JP2010504342A5 - - Google Patents
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- Publication number
- JP2010504342A5 JP2010504342A5 JP2009529306A JP2009529306A JP2010504342A5 JP 2010504342 A5 JP2010504342 A5 JP 2010504342A5 JP 2009529306 A JP2009529306 A JP 2009529306A JP 2009529306 A JP2009529306 A JP 2009529306A JP 2010504342 A5 JP2010504342 A5 JP 2010504342A5
- Authority
- JP
- Japan
- Prior art keywords
- oxo
- dihydro
- isoquinolin
- chloro
- alkyl
- 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.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 140
- 125000003118 aryl group Chemical group 0.000 claims 60
- 125000001072 heteroaryl group Chemical group 0.000 claims 32
- 229910052739 hydrogen Inorganic materials 0.000 claims 26
- 125000000623 heterocyclic group Chemical group 0.000 claims 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 17
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 16
- 125000003545 alkoxy group Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 16
- 229910052736 halogen Inorganic materials 0.000 claims 16
- 150000002367 halogens Chemical class 0.000 claims 16
- 229910052757 nitrogen Inorganic materials 0.000 claims 16
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 14
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 12
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 10
- -1 tetrahydropyran-4-ylmethyl Chemical group 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 9
- 125000003277 amino group Chemical group 0.000 claims 8
- 239000008194 pharmaceutical composition Substances 0.000 claims 8
- 229910052801 chlorine Inorganic materials 0.000 claims 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 6
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 6
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 5
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 229910052731 fluorine Inorganic materials 0.000 claims 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- JEVASONHRDRRRF-UHFFFAOYSA-N 2-chloro-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-4-nitrobenzamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 JEVASONHRDRRRF-UHFFFAOYSA-N 0.000 claims 4
- WHXKGHDWNQPZNP-UHFFFAOYSA-N 4-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)cyclohexane-1-carboxamide Chemical compound C1CC(N)CCC1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 WHXKGHDWNQPZNP-UHFFFAOYSA-N 0.000 claims 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 4
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- 125000005110 aryl thio group Chemical group 0.000 claims 4
- 125000004104 aryloxy group Chemical group 0.000 claims 4
- 125000001475 halogen functional group Chemical group 0.000 claims 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 4
- WMXFMQUBMUSJBJ-UHFFFAOYSA-N n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-1-methylpiperidine-4-carboxamide Chemical compound C1CN(C)CCC1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 WMXFMQUBMUSJBJ-UHFFFAOYSA-N 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 4
