JP2012514601A5 - - Google Patents
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- JP2012514601A5 JP2012514601A5 JP2011544638A JP2011544638A JP2012514601A5 JP 2012514601 A5 JP2012514601 A5 JP 2012514601A5 JP 2011544638 A JP2011544638 A JP 2011544638A JP 2011544638 A JP2011544638 A JP 2011544638A JP 2012514601 A5 JP2012514601 A5 JP 2012514601A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrimido
- diazepine
- methyl
- methoxy
- phenylamino
- 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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- -1 carbocycle Chemical group 0.000 claims 38
- 125000000217 alkyl group Chemical group 0.000 claims 34
- 125000003118 aryl group Chemical group 0.000 claims 27
- 229910052739 hydrogen Inorganic materials 0.000 claims 27
- 239000001257 hydrogen Substances 0.000 claims 27
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 21
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- 125000000623 heterocyclic group Chemical group 0.000 claims 17
- 125000000547 substituted alkyl group Chemical group 0.000 claims 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims 12
- 125000003342 alkenyl group Chemical group 0.000 claims 11
- 150000002148 esters Chemical class 0.000 claims 9
- 239000000651 prodrug Substances 0.000 claims 9
- 229940002612 prodrug Drugs 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 7
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- PKVNVXXWANAAFP-UHFFFAOYSA-N 1,7-dihydro-1,4-diazepin-6-one Chemical compound O=C1CNC=CN=C1 PKVNVXXWANAAFP-UHFFFAOYSA-N 0.000 claims 3
- AZQDLBJZOAHSAZ-UHFFFAOYSA-N 1,7-dihydrodiazepin-6-one Chemical compound O=C1CNN=CC=C1 AZQDLBJZOAHSAZ-UHFFFAOYSA-N 0.000 claims 3
- 101000950687 Homo sapiens Mitogen-activated protein kinase 7 Proteins 0.000 claims 3
- 102100037805 Mitogen-activated protein kinase 7 Human genes 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- BUBBBFSEOYHUQA-UHFFFAOYSA-N 2,5-dihydrooxazepin-6-one Chemical compound O1NC=CCC(C1)=O BUBBBFSEOYHUQA-UHFFFAOYSA-N 0.000 claims 2
- VVPYTOVXFOGRIN-UHFFFAOYSA-N 2-[2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N(CC1)CCC1N1CCN(C)CC1 VVPYTOVXFOGRIN-UHFFFAOYSA-N 0.000 claims 2
- LZNDHLKMOBVBFV-UHFFFAOYSA-N 4-[(2-cyclopentyl-9-methyl-8-oxo-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-13-yl)amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C2C(CCC2)N2C3CCCC3)C2=N1 LZNDHLKMOBVBFV-UHFFFAOYSA-N 0.000 claims 2
- 101100268648 Mus musculus Abl1 gene Proteins 0.000 claims 2
- QAPAJIZPZGWAND-UHFFFAOYSA-N XMD8-92 Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OCC)=CC=1N1CCC(O)CC1 QAPAJIZPZGWAND-UHFFFAOYSA-N 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- KPPVNWGJXFMGAM-UUILKARUSA-N (e)-2-methyl-1-(6-methyl-3,4-dihydro-2h-quinolin-1-yl)but-2-en-1-one Chemical compound CC1=CC=C2N(C(=O)C(/C)=C/C)CCCC2=C1 KPPVNWGJXFMGAM-UUILKARUSA-N 0.000 claims 1
