JP2006502134A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2006502134A5 JP2006502134A5 JP2004527914A JP2004527914A JP2006502134A5 JP 2006502134 A5 JP2006502134 A5 JP 2006502134A5 JP 2004527914 A JP2004527914 A JP 2004527914A JP 2004527914 A JP2004527914 A JP 2004527914A JP 2006502134 A5 JP2006502134 A5 JP 2006502134A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- oxadiazol
- ylmethyl
- piperidin
- benzonitrile
- 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.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims 111
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 44
- -1 3- (2,3-dimethoxyphenyl) -5- [1- (phenylmethyl) -2-pyrrolidinyl] -1,2,4-oxadiazole Chemical compound 0.000 claims 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 15
- 201000010099 disease Diseases 0.000 claims 12
- 125000004429 atom Chemical group 0.000 claims 9
- 229910052799 carbon Inorganic materials 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 9
- 229910052760 oxygen Inorganic materials 0.000 claims 9
- 229910052717 sulfur Inorganic materials 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 102000012777 Metabotropic Glutamate 5 Receptor Human genes 0.000 claims 7
- 108010065028 Metabotropic Glutamate 5 Receptor Proteins 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 7
- 230000001404 mediated effect Effects 0.000 claims 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims 6
- 125000001475 halogen functional group Chemical group 0.000 claims 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 6
- 125000004043 oxo group Chemical group O=* 0.000 claims 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- JRSWALOPXPBCPG-UHFFFAOYSA-N 3-(3-methylphenyl)-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound CC1=CC=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 JRSWALOPXPBCPG-UHFFFAOYSA-N 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 208000019901 Anxiety disease Diseases 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 206010019196 Head injury Diseases 0.000 claims 2
- 208000013016 Hypoglycemia Diseases 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 208000018737 Parkinson disease Diseases 0.000 claims 2
- 208000027418 Wounds and injury Diseases 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 230000036506 anxiety Effects 0.000 claims 2
- 230000006378 damage Effects 0.000 claims 2
- 206010015037 epilepsy Diseases 0.000 claims 2
- 230000002218 hypoglycaemic effect Effects 0.000 claims 2
- 208000014674 injury Diseases 0.000 claims 2
- 208000037906 ischaemic injury Diseases 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 208000004296 neuralgia Diseases 0.000 claims 2
- 230000004770 neurodegeneration Effects 0.000 claims 2
- 208000015122 neurodegenerative disease Diseases 0.000 claims 2
- 208000021722 neuropathic pain Diseases 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- SOQLQSYJDARMFJ-UHFFFAOYSA-N 2-[[2-[3-(3-cyanophenyl)-1,2,4-oxadiazol-5-yl]piperidin-1-yl]methyl]-1,3-thiazole-4-carbonitrile Chemical compound N#CC1=CSC(CN2C(CCCC2)C=2ON=C(N=2)C=2C=C(C=CC=2)C#N)=N1 SOQLQSYJDARMFJ-UHFFFAOYSA-N 0.000 claims 1
- CRHDBAIOECFMNV-UHFFFAOYSA-N 3-(3-chlorophenyl)-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound ClC1=CC=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 CRHDBAIOECFMNV-UHFFFAOYSA-N 0.000 claims 1
