JP2013522238A5 - - Google Patents
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- JP2013522238A5 JP2013522238A5 JP2012557294A JP2012557294A JP2013522238A5 JP 2013522238 A5 JP2013522238 A5 JP 2013522238A5 JP 2012557294 A JP2012557294 A JP 2012557294A JP 2012557294 A JP2012557294 A JP 2012557294A JP 2013522238 A5 JP2013522238 A5 JP 2013522238A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- imidazo
- alkyl
- amine
- indazol
- 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 3- (4- (tert-butyl) benzamido) -2-methylphenyl Chemical group 0.000 claims description 118
- 125000000217 alkyl group Chemical group 0.000 claims description 91
- 239000000126 substance Substances 0.000 claims description 39
- 230000000694 effects Effects 0.000 claims description 28
- 230000002401 inhibitory effect Effects 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 24
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 24
- 201000010099 disease Diseases 0.000 claims description 20
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 20
- 125000004076 pyridyl group Chemical group 0.000 claims description 20
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 20
- 125000000335 thiazolyl group Chemical group 0.000 claims description 20
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 125000000623 heterocyclic group Chemical group 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 claims description 6
- 238000006460 hydrolysis reaction Methods 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 4
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 238000000338 in vitro Methods 0.000 claims description 4
- 200000000018 inflammatory disease Diseases 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- CJWSQMSEHQXXCY-UHFFFAOYSA-N 1-[2-[[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-5-yl]ethanone Chemical compound N1=C2C=CNC2=CC(C=2C=C(C3=NC=CN3C=2)NC2=NN3CCN(CC3=C2)C(=O)C)=C1 CJWSQMSEHQXXCY-UHFFFAOYSA-N 0.000 claims description 2
- AAHVXELFAIWJBK-UHFFFAOYSA-N 1-[4-[6-[[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=CC3=NC=2)=CN2C1=NC=C2 AAHVXELFAIWJBK-UHFFFAOYSA-N 0.000 claims description 2
- HHZJQTQNJPCNPC-UHFFFAOYSA-N 1-[4-[6-[[6-[3-(2-hydroxyethyl)-1H-indol-6-yl]imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=C(CCO)C3=CC=2)=CN2C1=NC=C2 HHZJQTQNJPCNPC-UHFFFAOYSA-N 0.000 claims description 2
- AMKMRSDGPQZQLS-UHFFFAOYSA-N 1-[6-[[6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]-3-methylazetidin-3-ol Chemical compound C1C(C)(O)CN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 AMKMRSDGPQZQLS-UHFFFAOYSA-N 0.000 claims description 2
- UYCXAUWDQCPVMY-UHFFFAOYSA-N 1-[6-[[6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]-4-methylpiperidin-4-ol Chemical compound C1CC(C)(O)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 UYCXAUWDQCPVMY-UHFFFAOYSA-N 0.000 claims description 2
- MODZHSLQBONCHV-UHFFFAOYSA-N 1-[6-[[6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]azetidin-3-ol Chemical compound C1C(O)CN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 MODZHSLQBONCHV-UHFFFAOYSA-N 0.000 claims description 2
- IVHDGESMIPKUEO-UHFFFAOYSA-N 1-methyl-6-[5-methyl-8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridin-6-yl]-3H-indol-2-one Chemical compound C1=C2N(C)C(=O)CC2=CC=C1C(=C(N1C=CN=C11)C)C=C1NC(N=C1)=CC=C1N1CCOCC1 IVHDGESMIPKUEO-UHFFFAOYSA-N 0.000 claims description 2
