MX2014005140A - Derivado de azol. - Google Patents
Derivado de azol.Info
- Publication number
- MX2014005140A MX2014005140A MX2014005140A MX2014005140A MX2014005140A MX 2014005140 A MX2014005140 A MX 2014005140A MX 2014005140 A MX2014005140 A MX 2014005140A MX 2014005140 A MX2014005140 A MX 2014005140A MX 2014005140 A MX2014005140 A MX 2014005140A
- Authority
- MX
- Mexico
- Prior art keywords
- disease
- cerebral
- provides
- azole derivative
- avp
- Prior art date
Links
- 150000007980 azole derivatives Chemical class 0.000 title 1
- KBZOIRJILGZLEJ-LGYYRGKSSA-N argipressin Chemical compound C([C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@@H](C(N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1)=O)N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(N)=O)C1=CC=CC=C1 KBZOIRJILGZLEJ-LGYYRGKSSA-N 0.000 abstract 2
- 206010008118 cerebral infarction Diseases 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 201000004384 Alopecia Diseases 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- 101800001144 Arg-vasopressin Proteins 0.000 abstract 1
- 201000006474 Brain Ischemia Diseases 0.000 abstract 1
- 206010048962 Brain oedema Diseases 0.000 abstract 1
- 206010008120 Cerebral ischaemia Diseases 0.000 abstract 1
- 208000030814 Eating disease Diseases 0.000 abstract 1
- 208000019454 Feeding and Eating disease Diseases 0.000 abstract 1
- 208000018522 Gastrointestinal disease Diseases 0.000 abstract 1
- 206010019196 Head injury Diseases 0.000 abstract 1
- 208000023105 Huntington disease Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 208000019022 Mood disease Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical class C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 1
- 102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 abstract 1
- 231100000360 alopecia Toxicity 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- 208000006752 brain edema Diseases 0.000 abstract 1
- 208000026106 cerebrovascular disease Diseases 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 208000010643 digestive system disease Diseases 0.000 abstract 1
- 235000014632 disordered eating Nutrition 0.000 abstract 1
- 206010013663 drug dependence Diseases 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 208000018685 gastrointestinal system disease Diseases 0.000 abstract 1
- 230000036039 immunity Effects 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 102000005962 receptors Human genes 0.000 abstract 1
- 108020003175 receptors Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
- 208000011117 substance-related disease Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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Abstract
La presente invención proporciona agentes para tratar o prevenir enfermedades tales como el trastorno del estado de ánimo, trastorno de ansiedad, esquizofrenia, enfermedad de Alzheimer, enfermedad de Parkinson, corea de Huntington, trastornos de la alimentación, hipertensión, enfermedad gastrointestinal, adicción a fármacos, epilepsia, infarto cerebral, isquemia cerebral, edema cerebral, lesión de la cabeza, inflamación, enfermedades relacionadas con la inmunidad, alopecia y así sucesivamente; de manera específica, la invención proporciona derivados de azol representados por la fórmula general (I), o sales farmacéuticamente aceptables del mismo que tienen una acción antagonista contra el receptor V1b de la arginina-vasopresina (AVP): Quím. 1 (ver Fórmula).
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JP2011236487 | 2011-10-27 | ||
PCT/JP2012/077541 WO2013062027A1 (ja) | 2011-10-27 | 2012-10-25 | アゾール誘導体 |
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AU2011308403B2 (en) * | 2010-10-01 | 2014-08-21 | Taisho Pharmaceutical Co., Ltd. | 1,2,4-triazolone derivative |
JP6387669B2 (ja) * | 2013-04-26 | 2018-09-12 | 大正製薬株式会社 | アゾール誘導体を含有する医薬 |
US9663457B2 (en) * | 2014-04-09 | 2017-05-30 | Allergan, Inc. | Carbamoyl hydrazine derivatives as formyl peptide modulators |
CN107922390B (zh) | 2015-07-06 | 2019-05-10 | 吉利德科学公司 | Cot调节剂及其使用方法 |
KR20190028763A (ko) | 2016-07-12 | 2019-03-19 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 바이시클릭 화합물 |
CN106831712B (zh) * | 2017-01-13 | 2019-04-02 | 深圳大学 | 一种多靶点Aβ寡聚化抑制剂 |
CN106831713B (zh) * | 2017-01-13 | 2019-04-02 | 深圳大学 | 一种多靶点Aβ寡聚化抑制剂的合成方法及应用 |
CN107434778A (zh) * | 2017-05-23 | 2017-12-05 | 重庆文理学院 | 一种4‑羟基‑2h‑吡咯‑2‑酮衍生物的制备方法 |
CN107857729B (zh) * | 2017-12-25 | 2019-10-15 | 福州大学 | 一种4-碘化-n-芳基化的吡唑类化合物的合成方法 |
