JP5320291B2 - トリアゾリルピリジルベンゼンスルホンアミド類 - Google Patents
トリアゾリルピリジルベンゼンスルホンアミド類 Download PDFInfo
- Publication number
- JP5320291B2 JP5320291B2 JP2009520761A JP2009520761A JP5320291B2 JP 5320291 B2 JP5320291 B2 JP 5320291B2 JP 2009520761 A JP2009520761 A JP 2009520761A JP 2009520761 A JP2009520761 A JP 2009520761A JP 5320291 B2 JP5320291 B2 JP 5320291B2
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- chloro
- unsubstituted
- triazol
- benzenesulfonamide
- 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.)
- Active
Links
- 0 **=*C(NS([Al])(=O)=O)=C(*=C)c1nnc(*)[n]1* Chemical compound **=*C(NS([Al])(=O)=O)=C(*=C)c1nnc(*)[n]1* 0.000 description 12
- LJUSDRSLNKXAEQ-UHFFFAOYSA-N CC#S(c(cc1C(F)(F)F)ccc1Cl)Nc1c(-c2nnc(CO)[n]2-c2n[o]cc2)ncc(Cl)c1 Chemical compound CC#S(c(cc1C(F)(F)F)ccc1Cl)Nc1c(-c2nnc(CO)[n]2-c2n[o]cc2)ncc(Cl)c1 LJUSDRSLNKXAEQ-UHFFFAOYSA-N 0.000 description 1
- BDOGEYWVLAICGC-UHFFFAOYSA-N CC(C)(C)C(Nc1n[nH]cc1)=O Chemical compound CC(C)(C)C(Nc1n[nH]cc1)=O BDOGEYWVLAICGC-UHFFFAOYSA-N 0.000 description 1
- IQGPBRIVOHZFRH-UHFFFAOYSA-N CC(C)(C)c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2C(F)(F)F)ccc2Cl)(=O)=O)[n]1-c1n[nH]cc1 Chemical compound CC(C)(C)c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2C(F)(F)F)ccc2Cl)(=O)=O)[n]1-c1n[nH]cc1 IQGPBRIVOHZFRH-UHFFFAOYSA-N 0.000 description 1
- GLPBBQXLWAJSGC-UHFFFAOYSA-N CC(C)[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 Chemical compound CC(C)[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 GLPBBQXLWAJSGC-UHFFFAOYSA-N 0.000 description 1
- DUYKFRUVJBXMQQ-UHFFFAOYSA-N CC(C)[n]1c(Br)nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O Chemical compound CC(C)[n]1c(Br)nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O DUYKFRUVJBXMQQ-UHFFFAOYSA-N 0.000 description 1
- APMHVCCHQQAWKF-UHFFFAOYSA-N CC(C)[n]1c(Cl)nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O Chemical compound CC(C)[n]1c(Cl)nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O APMHVCCHQQAWKF-UHFFFAOYSA-N 0.000 description 1
- JTDBSXSLPVDHRS-UHFFFAOYSA-N CC(C)[n]1c(N)nnc1-c(ncc(Cl)c1)c1NS(c(cc1C(F)(F)F)ccc1Cl)(=O)=O Chemical compound CC(C)[n]1c(N)nnc1-c(ncc(Cl)c1)c1NS(c(cc1C(F)(F)F)ccc1Cl)(=O)=O JTDBSXSLPVDHRS-UHFFFAOYSA-N 0.000 description 1
- MRPYYDJYKUEABC-UHFFFAOYSA-N CC(C)c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)[n]1-c1n[nH]cc1 Chemical compound CC(C)c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)[n]1-c1n[nH]cc1 MRPYYDJYKUEABC-UHFFFAOYSA-N 0.000 description 1
- AIVZUXWPSBAONO-UHFFFAOYSA-N CC(CN=C1)=C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)N1c(cc(cc1)F)c1OC Chemical compound CC(CN=C1)=C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)N1c(cc(cc1)F)c1OC AIVZUXWPSBAONO-UHFFFAOYSA-N 0.000 description 1
- BDXRIXPBGRRJPZ-UHFFFAOYSA-N CCC1=C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)N(c2n[o]cc2)C(C(OCC)=O)=NC1 Chemical compound CCC1=C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)N(c2n[o]cc2)C(C(OCC)=O)=NC1 BDXRIXPBGRRJPZ-UHFFFAOYSA-N 0.000 description 1