- NFNBVXVXMQZSGB-UHFFFAOYSA-N 11-cyclopentyl-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5-methylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound COC1=CC(N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C1=CC=CC=C1N2C1CCCC1 NFNBVXVXMQZSGB-UHFFFAOYSA-N 0.000 claims 1
- JGVXSQJYBQAPAE-UHFFFAOYSA-N 11-ethyl-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5-methylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound N1=C2N(CC)C3=CC=CC=C3C(=O)N(C)C2=CN=C1NC(C(=C1)OC)=CC=C1N1CCN(C)CC1 JGVXSQJYBQAPAE-UHFFFAOYSA-N 0.000 claims 1
- ASAFHHFHFUCJHM-UHFFFAOYSA-N 11-methyl-2-[4-(4-methylpiperazin-1-yl)-2-propan-2-yloxyanilino]-5h-pyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)NC3=CN=2)C(OC(C)C)=CC=1N1CCN(C)CC1 ASAFHHFHFUCJHM-UHFFFAOYSA-N 0.000 claims 1
- LHBAORXBTTWPDF-UHFFFAOYSA-N 2-[2-ethoxy-4-(4-hydroxypiperidin-1-yl)anilino]-5-methyl-9-phenyl-7,8-dihydropyrimido[4,5-b][1,4]diazepin-6-one Chemical compound CCOC1=CC(N2CCC(O)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)CCN2C1=CC=CC=C1 LHBAORXBTTWPDF-UHFFFAOYSA-N 0.000 claims 1
- DDTPGANIPBKTNU-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methyl-1-piperazinyl)anilino]-5,11-dimethyl-6-pyrimido[4,5-b][1,4]benzodiazepinone Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 DDTPGANIPBKTNU-UHFFFAOYSA-N 0.000 claims 1
- KXCGZEPWZFXPSC-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-4,11-dimethyl-5h-pyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)NC3=C(C)N=2)C(OC)=CC=1N1CCN(C)CC1 KXCGZEPWZFXPSC-UHFFFAOYSA-N 0.000 claims 1
- OXTSNXXVWGKOMB-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-4,5,11-trimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=C(C)N=2)C(OC)=CC=1N1CCN(C)CC1 OXTSNXXVWGKOMB-UHFFFAOYSA-N 0.000 claims 1
- WBPCKVJWZORAAO-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5,11-dihydropyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3NC4=CC=CC=C4C(=O)NC3=CN=2)C(OC)=CC=1N1CCN(C)CC1 WBPCKVJWZORAAO-UHFFFAOYSA-N 0.000 claims 1
- NYHLZQOMTUZDHV-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5,8,11-trimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=C(C)C=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 NYHLZQOMTUZDHV-UHFFFAOYSA-N 0.000 claims 1
- YYTFTZONXCQXLW-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5-methyl-11-propan-2-ylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C(C)C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 YYTFTZONXCQXLW-UHFFFAOYSA-N 0.000 claims 1
- GTCWEOILNAZCDT-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5-methyl-11h-pyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3NC4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 GTCWEOILNAZCDT-UHFFFAOYSA-N 0.000 claims 1
- NTRCYAXJQIZACU-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5-methylpyrimido[4,5-b][1,4]benzothiazepin-6-one Chemical compound C=1C=C(NC=2N=C3SC4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 NTRCYAXJQIZACU-UHFFFAOYSA-N 0.000 claims 1
