JP2008519087A5 - - Google Patents
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- JP2008519087A5 JP2008519087A5 JP2007540710A JP2007540710A JP2008519087A5 JP 2008519087 A5 JP2008519087 A5 JP 2008519087A5 JP 2007540710 A JP2007540710 A JP 2007540710A JP 2007540710 A JP2007540710 A JP 2007540710A JP 2008519087 A5 JP2008519087 A5 JP 2008519087A5
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- 150000001875 compounds Chemical class 0.000 claims 37
- 125000004429 atom Chemical group 0.000 claims 23
- 229910052760 oxygen Inorganic materials 0.000 claims 21
- 229910052757 nitrogen Inorganic materials 0.000 claims 20
- 229910052739 hydrogen Inorganic materials 0.000 claims 19
- 239000001257 hydrogen Substances 0.000 claims 19
- 125000005842 heteroatom Chemical group 0.000 claims 14
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 13
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 12
- 125000005647 linker group Chemical group 0.000 claims 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 10
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- -1 cyano, nitro, carboxy, amino Chemical group 0.000 claims 9
- 229910052736 halogen Inorganic materials 0.000 claims 9
- 150000002367 halogens Chemical class 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 238000006243 chemical reaction Methods 0.000 claims 8
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 6
- 150000001204 N-oxides Chemical class 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 229910052731 fluorine Inorganic materials 0.000 claims 6
- 239000011737 fluorine Substances 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 5
- 229910052794 bromium Inorganic materials 0.000 claims 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 125000004043 oxo group Chemical group O=* 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 239000012453 solvate Substances 0.000 claims 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 125000004423 acyloxy group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 230000002265 prevention Effects 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 2
- 102000008130 Cyclic AMP-Dependent Protein Kinases Human genes 0.000 claims 2
- 108010049894 Cyclic AMP-Dependent Protein Kinases Proteins 0.000 claims 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 2
- 108091008611 Protein Kinase B Proteins 0.000 claims 2
- 102000005765 Proto-Oncogene Proteins c-akt Human genes 0.000 claims 2
- 230000002159 abnormal effect Effects 0.000 claims 2
- 150000001450 anions Chemical class 0.000 claims 2
- 125000002527 bicyclic carbocyclic group Chemical group 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 239000010949 copper Substances 0.000 claims 2
- 230000001419 dependent effect Effects 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 229910052763 palladium Inorganic materials 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000003386 piperidinyl group Chemical group 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 2
- 125000000586 2-(4-morpholinyl)ethoxy group Chemical group [H]C([H])(O*)C([H])([H])N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 claims 1
- JPAOSCNZYJIWGU-UHFFFAOYSA-N 4-(4-chlorophenyl)-n-(4-oxo-1h-quinazolin-7-yl)piperidine-4-carboxamide Chemical compound C1=CC(Cl)=CC=C1C1(C(=O)NC=2C=C3C(C(NC=N3)=O)=CC=2)CCNCC1 JPAOSCNZYJIWGU-UHFFFAOYSA-N 0.000 claims 1
- LKLACGZUXOSYME-UHFFFAOYSA-N 4-amino-2-(3,4-dichlorophenyl)-n-(4-oxo-1h-quinazolin-7-yl)butanamide Chemical compound C=1C=C(C(NC=N2)=O)C2=CC=1NC(=O)C(CCN)C1=CC=C(Cl)C(Cl)=C1 LKLACGZUXOSYME-UHFFFAOYSA-N 0.000 claims 1
- 125000006164 6-membered heteroaryl group Chemical group 0.000 claims 1