- JCQVILDTFNPCQD-UHFFFAOYSA-N 3-(3-ethylphenyl)-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound CCC1=CC=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 JCQVILDTFNPCQD-UHFFFAOYSA-N 0.000 claims 1
- KMCWHZPMGGCHIK-UHFFFAOYSA-N 3-(3-fluoro-5-imidazol-1-ylphenyl)-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound C=1C(F)=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=CC=CC=2)=CC=1N1C=CN=C1 KMCWHZPMGGCHIK-UHFFFAOYSA-N 0.000 claims 1
- UEUYNVNBEXGSOM-UHFFFAOYSA-N 3-(3-methoxyphenyl)-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound COC1=CC=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 UEUYNVNBEXGSOM-UHFFFAOYSA-N 0.000 claims 1
- MUWLZOUUKMVYEQ-UHFFFAOYSA-N 3-[3-(3-chlorophenyl)-1,2,4-oxadiazol-5-yl]-4-(1,3-thiazol-2-ylmethyl)morpholine Chemical compound ClC1=CC=CC(C=2N=C(ON=2)C2N(CCOC2)CC=2SC=CN=2)=C1 MUWLZOUUKMVYEQ-UHFFFAOYSA-N 0.000 claims 1
- GTZFPOKFRGLTNQ-AWEZNQCLSA-N 3-[5-[(2s)-1-(1,3-thiazol-2-ylmethyl)pyrrolidin-2-yl]-1,2,4-oxadiazol-3-yl]benzonitrile Chemical compound N#CC1=CC=CC(C=2N=C(ON=2)[C@H]2N(CCC2)CC=2SC=CN=2)=C1 GTZFPOKFRGLTNQ-AWEZNQCLSA-N 0.000 claims 1
- NFDNFXGXISIHBR-UHFFFAOYSA-N 3-[5-[1-(quinolin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazol-3-yl]benzonitrile Chemical compound N#CC1=CC=CC(C=2N=C(ON=2)C2N(CCCC2)CC=2N=C3C=CC=CC3=CC=2)=C1 NFDNFXGXISIHBR-UHFFFAOYSA-N 0.000 claims 1
- ZLJYWKHFOAZQKU-UHFFFAOYSA-N 3-methoxy-5-[3-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazol-5-yl]benzonitrile Chemical compound COC1=CC(C#N)=CC(C=2ON=C(N=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 ZLJYWKHFOAZQKU-UHFFFAOYSA-N 0.000 claims 1
- HSHDPJHECYAPOJ-UHFFFAOYSA-N 3-phenyl-5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound C=1C=CC=NC=1CN1CCCCC1C(ON=1)=NC=1C1=CC=CC=C1 HSHDPJHECYAPOJ-UHFFFAOYSA-N 0.000 claims 1
- MQNJRODJEBAUQQ-UHFFFAOYSA-N 5-(3-methoxyphenyl)-3-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound COC1=CC=CC(C=2ON=C(N=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 MQNJRODJEBAUQQ-UHFFFAOYSA-N 0.000 claims 1
- JZALMAHWFNMKOZ-UHFFFAOYSA-N 5-(3-methylphenyl)-3-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-1,2,4-oxadiazole Chemical compound CC1=CC=CC(C=2ON=C(N=2)C2N(CCCC2)CC=2N=CC=CC=2)=C1 JZALMAHWFNMKOZ-UHFFFAOYSA-N 0.000 claims 1
- SGVJZWFVMHFQJK-UHFFFAOYSA-N 5-[1-(pyridin-2-ylmethyl)piperidin-2-yl]-3-thiophen-2-yl-1,2,4-oxadiazole Chemical compound C=1C=CC=NC=1CN1CCCCC1C(ON=1)=NC=1C1=CC=CS1 SGVJZWFVMHFQJK-UHFFFAOYSA-N 0.000 claims 1
- DAGHUOKMGWCJLR-UHFFFAOYSA-N 6-[[2-[3-(3-cyanophenyl)-1,2,4-oxadiazol-5-yl]piperidin-1-yl]methyl]pyridine-3-carbonitrile Chemical compound N1=CC(C#N)=CC=C1CN1C(C=2ON=C(N=2)C=2C=C(C=CC=2)C#N)CCCC1 DAGHUOKMGWCJLR-UHFFFAOYSA-N 0.000 claims 1
- 206010065390 Inflammatory pain Diseases 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 208000019695 Migraine disease Diseases 0.000 claims 1
- 208000012902 Nervous system disease Diseases 0.000 claims 1
- 208000025966 Neurological disease Diseases 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 208000005298 acute pain Diseases 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 208000022371 chronic pain syndrome Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 206010027599 migraine Diseases 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 208000020016 psychiatric disease Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40203802P | 2002-08-09 | 2002-08-09 | |