- OGHDOVJGVKNHRQ-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5h-pyrimido[4,5-b][1,4]benzothiazepin-6-one Chemical compound C=1C=C(NC=2N=C3SC4=CC=CC=C4C(=O)NC3=CN=2)C(OC)=CC=1N1CCN(C)CC1 OGHDOVJGVKNHRQ-UHFFFAOYSA-N 0.000 claims 1
- KBULREVCYROFNX-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-8,11-dimethyl-5h-pyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=C(C)C=C4C(=O)NC3=CN=2)C(OC)=CC=1N1CCN(C)CC1 KBULREVCYROFNX-UHFFFAOYSA-N 0.000 claims 1
- HQHQZEUABJAAMZ-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-9-phenyl-7,8-dihydro-5h-pyrimido[4,5-b][1,4]diazepin-6-one Chemical compound COC1=CC(N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1NC(=O)CCN2C1=CC=CC=C1 HQHQZEUABJAAMZ-UHFFFAOYSA-N 0.000 claims 1
- UDMGPKXTQNCFIO-UHFFFAOYSA-N 2-[2-methoxy-4-(4-methylpiperazine-1-carbonyl)anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1C(=O)N1CCN(C)CC1 UDMGPKXTQNCFIO-UHFFFAOYSA-N 0.000 claims 1
- XYKSVLLNDQRZDK-UHFFFAOYSA-N 2-[2-methoxy-5-[4-(4-methylpiperazin-1-yl)piperidine-1-carbonyl]anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C1=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=C1C(=O)N(CC1)CCC1N1CCN(C)CC1 XYKSVLLNDQRZDK-UHFFFAOYSA-N 0.000 claims 1
- YSFFGUHMDPYPAW-UHFFFAOYSA-N 2-[4-(4-hydroxypiperidin-1-yl)-2-methoxyanilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCC(O)CC1 YSFFGUHMDPYPAW-UHFFFAOYSA-N 0.000 claims 1
- NPRYKZQCTXZUKH-UHFFFAOYSA-N 2-[4-(4-hydroxypiperidin-1-yl)-2-propan-2-yloxyanilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC(C)C)=CC=1N1CCC(O)CC1 NPRYKZQCTXZUKH-UHFFFAOYSA-N 0.000 claims 1
- NGXGUOYOCNOKJO-UHFFFAOYSA-N 2-[4-(4-hydroxypiperidin-1-yl)-2-propan-2-yloxyanilino]-5-methyl-9-phenyl-7,8-dihydropyrimido[4,5-b][1,4]diazepin-6-one Chemical compound CC(C)OC1=CC(N2CCC(O)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)CCN2C1=CC=CC=C1 NGXGUOYOCNOKJO-UHFFFAOYSA-N 0.000 claims 1
- RUSIEYRQPZZDCO-UHFFFAOYSA-N 2-[4-[4-(2-hydroxyethyl)piperazine-1-carbonyl]-2-methoxyanilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1C(=O)N1CCN(CCO)CC1 RUSIEYRQPZZDCO-UHFFFAOYSA-N 0.000 claims 1
- YMOOMBLIPWGVAG-UHFFFAOYSA-N 2-[[5-(4-hydroxypiperidin-1-yl)pyridin-2-yl]amino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound N1=C2N(C)C3=CC=CC=C3C(=O)N(C)C2=CN=C1NC(N=C1)=CC=C1N1CCC(O)CC1 YMOOMBLIPWGVAG-UHFFFAOYSA-N 0.000 claims 1
- FMJVGPKPZYQCHQ-UHFFFAOYSA-N 2-cyclopentyl-13-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-9-methyl-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-8-one Chemical compound COC1=CC(N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C1CCCC1N2C1CCCC1 FMJVGPKPZYQCHQ-UHFFFAOYSA-N 0.000 claims 1
- FWCFYOYWYWAYRZ-UHFFFAOYSA-N 2-cyclopentyl-13-[2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]anilino]-9-methyl-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-8-one Chemical compound COC1=CC(N2CCC(CC2)N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C1CCCC1N2C1CCCC1 FWCFYOYWYWAYRZ-UHFFFAOYSA-N 0.000 claims 1