- AKWWVGIPWJYWOJ-UHFFFAOYSA-N 7-[2-[4-(4-chlorophenyl)piperidin-4-yl]ethenyl]-1h-quinazolin-4-one Chemical compound C1=CC(Cl)=CC=C1C1(C=CC=2C=C3C(C(NC=N3)=O)=CC=2)CCNCC1 AKWWVGIPWJYWOJ-UHFFFAOYSA-N 0.000 claims 1
- CQCZVSPWCJSNOE-UHFFFAOYSA-N 7-[4-(aminomethyl)-4-(4-chlorophenyl)piperidin-1-yl]-1h-quinazolin-4-one Chemical compound C1CN(C=2C=C3C(C(NC=N3)=O)=CC=2)CCC1(CN)C1=CC=C(Cl)C=C1 CQCZVSPWCJSNOE-UHFFFAOYSA-N 0.000 claims 1
- CNOUMTJGSIBEDM-UHFFFAOYSA-N 7-[4-(aminomethyl)-4-(4-chlorophenyl)piperidin-1-yl]-2-methyl-1h-quinazolin-4-one Chemical compound C=1C=C2C(=O)NC(C)=NC2=CC=1N(CC1)CCC1(CN)C1=CC=C(Cl)C=C1 CNOUMTJGSIBEDM-UHFFFAOYSA-N 0.000 claims 1
- PIXXOEINPBZHFJ-UHFFFAOYSA-N 7-[4-(aminomethyl)-4-[(4-chlorophenyl)methyl]piperidin-1-yl]-1-methylquinazoline-2,4-dione Chemical compound C=1C=C2C(=O)NC(=O)N(C)C2=CC=1N(CC1)CCC1(CN)CC1=CC=C(Cl)C=C1 PIXXOEINPBZHFJ-UHFFFAOYSA-N 0.000 claims 1
- PCQFKJJJPQIJHA-UHFFFAOYSA-N 7-[4-(aminomethyl)-4-[(4-chlorophenyl)methyl]piperidin-1-yl]-1h-quinazolin-4-one Chemical compound C1CN(C=2C=C3C(C(NC=N3)=O)=CC=2)CCC1(CN)CC1=CC=C(Cl)C=C1 PCQFKJJJPQIJHA-UHFFFAOYSA-N 0.000 claims 1
- AHCDLSCQWMMXGO-UHFFFAOYSA-N 7-[4-[amino-(4-chlorophenyl)methyl]piperidin-1-yl]-1h-quinazolin-4-one Chemical compound C1CN(C=2C=C3C(C(NC=N3)=O)=CC=2)CCC1C(N)C1=CC=C(Cl)C=C1 AHCDLSCQWMMXGO-UHFFFAOYSA-N 0.000 claims 1
- BYPCNAQSAXHLDB-UHFFFAOYSA-N 7-[4-amino-4-(4-chlorophenyl)piperidin-1-yl]-1h-quinazolin-4-one Chemical compound C1CN(C=2C=C3C(C(NC=N3)=O)=CC=2)CCC1(N)C1=CC=C(Cl)C=C1 BYPCNAQSAXHLDB-UHFFFAOYSA-N 0.000 claims 1
- IDKVLXLJSXYUOF-UHFFFAOYSA-N 7-[4-amino-4-[(4-chlorophenyl)methyl]piperidin-1-yl]-1h-quinazolin-4-one Chemical compound C1CN(C=2C=C3C(C(NC=N3)=O)=CC=2)CCC1(N)CC1=CC=C(Cl)C=C1 IDKVLXLJSXYUOF-UHFFFAOYSA-N 0.000 claims 1
- NQKSXMPLSLVNNT-UHFFFAOYSA-N 7-[[4-(4-chlorophenyl)piperidin-4-yl]methoxy]-1-methylquinazoline-2,4-dione Chemical compound C=1C=C2C(=O)NC(=O)N(C)C2=CC=1OCC1(C=2C=CC(Cl)=CC=2)CCNCC1 NQKSXMPLSLVNNT-UHFFFAOYSA-N 0.000 claims 1
- 238000001321 HNCO Methods 0.000 claims 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical group N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- 125000004442 acylamino group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 230000030833 cell death Effects 0.000 claims 1
- 230000010261 cell growth Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000006518 morpholino carbonyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])N(C(*)=O)C1([H])[H] 0.000 claims 1
- WUUXBBLJAGVZKB-UHFFFAOYSA-N n-(4-oxo-1h-quinazolin-7-yl)-4-phenylpiperidine-4-carboxamide Chemical compound C=1C=C(C(NC=N2)=O)C2=CC=1NC(=O)C1(C=2C=CC=CC=2)CCNCC1 WUUXBBLJAGVZKB-UHFFFAOYSA-N 0.000 claims 1
- QAMJPJFFOJCDKP-UHFFFAOYSA-N n-[3-amino-1-(4-chlorophenyl)propyl]-4-oxo-1h-quinazoline-7-carboxamide Chemical compound C=1C=C(C(NC=N2)=O)C2=CC=1C(=O)NC(CCN)C1=CC=C(Cl)C=C1 QAMJPJFFOJCDKP-UHFFFAOYSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62640304P | 2004-11-09 | 2004-11-09 | |
| GB0424742A GB0424742D0 (en) | 2004-11-09 | 2004-11-09 | Pharmaceutical compounds |
| PCT/GB2005/004323 WO2006051290A2 (en) | 2004-11-09 | 2005-11-09 | Compounds for treating protein-kinase mediated disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008519087A JP2008519087A (ja) | 2008-06-05 |
| JP2008519087A5 true JP2008519087A5 (https=) | 2008-12-25 |
Family
ID=35695751
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007540710A Withdrawn JP2008519087A (ja) | 2004-11-09 | 2005-11-09 | 医薬品 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20080275029A1 (https=) |
| EP (1) | EP1814552A2 (https=) |
| JP (1) | JP2008519087A (https=) |
