JP6038037B2 - キナーゼ活性を増加させるための化合物とその応用 - Google Patents
キナーゼ活性を増加させるための化合物とその応用 Download PDFInfo
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- JP6038037B2 JP6038037B2 JP2013538052A JP2013538052A JP6038037B2 JP 6038037 B2 JP6038037 B2 JP 6038037B2 JP 2013538052 A JP2013538052 A JP 2013538052A JP 2013538052 A JP2013538052 A JP 2013538052A JP 6038037 B2 JP6038037 B2 JP 6038037B2
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- Prior art keywords
- pyridin
- methyl
- ylamino
- phenoxy
- methylsulfonyl
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims description 66
- 230000000694 effects Effects 0.000 title claims description 13
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
- 229910052757 nitrogen Inorganic materials 0.000 claims description 46
- 108010021582 Glucokinase Proteins 0.000 claims description 38
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 29
- 125000003545 alkoxy group Chemical group 0.000 claims description 27
- 201000010099 disease Diseases 0.000 claims description 23
- 239000003814 drug Substances 0.000 claims description 22
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 21
- -1 6- (methoxymethyl) pyridin-3-yloxy Chemical group 0.000 claims description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
- 125000003342 alkenyl group Chemical group 0.000 claims description 15
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 125000000304 alkynyl group Chemical group 0.000 claims description 13
- 239000008194 pharmaceutical composition Substances 0.000 claims description 12
- 230000002265 prevention Effects 0.000 claims description 12
- 125000001188 haloalkyl group Chemical group 0.000 claims description 11
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 8
- 241001465754 Metazoa Species 0.000 claims description 7
- 208000008589 Obesity Diseases 0.000 claims description 7
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 7
- 235000020824 obesity Nutrition 0.000 claims description 7
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 125000004429 atom Chemical group 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 4
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 4
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 4
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 4
- VLNCVNYQKBAVSD-UHFFFAOYSA-N 1-[[2-(6-methylsulfonylpyridin-3-yl)oxy-5-(pyridin-2-ylamino)phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=CC=N1 VLNCVNYQKBAVSD-UHFFFAOYSA-N 0.000 claims description 3
- JJOGSDYXKYYTFL-UHFFFAOYSA-N 4-(4-methylsulfonylphenoxy)-3-n-(oxan-4-yl)-1-n-pyridin-2-ylbenzene-1,3-diamine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1OC(C(=C1)NC2CCOCC2)=CC=C1NC1=CC=CC=N1 JJOGSDYXKYYTFL-UHFFFAOYSA-N 0.000 claims description 3
- LJNHUGBNRAVAFO-UHFFFAOYSA-N 6-(4-methylsulfonylphenoxy)-5-(oxolan-3-ylmethyl)-n-pyridin-2-ylpyridin-3-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1OC(C(=C1)CC2COCC2)=NC=C1NC1=CC=CC=N1 LJNHUGBNRAVAFO-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000012453 solvate Substances 0.000 claims description 3