| PCT/US2003/024915 WO2004014902A2 (en) | 2002-08-09 | 2003-08-08 | Compounds having an activity at metabotropic glutamate receptors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006502134A JP2006502134A (ja) | 2006-01-19 |
| JP2006502134A5 true JP2006502134A5 (enExample) | 2006-09-28 |
Family
ID=31715775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004527914A Pending JP2006502134A (ja) | 2002-08-09 | 2003-08-08 | 代謝調節型グルタミン酸受容体において活性を有する化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7074809B2 (enExample) |
| EP (1) | EP1581525A2 (enExample) |
| JP (1) | JP2006502134A (enExample) |
| AU (1) | AU2003264018A1 (enExample) |
| CA (1) | CA2495179A1 (enExample) |
| MX (1) | MXPA05001590A (enExample) |
| WO (1) | WO2004014902A2 (enExample) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2887054T3 (es) | 2003-04-11 | 2021-12-21 | Ptc Therapeutics Inc | Compuesto de ácido 1,2,4-oxadiazol benzoico y su uso para la supresión sin sentido y el tratamiento de enfermedades |
| GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
| WO2005077368A2 (en) * | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
| EP1720860A1 (en) * | 2004-02-18 | 2006-11-15 | AstraZeneca AB | Triazole compounds and their use as metabotropic glutamate receptor antagonists |
| AU2005214378A1 (en) * | 2004-02-18 | 2005-09-01 | Astrazeneca Ab | Polyheterocyclic compounds and their use as metabotropic glutamate receptor antagonists |
| US20070185095A1 (en) * | 2004-02-18 | 2007-08-09 | Astrazeneca Ab | Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists |
| US7585881B2 (en) * | 2004-02-18 | 2009-09-08 | Astrazeneca Ab | Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
| TW200538108A (en) | 2004-02-19 | 2005-12-01 | Astrazeneca Ab | Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists |
| CA2593439C (en) * | 2005-01-14 | 2014-02-25 | F. Hoffmann-La Roche Ag | Thiazole-4-carboxamide derivatives as mglur5 antagonists |
| GB0510142D0 (en) * | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds A1 |
| GB0510139D0 (en) * | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B1 |
| GB0510141D0 (en) * | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B3 |
| AR058807A1 (es) | 2005-09-29 | 2008-02-27 | Astrazeneca Ab | 5-(fenilisoxazoletoxi)-triazol-3-il piridinas sustituidas, para el tratamiento de trastornos mediados por el receptor mglur5 |
| HUP0500920A2 (en) * | 2005-10-05 | 2007-07-30 | Richter Gedeon Nyrt | Oxadiazole derivatives, process for their preparation and their use |
| IN2014CN04406A (enExample) | 2006-03-30 | 2015-09-04 | Ptc Therapeutics Inc | |
| MX2008011968A (es) * | 2006-03-31 | 2008-10-01 | Astrazeneca Ab | Compuestos biciclicos de bencimidazol y su uso como potenciadores del receptor metabotropico de glutamato. |
| MX2008012738A (es) * | 2006-04-03 | 2009-02-06 | Astellas Pharma Inc | Heterocompuesto. |
| KR100681911B1 (ko) | 2006-04-03 | 2007-02-15 | 재단법인서울대학교산학협력재단 | 5,10,15,20―테트라키스―（2―플루오로―피리딘―3―일）―포르피린,5,10,15,20―테트라키스―（3,5―다이플루오로―피리딘―4―일）―포르피린과 이들의 ｎ―알킬염 및 이들의 제조방법 |