| AR (1) | AR053778A1 (https=) |
| UY (1) | UY29198A1 (https=) |
| WO (1) | WO2006051290A2 (https=) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007008926A1 (en) | 2005-07-11 | 2007-01-18 | Aerie Pharmaceuticals, Inc. | Isoquinoline compounds |
| US7618985B2 (en) | 2005-12-08 | 2009-11-17 | N.V. Organon | Isoquinoline derivatives |
| US7893088B2 (en) | 2006-08-18 | 2011-02-22 | N.V. Organon | 6-substituted isoquinoline derivatives |
| WO2008036540A2 (en) | 2006-09-20 | 2008-03-27 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| US8455513B2 (en) | 2007-01-10 | 2013-06-04 | Aerie Pharmaceuticals, Inc. | 6-aminoisoquinoline compounds |
| US8455514B2 (en) * | 2008-01-17 | 2013-06-04 | Aerie Pharmaceuticals, Inc. | 6-and 7-amino isoquinoline compounds and methods for making and using the same |
| US8450344B2 (en) | 2008-07-25 | 2013-05-28 | Aerie Pharmaceuticals, Inc. | Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds |
| EP3053913B1 (en) | 2009-05-01 | 2018-03-07 | Aerie Pharmaceuticals, Inc. | Dual mechanism inhibitors for the treatment of disease |
| RU2451010C1 (ru) * | 2011-01-11 | 2012-05-20 | Закрытое Акционерное Общество "Ива Фарм" | Палладиево-медные катализаторы гомогенного селективного окисления тиольных групп, комбинация и композиция на их основе и способ терапевтического воздействия |
| DK3811943T3 (da) | 2013-03-15 | 2023-04-03 | Aerie Pharmaceuticals Inc | Forbindelse til anvendelse til behandling af øjenlidelser |
| CN103524431B (zh) * | 2013-09-24 | 2016-01-13 | 西安交通大学 | 3-苄基-4-喹唑啉酮类化合物及其合成方法和应用 |
| RU2743074C2 (ru) | 2014-08-01 | 2021-02-15 | Нуэволюшон А/С | Соединения, активные по отношению к бромодоменам |
| SG11201708622UA (en) | 2015-02-02 | 2017-11-29 | Forma Therapeutics Inc | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
| WO2016126726A1 (en) | 2015-02-02 | 2016-08-11 | Forma Therapeutics, Inc. | Bicyclic [4,6,0] hydroxamic acids as hdac6 inhibitors |
| US10550087B2 (en) | 2015-11-17 | 2020-02-04 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| US9643927B1 (en) | 2015-11-17 | 2017-05-09 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| EP3472131B1 (en) | 2016-06-17 | 2020-02-19 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors |
| KR102568079B1 (ko) | 2016-08-31 | 2023-08-17 | 에어리 파마슈티컬즈, 인코포레이티드 | 안과용 조성물 |
| KR20190135027A (ko) | 2017-03-31 | 2019-12-05 | 에어리 파마슈티컬즈, 인코포레이티드 | 아릴 시클로프로필-아미노-이소퀴놀리닐 아미드 화합물 |
| US20220089609A1 (en) | 2018-07-26 | 2022-03-24 | Domain Therapeutics | Substituted quinazolinone derivatives and their use as positive allosteric modulators of mglur4 |
| AU2019337703B2 (en) | 2018-09-14 | 2023-02-02 | Aerie Pharmaceuticals, Inc. | Aryl cyclopropyl-amino-isoquinolinyl amide compounds |
| TWI829003B (zh) | 2020-08-12 | 2024-01-11 | 美商建南德克公司 | 喹唑啉化合物之合成 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4281127A (en) * | 1979-07-09 | 1981-07-28 | Hoffmann-La Roche Inc. | Trans-3-(4-oxo-4H-quinazolin-3-yl)-2-propenoic acid derivatives |
| UA73993C2 (uk) * | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
| TW200301123A (en) * | 2001-12-21 | 2003-07-01 | Astrazeneca Uk Ltd | New use |
-
2005
- 2005-11-08 UY UY29198A patent/UY29198A1/es not_active Application Discontinuation
- 2005-11-09 WO PCT/GB2005/004323 patent/WO2006051290A2/en not_active Ceased
- 2005-11-09 US US11/718,943 patent/US20080275029A1/en not_active Abandoned
- 2005-11-09 JP JP2007540710A patent/JP2008519087A/ja not_active Withdrawn
- 2005-11-09 EP EP05801609A patent/EP1814552A2/en not_active Withdrawn
- 2005-11-09 AR ARP050104700A patent/AR053778A1/es not_active Application Discontinuation
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