- YXQSBQOOYOWCJL-UHFFFAOYSA-N 3-[(5,11-dimethyl-6-oxopyrimido[4,5-b][1,4]benzodiazepin-2-yl)amino]-4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1NC1=NC=C(N(C)C(=O)C=2C(=CC=CC=2)N2C)C2=N1 YXQSBQOOYOWCJL-UHFFFAOYSA-N 0.000 claims 1
- WEVYNIUIFUYDGI-UHFFFAOYSA-N 3-[6-[4-(trifluoromethoxy)anilino]-4-pyrimidinyl]benzamide Chemical compound NC(=O)C1=CC=CC(C=2N=CN=C(NC=3C=CC(OC(F)(F)F)=CC=3)C=2)=C1 WEVYNIUIFUYDGI-UHFFFAOYSA-N 0.000 claims 1
- XBWVKVCSCJYKTP-UHFFFAOYSA-N 4-[(2-cyclopentyl-9-methyl-8-oxo-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-13-yl)amino]-3-methoxy-N-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C2C(CCC2)N2C3CCCC3)C2=N1 XBWVKVCSCJYKTP-UHFFFAOYSA-N 0.000 claims 1
- REFAILJSNNDVNL-UHFFFAOYSA-N 4-[(2-cyclopentyl-9-methyl-8-oxo-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-13-yl)amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C2C(CCC2)N2C3CCCC3)C2=N1 REFAILJSNNDVNL-UHFFFAOYSA-N 0.000 claims 1
- WSLOEKAMNQLCHA-UHFFFAOYSA-N 4-[(5,11-dimethyl-6-oxopyrimido[4,5-b][1,4]benzodiazepin-2-yl)amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C=2C(=CC=CC=2)N2C)C2=N1 WSLOEKAMNQLCHA-UHFFFAOYSA-N 0.000 claims 1
- JFRNFMQDZRWAQB-UHFFFAOYSA-N 4-[(9-cyclopentyl-5-methyl-6-oxo-7,8-dihydropyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)CCN2C1CCCC1 JFRNFMQDZRWAQB-UHFFFAOYSA-N 0.000 claims 1
- YPTCBEGMGVTHLV-UHFFFAOYSA-N 4-[(9-cyclopentyl-6-oxo-7,8-dihydro-5h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1NC(=O)CCN2C1CCCC1 YPTCBEGMGVTHLV-UHFFFAOYSA-N 0.000 claims 1
- 102100022681 40S ribosomal protein S27 Human genes 0.000 claims 1
- HGOKWKGWPGOSCA-UHFFFAOYSA-N 5-ethyl-2-[4-(4-hydroxypiperidin-1-yl)-2-methoxyanilino]-11-methylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound N1=C2N(C)C3=CC=CC=C3C(=O)N(CC)C2=CN=C1NC(C(=C1)OC)=CC=C1N1CCC(O)CC1 HGOKWKGWPGOSCA-UHFFFAOYSA-N 0.000 claims 1
- UJDYKWMGSWQRHC-UHFFFAOYSA-N 5-ethyl-2-[[5-(4-hydroxypiperidin-1-yl)pyridin-2-yl]amino]-11-methylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound N1=C2N(C)C3=CC=CC=C3C(=O)N(CC)C2=CN=C1NC(N=C1)=CC=C1N1CCC(O)CC1 UJDYKWMGSWQRHC-UHFFFAOYSA-N 0.000 claims 1
- NGLWEPBNFIVDCQ-UHFFFAOYSA-N 6-[(2-cyclopentyl-9-methyl-8-oxo-2,9,12,14-tetrazatricyclo[8.4.0.03,7]tetradeca-1(14),10,12-trien-13-yl)amino]-N-methylpyridine-3-carboxamide Chemical compound N1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C2C(CCC2)N2C3CCCC3)C2=N1 NGLWEPBNFIVDCQ-UHFFFAOYSA-N 0.000 claims 1
- MUKRTRBUCKPVNQ-UHFFFAOYSA-N 8-chloro-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-11-methyl-5h-pyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=C(Cl)C=C4C(=O)NC3=CN=2)C(OC)=CC=1N1CCN(C)CC1 MUKRTRBUCKPVNQ-UHFFFAOYSA-N 0.000 claims 1
- VHGSQSKYNALGRI-UHFFFAOYSA-N 8-chloro-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC=C(Cl)C=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 VHGSQSKYNALGRI-UHFFFAOYSA-N 0.000 claims 1
