JP2011509280A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011509280A5 JP2011509280A5 JP2010541800A JP2010541800A JP2011509280A5 JP 2011509280 A5 JP2011509280 A5 JP 2011509280A5 JP 2010541800 A JP2010541800 A JP 2010541800A JP 2010541800 A JP2010541800 A JP 2010541800A JP 2011509280 A5 JP2011509280 A5 JP 2011509280A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- benzamide
- phenylamino
- phenyl
- diethylamino
- 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
Links
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 43
- 150000001875 compounds Chemical class 0.000 claims 31
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 16
- 201000010099 disease Diseases 0.000 claims 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 14
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 239000003795 chemical substances by application Substances 0.000 claims 11
- 229910052757 nitrogen Inorganic materials 0.000 claims 11
- 125000005843 halogen group Chemical group 0.000 claims 9
- 125000004432 carbon atom Chemical group C* 0.000 claims 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims 5
- -1 4-diethylaminomethyl- [1,2,3] triazol-1-yl Chemical group 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims 2
- USZCQHMQZZEHAM-UHFFFAOYSA-N 2-[2-(diethylamino)ethylamino]-n-pyridin-4-ylbenzamide Chemical compound CCN(CC)CCNC1=CC=CC=C1C(=O)NC1=CC=NC=C1 USZCQHMQZZEHAM-UHFFFAOYSA-N 0.000 claims 2
- 206010006187 Breast cancer Diseases 0.000 claims 2
- 208000026310 Breast neoplasm Diseases 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 206010013801 Duchenne Muscular Dystrophy Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 2
- 206010060862 Prostate cancer Diseases 0.000 claims 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 2
- 208000002495 Uterine Neoplasms Diseases 0.000 claims 2
- 230000032683 aging Effects 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 208000029742 colonic neoplasm Diseases 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 230000003834 intracellular effect Effects 0.000 claims 2
- 201000007270 liver cancer Diseases 0.000 claims 2
- 208000014018 liver neoplasm Diseases 0.000 claims 2
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 2
- 208000037819 metastatic cancer Diseases 0.000 claims 2
- 208000011575 metastatic malignant neoplasm Diseases 0.000 claims 2
- 230000035772 mutation Effects 0.000 claims 2
- NOCSCLVSJBOTTB-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-3-[3-[(3-methoxybenzoyl)amino]anilino]benzamide Chemical compound CCN(CC)CCCNC(=O)C1=CC=CC(NC=2C=C(NC(=O)C=3C=C(OC)C=CC=3)C=CC=2)=C1 NOCSCLVSJBOTTB-UHFFFAOYSA-N 0.000 claims 2
- 230000007171 neuropathology Effects 0.000 claims 2
- 229960003966 nicotinamide Drugs 0.000 claims 2
- 239000011570 nicotinamide Substances 0.000 claims 2
- 201000002528 pancreatic cancer Diseases 0.000 claims 2
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 claims 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 2
- 206010046766 uterine cancer Diseases 0.000 claims 2
- NMQCPIGNFXJPNZ-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCCN2C=NC=C2)=C1 NMQCPIGNFXJPNZ-UHFFFAOYSA-N 0.000 claims 1
- GNJQUDMOXXKPIX-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-(4-methoxyphenyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC(=O)C1=CC=CC=C1NCCCN1C=NC=C1 GNJQUDMOXXKPIX-UHFFFAOYSA-N 0.000 claims 1
- SJEYVWNLCVTNLP-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)C1=CC=CC=C1NCCCN1C=NC=C1 SJEYVWNLCVTNLP-UHFFFAOYSA-N 0.000 claims 1
- OQDNVIOBMWGPRV-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)C1=CC=CN=C1NCCCN1C=NC=C1 OQDNVIOBMWGPRV-UHFFFAOYSA-N 0.000 claims 1
- LTPCCUQYOBVIRZ-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-pyridin-4-ylbenzamide Chemical compound C=1C=CC=C(NCCCN2C=NC=C2)C=1C(=O)NC1=CC=NC=C1 LTPCCUQYOBVIRZ-UHFFFAOYSA-N 0.000 claims 1
- KMWYKVYOUACXOJ-UHFFFAOYSA-N 2-(3-imidazol-1-ylpropylamino)-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound C=1C=CN=C(NCCCN2C=NC=C2)C=1C(=O)NC1=CC=NC=C1 KMWYKVYOUACXOJ-UHFFFAOYSA-N 0.000 claims 1
- WYLLXNFJCIEZGL-UHFFFAOYSA-N 2-(4-hydroxybutylamino)-n-(3-methoxyphenyl)benzamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=CC=CC=2)NCCCCO)=C1 WYLLXNFJCIEZGL-UHFFFAOYSA-N 0.000 claims 1
- KGFLIMXLAWGSBC-UHFFFAOYSA-N 2-(4-hydroxybutylamino)-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCCCO)=C1 KGFLIMXLAWGSBC-UHFFFAOYSA-N 0.000 claims 1
- XFKRBVLYOLMZNC-UHFFFAOYSA-N 2-(4-hydroxybutylamino)-n-(4-methoxyphenyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC(=O)C1=CC=CC=C1NCCCCO XFKRBVLYOLMZNC-UHFFFAOYSA-N 0.000 claims 1
- WZBFHKXPCGPMBM-UHFFFAOYSA-N 2-(4-hydroxybutylamino)-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound OCCCCNC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 WZBFHKXPCGPMBM-UHFFFAOYSA-N 0.000 claims 1
- DYPFRGBASAWOEN-UHFFFAOYSA-N 2-(4-hydroxybutylamino)-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound OCCCCNC1=NC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 DYPFRGBASAWOEN-UHFFFAOYSA-N 0.000 claims 1
- JFFIHEJJKXROJR-UHFFFAOYSA-N 2-(5-hydroxypentylamino)-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCCCCO)=C1 JFFIHEJJKXROJR-UHFFFAOYSA-N 0.000 claims 1
