EA201071272A1 - Новые производные аминокислот, способ их получения и применение - Google Patents
Новые производные аминокислот, способ их получения и применениеInfo
- Publication number
- EA201071272A1 EA201071272A1 EA201071272A EA201071272A EA201071272A1 EA 201071272 A1 EA201071272 A1 EA 201071272A1 EA 201071272 A EA201071272 A EA 201071272A EA 201071272 A EA201071272 A EA 201071272A EA 201071272 A1 EA201071272 A1 EA 201071272A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- phenyl
- formula
- hydrogen
- benzyl radical
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/64—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
- C07C323/65—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfone or sulfoxide groups bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Addiction (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Изобретение относится к новым соединениям формулы (I) RNH-CH(R)-CH-S-S-CH-C(R)(R)-CONH-C(R)(R)-COOR, в которых Rпредставляет собой (ацилокси)алкилкарбаматную группу -C(O)-O-C(R)(R)-OC(O)-R; Rпредставляет собой углеводородную цепь, метиленовый радикал, замещенный гетероциклом; Rпредставляет собой атом водорода и Rпредставляет собой фенильный или бензильный радикал, гетероарил, метиленовую группу, замещенную гетероциклом, либо Rи Rобразуют вместе насыщенный цикл; Rи Rпредставляют собой атом водорода, углеводородную цепь, фенильный или бензильный радикал, либо Rи Rобразуют вместе насыщенный цикл; Rпредставляет собой атом водорода, фенильный или бензильный радикал, группу формулы CR(R)C(O)ORили OCR(R)OC(O)Rили OCR(R)OC(O)OR. Изобретение также относится к применению этих соединений в качестве лекарства и к фармацевтической композиции, содержащей эти соединения и фармацевтически приемлемый носитель. Далее изобретение относится к комбинированному применению по меньшей мере одного производного каннабиноидов и/или морфина или одного его производного и/или производных ГАМК для усиления анальгезирующего и антидепрессивного эффекта новых соединений формулы (I).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0853092A FR2931151A1 (fr) | 2008-05-13 | 2008-05-13 | Nouveaux derives d'amino-acides, leur procede de preparation et leur utilisation therapeutique |
PCT/EP2009/055787 WO2009138436A1 (fr) | 2008-05-13 | 2009-05-13 | Nouveaux dérivés d'amino-acides, leur procédé de préparation et leur utilisation thérapeutique |
Publications (1)
Publication Number | Publication Date |
---|---|
EA201071272A1 true EA201071272A1 (ru) | 2011-04-29 |
Family
ID=40225670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201071272A EA201071272A1 (ru) | 2008-05-13 | 2009-05-13 | Новые производные аминокислот, способ их получения и применение |
Country Status (16)
Country | Link |
---|---|
US (1) | US8466309B2 (ru) |
EP (1) | EP2297095B9 (ru) |
JP (1) | JP5642664B2 (ru) |
KR (1) | KR20110008325A (ru) |
CN (2) | CN103739531B (ru) |
AT (1) | ATE555084T1 (ru) |
AU (1) | AU2009248056A1 (ru) |
BR (1) | BRPI0912398A2 (ru) |
CA (1) | CA2722840C (ru) |
EA (1) | EA201071272A1 (ru) |
FR (1) | FR2931151A1 (ru) |
IL (1) | IL209214A (ru) |
MX (1) | MX2010012273A (ru) |
NZ (1) | NZ588955A (ru) |
WO (1) | WO2009138436A1 (ru) |
ZA (1) | ZA201008029B (ru) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2934267B1 (fr) * | 2008-07-23 | 2010-08-13 | Pharmaleads | Derives aminophosphiniques utiles dans le traitement de la douleur |
FR2997080B1 (fr) * | 2012-10-23 | 2015-11-27 | Pharmaleads | Inhibiteurs de neprilysine |
FR2997081B1 (fr) * | 2012-10-23 | 2015-11-27 | Pharmaleads | Inhibiteurs mixtes de l'aminopeptidase n et de la neprilysine |
TWI712582B (zh) * | 2015-10-14 | 2020-12-11 | 法商領先藥物公司 | 用來製備(5s,10s)-10-苄基-16-甲基-11,14,18-三側氧基-15,17,19-三氧雜-2,7,8-三噻基-12-氮二十一烷基-5-銨基(e)-3-羧基丙烯酸鹽的工業方法 |
