Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2005-03-02
2008-10-14
Stockton, Laura L. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
07435830
ABSTRACT:
Compounds are provided that act as potent modulators of one or more of the CCR1, CCR2 and CCR3 receptors. The compounds are generally fused-, spiro- or bridged-nitrogen heterocycles having an aryl and heteroaryl component and are useful in pharmaceutical compositions, methods for the treatment of CCR1-, CCR2- and/or CCR3-mediated diseases, and as controls in assays for the identification of competitive receptor antagonists for the above chemokine receptors.
REFERENCES:
patent: 3362956 (1968-01-01), Archer
patent: 3478032 (1969-11-01), Arya
patent: 3491098 (1970-01-01), Archer
patent: 3723433 (1973-03-01), Ueno et al.
patent: 3950354 (1976-04-01), Wenselburger et al.
patent: 3994890 (1976-11-01), Fujimura et al.
patent: 4166452 (1979-09-01), Generales, Jr.
patent: 4174393 (1979-11-01), Van Daalen et al.
patent: 4256108 (1981-03-01), Theeuwes
patent: 4265874 (1981-05-01), Bonsen et al.
patent: 4310429 (1982-01-01), Lai
patent: 4442102 (1984-04-01), Heinemann et al.
patent: 4547505 (1985-10-01), Oepen et al.
patent: 4559341 (1985-12-01), Petersen et al.
patent: 4562189 (1985-12-01), Tomcufcik et al.
patent: 4672063 (1987-06-01), Jasserand et al.
patent: 4772604 (1988-09-01), Van Wijngaarden et al.
patent: 4880809 (1989-11-01), Sugihara et al.
patent: 4997836 (1991-03-01), Sugihara et al.
patent: 5011928 (1991-04-01), Venero et al.
patent: 5177078 (1993-01-01), Ward et al.
patent: 5215989 (1993-06-01), Baldwin et al.
patent: 5227486 (1993-07-01), Merce-Vidal et al.
patent: 5292739 (1994-03-01), Merce Vidal et al.
patent: 5346896 (1994-09-01), Ward et al.
patent: 5382586 (1995-01-01), Merce Vidal et al.
patent: 5464788 (1995-11-01), Bock et al.
patent: 5580985 (1996-12-01), Lee et al.
patent: 5607936 (1997-03-01), Chiang et al.
patent: 5646151 (1997-07-01), Kruse et al.
patent: 5681954 (1997-10-01), Yamamoto et al.
patent: 5719156 (1998-02-01), Shue et al.
patent: 5756504 (1998-05-01), Bock et al.
patent: 5760028 (1998-06-01), Jadhav et al.
patent: 5760225 (1998-06-01), Yuan
patent: 5780475 (1998-07-01), Baker et al.
patent: 5798359 (1998-08-01), Shue et al.
patent: 5968938 (1999-10-01), Williams et al.
patent: 6043246 (2000-03-01), Fukami et al.
patent: 6114334 (2000-09-01), Kerrigan et al.
patent: 6191159 (2001-02-01), Pinto
patent: 6207665 (2001-03-01), Bauman et al.
patent: 6288083 (2001-09-01), Luly et al.
patent: 6329385 (2001-12-01), Luly et al.
patent: 6384035 (2002-05-01), Hutchings et al.
patent: 6451399 (2002-09-01), Boyce
patent: 6455544 (2002-09-01), Friedhoff et al.
patent: 6469041 (2002-10-01), Yuan
patent: 6492375 (2002-12-01), Snutch
patent: 6518273 (2003-02-01), Chapman et al.
patent: 7157464 (2007-01-01), Pennell et al.
patent: 2002/0022624 (2002-02-01), Dinnell et al.
patent: 2002/0040020 (2002-04-01), Bretenbucher et al.
patent: 2002/0045613 (2002-04-01), Pauls et al.
patent: 2002/0045749 (2002-04-01), Lai
patent: 2002/0049205 (2002-04-01), Li et al.
patent: 2002/0077321 (2002-06-01), Khanna et al.
patent: 2002/0107255 (2002-08-01), Bllumberg et al.
patent: 2002/0119961 (2002-08-01), Blumberg et al.
patent: 2003/0008893 (2003-01-01), Colon-Cruz et al.
patent: 2003/0087917 (2003-05-01), Starck et al.
patent: 2003/0139425 (2003-07-01), Bauman et al.
patent: 2003/0149021 (2003-08-01), Li et al.
patent: 2004/0162282 (2004-08-01), Pennell et al.
patent: 2005/0234034 (2005-10-01), Pennell et al.
patent: 2005/0256130 (2005-11-01), Pennell et al.
patent: 2006/0106218 (2006-05-01), Pennell et al.