- REGHLIZBPJTLDX-UHFFFAOYSA-N 2-(6-aminohexylamino)-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCCCCCN)=C1 REGHLIZBPJTLDX-UHFFFAOYSA-N 0.000 claims 1
- DBRLDAZIPHQPNA-UHFFFAOYSA-N 2-(6-aminohexylamino)-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound NCCCCCCNC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 DBRLDAZIPHQPNA-UHFFFAOYSA-N 0.000 claims 1
- QGUGGCODWYLPCV-UHFFFAOYSA-N 2-[2-(diethylamino)ethylamino]-n-(3-methoxyphenyl)benzamide Chemical compound CCN(CC)CCNC1=CC=CC=C1C(=O)NC1=CC=CC(OC)=C1 QGUGGCODWYLPCV-UHFFFAOYSA-N 0.000 claims 1
- YMTWNLGBVZGFCB-UHFFFAOYSA-N 2-[2-(diethylamino)ethylamino]-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound CCN(CC)CCNC1=NC=CC=C1C(=O)NC1=CC=CC(OC)=C1 YMTWNLGBVZGFCB-UHFFFAOYSA-N 0.000 claims 1
- ZHRFWLXMFRPTAA-UHFFFAOYSA-N 2-[2-(diethylamino)ethylamino]-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound CCN(CC)CCNC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 ZHRFWLXMFRPTAA-UHFFFAOYSA-N 0.000 claims 1
- HXIOZFFLVOUFPT-UHFFFAOYSA-N 2-[2-(diethylamino)ethylamino]-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound CCN(CC)CCNC1=NC=CC=C1C(=O)NC1=CC=NC=C1 HXIOZFFLVOUFPT-UHFFFAOYSA-N 0.000 claims 1
- FNOJGPGVTOCRRD-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-(3-methoxyphenyl)benzamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=CC=CC=2)NCCN(C)C)=C1 FNOJGPGVTOCRRD-UHFFFAOYSA-N 0.000 claims 1
- TXQLNHYTRZUJGM-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCN(C)C)=C1 TXQLNHYTRZUJGM-UHFFFAOYSA-N 0.000 claims 1
- JIBVWNRZPCYONC-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-(4-methoxyphenyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC(=O)C1=CC=CC=C1NCCN(C)C JIBVWNRZPCYONC-UHFFFAOYSA-N 0.000 claims 1
- RHODVADTHOPEOS-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-(4-methoxyphenyl)pyridine-3-carboxamide Chemical compound C1=CC(OC)=CC=C1NC(=O)C1=CC=CN=C1NCCN(C)C RHODVADTHOPEOS-UHFFFAOYSA-N 0.000 claims 1
- QNRFETAIXFVWEM-UHFFFAOYSA-N 2-[2-(dimethylamino)ethylamino]-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound CN(C)CCNC1=NC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 QNRFETAIXFVWEM-UHFFFAOYSA-N 0.000 claims 1
- YEBCJENRTNXSSZ-UHFFFAOYSA-N 2-[3-(diethylamino)propylamino]-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound CCN(CC)CCCNC1=NC=CC=C1C(=O)NC1=CC=CC(OC)=C1 YEBCJENRTNXSSZ-UHFFFAOYSA-N 0.000 claims 1
- UOJNSUFAUJMTHW-UHFFFAOYSA-N 2-[3-(diethylamino)propylamino]-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound CCN(CC)CCCNC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 UOJNSUFAUJMTHW-UHFFFAOYSA-N 0.000 claims 1
- BRZATTRACHIJHI-UHFFFAOYSA-N 2-[3-(diethylamino)propylamino]-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound CCN(CC)CCCNC1=NC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 BRZATTRACHIJHI-UHFFFAOYSA-N 0.000 claims 1
- UKJMANVTJCAMAT-UHFFFAOYSA-N 2-[3-(diethylamino)propylamino]-n-pyridin-4-ylbenzamide Chemical compound CCN(CC)CCCNC1=CC=CC=C1C(=O)NC1=CC=NC=C1 UKJMANVTJCAMAT-UHFFFAOYSA-N 0.000 claims 1
- ZREMPGYRQSWPTH-UHFFFAOYSA-N 2-[3-(diethylamino)propylamino]-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound CCN(CC)CCCNC1=NC=CC=C1C(=O)NC1=CC=NC=C1 ZREMPGYRQSWPTH-UHFFFAOYSA-N 0.000 claims 1
- LANZFGWNGPWWNO-UHFFFAOYSA-N 2-[3-(dimethylamino)propylamino]-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)NCCCN(C)C)=C1 LANZFGWNGPWWNO-UHFFFAOYSA-N 0.000 claims 1
- VTXKUAGOFKFCNL-UHFFFAOYSA-N 2-[3-(dimethylamino)propylamino]-n-(4-methoxyphenyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC(=O)C1=CC=CC=C1NCCCN(C)C VTXKUAGOFKFCNL-UHFFFAOYSA-N 0.000 claims 1
- OUZLNSLVSSRMNU-UHFFFAOYSA-N 2-[3-(dimethylamino)propylamino]-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound CN(C)CCCNC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 OUZLNSLVSSRMNU-UHFFFAOYSA-N 0.000 claims 1
- RRFODRCTTKIXJQ-UHFFFAOYSA-N 2-[3-(dimethylamino)propylamino]-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound CN(C)CCCNC1=NC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 RRFODRCTTKIXJQ-UHFFFAOYSA-N 0.000 claims 1
- IAFAOPWJFZTZQK-UHFFFAOYSA-N 2-[3-(dimethylamino)propylamino]-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound CN(C)CCCNC1=NC=CC=C1C(=O)NC1=CC=NC=C1 IAFAOPWJFZTZQK-UHFFFAOYSA-N 0.000 claims 1
- WJGLFEUAYGIPRN-UHFFFAOYSA-N 2-[4-(dimethylamino)anilino]-n-(3-imidazol-1-ylpropyl)benzamide Chemical compound C1=CC(N(C)C)=CC=C1NC1=CC=CC=C1C(=O)NCCCN1C=NC=C1 WJGLFEUAYGIPRN-UHFFFAOYSA-N 0.000 claims 1
- RWRPQAAVWLLUAU-UHFFFAOYSA-N 2-[5-(diethylamino)pentan-2-ylamino]-n-(3-methoxyphenyl)benzamide Chemical compound CCN(CC)CCCC(C)NC1=CC=CC=C1C(=O)NC1=CC=CC(OC)=C1 RWRPQAAVWLLUAU-UHFFFAOYSA-N 0.000 claims 1
- GYNKBIZJQNDMGT-UHFFFAOYSA-N 2-[5-(diethylamino)pentan-2-ylamino]-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound CCN(CC)CCCC(C)NC1=CC=CC=C1C(=O)NC1=CC=C(OC(F)(F)F)C=C1 GYNKBIZJQNDMGT-UHFFFAOYSA-N 0.000 claims 1
- KJBDNSBCXSIQMA-UHFFFAOYSA-N 2-bromo-N-(3-methoxyphenyl)benzamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=CC=CC=2)Br)=C1 KJBDNSBCXSIQMA-UHFFFAOYSA-N 0.000 claims 1