- 125000003386 piperidinyl group Chemical group 0.000 claims 4
- 125000004076 pyridyl group Chemical group 0.000 claims 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 4
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims 4
- VARKGNSLBZWGKS-MDOMKXGZSA-N (1R,3S)-3-amino-N-(7-chloro-1-oxo-2H-isoquinolin-6-yl)cyclopentane-1-carboxamide [4-[(7-chloro-1-oxo-2H-isoquinolin-6-yl)carbamoyl]cyclohexyl] acetate Chemical compound ClC1=C(C=C2C=CNC(C2=C1)=O)NC(=O)[C@H]1C[C@H](CC1)N.ClC1=C(C=C2C=CNC(C2=C1)=O)NC(=O)C1CCC(CC1)OC(C)=O VARKGNSLBZWGKS-MDOMKXGZSA-N 0.000 claims 2
- JQLLYNHFEVAHHJ-MNOVXSKESA-N (1r,3s)-3-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)cyclohexane-1-carboxamide Chemical compound C1[C@@H](N)CCC[C@H]1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 JQLLYNHFEVAHHJ-MNOVXSKESA-N 0.000 claims 2
- PQDMNMYSDXMLIL-NEPJUHHUSA-N (1r,3s)-3-amino-n-(7-methoxy-1-oxo-2h-isoquinolin-6-yl)cyclohexane-1-carboxamide Chemical compound COC1=CC(C(NC=C2)=O)=C2C=C1NC(=O)[C@@H]1CCC[C@H](N)C1 PQDMNMYSDXMLIL-NEPJUHHUSA-N 0.000 claims 2
- INIUJLPVWFLHOO-CABZTGNLSA-N (1s,2s)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-methyl-4-oxocyclohexane-1-carboxamide Chemical compound C[C@H]1CC(=O)CC[C@@H]1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 INIUJLPVWFLHOO-CABZTGNLSA-N 0.000 claims 2
- JQLLYNHFEVAHHJ-QWRGUYRKSA-N (1s,3s)-3-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)cyclohexane-1-carboxamide Chemical compound C1[C@@H](N)CCC[C@@H]1C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 JQLLYNHFEVAHHJ-QWRGUYRKSA-N 0.000 claims 2
- QWFCVBMSMZUVFU-NGQZWQHPSA-N (1s,5r)-3-azoniabicyclo[3.1.0]hexane-6-carboxylate Chemical compound C1NC[C@H]2C(C(=O)O)[C@H]21 QWFCVBMSMZUVFU-NGQZWQHPSA-N 0.000 claims 2
- FJWKKOVBOJSOMJ-QGZVFWFLSA-N (2r)-2-(4-chlorophenyl)-2-hydroxy-n-(4-oxo-1h-quinazolin-7-yl)propanamide Chemical compound C1([C@@](O)(C(=O)NC=2C=C3C(C(NC=N3)=O)=CC=2)C)=CC=C(Cl)C=C1 FJWKKOVBOJSOMJ-QGZVFWFLSA-N 0.000 claims 2
- ZHVIWNFGNBYNDX-OAHLLOKOSA-N (2r)-2-amino-2-cyclohexyl-n-(1-oxo-2h-isoquinolin-6-yl)acetamide Chemical compound C1([C@@H](N)C(=O)NC=2C=C3C(C(NC=C3)=O)=CC=2)CCCCC1 ZHVIWNFGNBYNDX-OAHLLOKOSA-N 0.000 claims 2
- MARASEZVJVDXJQ-MRXNPFEDSA-N (2r)-2-amino-2-cyclohexyl-n-(7-methoxy-1-oxo-2h-isoquinolin-6-yl)acetamide Chemical compound C1([C@@H](N)C(=O)NC2=CC3=C(C(NC=C3)=O)C=C2OC)CCCCC1 MARASEZVJVDXJQ-MRXNPFEDSA-N 0.000 claims 2
- KTCLKJWKHZTJLE-LLVKDONJSA-N (2r)-2-amino-3-methyl-n-(4-oxo-1h-quinazolin-7-yl)butanamide Chemical compound N1=CNC(=O)C=2C1=CC(NC(=O)[C@H](N)C(C)C)=CC=2 KTCLKJWKHZTJLE-LLVKDONJSA-N 0.000 claims 2
- NJZMIVUSGDNAHG-OAHLLOKOSA-N (2r)-2-amino-n-(1-oxo-2h-isoquinolin-6-yl)-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C=C3C(C(NC=C3)=O)=CC=2)N)=CC=CC=C1 NJZMIVUSGDNAHG-OAHLLOKOSA-N 0.000 claims 2
- OGWZKLROEMTEBA-CQSZACIVSA-N (2r)-2-amino-n-(4-oxo-1h-quinazolin-7-yl)-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C=C3C(C(NC=N3)=O)=CC=2)N)=CC=CC=C1 OGWZKLROEMTEBA-CQSZACIVSA-N 0.000 claims 2
