CL2013001810A1 - Compuestos derivados de 2-amino-4-ariltiazol, antagonistas del receptor trpa1; composicion farmaceutica que los comprende; metodo de tratamiento de una enfermedad o estado de salud asociados con dolor cronico, dolor neuropatico, dolor artritico reumatoide o dolor osteoartritico. - Google Patents
Compuestos derivados de 2-amino-4-ariltiazol, antagonistas del receptor trpa1; composicion farmaceutica que los comprende; metodo de tratamiento de una enfermedad o estado de salud asociados con dolor cronico, dolor neuropatico, dolor artritico reumatoide o dolor osteoartritico.Info
- Publication number
- CL2013001810A1 CL2013001810A1 CL2013001810A CL2013001810A CL2013001810A1 CL 2013001810 A1 CL2013001810 A1 CL 2013001810A1 CL 2013001810 A CL2013001810 A CL 2013001810A CL 2013001810 A CL2013001810 A CL 2013001810A CL 2013001810 A1 CL2013001810 A1 CL 2013001810A1
- Authority
- CL
- Chile
- Prior art keywords
- pain
- arylthiazole
- disease
- amino
- pharmaceutical composition
- Prior art date
Links
- 208000002193 Pain Diseases 0.000 title 3
- 101100482465 Caenorhabditis elegans trpa-1 gene Proteins 0.000 title 1
- 208000000094 Chronic Pain Diseases 0.000 title 1
- 230000002917 arthritic effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 208000004296 neuralgia Diseases 0.000 title 1
- 208000021722 neuropathic pain Diseases 0.000 title 1
- 230000003349 osteoarthritic effect Effects 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
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- C07D487/04—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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- C07D495/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Vascular Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN3451MU2010 | 2010-12-20 | ||
US201061428327P | 2010-12-30 | 2010-12-30 | |
IN748MU2011 | 2011-03-16 | ||
US201161466535P | 2011-03-23 | 2011-03-23 | |
IN1569MU2011 | 2011-05-25 | ||
US201161459002P | 2011-06-09 | 2011-06-09 | |
IN2741MU2011 | 2011-09-28 | ||
US201161552076P | 2011-10-27 | 2011-10-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2013001810A1 true CL2013001810A1 (es) | 2014-01-24 |
Family
ID=46235162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2013001810A CL2013001810A1 (es) | 2010-12-20 | 2013-06-19 | Compuestos derivados de 2-amino-4-ariltiazol, antagonistas del receptor trpa1; composicion farmaceutica que los comprende; metodo de tratamiento de una enfermedad o estado de salud asociados con dolor cronico, dolor neuropatico, dolor artritico reumatoide o dolor osteoartritico. |
Country Status (20)
Country | Link |
---|---|
US (3) | US8592398B2 (es) |
EP (1) | EP2655377B1 (es) |
JP (1) | JP5694560B2 (es) |
KR (1) | KR101591153B1 (es) |
CN (1) | CN103261201B (es) |
AP (1) | AP3391A (es) |
AR (1) | AR084294A1 (es) |
AU (1) | AU2011346763B2 (es) |
BR (1) | BR112013014692A2 (es) |
CA (1) | CA2820448A1 (es) |
CL (1) | CL2013001810A1 (es) |
EA (1) | EA023141B1 (es) |
HK (1) | HK1191008A1 (es) |
MX (1) | MX336549B (es) |
MY (1) | MY159059A (es) |
PE (1) | PE20140234A1 (es) |
SG (1) | SG191173A1 (es) |
TW (1) | TWI515199B (es) |
UA (1) | UA109916C2 (es) |
WO (1) | WO2012085662A1 (es) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10189802B2 (en) | 2008-11-07 | 2019-01-29 | Massachusetts Institute Of Technology | Aminoalcohol lipidoids and uses thereof |
US10201618B2 (en) | 2015-06-19 | 2019-02-12 | Massachusetts Institute Of Technology | Alkenyl substituted 2,5-piperazinediones, compositions, and uses thereof |
