UA106580C2 - Фармацевтично прийнятні солі тимодепресину і спосіб їх виробництва - Google Patents
Фармацевтично прийнятні солі тимодепресину і спосіб їх виробництваInfo
- Publication number
- UA106580C2 UA106580C2 UAA200907340A UAA200907340A UA106580C2 UA 106580 C2 UA106580 C2 UA 106580C2 UA A200907340 A UAA200907340 A UA A200907340A UA A200907340 A UAA200907340 A UA A200907340A UA 106580 C2 UA106580 C2 UA 106580C2
- Authority
- UA
- Ukraine
- Prior art keywords
- isoglutamyl
- tryptophan
- pharmaceutically acceptable
- timodepresinu
- production
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 150000003839 salts Chemical class 0.000 title abstract 2
- KSOCSOONUPBQDP-DGCLKSJQSA-N (2r)-2-[[(4r)-4,5-diamino-5-oxopentanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical class C1=CC=C2C(C[C@@H](NC(=O)CC[C@@H](N)C(N)=O)C(O)=O)=CNC2=C1 KSOCSOONUPBQDP-DGCLKSJQSA-N 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- OIXHJWJUSXFMKC-ROWAJOCBSA-L [Mg+2].N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O.N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O Chemical compound [Mg+2].N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O.N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O OIXHJWJUSXFMKC-ROWAJOCBSA-L 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- JZENWTWVDAMJOJ-LOCPCMAASA-N calcium;(2r)-2-[[(4r)-4,5-diamino-5-oxopentanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical class [Ca].C1=CC=C2C(C[C@@H](NC(=O)CC[C@@H](N)C(N)=O)C(O)=O)=CNC2=C1 JZENWTWVDAMJOJ-LOCPCMAASA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- LWGOOJLOALCXIG-LOCPCMAASA-M lithium (2R)-2-[[(4R)-4,5-diamino-5-oxopentanoyl]amino]-3-(1H-indol-3-yl)propanoate Chemical compound [Li+].N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O LWGOOJLOALCXIG-LOCPCMAASA-M 0.000 abstract 1
- JTCHENATDQSTCS-LOCPCMAASA-M potassium (2R)-2-[[(4R)-4,5-diamino-5-oxopentanoyl]amino]-3-(1H-indol-3-yl)propanoate Chemical compound [K+].N[C@H](CCC(=O)N[C@H](CC1=CNC2=CC=CC=C12)C(=O)[O-])C(N)=O JTCHENATDQSTCS-LOCPCMAASA-M 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0215—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing natural amino acids, forming a peptide bond via their side chain functional group, e.g. epsilon-Lys, gamma-Glu
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmacology & Pharmacy (AREA)
- Immunology (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Dermatology (AREA)
- Transplantation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Indole Compounds (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
Даний належить до фармацевтично прийнятних кристалічних або аморфних солей D-ізоглутаміл-D-триптофану, а також способів їх виробництва, фармацевтичних композицій, що їх містять, та їх застосування для одержання фармацевтичних композицій для лікування різних станів та/або захворювань. Зокрема, даний винахід стосується калієвої солі D-ізоглутаміл-D-триптофану (1:1), літієвої солі D-ізоглутаміл-D-триптофану (1:1), кальцієвої солі D-ізоглутаміл-D-триптофану (2:1), магнієвої солі D-ізоглутаміл-D-триптофану (2:1).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002571645A CA2571645A1 (en) | 2006-12-19 | 2006-12-19 | Pharmaceutically acceptable salts of thymodepressin and processes for their manufacture |
PCT/CA2007/002235 WO2008074128A1 (en) | 2006-12-19 | 2007-12-13 | Pharmaceutically acceptable salts of thymodepressin and processes for their manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
UA106580C2 true UA106580C2 (uk) | 2014-09-25 |
Family
ID=39535926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UAA200907340A UA106580C2 (uk) | 2006-12-19 | 2007-12-13 | Фармацевтично прийнятні солі тимодепресину і спосіб їх виробництва |
Country Status (14)
Country | Link |
---|---|
US (2) | US8138221B2 (uk) |
EP (1) | EP2121729A4 (uk) |
KR (1) | KR20090108034A (uk) |
CN (2) | CN103554004A (uk) |
AU (1) | AU2007335212B2 (uk) |
CA (2) | CA2571645A1 (uk) |
CL (1) | CL2007003680A1 (uk) |
MX (1) | MX2009006673A (uk) |
PE (2) | PE20121642A1 (uk) |
RU (1) | RU2536685C2 (uk) |
TW (1) | TWI406872B (uk) |
UA (1) | UA106580C2 (uk) |
UY (1) | UY30798A1 (uk) |
WO (1) | WO2008074128A1 (uk) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2579119C (en) | 2007-02-16 | 2013-03-05 | Apotex Technologies Inc. | Crystalline forms of the mono-sodium salt of d-isoglutamyl-d-tryptophan |
EP2062909A1 (en) * | 2007-11-21 | 2009-05-27 | SOLVAY (Société Anonyme) | Peptide production and purification process |