- XAFGHLJJPKUZKI-CQSZACIVSA-N (2r)-2-amino-n-(4-oxo-1h-quinazolin-7-yl)-3-phenylpropanamide Chemical compound C([C@@H](N)C(=O)NC=1C=C2C(C(NC=N2)=O)=CC=1)C1=CC=CC=C1 XAFGHLJJPKUZKI-CQSZACIVSA-N 0.000 claims 2
- XQWKVQZDJHYNTI-MRXNPFEDSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-(4-methylphenyl)acetamide Chemical compound C1=CC(C)=CC=C1[C@@H](N)C(=O)NC(C(=C1)Cl)=CC2=C1C(=O)NC=C2 XQWKVQZDJHYNTI-MRXNPFEDSA-N 0.000 claims 2
- LZKXNZXRQFFQAH-OAHLLOKOSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)N)=CC=CC=C1 LZKXNZXRQFFQAH-OAHLLOKOSA-N 0.000 claims 2
- FFOBQEHTKMMYOK-OAHLLOKOSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-(4-chlorophenyl)propanamide Chemical compound C([C@@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1=CC=C(Cl)C=C1 FFOBQEHTKMMYOK-OAHLLOKOSA-N 0.000 claims 2
- BHVXQQAOHUXHJX-OAHLLOKOSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-cyclohexylpropanamide Chemical compound C([C@@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1CCCCC1 BHVXQQAOHUXHJX-OAHLLOKOSA-N 0.000 claims 2
- WXRZSOWZRRRJSB-GFCCVEGCSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-methylbutanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@H](N)C(C)C)C(Cl)=C2 WXRZSOWZRRRJSB-GFCCVEGCSA-N 0.000 claims 2
- BRUWZKPRMONCGZ-LJQANCHMSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-naphthalen-1-ylpropanamide Chemical compound C1=CNC(=O)C(C=C2Cl)=C1C=C2NC(=O)[C@H](N)CC1=CC=CC2=CC=CC=C12 BRUWZKPRMONCGZ-LJQANCHMSA-N 0.000 claims 2
- FIYBSFIXYPPGOK-LJQANCHMSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-naphthalen-2-ylpropanamide Chemical compound C1=CNC(=O)C(C=C2Cl)=C1C=C2NC(=O)[C@H](N)CC1=CC=C(C=CC=C2)C2=C1 FIYBSFIXYPPGOK-LJQANCHMSA-N 0.000 claims 2
- MPPLZNXMOACWRV-OAHLLOKOSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-phenylpropanamide Chemical compound C([C@@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1=CC=CC=C1 MPPLZNXMOACWRV-OAHLLOKOSA-N 0.000 claims 2
- CPEUVOVIKQEOHO-CQSZACIVSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-pyridin-4-ylpropanamide Chemical compound C([C@@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1=CC=NC=C1 CPEUVOVIKQEOHO-CQSZACIVSA-N 0.000 claims 2
- DEUSPAYNLHIUSL-GFCCVEGCSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-4,4-dimethylpentanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@H](N)CC(C)(C)C)C(Cl)=C2 DEUSPAYNLHIUSL-GFCCVEGCSA-N 0.000 claims 2
- RADQDLRYXIUSGX-GFCCVEGCSA-N (2r)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-4-methylpentanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@H](N)CC(C)C)C(Cl)=C2 RADQDLRYXIUSGX-GFCCVEGCSA-N 0.000 claims 2
- OZTWJDXASSVZPZ-QGZVFWFLSA-N (2r)-2-methoxy-n-(7-methoxy-1-oxo-2h-isoquinolin-6-yl)-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)OC)OC)=CC=CC=C1 OZTWJDXASSVZPZ-QGZVFWFLSA-N 0.000 claims 2
- GJDXVSJQDCVVJF-SNVBAGLBSA-N (2r)-n-(4-oxo-1h-quinazolin-7-yl)pyrrolidine-2-carboxamide Chemical compound C=1C=C(C(NC=N2)=O)C2=CC=1NC(=O)[C@H]1CCCN1 GJDXVSJQDCVVJF-SNVBAGLBSA-N 0.000 claims 2
- DQXBCWGHRZOBIA-QGZVFWFLSA-N (2r)-n-(6-chloro-4-oxo-1h-quinazolin-7-yl)-2-(4-chlorophenyl)-2-hydroxypropanamide Chemical compound C1([C@@](O)(C(=O)NC=2C(=CC=3C(=O)NC=NC=3C=2)Cl)C)=CC=C(Cl)C=C1 DQXBCWGHRZOBIA-QGZVFWFLSA-N 0.000 claims 2