- GVZHUWSLJZJBOW-UHFFFAOYSA-N 2-N-[6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-yl]-5-N-(2-methoxyethyl)-5-N-methylpyridine-2,5-diamine Chemical compound N1=CC(N(C)CCOC)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 GVZHUWSLJZJBOW-UHFFFAOYSA-N 0.000 claims description 2
- VYICWLIDANWXNE-UHFFFAOYSA-N 2-[1-methyl-6-[5-methyl-8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridin-6-yl]indol-3-yl]ethanol Chemical compound C12=NC=CN2C(C)=C(C=2C=C3N(C)C=C(CCO)C3=CC=2)C=C1NC(N=C1)=CC=C1N1CCOCC1 VYICWLIDANWXNE-UHFFFAOYSA-N 0.000 claims description 2
- COXUVLHFSMGTNO-UHFFFAOYSA-N 2-[4-[[6-[3-(2-hydroxyethyl)-1H-indol-6-yl]imidazo[1,2-a]pyridin-8-yl]amino]phenyl]-2-methylpropan-1-ol Chemical compound C1=CC(C(C)(CO)C)=CC=C1NC1=CC(C=2C=C3NC=C(CCO)C3=CC=2)=CN2C1=NC=C2 COXUVLHFSMGTNO-UHFFFAOYSA-N 0.000 claims description 2
- QWHKXQBDXJJCHD-UHFFFAOYSA-N 2-[5-methyl-3-[[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyrazol-1-yl]ethanol Chemical compound OCCN1C(C)=CC(NC=2C3=NC=CN3C=C(C=2)C=2C=C3NC=CC3=NC=2)=N1 QWHKXQBDXJJCHD-UHFFFAOYSA-N 0.000 claims description 2
- LUWFEEPUDGWECA-UHFFFAOYSA-N 2-[6-[5-chloro-8-[[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]amino]imidazo[1,2-a]pyridin-6-yl]-1-methylindol-3-yl]ethanol Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3N(C)C=C(CCO)C3=CC=2)=C(Cl)N2C1=NC=C2 LUWFEEPUDGWECA-UHFFFAOYSA-N 0.000 claims description 2
- WCSIPHYOIZRNNZ-UHFFFAOYSA-N 2-[6-[5-chloro-8-[[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]amino]imidazo[1,2-a]pyridin-6-yl]-1H-indol-3-yl]ethanol Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=C(CCO)C3=CC=2)=C(Cl)N2C1=NC=C2 WCSIPHYOIZRNNZ-UHFFFAOYSA-N 0.000 claims description 2
- CPYZUOJAUGIHIA-UHFFFAOYSA-N 2-[6-[5-chloro-8-[[5-(4-propan-2-ylpiperazin-1-yl)pyridin-2-yl]amino]imidazo[1,2-a]pyridin-6-yl]-1-methylindol-3-yl]ethanol Chemical compound C1CN(C(C)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3N(C)C=C(CCO)C3=CC=2)=C(Cl)N2C1=NC=C2 CPYZUOJAUGIHIA-UHFFFAOYSA-N 0.000 claims description 2
- OEZWQIKWWVKAJI-UHFFFAOYSA-N 2-[6-[5-chloro-8-[[5-(4-propan-2-ylpiperazin-1-yl)pyridin-2-yl]amino]imidazo[1,2-a]pyridin-6-yl]-1H-indol-3-yl]ethanol Chemical compound C1CN(C(C)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=C(CCO)C3=CC=2)=C(Cl)N2C1=NC=C2 OEZWQIKWWVKAJI-UHFFFAOYSA-N 0.000 claims description 2
- UJLCAUDXTUPBJP-UHFFFAOYSA-N 2-[6-[8-(6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazin-2-ylamino)imidazo[1,2-a]pyridin-6-yl]-1H-indol-3-yl]ethanol Chemical compound C1=C2COCCN2N=C1NC1=CC(C=2C=C3NC=C(C3=CC=2)CCO)=CN2C=CN=C21 UJLCAUDXTUPBJP-UHFFFAOYSA-N 0.000 claims description 2
- XMRNHTWGJJNSMS-UHFFFAOYSA-N 2-[6-[8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridin-6-yl]-1H-indol-3-yl]ethanol Chemical compound C=1C=C2C(CCO)=CNC2=CC=1C(=CN1C=CN=C11)C=C1NC(N=C1)=CC=C1N1CCOCC1 XMRNHTWGJJNSMS-UHFFFAOYSA-N 0.000 claims description 2
- JLQXRJUDGNOZIR-UHFFFAOYSA-N 2-[6-[8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridin-6-yl]-2H-indazol-3-yl]ethanol Chemical compound C=1C=C2C(CCO)=NNC2=CC=1C(=CN1C=CN=C11)C=C1NC(N=C1)=CC=C1N1CCOCC1 JLQXRJUDGNOZIR-UHFFFAOYSA-N 0.000 claims description 2
- VMJQTHKIUMLGNI-UHFFFAOYSA-N 2-[6-[8-[[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]amino]-5-methylimidazo[1,2-a]pyridin-6-yl]-1H-indol-3-yl]ethanol Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=C(CCO)C3=CC=2)=C(C)N2C1=NC=C2 VMJQTHKIUMLGNI-UHFFFAOYSA-N 0.000 claims description 2
