JP2008510712A5 - - Google Patents
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- Publication number
- JP2008510712A5 JP2008510712A5 JP2007528007A JP2007528007A JP2008510712A5 JP 2008510712 A5 JP2008510712 A5 JP 2008510712A5 JP 2007528007 A JP2007528007 A JP 2007528007A JP 2007528007 A JP2007528007 A JP 2007528007A JP 2008510712 A5 JP2008510712 A5 JP 2008510712A5
- Authority
- JP
- Japan
- Prior art keywords
- carboxylic acid
- acid amide
- thieno
- pyrrole
- alkyl
- 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
- 150000001875 compounds Chemical class 0.000 claims 17
- 229910052799 carbon Inorganic materials 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 15
- 229910052717 sulfur Inorganic materials 0.000 claims 7
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 6
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 102000005403 Casein Kinases Human genes 0.000 claims 2
- 108010031425 Casein Kinases Proteins 0.000 claims 2
- -1 Pyridin-2-ylsulfanyl Chemical group 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
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 239000002798 polar solvent Substances 0.000 claims 2
- OICWBDMISQRIEM-UHFFFAOYSA-N 2,6-bis(phenylsulfanyl)-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound N=1C=2C(SC=3C=CC=CC=3)=C(C(=O)N)NC=2SC=1SC1=CC=CC=C1 OICWBDMISQRIEM-UHFFFAOYSA-N 0.000 claims 1
- SVGBHSTYOGQVPE-UHFFFAOYSA-N 2,6-bis[(3-methoxyphenyl)sulfanyl]-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound COC1=CC=CC(SC=2SC=3NC(=C(SC=4C=C(OC)C=CC=4)C=3N=2)C(N)=O)=C1 SVGBHSTYOGQVPE-UHFFFAOYSA-N 0.000 claims 1
- KHLCUPKDEHFRCJ-UHFFFAOYSA-N 2-methyl-6-[3-(trifluoromethoxy)phenyl]sulfanyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC(C)=NC=2C=1SC1=CC=CC(OC(F)(F)F)=C1 KHLCUPKDEHFRCJ-UHFFFAOYSA-N 0.000 claims 1
- HJYHRWTZEFNDSI-UHFFFAOYSA-N 2-methyl-6-phenyl-4-sulfanylpyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1N(S)C=2SC(C)=NC=2C=1C1=CC=CC=C1 HJYHRWTZEFNDSI-UHFFFAOYSA-N 0.000 claims 1
- KARMTEAISSCLNV-UHFFFAOYSA-N 4-(2-methoxyphenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound COC1=CC=CC=C1SC1=C(C(N)=O)NC2=C1C=CS2 KARMTEAISSCLNV-UHFFFAOYSA-N 0.000 claims 1
- LLODQNWTXWAEHQ-UHFFFAOYSA-N 4-(3,5-dichlorophenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC(Cl)=CC(Cl)=C1 LLODQNWTXWAEHQ-UHFFFAOYSA-N 0.000 claims 1
- HOQJCJIERRLTCY-UHFFFAOYSA-N 4-(3-bromophenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=CC(Br)=C1 HOQJCJIERRLTCY-UHFFFAOYSA-N 0.000 claims 1
- GHMABAHOMNASAZ-UHFFFAOYSA-N 4-(3-chlorophenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=CC(Cl)=C1 GHMABAHOMNASAZ-UHFFFAOYSA-N 0.000 claims 1
- YKZLNVSFLNFVOY-UHFFFAOYSA-N 4-(3-methoxyphenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound COC1=CC=CC(SC=2C=3C=CSC=3NC=2C(N)=O)=C1 YKZLNVSFLNFVOY-UHFFFAOYSA-N 0.000 claims 1
- UVOWKGFSUGZCGS-UHFFFAOYSA-N 4-(3-methylphenyl)sulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound CC1=CC=CC(SC=2C=3C=CSC=3NC=2C(N)=O)=C1 UVOWKGFSUGZCGS-UHFFFAOYSA-N 0.000 claims 1
