JP2014526501A5 - - Google Patents
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- Publication number
- JP2014526501A5 JP2014526501A5 JP2014530371A JP2014530371A JP2014526501A5 JP 2014526501 A5 JP2014526501 A5 JP 2014526501A5 JP 2014530371 A JP2014530371 A JP 2014530371A JP 2014530371 A JP2014530371 A JP 2014530371A JP 2014526501 A5 JP2014526501 A5 JP 2014526501A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- trifluoromethyl
- amino
- optionally substituted
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 62
- 125000003118 aryl group Chemical group 0.000 claims description 38
- 125000005843 halogen group Chemical group 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 28
- 229910052760 oxygen Inorganic materials 0.000 claims description 27
- 125000005842 heteroatom Chemical group 0.000 claims description 26
- 229910052717 sulfur Inorganic materials 0.000 claims description 26
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 24
- 229910052736 halogen Inorganic materials 0.000 claims description 23
- 150000002367 halogens Chemical class 0.000 claims description 23
- 125000001424 substituent group Chemical group 0.000 claims description 23
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 13
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 12
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 12
- -1 R 14 Chemical compound 0.000 claims description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims description 12
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 11
- 239000012453 solvate Substances 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 7
- 208000035475 disorder Diseases 0.000 claims description 7
- JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 claims description 6
- 102000016911 Deoxyribonucleases Human genes 0.000 claims description 6
- 108010053770 Deoxyribonucleases Proteins 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 229940079593 drug Drugs 0.000 claims description 6
- 230000000954 anitussive effect Effects 0.000 claims description 5
- 239000003242 anti bacterial agent Substances 0.000 claims description 5
- 229940121363 anti-inflammatory agent Drugs 0.000 claims description 5
- 239000002260 anti-inflammatory agent Substances 0.000 claims description 5
- 229940088710 antibiotic agent Drugs 0.000 claims description 5
- 229940125715 antihistaminic agent Drugs 0.000 claims description 5
- 239000000739 antihistaminic agent Substances 0.000 claims description 5
- 239000003434 antitussive agent Substances 0.000 claims description 5
- 229940124584 antitussives Drugs 0.000 claims description 5
- 229940124630 bronchodilator Drugs 0.000 claims description 5
- 239000000168 bronchodilator agent Substances 0.000 claims description 5
- 239000002713 epithelial sodium channel blocking agent Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 239000002357 osmotic agent Substances 0.000 claims description 5
- 239000013543 active substance Substances 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 230000036571 hydration Effects 0.000 claims description 4
- 238000006703 hydration reaction Methods 0.000 claims description 4
- 230000002757 inflammatory effect Effects 0.000 claims description 4
- 230000000414 obstructive effect Effects 0.000 claims description 4
- 208000023504 respiratory system disease Diseases 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 2
- HKHAXZAOTYRNJR-UHFFFAOYSA-N 2-amino-5-iodo-n-(1h-pyrazol-5-yl)-4-(trifluoromethyl)benzamide Chemical compound NC1=CC(C(F)(F)F)=C(I)C=C1C(=O)NC1=CC=NN1 HKHAXZAOTYRNJR-UHFFFAOYSA-N 0.000 claims description 2
- RISQBVZZZVJMCQ-UHFFFAOYSA-N 3-[[3-amino-6-bromo-5-(trifluoromethyl)pyrazine-2-carbonyl]amino]-1h-1,2,4-triazole-5-carboxylic acid Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=NNC(C(O)=O)=N1 RISQBVZZZVJMCQ-UHFFFAOYSA-N 0.000 claims description 2
- FXFCABCHYDSYGA-UHFFFAOYSA-N 3-amino-6-(dimethylamino)-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound N1=C(C(F)(F)F)C(N(C)C)=NC(C(=O)NC=2NN=CC=2)=C1N FXFCABCHYDSYGA-UHFFFAOYSA-N 0.000 claims description 2
- KIXVSTSXVKRPDJ-UHFFFAOYSA-N 3-amino-6-[3-[(2-oxopyrrolidin-1-yl)methyl]phenyl]-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyridine-2-carboxamide Chemical compound NC1=CC(C(F)(F)F)=C(C=2C=C(CN3C(CCC3)=O)C=CC=2)N=C1C(=O)NC1=CC=NN1 KIXVSTSXVKRPDJ-UHFFFAOYSA-N 0.000 claims description 2
- FUPSDNHEPZDUQN-UHFFFAOYSA-N 3-amino-6-[4-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyridine-2-carboxamide Chemical compound O1C(C)=NN=C1C1=CC=C(C=2C(=CC(N)=C(C(=O)NC=3NN=CC=3)N=2)C(F)(F)F)C=C1 FUPSDNHEPZDUQN-UHFFFAOYSA-N 0.000 claims description 2
- NOOJJZQLLTVMPE-UHFFFAOYSA-N 3-amino-6-bromo-5-(trifluoromethyl)-n-[5-(trifluoromethyl)-1h-pyrazol-3-yl]pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=CC(C(F)(F)F)=NN1 NOOJJZQLLTVMPE-UHFFFAOYSA-N 0.000 claims description 2
- ZUCIZZYAIRXYRO-UHFFFAOYSA-N 3-amino-6-bromo-5-(trifluoromethyl)-n-[5-(trifluoromethyl)-1h-pyrazol-3-yl]pyridine-2-carboxamide Chemical compound NC1=CC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=NNC(C(F)(F)F)=C1 ZUCIZZYAIRXYRO-UHFFFAOYSA-N 0.000 claims description 2
- IAPZDLKJYLUBAQ-UHFFFAOYSA-N 3-amino-6-bromo-n-(1h-1,2,4-triazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=NC=NN1 IAPZDLKJYLUBAQ-UHFFFAOYSA-N 0.000 claims description 2
- HVFUYNVQJNXAHU-UHFFFAOYSA-N 3-amino-6-bromo-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=CC=NN1 HVFUYNVQJNXAHU-UHFFFAOYSA-N 0.000 claims description 2
- FSCUPLKDZUDDSF-UHFFFAOYSA-N 3-amino-6-bromo-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyridine-2-carboxamide Chemical compound NC1=CC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=CC=NN1 FSCUPLKDZUDDSF-UHFFFAOYSA-N 0.000 claims description 2
- PWQUBOXPGHABEZ-UHFFFAOYSA-N 3-amino-6-bromo-n-(2h-pyrazolo[3,4-b]pyrazin-3-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=C2N=CC=NC2=NN1 PWQUBOXPGHABEZ-UHFFFAOYSA-N 0.000 claims description 2
- BXJFJPYRITVCEQ-UHFFFAOYSA-N 3-amino-6-bromo-n-(2h-pyrazolo[3,4-b]pyrazin-3-yl)-5-(trifluoromethyl)pyridine-2-carboxamide Chemical compound NC1=CC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=C2N=CC=NC2=NN1 BXJFJPYRITVCEQ-UHFFFAOYSA-N 0.000 claims description 2
- XMAZQJKAZLMNOJ-UHFFFAOYSA-N 3-amino-6-bromo-n-(2h-pyrazolo[3,4-b]pyridin-3-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=C2C=CC=NC2=NN1 XMAZQJKAZLMNOJ-UHFFFAOYSA-N 0.000 claims description 2
- QQYUTQVCAIWUGU-UHFFFAOYSA-N 3-amino-6-bromo-n-(4-pyridin-2-yl-1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=C(C=2N=CC=CC=2)C=NN1 QQYUTQVCAIWUGU-UHFFFAOYSA-N 0.000 claims description 2
- XMADKJUWROCHFU-UHFFFAOYSA-N 3-amino-6-bromo-n-(5-cyclopropyl-1h-pyrazol-3-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=NNC(C2CC2)=C1 XMADKJUWROCHFU-UHFFFAOYSA-N 0.000 claims description 2
- JYSRWFAZAJZCDA-UHFFFAOYSA-N 3-amino-6-bromo-n-(5-methyl-1h-pyrazol-3-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound N1C(C)=CC(NC(=O)C=2C(=NC(=C(Br)N=2)C(F)(F)F)N)=N1 JYSRWFAZAJZCDA-UHFFFAOYSA-N 0.000 claims description 2
- HTXQNEPOJZQZBM-UHFFFAOYSA-N 3-amino-6-bromo-n-(5-tert-butyl-1h-pyrazol-3-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound N1C(C(C)(C)C)=CC(NC(=O)C=2C(=NC(=C(Br)N=2)C(F)(F)F)N)=N1 HTXQNEPOJZQZBM-UHFFFAOYSA-N 0.000 claims description 2
- LXIZAXFAWNODOI-UHFFFAOYSA-N 3-amino-6-bromo-n-[5-(piperidin-1-ylmethyl)-1h-pyrazol-3-yl]-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Br)N=C1C(=O)NC1=NNC(CN2CCCCC2)=C1 LXIZAXFAWNODOI-UHFFFAOYSA-N 0.000 claims description 2