- AKSMMQPOWIFLJO-UHFFFAOYSA-N 2-[6-[8-[[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]amino]imidazo[1,2-a]pyridin-6-yl]-2H-indazol-3-yl]ethanol Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=C(CCO)C3=CC=2)=CN2C1=NC=C2 AKSMMQPOWIFLJO-UHFFFAOYSA-N 0.000 claims description 2
- XIQBMHMYQXKVNB-UHFFFAOYSA-N 2-[ethyl-[6-[[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]amino]ethanol Chemical compound N1=CC(N(CCO)CC)=CC=C1NC1=CC(C=2C=C3NC=CC3=NC=2)=CN2C1=NC=C2 XIQBMHMYQXKVNB-UHFFFAOYSA-N 0.000 claims description 2
- XLWBHWLYRXBZRX-UHFFFAOYSA-N 2-hydroxy-1-[4-[6-[[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]amino]pyridin-3-yl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)CO)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=CC3=NC=2)=CN2C1=NC=C2 XLWBHWLYRXBZRX-UHFFFAOYSA-N 0.000 claims description 2
- KEZHRKOVLKUYCQ-UHFFFAOYSA-N 3,3-dimethyl-1H-indol-2-one Chemical compound C1=CC=C2C(C)(C)C(=O)NC2=C1 KEZHRKOVLKUYCQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 2
- ARLTZSGJPGABLS-UHFFFAOYSA-N 3-(2-hydroxyethyl)-6-[8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridin-6-yl]-1H-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCO)C2=CC=C1C(=CN1C=CN=C11)C=C1NC(N=C1)=CC=C1N1CCOCC1 ARLTZSGJPGABLS-UHFFFAOYSA-N 0.000 claims description 2
- IJNYKXPIMNKCBK-UHFFFAOYSA-N 5-chloro-6-(1H-indazol-6-yl)-N-[5-(4-propan-2-ylpiperazin-1-yl)pyridin-2-yl]imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(C(C)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=C(Cl)N2C1=NC=C2 IJNYKXPIMNKCBK-UHFFFAOYSA-N 0.000 claims description 2
- TTXXVRQVMWILOX-UHFFFAOYSA-N 5-chloro-N-[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]-6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=C(Cl)N2C1=NC=C2 TTXXVRQVMWILOX-UHFFFAOYSA-N 0.000 claims description 2
- JCGQOBWKAYVSHM-UHFFFAOYSA-N 5-chloro-N-[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]-6-(1H-indol-6-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=CC3=CC=2)=C(Cl)N2C1=NC=C2 JCGQOBWKAYVSHM-UHFFFAOYSA-N 0.000 claims description 2
- NGNYRZRWQFOUFK-UHFFFAOYSA-N 5-ethyl-N-[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]-6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=C(CC)N2C1=NC=C2 NGNYRZRWQFOUFK-UHFFFAOYSA-N 0.000 claims description 2
- HYULMKQXSAMIIE-UHFFFAOYSA-N 5-ethyl-N-[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]-6-(1H-indol-6-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(CC)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NC=CC3=CC=2)=C(CC)N2C1=NC=C2 HYULMKQXSAMIIE-UHFFFAOYSA-N 0.000 claims description 2
- FVPPJLAQPIKWLT-UHFFFAOYSA-N 5-fluoro-6-(1H-indazol-6-yl)-N-[5-(4-propan-2-ylpiperazin-1-yl)pyridin-2-yl]imidazo[1,2-a]pyridin-8-amine Chemical compound C1CN(C(C)C)CCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=C(F)N2C1=NC=C2 FVPPJLAQPIKWLT-UHFFFAOYSA-N 0.000 claims description 2
- SMDZKFNTPDKVCD-UHFFFAOYSA-N 5-methyl-N-(5-morpholin-4-ylpyridin-2-yl)-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C12=NC=CN2C(C)=C(C=2C=C3C=CNC3=NC=2)C=C1NC(N=C1)=CC=C1N1CCOCC1 SMDZKFNTPDKVCD-UHFFFAOYSA-N 0.000 claims description 2
- NESGFBOLRFKZDH-UHFFFAOYSA-N 5-methyl-N-(5-morpholin-4-ylpyridin-2-yl)-6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C12=NC=CN2C(C)=C(C=2C=C3NC=CC3=NC=2)C=C1NC(N=C1)=CC=C1N1CCOCC1 NESGFBOLRFKZDH-UHFFFAOYSA-N 0.000 claims description 2
