JP2009514980A5 - - Google Patents
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- JP2009514980A5 JP2009514980A5 JP2008540217A JP2008540217A JP2009514980A5 JP 2009514980 A5 JP2009514980 A5 JP 2009514980A5 JP 2008540217 A JP2008540217 A JP 2008540217A JP 2008540217 A JP2008540217 A JP 2008540217A JP 2009514980 A5 JP2009514980 A5 JP 2009514980A5
- Authority
- JP
- Japan
- Prior art keywords
- diazabicyclo
- carbon atoms
- ylcarbonyl
- alkyl
- cycloalkyl
- 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.)
- Pending
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- 125000004432 carbon atom Chemical group C* 0.000 claims 106
- 229910005965 SO 2 Inorganic materials 0.000 claims 77
- 125000000217 alkyl group Chemical group 0.000 claims 52
- 150000001875 compounds Chemical class 0.000 claims 44
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 42
- 229910052794 bromium Inorganic materials 0.000 claims 39
- 229910052801 chlorine Inorganic materials 0.000 claims 39
- 229910052731 fluorine Inorganic materials 0.000 claims 39
- 229910052740 iodine Inorganic materials 0.000 claims 39
- -1 Cyano, Hydroxy Chemical group 0.000 claims 36
- 125000003545 alkoxy group Chemical group 0.000 claims 20
- 125000004663 dialkyl amino group Chemical group 0.000 claims 19
- 229910052736 halogen Inorganic materials 0.000 claims 19
- 150000002367 halogens Chemical class 0.000 claims 19
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 claims 13
- 125000004043 oxo group Chemical group O=* 0.000 claims 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 12
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 12
- 239000012453 solvate Substances 0.000 claims 11
- 150000001350 alkyl halides Chemical class 0.000 claims 10
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 9
- 239000012458 free base Substances 0.000 claims 9
- 229920006395 saturated elastomer Polymers 0.000 claims 8
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 150000001204 N-oxides Chemical class 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- CDQFTKBQYMHUKI-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-morpholin-4-yl-1h-indazol-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2N1CCOCC1 CDQFTKBQYMHUKI-UHFFFAOYSA-N 0.000 claims 3
- PGHTXZVHWVYKII-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-pyrrolidin-1-yl-1h-indazol-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2N1CCCC1 PGHTXZVHWVYKII-UHFFFAOYSA-N 0.000 claims 3
- XDLAJOHFJBFDBR-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-thiomorpholin-4-yl-1h-indazol-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2N1CCSCC1 XDLAJOHFJBFDBR-UHFFFAOYSA-N 0.000 claims 3
- YANZINWIXKAPBJ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(1,4-oxazepan-4-yl)-1h-indazol-3-yl]methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2N1CCCOCC1 YANZINWIXKAPBJ-UHFFFAOYSA-N 0.000 claims 3
- SDGFKGORCOJBTQ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(3-methoxypyrrolidin-1-yl)-1h-indazol-3-yl]methanone Chemical compound C1C(OC)CCN1C1=CC=C(C(=NN2)C(=O)N3C4CCN(CC4)CC3)C2=C1 SDGFKGORCOJBTQ-UHFFFAOYSA-N 0.000 claims 3
