PE20081485A1 - Derivados de sulfonamida - Google Patents
Derivados de sulfonamidaInfo
- Publication number
- PE20081485A1 PE20081485A1 PE2007001806A PE2007001806A PE20081485A1 PE 20081485 A1 PE20081485 A1 PE 20081485A1 PE 2007001806 A PE2007001806 A PE 2007001806A PE 2007001806 A PE2007001806 A PE 2007001806A PE 20081485 A1 PE20081485 A1 PE 20081485A1
- Authority
- PE
- Peru
- Prior art keywords
- hydroxy
- halogen
- indol
- aryl
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/58—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE X ES -NHC(O)-, C(O)NH-; Y ES -C(R4R5)-, -C(R4R5)C(R6R7)-, -CR4=CR6, ENTRE OTROS; R1 ES ARILO, HETEROARILO SUSTITUIDOS O NO; R2 ES H, ALQUILO INFERIOR, HIDROXI, HALOGENO, ALCOXI INFERIOR, ENTRE OTROS; R3 ES ARILO, SUSTITUIDO POR 1-3 SUSTITUYENTES SELECCIONADOS ENTRE HALOGENO, CIANO, HIDROXI, ENTRE OTROS; R4, R5, R6 Y R7 SON CADA UNO H, HALOGENO, ALQUILO INFERIOR, HIDROXI, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ACIDO (4-{[1-(5-CLORO-2-METOXI-BENCENOSULFONIL)-1H-INDOL-6-CARBOMIL]-AMINO}-FENIL)-ACETICO; ACIDO (2-{[1-(3,5-DIMETIL-BENCENOSULFONIL)-2,3-DIHIDRO-1H-INDOL-6-CARBONIL]-AMINO}-TIAZOL-4-IL)-ACETICO; ENTRE OTROS. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PALMITOIL-TRANSFERASA DE CARNITINA DEL HIGADO 1 (L-CPT1), UTILES EN EL TRATAMIENTO DE ENFERMEDADES Y/O TRASTORNOS DE TOLERANCIA A LA GLUCOSA TALES COMO DIABETES Y PATOLOGIAS ASOCIADAS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06126920 | 2006-12-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20081485A1 true PE20081485A1 (es) | 2008-10-18 |
Family
ID=39273549
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007001806A PE20081485A1 (es) | 2006-12-21 | 2007-12-14 | Derivados de sulfonamida |
Country Status (17)
Country | Link |
---|---|
US (1) | US7799933B2 (es) |
EP (1) | EP2097373B1 (es) |
JP (1) | JP5089707B2 (es) |
KR (1) | KR101139211B1 (es) |
CN (1) | CN101583597B (es) |
AR (1) | AR064459A1 (es) |
AT (1) | ATE477240T1 (es) |
AU (1) | AU2007336364B2 (es) |
BR (1) | BRPI0720524A2 (es) |
CA (1) | CA2672761A1 (es) |
CL (1) | CL2007003697A1 (es) |
DE (1) | DE602007008467D1 (es) |
ES (1) | ES2348270T3 (es) |
MX (1) | MX2009006598A (es) |
PE (1) | PE20081485A1 (es) |
TW (1) | TW200833324A (es) |
WO (1) | WO2008074692A1 (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010017827A1 (en) * | 2008-08-14 | 2010-02-18 | European Molecular Biology Laboratory | 6-substituted 1-sulfonyl-2, 3-dihydro-indole derivatives for the treatment of proliferative diseases |
EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
EP2638014B1 (en) | 2010-11-08 | 2017-01-04 | Lycera Corporation | N-sulfonylated tetrahydroquinolines and related bicyclic compounds for inhibition of ror-gamma activity and the treatment of diseases |
EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
AU2013259624B2 (en) | 2012-05-08 | 2017-10-19 | Lycera Corporation | Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORy and the treatment of disease |
KR20150007300A (ko) | 2012-05-08 | 2015-01-20 | 머크 샤프 앤드 돔 코포레이션 | Ror감마 활성의 억제를 위한 테트라히드로나프티리딘 및 관련 비시클릭 화합물 및 질환의 치료 |
KR20150013500A (ko) * | 2012-05-08 | 2015-02-05 | 머크 샤프 앤드 돔 코포레이션 | Ror감마 활성의 억제를 위한 비시클릭 술폰 화합물 및 질환의 치료 |
WO2015095788A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | 2-ACYLAMIDOMETHYL AND SULFONYLAMIDOMETHYL BENZOXAZINE CARBAMATES FOR INHIBITION OF RORgamma ACTIVITY AND THE TREATMENT OF DISEASE |
US9809561B2 (en) | 2013-12-20 | 2017-11-07 | Merck Sharp & Dohme Corp. | Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease |
WO2015095792A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Carbamate benzoxaxine propionic acids and acid derivatives for modulation of rorgamma activity and the treatment of disease |
JP2017507950A (ja) | 2014-02-27 | 2017-03-23 | リセラ・コーポレイションLycera Corporation | レチノイン酸受容体関連オーファン受容体ガンマのアゴニストを使用する養子細胞療法及び関連治療方法 |
WO2015171558A2 (en) | 2014-05-05 | 2015-11-12 | Lycera Corporation | BENZENESULFONAMIDO AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORγ AND THE TREATEMENT OF DISEASE |