| TW200811137A (en) * | 2006-05-05 | 2008-03-01 | Astrazeneca Ab | mGluR5 modulators II |
| TW200811157A (en) * | 2006-05-05 | 2008-03-01 | Astrazeneca Ab | mGluR5 modulators I |
| TW200808777A (en) * | 2006-05-05 | 2008-02-16 | Astrazeneca Ab | MGLUR5 modulators III |
| TW200808800A (en) * | 2006-05-05 | 2008-02-16 | Astrazeneca Ab | MGluR5 modulators V |
| TW200811179A (en) * | 2006-05-05 | 2008-03-01 | Astrazeneca Ab | mGluR5 modulators VI |
| FR2903405B1 (fr) * | 2006-07-04 | 2011-09-09 | Pasteur Institut | Composes a effet potentialisateur de l'activite de l'ethionamide et leurs applications |
| JP5448164B2 (ja) | 2006-07-28 | 2014-03-19 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃｂ２受容体を変調する化合物 |
| US7985753B2 (en) * | 2006-08-04 | 2011-07-26 | Merz Pharma Gmbh & Co. Kgaa | Substituted pyrazolo[1,5-A]pyrimidines as metabotropic glutamate receptor modulators |
| HUE036519T2 (hu) | 2007-08-13 | 2018-07-30 | Monsanto Technology Llc | Készítmények és eljárások nematódák irtására |
| JP5492092B2 (ja) | 2007-11-07 | 2014-05-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃｂ２受容体を調節する化合物 |
| EP2300437B1 (en) | 2008-06-05 | 2013-11-20 | Glaxo Group Limited | Benzpyrazol derivatives as inhibitors of pi3 kinases |
| EP2280705B1 (en) | 2008-06-05 | 2014-10-08 | Glaxo Group Limited | Novel compounds |
| JP5502077B2 (ja) | 2008-06-05 | 2014-05-28 | グラクソ グループ リミテッド | 新規な化合物 |
| US8178568B2 (en) | 2008-07-10 | 2012-05-15 | Boehringer Ingelheim International Gmbh | Sulfone compounds which modulate the CB2 receptor |
| US8048899B2 (en) | 2008-09-25 | 2011-11-01 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
| DE102008057344A1 (de) | 2008-11-14 | 2010-05-20 | Bayer Schering Pharma Aktiengesellschaft | Aminoalkyl-substituierte Aryl-Verbindungen und ihre Verwendung |
| DE102009041242A1 (de) | 2009-09-11 | 2011-12-15 | Bayer Schering Pharma Aktiengesellschaft | Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung |
| DE102009041241A1 (de) | 2009-09-11 | 2011-08-04 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Substituierte Aryl-Verbindungen und ihre Verwendung |
| DE102008057364A1 (de) | 2008-11-14 | 2010-05-20 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Aryl-Verbindungen und ihre Verwendung |
| DE102008057343A1 (de) | 2008-11-14 | 2010-05-20 | Bayer Schering Pharma Aktiengesellschaft | Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung |
| JP5705748B2 (ja) | 2009-02-18 | 2015-04-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃｂ２受容体を変調する複素環化合物 |
| EP2406255B1 (en) | 2009-03-09 | 2015-04-29 | Glaxo Group Limited | 4-oxadiazol-2-yl-indazoles as inhibitors of pi3 kinases |
| AR076435A1 (es) | 2009-04-30 | 2011-06-08 | Glaxo Group Ltd | Compuestos de indazoles sustituidos, composiciones farmaceuticas que los contienen y procesos de obtencion de los mismos |
| SG176628A1 (en) | 2009-06-05 | 2012-01-30 | Link Medicine Corp | Aminopyrrolidinone derivatives and uses thereof |
| US8299103B2 (en) | 2009-06-15 | 2012-10-30 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
| US8383615B2 (en) | 2009-06-16 | 2013-02-26 | Boehringer Ingelheim International Gmbh | Azetidine 2-carboxamide derivatives which modulate the CB2 receptor |