- LTVXRMDSQZMXSR-UHFFFAOYSA-N 1-[2-[[2-(4-methylsulfonylphenoxy)-5-(pyrazin-2-ylamino)phenyl]methyl]pyrrolidin-1-yl]ethanone Chemical compound CC(=O)N1CCCC1CC1=CC(NC=2N=CC=NC=2)=CC=C1OC1=CC=C(S(C)(=O)=O)C=C1 LTVXRMDSQZMXSR-UHFFFAOYSA-N 0.000 claims description 2
- HDCIFOMMIXJNQZ-UHFFFAOYSA-N 1-[2-[[2-(4-methylsulfonylphenoxy)-5-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenyl]methyl]pyrrolidin-1-yl]ethanone Chemical compound CC(=O)N1CCCC1CC1=CC(NC=2N=CC(=CC=2)C(F)(F)F)=CC=C1OC1=CC=C(S(C)(=O)=O)C=C1 HDCIFOMMIXJNQZ-UHFFFAOYSA-N 0.000 claims description 2
- GGFFJTWKEJFDFK-UHFFFAOYSA-N 1-[[2-(5-chloro-6-methylpyridin-3-yl)oxy-5-[(5-chloropyridin-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=C(Cl)C(C)=NC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(Cl)C=N1 GGFFJTWKEJFDFK-UHFFFAOYSA-N 0.000 claims description 2
- QUFOWARVMDUBPC-UHFFFAOYSA-N 1-[[2-(6-methylsulfonylpyridin-3-yl)oxy-5-(pyrazin-2-ylamino)phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CN=CC=N1 QUFOWARVMDUBPC-UHFFFAOYSA-N 0.000 claims description 2
- JVEAZPHPKYFEQV-UHFFFAOYSA-N 1-[[2-(6-methylsulfonylpyridin-3-yl)oxy-5-[(5-methyl-1,3-thiazol-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound S1C(C)=CN=C1NC(C=C1CN2C(CCC2)=O)=CC=C1OC1=CC=C(S(C)(=O)=O)N=C1 JVEAZPHPKYFEQV-UHFFFAOYSA-N 0.000 claims description 2
- ZLAKPJHVODSQLN-UHFFFAOYSA-N 1-[[2-(6-methylsulfonylpyridin-3-yl)oxy-5-[(5-phenylpyridin-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C=2C=CC=CC=2)C=N1 ZLAKPJHVODSQLN-UHFFFAOYSA-N 0.000 claims description 2
- QJMOGGHSUCRKLB-UHFFFAOYSA-N 1-[[2-(6-methylsulfonylpyridin-3-yl)oxy-5-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C(F)(F)F)C=N1 QJMOGGHSUCRKLB-UHFFFAOYSA-N 0.000 claims description 2
- MKUVNIYWWVEOGR-UHFFFAOYSA-N 1-[[2-(6-morpholin-4-ylsulfonylpyridin-3-yl)oxy-5-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenyl]methyl]pyrrolidin-2-one Chemical compound N1=CC(C(F)(F)F)=CC=C1NC(C=C1CN2C(CCC2)=O)=CC=C1OC1=CC=C(S(=O)(=O)N2CCOCC2)N=C1 MKUVNIYWWVEOGR-UHFFFAOYSA-N 0.000 claims description 2
- INHBBNSVPHXBTC-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-(pyrazin-2-ylamino)phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CN=CC=N1 INHBBNSVPHXBTC-UHFFFAOYSA-N 0.000 claims description 2
- LJSXFMKJRNWTBT-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-(pyridin-2-ylamino)phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=CC=N1 LJSXFMKJRNWTBT-UHFFFAOYSA-N 0.000 claims description 2
- ZEZWUIDOZZEYLK-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-[(5-methyl-1,3-thiazol-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=NC=C(C)S1 ZEZWUIDOZZEYLK-UHFFFAOYSA-N 0.000 claims description 2
- WNWKDPVHKWIRKI-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-[(5-methylpyridin-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C)C=N1 WNWKDPVHKWIRKI-UHFFFAOYSA-N 0.000 claims description 2