- PMVOMXDSKUVNOM-OAHLLOKOSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-(2-chlorophenyl)-2-hydroxyacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)O)=CC=CC=C1Cl PMVOMXDSKUVNOM-OAHLLOKOSA-N 0.000 claims 2
- QPXDNPWJKQEBFD-OAHLLOKOSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-(3-chlorophenyl)-2-hydroxyacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)O)=CC=CC(Cl)=C1 QPXDNPWJKQEBFD-OAHLLOKOSA-N 0.000 claims 2
- IFLCAMSZRCEJTF-GOSISDBHSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-(4-chlorophenyl)-2-hydroxypropanamide Chemical compound C1([C@@](O)(C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)C)=CC=C(Cl)C=C1 IFLCAMSZRCEJTF-GOSISDBHSA-N 0.000 claims 2
- BXYBHROBEQFUAY-OAHLLOKOSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-cyclohexyl-2-hydroxyacetamide Chemical compound C1([C@@H](O)C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)CCCCC1 BXYBHROBEQFUAY-OAHLLOKOSA-N 0.000 claims 2
- LUYZNSYWWRRMFY-OAHLLOKOSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-hydroxy-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)O)=CC=CC=C1 LUYZNSYWWRRMFY-OAHLLOKOSA-N 0.000 claims 2
- MDVFBZHBVUQEFG-GOSISDBHSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-hydroxy-2-phenylpropanamide Chemical compound C1([C@@](O)(C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)C)=CC=CC=C1 MDVFBZHBVUQEFG-GOSISDBHSA-N 0.000 claims 2
- LBUGZWJPFXKNGX-GFCCVEGCSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-hydroxy-3-methylbutanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@H](O)C(C)C)C(Cl)=C2 LBUGZWJPFXKNGX-GFCCVEGCSA-N 0.000 claims 2
- ZIZDTBAFVYQRCD-MRXNPFEDSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-methoxy-2-phenylacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)OC)=CC=CC=C1 ZIZDTBAFVYQRCD-MRXNPFEDSA-N 0.000 claims 2
- DXMAQMGWRMJOAX-LLVKDONJSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-phenoxypropanamide Chemical compound O([C@H](C)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1=CC=CC=C1 DXMAQMGWRMJOAX-LLVKDONJSA-N 0.000 claims 2
- NCWXQEQIDGEPAD-GOSISDBHSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-phenyl-2-propan-2-yloxyacetamide Chemical compound C1([C@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)OC(C)C)=CC=CC=C1 NCWXQEQIDGEPAD-GOSISDBHSA-N 0.000 claims 2
- QIXIMQMDBYEQGJ-GFCCVEGCSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)oxolane-2-carboxamide Chemical compound ClC1=CC(C(NC=C2)=O)=C2C=C1NC(=O)[C@H]1CCCO1 QIXIMQMDBYEQGJ-GFCCVEGCSA-N 0.000 claims 2
- CIJSISGZZDYHIK-GFCCVEGCSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)piperidine-2-carboxamide Chemical compound ClC1=CC(C(NC=C2)=O)=C2C=C1NC(=O)[C@H]1CCCCN1 CIJSISGZZDYHIK-GFCCVEGCSA-N 0.000 claims 2
- ASOKPJKABROLOA-LLVKDONJSA-N (2r)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)pyrrolidine-2-carboxamide Chemical compound ClC1=CC(C(NC=C2)=O)=C2C=C1NC(=O)[C@H]1CCCN1 ASOKPJKABROLOA-LLVKDONJSA-N 0.000 claims 2