- DDTYMWFASCHUPO-UHFFFAOYSA-N CCNC(c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)[n]1-c1n[o]cc1)=O Chemical compound CCNC(c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)[n]1-c1n[o]cc1)=O DDTYMWFASCHUPO-UHFFFAOYSA-N 0.000 description 1
- ZUBYYFJNPNPEBE-QSCXIMFFSA-N CCOC(c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2C(F)(F)F)ccc2Cl)(=O)=O)[n]1C(/C=C\O)=N)=O Chemical compound CCOC(c1nnc(-c(ncc(Cl)c2)c2NS(c(cc2C(F)(F)F)ccc2Cl)(=O)=O)[n]1C(/C=C\O)=N)=O ZUBYYFJNPNPEBE-QSCXIMFFSA-N 0.000 description 1
- ZMYGHNYGVNSZIN-UHFFFAOYSA-N CN(c1c[o]nc1-[n]1c2nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O)C2=O Chemical compound CN(c1c[o]nc1-[n]1c2nnc1-c(ncc(Cl)c1)c1NS(c(cc1)cc(C(F)(F)F)c1Cl)(=O)=O)C2=O ZMYGHNYGVNSZIN-UHFFFAOYSA-N 0.000 description 1
- ZTCWESBVZFHHRS-UHFFFAOYSA-N Cc(cccc1)c1N1C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=C2CC2)=O)=CCCN=C1 Chemical compound Cc(cccc1)c1N1C(c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=C2CC2)=O)=CCCN=C1 ZTCWESBVZFHHRS-UHFFFAOYSA-N 0.000 description 1
- FZFLWOHYWMSSFG-UHFFFAOYSA-N Cc1c[nH]nc1-[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 Chemical compound Cc1c[nH]nc1-[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 FZFLWOHYWMSSFG-UHFFFAOYSA-N 0.000 description 1
- VBQYUEZVUVOZKU-UHFFFAOYSA-N Cc1cc(NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)c(-c2nnc[n]2-c2n[nH]cc2)nc1 Chemical compound Cc1cc(NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)c(-c2nnc[n]2-c2n[nH]cc2)nc1 VBQYUEZVUVOZKU-UHFFFAOYSA-N 0.000 description 1
- FSVGXDUCCAPWHU-UHFFFAOYSA-N Cc1n[nH]cc1-[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 Chemical compound Cc1n[nH]cc1-[n]1c(-c(ncc(Cl)c2)c2NS(c(cc2)cc(C(F)(F)F)c2Cl)(=O)=O)nnc1 FSVGXDUCCAPWHU-UHFFFAOYSA-N 0.000 description 1
- JRNVZBWKYDBUCA-UHFFFAOYSA-N O=C(CCC1=O)N1Cl Chemical compound O=C(CCC1=O)N1Cl JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 1
- FNMHSWRHHGHJBG-UHFFFAOYSA-N O=S(c(cc1)cc(C(F)(F)F)c1Cl)(Nc1c(-c2nnc(C(F)(F)F)[n]2-c2n[nH]cc2)ncc(Cl)c1)=O Chemical compound O=S(c(cc1)cc(C(F)(F)F)c1Cl)(Nc1c(-c2nnc(C(F)(F)F)[n]2-c2n[nH]cc2)ncc(Cl)c1)=O FNMHSWRHHGHJBG-UHFFFAOYSA-N 0.000 description 1
- RLTLCLAXQQFSBJ-UHFFFAOYSA-N O=S(c(cc1C(F)(F)F)ccc1Cl)(Nc1c(-c2nnc[n]2-c2c[nH]nc2)ncc(Cl)c1)=O Chemical compound O=S(c(cc1C(F)(F)F)ccc1Cl)(Nc1c(-c2nnc[n]2-c2c[nH]nc2)ncc(Cl)c1)=O RLTLCLAXQQFSBJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83104206P | 2006-07-14 | 2006-07-14 | |
| US60/831,042 | 2006-07-14 | ||
| US94585407P | 2007-06-22 | 2007-06-22 | |
| US60/945,854 | 2007-06-22 | ||
| PCT/US2007/015786 WO2008008375A2 (en) | 2006-07-14 | 2007-07-10 | Triazolyl pyridyl benzenesulfonamides as ccr2 or ccr9 modulators for the treatment of inflammation |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010504280A JP2010504280A (ja) | 2010-02-12 |