| GB0912946D0 (en) * | 2009-07-24 | 2009-09-02 | Addex Pharmaceuticals Sa | New compounds 5 |
| EP2480544A1 (en) | 2009-09-22 | 2012-08-01 | Boehringer Ingelheim International GmbH | Compounds which selectively modulate the cb2 receptor |
| JP2013517271A (ja) | 2010-01-15 | 2013-05-16 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃｂ２受容体を調節する化合物 |
| US8329735B2 (en) | 2010-03-05 | 2012-12-11 | Boehringer Ingelheim International Gmbh | Tetrazole compounds which selectively modulate the CB2 receptor |
| EP2595959B1 (en) | 2010-07-22 | 2015-11-04 | Boehringer Ingelheim International GmbH | Sulfonyl compounds which modulate the cb2 receptor |
| GB201018124D0 (en) | 2010-10-27 | 2010-12-08 | Glaxo Group Ltd | Polymorphs and salts |
| RU2612217C2 (ru) | 2011-05-04 | 2017-03-03 | Мерк Шарп И Доум Корп. | Аминопиридинсодержащие ингибиторы тирозинкиназы селезенки (syk) |
| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| AU2012322660B2 (en) | 2011-10-11 | 2017-07-06 | Dana Farber Cancer Institute, Inc. | Pyrazol-3-ones that activate pro-apoptotic BAX |
| US8729263B2 (en) | 2012-08-13 | 2014-05-20 | Novartis Ag | 1,4-disubstituted pyridazine analogs there of and methods for treating SMN-deficiency-related conditions |
| US9040712B2 (en) | 2013-01-23 | 2015-05-26 | Novartis Ag | Thiadiazole analogs thereof and methods for treating SMN-deficiency-related-conditions |
| KR102280614B1 (ko) | 2013-03-15 | 2021-07-21 | 글로벌 블러드 테라퓨틱스, 인크. | 헤모글로빈 조정을 위한 화합물 및 이의 용도 |
| EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
| KR102318727B1 (ko) | 2013-07-31 | 2021-10-28 | 노파르티스 아게 | 1,4-이치환된 피리다진 유사체 및 smn-결핍-관련 상태를 치료하기 위한 그의 용도 |
| EA201992707A1 (ru) | 2013-11-18 | 2020-06-30 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
| GB201402277D0 (en) | 2014-02-10 | 2014-03-26 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| TWI695717B (zh) | 2014-03-06 | 2020-06-11 | 美商 Ptc 治療公司 | １,２,４-二唑苯甲酸之鹽及醫藥組合物 |
| JP2018531924A (ja) | 2015-09-24 | 2018-11-01 | ファイザー・インク | テトラヒドロピラノ［３，４−ｄ］［１，３］オキサジン誘導体、およびｂａｃｅ阻害剤としてのその使用 |
| HK1251965A1 (zh) | 2015-10-30 | 2019-05-10 | Ptc医疗公司 | 用於治疗癫痫的方法 |
| CA3252823A1 (en) | 2016-06-13 | 2025-02-25 | Gilead Sciences, Inc. | Substituted tert-butyl-3-(2-chloro-phenyl)-3-hydroxyazetidine-1-carboxylate compounds |
| BR112018075734A2 (pt) | 2016-06-13 | 2019-04-02 | Gilead Sciences, Inc. | composto, composição farmacêutica, método para tratar um paciente com uma doença ou condição mediada pelo menos em parte por fxr, e, uso de um composto. |
| CA3027500A1 (en) * | 2016-06-21 | 2017-12-28 | X4 Pharmaceuticals, Inc. | Cxcr4 inhibitors and uses thereof |
| JP7054529B2 (ja) | 2016-06-21 | 2022-04-14 | エックス４ ファーマシューティカルズ， インコーポレイテッド | Ｃｘｃｒ４阻害剤およびその使用 |
| JP2019533022A (ja) | 2016-10-24 | 2019-11-14 | ユマニティ セラピューティクス，インコーポレーテッド | 化合物及びその使用 |
| CA3049010A1 (en) | 2017-01-06 | 2018-07-12 | Yumanity Therapeutics, Inc. | Methods for the treatment of neurological disorders |
| CN110461328A (zh) | 2017-03-28 | 2019-11-15 | 吉利德科学公司 | 治疗肝疾病的治疗组合 |
| SG11202001684PA (en) | 2017-10-06 | 2020-03-30 | Forma Therapeutics Inc | Inhibiting ubiquitin specific peptidase 30 |
| CA3083000A1 (en) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
| WO2019089667A1 (en) | 2017-11-01 | 2019-05-09 | Bristol-Myers Squibb Company | Bridged bicyclic compounds as farnesoid x receptor modulators |