FR3077201B1 (fr) | 2018-01-26 | 2020-01-17 | Pharmaleads | Derives aminoacides contenant un groupement disulfanyle sous forme d'un inhibiteur de nep et d'apn pour la prevention et le traitement des douleurs relatives au nerf trijumeau |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2480747A1 (fr) * | 1980-04-17 | 1981-10-23 | Roques Bernard | Derives d'acides amines et leur application therapeutique |
FR2488253A1 (fr) * | 1980-08-08 | 1982-02-12 | Roques Bernard | Nouveaux peptides et leur application en therapeutique |
FR2518088B1 (fr) | 1981-12-16 | 1987-11-27 | Roques Bernard | Nouveaux derives d'aminoacides, et leur application therapeutique |
US4426391A (en) * | 1982-09-15 | 1984-01-17 | Merck & Co., Inc. | [(Alkoxycarbonyl)oxy]alkyl esters of methyldopa |
DE3475065D1 (en) * | 1983-06-23 | 1988-12-15 | Merck & Co Inc | (acyloxyalkoxy) carbonyl derivatives as bioreversible prodrug moieties for primary and secondary amine functions in drugs, their preparation and pharmaceutical compositions containing said derivatives |
US4916230A (en) * | 1984-07-02 | 1990-04-10 | Merck & Co., Inc. | Process for preparing novel N-(acyloxy-alkoxy)carbonyl derivatives useful as bioreversible prodrug moieties for primary and secondary amine functions in drugs |
FR2605004B1 (fr) | 1986-09-25 | 1989-01-13 | Centre Nat Rech Scient | Nouveaux derives d'amino-acides, leur procede de preparation et composition pharmaceutiques les contenant |
FR2611722B1 (fr) * | 1987-03-02 | 1989-08-11 | Inst Nat Sante Rech Med | Nouveaux peptides derives de la cck8, leur preparation et les compositions pharmaceutiques qui les contiennent |
FR2634763B1 (fr) * | 1988-08-01 | 1991-07-12 | Inst Nat Sante Rech Med | Amino-acides et peptides presentant un residu tyrosine modifiee, leur preparation et leur application comme medicaments |
FR2651229B1 (fr) | 1989-08-24 | 1991-12-13 | Inst Nat Sante Rech Med | Nouveaux derives d'amino-acides, leur procede de preparation et leur application therapeutique. |
FR2679564A1 (fr) * | 1991-07-23 | 1993-01-29 | Inst Nat Sante Rech Med | Nouveaux acylmercaptoalcanoldipeptides, leur preparation et les compositions qui les contiennent. |
FR2729668A1 (fr) * | 1995-01-23 | 1996-07-26 | Adir | Nouveaux derives de mercaptoalcanoyldipeptides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
FR2745571B1 (fr) * | 1996-03-04 | 1998-06-19 | Inst Nat Sante Rech Med | Nouveaux derives soufres comportant une liaison amide, leur procede de preparation, leur application a titre de medicaments, et les compositions pharmaceutiques les renfermant |
FR2755135B1 (fr) * | 1996-10-25 | 2002-12-27 | Inst Nat Sante Rech Med | Nouveaux derives d'(alpha-aminophosphino)peptides, leur procede de preparation et les compositions qui les contiennent |
FR2773712B1 (fr) * | 1998-01-16 | 2000-06-02 | Inst Nat Sante Rech Med | Composition pharmaceutique comprenant au moins un inhibiteur de l'aminopeptidase a |
FR2777780B1 (fr) | 1998-04-22 | 2001-05-04 | Inst Nat Sante Rech Med | Derives d'(alpha-aminophosphino) peptides, leur procede de preparation et les compositions qui les contiennent |
US20020055463A1 (en) * | 1998-12-24 | 2002-05-09 | Christiane Garbay | Pseudopeptide compounds having an inhibiting activity with respect to paths activated by proteins with active tyrosine kinase activity and pharmaceutical compositions containing same |
FR2788526B1 (fr) * | 1999-01-20 | 2002-07-05 | Inst Nat Sante Rech Med | Composes tripeptidiques utiles a titre d'hinhibiteurs selectifs de l'aminopeptidase a et compositions pharmaceutiques correspondantes |
FR2805259B1 (fr) * | 2000-02-17 | 2002-03-29 | Inst Nat Sante Rech Med | Nouveaux derives d'aminoacides n-mercaptoacyles, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
FR2807523B1 (fr) * | 2000-04-07 | 2002-08-30 | Inst Nat Sante Rech Med | UTILISATION D'UN RESTE PyA-(Z)x-pNF A DES FINS DE DETECTION, IDENTIFICATION ET/OU DOSAGE PAR FLUORESCENCE |
GB2362646A (en) * | 2000-05-26 | 2001-11-28 | Warner Lambert Co | Cyclic amino acid derivatives useful as pharmaceutical agents |
