylamino, heteroaryl, or aryl.
REFERENCES:
patent: 5817677 (1998-10-01), Linz
patent: 2004/0259877 (2004-12-01), Muto
patent: 2005/0153962 (2005-07-01), Nettekoven
patent: 2006/0069102 (2006-03-01), Leban et al.
patent: 2006/0100224 (2006-05-01), Svenstrup
patent: 10208256 (2003-09-01), None
patent: 1 352 650 (2003-10-01), None
patent: 1352650 (2003-10-01), None
patent: 1637529 (2006-03-01), None
patent: 1516777 (1968-02-01), None
patent: 2270848 (1975-12-01), None
patent: 1487007 (1977-09-01), None
patent: WO9715567 (1997-05-01), None
patent: WO/2004/014882 (2004-02-01), None
patent: WO2004018453 (2004-03-01), None
patent: WO2004041815 (2004-07-01), None
patent: WO2004058750 (2004-07-01), None
patent: WO2004058751 (2004-07-01), None
patent: 2005/003128 (2005-01-01), None
patent: WO2005003128 (2005-01-01), None
patent: WO2005079791 (2005-01-01), None
patent: WO2005/005887 (2005-06-01), None
patent: WO2005077924 (2005-08-01), None
patent: 2006/032322 (2006-03-01), None
patent: WO2006032322 (2006-03-01), None
Wolff, Manfred E., Burger's Medicinal Chemistry and Drug Discovery, Fifth Ed., vol. 1: Principles and Practice, John Wiley & Sons, 1995, 975.
Banker, Gilbert S. et al., Modem Pharmaceutics, Marcel Dekker, New York, 1996.
Dale L. Boger, et al., “A new Class of Highly Cytotoxic Diketopiperazines”, Bioorganic & Medicinal Chemistry Letters, vol. 10, No. 10, XP-004204595m, May 2000, pp. 1019-1020.
Udo E. Lange, et al., “Synthesis of Highly Potent and Selective Hetaryl Ureas as Integrin xvβ3—Receptor Antagonists”, Bioorganic & Medicinal Chemistry Letters, vol. 12, XP-002289253,2002 pp. 1379-1382.
Hi El-Subbagh, et al., “2,4—Disubstituted thiazoles II. * A novel class of antitumor agents, synthesis and biological evaluation” European Journal of Medicinal Chemistry, vol. 31, No. 12, XP-004071797, 1996, pp. 1017-1021.
K. Ekambareswara RAO, et al. Synthesis of Novel Thiazole—Containing DNA Minor Grrove Binding Oligopeptides Related to the Antibiotic Distamycin, Journal of Organic Chemistry, American Chemical Society, vol. 55, No. 2 XP-002255609, 1990, pp. 728-737.
Rohtash Kumar, et al., “Synthesis and Antitumor Cytotoxcity Evluation of Novel hiazole-Contraining Flycosylated Polyamides”, Eur. J. Org. Chem., vol. 24 XP-00234691,2003. pp. 4842-4851.
Abedawbn I. Khalaf, et al., “Distamycin Analogues with Enchanced Lipophilicity: Syntheisis and Antimicrobial Activity”, J. Med. CHem., vol. 47, No. 8 XP-002346492, Mar. 5, 2004, pp. 2133-2156.
Paknarisa Ranchetti, et al., “A New C-Nucleoside Analogue of Tiazofurin: Synthesis and Biological Evaluation of 2-β-D- Ribofuranosylimidazole—4—carboxamide (Imidazofurin)”, Bioorganix & Medicinal Chemistry Letters, vol. 11, No. 1, XP-004225324, Jan. 8, 2001 pp. 67-69.
Richard J. Boyce et al.,“Naturally Occurring 4-Methylthiazolines. A total Synthesis of (-)-[4R, 4S']—Didehydromirabazole A” vol. 51, No. 26, XP-002346493, 1995, pp. 7313-7320.
Rodney L. Parsons Jr., et al., “Total Synthesis of (-)—Thiangazole, a Naturally- Occurring HIV-1 Inhibitor”, J. Org. Chem., vol. 59, XP-002346494, pp. 4733-4734.
Peter WIPF, et al., “Total Synthesis of (-)—Thiangazole and Structurally Related Polyazoles”, J. Org. Chem., vol. 60, XP-002346495, 1995, pp. 7224-7229.
Cornelia Hahnemann, et al., “On the Reaction of Thiazole-2,4-diamines with Isothiocyanates—Preparation and Transformation of 2,4 Diaminothiazole-5 carbothioamides”, Helvetic Chimica Acta, vol. 86, XP-002346496, 2003, pp. 1949-1965.
Pierre-Yves Coqueron, et al., “Iterativer Aufbau von Oxazolringen uber α-chlorglycinate: Totalsynthese von (-)-Muscorid A **”Angewandte Chemie, vol. 1 XP-002346498, 1997, pp. 1-10.
Peter, WIPF, et al., “From Aziridines to Oxazolines and Thiazolines: The heterocrylic Route to Thiangazole”, Synlett, vol. 1. XP-002346499, 1999, pp. 3381-3392.
Martina Herrmann, et al., “Chemical Modification of Thiangazole A in the Oxazole and Styryl Region”, Eur. J. Org Chem., vol. 12, XP-002346499, 1999, pp. 3381-3392.
Jagabandhu Das, et al., “Thromboxane A2/ Endoperoxide Receptor Antagonist: 1,3 Dioxane and 1,3 Analogs”, Bioorganic & Chemistry Letters, vol. 3, No. 6, XP-002346707, 1993, pp. 1271-1276.
European Patent Office Communication, Mar. 15, 2005.
International Search Report for PCT/EP2005/008261, Dated Oct. 11, 2005.
Leban Johann
Pegoraro Stefano
Schmitt Harald
Wolf Kristina
Wuzik Andreas
4SC AG
Baker, Donelson, Bearman, Caldwell and Berkowitz, P.C.
Leeser Erich A
Wilson James O
LandOfFree
Heterocyclic NF-kB inhibitors does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Heterocyclic NF-kB inhibitors, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Heterocyclic NF-kB inhibitors will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-4102811