- BDJQBBPBWIKLPI-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(4-methyl-1,4-diazepan-1-yl)-1h-indazol-3-yl]methanone Chemical compound C1CN(C)CCCN1C1=CC=C(C(=NN2)C(=O)N3C4CCN(CC4)CC3)C2=C1 BDJQBBPBWIKLPI-UHFFFAOYSA-N 0.000 claims 3
- CZUBGJIEWJEYLG-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(4-methylpiperazin-1-yl)-1h-indazol-3-yl]methanone Chemical compound C1CN(C)CCN1C1=CC=C(C(=NN2)C(=O)N3C4CCN(CC4)CC3)C2=C1 CZUBGJIEWJEYLG-UHFFFAOYSA-N 0.000 claims 3
- KGLWXAZNCVRDSK-UHFFFAOYSA-N 1-[3-(1,4-diazabicyclo[3.2.2]nonane-4-carbonyl)-1h-indazol-6-yl]-3-propylimidazolidin-2-one Chemical compound O=C1N(CCC)CCN1C1=CC=C(C(=NN2)C(=O)N3C4CCN(CC4)CC3)C2=C1 KGLWXAZNCVRDSK-UHFFFAOYSA-N 0.000 claims 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 3
- FOPHMSZZCWXLSE-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-pyrrolidin-1-yl-1,2-benzothiazol-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NSC1=CC=2N1CCCC1 FOPHMSZZCWXLSE-UHFFFAOYSA-N 0.000 claims 2
- IVDYMQJQBOZDLZ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[5-(oxan-3-yloxy)-1h-indazol-3-yl]methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=C2)=NNC1=CC=C2OC1CCCOC1 IVDYMQJQBOZDLZ-UHFFFAOYSA-N 0.000 claims 2
- VKKAITWTUBGNFK-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[5-[4-(2,2,2-trifluoroethyl)-1,4-diazepan-1-yl]-1h-indazol-3-yl]methanone Chemical compound C1CN(CC(F)(F)F)CCCN1C1=CC=C(NN=C2C(=O)N3C4CCN(CC4)CC3)C2=C1 VKKAITWTUBGNFK-UHFFFAOYSA-N 0.000 claims 2
- IOUAQUSNNJXIFQ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(1-methyl-4,5-dihydroimidazol-2-yl)-1h-indazol-3-yl]methanone Chemical compound CN1CCN=C1C1=CC=C(C(=NN2)C(=O)N3C4CCN(CC4)CC3)C2=C1 IOUAQUSNNJXIFQ-UHFFFAOYSA-N 0.000 claims 2
- MODJKVLWMQXWNQ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(1-methylpyrrolidin-3-yl)oxy-1,2-benzothiazol-3-yl]methanone Chemical compound C1N(C)CCC1OC1=CC=C(C(=NS2)C(=O)N3C4CCN(CC4)CC3)C2=C1 MODJKVLWMQXWNQ-UHFFFAOYSA-N 0.000 claims 2
- XEKACKLBOIHKMY-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(4-methyl-1,4-diazepan-1-yl)-1,2-benzothiazol-3-yl]methanone Chemical compound C1CN(C)CCCN1C1=CC=C(C(=NS2)C(=O)N3C4CCN(CC4)CC3)C2=C1 XEKACKLBOIHKMY-UHFFFAOYSA-N 0.000 claims 2
- OTCDNWYAYRJYFI-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(4-methylpiperazin-1-yl)-1,2-benzothiazol-3-yl]methanone Chemical compound C1CN(C)CCN1C1=CC=C(C(=NS2)C(=O)N3C4CCN(CC4)CC3)C2=C1 OTCDNWYAYRJYFI-UHFFFAOYSA-N 0.000 claims 2
- OPBMDLXCLRKRON-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(5-methyl-2,5-diazabicyclo[2.2.2]octan-2-yl)-1,2-benzothiazol-3-yl]methanone Chemical compound CN1CC2CCC1CN2C(C=C1SN=2)=CC=C1C=2C(=O)N1CCN2CCC1CC2 OPBMDLXCLRKRON-UHFFFAOYSA-N 0.000 claims 2
- BHNLNIXBMVMWBJ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(oxan-3-yloxy)-1h-indazol-3-yl]methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2OC1CCCOC1 BHNLNIXBMVMWBJ-UHFFFAOYSA-N 0.000 claims 2
- UKVXPHCQATZHCH-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-(oxan-4-yloxy)-1h-indazol-3-yl]methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2OC1CCOCC1 UKVXPHCQATZHCH-UHFFFAOYSA-N 0.000 claims 2