- AKEQDKIMDBCGSA-UHFFFAOYSA-N 2-bromo-n-[4-(dimethylamino)phenyl]benzamide Chemical compound C1=CC(N(C)C)=CC=C1NC(=O)C1=CC=CC=C1Br AKEQDKIMDBCGSA-UHFFFAOYSA-N 0.000 claims 1
- PAFQKZAUYMWWHG-UHFFFAOYSA-N 2-bromo-n-[4-(trifluoromethoxy)phenyl]benzamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)C1=CC=CC=C1Br PAFQKZAUYMWWHG-UHFFFAOYSA-N 0.000 claims 1
- REDJPCIUXHKTFR-UHFFFAOYSA-N 2-bromo-n-pyridin-4-ylbenzamide Chemical compound BrC1=CC=CC=C1C(=O)NC1=CC=NC=C1 REDJPCIUXHKTFR-UHFFFAOYSA-N 0.000 claims 1
- CVCAWLQDFRMHFV-UHFFFAOYSA-N 2-chloro-n-(3-methoxyphenyl)pyridine-3-carboxamide Chemical compound COC1=CC=CC(NC(=O)C=2C(=NC=CC=2)Cl)=C1 CVCAWLQDFRMHFV-UHFFFAOYSA-N 0.000 claims 1
- WGNNXHGHEGCGDV-UHFFFAOYSA-N 2-chloro-n-[4-(dimethylamino)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(N(C)C)=CC=C1NC(=O)C1=CC=CN=C1Cl WGNNXHGHEGCGDV-UHFFFAOYSA-N 0.000 claims 1
- SHMTXVLNVCIHGF-UHFFFAOYSA-N 2-chloro-n-[4-(trifluoromethoxy)phenyl]pyridine-3-carboxamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)C1=CC=CN=C1Cl SHMTXVLNVCIHGF-UHFFFAOYSA-N 0.000 claims 1
- YMMKGFFYVNSGPC-UHFFFAOYSA-N 2-chloro-n-pyridin-4-ylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=NC=C1 YMMKGFFYVNSGPC-UHFFFAOYSA-N 0.000 claims 1
- GNISBZMJFHJXNU-MDZDMXLPSA-N 3-[1-[3-[3-[(e)-2-pyridin-4-ylethenyl]anilino]phenyl]triazol-4-yl]propan-1-ol Chemical compound N1=NC(CCCO)=CN1C1=CC=CC(NC=2C=C(\C=C\C=3C=CN=CC=3)C=CC=2)=C1 GNISBZMJFHJXNU-MDZDMXLPSA-N 0.000 claims 1
- DIIZSPAUXGEYBF-UHFFFAOYSA-N 3-[1-[3-[4-(dimethylamino)anilino]phenyl]triazol-4-yl]propan-1-ol Chemical compound C1=CC(N(C)C)=CC=C1NC1=CC=CC(N2N=NC(CCCO)=C2)=C1 DIIZSPAUXGEYBF-UHFFFAOYSA-N 0.000 claims 1
- VHXLOICSLKMMJZ-UHFFFAOYSA-N 3-[1-[3-[4-(trifluoromethoxy)anilino]phenyl]triazol-4-yl]propan-1-ol Chemical compound N1=NC(CCCO)=CN1C1=CC=CC(NC=2C=CC(OC(F)(F)F)=CC=2)=C1 VHXLOICSLKMMJZ-UHFFFAOYSA-N 0.000 claims 1
- QDVCMXVFTFQFBN-VOTSOKGWSA-N 3-[1-[3-[4-[(e)-2-pyridin-4-ylethenyl]anilino]phenyl]triazol-4-yl]propan-1-ol Chemical compound N1=NC(CCCO)=CN1C1=CC=CC(NC=2C=CC(\C=C\C=3C=CN=CC=3)=CC=2)=C1 QDVCMXVFTFQFBN-VOTSOKGWSA-N 0.000 claims 1
- RYZMHJCWSQMDPT-UHFFFAOYSA-N 3-[1-[4-(4-methoxyanilino)phenyl]triazol-4-yl]propan-1-ol Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(N2N=NC(CCCO)=C2)C=C1 RYZMHJCWSQMDPT-UHFFFAOYSA-N 0.000 claims 1
- VOQKSODWFALURE-ONEGZZNKSA-N 3-[1-[4-[4-[(e)-2-pyridin-4-ylethenyl]anilino]phenyl]triazol-4-yl]propan-1-ol Chemical compound N1=NC(CCCO)=CN1C(C=C1)=CC=C1NC(C=C1)=CC=C1\C=C\C1=CC=NC=C1 VOQKSODWFALURE-ONEGZZNKSA-N 0.000 claims 1
- QSAZGUXUFYSUFB-UHFFFAOYSA-N 3-[4-[(3-methoxybenzoyl)amino]anilino]-n-(3-methylbutyl)benzamide Chemical compound COC1=CC=CC(C(=O)NC=2C=CC(NC=3C=C(C=CC=3)C(=O)NCCC(C)C)=CC=2)=C1 QSAZGUXUFYSUFB-UHFFFAOYSA-N 0.000 claims 1
- UEUHRHHHIWCCFK-UHFFFAOYSA-N 3-[4-[diethylamino(methyl)amino]triazol-1-yl]-n-(4-methoxyphenyl)aniline Chemical compound N1=NC(N(C)N(CC)CC)=CN1C1=CC=CC(NC=2C=CC(OC)=CC=2)=C1 UEUHRHHHIWCCFK-UHFFFAOYSA-N 0.000 claims 1
- ZEJFPRRKAYPBRR-UHFFFAOYSA-N 3-methoxy-n-[3-[4-(3-methylbutylcarbamoyl)anilino]phenyl]benzamide Chemical compound COC1=CC=CC(C(=O)NC=2C=C(NC=3C=CC(=CC=3)C(=O)NCCC(C)C)C=CC=2)=C1 ZEJFPRRKAYPBRR-UHFFFAOYSA-N 0.000 claims 1
- IKKACGVZFOLYAM-ZRDIBKRKSA-N 3-methyl-n-(3-methylbutyl)-4-[3-[(e)-2-pyridin-2-ylethenyl]anilino]benzamide Chemical compound CC1=CC(C(=O)NCCC(C)C)=CC=C1NC1=CC=CC(\C=C\C=2N=CC=CC=2)=C1 IKKACGVZFOLYAM-ZRDIBKRKSA-N 0.000 claims 1
- RRNFHBAWFDBTBS-UHFFFAOYSA-N 3-methyl-n-(3-methylbutyl)-4-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CC1=CC(C(=O)NCCC(C)C)=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 RRNFHBAWFDBTBS-UHFFFAOYSA-N 0.000 claims 1
- VXOLWJRLEHQZSP-SNAWJCMRSA-N 3-methyl-n-(3-methylbutyl)-4-[4-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC1=CC(C(=O)NCCC(C)C)=CC=C1NC(C=C1)=CC=C1\C=C\C1=CC=NC=C1 VXOLWJRLEHQZSP-SNAWJCMRSA-N 0.000 claims 1
- MJNPBAIZWHGFQN-UHFFFAOYSA-N 4-(4-methoxyanilino)-3-methyl-n-(3-methylbutyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(C(=O)NCCC(C)C)C=C1C MJNPBAIZWHGFQN-UHFFFAOYSA-N 0.000 claims 1
- ARKWELBWICHKGK-UHFFFAOYSA-N 4-(4-methoxyanilino)-n-(3-methylbutyl)benzamide Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(C(=O)NCCC(C)C)C=C1 ARKWELBWICHKGK-UHFFFAOYSA-N 0.000 claims 1
- QUEACOJWZZCAIP-UHFFFAOYSA-N 4-(5-chloro-1h-imidazol-2-yl)-n-(4-methoxyphenyl)-2-methylaniline Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(C=2NC(Cl)=CN=2)C=C1C QUEACOJWZZCAIP-UHFFFAOYSA-N 0.000 claims 1
- ZCRNEOWAENGMKO-UHFFFAOYSA-N 4-[3-[(4-methoxybenzoyl)amino]anilino]-3-methyl-n-(3-methylbutyl)benzamide Chemical compound C1=CC(OC)=CC=C1C(=O)NC1=CC=CC(NC=2C(=CC(=CC=2)C(=O)NCCC(C)C)C)=C1 ZCRNEOWAENGMKO-UHFFFAOYSA-N 0.000 claims 1
- LWHFMYOAENSUMW-UHFFFAOYSA-N 4-[4-(dimethylamino)anilino]-n-[2-(dimethylamino)ethyl]benzamide Chemical compound C1=CC(C(=O)NCCN(C)C)=CC=C1NC1=CC=C(N(C)C)C=C1 LWHFMYOAENSUMW-UHFFFAOYSA-N 0.000 claims 1
- ODJWKTMPQRXFOP-UHFFFAOYSA-N 4-[4-[(3-methoxybenzoyl)amino]anilino]-3-methyl-n-(3-methylbutyl)benzamide Chemical compound COC1=CC=CC(C(=O)NC=2C=CC(NC=3C(=CC(=CC=3)C(=O)NCCC(C)C)C)=CC=2)=C1 ODJWKTMPQRXFOP-UHFFFAOYSA-N 0.000 claims 1
- OLQDONPZUXJKHK-UHFFFAOYSA-N 4-[4-[diethylamino(methyl)amino]triazol-1-yl]-n-(4-methoxyphenyl)aniline Chemical compound N1=NC(N(C)N(CC)CC)=CN1C(C=C1)=CC=C1NC1=CC=C(OC)C=C1 OLQDONPZUXJKHK-UHFFFAOYSA-N 0.000 claims 1
