JP2009515995A5 - - Google Patents
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- Publication number
- JP2009515995A5 JP2009515995A5 JP2008541376A JP2008541376A JP2009515995A5 JP 2009515995 A5 JP2009515995 A5 JP 2009515995A5 JP 2008541376 A JP2008541376 A JP 2008541376A JP 2008541376 A JP2008541376 A JP 2008541376A JP 2009515995 A5 JP2009515995 A5 JP 2009515995A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- carbonyl
- amino
- triazin
- pyrrolo
- 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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- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims 12
- 125000004104 aryloxy group Chemical group 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 12
- 125000001072 heteroaryl group Chemical group 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 10
- 150000002367 halogens Chemical class 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 125000003107 substituted aryl group Chemical group 0.000 claims 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 8
- 239000008194 pharmaceutical composition Substances 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- 241000124008 Mammalia Species 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 239000002254 cytotoxic agent Substances 0.000 claims 5
- 229940127089 cytotoxic agent Drugs 0.000 claims 5
- 231100000599 cytotoxic agent Toxicity 0.000 claims 5
- 229940127084 other anti-cancer agent Drugs 0.000 claims 5
- -1 C 1 -C 6 alkyl Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 230000002062 proliferating effect Effects 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 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 3
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 150000001602 bicycloalkyls Chemical group 0.000 claims 3
- 239000003937 drug carrier Substances 0.000 claims 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 3
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 claims 2
- 125000006728 (C1-C6) alkynyl group Chemical group 0.000 claims 2
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 108091008598 receptor tyrosine kinases Proteins 0.000 claims 2
- 102000027426 receptor tyrosine kinases Human genes 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 2
- WRQIIHFURAGCIR-UHFFFAOYSA-N 1-[3-(4-amino-7-bromopyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(2,4-dichlorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(Br)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(Cl)C=C1Cl WRQIIHFURAGCIR-UHFFFAOYSA-N 0.000 claims 1
- XTLOABAAKWDWKF-UHFFFAOYSA-N 1-[3-(4-amino-7-bromopyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(5-cyclopropyl-2-methylpyrazol-3-yl)urea Chemical compound C1=C(NC(=O)NC=2C=C(C=CC=2)C(=O)C2=C3C(N)=NC=NN3C(Br)=C2)N(C)N=C1C1CC1 XTLOABAAKWDWKF-UHFFFAOYSA-N 0.000 claims 1
- JSLIJLUSLPYLEM-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(2,4-dichlorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(Cl)C=C1Cl JSLIJLUSLPYLEM-UHFFFAOYSA-N 0.000 claims 1
- DSEJPAOKMPFSDR-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(2,4-dimethylphenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(C)C=C1C DSEJPAOKMPFSDR-UHFFFAOYSA-N 0.000 claims 1
- VPMQPJSTRSFLBC-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(2-methoxyphenyl)urea Chemical compound COC1=CC=CC=C1NC(=O)NC1=CC=CC(C(=O)C2=C3C(N)=NC=NN3C(C(C)C)=C2)=C1 VPMQPJSTRSFLBC-UHFFFAOYSA-N 0.000 claims 1
- KSVJBSVMTUNSBX-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(2-phenylphenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=CC=C1C1=CC=CC=C1 KSVJBSVMTUNSBX-UHFFFAOYSA-N 0.000 claims 1
- QZIROKOVAVXJCK-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(3-methoxyphenyl)urea Chemical compound COC1=CC=CC(NC(=O)NC=2C=C(C=CC=2)C(=O)C2=C3C(N)=NC=NN3C(C(C)C)=C2)=C1 QZIROKOVAVXJCK-UHFFFAOYSA-N 0.000 claims 1
- FOFRCQWXOKHOIE-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(3-methylphenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=CC(C)=C1 FOFRCQWXOKHOIE-UHFFFAOYSA-N 0.000 claims 1
- CZMBZBLFVFIDHB-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(4-bromophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(Br)C=C1 CZMBZBLFVFIDHB-UHFFFAOYSA-N 0.000 claims 1
- GQLXAGSDBDRKKH-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(4-fluorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(F)C=C1 GQLXAGSDBDRKKH-UHFFFAOYSA-N 0.000 claims 1
- KDQFJIOVEHPENA-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(4-phenoxyphenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC(C=C1)=CC=C1OC1=CC=CC=C1 KDQFJIOVEHPENA-UHFFFAOYSA-N 0.000 claims 1