- YYMONJYIJHVWEZ-IAGOWNOFSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-[(1r,4r)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazol-3-yl]methanone Chemical compound C([C@@]1(N(C[C@@]2([H])C1)C)[H])N2C(C=C1SN=2)=CC=C1C=2C(=O)N1CCN2CCC1CC2 YYMONJYIJHVWEZ-IAGOWNOFSA-N 0.000 claims 2
- YYMONJYIJHVWEZ-IRXDYDNUSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazol-3-yl]methanone Chemical compound C([C@]1(N(C[C@]2([H])C1)C)[H])N2C(C=C1SN=2)=CC=C1C=2C(=O)N1CCN2CCC1CC2 YYMONJYIJHVWEZ-IRXDYDNUSA-N 0.000 claims 2
- DXGBMYLWFPPWLO-MRXNPFEDSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-[(3r)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazol-3-yl]methanone Chemical compound C1[C@H](OC)CCN1C1=CC=C(C(=NS2)C(=O)N3C4CCN(CC4)CC3)C2=C1 DXGBMYLWFPPWLO-MRXNPFEDSA-N 0.000 claims 2
- DXGBMYLWFPPWLO-INIZCTEOSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-[6-[(3s)-3-methoxypyrrolidin-1-yl]-1,2-benzothiazol-3-yl]methanone Chemical compound C1[C@@H](OC)CCN1C1=CC=C(C(=NS2)C(=O)N3C4CCN(CC4)CC3)C2=C1 DXGBMYLWFPPWLO-INIZCTEOSA-N 0.000 claims 2
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 101100349077 Caenorhabditis elegans nrf-6 gene Proteins 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- HPELPVSEHNCJLX-UHFFFAOYSA-N [6-(3,4,6,7,8,8a-hexahydro-1h-pyrrolo[1,2-a]pyrazin-2-yl)-1,2-benzothiazol-3-yl]-(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone Chemical compound N=1SC2=CC(N3CC4CCCN4CC3)=CC=C2C=1C(=O)N1CCN2CCC1CC2 HPELPVSEHNCJLX-UHFFFAOYSA-N 0.000 claims 2
- AZIYSLGXZWNCRO-OALUTQOASA-N [6-[(1s,4s)-5-cyclopropyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazol-3-yl]-(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone Chemical compound C([C@]1(N(C=2C=C3SN=C(C3=CC=2)C(=O)N2C3CCN(CC3)CC2)C[C@@]2(C1)[H])[H])N2C1CC1 AZIYSLGXZWNCRO-OALUTQOASA-N 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000005110 aryl thio group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 2
- 125000005959 diazepanyl group Chemical group 0.000 claims 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- 125000002632 imidazolidinyl group Chemical group 0.000 claims 2
- 125000004193 piperazinyl group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- LNPMTXRDMQWIPO-OALUTQOASA-N tert-butyl (1s,4s)-5-[3-(1,4-diazabicyclo[3.2.2]nonane-4-carbonyl)-1,2-benzothiazol-6-yl]-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate Chemical compound C([C@]1(N(C[C@]2([H])C1)C(=O)OC(C)(C)C)[H])N2C(C=C1SN=2)=CC=C1C=2C(=O)N1CCN2CCC1CC2 LNPMTXRDMQWIPO-OALUTQOASA-N 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- YRXUTSNTOGXCAG-UHFFFAOYSA-N 1,2-benzothiazol-3-yl(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone Chemical compound N=1SC2=CC=CC=C2C=1C(=O)N1CCN2CCC1CC2 YRXUTSNTOGXCAG-UHFFFAOYSA-N 0.000 claims 1
- FZSKECBLOWFYPD-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(1-ethyl-6-methoxyindazol-3-yl)methanone Chemical compound C12=CC=C(OC)C=C2N(CC)N=C1C(=O)N1CCN2CCC1CC2 FZSKECBLOWFYPD-UHFFFAOYSA-N 0.000 claims 1