- OSUMFHIKSGBWLE-UHFFFAOYSA-N 3-amino-6-chloro-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(Cl)N=C1C(=O)NC1=CC=NN1 OSUMFHIKSGBWLE-UHFFFAOYSA-N 0.000 claims description 2
- ZTFYPFHFEGGAJX-UHFFFAOYSA-N 3-amino-6-morpholin-4-yl-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(N2CCOCC2)N=C1C(=O)NC1=CC=NN1 ZTFYPFHFEGGAJX-UHFFFAOYSA-N 0.000 claims description 2
- CASMOHLSJQKMGI-UHFFFAOYSA-N 3-amino-6-pyrrolidin-1-yl-5-(trifluoromethyl)-n-[5-(trifluoromethyl)-1h-pyrazol-3-yl]pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=C(N2CCCC2)N=C1C(=O)NC=1C=C(C(F)(F)F)NN=1 CASMOHLSJQKMGI-UHFFFAOYSA-N 0.000 claims description 2
- NMSPFFAERNQCAK-UHFFFAOYSA-N 3-amino-n-(1h-pyrazol-5-yl)-5-(trifluoromethyl)pyrazine-2-carboxamide Chemical compound NC1=NC(C(F)(F)F)=CN=C1C(=O)NC1=CC=NN1 NMSPFFAERNQCAK-UHFFFAOYSA-N 0.000 claims description 2
- GKZILYYYGAHEGB-UHFFFAOYSA-N 3-amino-n-(4-methyl-1h-pyrazol-5-yl)-5,6-bis(trifluoromethyl)pyrazine-2-carboxamide Chemical compound C1=NNC(NC(=O)C=2C(=NC(=C(N=2)C(F)(F)F)C(F)(F)F)N)=C1C GKZILYYYGAHEGB-UHFFFAOYSA-N 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 2
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 108010079245 Cystic Fibrosis Transmembrane Conductance Regulator Proteins 0.000 description 4
- 102000008371 intracellularly ATP-gated chloride channel activity proteins Human genes 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
- 125000005330 8 membered heterocyclic group Chemical group 0.000 description 1
- 206010006458 Bronchitis chronic Diseases 0.000 description 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 description 1
- 206010010774 Constipation Diseases 0.000 description 1
- 201000003883 Cystic fibrosis Diseases 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 206010057190 Respiratory tract infections Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 206010006451 bronchitis Diseases 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 208000007451 chronic bronchitis Diseases 0.000 description 1
- 230000001886 ciliary effect Effects 0.000 description 1
- 206010013781 dry mouth Diseases 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- FZWBNHMXJMCXLU-BLAUPYHCSA-N isomaltotriose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)O1 FZWBNHMXJMCXLU-BLAUPYHCSA-N 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161535671P | 2011-09-16 | 2011-09-16 | |
| US61/535,671 | 2011-09-16 | ||
| PCT/IB2012/054832 WO2013038390A1 (en) | 2011-09-16 | 2012-09-14 | N-substituted heterocyclyl carboxamides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014526501A JP2014526501A (ja) | 2014-10-06 |
| JP2014526501A5 true JP2014526501A5 (cg-RX-API-DMAC10.html) | 2017-06-22 |
| JP6165733B2 JP6165733B2 (ja) | 2017-07-19 |
Family
ID=47143991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014530371A Expired - Fee Related JP6165733B2 (ja) | 2011-09-16 | 2012-09-14 | Ｎ−置換ヘテロシクリルカルボキサミド類 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9056867B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP2755652B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP6165733B2 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2882807T3 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2013038390A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8563573B2 (en) | 2007-11-02 | 2013-10-22 | Vertex Pharmaceuticals Incorporated | Azaindole derivatives as CFTR modulators |
| US8802868B2 (en) | 2010-03-25 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of (R)-1(2,2-difluorobenzo[D][1,3]dioxo1-5-yl)-N-(1-(2,3-dihydroxypropyl-6-fluoro-2-(1-hydroxy-2-methylpropan2-yl)-1H-Indol-5-yl)-Cyclopropanecarboxamide |
| EP3381899B1 (en) | 2010-04-22 | 2021-01-06 | Vertex Pharmaceuticals Incorporated | Intermediate compound for process of producing cycloalkylcarboxamido-indole compounds |
| WO2013038386A1 (en) | 2011-09-16 | 2013-03-21 | Novartis Ag | Heterocyclic compounds for the treatment of cystic fibrosis |
| JP6543268B2 (ja) | 2014-04-15 | 2019-07-10 | バーテックス ファーマシューティカルズ インコーポレイテッドＶｅｒｔｅｘ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｉｎｃｏｒｐｏｒａｔｅｄ | 嚢胞性線維症膜コンダクタンス調節因子が媒介する疾患を処置するための医薬組成物 |
| EP3140298A1 (en) | 2014-05-07 | 2017-03-15 | Pfizer Inc. | Tropomyosin-related kinase inhibitors |
| WO2015196071A1 (en) | 2014-06-19 | 2015-12-23 | Proteostasis Therapeutics, Inc. | Compounds, compositions and methods of increasing cftr activity |
| SMT202000540T1 (it) | 2014-10-06 | 2020-11-10 | Vertex Pharma | Modulatori di regolatore di conduttanza transmembrana di fibrosi cistica |
| US9567322B2 (en) | 2014-10-31 | 2017-02-14 | Abbvie S.Á.R.L. | Substituted tetrahydropyrans and method of use |
| CA2971835A1 (en) | 2014-12-23 | 2016-06-30 | Proteostasis Therapeutics, Inc. | Derivatives of 3-heteroarylisoxazol-5-carboxylic amide useful for the treatment of inter alia cystic fibrosis |
| MA41253A (fr) | 2014-12-23 | 2017-10-31 | Proteostasis Therapeutics Inc | Composés, compositions et procédés pour augmenter l'activité du cftr |
| US10392378B2 (en) | 2014-12-23 | 2019-08-27 | Proteostasis Therapeutics, Inc. | Derivatives of 5-phenyl- or 5-heteroarylathiazol-2-carboxylic amide useful for the treatment of inter alia cystic fibrosis |
| BR112017026132A2 (pt) * | 2015-06-02 | 2018-08-28 | AbbVie S.à.r.l. | piridinas substituídas e métodos de uso |
| HRP20211864T1 (hr) * | 2015-07-06 | 2022-03-04 | Alkermes, Inc. | Inhibitori hetero-halo histonske deacetilaze |
| US9840513B2 (en) | 2015-07-16 | 2017-12-12 | Abbvie S.Á.R.L. | Substituted tricyclics and method of use |
| WO2017019589A1 (en) | 2015-07-24 | 2017-02-02 | Proteostasis Therapeutics, Inc. | Compounds, compositions and methods of increasing cftr activity |
| SG11201802798WA (en) | 2015-10-06 | 2018-05-30 | Proteostasis Therapeutics Inc | Compounds, compositions, and methods for modulating cftr |
| BR112018007165A2 (pt) | 2015-10-09 | 2019-01-22 | AbbVie S.à.r.l. | novos compostos para tratamento da fibrose cística |
| WO2017060873A1 (en) | 2015-10-09 | 2017-04-13 | AbbVie S.à.r.l. | Substituted pyrazolo[3,4-b]pyridin-6-carboxylic acids and their use |
| PE20181348A1 (es) | 2015-10-09 | 2018-08-22 | Abbvie Sarl | PIRAZOLO[3,4-b]PIRIDIN-6-CARBOXAMIDAS N-SULFONILADAS Y METODO DE USO |
| CN108463223A (zh) * | 2015-10-09 | 2018-08-28 | 艾伯维公司 | 用于治疗囊性纤维化的增效剂-校正剂组合 |
| US10662207B2 (en) | 2016-04-07 | 2020-05-26 | Proteostasis Therapeutics, Inc. | Compounds, compositions, and methods for modulating CFTR |
| CN109219602A (zh) | 2016-04-26 | 2019-01-15 | 艾伯维公司 | 囊性纤维化跨膜传导调节物蛋白的调节剂 |
| JP2019112306A (ja) * | 2016-04-28 | 2019-07-11 | 宇部興産株式会社 | 慢性閉塞性肺疾患の治療または予防のための医薬組成物 |
| US10138227B2 (en) | 2016-06-03 | 2018-11-27 | Abbvie S.Á.R.L. | Heteroaryl substituted pyridines and methods of use |
| ES2954658T3 (es) | 2016-06-21 | 2023-11-23 | Proteostasis Therapeutics Inc | Compuestos, composiciones y procedimientos para aumentar la actividad de CFTR |
| TW201811766A (zh) * | 2016-08-29 | 2018-04-01 | 瑞士商諾華公司 | N-(吡啶-2-基)吡啶-磺醯胺衍生物及其用於疾病治療之用途 |
| US10399940B2 (en) | 2016-10-07 | 2019-09-03 | Abbvie S.Á.R.L. | Substituted pyrrolidines and methods of use |
| US9981910B2 (en) | 2016-10-07 | 2018-05-29 | Abbvie S.Á.R.L. | Substituted pyrrolidines and methods of use |
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2012
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- 2012-09-14 JP JP2014530371A patent/JP6165733B2/ja not_active Expired - Fee Related
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- 2012-09-14 ES ES12783311T patent/ES2882807T3/es active Active