- KKVKEHQMNCTHOL-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(4-phenylmethoxyphenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC(C=C1)=CC=C1OCC1=CC=CC=C1 KKVKEHQMNCTHOL-UHFFFAOYSA-N 0.000 claims 1
- BZEWXXDOPRVKCS-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(5-cyclopropyl-2-methylpyrazol-3-yl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC(N(N=1)C)=CC=1C1CC1 BZEWXXDOPRVKCS-UHFFFAOYSA-N 0.000 claims 1
- DIGSKJLFEXFWAC-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-(5-tert-butyl-2-methylpyrazol-3-yl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC(C(C)(C)C)=NN1C DIGSKJLFEXFWAC-UHFFFAOYSA-N 0.000 claims 1
- ADYFANLDRLLPSL-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-[2-(trifluoromethyl)phenyl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=CC=C1C(F)(F)F ADYFANLDRLLPSL-UHFFFAOYSA-N 0.000 claims 1
- JVXQFWTWKPFZOB-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-[4-(dimethylamino)phenyl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(N(C)C)C=C1 JVXQFWTWKPFZOB-UHFFFAOYSA-N 0.000 claims 1
- XPCDUPMKQGWWSS-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-[4-(trifluoromethyl)phenyl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=C(C(F)(F)F)C=C1 XPCDUPMKQGWWSS-UHFFFAOYSA-N 0.000 claims 1
- SMZVSSCASPEMIK-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-[5-cyclopropyl-2-(2-morpholin-4-ylethyl)pyrazol-3-yl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC(C2CC2)=NN1CCN1CCOCC1 SMZVSSCASPEMIK-UHFFFAOYSA-N 0.000 claims 1
- MVRBPFWJIWRIQL-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-[5-tert-butyl-2-(2-hydroxyethyl)pyrazol-3-yl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC(C(C)(C)C)=NN1CCO MVRBPFWJIWRIQL-UHFFFAOYSA-N 0.000 claims 1
- DYZUVHQBGUMLKY-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-naphthalen-1-ylurea Chemical compound NC1=NC=NN2C(C(C)C)=CC(C(=O)C=3C=C(NC(=O)NC=4C5=CC=CC=C5C=CC=4)C=CC=3)=C21 DYZUVHQBGUMLKY-UHFFFAOYSA-N 0.000 claims 1
- DFQXDYVZCOUQOI-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-naphthalen-2-ylurea Chemical compound NC1=NC=NN2C(C(C)C)=CC(C(=O)C=3C=C(NC(=O)NC=4C=C5C=CC=CC5=CC=4)C=CC=3)=C21 DFQXDYVZCOUQOI-UHFFFAOYSA-N 0.000 claims 1
- YASCKFXNGQOGHI-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-phenylurea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=CC=C1 YASCKFXNGQOGHI-UHFFFAOYSA-N 0.000 claims 1
- QWFUHFFGAOBQJP-UHFFFAOYSA-N 1-[3-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)phenyl]-3-pyridin-3-ylurea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC1=CC=CN=C1 QWFUHFFGAOBQJP-UHFFFAOYSA-N 0.000 claims 1
- ZJDBIGLNRMGKMD-UHFFFAOYSA-N 1-[3-[4-amino-7-[3-(dimethylamino)prop-1-ynyl]pyrrolo[2,1-f][1,2,4]triazine-5-carbonyl]phenyl]-3-(5-cyclopropyl-2-methylpyrazol-3-yl)urea Chemical compound C=12C(N)=NC=NN2C(C#CCN(C)C)=CC=1C(=O)C(C=1)=CC=CC=1NC(=O)NC(N(N=1)C)=CC=1C1CC1 ZJDBIGLNRMGKMD-UHFFFAOYSA-N 0.000 claims 1
- ZAUDXAUEKJIQSN-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(2,4-dichlorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=C(Cl)C=C1Cl ZAUDXAUEKJIQSN-UHFFFAOYSA-N 0.000 claims 1
- HQQXLNNMPJFQTN-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(2,4-difluorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=C(F)C=C1F HQQXLNNMPJFQTN-UHFFFAOYSA-N 0.000 claims 1
- UMKGTOFMRRZZJG-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(2-cyanophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=CC=C1C#N UMKGTOFMRRZZJG-UHFFFAOYSA-N 0.000 claims 1
- SJQRRVUSTOILCH-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(2-fluorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=CC=C1F SJQRRVUSTOILCH-UHFFFAOYSA-N 0.000 claims 1
- XLUCVCLBQLSBSS-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(2-methyl-5-propan-2-ylpyrazol-3-yl)urea Chemical compound CN1N=C(C(C)C)C=C1NC(=O)NC1=CN=CC(C(=O)C2=C3C(N)=NC=NN3C(C(C)C)=C2)=C1 XLUCVCLBQLSBSS-UHFFFAOYSA-N 0.000 claims 1
- NJLDTRRPLUMIPI-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-(4-chlorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=C(Cl)C=C1 NJLDTRRPLUMIPI-UHFFFAOYSA-N 0.000 claims 1
- XSHPLAKMCBWMPR-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-[2-(trifluoromethyl)phenyl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=CC=C1C(F)(F)F XSHPLAKMCBWMPR-UHFFFAOYSA-N 0.000 claims 1
- IAPIEYZPBDFEHD-UHFFFAOYSA-N 1-[5-(4-amino-7-propan-2-ylpyrrolo[2,1-f][1,2,4]triazine-5-carbonyl)pyridin-3-yl]-3-[4-(dimethylamino)phenyl]urea Chemical compound C=12C(N)=NC=NN2C(C(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=C(N(C)C)C=C1 IAPIEYZPBDFEHD-UHFFFAOYSA-N 0.000 claims 1