US10039749B1 (en) | 2018-01-15 | 2018-08-07 | King Saud University | Substituted pyrazole derivatives |
EP3886854A4 (en) | 2018-11-30 | 2022-07-06 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
TWI770527B (zh) | 2019-06-14 | 2022-07-11 | 美商基利科學股份有限公司 | Cot 調節劑及其使用方法 |
RU2730492C1 (ru) * | 2019-12-27 | 2020-08-24 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Российский химико-технологический университет имени Д.И. Менделеева" | Способ получения алкил 2-[([1,1'-бифенил]-4-карбонил)амино]-3-(1н-азол-1-ил) пропаноатов |
JP7637121B2 (ja) | 2020-03-17 | 2025-02-27 | 住友ファーマ株式会社 | オキサジアゾール誘導体 |
CN115397511A (zh) | 2020-03-30 | 2022-11-25 | 吉利德科学公司 | Cot抑制剂化合物(s)-6-(((1-(双环[1.1.1]戊-1-基)-1h-1,2,3-三唑-4-基)2-甲基-1-氧代-1,2-二氢异喹啉-5-基)甲基)))氨基8-氯-(新戊基氨基)喹啉-3-甲腈的固体形式 |
CN115397824B (zh) | 2020-04-02 | 2024-10-22 | 吉利德科学公司 | 用于制备cot抑制剂化合物的方法 |
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JP2000063363A (ja) * | 1998-08-12 | 2000-02-29 | Yamanouchi Pharmaceut Co Ltd | 新規なトリアゾール誘導体 |
FR2804114B1 (fr) | 2000-01-25 | 2002-03-08 | Sanofi Synthelabo | Nouveaux derives de 1,3-dihydro-2h-indol-2-one, un procede pour leur preparation et les compositions pharmaceutiques en contenant |
US7528124B2 (en) | 2003-08-28 | 2009-05-05 | Taisho Pharmaceutical Co., Ltd. | 1,3-dihydro-2H-indol-2-one derivative |
US20050070718A1 (en) | 2003-09-30 | 2005-03-31 | Abbott Gmbh & Co. Kg | Heteroaryl-substituted 1,3-dihydroindol-2-one derivatives and medicaments containing them |
CA2578075A1 (en) | 2004-08-26 | 2006-03-02 | Pfizer Inc. | Aminoheteroaryl compounds as protein tyrosine kinase inhibitors |
AR052342A1 (es) * | 2004-12-21 | 2007-03-14 | Janssen Pharmaceutica Nv | Derivados sustituidos de triazolona,tetrazolona e imidazolona con actividad selectiva antagonista de alfa2c-adenoreceptores |
TW200643015A (en) | 2005-03-11 | 2006-12-16 | Akzo Nobel Nv | 2-(4-oxo-4H-quinazolin-3-yl)acetamide derivatives |
CN104922117A (zh) | 2005-03-22 | 2015-09-23 | 阿泽范药品公司 | 用于治疗月经前病症的β-内酰氨基链烷酸 |
US8350043B2 (en) | 2005-06-07 | 2013-01-08 | Pharmacopeia, Inc. | Azinone and diazinone V3 inhibitors for depression and stress disorders |
WO2007109098A2 (en) | 2006-03-16 | 2007-09-27 | Azevan Pharmaceuticals, Inc. | HYDROXY AND KETO-SUBSTITUTED β-LACTAMYL ALKANEDIOIC ACIDS |
DE102006024024A1 (de) | 2006-05-23 | 2007-11-29 | Bayer Healthcare Aktiengesellschaft | Substituierte Arylimidazolone und -triazolone sowie ihre Verwendung |
EP2061769A1 (en) | 2006-08-26 | 2009-05-27 | Abbott GmbH & Co. KG | Substituted benzimidazolone derivatives, medicaments comprising them and their use |
MX2009002685A (es) | 2006-09-11 | 2009-10-13 | Organon Nv | Derivados de acetamida de (2- (1-oxo-1h-isoquinolin-2-il). |
CA2663161C (en) | 2006-09-11 | 2014-10-28 | N.V. Organon | Quinazolinone and isoquinolinone acetamide derivatives |
JP2010229035A (ja) * | 2007-08-01 | 2010-10-14 | Taisho Pharmaceutical Co Ltd | ピリドピリミジン−4−オン誘導体 |
WO2009130231A1 (en) | 2008-04-24 | 2009-10-29 | Glaxo Group Limited | Pyrrolo [1, 2-a] pyrazine derivatives as vasopressin vib receptor antagonists |
WO2009130232A1 (en) * | 2008-04-24 | 2009-10-29 | Glaxo Group Limited | Pyrazolo [1, 5 -a] pyrazine derivatives as antagonists of v1b receptors |
JP5369721B2 (ja) * | 2009-01-30 | 2013-12-18 | 大正製薬株式会社 | ピリドピリミジン−4−オン誘導体 |
DE102009013642A1 (de) * | 2009-03-18 | 2010-09-23 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Phenylalaninderivate und deren Verwendung |
JP2013075830A (ja) | 2010-02-03 | 2013-04-25 | Taisho Pharmaceutical Co Ltd | キノリン誘導体 |
CN103189363B (zh) | 2010-02-27 | 2015-07-29 | 拜耳知识产权有限责任公司 | 双芳基连接的芳基三唑酮及其用途 |
AU2011308403B2 (en) * | 2010-10-01 | 2014-08-21 | Taisho Pharmaceutical Co., Ltd. | 1,2,4-triazolone derivative |
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- 2012-10-25 US US14/353,447 patent/US9522914B2/en not_active Expired - Fee Related
- 2012-10-25 MY MYPI2014701021A patent/MY168930A/en unknown
- 2012-10-26 TW TW101139716A patent/TWI543971B/zh not_active IP Right Cessation
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2014
- 2014-04-24 ZA ZA2014/03000A patent/ZA201403000B/en unknown
- 2014-04-24 IL IL232217A patent/IL232217A/en active IP Right Grant
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2016
- 2016-05-24 CY CY20161100454T patent/CY1118021T1/el unknown
- 2016-05-31 SM SM201600153T patent/SMT201600153B/it unknown
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