- MARASEZVJVDXJQ-INIZCTEOSA-N (2s)-2-amino-2-cyclohexyl-n-(7-methoxy-1-oxo-2h-isoquinolin-6-yl)acetamide Chemical compound C1([C@H](N)C(=O)NC2=CC3=C(C(NC=C3)=O)C=C2OC)CCCCC1 MARASEZVJVDXJQ-INIZCTEOSA-N 0.000 claims 2
- XAFGHLJJPKUZKI-AWEZNQCLSA-N (2s)-2-amino-n-(4-oxo-1h-quinazolin-7-yl)-3-phenylpropanamide Chemical compound C([C@H](N)C(=O)NC=1C=C2C(C(NC=N2)=O)=CC=1)C1=CC=CC=C1 XAFGHLJJPKUZKI-AWEZNQCLSA-N 0.000 claims 2
- LEQCZRIIDQNHNS-HNNXBMFYSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-cyclohexylacetamide Chemical compound C1([C@H](N)C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)CCCCC1 LEQCZRIIDQNHNS-HNNXBMFYSA-N 0.000 claims 2
- BHVXQQAOHUXHJX-HNNXBMFYSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-cyclohexylpropanamide Chemical compound C([C@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1CCCCC1 BHVXQQAOHUXHJX-HNNXBMFYSA-N 0.000 claims 2
- WXRZSOWZRRRJSB-LBPRGKRZSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-methylbutanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@@H](N)C(C)C)C(Cl)=C2 WXRZSOWZRRRJSB-LBPRGKRZSA-N 0.000 claims 2
- MPPLZNXMOACWRV-HNNXBMFYSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-3-phenylpropanamide Chemical compound C([C@H](N)C(=O)NC=1C(=CC=2C(=O)NC=CC=2C=1)Cl)C1=CC=CC=C1 MPPLZNXMOACWRV-HNNXBMFYSA-N 0.000 claims 2
- DEUSPAYNLHIUSL-LBPRGKRZSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-4,4-dimethylpentanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@@H](N)CC(C)(C)C)C(Cl)=C2 DEUSPAYNLHIUSL-LBPRGKRZSA-N 0.000 claims 2
- RADQDLRYXIUSGX-LBPRGKRZSA-N (2s)-2-amino-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-4-methylpentanamide Chemical compound C1=CNC(=O)C2=C1C=C(NC(=O)[C@@H](N)CC(C)C)C(Cl)=C2 RADQDLRYXIUSGX-LBPRGKRZSA-N 0.000 claims 2
- OZTWJDXASSVZPZ-KRWDZBQOSA-N (2s)-2-methoxy-n-(7-methoxy-1-oxo-2h-isoquinolin-6-yl)-2-phenylacetamide Chemical compound C1([C@@H](C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)OC)OC)=CC=CC=C1 OZTWJDXASSVZPZ-KRWDZBQOSA-N 0.000 claims 2
- ZDTCHBCAYSXSNH-SFHVURJKSA-N (2s)-n-(7-chloro-1-oxo-2h-isoquinolin-6-yl)-2-cyclohexyl-2-(propan-2-ylamino)acetamide Chemical compound C1([C@H](NC(C)C)C(=O)NC=2C(=CC=3C(=O)NC=CC=3C=2)Cl)CCCCC1 ZDTCHBCAYSXSNH-SFHVURJKSA-N 0.000 claims 2
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| EP2066619A2 (en) * | 2006-11-02 | 2009-06-10 | Arete Therapeutics, INC. | Soluble epoxide hydrolase inhibitors |
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| US8455514B2 (en) | 2008-01-17 | 2013-06-04 | Aerie Pharmaceuticals, Inc. | 6-and 7-amino isoquinoline compounds and methods for making and using the same |
| ES2434121T3 (es) * | 2008-06-24 | 2013-12-13 | Sanofi | Derivados de isoquinolina e isoquinolinona bi- y policíclicos sustituidos como inhibidores de rho cinasa |
| US8450344B2 (en) | 2008-07-25 | 2013-05-28 | Aerie Pharmaceuticals, Inc. | Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds |
| WO2010021882A2 (en) | 2008-08-19 | 2010-02-25 | Janssen Pharmaceutica Nv | Cold menthol receptor antagonists |