RU2634258C1 (ru) * | 2016-11-08 | 2017-10-24 | федеральное государственное автономное образовательное учреждение высшего образования "Российский университет дружбы народов" (РУДН) | Наполнитель для капсульного ингалятора |
RU2703991C1 (ru) * | 2019-02-12 | 2019-10-23 | Акционерное общество "Медико-биологический научно-производственный комплекс "Цитомед" (АО "МБНПК "Цитомед") | Способ получения мононатриевой соли изоглутамил-триптофана |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3238118A1 (de) | 1982-10-14 | 1984-04-19 | Verla-Pharm, Arzneimittelfabrik Apotheker H.J. v. Ehrlich GmbH & Co KG, 8132 Tutzing | Verfahren zur herstellung von komplexverbindungen aus aminodicarbonsaeuren, zweiwertigen metallionen und halogenidionen |
AU566747B2 (en) | 1984-01-10 | 1987-10-29 | Mitsui Chemicals, Inc. | Method of separating l-tryptophan |
US5902790A (en) * | 1995-10-03 | 1999-05-11 | Cytran, Inc. | Pharmaceutical angiostatic dipeptide compositions and method of use thereof |
RU2107692C1 (ru) * | 1995-06-07 | 1998-03-27 | Дейгин Владислав Исакович | Пептид и способ его получения |
RU2107691C1 (ru) * | 1995-03-02 | 1998-03-27 | Дейгин Владислав Исакович | Пептид и способ его получения |
US6103699A (en) * | 1996-06-07 | 2000-08-15 | Immunotech Developments Inc. | Peptide, a method for its preparation and a pharmaceutical composition containing the peptide |
DE19540788A1 (de) * | 1995-11-02 | 1997-05-07 | Degussa | Verwendung von wässrigen L-Tryptophan- und/oder L-Threonin-Salzlösungen |
US5744452A (en) * | 1995-11-28 | 1998-04-28 | Edward T. Wei | γ-L-glutamyl containing immunomodulator compounds and methods therewith |
US5916878A (en) * | 1995-11-28 | 1999-06-29 | Edward T. Wei | γ-glutamyl and β-aspartyl containing immunomodulator compounds and methods therewith |
IL120923A0 (en) * | 1997-05-27 | 1997-09-30 | Amylum Nv | A combined process for the production of lysine and its salts and of a further weak acid and a salt thereof |
EP2046778B1 (en) * | 2006-08-04 | 2013-12-04 | Manus Pharmaceuticals (Canada) Ltd. | Multifunctional bioactive compounds |
CA2569204A1 (en) * | 2006-11-28 | 2008-05-28 | Apotex Technologies Inc. | Crystalline d-isoglutamyl-d-tryptophan and the mono ammonium salt of d-isoglutamyl-d-tryptophan |
-
2006
- 2006-12-19 CA CA002571645A patent/CA2571645A1/en not_active Abandoned
-
2007
- 2007-12-13 CN CN201310459336.XA patent/CN103554004A/zh active Pending
- 2007-12-13 WO PCT/CA2007/002235 patent/WO2008074128A1/en active Application Filing
- 2007-12-13 KR KR1020097014834A patent/KR20090108034A/ko not_active Application Discontinuation
- 2007-12-13 TW TW096147768A patent/TWI406872B/zh not_active IP Right Cessation
- 2007-12-13 US US12/520,337 patent/US8138221B2/en not_active Expired - Fee Related
- 2007-12-13 MX MX2009006673A patent/MX2009006673A/es active IP Right Grant
- 2007-12-13 UA UAA200907340A patent/UA106580C2/uk unknown
- 2007-12-13 RU RU2009127795/04A patent/RU2536685C2/ru not_active IP Right Cessation
- 2007-12-13 EP EP07855517.4A patent/EP2121729A4/en not_active Withdrawn
- 2007-12-13 CN CN2007800508835A patent/CN101611050B/zh not_active Expired - Fee Related
- 2007-12-13 AU AU2007335212A patent/AU2007335212B2/en not_active Ceased
- 2007-12-13 CA CA002673421A patent/CA2673421A1/en not_active Abandoned
- 2007-12-14 UY UY30798A patent/UY30798A1/es not_active Application Discontinuation
- 2007-12-14 PE PE2012000979A patent/PE20121642A1/es not_active Application Discontinuation
- 2007-12-14 PE PE2007001794A patent/PE20081402A1/es not_active Application Discontinuation
- 2007-12-18 CL CL200703680A patent/CL2007003680A1/es unknown
-
2012
- 2012-03-19 US US13/424,343 patent/US8735602B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
PE20081402A1 (es) | 2008-11-16 |
CN101611050A (zh) | 2009-12-23 |
CL2007003680A1 (es) | 2008-03-14 |
MX2009006673A (es) | 2009-11-02 |
RU2536685C2 (ru) | 2014-12-27 |
EP2121729A1 (en) | 2009-11-25 |
CA2571645A1 (en) | 2008-06-19 |
CN101611050B (zh) | 2013-10-30 |
AU2007335212B2 (en) | 2013-09-05 |
US20130072692A1 (en) | 2013-03-21 |
CA2673421A1 (en) | 2008-06-26 |
RU2009127795A (ru) | 2011-01-27 |
KR20090108034A (ko) | 2009-10-14 |
PE20121642A1 (es) | 2012-12-16 |
CN103554004A (zh) | 2014-02-05 |
TWI406872B (zh) | 2013-09-01 |
US20100056803A1 (en) | 2010-03-04 |
UY30798A1 (es) | 2008-07-03 |
WO2008074128A1 (en) | 2008-06-26 |
US8735602B2 (en) | 2014-05-27 |
AU2007335212A1 (en) | 2008-06-26 |
EP2121729A4 (en) | 2013-07-31 |
US8138221B2 (en) | 2012-03-20 |
TW200833708A (en) | 2008-08-16 |
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