patent: 0 479 546 (1992-04-01), None
patent: 1 006 110 (2000-06-01), None
patent: WO 97/10219 (1997-03-01), None
patent: WO 97/44329 (1997-11-01), None
patent: WO 98/25617 (1998-06-01), None
patent: WO 98/39000 (1998-09-01), None
patent: WO 98/56771 (1998-12-01), None
patent: WO 99/07351 (1999-02-01), None
patent: WO 99/09984 (1999-03-01), None
patent: WO 99/25686 (1999-05-01), None
patent: WO 99/32468 (1999-07-01), None
patent: WO 99/37619 (1999-07-01), None
patent: WO 99/37651 (1999-07-01), None
patent: WO 00/31032 (2000-06-01), None
patent: WO 00/46195 (2000-08-01), None
patent: WO 00/46196 (2000-08-01), None
patent: WO 00/46197 (2000-08-01), None
patent: WO 00/46198 (2000-08-01), None
patent: WO 00/46199 (2000-08-01), None
patent: WO 00/47539 (2000-08-01), None
patent: WO 00/53600 (2000-09-01), None
patent: WO 00/69815 (2000-11-01), None
patent: WO 00/69820 (2000-11-01), None
patent: WO 00/69848 (2000-11-01), None
patent: WO 02/008221 (2002-01-01), None
patent: WO 02/14314 (2002-02-01), None
patent: WO 02/070523 (2002-09-01), None
patent: WO 03/008395 (2003-01-01), None
patent: WO 03/024450 (2003-03-01), None
patent: WO 03/0051842 (2003-06-01), None
patent: WO 03/105853 (2003-12-01), None
patent: WO 2004/009550 (2004-01-01), None
patent: WO 2005/084667 (2005-09-01), None
International Search Report mailed on Jun. 24, 2005, for PCT Application No. PCT/US05/07166 filed on Mar. 2, 2005, three pages.
International Search Report mailed on Mar. 9, 2007, for PCT Application No. PCT/US06/33803 filed Aug. 29, 2006, three pages.
Anders, et al., A chemokine receptor CCR-1 antagonist reduces renal fibrosis after unilateral ureter ligation. J Clin Invest. (2002) 109(2):251-9.
Badran, M. et al., “Indazole derivatives (part III): synthesis of pyrazolo-[1,2-a]indazole-1,9-dione,[1,2,4]triazino[1,2-a]indazole-1, 10-dione, 3-(Indazol-1-yl)propionic acid amides and hydrazides possessing potential biological activity”Alex. J. Pharm. Sci. (1999) 13(2):101-106.
Bebernitz, G. et al., “The effect of 1,3-diaryl-[1H]-pyrazole-4-acetamides on glucose utilization in on/ob mice”J. Med. Chem. (2001) 44:2601-2611.
Bendele, et al., Animal models of arthritis: relevance to human disease, Toxicologic Pathol. (1999) 27:134-142.
Berge, S.M., et al., Pharmaceutical Salts, Journal of Pharmaceutical Sciences (1977) 66:1-19.
CHEMCATS Database, Chemical Abstracting Service, Accession No. 2003:2855298, Jan. 1, 2004 for CAS Registry No. 492422-98-7.
CHEMCATS Database, Chemical Abstracting Service, Accession No. 2001:2759474, Oct. 20, 2003 for CAS Registry No. 351986-92-0.
Czarnocka-Janowicz, A. et al., “Synthesis and pharmacological activity of 5-substituted-s-triazole-3-thiols”Pharmazie(1991) 46:109-112.
Database Crossfire Beilstein ′Online! Beilstein Institut zur Forderung der Chemischen Wissenschaften, Frankfurt am Main, DE; Database accession No. BRN 6982047 XP002254060 abstract & Varasi et al.,Farmaco Ed. Sci. (1987) 42(6):425-436.
Database Crossfire Beilstein ′Online! Beilstein Institut zur Forderung der Chemischen Wissenschaften, Frankfurt am Main, DE; Database accession No. BRN 1159762 XP002254062 abstract & Zotta et al.FARMACIA(1977) 25:129-134.
Database Crossfire Beilstein !Online! Beilstein Institut zur Forderung der Chemischen Wissenschaften, Frankfurt am Main, DE; Database accession No. BRN 6000843 XP002254061 abstract & Toja et al.,Heterocycles(1987) 26(8):2129-2138.
Database Crossfire Beilstein ′Online! Beilstein Institut zur Forderung der Chemischen Wissenschaften, Frankfurt am Main, DE; Database accession No. BRN 9229443 XP002254063 abstract & Vovk, et al.,Russ. J. Org. Chem. (2001) 37(12).
Devries, M. et al., “On the edge: the physiological and pathophysiological role of chemokines during inflammatory and immunological responses”Sem. Immun. (1999) 11:95-104.
Fischer, F. et al., “Modulation of experimental autoimmune encephalomyelitis: effect of altered peptide ligand on chemokine and chemokine receptor expression”J. Neuroimmun. (2000) 110:195-208.
Foks, H. et al., “Synthesis of new 5-substituted 1,2,4-triazole-3-thione derivatives”Phosphorus, Sulfur and Silicon(2000) 164:67-81.
Gao, et al., Targeting of the chemokine receptor CCR1 suppresses development of acute and chronic cardiac allograft rejection, J Clin Invest. (2000) 105(1):35-44.
Hayao, S. et al., “New antihypertensive aminoalkyltetrazoles”J. Med. Chem. (1967) 10:400-402.
HCAPLUS; Accession No. 1984:630511, Document No. 101:230511; Japanese Patent No. 59130890, issued Jul. 27, 1984; Abstract, 4 pages.
H
Aggen James B.
Chen Wei
Dairaghi Daniel Joseph
Pennell Andrew M. K.
Sen Subhabrata
ChemoCentryx, Inc.
Stockton Laura L.
Townsend and Townsend / and Crew LLP
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