- RHSOYHKODVPGTH-UHFFFAOYSA-N 9-chloro-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one Chemical compound C=1C=C(NC=2N=C3N(C)C4=CC(Cl)=CC=C4C(=O)N(C)C3=CN=2)C(OC)=CC=1N1CCN(C)CC1 RHSOYHKODVPGTH-UHFFFAOYSA-N 0.000 claims 1
- ACHCMXBSPWFSTG-UHFFFAOYSA-N 9-cyclopentyl-2-[2-ethoxy-4-(4-hydroxypiperidin-1-yl)anilino]-5-ethyl-7,8-dihydropyrimido[4,5-b][1,4]diazepin-6-one Chemical compound CCOC1=CC(N2CCC(O)CC2)=CC=C1NC(N=C12)=NC=C1N(CC)C(=O)CCN2C1CCCC1 ACHCMXBSPWFSTG-UHFFFAOYSA-N 0.000 claims 1
- JPPAAAXZOZVWJV-UHFFFAOYSA-N 9-cyclopentyl-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-5,8-dimethyl-7,8-dihydropyrimido[4,5-b][1,4]diazepin-6-one Chemical compound COC1=CC(N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)CC(C)N2C1CCCC1 JPPAAAXZOZVWJV-UHFFFAOYSA-N 0.000 claims 1
- OJWZTBKXQCIUGC-UHFFFAOYSA-N 9-cyclopentyl-2-[2-methoxy-4-(4-methylpiperazin-1-yl)anilino]-8-methyl-7,8-dihydro-5h-pyrimido[4,5-b][1,4]diazepin-6-one Chemical compound COC1=CC(N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1NC(=O)CC(C)N2C1CCCC1 OJWZTBKXQCIUGC-UHFFFAOYSA-N 0.000 claims 1
- DIKJXQJRGJEYBE-UHFFFAOYSA-N 9-cyclopentyl-2-[2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]anilino]-5,8-dimethyl-7,8-dihydropyrimido[4,5-b][1,4]diazepin-6-one Chemical compound COC1=CC(N2CCC(CC2)N2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)CC(C)N2C1CCCC1 DIKJXQJRGJEYBE-UHFFFAOYSA-N 0.000 claims 1
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| WO2014031872A2 (en) * | 2012-08-23 | 2014-02-27 | The Broad Institute, Inc. | Small molecule inhibitors for treating parasitic infections |
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| US9714946B2 (en) | 2013-03-14 | 2017-07-25 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
| EP3738964A1 (en) * | 2013-03-15 | 2020-11-18 | Dana Farber Cancer Institute, Inc. | Pyrimido-diazepinone compounds and methods of treating disorders |
| UA120248C2 (uk) | 2013-03-15 | 2019-11-11 | Селджен Кар Ллс | Гетероарильні сполуки та їх застосування |
| JP6576325B2 (ja) | 2013-03-15 | 2019-09-18 | セルジーン シーエーアール エルエルシー | ヘテロアリール化合物およびそれらの使用 |
| AR095464A1 (es) | 2013-03-15 | 2015-10-21 | Celgene Avilomics Res Inc | Compuestos de heteroarilo y usos de los mismos |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| MY181497A (en) | 2013-04-19 | 2020-12-23 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| CA2902686C (en) | 2013-04-25 | 2017-01-24 | Beigene, Ltd. | Fused heterocyclic compounds as protein kinase inhibitors |
| JP2016531113A (ja) | 2013-07-25 | 2016-10-06 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | 転写因子の阻害剤およびその使用 |
| CN108715615B (zh) | 2013-09-13 | 2020-11-27 | 百济神州(广州)生物科技有限公司 | 抗pd1抗体及其作为治疗剂与诊断剂的用途 |
| MX379463B (es) | 2013-11-08 | 2025-03-10 | Dana Farber Cancer Inst Inc | Terapia de combinación para el cáncer usando inhibidores de la proteína bromodominio y extra-terminal. |