- JOQVMBXCUQJRSB-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-phenyl-2h-pyrazolo[3,4-b]pyridin-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=NC=2C1=CC=CC=C1 JOQVMBXCUQJRSB-UHFFFAOYSA-N 0.000 claims 1
- CHVCZOHUBWQHTK-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(6-phenylmethoxy-1h-indazol-3-yl)methanone Chemical compound C1CN(CC2)CCC2N1C(=O)C(C1=CC=2)=NNC1=CC=2OCC1=CC=CC=C1 CHVCZOHUBWQHTK-UHFFFAOYSA-N 0.000 claims 1
- VXAYFZPZFVZCPZ-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonan-4-yl-(7-fluoro-6-methoxy-1,2-benzothiazol-3-yl)methanone Chemical compound N=1SC2=C(F)C(OC)=CC=C2C=1C(=O)N1CCN2CCC1CC2 VXAYFZPZFVZCPZ-UHFFFAOYSA-N 0.000 claims 1
- LLSRLLPHUVVLQJ-UHFFFAOYSA-N 1-cycloheptyldiazepane Chemical group C1CCCCCC1N1NCCCCC1 LLSRLLPHUVVLQJ-UHFFFAOYSA-N 0.000 claims 1
- PPNCOQHHSGMKGI-UHFFFAOYSA-N 1-cyclononyldiazonane Chemical group C1CCCCCCCC1N1NCCCCCCC1 PPNCOQHHSGMKGI-UHFFFAOYSA-N 0.000 claims 1
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical group C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 claims 1
- 229910014033 C-OH Inorganic materials 0.000 claims 1
- 229910014570 C—OH Inorganic materials 0.000 claims 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 claims 1
- DOGJICDABWIVPC-BBRMVZONSA-N [6-[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazol-3-yl]-(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2C(C=C1SN=2)=CC=C1C=2C(=O)N1CCN2CCC1CC2 DOGJICDABWIVPC-BBRMVZONSA-N 0.000 claims 1
- OXDKBEYNLGGKKV-PMACEKPBSA-N [6-[(1s,4s)-5-(cyclopropylmethyl)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1,2-benzothiazol-3-yl]-(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone Chemical compound C([C@]1(N(C=2C=C3SN=C(C3=CC=2)C(=O)N2C3CCN(CC3)CC2)C[C@@]2(C1)[H])[H])N2CC1CC1 OXDKBEYNLGGKKV-PMACEKPBSA-N 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 125000002636 imidazolinyl group Chemical group 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 125000005961 oxazepanyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73476105P | 2005-11-09 | 2005-11-09 | |
| PCT/US2006/043818 WO2007056582A1 (en) | 2005-11-09 | 2006-11-09 | 1 h-indazoles, benzothiazoles, 1,2-benzoisoxazoles, 1,2-benzoisothiazoles, and chromones and preparation and uses thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009514980A JP2009514980A (ja) | 2009-04-09 |
| JP2009514980A5 true JP2009514980A5 (enExample) | 2009-11-26 |
Family
ID=37745197
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008540217A Pending JP2009514980A (ja) | 2005-11-09 | 2006-11-09 | １ｈ−インダゾール類、ベンゾチアゾール類、１，２−ベンゾイソオキサゾール類、１，２−ベンゾイソチアゾール類、および／クロモン類と、それらの製造と用途 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7932248B2 (enExample) |
| EP (1) | EP1963332A1 (enExample) |
| JP (1) | JP2009514980A (enExample) |
| KR (1) | KR20080067339A (enExample) |
| CN (1) | CN101316849A (enExample) |
| AU (1) | AU2006311422A1 (enExample) |
| BR (1) | BRPI0619672A2 (enExample) |
| CA (1) | CA2627089A1 (enExample) |
| IL (1) | IL190874A0 (enExample) |
| WO (1) | WO2007056582A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20070015607A (ko) * | 2004-05-07 | 2007-02-05 | 메모리 파마슈티칼스 코포레이션 | 1ｈ-인다졸, 벤조티아졸, 1,2-벤조이속사졸,1,2-벤조이소티아졸, 및 크로몬 및 그의 제조법 및 용도 |