- RWXUROFIQSIUQV-UHFFFAOYSA-N 4-phenylsulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=CC=C1 RWXUROFIQSIUQV-UHFFFAOYSA-N 0.000 claims 1
- FNWSTCZNXVPFRZ-UHFFFAOYSA-N 4-pyridin-2-ylsulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=CC=N1 FNWSTCZNXVPFRZ-UHFFFAOYSA-N 0.000 claims 1
- NTLRFOPPLIJBSC-UHFFFAOYSA-N 4-pyridin-4-ylsulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=NC=C1 NTLRFOPPLIJBSC-UHFFFAOYSA-N 0.000 claims 1
- JYSYZRVJGHEJDK-UHFFFAOYSA-N 4-thiophen-2-ylsulfanyl-6h-thieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=CC=2C=1SC1=CC=CS1 JYSYZRVJGHEJDK-UHFFFAOYSA-N 0.000 claims 1
- PKGPYNAWHYBFKC-UHFFFAOYSA-N 6-(2,3-dichlorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC(Cl)=C1Cl PKGPYNAWHYBFKC-UHFFFAOYSA-N 0.000 claims 1
- ZGLKUVLANMUNDL-UHFFFAOYSA-N 6-(2,5-dichlorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC(Cl)=CC=C1Cl ZGLKUVLANMUNDL-UHFFFAOYSA-N 0.000 claims 1
- IAGGBMKLGCTCCG-UHFFFAOYSA-N 6-(2-aminophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC=C1N IAGGBMKLGCTCCG-UHFFFAOYSA-N 0.000 claims 1
- PTCCVJFAQYJGKI-UHFFFAOYSA-N 6-(2-ethylphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound CCC1=CC=CC=C1SC1=C(C(N)=O)NC2=C1SC=C2 PTCCVJFAQYJGKI-UHFFFAOYSA-N 0.000 claims 1
- UELCIDRHHFSPMJ-UHFFFAOYSA-N 6-(2-fluorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC=C1F UELCIDRHHFSPMJ-UHFFFAOYSA-N 0.000 claims 1
- ZZCCDNLZKPNSCR-UHFFFAOYSA-N 6-(2-methoxyphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound COC1=CC=CC=C1SC1=C(C(N)=O)NC2=C1SC=C2 ZZCCDNLZKPNSCR-UHFFFAOYSA-N 0.000 claims 1
- SLYFMXMWIGEZPA-UHFFFAOYSA-N 6-(2-methylphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound CC1=CC=CC=C1SC1=C(C(N)=O)NC2=C1SC=C2 SLYFMXMWIGEZPA-UHFFFAOYSA-N 0.000 claims 1
- JBLCKTNGYXHRDT-UHFFFAOYSA-N 6-(3,5-dichlorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC(Cl)=CC(Cl)=C1 JBLCKTNGYXHRDT-UHFFFAOYSA-N 0.000 claims 1
- OSBJUNASPBRUBU-UHFFFAOYSA-N 6-(3,5-dimethylphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound CC1=CC(C)=CC(SC=2C=3SC=CC=3NC=2C(N)=O)=C1 OSBJUNASPBRUBU-UHFFFAOYSA-N 0.000 claims 1
- GJSSWWBRWAOAHD-UHFFFAOYSA-N 6-(3-bromophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC(Br)=C1 GJSSWWBRWAOAHD-UHFFFAOYSA-N 0.000 claims 1
- KVNUDRZMWWEVIU-UHFFFAOYSA-N 6-(3-chlorophenyl)sulfanyl-2-methyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC(C)=NC=2C=1SC1=CC=CC(Cl)=C1 KVNUDRZMWWEVIU-UHFFFAOYSA-N 0.000 claims 1
- VKJKCISGARMRPR-UHFFFAOYSA-N 6-(3-fluorophenyl)sulfanyl-2-methyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC(C)=NC=2C=1SC1=CC=CC(F)=C1 VKJKCISGARMRPR-UHFFFAOYSA-N 0.000 claims 1
- XUZZYHHHPFOTDR-UHFFFAOYSA-N 6-(3-fluorophenyl)sulfanyl-4h-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2N=CSC=2C=1SC1=CC=CC(F)=C1 XUZZYHHHPFOTDR-UHFFFAOYSA-N 0.000 claims 1
- ZNYIUWSBBGOLAV-UHFFFAOYSA-N 6-(3-fluorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC(F)=C1 ZNYIUWSBBGOLAV-UHFFFAOYSA-N 0.000 claims 1
- RQWWELNBPALKAG-UHFFFAOYSA-N 6-(3-fluorophenyl)sulfanylthieno[2,3-b]pyrrole-5-carboxamide Chemical compound NC(=O)C1=CC=2C=CSC=2N1SC1=CC=CC(F)=C1 RQWWELNBPALKAG-UHFFFAOYSA-N 0.000 claims 1