| JP6992960B2 (ja) * | 2013-12-02 | 2022-02-03 | ベルゲンビオ アーエスアー | キナーゼ阻害剤の用途 |
| ES2663622T3 (es) | 2013-12-17 | 2018-04-16 | Pfizer Inc. | Novedosas 1H-pirrolo[2,3-b]piridinas 3,4-disustituidas y 7H-pirrolo[2,3-c]piridacinas 4,5-disustituidas como inhibidores de LRRK2 |
| EP3099693A4 (en) * | 2014-01-31 | 2017-08-16 | Dana-Farber Cancer Institute, Inc. | Uses of diazepane derivatives |
| MX2016009976A (es) | 2014-01-31 | 2016-11-15 | Dana Farber Cancer Inst Inc | Derivados de diazepam y sus usos. |
| CA2936865A1 (en) | 2014-01-31 | 2015-08-06 | Dana-Farber Cancer Institute, Inc. | Diaminopyrimidine benzenesulfone derivatives and uses thereof |
| EP3110819A4 (en) * | 2014-02-26 | 2017-08-02 | Kyorin Pharmaceutical Co., Ltd. | Heterocyclic compounds |
| WO2015131113A1 (en) | 2014-02-28 | 2015-09-03 | Tensha Therapeutics, Inc. | Treatment of conditions associated with hyperinsulinaemia |
| GB201411581D0 (en) * | 2014-06-30 | 2014-08-13 | Inst Europ Di Oncologia S R L | Compounds inhibiting the enzyme monopolar spindle 1 kinase, pharmaceutical compositions and uses thereof |
| CN110156892B (zh) | 2014-07-03 | 2023-05-16 | 百济神州有限公司 | 抗pd-l1抗体及其作为治疗剂及诊断剂的用途 |
| EP3166637B1 (en) | 2014-07-10 | 2020-01-29 | The J. David Gladstone Institutes | Compositions and methods for treating dengue virus infection |
| CA2955077A1 (en) | 2014-08-08 | 2016-02-11 | Dana-Farber Cancer Institute, Inc. | Dihydropteridinone derivatives and uses thereof |
| BR112017002369A2 (pt) * | 2014-08-08 | 2017-12-05 | Dana Farber Cancer Inst Inc | derivados de diazepana e usos dos mesmos |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MX376748B (es) | 2014-10-27 | 2025-03-07 | Tensha Therapeutics Inc | Inhibidores del bromodominio. |
| TW201632520A (zh) | 2014-11-25 | 2016-09-16 | 拜耳製藥股份有限公司 | 經取代之吡啶並苯並二氮呯酮衍生物及其用途 |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| PE20171514A1 (es) | 2015-02-20 | 2017-10-20 | Incyte Corp | Heterociclos biciclicos como inhibidores de fgfr |
| CN107567503B (zh) | 2015-04-17 | 2022-03-22 | 荷兰转化研究中心有限责任公司 | 用于ttk抑制剂化疗的预后生物标记 |
| AU2016276963C1 (en) | 2015-06-12 | 2021-08-05 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| BR112018004617A2 (pt) | 2015-09-11 | 2018-09-25 | Dana Farber Cancer Inst Inc | acetamida tienotriazoldiazepinas e usos das mesmas |
| JP2018526421A (ja) | 2015-09-11 | 2018-09-13 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | シアノチエノトリアゾロジアゼピンおよびこれらの使用 |
| WO2017046675A1 (en) | 2015-09-14 | 2017-03-23 | Pfizer Inc. | Novel imidazo [4,5-c] quinoline and imidazo [4,5-c][1,5] naphthyridine derivatives as lrrk2 inhibitors |
| WO2017066193A1 (en) | 2015-10-15 | 2017-04-20 | Princeton Drug Discovery, Llc | Novel inhibitors of protein kinases |
| CN108431004B (zh) * | 2015-10-23 | 2021-02-12 | 武田药品工业株式会社 | 杂环化合物 |
| CN108472295B (zh) | 2015-11-25 | 2022-04-15 | 达纳-法伯癌症研究所股份有限公司 | 二价溴结构域抑制剂及其用途 |