- LPSBJYKYVDWTGE-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-[(5-phenylpyridin-2-yl)amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C=2C=CC=CC=2)C=N1 LPSBJYKYVDWTGE-UHFFFAOYSA-N 0.000 claims description 2
- UNKRZHQNKZUENO-UHFFFAOYSA-N 1-[[2-[6-(methoxymethyl)pyridin-3-yl]oxy-5-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C(F)(F)F)C=N1 UNKRZHQNKZUENO-UHFFFAOYSA-N 0.000 claims description 2
- ZMFFIGGQSFTJIM-UHFFFAOYSA-N 1-[[5-(1h-imidazol-5-ylamino)-2-(6-methylsulfonylpyridin-3-yl)oxyphenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CNC=N1 ZMFFIGGQSFTJIM-UHFFFAOYSA-N 0.000 claims description 2
- BNAWXFBWNNQVHB-UHFFFAOYSA-N 1-[[5-(1h-imidazol-5-ylamino)-2-[6-(methoxymethyl)pyridin-3-yl]oxyphenyl]methyl]pyrrolidin-2-one Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CNC=N1 BNAWXFBWNNQVHB-UHFFFAOYSA-N 0.000 claims description 2
- WLLRTWTWIVPGKA-UHFFFAOYSA-N 1-[[5-[(5-methoxypyridin-2-yl)amino]-2-(6-methylsulfonylpyridin-3-yl)oxyphenyl]methyl]pyrrolidin-2-one Chemical compound N1=CC(OC)=CC=C1NC(C=C1CN2C(CCC2)=O)=CC=C1OC1=CC=C(S(C)(=O)=O)N=C1 WLLRTWTWIVPGKA-UHFFFAOYSA-N 0.000 claims description 2
- LRLIZXVXQXACEY-UHFFFAOYSA-N 1-[[5-[(5-methylpyridin-2-yl)amino]-2-(6-methylsulfonylpyridin-3-yl)oxyphenyl]methyl]pyrrolidin-2-one Chemical compound N1=CC(C)=CC=C1NC(C=C1CN2C(CCC2)=O)=CC=C1OC1=CC=C(S(C)(=O)=O)N=C1 LRLIZXVXQXACEY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- DSRLBHGRJVWYKJ-UHFFFAOYSA-N 2-[6-[3-[(1-acetylpyrrolidin-2-yl)methyl]-4-[4-(dimethylcarbamoyl)phenoxy]anilino]pyridin-3-yl]acetic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2N(CCC2)C(C)=O)=CC=C1NC1=CC=C(CC(O)=O)C=N1 DSRLBHGRJVWYKJ-UHFFFAOYSA-N 0.000 claims description 2
- QXFMFGSNQRBBRR-UHFFFAOYSA-N 2-[6-[4-(6-methylsulfonylpyridin-3-yl)oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]acetic acid Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CC(O)=O)C=N1 QXFMFGSNQRBBRR-UHFFFAOYSA-N 0.000 claims description 2
- CFKMLKZFSOJNHJ-UHFFFAOYSA-N 2-[6-[4-[4-(dimethylcarbamoyl)phenoxy]-3-(oxan-4-ylmethyl)anilino]pyridin-3-yl]acetic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2CCOCC2)=CC=C1NC1=CC=C(CC(O)=O)C=N1 CFKMLKZFSOJNHJ-UHFFFAOYSA-N 0.000 claims description 2
- FUJWNXLHPIKXCY-UHFFFAOYSA-N 2-[6-[4-[6-(dimethylcarbamoyl)pyridin-3-yl]oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]acetic acid Chemical compound C1=NC(C(=O)N(C)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CC(O)=O)C=N1 FUJWNXLHPIKXCY-UHFFFAOYSA-N 0.000 claims description 2
- VEQNMWXAZFNTKD-UHFFFAOYSA-N 2-[6-[4-[6-(methoxymethyl)pyridin-3-yl]oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]acetic acid Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CC(O)=O)C=N1 VEQNMWXAZFNTKD-UHFFFAOYSA-N 0.000 claims description 2
- VJFGMLNMDJEWFQ-UHFFFAOYSA-N 2-[6-[[6-[4-(dimethylcarbamoyl)phenoxy]-5-(oxolan-3-ylmethyl)pyridin-3-yl]amino]pyridin-3-yl]acetic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2COCC2)=NC=C1NC1=CC=C(CC(O)=O)C=N1 VJFGMLNMDJEWFQ-UHFFFAOYSA-N 0.000 claims description 2