FR2809733B1 (fr) * | 2000-06-02 | 2004-04-30 | Inst Nat Sante Rech Med | Substrat peptidique reconnu par la toxine botulique de type bont/b et son utilisation pour doser et/ou detecter ladite toxine ou des inhibiteurs correspondants |
ES2369256T3 (es) * | 2000-06-26 | 2011-11-28 | Helen Of Troy Limited | Sistema de lámpara recargable. |
GB2365425A (en) * | 2000-08-01 | 2002-02-20 | Parke Davis & Co Ltd | Alkyl amino acid derivatives useful as pharmaceutical agents |
DE60136747D1 (de) * | 2000-09-11 | 2009-01-08 | Pasteur Institut | Mitochondrialen membrane permeabilisierung durch hiv-1 vpr und screeningsverfahren |
FR2823212B1 (fr) * | 2001-04-10 | 2005-12-02 | Inst Nat Sante Rech Med | Inhibiteurs de la toxine botulique de type b |
SI1525188T1 (sl) * | 2002-07-16 | 2008-12-31 | Edicale Inserm Inst Nat De La | Novi derivati 4,4-ditiobis-(3-aminobutan-1-sulfonatov) in sestavki, ki jih vsebujejo |
FR2858617A1 (fr) * | 2003-08-06 | 2005-02-11 | Inst Nat Sante Rech Med | Derives de 4',4'-dithiobis-(3-aminobutane-1-sulfonate-1- sulfonates) nouveaux et compositions les contenant |
US7875436B2 (en) * | 2004-05-05 | 2011-01-25 | Pharmaleads | Peptide substrates recognizable by a botulinum toxin A, BoNT/A and the use thereof |
US20070049627A1 (en) * | 2005-08-23 | 2007-03-01 | Tran Pierre V | Treating vulvodynia using prodrugs of GABA analogs |
US8247609B2 (en) * | 2005-10-25 | 2012-08-21 | Pharamleads | Aminoacid derivatives containing a disulfanyl group in the form of mixed disulfanyl and aminopeptidase N inhibitors |
WO2007048787A1 (fr) * | 2005-10-25 | 2007-05-03 | Pharmaleads | Derives d'amino-acides contenant un groupement disulfanyle comme inhibiteurs mixtes de la neprilysine et de l 'aminopeptidase n |
-
2008
- 2008-05-13 FR FR0853092A patent/FR2931151A1/fr not_active Withdrawn
-
2009
- 2009-05-13 NZ NZ588955A patent/NZ588955A/en not_active IP Right Cessation
- 2009-05-13 JP JP2011508908A patent/JP5642664B2/ja active Active
- 2009-05-13 KR KR1020107028001A patent/KR20110008325A/ko not_active Application Discontinuation
- 2009-05-13 AU AU2009248056A patent/AU2009248056A1/en not_active Abandoned
- 2009-05-13 EP EP09745768A patent/EP2297095B9/fr active Active
- 2009-05-13 AT AT09745768T patent/ATE555084T1/de active
- 2009-05-13 BR BRPI0912398A patent/BRPI0912398A2/pt not_active IP Right Cessation
- 2009-05-13 WO PCT/EP2009/055787 patent/WO2009138436A1/fr active Application Filing
- 2009-05-13 US US12/991,999 patent/US8466309B2/en active Active
- 2009-05-13 MX MX2010012273A patent/MX2010012273A/es not_active Application Discontinuation
- 2009-05-13 CA CA2722840A patent/CA2722840C/fr active Active
- 2009-05-13 CN CN201310736987.9A patent/CN103739531B/zh active Active
- 2009-05-13 EA EA201071272A patent/EA201071272A1/ru unknown
- 2009-05-13 CN CN200980116831.2A patent/CN102026966B/zh active Active
-
2010
- 2010-11-09 IL IL209214A patent/IL209214A/en active IP Right Grant
- 2010-11-09 ZA ZA2010/08029A patent/ZA201008029B/en unknown
Also Published As
Publication number | Publication date |
---|---|
MX2010012273A (es) | 2010-12-02 |
EP2297095B9 (fr) | 2013-01-09 |
US20110071218A1 (en) | 2011-03-24 |
CA2722840A1 (fr) | 2009-11-19 |
JP5642664B2 (ja) | 2014-12-17 |
ATE555084T1 (de) | 2012-05-15 |
US8466309B2 (en) | 2013-06-18 |
CN103739531B (zh) | 2016-09-14 |
KR20110008325A (ko) | 2011-01-26 |
AU2009248056A1 (en) | 2009-11-19 |
CA2722840C (fr) | 2017-04-11 |
IL209214A (en) | 2014-08-31 |
ZA201008029B (en) | 2011-08-31 |
JP2011522797A (ja) | 2011-08-04 |
IL209214A0 (en) | 2011-01-31 |
FR2931151A1 (fr) | 2009-11-20 |
CN103739531A (zh) | 2014-04-23 |
EP2297095A1 (fr) | 2011-03-23 |
CN102026966B (zh) | 2014-02-12 |
NZ588955A (en) | 2012-07-27 |
WO2009138436A1 (fr) | 2009-11-19 |
CN102026966A (zh) | 2011-04-20 |
EP2297095B1 (fr) | 2012-04-25 |
BRPI0912398A2 (pt) | 2016-03-15 |
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