| CA3012516A1 (en) * | 2016-03-04 | 2017-09-08 | Anhui New Star Pharmaceutical Development Co., Ltd | Pyrimidine seven-membered-ring compounds, preparation method therefor, pharmaceutical composition therefor, and uses thereof |
| KR20180132812A (ko) * | 2016-04-07 | 2018-12-12 | 다나-파버 캔서 인스티튜트 인크. | 피리미도-디아제피논 키나아제 스캐폴드 화합물 및 pi3k-매개된 장애의 치료 방법 |
| JP6993056B2 (ja) | 2016-07-05 | 2022-02-15 | ベイジーン リミテッド | 癌治療のためのpd-1アンタゴニスト及びraf阻害剤の組合せ |
| SG11201900515PA (en) | 2016-07-21 | 2019-02-27 | Biogen Ma Inc | Succinate forms and compositions of bruton's tyrosine kinase inhibitors |
| EP3490552B1 (en) * | 2016-07-26 | 2022-11-23 | University of Southern California | Selective bromodomain inhibition of fungal bdf1 |
| CN116478166A (zh) | 2016-08-16 | 2023-07-25 | 百济神州(苏州)生物科技有限公司 | 一种化合物的晶型、其制备和用途 |
| DK3500299T3 (da) | 2016-08-19 | 2024-01-29 | Beigene Switzerland Gmbh | Kombination af zanubrutinib med et anti-CD20- eller et anti-PD-1-antistof til anvendelse i behandling af cancer |
| MX390121B (es) | 2016-09-19 | 2025-03-20 | Mei Pharma Inc | Combinaciones de un inhibidor de btk y un inhibidor de pi3k para tratar neoplasias malignas hematológicas. |
| JP7086948B2 (ja) * | 2016-10-18 | 2022-06-20 | ダナ-ファーバー キャンサー インスティテュート,インコーポレイテッド | ピリミド-ジアゼピノンキナーゼ骨格化合物およびdclk1/2媒介性障害の治療方法 |
| US11555038B2 (en) | 2017-01-25 | 2023-01-17 | Beigene, Ltd. | Crystalline forms of (S)-7-(1-(but-2-ynoyl)piperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide, preparation, and uses thereof |
| JP6728503B2 (ja) * | 2017-02-24 | 2020-07-22 | テグ−キョンプク メディカル イノベーション ファウンデーション | 血液脳関門を通過することができる化合物を有効成分として含有する脳腫瘍の予防または治療用薬学的組成物 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CN110799543A (zh) | 2017-06-26 | 2020-02-14 | 百济神州有限公司 | 肝细胞癌的免疫治疗 |
| US11377449B2 (en) | 2017-08-12 | 2022-07-05 | Beigene, Ltd. | BTK inhibitors with improved dual selectivity |
| CN111801334B (zh) | 2017-11-29 | 2023-06-09 | 百济神州瑞士有限责任公司 | 使用包含btk抑制剂的组合治疗惰性或侵袭性b-细胞淋巴瘤 |
| WO2019164947A1 (en) * | 2018-02-20 | 2019-08-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of egfr and methods of use thereof |
| US20200390783A1 (en) * | 2018-02-20 | 2020-12-17 | Dana-Farber Cancer Institute, Inc. | Inhibitors of egfr and methods of use thereof |
| JP7568512B2 (ja) | 2018-05-04 | 2024-10-16 | インサイト・コーポレイション | Fgfr阻害剤の塩 |
| CN112867716B (zh) | 2018-05-04 | 2024-09-13 | 因赛特公司 | Fgfr抑制剂的固体形式和其制备方法 |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| CN109999763A (zh) * | 2019-03-20 | 2019-07-12 | 广西民族大学 | 一种去除糖浆中钙镁离子的方法 |
| ES3034869T3 (en) * | 2019-04-22 | 2025-08-25 | Univ Pittsburgh Commonwealth Sys Higher Education | Tg02 for use in treating gliomas in pediatric subjects |
| WO2020231726A1 (en) * | 2019-05-10 | 2020-11-19 | Dana-Farber Cancer Institute, Inc. | Small-molecule focal adhesion kinase (fak) inhibitors |