- BDXJTQWQCQIXNA-UHFFFAOYSA-N 3-[6-[3-[(1-acetylpyrrolidin-2-yl)methyl]-4-[4-(dimethylcarbamoyl)phenoxy]anilino]pyridin-3-yl]propanoic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2N(CCC2)C(C)=O)=CC=C1NC1=CC=C(CCC(O)=O)C=N1 BDXJTQWQCQIXNA-UHFFFAOYSA-N 0.000 claims description 2
- AXXRMULPISHBIZ-UHFFFAOYSA-N 3-[6-[4-(6-methylsulfonylpyridin-3-yl)oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]propanoic acid Chemical compound C1=NC(S(=O)(=O)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CCC(O)=O)C=N1 AXXRMULPISHBIZ-UHFFFAOYSA-N 0.000 claims description 2
- YGBNRXAQPZYEHV-UHFFFAOYSA-N 3-[6-[4-[4-(dimethylcarbamoyl)phenoxy]-3-(oxan-4-ylmethyl)anilino]pyridin-3-yl]propanoic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2CCOCC2)=CC=C1NC1=CC=C(CCC(O)=O)C=N1 YGBNRXAQPZYEHV-UHFFFAOYSA-N 0.000 claims description 2
- UQGGNOAQMJSJGS-UHFFFAOYSA-N 3-[6-[4-[6-(dimethylcarbamoyl)pyridin-3-yl]oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]propanoic acid Chemical compound C1=NC(C(=O)N(C)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CCC(O)=O)C=N1 UQGGNOAQMJSJGS-UHFFFAOYSA-N 0.000 claims description 2
- APMAUEXRWGWXEZ-UHFFFAOYSA-N 3-[6-[4-[6-(methoxymethyl)pyridin-3-yl]oxy-3-[(2-oxopyrrolidin-1-yl)methyl]anilino]pyridin-3-yl]propanoic acid Chemical compound C1=NC(COC)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(CCC(O)=O)C=N1 APMAUEXRWGWXEZ-UHFFFAOYSA-N 0.000 claims description 2
- XUCDRHIBIXMSCU-UHFFFAOYSA-N 3-[6-[[6-[4-(dimethylcarbamoyl)phenoxy]-5-(oxolan-3-ylmethyl)pyridin-3-yl]amino]pyridin-3-yl]propanoic acid Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2COCC2)=NC=C1NC1=CC=C(CCC(O)=O)C=N1 XUCDRHIBIXMSCU-UHFFFAOYSA-N 0.000 claims description 2
- BAVATAKQLFMZSI-UHFFFAOYSA-N 3-[[2-(4-methylsulfonylphenoxy)-5-(pyrazin-2-ylamino)phenyl]methyl]cyclopentan-1-one Chemical compound C1=CC(S(=O)(=O)C)=CC=C1OC(C(=C1)CC2CC(=O)CC2)=CC=C1NC1=CN=CC=N1 BAVATAKQLFMZSI-UHFFFAOYSA-N 0.000 claims description 2
- UMXOMJUHDJQIML-UHFFFAOYSA-N 3-[[2-(4-methylsulfonylphenoxy)-5-[(5-methyl-1,3-thiazol-2-yl)amino]phenyl]methyl]cyclopentan-1-one Chemical compound S1C(C)=CN=C1NC(C=C1CC2CC(=O)CC2)=CC=C1OC1=CC=C(S(C)(=O)=O)C=C1 UMXOMJUHDJQIML-UHFFFAOYSA-N 0.000 claims description 2
- ZEQHSWVZIZHZGM-UHFFFAOYSA-N 3-[[2-(4-methylsulfonylphenoxy)-5-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenyl]methyl]cyclopentan-1-one Chemical compound C1=CC(S(=O)(=O)C)=CC=C1OC(C(=C1)CC2CC(=O)CC2)=CC=C1NC1=CC=C(C(F)(F)F)C=N1 ZEQHSWVZIZHZGM-UHFFFAOYSA-N 0.000 claims description 2
- LWRBCBWRGYXKQJ-UHFFFAOYSA-N 4-(4-methylsulfonylphenoxy)-3-n-(oxan-4-yl)-1-n-[5-(trifluoromethyl)pyridin-2-yl]benzene-1,3-diamine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1OC(C(=C1)NC2CCOCC2)=CC=C1NC1=CC=C(C(F)(F)F)C=N1 LWRBCBWRGYXKQJ-UHFFFAOYSA-N 0.000 claims description 2
- SGBSEWKVQLFXDI-UHFFFAOYSA-N 4-[2-[(1-acetylpyrrolidin-2-yl)methyl]-4-(pyrazin-2-ylamino)phenoxy]-n,n-dimethylbenzamide Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2N(CCC2)C(C)=O)=CC=C1NC1=CN=CC=N1 SGBSEWKVQLFXDI-UHFFFAOYSA-N 0.000 claims description 2