| CA3094527A1 (en) | 2018-03-23 | 2019-09-26 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
| WO2019209962A1 (en) | 2018-04-25 | 2019-10-31 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
| WO2019209948A1 (en) * | 2018-04-25 | 2019-10-31 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
| ES2988920T3 (es) | 2018-05-17 | 2024-11-22 | Forma Therapeutics Inc | Compuestos bicíclicos fusionados útiles como inhibidores de la peptidasa 30 específica de ubiquitina |
| PL3860989T3 (pl) | 2018-10-05 | 2023-07-10 | Forma Therapeutics, Inc. | Sprzężone piroliny, które działają jako inhibitory proteazy 30 swoistej dla ubikwityny (usp30) |
| EP4360632B1 (en) | 2019-01-15 | 2025-10-29 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
| US12098146B2 (en) | 2019-01-24 | 2024-09-24 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| MX2021009276A (es) | 2019-01-31 | 2021-08-24 | Pfizer | Compuestos de 3-carbonilamino-5-ciclopentil-1h-pirazol que tienen actividad inhibidora sobre cdk2. |
| US11524005B2 (en) | 2019-02-19 | 2022-12-13 | Gilead Sciences, Inc. | Solid forms of FXR agonists |
| EA202192047A1 (ru) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
| EP4514782B1 (en) | 2022-05-19 | 2025-09-10 | Astrazeneca AB | Amido heteroaromatic compounds useful in the treatment of liver diseases |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3740434A (en) | 1966-12-23 | 1973-06-19 | American Cyanamid Co | Substituted nitroimidazolylthiadiazoles and oxadiazoles as antiprotozoal agents |
| US3647809A (en) * | 1968-04-26 | 1972-03-07 | Chinoin Gyogyszer Es Vegyeszet | Certain pyridyl-1 2 4-oxadiazole derivatives |
| US3816426A (en) * | 1970-10-27 | 1974-06-11 | Abbott Lab | 1-(5-phenyl-4-oxo-2-oxazolin-2-yl)piperazines |
| US4022901A (en) | 1975-03-05 | 1977-05-10 | E. R. Squibb & Sons, Inc. | 3-Pyridinyl-5-isothiocyanophenyl oxadiazoles |
| JPS56127364A (en) | 1980-03-01 | 1981-10-06 | Mitsui Toatsu Chem Inc | Novel piperazine compound, its preparation and utilization |
| JP3003148B2 (ja) * | 1989-01-05 | 2000-01-24 | 藤沢薬品工業株式会社 | チアゾール化合物、その製造法およびそれを含有する医薬組成物 |
| IL96891A0 (en) | 1990-01-17 | 1992-03-29 | Merck Sharp & Dohme | Indole-substituted five-membered heteroaromatic compounds,their preparation and pharmaceutical compositions containing them |
| JPH08502508A (ja) | 1992-10-23 | 1996-03-19 | メルク シヤープ エンド ドーム リミテツド | ドーパミンレセプターサブタイプリガンド |
| US6589969B1 (en) * | 1998-10-16 | 2003-07-08 | Ono Pharmaceutical Co., Ltd. | Carboxylic acid derivatives and drugs containing the same as the active ingredient |
| DE19858191A1 (de) * | 1998-12-17 | 2000-06-21 | Aventis Cropscience Gmbh | 4-Haloalkyl-3-heterocyclylpyridine und 4-Haloalkyl-5-heterocyclyl-pyrimidine und ihre Verwendung als Repellentien |
| CO5170501A1 (es) * | 1999-04-14 | 2002-06-27 | Novartis Ag | AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO |
| CN1313465C (zh) | 1999-08-19 | 2007-05-02 | Nps药物有限公司 | 杂多环化合物及其用于制备代谢性谷氨酸受体拮抗剂的应用 |
| TWI283577B (en) | 1999-10-11 | 2007-07-11 | Sod Conseils Rech Applic | Pharmaceutical composition of imidazole derivatives acting as modulators of sodium channels and the use thereof |
