EA200900496A1 - Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой - Google Patents

Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой

Info

Publication number
EA200900496A1
EA200900496A1 EA200900496A EA200900496A EA200900496A1 EA 200900496 A1 EA200900496 A1 EA 200900496A1 EA 200900496 A EA200900496 A EA 200900496A EA 200900496 A EA200900496 A EA 200900496A EA 200900496 A1 EA200900496 A1 EA 200900496A1
Authority
EA
Eurasian Patent Office
Prior art keywords
mediated
epoxydhydrolase
options
solutions
pharmaceutical composition
Prior art date
Application number
EA200900496A
Other languages
English (en)
Inventor
Ричард Д. мл. Глесс
Original Assignee
Эрет Терэпьютикс, Инк.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Эрет Терэпьютикс, Инк. filed Critical Эрет Терэпьютикс, Инк.
Publication of EA200900496A1 publication Critical patent/EA200900496A1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
    • C07C311/47Y being a hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/125Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/13Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/70Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74Adamantanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

В настоящем изобретении раскрываются сульфонамидные соединения и композиции, которые ингибируют растворимую эпоксидгидролазу (sEH), способы получения соединений и композиций и способы лечения пациентов данными соединениями и композициями. Соединения, композиции и способы используют для лечения ряда sEH-опосредованных заболеваний, включая гипертензивные, сердечно-сосудистые, воспалительные, легочные и связанные с диабетом заболевания.
EA200900496A 2006-09-28 2007-09-28 Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой EA200900496A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84850306P 2006-09-28 2006-09-28
PCT/US2007/079946 WO2008040000A2 (en) 2006-09-28 2007-09-28 Soluble epoxide hydrolase inhibitors

Publications (1)

Publication Number Publication Date
EA200900496A1 true EA200900496A1 (ru) 2009-08-28

Family

ID=38982713

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200900496A EA200900496A1 (ru) 2006-09-28 2007-09-28 Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой

Country Status (10)

Country Link
US (1) US20080207621A1 (ru)
EP (1) EP2068857A2 (ru)
JP (1) JP2010505768A (ru)
CN (1) CN101516361A (ru)
AU (1) AU2007299993A1 (ru)
BR (1) BRPI0717327A2 (ru)
CA (1) CA2664365A1 (ru)
EA (1) EA200900496A1 (ru)
IL (1) IL197091A0 (ru)
WO (1) WO2008040000A2 (ru)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2558928T3 (es) 2007-01-31 2016-02-09 Dana-Farber Cancer Institute, Inc. Péptidos p53 estabilizados y usos de los mismos
US8592377B2 (en) 2007-03-28 2013-11-26 President And Fellows Of Harvard College Stitched polypeptides
AR071377A1 (es) * 2008-04-18 2010-06-16 Arete Therapeutics Inc Inhibidores de epoxido hidrolasa soluble
WO2012021963A1 (en) * 2010-07-09 2012-02-23 Metasignal Therapeutics Inc. Novel sulfonamide compounds for inhibition of metastatic tumor growth
CN102464631B (zh) * 2010-11-08 2016-08-10 中国科学院上海药物研究所 哌嗪取代的1,3-二取代脲类化合物及哌嗪取代的酰胺类化合物及其制备方法和用途
TW201806968A (zh) 2011-10-18 2018-03-01 艾利倫治療公司 擬肽巨環化合物
CN104159595A (zh) 2012-02-15 2014-11-19 爱勒让治疗公司 拟肽大环化合物
WO2013123267A1 (en) 2012-02-15 2013-08-22 Aileron Therapeutics, Inc. Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles
WO2014138429A2 (en) 2013-03-06 2014-09-12 Aileron Therapeutics, Inc. Peptidomimetic macrocycles and use thereof in regulating hif1alpha
SG11201509194SA (en) 2013-05-07 2015-12-30 Univ California Radiomitigating pharmaceutical formulations
AU2015320549A1 (en) 2014-09-24 2017-04-13 Aileron Therapeutics, Inc. Peptidomimetic macrocycles and uses thereof
CN105820076A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-[2,5-二乙氧基-4-(3-对-甲苯基-脲基甲基)-苯基]-甲磺酰胺新化合物、制备方法及用途
CN105820084A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-丙氧基-苯甲酸甲基酯新化合物、制备方法及用途
CN105820085A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种乙磺酸{4-[3-(3-溴-苯基)-脲基甲基]-2,5-二乙氧基-苯基}-酰胺新化合物、制备方法及用途
CN105820087A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-乙氧基-n-对甲苯基-苯甲酰胺新化合物、制备方法及用途
CN105820090A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-乙氧基-n-(3-甲氧基-苯基)-苯甲酰胺新化合物、制备方法及用途
CN105820073A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-{[2,5-二乙氧基-4-[3-(3-甲氧基-苯基)-脲基甲基]-苯基}-甲磺酰胺新化合物、制备方法及用途
CN105820067A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-{[2,5-二乙氧基-4-[(3-苯基-脲基)-甲基]-苯基}-甲磺酰胺新化合物、制备方法及用途
CN105820091A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种基于3,4-二甲氧基苯基的取代苯甲酰胺新化合物、制备方法及用途
CN105820074A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-[4-(3-苄基-脲基甲基)-2,5-二乙氧基苯基]甲磺酰胺新化合物、制备方法及用途
CN105820066A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种基于3-甲氧基-苄基的取代苯甲酰胺新化合物、制备方法及用途
CN105820088A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-(4-溴-苯基)-5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-乙氧基苯甲酰胺新化合物、制备方法及用途
CN105820075A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-{4-[3-(3,4-二甲氧基-苯基)-脲基甲基]-2,5-二乙氧基-苯基}-甲磺酰胺新化合物、制备方法及用途
CN105820078A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种2-苄氧基-5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-苯甲酸甲酯新化合物、制备方法及用途
CN105820083A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-乙氧基-n-苯基-苯甲酰胺新化合物、制备方法及用途
CN105820069A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种n-{4-[3-(3-溴-苯基)-脲基甲基]-2,5-二丁氧基-苯基}-甲磺酰胺新化合物、制备方法及用途
CN105820079A (zh) * 2015-01-05 2016-08-03 齐鲁工业大学 一种5-[3-(2,5-二乙氧基-4-甲磺酰基-苄基)-脲基]-2-乙氧基-n-甲基-苯甲酰胺新化合物、制备方法及用途
CN105837476A (zh) * 2015-01-12 2016-08-10 齐鲁工业大学 一种n-{4-[3-(3-溴-苯基)-脲基甲基]-2,5-二乙氧基-苯基}-甲磺酰胺新化合物、制备方法及用途
BR112017019738A2 (pt) 2015-03-20 2018-05-29 Aileron Therapeutics Inc macrociclos peptidomiméticos e usos dos mesmos
CN106167456A (zh) * 2015-05-20 2016-11-30 齐鲁工业大学 新型脲类蛋白酪氨酸磷酸酯酶1b抑制剂及其制备方法、药物组合物和用途
US10023613B2 (en) 2015-09-10 2018-07-17 Aileron Therapeutics, Inc. Peptidomimetic macrocycles as modulators of MCL-1
US20200317813A1 (en) 2016-05-25 2020-10-08 Johann Wolfgang Goethe-Universitat Frankfurt Am Main Treatment and diagnosis of non-proliferative diabetic retinopathy
EP3863639A1 (en) * 2018-10-10 2021-08-18 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and topical pharmaceutical compositions for the treatment of skin microvascular dysfunction
CN113185451B (zh) * 2021-04-28 2023-09-12 沈阳药科大学 美金刚脲类衍生物及其制备方法和应用
WO2023114366A2 (en) * 2021-12-16 2023-06-22 The United States Of America, As Represented By The Secretary, Dept. Of Health And Human Services Sulfonamide derivatives and their use as soluble epoxide hydrolase inhibitors

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5571821A (en) * 1993-05-20 1996-11-05 Texas Biotechnology Corporation Sulfonamides and derivatives thereof that modulate the activity of endothelin
US6506901B2 (en) * 2000-07-17 2003-01-14 Wyeth Substituted 2-(S)-hydroxy-3-(piperidin-4-yl-methylamino)-propyl ethers and substituted 2-aryl-2-(R)-hydroxy-1-(piperidin-4-yl-methyl)-ethylamine β-3 adrenergic receptor agonists

Also Published As

Publication number Publication date
BRPI0717327A2 (pt) 2014-09-30
EP2068857A2 (en) 2009-06-17
IL197091A0 (en) 2009-11-18
CN101516361A (zh) 2009-08-26
WO2008040000A2 (en) 2008-04-03
US20080207621A1 (en) 2008-08-28
JP2010505768A (ja) 2010-02-25
CA2664365A1 (en) 2008-04-03
WO2008040000A3 (en) 2008-10-23
AU2007299993A1 (en) 2008-04-03

Similar Documents

Publication Publication Date Title
EA200900496A1 (ru) Сульфонамидные соединения (варианты), содержащая их фармацевтическая композиция, способ ингибирования растворимой эпоксидгидролазы и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой
EA200900258A1 (ru) Ингибиторы растворимой эпоксидгидролазы, фармацевтическая композиция на их основе и способ лечения заболеваний, опосредованных растворимой эпоксидгидролазой
DK2358717T3 (da) Aminotetrahydropyraner som dipeptidylpeptidase-iv-inhibitorer tilbehandling eller forebyggelse af diabetes
EA200870380A1 (ru) Аминотетрагидропираны в качестве ингибиторов дипептидилпептидазы-vi для лечения или предупреждения диабета
EA200900959A1 (ru) Ингибиторы мек
NO20091599L (no) Kjemiske forbindelser
WO2008086188A3 (en) Thiophene carboxamides as factor xa inhibitors
NO20064347L (no) Substituerte 1,2,3,4-tetrahydroisokinolinderivater
EA201070328A1 (ru) Соединения триазолопиридина и их применение в качестве ингибиторов ask
MX2009009754A (es) Compuestos de 4-piperidinilurea como inhibidores de epoxido hidrolasa soluble.
EA201270520A1 (ru) Новые соединения, эффективные в качестве ингибиторов ксантиноксидазы, способ их получения и содержащая их фармацевтическая композиция
WO2007098270A3 (en) Co-crystals comprising vx-950 and pharmaceutical compositions comprising the same
DE602006010564D1 (de) Pyridoä2,3-düpyrimidin-2,4-diamin-verbindungen als ptpib-hemmer
EA200970337A1 (ru) Ингибиторы котранспортера натрий-глюкозы 2 и способы их применения
EA200970156A1 (ru) Пиридизиноновые производные
WO2008086226A3 (en) Factor xa inhibitors
WO2007087231A3 (en) Aminocyclohexanes as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes
EA200700851A1 (ru) Получение и применение бифенил-4-илкарбониламинокислотных производных для лечения ожирения
EA201100750A1 (ru) Замещенные диоксопиперидинилфталимидные производные
EA201270666A1 (ru) Соединения и фармацевтические композиции для снижения уровня мочевой кислоты
NO20093009L (no) Kondensert ring heterocykel kinase modulatorer
EA201070039A1 (ru) Спироциклы в качестве ингибиторов 11-бета гидроксилстероиддегидрогеназы типа 1
EA201200323A1 (ru) Соединения и композиции, как ингибиторы протеинкиназы
EA200900213A1 (ru) Ингибиторы обратной транскриптазы вич (варианты), фармацевтическая композиция на их основе, способ ингибирования репликации ретровируса с их помощью и названные ингибиторы для изготовления лекарственного средства для ингибирования обратной транскриптазы вич и для лечения или профилактики инфекционного вич
EA200801997A1 (ru) Новые соединения