- AGFWNTDVNNXOAL-UHFFFAOYSA-N 4-[2-[(1-acetylpyrrolidin-2-yl)methyl]-4-[[5-(trifluoromethyl)pyridin-2-yl]amino]phenoxy]-n,n-dimethylbenzamide Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2N(CCC2)C(C)=O)=CC=C1NC1=CC=C(C(F)(F)F)C=N1 AGFWNTDVNNXOAL-UHFFFAOYSA-N 0.000 claims description 2
- OHJOPXBCGXRBRD-UHFFFAOYSA-N 4-[4-(1h-imidazol-5-ylamino)-2-(oxan-4-ylmethyl)phenoxy]-n,n-dimethylbenzamide Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2CCOCC2)=CC=C1NC1=CNC=N1 OHJOPXBCGXRBRD-UHFFFAOYSA-N 0.000 claims description 2
- DXQLXRKGTSAGGN-UHFFFAOYSA-N 4-[4-(1h-imidazol-5-ylamino)-2-[(3-oxocyclopentyl)methyl]phenoxy]-n,n-dimethylbenzamide Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2CC(=O)CC2)=CC=C1NC1=CNC=N1 DXQLXRKGTSAGGN-UHFFFAOYSA-N 0.000 claims description 2
- BFEISNSIJOLCQI-UHFFFAOYSA-N 4-[5-[(5-cyanopyridin-2-yl)amino]-3-(oxolan-3-ylmethyl)pyridin-2-yl]oxy-n,n-dimethylbenzamide Chemical compound C1=CC(C(=O)N(C)C)=CC=C1OC(C(=C1)CC2COCC2)=NC=C1NC1=CC=C(C#N)C=N1 BFEISNSIJOLCQI-UHFFFAOYSA-N 0.000 claims description 2
- QBPJGNLJRBLHIH-UHFFFAOYSA-N 5-[4-(1h-imidazol-5-ylamino)-2-[(2-oxopyrrolidin-1-yl)methyl]phenoxy]-n,n-dimethylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)N(C)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CNC=N1 QBPJGNLJRBLHIH-UHFFFAOYSA-N 0.000 claims description 2
- DSYNIKWVJPVBSO-UHFFFAOYSA-N 5-[4-[(5-cyanopyridin-2-yl)amino]-2-[(2-oxopyrrolidin-1-yl)methyl]phenoxy]-n,n-dimethylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)N(C)C)=CC=C1OC(C(=C1)CN2C(CCC2)=O)=CC=C1NC1=CC=C(C#N)C=N1 DSYNIKWVJPVBSO-UHFFFAOYSA-N 0.000 claims description 2
- OAMYWEBCPWCKBQ-UHFFFAOYSA-N 5-[4-[(5-methoxypyridin-2-yl)amino]-2-[(2-oxopyrrolidin-1-yl)methyl]phenoxy]-n,n-dimethylpyridine-2-carboxamide Chemical compound N1=CC(OC)=CC=C1NC(C=C1CN2C(CCC2)=O)=CC=C1OC1=CC=C(C(=O)N(C)C)N=C1 OAMYWEBCPWCKBQ-UHFFFAOYSA-N 0.000 claims description 2
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Images
Classifications
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- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/08—1,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
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- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Epidemiology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201010535640.4 | 2010-11-09 | ||
| CN201010535640 | 2010-11-09 | ||
| PCT/CN2011/082004 WO2012062210A1 (en) | 2010-11-09 | 2011-11-09 | Compound for increasing kinase active and application thereof |
Publications (3)
| Publication Number | Publication Date |
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| JP2014500252A JP2014500252A (ja) | 2014-01-09 |
| JP2014500252A5 JP2014500252A5 (enExample) | 2014-12-25 |
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| SG (2) | SG10201509157QA (enExample) |
| WO (1) | WO2012062210A1 (enExample) |
Families Citing this family (1)
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| CN118234867A (zh) | 2021-09-17 | 2024-06-21 | 旗舰创业创新六公司 | 用于产生环状多核糖核苷酸的组合物和方法 |