- FUHFQPLBCITXQI-UHFFFAOYSA-N 6-(3-methoxyphenyl)sulfanyl-2-methyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound COC1=CC=CC(SC=2C=3N=C(C)SC=3NC=2C(N)=O)=C1 FUHFQPLBCITXQI-UHFFFAOYSA-N 0.000 claims 1
- DZRGVTJILNYAEW-UHFFFAOYSA-N 6-(3-methoxyphenyl)sulfanyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical class COC1=CC=CC(SC=2C=3N=CSC=3NC=2C(N)=O)=C1 DZRGVTJILNYAEW-UHFFFAOYSA-N 0.000 claims 1
- DJCKEACUJYXBFG-UHFFFAOYSA-N 6-(3-methoxyphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound COC1=CC=CC(SC=2C=3SC=CC=3NC=2C(N)=O)=C1 DJCKEACUJYXBFG-UHFFFAOYSA-N 0.000 claims 1
- QZAPRLOGXQRWDW-UHFFFAOYSA-N 6-(3-methylphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound CC1=CC=CC(SC=2C=3SC=CC=3NC=2C(N)=O)=C1 QZAPRLOGXQRWDW-UHFFFAOYSA-N 0.000 claims 1
- KHHVIGWHUFDFSL-UHFFFAOYSA-N 6-(4-chlorophenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=C(Cl)C=C1 KHHVIGWHUFDFSL-UHFFFAOYSA-N 0.000 claims 1
- FPYSUIWAQIUWQH-UHFFFAOYSA-N 6-(4-methylphenyl)sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound C1=CC(C)=CC=C1SC1=C(C(N)=O)NC2=C1SC=C2 FPYSUIWAQIUWQH-UHFFFAOYSA-N 0.000 claims 1
- HPKXRVROTCZNPM-UHFFFAOYSA-N 6-[2-(trifluoromethyl)phenyl]sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC=C1C(F)(F)F HPKXRVROTCZNPM-UHFFFAOYSA-N 0.000 claims 1
- DBFNMLATEPIVEF-UHFFFAOYSA-N 6-[3-(trifluoromethoxy)phenyl]sulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC(OC(F)(F)F)=C1 DBFNMLATEPIVEF-UHFFFAOYSA-N 0.000 claims 1
- ZURZOOVHMHWWTI-UHFFFAOYSA-N 6-phenylsulfanyl-4h-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2N=CSC=2C=1SC1=CC=CC=C1 ZURZOOVHMHWWTI-UHFFFAOYSA-N 0.000 claims 1
- ZNXHNYLEVPGVHR-UHFFFAOYSA-N 6-phenylsulfanyl-4h-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2SC=NC=2C=1SC1=CC=CC=C1 ZNXHNYLEVPGVHR-UHFFFAOYSA-N 0.000 claims 1
- PYQIOYKMCRUWPT-UHFFFAOYSA-N 6-phenylsulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CC=C1 PYQIOYKMCRUWPT-UHFFFAOYSA-N 0.000 claims 1
- VFCHWLOHRQUEDF-UHFFFAOYSA-N 6-pyridin-2-ylsulfanyl-4h-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide Chemical compound NC(=O)C=1NC=2N=CSC=2C=1SC1=CC=CC=N1 VFCHWLOHRQUEDF-UHFFFAOYSA-N 0.000 claims 1
- RAABJMMDMKLJDD-UHFFFAOYSA-N 6-pyridin-4-ylsulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=NC=C1 RAABJMMDMKLJDD-UHFFFAOYSA-N 0.000 claims 1
- AQSXTNJWWMGTSG-UHFFFAOYSA-N 6-thiophen-2-ylsulfanyl-4h-thieno[3,2-b]pyrrole-5-carboxamide Chemical compound NC(=O)C=1NC=2C=CSC=2C=1SC1=CC=CS1 AQSXTNJWWMGTSG-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- 230000001668 ameliorated effect Effects 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical group [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 claims 1
- 229910000024 caesium carbonate Inorganic materials 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000027288 circadian rhythm Effects 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 230000002035 prolonged effect Effects 0.000 claims 1
- 208000019116 sleep disease Diseases 0.000 claims 1
