JP2007534678A - Ccr−1アンタゴニストとしての化合物 - Google Patents
Ccr−1アンタゴニストとしての化合物 Download PDFInfo
- Publication number
- JP2007534678A JP2007534678A JP2007508868A JP2007508868A JP2007534678A JP 2007534678 A JP2007534678 A JP 2007534678A JP 2007508868 A JP2007508868 A JP 2007508868A JP 2007508868 A JP2007508868 A JP 2007508868A JP 2007534678 A JP2007534678 A JP 2007534678A
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- phenyl
- oxo
- compound
- mmol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 0 C*([C@]1(*)N(*C2=C(*)C=C(*)C(C*3=CC3)C2)CC*(*c2ccc(*)cc2)C1)I Chemical compound C*([C@]1(*)N(*C2=C(*)C=C(*)C(C*3=CC3)C2)CC*(*c2ccc(*)cc2)C1)I 0.000 description 3
- LQJHAFSQBOBMAT-UHFFFAOYSA-N C=CC(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O Chemical compound C=CC(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O LQJHAFSQBOBMAT-UHFFFAOYSA-N 0.000 description 2
- DSALFNANMWKNOY-NSCUHMNNSA-N CC(Nc(c(/C=C/C(O)=O)c1)cc(Cl)c1-c1nccnc1)=O Chemical compound CC(Nc(c(/C=C/C(O)=O)c1)cc(Cl)c1-c1nccnc1)=O DSALFNANMWKNOY-NSCUHMNNSA-N 0.000 description 2
- NJVOIIPGERUENG-RUDMXATFSA-N Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(N)c1)c1Cl Chemical compound Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(N)c1)c1Cl NJVOIIPGERUENG-RUDMXATFSA-N 0.000 description 2
- DSSOKHMZIFURBX-VMPITWQZSA-N Nc(c(/C=C/C(N1C2COCC1CN(Cc(cc1)ccc1F)C2)=O)c1)cc(Cl)c1OCC1CC1 Chemical compound Nc(c(/C=C/C(N1C2COCC1CN(Cc(cc1)ccc1F)C2)=O)c1)cc(Cl)c1OCC1CC1 DSSOKHMZIFURBX-VMPITWQZSA-N 0.000 description 2
- ZYPPEOPTMSIIND-YRNVUSSQSA-N O=C(CCl)Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1 Chemical compound O=C(CCl)Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1 ZYPPEOPTMSIIND-YRNVUSSQSA-N 0.000 description 2
- ZCFBGYBOYFTJJJ-RUDMXATFSA-N CC(C(N1c(c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CC3)=O)c2)cc(Cl)c2OC(F)(F)F)=O)NC1=O Chemical compound CC(C(N1c(c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CC3)=O)c2)cc(Cl)c2OC(F)(F)F)=O)NC1=O ZCFBGYBOYFTJJJ-RUDMXATFSA-N 0.000 description 1
- LFKDJXLFVYVEFG-UHFFFAOYSA-N CC(C)(C)OC(N)=O Chemical compound CC(C)(C)OC(N)=O LFKDJXLFVYVEFG-UHFFFAOYSA-N 0.000 description 1
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- MCFHKVLPHCQBNP-ONEGZZNKSA-N CCOC(/C=C/c(c(N)c1)cc(-c2cnccn2)c1Cl)=O Chemical compound CCOC(/C=C/c(c(N)c1)cc(-c2cnccn2)c1Cl)=O MCFHKVLPHCQBNP-ONEGZZNKSA-N 0.000 description 1
- NBRWNNLCIUDIOA-AATRIKPKSA-N CCOC(/C=C/c(c(S(N(C)C)(=O)=O)c1)cc(OC(F)(F)F)c1Cl)=O Chemical compound CCOC(/C=C/c(c(S(N(C)C)(=O)=O)c1)cc(OC(F)(F)F)c1Cl)=O NBRWNNLCIUDIOA-AATRIKPKSA-N 0.000 description 1
