CY1109693T1 - ΥΠΟΚΑΤΕΣΤΗΜΕΝΑ ΙΜΙΔΑΖΟΛΙΑ ΩΣ ΑΝΑΣΤΟΛΕΙΣ TAFIa - Google Patents
ΥΠΟΚΑΤΕΣΤΗΜΕΝΑ ΙΜΙΔΑΖΟΛΙΑ ΩΣ ΑΝΑΣΤΟΛΕΙΣ TAFIaInfo
- Publication number
- CY1109693T1 CY1109693T1 CY20091101349T CY091101349T CY1109693T1 CY 1109693 T1 CY1109693 T1 CY 1109693T1 CY 20091101349 T CY20091101349 T CY 20091101349T CY 091101349 T CY091101349 T CY 091101349T CY 1109693 T1 CY1109693 T1 CY 1109693T1
- Authority
- CY
- Cyprus
- Prior art keywords
- tafia
- suspensions
- substituted imidazoles
- compounds
- conditions
- Prior art date
Links
- 150000002460 imidazoles Chemical class 0.000 title 1
- 239000000725 suspension Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 101800004538 Bradykinin Proteins 0.000 abstract 1
- QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 abstract 1
- 102100035792 Kininogen-1 Human genes 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 206010039580 Scar Diseases 0.000 abstract 1
- QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 230000003176 fibrotic effect Effects 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Reproductive Health (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Gynecology & Obstetrics (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Pregnancy & Childbirth (AREA)
- Urology & Nephrology (AREA)
- Endocrinology (AREA)
- Surgery (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
Abstract
Η παρούσα εφεύρεση παρέχει ενώσεις του τύπου (I). Αυτές οι ενώσεις είναι μια κατηγορία αναστολέων TAFIa, αθηροσκλήρωσης, συμφύσεων, δερματικής ουλής, καρκίνου, ινωτικών καταστάσεων, φλεγμονωδών ασθενειών και αυτών των καταστάσεων οι οποίες ευεργετούνται από διατήρηση ή ενίσχυση επιπέδων βραδυκινίνης στο σώμα.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0020346A GB0020346D0 (en) | 2000-08-17 | 2000-08-17 | Pharmaceuticals |
| GB0027409A GB0027409D0 (en) | 2000-11-09 | 2000-11-09 | Pharmaceuticals |
| GB0029556A GB0029556D0 (en) | 2000-12-04 | 2000-12-04 | Pharmaceuticals |
| EP01954264A EP1311488B1 (en) | 2000-08-17 | 2001-08-08 | Substituted imidazoles as tafia inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1109693T1 true CY1109693T1 (el) | 2014-08-13 |
Family
ID=27255849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY20091101349T CY1109693T1 (el) | 2000-08-17 | 2009-12-30 | ΥΠΟΚΑΤΕΣΤΗΜΕΝΑ ΙΜΙΔΑΖΟΛΙΑ ΩΣ ΑΝΑΣΤΟΛΕΙΣ TAFIa |
Country Status (38)
| Country | Link |
|---|---|
| EP (1) | EP1311488B1 (el) |
| JP (2) | JP4119746B2 (el) |
| KR (1) | KR20030022412A (el) |
| CN (1) | CN1443173A (el) |
| AP (1) | AP1375A (el) |
| AR (1) | AR035580A1 (el) |
| AT (1) | ATE447557T1 (el) |
| AU (1) | AU2001276605A1 (el) |
| BG (1) | BG107330A (el) |
| BR (1) | BR0113289A (el) |
| CA (1) | CA2419633C (el) |
| CY (1) | CY1109693T1 (el) |
| CZ (1) | CZ2003388A3 (el) |
| DE (1) | DE60140368D1 (el) |
| DK (1) | DK1311488T3 (el) |
| DO (1) | DOP2001000233A (el) |
| EA (1) | EA005532B1 (el) |
| EE (1) | EE200300070A (el) |
| ES (1) | ES2334101T3 (el) |
| HR (1) | HRP20030103A2 (el) |
| HU (1) | HUP0303763A3 (el) |
| IL (1) | IL153225A0 (el) |
| IS (1) | IS6638A (el) |
| MA (1) | MA26940A1 (el) |
| MX (1) | MXPA03001425A (el) |
| NO (1) | NO20030706L (el) |
| NZ (1) | NZ522823A (el) |
| OA (1) | OA12362A (el) |
| PA (1) | PA8525401A1 (el) |
| PE (1) | PE20020352A1 (el) |
| PL (1) | PL361054A1 (el) |
| PT (1) | PT1311488E (el) |
| SI (1) | SI1311488T1 (el) |