- IKXUYEHWXOXZSD-UHFFFAOYSA-N 4-[4-[diethylamino(methyl)amino]triazol-1-yl]-n-[4-(trifluoromethoxy)phenyl]aniline Chemical compound N1=NC(N(C)N(CC)CC)=CN1C(C=C1)=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 IKXUYEHWXOXZSD-UHFFFAOYSA-N 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- PJBPBHKZDXGKJG-CMDGGOBGSA-N 4-methyl-n-(3-methylbutyl)-3-[3-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC(C)CCNC(=O)C1=CC=C(C)C(NC=2C=C(\C=C\C=3C=CN=CC=3)C=CC=2)=C1 PJBPBHKZDXGKJG-CMDGGOBGSA-N 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- 125000004863 4-trifluoromethoxyphenyl group Chemical group [H]C1=C([H])C(OC(F)(F)F)=C([H])C([H])=C1* 0.000 claims 1
- 208000030507 AIDS Diseases 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000014644 Brain disease Diseases 0.000 claims 1
- 201000009030 Carcinoma Diseases 0.000 claims 1
- 208000002177 Cataract Diseases 0.000 claims 1
- 201000003883 Cystic fibrosis Diseases 0.000 claims 1
- 101000869592 Daucus carota Major allergen Dau c 1 Chemical group 0.000 claims 1
- 208000032274 Encephalopathy Diseases 0.000 claims 1
- 208000007982 Frasier Syndrome Diseases 0.000 claims 1
- 201000011240 Frontotemporal dementia Diseases 0.000 claims 1
- 101000650136 Homo sapiens WAS/WASL-interacting protein family member 3 Chemical group 0.000 claims 1
- 208000026350 Inborn Genetic disease Diseases 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 208000006136 Leigh Disease Diseases 0.000 claims 1
- 208000017507 Leigh syndrome Diseases 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- 206010058799 Mitochondrial encephalomyopathy Diseases 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 241000700605 Viruses Species 0.000 claims 1
- 102100027539 WAS/WASL-interacting protein family member 3 Human genes 0.000 claims 1
- 125000002009 alkene group Chemical group 0.000 claims 1
- 125000003368 amide group Chemical group 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 210000004027 cell Anatomy 0.000 claims 1
- 210000000349 chromosome Anatomy 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000008482 dysregulation Effects 0.000 claims 1
- 208000016361 genetic disease Diseases 0.000 claims 1
- 108020004999 messenger RNA Proteins 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 210000002161 motor neuron Anatomy 0.000 claims 1
- 201000000585 muscular atrophy Diseases 0.000 claims 1
- BASNBMRFRNZZRC-UHFFFAOYSA-N n-(3-imidazol-1-ylpropyl)-2-(4-methoxyanilino)benzamide Chemical compound C1=CC(OC)=CC=C1NC1=CC=CC=C1C(=O)NCCCN1C=NC=C1 BASNBMRFRNZZRC-UHFFFAOYSA-N 0.000 claims 1
- RPIINHOYBAFYGL-UHFFFAOYSA-N n-(3-imidazol-1-ylpropyl)-2-[4-(trifluoromethoxy)anilino]benzamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC1=CC=CC=C1C(=O)NCCCN1C=NC=C1 RPIINHOYBAFYGL-UHFFFAOYSA-N 0.000 claims 1
- NLNIABZQDKVDNC-UHFFFAOYSA-N n-(3-imidazol-1-ylpropyl)-4-[4-(trifluoromethoxy)anilino]benzamide Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC1=CC=C(C(=O)NCCCN2C=NC=C2)C=C1 NLNIABZQDKVDNC-UHFFFAOYSA-N 0.000 claims 1
- CMMZCLJIEKWYSE-OUKQBFOZSA-N n-(3-methylbutyl)-3-[3-[(e)-2-pyridin-2-ylethenyl]anilino]benzamide Chemical compound CC(C)CCNC(=O)C1=CC=CC(NC=2C=C(\C=C\C=3N=CC=CC=3)C=CC=2)=C1 CMMZCLJIEKWYSE-OUKQBFOZSA-N 0.000 claims 1
- YQCSORIIPSUFJA-MDZDMXLPSA-N n-(3-methylbutyl)-3-[3-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC(C)CCNC(=O)C1=CC=CC(NC=2C=C(\C=C\C=3C=CN=CC=3)C=CC=2)=C1 YQCSORIIPSUFJA-MDZDMXLPSA-N 0.000 claims 1
- LYFSTPNZBYZVEJ-VOTSOKGWSA-N n-(3-methylbutyl)-3-[4-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC(C)CCNC(=O)C1=CC=CC(NC=2C=CC(\C=C\C=3C=CN=CC=3)=CC=2)=C1 LYFSTPNZBYZVEJ-VOTSOKGWSA-N 0.000 claims 1
- DTMOKOVLSJWVHF-VOTSOKGWSA-N n-(3-methylbutyl)-4-[3-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound C1=CC(C(=O)NCCC(C)C)=CC=C1NC1=CC=CC(\C=C\C=2C=CN=CC=2)=C1 DTMOKOVLSJWVHF-VOTSOKGWSA-N 0.000 claims 1
- OGWMDNOQYLEVCB-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-2-(4-methoxyanilino)benzamide Chemical compound CCN(CC)CCNC(=O)C1=CC=CC=C1NC1=CC=C(OC)C=C1 OGWMDNOQYLEVCB-UHFFFAOYSA-N 0.000 claims 1
- QOWOCAIBBUSUOK-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-2-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CCN(CC)CCNC(=O)C1=CC=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 QOWOCAIBBUSUOK-UHFFFAOYSA-N 0.000 claims 1
- PTKYZEPYEYWXST-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-4-(4-methoxyanilino)benzamide Chemical compound C1=CC(C(=O)NCCN(CC)CC)=CC=C1NC1=CC=C(OC)C=C1 PTKYZEPYEYWXST-UHFFFAOYSA-N 0.000 claims 1
- GFJGXGKCRUYVJH-UHFFFAOYSA-N n-[2-(diethylamino)propyl]-2-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CCN(CC)C(C)CNC(=O)C1=CC=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 GFJGXGKCRUYVJH-UHFFFAOYSA-N 0.000 claims 1
- FTCSDXMVZJRNLK-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-(4-methoxyanilino)benzamide Chemical compound C1=CC(OC)=CC=C1NC1=CC=CC=C1C(=O)NCCN(C)C FTCSDXMVZJRNLK-UHFFFAOYSA-N 0.000 claims 1
- XOKDWZOUYOXSBJ-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CN(C)CCNC(=O)C1=CC=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 XOKDWZOUYOXSBJ-UHFFFAOYSA-N 0.000 claims 1