JP6728061B2 (ja) | 2014-05-05 | 2020-07-22 | リセラ・コーポレイションLycera Corporation | RORγアゴニストとして用いるテトラヒドロキノリンスルホンアミド及び関連化合物ならびに疾患の治療 |
JP2018510135A (ja) | 2015-02-11 | 2018-04-12 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害剤としての置換ピラゾール化合物及びその使用 |
EP3292119A4 (en) | 2015-05-05 | 2018-10-03 | Lycera Corporation | DIHYDRO-2H-BENZO[b][1,4]OXAZINE SULFONAMIDE AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORy AND THE TREATMENT OF DISEASE |
US10611740B2 (en) | 2015-06-11 | 2020-04-07 | Lycera Corporation | Aryl dihydro-2H-benzo[b][1,4]oxazine sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease |
JP2018531958A (ja) | 2015-10-27 | 2018-11-01 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害薬としてのヘテロアリール置換安息香酸及びその使用 |
CA3002850A1 (en) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Substituted indazole compounds as rorgammat inhibitors and uses thereof |
AU2016344111A1 (en) | 2015-10-27 | 2018-05-10 | Merck Sharp & Dohme Corp. | Substituted bicyclic pyrazole compounds as RORgammaT inhibitors and uses thereof |
US20200172483A1 (en) * | 2017-06-22 | 2020-06-04 | Curadev Pharma Limited | Heterocyclic small molecule modulators of human sting |
CN110511182B (zh) * | 2019-09-03 | 2023-01-17 | 上海昕凯医药科技有限公司 | 一种连续流反应合成7-硝基-1,2,3,4-四氢喹啉的方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU7315700A (en) | 1999-09-20 | 2001-04-24 | Takeda Chemical Industries Ltd. | Melanin concentrating hormone antagonist |
WO2006131452A1 (en) | 2005-06-06 | 2006-12-14 | F. Hoffmann-La Roche Ag | SULFONAMIDE DERIVATIVES USEFUL AS LIVER CARNITINE PALMITOYL TRANSFERASE (L-CPTl) INHIBITORS |
ES2398111T3 (es) * | 2005-09-15 | 2013-03-13 | F. Hoffmann-La Roche Ag | Nuevos derivados heterobicíclicos útiles como inhibidores de carnitina palmitoiltranferasa del hígado |
-
2007
- 2007-12-06 US US11/951,426 patent/US7799933B2/en not_active Expired - Fee Related
- 2007-12-11 EP EP07857385A patent/EP2097373B1/en not_active Not-in-force
- 2007-12-11 WO PCT/EP2007/063696 patent/WO2008074692A1/en active Application Filing
- 2007-12-11 CN CN2007800471883A patent/CN101583597B/zh not_active Expired - Fee Related
- 2007-12-11 KR KR1020097012803A patent/KR101139211B1/ko not_active IP Right Cessation
- 2007-12-11 AT AT07857385T patent/ATE477240T1/de active
- 2007-12-11 DE DE602007008467T patent/DE602007008467D1/de active Active
- 2007-12-11 ES ES07857385T patent/ES2348270T3/es active Active
- 2007-12-11 MX MX2009006598A patent/MX2009006598A/es active IP Right Grant
- 2007-12-11 BR BRPI0720524-4A patent/BRPI0720524A2/pt not_active IP Right Cessation
- 2007-12-11 AU AU2007336364A patent/AU2007336364B2/en not_active Ceased
- 2007-12-11 JP JP2009541983A patent/JP5089707B2/ja not_active Expired - Fee Related
- 2007-12-11 CA CA002672761A patent/CA2672761A1/en not_active Abandoned
- 2007-12-14 PE PE2007001806A patent/PE20081485A1/es not_active Application Discontinuation
- 2007-12-18 TW TW096148490A patent/TW200833324A/zh unknown
- 2007-12-19 AR ARP070105736A patent/AR064459A1/es not_active Application Discontinuation
- 2007-12-19 CL CL200703697A patent/CL2007003697A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
JP2010513376A (ja) | 2010-04-30 |
CL2007003697A1 (es) | 2008-07-04 |
AR064459A1 (es) | 2009-04-01 |
AU2007336364B2 (en) | 2012-08-02 |
DE602007008467D1 (de) | 2010-09-23 |
US20080153805A1 (en) | 2008-06-26 |
EP2097373A1 (en) | 2009-09-09 |
TW200833324A (en) | 2008-08-16 |
CN101583597B (zh) | 2012-07-11 |
AU2007336364A1 (en) | 2008-06-26 |
KR20090080567A (ko) | 2009-07-24 |
MX2009006598A (es) | 2009-07-24 |
CA2672761A1 (en) | 2008-06-26 |
KR101139211B1 (ko) | 2012-04-26 |
JP5089707B2 (ja) | 2012-12-05 |
ATE477240T1 (de) | 2010-08-15 |
BRPI0720524A2 (pt) | 2014-01-07 |
EP2097373B1 (en) | 2010-08-11 |
CN101583597A (zh) | 2009-11-18 |
WO2008074692A1 (en) | 2008-06-26 |
US7799933B2 (en) | 2010-09-21 |
ES2348270T3 (es) | 2010-12-02 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |