EA201390947A1 - Соединения 2-амино-4-арилтиазола в качестве антагонистов trpa1 - Google Patents
Соединения 2-амино-4-арилтиазола в качестве антагонистов trpa1Info
- Publication number
- EA201390947A1 EA201390947A1 EA201390947A EA201390947A EA201390947A1 EA 201390947 A1 EA201390947 A1 EA 201390947A1 EA 201390947 A EA201390947 A EA 201390947A EA 201390947 A EA201390947 A EA 201390947A EA 201390947 A1 EA201390947 A1 EA 201390947A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- trpa1
- arylthiazole
- amino
- compounds
- antagonists
- Prior art date
Links
- 101000764872 Homo sapiens Transient receptor potential cation channel subfamily A member 1 Proteins 0.000 title abstract 3
- 102100026186 Transient receptor potential cation channel subfamily A member 1 Human genes 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 239000005557 antagonist Substances 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 4
- 201000010099 disease Diseases 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 102000005962 receptors Human genes 0.000 abstract 2
- 108020003175 receptors Proteins 0.000 abstract 2
- 230000001052 transient effect Effects 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
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- 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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- 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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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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- 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
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- 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
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- 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
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- 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
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- 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)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Otolaryngology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Psychiatry (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)
Abstract
В заявке описаны производные 2-амино-4-арилтиазола, которые являются модуляторами TRPA (действующего по механизму транзиторного рецепторного потенциала подсемейства А). В частности, описаны соединения, применимые для лечения или профилактики заболеваний, состояний и(или) нарушений, модулируемых TRPA1 (членом 1 действующего по механизму транзиторного рецепторного потенциала подсемейства А). Также описаны способы получения предложенных соединений, используемые для их синтеза промежуточные соединения, их фармацевтические композиции и способы лечения или профилактики заболеваний, состояний и(или) нарушений, модулируемых TRPA1.
Applications Claiming Priority (9)
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 | ||
US201161495002P | 2011-06-09 | 2011-06-09 | |
IN2741MU2011 | 2011-09-28 | ||
US201161552076P | 2011-10-27 | 2011-10-27 | |
PCT/IB2011/003224 WO2012085662A1 (en) | 2010-12-20 | 2011-12-15 | 2-amino-4-arylthiazole compounds as trpa1 antagonists |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201390947A1 true EA201390947A1 (ru) | 2014-07-30 |
EA023141B1 EA023141B1 (ru) | 2016-04-29 |
Family
ID=46235162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201390947A EA023141B1 (ru) | 2010-12-20 | 2011-12-15 | Соединения 2-амино-4-арилтиазола в качестве антагонистов trpa1 |
Country Status (20)
Country | Link |
---|---|
US (3) | US8592398B2 (ru) |
EP (1) | EP2655377B1 (ru) |
JP (1) | JP5694560B2 (ru) |
KR (1) | KR101591153B1 (ru) |
CN (1) | CN103261201B (ru) |
AP (1) | AP3391A (ru) |
AR (1) | AR084294A1 (ru) |
AU (1) | AU2011346763B2 (ru) |
BR (1) | BR112013014692A2 (ru) |
CA (1) | CA2820448A1 (ru) |