- NYNWBLCWWOFPFI-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-3-methyl-4-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CC1=CC(C(=O)NCCN(C)C)=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 NYNWBLCWWOFPFI-UHFFFAOYSA-N 0.000 claims 1
- PNZMAMKNMDRBAM-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-4-(4-methoxyanilino)-3-methylbenzamide Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(C(=O)NCCN(C)C)C=C1C PNZMAMKNMDRBAM-UHFFFAOYSA-N 0.000 claims 1
- FARHIFIXEBMFLL-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-4-[4-(trifluoromethoxy)anilino]benzamide Chemical compound C1=CC(C(=O)NCCN(C)C)=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 FARHIFIXEBMFLL-UHFFFAOYSA-N 0.000 claims 1
- KREXZWDGNXMIGX-FOCLMDBBSA-N n-[3-(diethylamino)propyl]-3-[3-[(e)-2-pyridin-2-ylethenyl]anilino]benzamide Chemical compound CCN(CC)CCCNC(=O)C1=CC=CC(NC=2C=C(\C=C\C=3N=CC=CC=3)C=CC=2)=C1 KREXZWDGNXMIGX-FOCLMDBBSA-N 0.000 claims 1
- YIZJTUSBTZHCIV-OUKQBFOZSA-N n-[3-(diethylamino)propyl]-3-[3-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CCN(CC)CCCNC(=O)C1=CC=CC(NC=2C=C(\C=C\C=3C=CN=CC=3)C=CC=2)=C1 YIZJTUSBTZHCIV-OUKQBFOZSA-N 0.000 claims 1
- RDRLQCQCSWDJGY-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-3-[4-[(3-methoxybenzoyl)amino]anilino]benzamide Chemical compound CCN(CC)CCCNC(=O)C1=CC=CC(NC=2C=CC(NC(=O)C=3C=C(OC)C=CC=3)=CC=2)=C1 RDRLQCQCSWDJGY-UHFFFAOYSA-N 0.000 claims 1
- ZESWQWOYEBKTBQ-MDZDMXLPSA-N n-[3-(diethylamino)propyl]-3-[4-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CCN(CC)CCCNC(=O)C1=CC=CC(NC=2C=CC(\C=C\C=3C=CN=CC=3)=CC=2)=C1 ZESWQWOYEBKTBQ-MDZDMXLPSA-N 0.000 claims 1
- TZDYLWZAPZHIHR-ZHACJKMWSA-N n-[3-(diethylamino)propyl]-3-methyl-4-[3-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=CC(\C=C\C=2C=CN=CC=2)=C1 TZDYLWZAPZHIHR-ZHACJKMWSA-N 0.000 claims 1
- CUUVIRNLGNFTPV-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-3-methyl-4-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=C(OC(F)(F)F)C=C1 CUUVIRNLGNFTPV-UHFFFAOYSA-N 0.000 claims 1
- ZAPRZCVJOPXSGS-BQYQJAHWSA-N n-[3-(diethylamino)propyl]-3-methyl-4-[4-[(e)-2-pyridin-4-ylethenyl]anilino]benzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC(C=C1)=CC=C1\C=C\C1=CC=NC=C1 ZAPRZCVJOPXSGS-BQYQJAHWSA-N 0.000 claims 1
- BQFHBXFWSZEKJI-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-4-(4-methoxyanilino)-3-methylbenzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=C(OC)C=C1 BQFHBXFWSZEKJI-UHFFFAOYSA-N 0.000 claims 1
- NEHAWPULKZRPDY-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-4-(4-methoxyanilino)benzamide Chemical compound C1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=C(OC)C=C1 NEHAWPULKZRPDY-UHFFFAOYSA-N 0.000 claims 1
- XXMMMCMUEOONLX-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-4-[3-[(3-methoxybenzoyl)amino]anilino]-3-methylbenzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=CC(NC(=O)C=2C=C(OC)C=CC=2)=C1 XXMMMCMUEOONLX-UHFFFAOYSA-N 0.000 claims 1
- WZYONDRBTGWZSD-NTCAYCPXSA-N n-[3-(diethylamino)propyl]-4-[3-[(e)-2-pyridin-2-ylethenyl]anilino]benzamide Chemical compound C1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=CC(\C=C\C=2N=CC=CC=2)=C1 WZYONDRBTGWZSD-NTCAYCPXSA-N 0.000 claims 1
- CVHIJLXXLCRDAQ-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-4-[4-(dimethylamino)anilino]-3-methylbenzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC1=CC=C(N(C)C)C=C1 CVHIJLXXLCRDAQ-UHFFFAOYSA-N 0.000 claims 1
- IWYIYEYQYJYWQV-UHFFFAOYSA-N n-[3-(diethylamino)propyl]-4-[4-[(3-methoxybenzoyl)amino]anilino]-3-methylbenzamide Chemical compound CC1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC(C=C1)=CC=C1NC(=O)C1=CC=CC(OC)=C1 IWYIYEYQYJYWQV-UHFFFAOYSA-N 0.000 claims 1
- FFSAKCDOKQPAEU-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-3-[4-(trifluoromethoxy)anilino]benzamide Chemical compound CN(C)CCCNC(=O)C1=CC=CC(NC=2C=CC(OC(F)(F)F)=CC=2)=C1 FFSAKCDOKQPAEU-UHFFFAOYSA-N 0.000 claims 1
- PGYVMLPHOHSYQD-UHFFFAOYSA-N n-[4-[4-[3-(diethylamino)propylcarbamoyl]anilino]phenyl]-3-methoxybenzamide Chemical compound C1=CC(C(=O)NCCCN(CC)CC)=CC=C1NC(C=C1)=CC=C1NC(=O)C1=CC=CC(OC)=C1 PGYVMLPHOHSYQD-UHFFFAOYSA-N 0.000 claims 1
- SGNNFTLSVFAJSQ-UHFFFAOYSA-N n-[5-(diethylamino)pentan-2-yl]-2-[4-(dimethylamino)anilino]benzamide Chemical compound CCN(CC)CCCC(C)NC(=O)C1=CC=CC=C1NC1=CC=C(N(C)C)C=C1 SGNNFTLSVFAJSQ-UHFFFAOYSA-N 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229940076279 serotonin Drugs 0.000 claims 1
- 102000013498 tau Proteins Human genes 0.000 claims 1
- 108010026424 tau Proteins Proteins 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0850144 | 2008-01-10 | ||
| FR0850144A FR2926297B1 (fr) | 2008-01-10 | 2008-01-10 | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
| PCT/EP2009/050280 WO2009087238A2 (en) | 2008-01-10 | 2009-01-12 | Chemical molecules that inhibit the slicing mechanism for treating diseases resulting from splicing anomalies |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011509280A JP2011509280A (ja) | 2011-03-24 |
| JP2011509280A5 true JP2011509280A5 (enExample) | 2012-04-12 |
| JP5784909B2 JP5784909B2 (ja) | 2015-09-24 |
Family
ID=39720243