- VVVAHIMKXLXSAZ-UHFFFAOYSA-N 5-methyl-N-[6-(1H-pyrazolo[4,3-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-2-amine Chemical compound N1=C2C=NNC2=CC(C=2C=C(C3=NC=CN3C=2)NC2=NN3CCN(CC3=C2)C)=C1 VVVAHIMKXLXSAZ-UHFFFAOYSA-N 0.000 claims description 2
- XGIBBFYEAXESGG-UHFFFAOYSA-N 5-methylsulfonyl-N-[6-(1H-pyrrolo[3,2-b]pyridin-6-yl)imidazo[1,2-a]pyridin-8-yl]-6,7-dihydro-4H-pyrazolo[1,5-a]pyrazin-2-amine Chemical compound N1=C2C=CNC2=CC(C=2C=C(C3=NC=CN3C=2)NC2=NN3CCN(CC3=C2)S(=O)(=O)C)=C1 XGIBBFYEAXESGG-UHFFFAOYSA-N 0.000 claims description 2
- HFLJFLGBUYZUQI-UHFFFAOYSA-N 6-(1,3-benzothiazol-5-yl)-N-(5,6-dimethoxypyridin-2-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound N1=C(OC)C(OC)=CC=C1NC1=CC(C=2C=C3N=CSC3=CC=2)=CN2C1=NC=C2 HFLJFLGBUYZUQI-UHFFFAOYSA-N 0.000 claims description 2
- AUNKAMCNRBZWGS-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-5-methyl-N-(5-morpholin-4-ylpyridin-2-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C12=NC=CN2C(C)=C(C=2C=C3NN=CC3=CC=2)C=C1NC(N=C1)=CC=C1N1CCOCC1 AUNKAMCNRBZWGS-UHFFFAOYSA-N 0.000 claims description 2
- AGCIFROCRUWKFH-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-5-methyl-N-(5-piperazin-1-ylpyridin-2-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C12=NC=CN2C(C)=C(C=2C=C3NN=CC3=CC=2)C=C1NC(N=C1)=CC=C1N1CCNCC1 AGCIFROCRUWKFH-UHFFFAOYSA-N 0.000 claims description 2
- VNVXBPDUZLOFDL-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-8-[(5-morpholin-4-ylpyridin-2-yl)amino]imidazo[1,2-a]pyridine-5-carboxylic acid Chemical compound C12=NC=CN2C(C(=O)O)=C(C=2C=C3NN=CC3=CC=2)C=C1NC(N=C1)=CC=C1N1CCOCC1 VNVXBPDUZLOFDL-UHFFFAOYSA-N 0.000 claims description 2
- MMVVVHCESUZDJQ-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-N-(1-methylpyrazol-3-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound CN1C=CC(NC=2C3=NC=CN3C=C(C=2)C=2C=C3NN=CC3=CC=2)=N1 MMVVVHCESUZDJQ-UHFFFAOYSA-N 0.000 claims description 2
- RXLYIOCBKNBFKY-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-N-(2-methoxypyrimidin-4-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound COC1=NC=CC(NC=2C3=NC=CN3C=C(C=2)C=2C=C3NN=CC3=CC=2)=N1 RXLYIOCBKNBFKY-UHFFFAOYSA-N 0.000 claims description 2
- ASOHWEMFUOHJIO-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-N-(5-morpholin-4-ylpyridin-2-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1COCCN1C(C=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 ASOHWEMFUOHJIO-UHFFFAOYSA-N 0.000 claims description 2
- SMDZVMZCRFMZLC-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-N-(6-morpholin-4-ylpyridazin-3-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound C1COCCN1C(N=N1)=CC=C1NC1=CC(C=2C=C3NN=CC3=CC=2)=CN2C1=NC=C2 SMDZVMZCRFMZLC-UHFFFAOYSA-N 0.000 claims description 2
- ZWZYOUWAHJEIEO-UHFFFAOYSA-N 6-(1H-indazol-6-yl)-N-pyrimidin-4-ylimidazo[1,2-a]pyridin-8-amine Chemical compound C=1C(C=2C=C3NN=CC3=CC=2)=CN2C=CN=C2C=1NC1=CC=NC=N1 ZWZYOUWAHJEIEO-UHFFFAOYSA-N 0.000 claims description 2
- WKMHWRRKVGSIQB-UHFFFAOYSA-N 6-(3,4-dihydro-2H-1,4-benzoxazin-6-yl)-N-(1,5-dimethylpyrazol-3-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound CN1C(C)=CC(NC=2C3=NC=CN3C=C(C=2)C=2C=C3NCCOC3=CC=2)=N1 WKMHWRRKVGSIQB-UHFFFAOYSA-N 0.000 claims description 2