US11458158B2 (en) | 2011-10-27 | 2022-10-04 | Massachusetts Institute Of Technology | Amino acid-, peptide- and polypeptide-lipids, isomers, compositions, and uses thereof |
US11655245B2 (en) | 2018-03-19 | 2023-05-23 | Genentech, Inc. | Oxadiazole transient receptor potential channel inhibitors |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2820448A1 (en) | 2010-12-20 | 2012-06-28 | Glenmark Pharmaceuticals, S.A. | 2-amino-4-arylthiazole compounds as trpa1 antagonists |
MX2014001551A (es) | 2011-08-09 | 2014-09-15 | Hydra Biosciences Inc | Inhibicion de canal ionico del potencial receptor transitorio a1 (trpa1). |
EP2805718B1 (en) | 2012-01-17 | 2018-04-04 | EA Pharma Co., Ltd. | Heterocyclic amide derivative and pharmaceutical product containing same |
KR20150015488A (ko) | 2012-06-08 | 2015-02-10 | 그렌마크 파머수티칼스 에스. 아. | 2-아미노-4-아릴티아졸 화합물의 아미드 및 그의 염 |
EP2903965B1 (en) | 2012-10-01 | 2017-03-01 | Orion Corporation | N-prop-2-ynyl carboxamide derivatives and their use as trpa1 antagonists |
US9394308B2 (en) | 2013-01-18 | 2016-07-19 | Merck Sharp & Dohme Corp. | Inhibiting the transient receptor potential A1 ion channel |
GB201309333D0 (en) * | 2013-05-23 | 2013-07-10 | Agency Science Tech & Res | Purine diones as WNT pathway modulators |
US9198898B2 (en) | 2013-06-24 | 2015-12-01 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
US8906951B1 (en) | 2013-06-24 | 2014-12-09 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
US9532988B2 (en) | 2013-10-15 | 2017-01-03 | Glenmark Pharmaceuticals S.A. | Pharmaceutical composition comprising a TRPA1 antagonist and an analgesic agent |
US11066455B2 (en) | 2014-02-24 | 2021-07-20 | The Johns Hopkins University | Tmem100 peptides and variants thereof and their use in treating or preventing diseases or conditions |
FR3037956B1 (fr) * | 2015-06-23 | 2017-08-04 | Servier Lab | Nouveaux derives d'acide amine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
WO2017060488A1 (en) | 2015-10-09 | 2017-04-13 | Almirall, S.A. | New trpa1 antagonists |
WO2017064068A1 (en) | 2015-10-14 | 2017-04-20 | Almirall, S.A. | New trpa1 antagonists |
CN108727400B (zh) * | 2017-05-24 | 2021-07-09 | 四川晶华生物科技有限公司 | 一种治疗肿瘤的化合物 |
US20220000966A1 (en) * | 2018-10-23 | 2022-01-06 | George Edward Hoag | Composition and method for treating the lungs |
TW202128705A (zh) * | 2019-10-15 | 2021-08-01 | 德商百靈佳殷格翰國際股份有限公司 | 新穎噻吩并嘧啶酮 |
MX2022004565A (es) * | 2019-10-15 | 2022-05-06 | Boehringer Ingelheim Int | Tienopirimidonas como inhibidores de trpa1. |
US20230355571A1 (en) * | 2020-04-22 | 2023-11-09 | George Edward Hoag | Method for treating viral and bacterial infection through inhalation therapy |
CN111437275B (zh) * | 2020-05-14 | 2021-03-19 | 黑龙江中医药大学 | 一种用于外科手术后抗炎和镇痛的药物及其应用 |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2004228668B2 (en) | 2003-04-03 | 2011-10-27 | Park Funding, Llc | PI-3 kinase inhibitor prodrugs |
TW200720264A (en) | 2005-04-25 | 2007-06-01 | Lundbeck & Co As H | Pro-drugs of n-thiazol-2-yl-benzamide derivatives |
AU2006327181A1 (en) | 2005-12-22 | 2007-06-28 | Hydra Biosciences, Inc. | TRPA1 inhibitors for treating pain |
JP2010530901A (ja) | 2007-06-22 | 2010-09-16 | ハイドラ バイオサイエンシズ インコーポレイテッド | 障害を治療するための方法および組成物 |
WO2009118596A2 (en) | 2008-03-26 | 2009-10-01 | Glenmark Pharmaceuticals, S. A. | Phthalimide derivatives as trpa1 modulators |