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- YMTYSIHCESLJLR-UKTHLTGXSA-N CN(C)CC(Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1)=O Chemical compound CN(C)CC(Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1)=O YMTYSIHCESLJLR-UKTHLTGXSA-N 0.000 description 1
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- RKWUZLAYCMYANV-OWQVCNQYSA-N CN(C)S(c(c(/C=C/C(N(/C(/C1)=C/N(C)Cc(cc2)ccc2F)/C1=C/N(C)S(C)(=O)=O)=O)c1)cc(Cl)c1OC(F)(F)F)(=O)=O Chemical compound CN(C)S(c(c(/C=C/C(N(/C(/C1)=C/N(C)Cc(cc2)ccc2F)/C1=C/N(C)S(C)(=O)=O)=O)c1)cc(Cl)c1OC(F)(F)F)(=O)=O RKWUZLAYCMYANV-OWQVCNQYSA-N 0.000 description 1
- PAEUVVPFLAULEO-UHFFFAOYSA-N CN(C)S(c(c(Br)c1)cc(Cl)c1OC(F)(F)F)(=O)=O Chemical compound CN(C)S(c(c(Br)c1)cc(Cl)c1OC(F)(F)F)(=O)=O PAEUVVPFLAULEO-UHFFFAOYSA-N 0.000 description 1
- UNVZPNPUCNYYLV-UHFFFAOYSA-N CN(C)S(c(c(Br)c1)cc(Cl)c1OC)(=O)=O Chemical compound CN(C)S(c(c(Br)c1)cc(Cl)c1OC)(=O)=O UNVZPNPUCNYYLV-UHFFFAOYSA-N 0.000 description 1
- NWEHILWQHPKVKA-RMKNXTFCSA-N CNC(Nc(c(/C=C/C(N1C2COCC1CN(Cc(cc1)ccc1F)C2)=O)c1)cc(Cl)c1OCC1CC1)=O Chemical compound CNC(Nc(c(/C=C/C(N1C2COCC1CN(Cc(cc1)ccc1F)C2)=O)c1)cc(Cl)c1OCC1CC1)=O NWEHILWQHPKVKA-RMKNXTFCSA-N 0.000 description 1
- VHCSJCFEYXNKHF-HWKANZROSA-N COC(/C=C/c(ccc(Cl)c1)c1N)=O Chemical compound COC(/C=C/c(ccc(Cl)c1)c1N)=O VHCSJCFEYXNKHF-HWKANZROSA-N 0.000 description 1
- AQQPBEREMDKHGG-GLSGQPPMSA-N COc(cc(/C=C/C(N1C(C2)COC[C@H]1C[C@H]2Nc(cc1)ccc1F)=O)c(N)c1)c1Cl Chemical compound COc(cc(/C=C/C(N1C(C2)COC[C@H]1C[C@H]2Nc(cc1)ccc1F)=O)c(N)c1)c1Cl AQQPBEREMDKHGG-GLSGQPPMSA-N 0.000 description 1
- FQTGKADQSLNZAR-RXMQYKEDSA-N C[C@H](C(OC)=O)NC(Nc(c(Br)c1)cc(Cl)c1OC(F)(F)F)=O Chemical compound C[C@H](C(OC)=O)NC(Nc(c(Br)c1)cc(Cl)c1OC(F)(F)F)=O FQTGKADQSLNZAR-RXMQYKEDSA-N 0.000 description 1
- SRAIDNXIYJWTIG-RUDMXATFSA-N Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(NC(N(CCN1)CC1=O)=O)c1)c1Cl Chemical compound Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(NC(N(CCN1)CC1=O)=O)c1)c1Cl SRAIDNXIYJWTIG-RUDMXATFSA-N 0.000 description 1
- PAGBTVXBVDPORE-NYYWCZLTSA-N Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(NC(NC1CC1)=O)c1)c1Cl Chemical compound Cc(cc(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c(NC(NC1CC1)=O)c1)c1Cl PAGBTVXBVDPORE-NYYWCZLTSA-N 0.000 description 1
- HLXVODXEFZJQBR-FUNVUKJBSA-N Fc(cc1)ccc1NC1C[C@H](CC2)N[C@H]2C1 Chemical compound Fc(cc1)ccc1NC1C[C@H](CC2)N[C@H]2C1 HLXVODXEFZJQBR-FUNVUKJBSA-N 0.000 description 1
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- UKJGNETYFLQDQI-UHFFFAOYSA-N Fc1ccc(CN2C(CCl)COCC2CCl)cc1 Chemical compound Fc1ccc(CN2C(CCl)COCC2CCl)cc1 UKJGNETYFLQDQI-UHFFFAOYSA-N 0.000 description 1