Family Cites Families (15)
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| DE3632042A1 (de) * | 1986-03-08 | 1987-09-10 | Bayer Ag | Diarylsulfidderivate |
| JPS62212378A (ja) * | 1986-03-08 | 1987-09-18 | バイエル・アクチエンゲゼルシヤフト | ジアリ−ルスルフイド誘導体 |
| US6719520B2 (en) | 1998-10-08 | 2004-04-13 | Smithkline Beecham Corporation | Method and compounds |
| DE69922526T2 (de) * | 1998-10-08 | 2005-06-02 | Smithkline Beecham Plc, Brentford | 3-(3-chloro-4-hydroxyphenylamino)-4-(2-nitrophenyl)-1h-pyrrol-2,5-dion als glykogen synthase kinase-3 inhibitor (gsk-3) |
| UA71945C2 (en) * | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
| EP1127882A1 (en) * | 2000-01-25 | 2001-08-29 | Pfizer Products Inc. | Tetrazole compounds as thyroid receptor ligands |
| GB0008264D0 (en) * | 2000-04-04 | 2000-05-24 | Smithkline Beecham Plc | Novel method and compounds |
| JP3598994B2 (ja) * | 2000-07-10 | 2004-12-08 | セイコーエプソン株式会社 | 電気光学装置の製造方法 |
| ATE330956T1 (de) * | 2001-04-13 | 2006-07-15 | Pfizer Prod Inc | Bizyklisch substituierte 4- aminopyridopyrimidinderivate |
| WO2003026666A1 (en) * | 2001-09-26 | 2003-04-03 | Bayer Pharmaceuticals Corporation | 2-phenylamino-4- (5-pyrazolylamino)-pyrimidine derivatives as kinase inhibitors, in particular, as src kinase inhibitors |
| DE10153396A1 (de) | 2001-11-01 | 2003-05-28 | Siemens Ag | Einrichtung zur Ansteuerung einer elektrischen Kraftstoffpumpe |
| BRPI0411867A (pt) * | 2003-07-09 | 2006-08-08 | Hoffmann La Roche | tiofenilaminoimidazolinas |
| KR20070083939A (ko) * | 2004-11-02 | 2007-08-24 | 반유 세이야꾸 가부시끼가이샤 | 아릴옥시 치환된 벤즈이미다졸 유도체 |
| JP2010540460A (ja) * | 2007-09-24 | 2010-12-24 | トラガラ ファーマシューティカルズ,インク. | COX‐2阻害薬と抗HER2[ErbB2]抗体の混合物又はCOX‐2阻害薬とHER2[ErbB2]受容体チロシンキナーゼ阻害薬の混合物を用いた癌の治療 |
| US8377924B2 (en) * | 2009-01-21 | 2013-02-19 | Rigel Pharmaceuticals Inc. | Protein kinase C inhibitors and uses thereof |
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2011
- 2011-11-09 KR KR1020157025687A patent/KR101643721B1/ko active Active
- 2011-11-09 WO PCT/CN2011/082004 patent/WO2012062210A1/en not_active Ceased
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- 2011-11-09 JP JP2013538052A patent/JP6038037B2/ja active Active
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Also Published As
| Publication number | Publication date |
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| EP2638036A4 (en) | 2014-09-03 |
| KR20140016245A (ko) | 2014-02-07 |
| WO2012062210A1 (en) | 2012-05-18 |
| CN103502244A (zh) | 2014-01-08 |
| JP2014500252A (ja) | 2014-01-09 |
| KR101643721B1 (ko) | 2016-07-28 |
| EP2638036A1 (en) | 2013-09-18 |
| AU2011328673A1 (en) | 2013-07-04 |
| SG10201509157QA (en) | 2015-12-30 |
| EP2638036B1 (en) | 2017-08-16 |
| US20130225587A1 (en) | 2013-08-29 |
| AU2011328673B2 (en) | 2016-02-25 |
| CN103502244B (zh) | 2014-10-08 |
| AU2011328673A8 (en) | 2013-07-25 |
| KR20150109501A (ko) | 2015-10-01 |
| SG190784A1 (en) | 2013-07-31 |
| US9409900B2 (en) | 2016-08-09 |
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