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010541800A Active JP5784909B2 (ja) | 2008-01-10 | 2009-01-12 | スプライシング異常からもたらされる疾患を処置する為のスライスする機構を阻害する化学分子 |
Country Status (12)
| Country | Link |
|---|---|
| US (4) | US8604063B2 (enExample) |
| EP (2) | EP3536691B1 (enExample) |
| JP (1) | JP5784909B2 (enExample) |
| CN (3) | CN104130242B (enExample) |
| CA (5) | CA2711652C (enExample) |
| DK (1) | DK2235000T3 (enExample) |
| ES (2) | ES2934810T3 (enExample) |
| FR (4) | FR2926297B1 (enExample) |
| HR (1) | HRP20201369T1 (enExample) |
| PL (1) | PL2235000T3 (enExample) |
| PT (1) | PT2235000T (enExample) |
| WO (1) | WO2009087238A2 (enExample) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8367669B2 (en) | 2005-06-15 | 2013-02-05 | Vanderbilt University | Inhibitors of hemeprotein-catalyzed lipid peroxidation |
| US9133212B1 (en) | 2005-06-15 | 2015-09-15 | Vanderbilt University | Inhibitors of hemeprotein-catalyzed lipid peroxidation |
| FR2926297B1 (fr) * | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
| TW201103904A (en) | 2009-06-11 | 2011-02-01 | Hoffmann La Roche | Janus kinase inhibitor compounds and methods |
| EP2266972A1 (en) * | 2009-06-12 | 2010-12-29 | Splicos | New chemical molecules that inhibit the splicing mechanism for treating diseases resulting from splicing anomalies |
| US10253020B2 (en) | 2009-06-12 | 2019-04-09 | Abivax | Compounds for preventing, inhibiting, or treating cancer, AIDS and/or premature aging |
| FI2440546T3 (fi) | 2009-06-12 | 2023-03-30 | Abivax | Ennenaikaisen vanhenemisen ja erityisesti progerian hoitamiseen hyödyllisiä yhdisteitä |
| JP5819305B2 (ja) | 2009-10-13 | 2015-11-24 | リガンド・ファーマシューティカルズ・インコーポレイテッド | 造血成長因子模倣小分子化合物およびそれらの使用 |
| WO2012001941A1 (ja) * | 2010-06-28 | 2012-01-05 | Hagiwara Masatoshi | 遺伝性疾患の予防・改善剤 |
| EP2465502A1 (en) | 2010-12-15 | 2012-06-20 | Société Splicos | Compounds useful for treating AIDS |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| EP2505198A1 (en) | 2011-04-01 | 2012-10-03 | Société Splicos | Compounds for use as therapeutic agents affecting p53 expression and/or activity |
| FR2987627B1 (fr) | 2012-03-05 | 2016-03-18 | Splicos | Utilisation de rbm39 comme biomarqueur |
| LT3495367T (lt) | 2012-06-13 | 2021-02-25 | Incyte Holdings Corporation | Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| EP2712862A1 (en) * | 2012-09-28 | 2014-04-02 | Splicos | New anti-invasive compounds |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| EP2757161A1 (en) | 2013-01-17 | 2014-07-23 | Splicos | miRNA-124 as a biomarker of viral infection |
| ITMI20130444A1 (it) * | 2013-03-22 | 2014-09-23 | S B M Science Of Biology In Medici Ne Srl | Composto di inclusione comprendente adjudin [1-(2,4-diclorobenzil) - 1h-indazolo-3-carboidrazide] e ciclodestrina, sua preparazione e utilizzo. |
| LT2986610T (lt) | 2013-04-19 | 2018-04-10 | Incyte Holdings Corporation | Bicikliniai heterociklai, kaip fgfr inhibitoriai |
| MX382692B (es) | 2013-07-05 | 2025-03-13 | Abivax | Compuestos bicíclicos útiles para el tratamiento de enfermedades causadas por retrovirus. |
| WO2015100322A1 (en) * | 2013-12-24 | 2015-07-02 | Oncotartis, Inc. | Benzamide and nicotinamide compounds and methods of using same |
| EP2974729A1 (en) | 2014-07-17 | 2016-01-20 | Abivax | Quinoline derivatives for use in the treatment of inflammatory diseases |
| JP2017523211A (ja) | 2014-08-04 | 2017-08-17 | ドレクセル ユニバーシティ | 新規化合物およびそれを用いてil−1r媒介性の疾患または障害を処置するかまたは寛解させる方法 |
| CN106714845A (zh) * | 2014-08-11 | 2017-05-24 | 得克萨斯州大学系统董事会 | 通过crispr/cas9介导的基因编辑预防肌营养不良 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | 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 |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| SG11201706287PA (en) | 2015-02-20 | 2017-09-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| CN110892069B (zh) * | 2017-03-30 | 2024-02-09 | 国立大学法人京都大学 | 基于基因组编辑的外显子跳跃诱导方法 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| KR20200142039A (ko) * | 2018-04-10 | 2020-12-21 | 스카이호크 테라퓨틱스, 인코포레이티드 | 암 치료용 화합물 |
| MX2020011718A (es) | 2018-05-04 | 2021-02-15 | Incyte Corp | Formas solidas de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr) y procesos para prepararlas. |
| ES3061844T3 (en) | 2018-05-04 | 2026-04-07 | Incyte Corp | Salts of an fgfr inhibitor |
| EP3594205A1 (en) * | 2018-07-09 | 2020-01-15 | Abivax | Phenyl-n-aryl derivatives for treating a rna virus infection |
| EP3594206A1 (en) | 2018-07-09 | 2020-01-15 | Abivax | Phenyl-n-quinoline derivatives for treating a rna virus infection |
| EP3669873A1 (en) | 2018-12-20 | 2020-06-24 | Abivax | Quinoline derivatives for use ine the traeatment of inflammation diseases |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| CN110172037A (zh) * | 2019-07-01 | 2019-08-27 | 华北理工大学 | 一种含吡啶结构的苯乙烯基吡啶化合物、制备方法及其制备抗肿瘤药物的应用 |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| EP3848356A1 (en) * | 2020-01-07 | 2021-07-14 | Abivax | Aryl-n-aryl derivatives for treating a rna virus infection |