- MVLRXQRLEYZCTJ-ONNFQVAWSA-N NC(Nc1c(/C=C/C(N2CC(CC3)N(Cc(cc4)ccc4F)C3C2)=O)ccc(Cl)c1)=O Chemical compound NC(Nc1c(/C=C/C(N2CC(CC3)N(Cc(cc4)ccc4F)C3C2)=O)ccc(Cl)c1)=O MVLRXQRLEYZCTJ-ONNFQVAWSA-N 0.000 description 1
- IIFVWLUQBAIPMJ-UHFFFAOYSA-N NCc(cc1)ccc1F Chemical compound NCc(cc1)ccc1F IIFVWLUQBAIPMJ-UHFFFAOYSA-N 0.000 description 1
- ZFMMHUQRTGLSLB-OWOJBTEDSA-N Nc(c(/C=C/C(Cl)=O)c1)cc(Cl)c1OC(F)(F)F Chemical compound Nc(c(/C=C/C(Cl)=O)c1)cc(Cl)c1OC(F)(F)F ZFMMHUQRTGLSLB-OWOJBTEDSA-N 0.000 description 1
- UCHBIYXTRRZASR-FPYGCLRLSA-N Nc(c(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c1)cc(Cl)c1OC(F)(F)F Chemical compound Nc(c(/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O)c1)cc(Cl)c1OC(F)(F)F UCHBIYXTRRZASR-FPYGCLRLSA-N 0.000 description 1
- JBPMERIUCWTDTB-AATRIKPKSA-N Nc(c(/C=C/C(O)=O)c1)cc(C2CC2)c1OCC1CC1 Chemical compound Nc(c(/C=C/C(O)=O)c1)cc(C2CC2)c1OCC1CC1 JBPMERIUCWTDTB-AATRIKPKSA-N 0.000 description 1
- LDCDTGUIDNWXCT-UHFFFAOYSA-N Nc(c(Br)c1)cc(Cl)c1-c1cnccn1 Chemical compound Nc(c(Br)c1)cc(Cl)c1-c1cnccn1 LDCDTGUIDNWXCT-UHFFFAOYSA-N 0.000 description 1
- QVWOKCMCWKQVLW-YRNVUSSQSA-N Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1 Chemical compound Nc1c(/C=C/C(N2C3CN(Cc(cc4)ccc4F)CC2CCC3)=O)ccc(Cl)c1 QVWOKCMCWKQVLW-YRNVUSSQSA-N 0.000 description 1
- OFUSIBAPZJAQIZ-ONNFQVAWSA-N Nc1c(/C=C/C(N2CC(CC3)N(Cc(cc4)ccc4F)C3C2)=O)ccc(Cl)c1 Chemical compound Nc1c(/C=C/C(N2CC(CC3)N(Cc(cc4)ccc4F)C3C2)=O)ccc(Cl)c1 OFUSIBAPZJAQIZ-ONNFQVAWSA-N 0.000 description 1
- JYTJEKYOZQRKGM-ONNFQVAWSA-N Nc1cc(Cl)ccc1/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O Chemical compound Nc1cc(Cl)ccc1/C=C/C(N1C2CN(Cc(cc3)ccc3F)CC1CC2)=O JYTJEKYOZQRKGM-ONNFQVAWSA-N 0.000 description 1
- WLHALLKXPAGJAL-FPYGCLRLSA-N O=C(/C=C/c(c(N(C(C1(CC1)N1)=O)C1=O)c1)cc(OC(F)(F)F)c1Cl)N1C2CN(Cc(cc3)ccc3F)CC1CC2 Chemical compound O=C(/C=C/c(c(N(C(C1(CC1)N1)=O)C1=O)c1)cc(OC(F)(F)F)c1Cl)N1C2CN(Cc(cc3)ccc3F)CC1CC2 WLHALLKXPAGJAL-FPYGCLRLSA-N 0.000 description 1
- CLLQAXBEKRTEME-ONNFQVAWSA-N O=C(/C=C/c(ccc(Cl)c1)c1NC(NC1CCOCC1)=O)N1C2CN(Cc(cc3)ccc3F)CC1CC2 Chemical compound O=C(/C=C/c(ccc(Cl)c1)c1NC(NC1CCOCC1)=O)N1C2CN(Cc(cc3)ccc3F)CC1CC2 CLLQAXBEKRTEME-ONNFQVAWSA-N 0.000 description 1
- IASXRVMBAPTGLH-UHFFFAOYSA-N O=C(C1(CC1)NC1=O)N1c(c(Br)c1)cc(Cl)c1OC(F)(F)F Chemical compound O=C(C1(CC1)NC1=O)N1c(c(Br)c1)cc(Cl)c1OC(F)(F)F IASXRVMBAPTGLH-UHFFFAOYSA-N 0.000 description 1
- ZECIYOYICFNUCZ-DUXPYHPUSA-N OC(/C=C/c(ccc(Cl)c1)c1NC(C(F)(F)F)=O)=O Chemical compound OC(/C=C/c(ccc(Cl)c1)c1NC(C(F)(F)F)=O)=O ZECIYOYICFNUCZ-DUXPYHPUSA-N 0.000 description 1
- NFEWTPJZELAVOQ-UHFFFAOYSA-N OCC1N(Cc(cc2)ccc2F)C(CO)COC1 Chemical compound OCC1N(Cc(cc2)ccc2F)C(CO)COC1 NFEWTPJZELAVOQ-UHFFFAOYSA-N 0.000 description 1