- 208000020685 sleep-wake disease Diseases 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60334704P | 2004-08-19 | 2004-08-19 | |
| US60/603,347 | 2004-08-19 | ||
| PCT/US2005/029383 WO2006021000A2 (en) | 2004-08-19 | 2005-08-18 | Substituted thienopyrrole carboxylic acid amides, pyrrolothiazole carboxylic acid amides, and related analogs as inhibitors of casein kinase i epsilon |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008510712A JP2008510712A (ja) | 2008-04-10 |
| JP2008510712A5 true JP2008510712A5 (enExample) | 2008-10-02 |
| JP4869232B2 JP4869232B2 (ja) | 2012-02-08 |
Family
ID=35695546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007528007A Expired - Fee Related JP4869232B2 (ja) | 2004-08-19 | 2005-08-18 | カゼイン・キナーゼＩε阻害剤としての、置換チエノピロールカルボン酸アミド、ピロロチアゾールカルボン酸アミド及び関連する類似化合物 |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US7393867B2 (enExample) |
| EP (1) | EP1784409B1 (enExample) |
| JP (1) | JP4869232B2 (enExample) |
| KR (1) | KR20070045263A (enExample) |
| CN (1) | CN100562521C (enExample) |
| AR (1) | AR051008A1 (enExample) |
| AT (1) | ATE471326T1 (enExample) |
| AU (1) | AU2005272584B2 (enExample) |
| BR (1) | BRPI0514419A (enExample) |
| CA (1) | CA2577879C (enExample) |
| CY (1) | CY1110775T1 (enExample) |
| DE (1) | DE602005021889D1 (enExample) |
| DK (1) | DK1784409T3 (enExample) |
| ES (1) | ES2347166T3 (enExample) |
| GT (1) | GT200500215A (enExample) |
| HR (1) | HRP20100475T1 (enExample) |
| IL (1) | IL181158A0 (enExample) |
| JO (1) | JO2629B1 (enExample) |
| MY (1) | MY139831A (enExample) |
| PA (1) | PA8642801A1 (enExample) |
| PE (1) | PE20060630A1 (enExample) |
| PL (1) | PL1784409T3 (enExample) |
| PT (1) | PT1784409E (enExample) |
| RS (1) | RS51413B (enExample) |
| RU (1) | RU2403257C2 (enExample) |
| SI (1) | SI1784409T1 (enExample) |
| SV (1) | SV2006002190A (enExample) |
| TW (1) | TWI372149B (enExample) |
| UY (1) | UY29077A1 (enExample) |
| WO (1) | WO2006021000A2 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ548212A (en) | 2003-12-29 | 2010-07-30 | Sepracor Inc | Pyrrole and pyrazole DAAO inhibitors |
| US8053603B2 (en) | 2006-01-06 | 2011-11-08 | Sunovion Pharmaceuticals Inc. | Tetralone-based monoamine reuptake inhibitors |
| KR101294014B1 (ko) | 2006-01-06 | 2013-08-09 | 선오비온 파마슈티컬스 인코포레이티드 | 모노아민 재흡수 저해제로서의 시클로알킬아민 |
| DK2816024T3 (en) | 2006-03-31 | 2017-10-30 | Sunovion Pharmaceuticals Inc | CHIRALE AMINER |
| US7884124B2 (en) | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| US7902252B2 (en) | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| EP1955699A1 (en) * | 2007-02-08 | 2008-08-13 | Boehringer Ingelheim Pharma GmbH & Co. KG | Use of flibanserin for the treatment of insomnia |
| MX2009012685A (es) | 2007-05-31 | 2009-12-14 | Sepracor Inc | Cicloalquilaminas sustituidas con fenilo como inhibidores de la reabsorcion de monoamina. |
| JP4748823B2 (ja) * | 2009-02-12 | 2011-08-17 | 株式会社ファルマデザイン | カゼインキナーゼ１δ及びカゼインキナーゼ１ε阻害剤 |
| UA106082C2 (uk) * | 2009-05-28 | 2014-07-25 | Вертекс Фармасьютікалз Інкорпорейтед | АМІНОПІРАЗОЛ ТРИАЗОЛОТІАДІАЗОЛЬНІ ІНГІБІТОРИ ПРОТЕЇНКІНАЗИ c-МЕТ |