| EP3981399A4 (en) | 2019-06-10 | 2023-05-31 | BeiGene Switzerland GmbH | ORAL SOLID TABLET WITH A TYROSINE KINAS INHIBITOR AND METHOD OF MANUFACTURE THEREOF |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CN114728009B (zh) * | 2019-08-08 | 2024-09-03 | 李晓祥 | 预防或治疗与组织损伤相关的疾病和紊乱 |
| CA3150316A1 (en) * | 2019-09-27 | 2021-04-01 | Dana-Farber Cancer Institute, Inc. | ERK5 DEGRADING AGENTS USED AS THERAPEUTIC AGENTS IN CANCER AND INFLAMMATORY DISEASES |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11607416B2 (en) | 2019-10-14 | 2023-03-21 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| WO2021113462A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| KR102498531B1 (ko) * | 2020-06-29 | 2023-02-13 | 한국과학기술연구원 | 단백질 카이네이즈 trkc에 선택적인 억제제로서의 신규 피리미도디아제핀 유도체 |
| US20230303499A1 (en) * | 2020-08-14 | 2023-09-28 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Inhibitors of ack1/tnk2 tyrosine kinase |
| CN116615429A (zh) * | 2020-10-14 | 2023-08-18 | 珃诺生物医药科技(杭州)有限公司 | 用于靶向蛋白降解的方法和组合物 |
| WO2022145989A1 (ko) * | 2020-12-31 | 2022-07-07 | (주) 업테라 | 선택적 plk1 억제제로서의 피리미도디아제핀 유도체 |
| CA3215903A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| JP2024522188A (ja) | 2021-06-09 | 2024-06-11 | インサイト・コーポレイション | Fgfr阻害剤としての三環式ヘテロ環 |
| US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| WO2023076404A1 (en) | 2021-10-27 | 2023-05-04 | Aria Pharmaceuticals, Inc. | Methods for treating systemic lupus erythematosus |
| CN114478539B (zh) * | 2022-02-09 | 2024-02-02 | 中国人民解放军海军军医大学 | 一种新型dclk1抑制剂及其制备方法和应用 |
| US11786531B1 (en) | 2022-06-08 | 2023-10-17 | Beigene Switzerland Gmbh | Methods of treating B-cell proliferative disorder |
| CN116173040B (zh) * | 2022-08-23 | 2025-05-23 | 杭州天玑济世生物科技有限公司 | Xmd17109作为arih1激动剂的用途 |
| CN116375713B (zh) * | 2023-03-07 | 2024-11-19 | 中国人民解放军海军军医大学 | 一种dclk1蛋白降解靶向嵌合体及其应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2310039T3 (es) * | 1998-05-26 | 2008-12-16 | Warner-Lambert Company Llc | Pirimidinas biciclicas y 3,4-dihidropirimidinas biciclicas como inhibidores de la proliferacion celular. |
| ES2287583T3 (es) * | 2003-02-26 | 2007-12-16 | BOEHRINGER INGELHEIM PHARMA GMBH & CO.KG | Dihidropteridinonas, procedimiento para su preparacion y su uso como medicamenteos. |
| DE102005061655A1 (de) * | 2005-12-22 | 2007-06-28 | Merck Patent Gmbh | Diazepinone |
| NZ570530A (en) * | 2006-02-14 | 2011-09-30 | Vertex Pharma | Pharmaceutical compositions comprising 6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4)diazepine derivatives |
| TW200808325A (en) * | 2006-07-06 | 2008-02-16 | Astrazeneca Ab | Novel compounds |
| WO2008113711A1 (en) | 2007-03-22 | 2008-09-25 | F. Hoffmann-La Roche Ag | Substituted pyrimidodiazepines useful as plk1 inhibitors |
| US20090291938A1 (en) * | 2007-11-19 | 2009-11-26 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| US9266890B2 (en) * | 2009-01-06 | 2016-02-23 | Dana-Farber Cancer Institute, Inc. | Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders |
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