| PE20061119A1 (es) | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
| FR2889526B1 (fr) | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
| WO2009055437A2 (en) * | 2007-10-22 | 2009-04-30 | Memory Pharmaceuticals Corporation | (1,4-diaza-bicyclo[3.2.2]non-6-en-4-yl)-heterocyclyl-methanone ligands for nicotinic acetylcholine receptors, useful for the treatment of disease |
| JO3250B1 (ar) | 2009-09-22 | 2018-09-16 | Novartis Ag | إستعمال منشطات مستقبل نيكوتينيك أسيتيل كولين ألفا 7 |
| CU24152B1 (es) | 2010-12-20 | 2016-02-29 | Irm Llc | 1,2 oxazol-8-azabiciclo[3,2,1]octano 8 il como moduladores de fxr |
| EP2548870A1 (en) * | 2011-07-20 | 2013-01-23 | Cytec Technology Corp. | Process for the Synthesis of Cyclic Alkylene Ureas |
| EP2548869A1 (en) * | 2011-07-20 | 2013-01-23 | Cytec Technology Corp. | Process for the Synthesis of N-substituted Cyclic Alkylene Ureas |
| US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| US9394285B2 (en) | 2013-03-15 | 2016-07-19 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
| CN106279119B (zh) * | 2015-05-27 | 2020-06-16 | 上海海和药物研究开发有限公司 | 一种新型激酶抑制剂的制备及其应用 |
| CN110494136A (zh) * | 2017-01-10 | 2019-11-22 | 瑞士苏黎世联邦理工学院 | 细胞保护性化合物及其用途 |
| US20240051939A1 (en) * | 2020-12-08 | 2024-02-15 | Disarm Therapeutics, Inc. | Benzopyrazole inhibitors of sarm1 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0202465D0 (sv) * | 2002-08-14 | 2002-08-14 | Astrazeneca Ab | New compounds |
| CA2499128C (en) * | 2002-09-25 | 2012-07-31 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, and benzoisothiazoles, and preparation and uses thereof |
| US7456171B2 (en) * | 2002-10-08 | 2008-11-25 | Sanofi-Aventis | 1,4-Diazabicyclo[3.2.2]nonanecarboxamide derivatives, preparation and therapeutic use thereof |
| FR2845388B1 (fr) * | 2002-10-08 | 2004-11-12 | Sanofi Synthelabo | Derives de 1,4-diazabicyclo[3.2.2]nonanecarboxamides, leur preparation et leur application en therapeutique |
| US7396833B2 (en) | 2003-12-22 | 2008-07-08 | Memory Pharmaceuticals Corporation | Indoles, 1H-indazoles, 1,2-benzisoxazoles, and 1,2-benzisothiazoles, and preparation and uses thereof |
| CN103724343A (zh) * | 2004-03-25 | 2014-04-16 | 记忆药物公司 | 吲唑、苯并噻唑、苯并异噻唑、苯并异噁唑及其制备和用途 |
-
2006
- 2006-11-09 CA CA002627089A patent/CA2627089A1/en not_active Abandoned
- 2006-11-09 JP JP2008540217A patent/JP2009514980A/ja active Pending
- 2006-11-09 BR BRPI0619672-1A patent/BRPI0619672A2/pt not_active IP Right Cessation
- 2006-11-09 US US11/594,993 patent/US7932248B2/en not_active Expired - Fee Related
- 2006-11-09 EP EP06837344A patent/EP1963332A1/en not_active Withdrawn
- 2006-11-09 KR KR1020087011073A patent/KR20080067339A/ko not_active Ceased
- 2006-11-09 AU AU2006311422A patent/AU2006311422A1/en not_active Abandoned
- 2006-11-09 WO PCT/US2006/043818 patent/WO2007056582A1/en not_active Ceased
- 2006-11-09 CN CNA2006800420321A patent/CN101316849A/zh active Pending
-
2008
- 2008-04-15 IL IL190874A patent/IL190874A0/en unknown
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