| US6800647B2 (en) * | 2000-05-26 | 2004-10-05 | Merck & Co., Inc. | 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3]bipyridinyl in pure crystalline form and process for synthesis |
| WO2002024680A1 (en) * | 2000-09-21 | 2002-03-28 | Smithkline Beecham P.L.C. | Imidazole derivatives as raf kinase inhibitors |
| MXPA03003868A (es) | 2000-10-30 | 2003-07-28 | Janssen Pharmaceutica Nv | Inhibidores de tripeptidil peptidasa. |
| ATE288898T1 (de) | 2000-12-04 | 2005-02-15 | Hoffmann La Roche | Phenylethenyl- oder phenylethinylderivate als glutamatrezeptorantagonisten |
| GB0113233D0 (en) * | 2001-05-31 | 2001-07-25 | Glaxo Group Ltd | Chemical compounds |
| GB0115862D0 (en) | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
| DE60204633T2 (de) * | 2001-07-05 | 2006-06-14 | Pfizer Prod Inc | Sulfonyl-Heteroaryl-Triazole als entzündungshemmende und analgetische Mittel |
| DK1406898T3 (da) | 2001-07-19 | 2005-05-30 | Cv Therapeutics Inc | Substituerede piperazinforbindelser og anvendelse af disse som fedtsyreoxidationsinhibitorer |
| AR036873A1 (es) * | 2001-09-07 | 2004-10-13 | Euro Celtique Sa | Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento |
| US6864268B2 (en) * | 2002-02-27 | 2005-03-08 | Pfizer Inc. | β3 adrenergic receptor agonists |
-
2003
- 2003-08-08 WO PCT/US2003/024915 patent/WO2004014902A2/en not_active Ceased
- 2003-08-08 MX MXPA05001590A patent/MXPA05001590A/es unknown
- 2003-08-08 US US10/636,977 patent/US7074809B2/en not_active Expired - Fee Related
- 2003-08-08 CA CA002495179A patent/CA2495179A1/en not_active Abandoned
- 2003-08-08 JP JP2004527914A patent/JP2006502134A/ja active Pending
- 2003-08-08 AU AU2003264018A patent/AU2003264018A1/en not_active Abandoned
- 2003-08-08 EP EP03785076A patent/EP1581525A2/en not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2006503009A5 (enExample) | ||
| RU2352568C2 (ru) | [1,2,4]оксадиазолы (варианты), способ их получения, фармацевтическая композиция и способ ингибирования активации метаботропных глютаматных рецепторов-5 | |
| RU2396269C2 (ru) | Производные гетероарилзамещенного пиперидина в качестве ингибиторов печеночной карнитин пальмитоилтрансферазы (l-cpt1) | |
| JP2020530446A5 (enExample) | ||
| JP2015509510A5 (enExample) | ||
| JP2022531932A5 (enExample) | ||
| JP2006506340A5 (enExample) | ||
| IL303196A (en) | Heteroaryl-substituted pyridines and methods of use | |
| RU2006127572A (ru) | Полигетероциклические соединения и их применение в качестве антагонистов метаботропного рецептора глутамата | |
| JP2007523181A5 (enExample) | ||
| JP2019517455A5 (enExample) | ||
| RU2006127575A (ru) | Соединение триазола и их применение в качестве антагонистов метаботропного рецептора глутамата | |
| HRP20211960T1 (hr) | Alosterični modulatori nikotinskih acetilcolinskih receptora | |
| JP2015533157A5 (enExample) | ||
| WO2008002570B1 (en) | Human protein tyrosine phosphatase inhibitors and methods of use | |
| RU2010137300A (ru) | Модуляторы бета-амилоида | |
| JP2014517833A5 (enExample) | ||
| RU2010136953A (ru) | Новое производное фенилпиррола | |
| RU2009111113A (ru) | Мидуляторы mglur5 | |
| JP2007508346A5 (enExample) | ||
| JP2006502134A (ja) | 代謝調節型グルタミン酸受容体において活性を有する化合物 | |
| US8399451B2 (en) | Heterocyclic compounds | |
| JP2004516295A5 (enExample) | ||
| JP2014523400A5 (enExample) | ||
| JP2009504791A5 (enExample) |