- ZKXXMWLEMLPDGZ-UHFFFAOYSA-N 1-[5-[4-amino-7-[3-(dimethylamino)prop-1-ynyl]pyrrolo[2,1-f][1,2,4]triazine-5-carbonyl]pyridin-3-yl]-3-(2,4-dichlorophenyl)urea Chemical compound C=12C(N)=NC=NN2C(C#CCN(C)C)=CC=1C(=O)C(C=1)=CN=CC=1NC(=O)NC1=CC=C(Cl)C=C1Cl ZKXXMWLEMLPDGZ-UHFFFAOYSA-N 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 208000000172 Medulloblastoma Diseases 0.000 claims 1
- 208000034578 Multiple myelomas Diseases 0.000 claims 1
- 101100335081 Mus musculus Flt3 gene Proteins 0.000 claims 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 1
- 101150111783 NTRK1 gene Proteins 0.000 claims 1
- 101150117329 NTRK3 gene Proteins 0.000 claims 1
- 206010029260 Neuroblastoma Diseases 0.000 claims 1
- 101150056950 Ntrk2 gene Proteins 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 108091000080 Phosphotransferase Proteins 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- 201000004681 Psoriasis Diseases 0.000 claims 1
- 208000024770 Thyroid neoplasm Diseases 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 210000000481 breast Anatomy 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 201000010989 colorectal carcinoma Diseases 0.000 claims 1
- 208000021045 exocrine pancreatic carcinoma Diseases 0.000 claims 1
- 210000004907 gland Anatomy 0.000 claims 1
- 208000005017 glioblastoma Diseases 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004404 heteroalkyl group Chemical group 0.000 claims 1
- 210000002429 large intestine Anatomy 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 201000005296 lung carcinoma Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 210000001672 ovary Anatomy 0.000 claims 1
- 210000000496 pancreas Anatomy 0.000 claims 1
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 1
- 102000020233 phosphotransferase Human genes 0.000 claims 1
- 210000002307 prostate Anatomy 0.000 claims 1
- 108020003175 receptors Proteins 0.000 claims 1
- 102000005962 receptors Human genes 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73826905P | 2005-11-18 | 2005-11-18 | |
| US60/738,269 | 2005-11-18 | ||
| US11/560,378 | 2006-11-16 | ||
| US11/560,378 US7514435B2 (en) | 2005-11-18 | 2006-11-16 | Pyrrolotriazine kinase inhibitors |
| PCT/US2006/044756 WO2007061882A2 (en) | 2005-11-18 | 2006-11-17 | Pyrrolotriazine kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009515995A JP2009515995A (ja) | 2009-04-16 |
| JP2009515995A5 true JP2009515995A5 (enExample) | 2009-11-26 |
| JP5095626B2 JP5095626B2 (ja) | 2012-12-12 |
Family
ID=38051768
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008541376A Expired - Fee Related JP5095626B2 (ja) | 2005-11-18 | 2006-11-17 | ピロロトリアジンキナーゼ阻害剤 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7514435B2 (enExample) |
| EP (1) | EP1948664B1 (enExample) |
| JP (1) | JP5095626B2 (enExample) |
| KR (1) | KR101392678B1 (enExample) |
| CN (1) | CN101365701B (enExample) |
| AT (1) | ATE512151T1 (enExample) |
| AU (1) | AU2006318682B2 (enExample) |
| NO (1) | NO20082023L (enExample) |
| WO (1) | WO2007061882A2 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UY28931A1 (es) | 2004-06-03 | 2005-12-30 | Bayer Pharmaceuticals Corp | Derivados de pirrolotriazina utiles para tratar trastornos hiper-proliferativos y enfermedades asociadas con angiogenesis |
| BRPI0619146A2 (pt) | 2005-12-02 | 2011-09-13 | Bayer Pharmaceuticals Corp | derivados de 4-amino-pirroltriazina substituìda úteis no tratamento de disordens e doenças hiperproliferativas associadas com angiogênesis |
| PE20070855A1 (es) | 2005-12-02 | 2007-10-14 | Bayer Pharmaceuticals Corp | Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas |
| US8124759B2 (en) * | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
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| US7102002B2 (en) * | 2004-06-16 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
| US7102003B2 (en) * | 2004-07-01 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
| US7151176B2 (en) * | 2004-10-21 | 2006-12-19 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
| JP5116687B2 (ja) * | 2005-11-02 | 2013-01-09 | バイエル・ファルマ・アクチェンゲゼルシャフト | がんおよび他の過剰増殖性疾患の処置のためのピロロ［２，１−ｆ］［１，２，４］トリアジン−４−イルアミンＩＧＦ−１Ｒキナーゼ阻害剤 |
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- 2006-11-17 CN CN2006800513398A patent/CN101365701B/zh not_active Expired - Fee Related
- 2006-11-17 AT AT06837967T patent/ATE512151T1/de not_active IP Right Cessation
- 2006-11-17 WO PCT/US2006/044756 patent/WO2007061882A2/en not_active Ceased
- 2006-11-17 EP EP06837967A patent/EP1948664B1/en active Active
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