WO2009144548A1 (en) | 2008-05-28 | 2009-12-03 | Glenmark Pharmaceuticals S.A. | Imidazo [2,1-b] purine derivatives as trpa1 modulators |
WO2010004390A1 (en) | 2008-06-17 | 2010-01-14 | Glenmark Pharmaceuticals, S.A. | Quinazoline dione derivatives as trpa1 modulators |
WO2009158719A2 (en) | 2008-06-27 | 2009-12-30 | Hydra Biosciences, Inc. | Methods and compositions for treating disorders |
WO2010075353A1 (en) | 2008-12-22 | 2010-07-01 | Hydra Biosciences, Inc. | Compositions useful for treating disorders related to trpa1 |
DK2411393T3 (da) * | 2009-03-23 | 2014-04-07 | Glenmark Pharmaceuticals Sa | Kondenserede pyrimidin-dionderivater som TRPA1-modulatorer |
PT2411397E (pt) | 2009-03-23 | 2013-06-06 | Glenmark Pharmaceuticals Sa | Derivados de isotiazolo-pirimidinadiona como moduladores de trpa1 |
ES2424341T3 (es) | 2009-03-23 | 2013-10-01 | Glenmark Pharmaceuticals S.A. | Derivados de furopirimidinadiona como moduladores de TRPA1 |
US8623880B2 (en) * | 2009-03-23 | 2014-01-07 | Glenmark Pharmaceuticals S.A. | Fused pyrimidine-dione derivatives as TRPA1 modulators |
WO2010125469A1 (en) * | 2009-04-29 | 2010-11-04 | Glenmark Pharmaceuticals, S.A. | Pyrimidinedione-fused heterocyclic compounds as trpa1 modulators |
WO2010132838A1 (en) | 2009-05-14 | 2010-11-18 | Hydra Biosciences, Inc. | Compounds useful for treating disorders related to trpa1 |
WO2011114184A1 (en) | 2010-03-15 | 2011-09-22 | Glenmark Pharmaceuticals S.A. | Amides of heterocyclic compounds as trpa1 inhibitors |
WO2011132017A1 (en) | 2010-04-19 | 2011-10-27 | Glenmark Pharmaceuticals S.A. | Pyrido[3,4-d]pyrimidinyl acetamide derivatives as trpa1 modulators |
CA2820448A1 (en) | 2010-12-20 | 2012-06-28 | Glenmark Pharmaceuticals, S.A. | 2-amino-4-arylthiazole compounds as trpa1 antagonists |
-
2011
- 2011-12-15 CA CA2820448A patent/CA2820448A1/en not_active Abandoned
- 2011-12-15 WO PCT/IB2011/003224 patent/WO2012085662A1/en active Application Filing
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- 2011-12-15 PE PE2013001454A patent/PE20140234A1/es not_active Application Discontinuation
- 2011-12-15 SG SG2013046073A patent/SG191173A1/en unknown
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- 2011-12-15 EA EA201390947A patent/EA023141B1/ru not_active IP Right Cessation
- 2011-12-15 UA UAA201306497A patent/UA109916C2/uk unknown
- 2011-12-15 AU AU2011346763A patent/AU2011346763B2/en not_active Ceased
- 2011-12-15 BR BR112013014692A patent/BR112013014692A2/pt not_active IP Right Cessation
- 2011-12-15 KR KR1020137014826A patent/KR101591153B1/ko not_active IP Right Cessation
- 2011-12-15 CN CN201180059690.2A patent/CN103261201B/zh not_active Expired - Fee Related
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10189802B2 (en) | 2008-11-07 | 2019-01-29 | Massachusetts Institute Of Technology | Aminoalcohol lipidoids and uses thereof |
US11414393B2 (en) | 2008-11-07 | 2022-08-16 | Massachusetts Institute Of Technology | Aminoalcohol lipidoids and uses thereof |
US11458158B2 (en) | 2011-10-27 | 2022-10-04 | Massachusetts Institute Of Technology | Amino acid-, peptide- and polypeptide-lipids, isomers, compositions, and uses thereof |
US10201618B2 (en) | 2015-06-19 | 2019-02-12 | Massachusetts Institute Of Technology | Alkenyl substituted 2,5-piperazinediones, compositions, and uses thereof |
US11655245B2 (en) | 2018-03-19 | 2023-05-23 | Genentech, Inc. | Oxadiazole transient receptor potential channel inhibitors |
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