| JP2010504280A5 JP2010504280A5 (enExample) | 2012-02-16 |
| JP5320291B2 true JP5320291B2 (ja) | 2013-10-23 |
Family
ID=38670575
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009520761A Active JP5320291B2 (ja) | 2006-07-14 | 2007-07-10 | トリアゾリルピリジルベンゼンスルホンアミド類 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US7683176B2 (enExample) |
| EP (1) | EP2049515B1 (enExample) |
| JP (1) | JP5320291B2 (enExample) |
| CN (1) | CN101511800B (enExample) |
| AT (1) | ATE496905T1 (enExample) |
| AU (1) | AU2007272972B2 (enExample) |
| CA (1) | CA2657670C (enExample) |
| DE (1) | DE602007012261D1 (enExample) |
| ES (2) | ES2358618T3 (enExample) |
| WO (1) | WO2008008375A2 (enExample) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1748989A2 (en) | 2004-05-12 | 2007-02-07 | ChemoCentryx Inc | Aryl sulfonamides |
| US7718683B2 (en) | 2006-07-14 | 2010-05-18 | Chemocentryx, Inc. | Triazolyl phenyl benzenesulfonamides |
| US7683176B2 (en) | 2006-07-14 | 2010-03-23 | Chemocentryx, Inc. | Triazolyl pyridyl benzenesulfonamides |
| US7776877B2 (en) | 2007-06-22 | 2010-08-17 | Chemocentryx, Inc. | N-(2-(hetaryl)aryl) arylsulfonamides and N-(2-(hetaryl) hetaryl arylsulfonamides |
| WO2009126675A1 (en) * | 2008-04-09 | 2009-10-15 | Boehringer Ingelheim International Gmbh | 2-sulfonylamino-4-heteroaryl butyramide antagonists of ccr10 |
| EP2598481B1 (en) | 2010-07-26 | 2016-08-31 | Bristol-Myers Squibb Company | Sulfonamide compounds useful as cyp17 inhibitors |
| UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
| KR20180059560A (ko) | 2010-10-29 | 2018-06-04 | 애브비 인코포레이티드 | 아폽토시스―유도제를 포함하는 고체 분산체 |
| US20140329809A1 (en) | 2011-10-28 | 2014-11-06 | Galderma Research & Development | New leukocyte infiltrate markers for rosacea and uses thereof |
| PT2953942T (pt) | 2013-02-06 | 2018-01-17 | Bayer Cropscience Ag | Derivados de pirazol substituídos com halogéneo como agentes pesticidas |
| JP6417415B2 (ja) | 2013-07-29 | 2018-11-07 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 1,3−二置換シクロペンタン誘導体 |
| ES2735360T3 (es) * | 2013-12-02 | 2019-12-18 | Chemocentryx Inc | Compuestos CCR6 |
| EP3087069B1 (en) | 2013-12-23 | 2019-01-30 | Norgine B.V. | Compounds useful as ccr9 modulators |
| EP3087074A1 (en) | 2013-12-23 | 2016-11-02 | Norgine BV | Benzene sulfonamides as ccr9 inhibitors |
| JP6556825B2 (ja) * | 2014-03-21 | 2019-08-07 | トビラ セラピューティクス, インコーポレイテッド | 線維症を処置するためのセニクリビロック |
| ES2971041T3 (es) | 2014-10-06 | 2024-06-03 | Chemocentryx Inc | Terapia combinada de inhibidores del receptor 9 de quimiocina C-C (CCR9) y anticuerpos bloqueadores anti-integrina alfa4beta7 para el tratamiento de la enfermedad inflamatoria intestinal |
| CN104341389A (zh) * | 2014-10-19 | 2015-02-11 | 湖南华腾制药有限公司 | 一种三唑哌啶盐酸盐的制备方法 |
| TN2017000483A1 (en) | 2015-05-20 | 2019-04-12 | Amgen Inc | Triazole agonists of the apj receptor. |
| US10000458B2 (en) * | 2016-03-31 | 2018-06-19 | Sumitomo Chemical Company, Limited | Production method of 1, 2, 4-triazole compound |
| WO2017192485A1 (en) | 2016-05-03 | 2017-11-09 | Amgen Inc. | Heterocyclic triazole compounds as agonists of the apj receptor |
| RU2740902C2 (ru) * | 2016-06-03 | 2021-01-21 | Хемоцентрикс, Инк. | Способ лечения фиброза печени |
| 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 |
| US10906890B2 (en) | 2016-11-16 | 2021-02-02 | Amgen Inc. | Triazole phenyl compounds as agonists of the APJ receptor |
| MA46827A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole à substitution cycloalkyle en tant qu'agonistes du récepteur apj |
| US11191762B2 (en) | 2016-11-16 | 2021-12-07 | Amgen Inc. | Alkyl substituted triazole compounds as agonists of the APJ Receptor |
| WO2018093580A1 (en) | 2016-11-16 | 2018-05-24 | Amgen Inc. | Triazole pyridyl compounds as agonists of the apj receptor |
| EP3541792B1 (en) | 2016-11-16 | 2020-12-23 | Amgen Inc. | Triazole furan compounds as agonists of the apj receptor |
| WO2018097945A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Heteroaryl-substituted triazoles as apj receptor agonists |
| EP3551034A1 (en) | 2016-12-07 | 2019-10-16 | Progenity, Inc. | Gastrointestinal tract detection methods, devices and systems |
| WO2018112264A1 (en) | 2016-12-14 | 2018-06-21 | Progenity Inc. | Treatment of a disease of the gastrointestinal tract with a chemokine/chemokine receptor inhibitor |
| TW201833108A (zh) | 2017-03-03 | 2018-09-16 | 大陸商江蘇豪森藥業集團有限公司 | 醯胺類衍生物抑制劑及其製備方法和應用 |
| GB201705263D0 (en) | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
| EP3655402A1 (de) | 2017-07-18 | 2020-05-27 | Bayer CropScience Aktiengesellschaft | Substituierte 3-heteroaryloxy-1h-pyrazole sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| WO2019089335A1 (en) | 2017-11-03 | 2019-05-09 | Amgen Inc. | Fused triazole agonists of the apj receptor |
| WO2019213006A1 (en) | 2018-05-01 | 2019-11-07 | Amgen Inc. | Substituted pyrimidinones as agonists of the apj receptor |
| JP2021534101A (ja) | 2018-08-09 | 2021-12-09 | ヴェルソー セラピューティクス, インコーポレイテッド | Ccr2及びcsf1rを標的とするためのオリゴヌクレオチド組成物ならびにその使用 |
| AU2019383976B2 (en) | 2018-11-19 | 2025-07-03 | Bt Bidco, Inc. | Methods and devices for treating a disease with biotherapeutics |
| EP3996711A4 (en) | 2019-07-10 | 2023-08-16 | ChemoCentryx, Inc. | Indanes as pd-l1 inhibitors |
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| JO2397B1 (en) | 2002-12-20 | 2007-06-17 | ميرك شارب اند دوم كوربوريشن | Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors |
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| CN101511800B (zh) | 2013-02-27 |
| CA2657670C (en) | 2012-04-17 |
| AU2007272972A1 (en) | 2008-01-17 |
| DE602007012261D1 (de) | 2011-03-10 |
| JP2010504280A (ja) | 2010-02-12 |
| EP2049515B1 (en) | 2011-01-26 |
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