- TVEGHVLNCAEJCT-UHFFFAOYSA-N 6-(3,4-dihydro-2H-1,4-benzoxazin-6-yl)-N-(5,6-dimethoxypyridin-2-yl)imidazo[1,2-a]pyridin-8-amine Chemical compound N1=C(OC)C(OC)=CC=C1NC1=CC(C=2C=C3NCCOC3=CC=2)=CN2C1=NC=C2 TVEGHVLNCAEJCT-UHFFFAOYSA-N 0.000 claims description 2
- PNUYPAFIVQXTMN-UHFFFAOYSA-N 6-N-[6-(1H-indazol-6-yl)imidazo[1,2-a]pyridin-8-yl]pyridine-2,6-diamine Chemical compound NC1=CC=CC(NC=2C3=NC=CN3C=C(C=2)C=2C=C3NN=CC3=CC=2)=N1 PNUYPAFIVQXTMN-UHFFFAOYSA-N 0.000 claims description 2
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| AU2014296308C1 (en) | 2013-07-30 | 2018-09-13 | Kronos Bio, Inc. | Polymorph of Syk inhibitors |
| TW201601728A (zh) | 2013-07-30 | 2016-01-16 | 吉李德康乃狄克公司 | 脾酪胺酸激酶（ＳｙＫ）抑制劑之調合物 |
| MX2016001427A (es) | 2013-07-31 | 2016-08-03 | Gilead Sciences Inc | Inhibidores de syk. |
| MX2016007311A (es) | 2013-12-04 | 2016-09-07 | Gilead Sciences Inc | Metodos para tratar canceres. |
| US9290505B2 (en) | 2013-12-23 | 2016-03-22 | Gilead Sciences, Inc. | Substituted imidazo[1,2-a]pyrazines as Syk inhibitors |
| TWI662037B (zh) | 2013-12-23 | 2019-06-11 | 美商基利科學股份有限公司 | 脾酪胺酸激酶抑制劑 |
| TW201617074A (zh) | 2014-07-14 | 2016-05-16 | 吉李德科學股份有限公司 | Ｓｙｋ（脾酪胺酸激酶）抑制劑 |
| BR112016028641A2 (pt) | 2014-07-14 | 2017-08-22 | Gilead Sciences Inc | ?método para tratar câncer? |
| TW201639573A (zh) | 2015-02-03 | 2016-11-16 | 吉李德科學股份有限公司 | 有關治療癌症之合併治療 |
| BR112017022323A2 (pt) | 2015-04-21 | 2018-07-03 | Gilead Sciences, Inc. | método para tratar doença do enxerto contra hospedeiro, uso de um composto, e, kit. |
| TW201822764A (zh) | 2016-09-14 | 2018-07-01 | 美商基利科學股份有限公司 | Syk抑制劑 |
| WO2018053190A1 (en) | 2016-09-14 | 2018-03-22 | Gilead Sciences, Inc. | Syk inhibitors |
-
2011
- 2011-03-11 KR KR1020127026472A patent/KR101717809B1/ko active IP Right Grant
- 2011-03-11 US US13/806,094 patent/US9562056B2/en active Active
- 2011-03-11 BR BR112012022943A patent/BR112012022943A2/pt not_active Application Discontinuation
- 2011-03-11 MX MX2012010418A patent/MX350010B/es active IP Right Grant
- 2011-03-11 JP JP2012557294A patent/JP5938352B2/ja active Active
- 2011-03-11 ES ES11709600T patent/ES2530449T3/es active Active
- 2011-03-11 EP EP11709600.8A patent/EP2545052B1/en active Active
- 2011-03-11 CA CA2792769A patent/CA2792769C/en active Active
- 2011-03-11 AU AU2011226689A patent/AU2011226689B2/en active Active
- 2011-03-11 PT PT117096008T patent/PT2545052E/pt unknown
- 2011-03-11 NZ NZ602362A patent/NZ602362A/en unknown
- 2011-03-11 WO PCT/US2011/028194 patent/WO2011112995A1/en active Application Filing
- 2011-03-11 CN CN201180023252.0A patent/CN103168039B/zh not_active Expired - Fee Related
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2013
- 2013-07-10 HK HK13108104.1A patent/HK1180689A1/xx unknown
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2015
- 2015-05-05 JP JP2015094508A patent/JP6177828B2/ja not_active Expired - Fee Related
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2016
- 2016-08-23 AU AU2016219585A patent/AU2016219585B2/en active Active
- 2016-12-21 US US15/387,557 patent/US10092583B2/en active Active
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2017
- 2017-07-13 JP JP2017136797A patent/JP2017222685A/ja not_active Withdrawn
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2018
- 2018-05-08 AU AU2018203210A patent/AU2018203210A1/en not_active Abandoned
- 2018-09-06 US US16/124,113 patent/US10842803B2/en active Active
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