- NKQOLGXECGOTQU-UHFFFAOYSA-N [O-][N+](c(c(Br)c1)cc(Cl)c1OCC1CC1)=O Chemical compound [O-][N+](c(c(Br)c1)cc(Cl)c1OCC1CC1)=O NKQOLGXECGOTQU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/14—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Steroid Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0409236.7A GB0409236D0 (en) | 2004-04-26 | 2004-04-26 | Organic compounds |
| PCT/EP2005/004422 WO2005103054A2 (en) | 2004-04-26 | 2005-04-25 | Bridged piperazine and piperidine derivatives as ccri antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007534678A true JP2007534678A (ja) | 2007-11-29 |
| JP2007534678A5 JP2007534678A5 (https=) | 2010-08-05 |
Family
ID=32344398
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007508868A Ceased JP2007534678A (ja) | 2004-04-26 | 2005-04-25 | Ccr−1アンタゴニストとしての化合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20070196270A1 (https=) |
| EP (1) | EP1794164A2 (https=) |
| JP (1) | JP2007534678A (https=) |
| KR (2) | KR100845356B1 (https=) |
| CN (1) | CN101238131A (https=) |
| AR (1) | AR052397A1 (https=) |
| AU (1) | AU2005235724B2 (https=) |
| BR (1) | BRPI0510313A (https=) |
| CA (1) | CA2559917A1 (https=) |
| GB (1) | GB0409236D0 (https=) |
| MX (1) | MXPA06012380A (https=) |
| RU (1) | RU2383548C2 (https=) |
| TW (1) | TW200603805A (https=) |
| WO (1) | WO2005103054A2 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2712211T3 (es) | 2013-06-20 | 2019-05-09 | Bayer Cropscience Ag | Derivados de arilsulfuro y arilsulfóxido acaricidas e insecticidas |
| MX368059B (es) | 2013-07-18 | 2019-09-18 | Novartis Ag | Inhibidores de autotaxina que comprenden un núcleo de anillo heteroaromático de bencil-amida cíclica. |
| CN115286637B (zh) * | 2022-08-11 | 2024-03-22 | 成都金博汇康医药科技有限公司 | 三氮杂桥环化合物及其中间体化合物、制备方法和应用 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998056771A2 (en) * | 1997-06-12 | 1998-12-17 | Schering Aktiengesellschaft | Piperazine derivatives and their use as anti-inflammatory agents |
| WO2001042245A1 (en) * | 1999-12-08 | 2001-06-14 | Bristol-Myers Squibb Company | Neurotrophic bicyclic diamides |
| WO2002032901A2 (en) * | 2000-10-19 | 2002-04-25 | Pfizer Products Inc. | Bridged piperazine derivatives |
| WO2002036581A1 (en) * | 2000-11-06 | 2002-05-10 | Schering Aktiengesellschaft | Radiopharmaceuticals for diagnosing alzheimer's disease |
| WO2004009588A1 (en) * | 2002-07-18 | 2004-01-29 | Pfizer Products Inc. | Bicyclic piperidine derivatives as antagonists of the ccr1 chemokine receptor |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2002100833A1 (ja) * | 2001-06-12 | 2004-09-24 | 住友製薬株式会社 | Rhoキナーゼ阻害剤 |