| MX2012004997A (es) * | 2009-10-28 | 2012-06-12 | Pfizer | Derivados de imidazol como inhibidores de la caseina quinasa. |
| DE102009058280A1 (de) * | 2009-12-14 | 2011-06-16 | Merck Patent Gmbh | Thiazolderivate |
| CN104803997A (zh) * | 2010-08-09 | 2015-07-29 | 株式会社创药分子设计 | 酪蛋白激酶1δ及酪蛋白激酶1ε抑制剂 |
| CN109748927A (zh) * | 2017-11-03 | 2019-05-14 | 上海交通大学医学院附属瑞金医院 | 杂芳基酰胺类化合物、其制备方法、药用组合物及其应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE9702001D0 (sv) * | 1997-05-28 | 1997-05-28 | Astra Pharma Prod | Novel compounds |
| KR100722176B1 (ko) * | 1999-06-08 | 2007-05-29 | 아벤티스 파마슈티칼스 인크. | 일주기 리듬 단백질을 변화시키기 위한 스크리닝 방법 |
| CN100439367C (zh) * | 2003-12-11 | 2008-12-03 | 安万特药物公司 | 作为酪蛋白激酶Iε抑制剂的取代的1H-吡咯并[3,2-b、3,2-c和2,3-c]吡啶-2-甲酰胺以及相关类似物 |
-
2005
- 2005-07-18 JO JO2005104A patent/JO2629B1/en active
- 2005-08-09 GT GT200500215A patent/GT200500215A/es unknown
- 2005-08-09 SV SV2005002190A patent/SV2006002190A/es not_active Application Discontinuation
- 2005-08-16 AR ARP050103439A patent/AR051008A1/es unknown
- 2005-08-17 PE PE2005000956A patent/PE20060630A1/es not_active Application Discontinuation
- 2005-08-18 CN CNB2005800269958A patent/CN100562521C/zh not_active Expired - Fee Related
- 2005-08-18 PT PT05826812T patent/PT1784409E/pt unknown
- 2005-08-18 JP JP2007528007A patent/JP4869232B2/ja not_active Expired - Fee Related
- 2005-08-18 BR BRPI0514419-1A patent/BRPI0514419A/pt not_active Application Discontinuation
- 2005-08-18 CA CA2577879A patent/CA2577879C/en not_active Expired - Fee Related
- 2005-08-18 WO PCT/US2005/029383 patent/WO2006021000A2/en not_active Ceased
- 2005-08-18 RS RSP-2010/0401A patent/RS51413B/sr unknown
- 2005-08-18 SI SI200531094T patent/SI1784409T1/sl unknown
- 2005-08-18 PL PL05826812T patent/PL1784409T3/pl unknown
- 2005-08-18 EP EP05826812A patent/EP1784409B1/en not_active Expired - Lifetime
- 2005-08-18 DK DK05826812.9T patent/DK1784409T3/da active
- 2005-08-18 AU AU2005272584A patent/AU2005272584B2/en not_active Ceased
- 2005-08-18 HR HR20100475T patent/HRP20100475T1/hr unknown
- 2005-08-18 KR KR1020077003865A patent/KR20070045263A/ko not_active Abandoned
- 2005-08-18 AT AT05826812T patent/ATE471326T1/de active
- 2005-08-18 RU RU2007109812/04A patent/RU2403257C2/ru not_active IP Right Cessation
- 2005-08-18 MY MYPI20053879A patent/MY139831A/en unknown
- 2005-08-18 DE DE602005021889T patent/DE602005021889D1/de not_active Expired - Lifetime
- 2005-08-18 ES ES05826812T patent/ES2347166T3/es not_active Expired - Lifetime
- 2005-08-19 TW TW094128282A patent/TWI372149B/zh not_active IP Right Cessation
- 2005-08-19 UY UY29077A patent/UY29077A1/es not_active Application Discontinuation
- 2005-08-19 PA PA20058642801A patent/PA8642801A1/es unknown
-
2007
- 2007-02-04 IL IL181158A patent/IL181158A0/en unknown
- 2007-02-13 US US11/674,349 patent/US7393867B2/en not_active Expired - Lifetime
-
2008
- 2008-05-22 US US12/125,450 patent/US7652046B2/en not_active Expired - Lifetime
-
2010
- 2010-09-09 CY CY20101100823T patent/CY1110775T1/el unknown
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