CL (1) | CL2013001810A1 (ru) |
EA (1) | EA023141B1 (ru) |
HK (1) | HK1191008A1 (ru) |
MX (1) | MX336549B (ru) |
MY (1) | MY159059A (ru) |
PE (1) | PE20140234A1 (ru) |
SG (1) | SG191173A1 (ru) |
TW (1) | TWI515199B (ru) |
UA (1) | UA109916C2 (ru) |
WO (1) | WO2012085662A1 (ru) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8969353B2 (en) | 2008-11-07 | 2015-03-03 | Massachusetts Institute Of Technology | Aminoalcohol lipidoids and uses thereof |
UA109916C2 (ru) | 2010-12-20 | 2015-10-26 | Гленмарк Фармасьютікалс С.А. | 2-амино-4-арилтиазольные соединения как антагонисты trpa1 |
WO2013023102A1 (en) | 2011-08-09 | 2013-02-14 | Hydra Biosciences, Inc. | Inhibiting transient receptor potential ion channel trpa1 |
NZ747501A (en) | 2011-10-27 | 2020-05-29 | Massachusetts Inst Technology | Amino acid derivatives functionalized on the n-terminal capable of forming drug encapsulating microspheres |
WO2013108857A1 (ja) | 2012-01-17 | 2013-07-25 | 味の素株式会社 | 複素環アミド誘導体及びそれを含有する医薬 |
CA2873570C (en) | 2012-06-08 | 2016-11-01 | Glenmark Pharmaceuticals S.A. | Amides of 2-amino-4-arylthiazole compounds and their salts as trpa1 modulators |
PL2903965T3 (pl) | 2012-10-01 | 2017-08-31 | Orion Corporation | Pochodne n-prop-2-ynylokarboksamidu i ich zastosowanie jako antagonistów trpa1 |
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 |
US8906951B1 (en) | 2013-06-24 | 2014-12-09 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
US9198898B2 (en) | 2013-06-24 | 2015-12-01 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
JP2016537322A (ja) * | 2013-10-15 | 2016-12-01 | グレンマーク ファーマシューティカルズ, エセ.アー. | Trpa1アンタゴニスト及び鎮痛剤を含む医薬組成物 |
EP3110453A4 (en) | 2014-02-24 | 2017-09-27 | The Johns Hopkins University | Tmem100 peptides and variants thereof and their use in treating or preventing diseases or conditions |
RS64331B1 (sr) | 2015-06-19 | 2023-08-31 | Massachusetts Inst Technology | Alkenil supstituisani 2,5-piperazindioni i njihova primena u sastavima za isporuku agensa u organizam ili ćeliju subjekta |
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 |
US10710994B2 (en) | 2018-03-19 | 2020-07-14 | Genentech, Inc. | Oxadiazole transient receptor potential channel inhibitors |
CA3117213A1 (en) * | 2018-10-23 | 2020-04-30 | George Edward Hoag | Composition and method for treating the lungs |
MX2022004565A (es) * | 2019-10-15 | 2022-05-06 | Boehringer Ingelheim Int | Tienopirimidonas como inhibidores de trpa1. |
BR112022003729A2 (pt) | 2019-10-15 | 2022-05-31 | Boehringer Ingelheim Int | Tienopirimidonas como inibidores de trpa1 |
CA3180979A1 (en) * | 2020-04-22 | 2021-10-28 | 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 |
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SG160211A1 (en) | 2003-04-03 | 2010-04-29 | Semafore Pharmaceuticals Inc | 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 |
CN101384261B (zh) | 2005-12-22 | 2011-12-07 | 海德拉生物科学公司 | 治疗疼痛的组合物 |
AU2008268463B2 (en) * | 2007-06-22 | 2015-03-05 | Eli Lilly And Company | Methods and compositions for treating disorders |
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 |
TW201026700A (en) | 2008-12-22 | 2010-07-16 | Hydra Biosciences Inc | Compositions useful for treating disorders related to TRPA1 |
MX2011009824A (es) | 2009-03-23 | 2012-01-25 | Glenmark Pharmaceuticals Sa | Derivados de pirimidina-diona fusionados como moduladores del trpa1. |
US8575178B2 (en) | 2009-03-23 | 2013-11-05 | Glenmark Pharmaceuticals S.A. | Isothiazolo-pyrimidinedione derivatives as TRPA1 modulators |
WO2010109329A1 (en) | 2009-03-23 | 2010-09-30 | Glenmark Pharmaceuticals, S.A. | Furopyrimidinedione derivatives as trpa1 modulators |
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 |
UA109916C2 (ru) | 2010-12-20 | 2015-10-26 | Гленмарк Фармасьютікалс С.А. | 2-амино-4-арилтиазольные соединения как антагонисты trpa1 |
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