| GB0224917D0 (en) * | 2002-10-25 | 2002-12-04 | Novartis Ag | Organic compounds |
-
2004
- 2004-04-26 GB GBGB0409236.7A patent/GB0409236D0/en not_active Ceased
-
2005
- 2005-04-25 CA CA002559917A patent/CA2559917A1/en not_active Abandoned
- 2005-04-25 WO PCT/EP2005/004422 patent/WO2005103054A2/en not_active Ceased
- 2005-04-25 CN CNA2005800132391A patent/CN101238131A/zh active Pending
- 2005-04-25 JP JP2007508868A patent/JP2007534678A/ja not_active Ceased
- 2005-04-25 KR KR1020067022181A patent/KR100845356B1/ko not_active Expired - Fee Related
- 2005-04-25 BR BRPI0510313-4A patent/BRPI0510313A/pt not_active IP Right Cessation
- 2005-04-25 EP EP05737794A patent/EP1794164A2/en not_active Withdrawn
- 2005-04-25 RU RU2006141702/04A patent/RU2383548C2/ru not_active IP Right Cessation
- 2005-04-25 AU AU2005235724A patent/AU2005235724B2/en not_active Ceased
- 2005-04-25 MX MXPA06012380A patent/MXPA06012380A/es not_active Application Discontinuation
- 2005-04-25 US US10/599,819 patent/US20070196270A1/en not_active Abandoned
- 2005-04-25 KR KR1020087002184A patent/KR20080015151A/ko not_active Ceased
- 2005-04-25 AR ARP050101623A patent/AR052397A1/es unknown
- 2005-04-25 TW TW094113108A patent/TW200603805A/zh unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998056771A2 (en) * | 1997-06-12 | 1998-12-17 | Schering Aktiengesellschaft | Piperazine derivatives and their use as anti-inflammatory agents |
| WO2001042245A1 (en) * | 1999-12-08 | 2001-06-14 | Bristol-Myers Squibb Company | Neurotrophic bicyclic diamides |
| WO2002032901A2 (en) * | 2000-10-19 | 2002-04-25 | Pfizer Products Inc. | Bridged piperazine derivatives |
| WO2002036581A1 (en) * | 2000-11-06 | 2002-05-10 | Schering Aktiengesellschaft | Radiopharmaceuticals for diagnosing alzheimer's disease |
| WO2004009588A1 (en) * | 2002-07-18 | 2004-01-29 | Pfizer Products Inc. | Bicyclic piperidine derivatives as antagonists of the ccr1 chemokine receptor |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20080015151A (ko) | 2008-02-18 |
| US20070196270A1 (en) | 2007-08-23 |
| GB0409236D0 (en) | 2004-05-26 |
| CN101238131A (zh) | 2008-08-06 |
| KR20070014154A (ko) | 2007-01-31 |
| MXPA06012380A (es) | 2007-01-17 |
| WO2005103054A2 (en) | 2005-11-03 |
| RU2383548C2 (ru) | 2010-03-10 |
| EP1794164A2 (en) | 2007-06-13 |
| AR052397A1 (es) | 2007-03-21 |
| AU2005235724A1 (en) | 2005-11-03 |
| BRPI0510313A (pt) | 2007-10-16 |
| CA2559917A1 (en) | 2005-11-03 |
| AU2005235724B2 (en) | 2008-10-30 |
| RU2006141702A (ru) | 2008-06-10 |
| WO2005103054A3 (en) | 2007-02-08 |
| KR100845356B1 (ko) | 2008-07-09 |
| TW200603805A (en) | 2006-02-01 |
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