| PL3999493T3 (pl) * | 2019-07-19 | 2024-04-22 | Abivax | Pochodne arylo-N-arylowe do leczenia zakażenia wirusem RNA |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| TWI891666B (zh) | 2019-10-14 | 2025-08-01 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| WO2021113462A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| US20230076977A1 (en) * | 2020-01-14 | 2023-03-09 | The Trustees Of The University Of Pennsylvania | Utrophin upregulation compounds for duchenne muscular dystrophy therapy |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| TW202304459A (zh) | 2021-04-12 | 2023-02-01 | 美商英塞特公司 | 包含fgfr抑制劑及nectin-4靶向劑之組合療法 |
| EP4352060A1 (en) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| JP2024522189A (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 |
| CA3237229A1 (en) | 2021-11-15 | 2023-05-19 | Narasimha Murthy Cheemala | Bicyclic heteroaromatic compounds and their use as pest control agents |
| WO2023173081A2 (en) * | 2022-03-11 | 2023-09-14 | The Johns Hopkins University | Targeting an eukaryotic initiation factor 2 alpha kinase to regulate translation under stress |
| WO2023218245A1 (en) * | 2022-05-13 | 2023-11-16 | Voronoi Inc. | Heteroaryl derivative compounds, and pharmaceutical composition comprising thereof |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR400973A (fr) | 1909-03-19 | 1909-08-13 | Jean Victor Massillon | Nouveau sertisseur à main pour la fabrication des cartouches |
| DE374291C (de) * | 1914-03-24 | 1923-04-21 | Alexei Ewgenjewitsch Tschitsch | Verfahren zur Darstellung von Aminosubstitutionsprodukten der Pyridin- und Chinolinreihe |
| US2274620A (en) * | 1940-01-02 | 1942-02-24 | S M A Corp | Substituted aryl amides of pyridine carboxylic acid |
| US2671805A (en) | 1952-07-02 | 1954-03-09 | Searle & Co | Basically substituted o-arylamino-benzamides |
| DE1168435B (de) * | 1961-12-09 | 1964-04-23 | Kali Chemie Ag | Verfahren zur Herstellung von 4-Oxo-3, 4-dihydrochinazolinen |
| NL132603C (enExample) * | 1964-08-29 | |||
| US3409668A (en) | 1964-11-07 | 1968-11-05 | Palazzo Giuseppe | Substituted anthranilamides and process for the preparation thereof |
| GB1318291A (en) * | 1970-04-15 | 1973-05-23 | Shell Int Research | Carboxamide derivatives and fungicidal compositions containing them |
| JPS5095285A (enExample) | 1973-12-26 | 1975-07-29 | ||
| DE2417216A1 (de) * | 1974-04-09 | 1975-11-06 | Basf Ag | Fungizide |
| JPS52133939A (en) * | 1976-04-30 | 1977-11-09 | Ihara Chem Ind Co Ltd | Preparation of 2-substituted benzanilides |
| FR2436786A1 (fr) | 1978-09-21 | 1980-04-18 | Anvar | Nouveaux derives des pyrido (4,3-b) carbazoles (ellipticines), substitues en position 1 par une chaine polyaminee, leur obtention et leur application a titre de medicaments |
| US4510139A (en) * | 1984-01-06 | 1985-04-09 | Sterling Drug Inc. | Substituted aminobenzamides and their use as agents which inhibit lipoxygenase activity |
| JPS62158252A (ja) * | 1985-12-28 | 1987-07-14 | Kirin Brewery Co Ltd | 4−アミノピリジンベンズアミド誘導体 |
| DE3819025A1 (de) * | 1987-09-01 | 1989-05-24 | Fuji Photo Film Co Ltd | Verfahren zur herstellung von alkoxybenzolverbindungen |
| US4855308A (en) * | 1987-12-04 | 1989-08-08 | Warner-Lambert Company | Method of treating senile cognitive decline with N'-substituted aminopyridine adrenergic agents |
| FR2627493B1 (fr) | 1988-02-23 | 1991-10-31 | Sanofi Sa | Procede de preparation de derives d'isoquinoleine |
| FR2645861A1 (fr) | 1989-04-17 | 1990-10-19 | Inst Nat Sante Rech Med | Utilisation de dipyrido (4,3-b) (3,4-f) indoles pour la preparation de medicaments utiles pour le traitement du sida |
| US5579033A (en) | 1992-05-20 | 1996-11-26 | International Business Machines Corporation | Pointing device for retrofitting onto the keyboard of an existing computer system |
| GB9715584D0 (en) * | 1997-07-23 | 1997-10-01 | Eisai Co Ltd | Compounds |
| US6268387B1 (en) * | 1997-12-23 | 2001-07-31 | Warner-Lambert Company | Thiourea and benzamide compounds, compositions and methods of treating or preventing inflammatory diseases and atherosclerosis |
| US7223879B2 (en) * | 1998-07-10 | 2007-05-29 | Massachusetts Institute Of Technology | Ligands for metals and improved metal-catalyzed processes based thereon |
| ATE360634T1 (de) * | 1998-07-10 | 2007-05-15 | Massachusetts Inst Technology | Ligande für metalle und verbesserte metall- katalysierte verfahren, die darauf basieren |
| FR2787444B1 (fr) | 1998-12-22 | 2001-02-09 | Rhodia Chimie Sa | Composition et procede d'inhibition de la polymerisation radicalaire de monomeres aliphatiques a insaturation ethylenique |
| CA2358091A1 (en) * | 1998-12-23 | 2000-07-06 | Eli Lilly And Company | Antithrombotic amides |
| FR2789576B1 (fr) | 1999-02-16 | 2002-04-26 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| US6878714B2 (en) * | 2001-01-12 | 2005-04-12 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| US7101948B2 (en) | 2001-12-21 | 2006-09-05 | Air Products And Chemicals, Inc. | Stabilizers to inhibit the polymerization of substituted cyclotetrasiloxane |
| FR2836917B1 (fr) * | 2002-03-11 | 2006-02-24 | Lipha | Derives nitroso de la diphenylamine, compositions pharmaceutiques les contenant en tant que medicaments utilisables dans le traitement des pathologies caracterisees par une situation de stress oxydatif |