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| FR2956816B1 (fr) | 2010-03-01 | 2012-05-18 | Univ Joseph Fourier | Utilisation de quinolones pour la preparation de medicaments, nouvelles quinolones et leur procede de synthese |
| US9079880B2 (en) | 2010-07-07 | 2015-07-14 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
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| CN103864684A (zh) * | 2012-12-07 | 2014-06-18 | 天津科技大学 | 一种新颖的3,4-二氢-1(2h)异喹啉类衍生物的合成与抗肿瘤药物的应用 |
| TW201443023A (zh) | 2013-01-18 | 2014-11-16 | 必治妥美雅史谷比公司 | 作爲ｒｏｃｋ抑制劑之酞□酮及異喹啉酮 |
| PT3811943T (pt) | 2013-03-15 | 2023-03-15 | Aerie Pharmaceuticals Inc | Composto para uso no tratamento de distúrbios oculares |
| US9902702B2 (en) | 2014-07-15 | 2018-02-27 | Bristol-Myers Squibb Company | Spirocycloheptanes as inhibitors of rock |
| JP6633618B2 (ja) | 2014-08-21 | 2020-01-22 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | 強力なｒｏｃｋ阻害剤としてのタイドバックのベンズアミド誘導体 |
| US10465188B2 (en) | 2014-08-22 | 2019-11-05 | Auckland Uniservices Limited | Channel modulators |
| US9643927B1 (en) | 2015-11-17 | 2017-05-09 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| US10550087B2 (en) | 2015-11-17 | 2020-02-04 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| UY37073A (es) | 2016-01-13 | 2017-07-31 | Bristol-Myers Squibb Company Una Corporación Del Estado De Delaware | Salicilamidas espiroheptanos y compuestos relacionados como inhibidores de rock, y las composiciones que los contienen |
| JP7155102B2 (ja) | 2016-07-07 | 2022-10-18 | ブリストル－マイヤーズ スクイブ カンパニー | Ｒｏｃｋ阻害剤としてのスピロ縮合環尿素 |
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| JP2020515583A (ja) | 2017-03-31 | 2020-05-28 | アエリエ ファーマシューティカルズ インコーポレイテッド | アリールシクロプロピル−アミノ−イソキノリニルアミド化合物 |
| EP3652164B1 (en) | 2017-07-12 | 2023-06-21 | Bristol-Myers Squibb Company | Phenylacetamides as inhibitors of rock |
| WO2019014304A1 (en) | 2017-07-12 | 2019-01-17 | Bristol-Myers Squibb Company | SPIROHEPTANYL HYDANTOIDS AS ROCK INHIBITORS |
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-
2007
- 2007-09-13 EP EP07814835.0A patent/EP2068878B1/en not_active Not-in-force
- 2007-09-13 EP EP12003567A patent/EP2526948A1/en not_active Withdrawn
- 2007-09-13 WO PCT/US2007/078343 patent/WO2008036540A2/en not_active Ceased
- 2007-09-13 ES ES07814835T patent/ES2729424T3/es active Active
- 2007-09-13 CA CA2664335A patent/CA2664335C/en active Active
- 2007-09-13 JP JP2009529306A patent/JP5235887B2/ja not_active Expired - Fee Related
- 2007-09-14 CL CL200702686A patent/CL2007002686A1/es unknown
- 2007-09-18 US US11/856,740 patent/US8809326B2/en active Active
- 2007-09-19 TW TW096134934A patent/TW200819133A/zh unknown
- 2007-09-19 AR ARP070104139A patent/AR062900A1/es not_active Application Discontinuation
-
2014
- 2014-08-18 US US14/461,597 patent/US20140357652A1/en not_active Abandoned
-
2015
- 2015-06-30 US US14/754,787 patent/US20150297581A1/en not_active Abandoned
-
2016
- 2016-04-29 US US15/142,448 patent/US20160243102A1/en not_active Abandoned
-
2017
- 2017-12-29 US US15/858,995 patent/US10624882B2/en active Active
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