| US20060040931A1 (en) * | 2002-12-06 | 2006-02-23 | Toray Industries, Inc. | Benzomorpholine derivatives |
| AU2003296326A1 (en) * | 2002-12-09 | 2004-06-30 | Massachusetts Institute Of Technology | Ligands for metals and improved metal-catalyzed processes based thereon |
| US7125997B2 (en) | 2002-12-20 | 2006-10-24 | Irm Llc | Differential tumor cytotoxicity compounds and compositions |
| FR2859475A1 (fr) * | 2003-09-04 | 2005-03-11 | Centre Nat Rech Scient | Utilisation de composes derives d'ellipticine et d'aza-ellipticine pour la preparation d'un medicament utile pour le traitement de maladies genetiques resultant de l'alteration des processus d'epissage |
| FR2859474B1 (fr) | 2003-09-04 | 2006-01-13 | Centre Nat Rech Scient | Utilisation de composes derives d'indole pour la preparation d'un medicament utile pour le traitement de maladies genetiques resultant de l'alteration des processus d'epissage |
| WO2005025498A2 (en) * | 2003-09-08 | 2005-03-24 | Corus Pharma | Substituted acetanilides and benzamides for the treatment of asthma and pulmonary inflammation |
| FR2862964B1 (fr) | 2003-11-27 | 2006-12-29 | Merck Sante Sas | Derives de la diphenylamine. |
| FR2862965B1 (fr) * | 2003-11-27 | 2007-09-07 | Merck Sante Sas | Nouveaux derives de phenoxyacetamides et leur utilisation pour la preparation de diphenylamides. |
| TWI380975B (zh) | 2004-03-25 | 2013-01-01 | Otsuka Pharma Co Ltd | 製造胺基酚類化合物的方法 |
| EP1845985A4 (en) | 2005-02-02 | 2011-10-12 | Nexuspharma Inc | AMIN DERIVATIVE COMPOSITIONS AND METHODS FOR TREATING VIRUS DISEASES RELATED TO CANCER Aetiology |
| WO2006133848A1 (en) | 2005-06-13 | 2006-12-21 | Dsm Ip Assets. B.V. | Additive composition comprising an amidized or imidized polymer |
| WO2007096647A2 (en) | 2006-02-27 | 2007-08-30 | Sterix Limited | Diaryl compounds as non-steroidal inhibitors of 17-beta hydroxysteroid dehydrogenase and/or steroid sulphatase for the treatment of oestrogen-related diseases such as hormone dependent breast cancer |
| US20090118135A1 (en) | 2007-06-08 | 2009-05-07 | The Burnham Institute | Methods and compounds for regulating apoptosis |
| FR2926297B1 (fr) | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
| EP2712862A1 (en) | 2012-09-28 | 2014-04-02 | Splicos | New anti-invasive compounds |
-
2008
- 2008-01-10 FR FR0850144A patent/FR2926297B1/fr active Active
-
2009
- 2009-01-12 DK DK09700499.8T patent/DK2235000T3/da active
- 2009-01-12 PT PT97004998T patent/PT2235000T/pt unknown
- 2009-01-12 ES ES19164367T patent/ES2934810T3/es active Active
- 2009-01-12 CA CA2711652A patent/CA2711652C/en active Active
- 2009-01-12 CA CA3072245A patent/CA3072245C/en active Active
- 2009-01-12 CA CA2946329A patent/CA2946329C/en active Active
- 2009-01-12 US US12/811,931 patent/US8604063B2/en active Active
- 2009-01-12 HR HRP20201369TT patent/HRP20201369T1/hr unknown
- 2009-01-12 JP JP2010541800A patent/JP5784909B2/ja active Active
- 2009-01-12 ES ES09700499T patent/ES2816178T3/es active Active
- 2009-01-12 CN CN201410301260.2A patent/CN104130242B/zh active Active
- 2009-01-12 EP EP19164367.5A patent/EP3536691B1/en active Active
- 2009-01-12 CN CN200980106361.1A patent/CN101965341B/zh active Active
- 2009-01-12 WO PCT/EP2009/050280 patent/WO2009087238A2/en not_active Ceased
- 2009-01-12 PL PL09700499T patent/PL2235000T3/pl unknown
- 2009-01-12 CA CA2946326A patent/CA2946326C/en active Active
- 2009-01-12 CA CA2946336A patent/CA2946336C/en active Active
- 2009-01-12 CN CN201410299552.7A patent/CN104086482B/zh active Active
- 2009-01-12 EP EP09700499.8A patent/EP2235000B1/en active Active
-
2013
- 2013-01-24 FR FR1350600A patent/FR2983196B1/fr active Active
- 2013-01-24 FR FR1350601A patent/FR2983200B1/fr active Active
- 2013-01-24 FR FR1350599A patent/FR2983199B1/fr active Active
- 2013-11-04 US US14/070,799 patent/US9233931B2/en active Active
-
2015
- 2015-12-03 US US14/958,602 patent/US10130595B2/en active Active
-
2018
- 2018-10-05 US US16/153,249 patent/US10654813B2/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA3072245C (en) | Chemical molecules that inhibit the slicing mechanism for treating diseases resulting from splicing anomalies | |
| HRP20140346T1 (hr) | DERIVATI 1,2,3-TRIAZOLA, NAMIJENJENI UPOTREBI KAO INHIBITORI STEAROIL-CoA-DESATURAZE | |
| JP2017522346A5 (enExample) | ||
| JP2009541270A5 (enExample) | ||
| TWI445701B (zh) | 經取代之苯甲醯胺衍生物 | |
| CN110678450B (zh) | 作为核受体激动剂的异噁唑衍生物及其用途 | |
| KR20160033726A (ko) | 헤테로방향족 고리-벤질-아미드-사이클 코어를 포함하는 오토탁신 억제제 | |
| JP2004503549A (ja) | 生体等配電子性ベンズアミド誘導体およびそのアポb−100分泌阻害剤としての使用 | |
| JP2008515992A5 (enExample) | ||
| JP2007511485A5 (enExample) | ||
| JP2010522770A5 (enExample) | ||
| JP2011518811A5 (enExample) | ||
| CN107848962A (zh) | 脲衍生物或其药理学上可接受的盐 | |
| JP2005521650A5 (enExample) | ||
| TW201332998A (zh) | 雜環衍生物 | |
| JP6937524B2 (ja) | アミド化合物およびその使用 | |
| JP2006522779A (ja) | 4−置換キノリン誘導体、その調製方法、中間体及び医薬組成物 | |
| CN101039904B (zh) | 适于治疗对于多巴胺d3受体调节有反应的病症的杂环化合物 | |
| ME02144B (me) | Jedinjenja aril triazola sa antitumorskom aktivnošću | |
| CN101423514A (zh) | 一种杂环取代三氮唑化合物及其合成方法 | |
| KR101657594B1 (ko) | 4,5-다이하이드로-1h-피라졸 유도체 또는 그의 염 및 이를 포함하는 약학 조성물 | |
| HK40017121B (en) | An isoxazole derivatives as nuclear receptor agonists and used thereof |