| SK (1) | SK1732003A3 (el) |
| SV (1) | SV2002000602A (el) |
| TN (1) | TNSN01126A1 (el) |
| UY (1) | UY26889A1 (el) |
| WO (1) | WO2002014285A1 (el) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0103272D0 (sv) | 2001-09-28 | 2001-09-28 | Astrazeneca Ab | Chemical compounds |
| US6713496B2 (en) | 2002-01-22 | 2004-03-30 | Pfizer Inc | 3-(imidazolyl)-2-alkoxypropanoic acids |
| IL162677A0 (en) * | 2002-01-22 | 2005-11-20 | Pfizer | 3-(Imidazolyl)-2-alkoxypropanoic acids as tafia inhibitors |
| MXPA04005940A (es) | 2002-01-22 | 2004-09-13 | Pfizer | Acidos 3-(imidazolil)-2-aminopropanoicos. |
| AU2004235488A1 (en) * | 2003-04-29 | 2004-11-11 | Universitat Zurich | Nepsilon and/or nalpha derivatized, metal and organic protected l-histidine for coupling to biomolecules for highly efficient labeling with [M(OH2)3(CO)3]+ by fac coordination |
| SE0302853D0 (sv) * | 2003-10-29 | 2003-10-29 | Astrazeneca Ab | Chemical compounds |
| AU2004290499C1 (en) * | 2003-11-03 | 2011-02-24 | Probiodrug Ag | Combinations useful for the treatment of neuronal disorders |
| WO2005051384A1 (en) * | 2003-11-25 | 2005-06-09 | Pfizer Limited | Stabilised pharmaceutical compositions |
| CA2604912A1 (en) * | 2005-04-18 | 2006-10-26 | Bayer Schering Pharma Aktiengesellschaft | Use of tafi inhibitors for enhanced myocardial reperfusion and facilitated pci |
| DE102005049385A1 (de) * | 2005-10-15 | 2007-04-19 | Sanofi-Aventis Deutschland Gmbh | Imidazolderivate als Inhibitoren von TAFIa |
| HRP20150514T1 (hr) * | 2006-12-06 | 2015-09-11 | Sanofi | DERIVATI SULFAMIDA KAO INHIBITORI TAFIa |
| EP2262783A2 (en) * | 2008-02-21 | 2010-12-22 | Sanofi-Aventis | Covalently binding imaging probes |
| JPWO2010050525A1 (ja) | 2008-10-29 | 2012-03-29 | 大正製薬株式会社 | TAFIa阻害活性を有する化合物 |
| FR2947266B1 (fr) * | 2009-06-26 | 2011-06-17 | Servier Lab | Nouveaux derives d'acide 2-mercaptocyclopentanecarboxylique, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| EP2548872B1 (en) | 2010-03-18 | 2016-09-28 | Daiichi Sankyo Company, Limited | Cyclopropanecarboxylic acid derivative |
| ES2643132T3 (es) * | 2010-03-18 | 2017-11-21 | Daiichi Sankyo Company, Limited | Derivado de imidazol cicloalquilo sustituido |
| GEP201706614B (en) * | 2011-05-17 | 2017-02-10 | Pharmasyntez | Compounds, pharmaceutical compositions and a method for the prophylaxis and treatment of the adhesion process |
| JP5996647B2 (ja) * | 2011-07-22 | 2016-09-21 | カンブレックス カルルスクーガ アクチ ボラケットCambrex Karlskoga Ab | 4−置換イミダゾールの新規な調製プロセス |
| WO2013039202A1 (ja) * | 2011-09-15 | 2013-03-21 | 第一三共株式会社 | 新規アクリル酸誘導体 |
| BR112015029667A2 (pt) | 2013-06-10 | 2017-07-25 | Sanofi Sa | derivados de ureia macrocíclica como inibidores de tafia, sua preparação e seus usos como produtos farmacêuticos |
| WO2017062468A1 (en) | 2015-10-07 | 2017-04-13 | Mitobridge, Inc. | Ppar agonists, compounds, pharmaceutical compositions, and methods of use thereof |
| FR3046793B1 (fr) * | 2016-01-14 | 2018-01-05 | Les Laboratoires Servier | Nouveaux derives de phosphinanes et azaphosphinanes, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US20190117624A1 (en) | 2016-03-29 | 2019-04-25 | Daiichi Sankyo Company, Limited | Therapeutic agent for inflammatory bowel diseases |
| JP6925367B2 (ja) | 2016-04-13 | 2021-08-25 | ミトブリッジ,インコーポレーテッド | Pparアゴニスト、化合物、医薬組成物、及びその使用方法 |
| CN113943255B (zh) * | 2020-07-17 | 2024-08-06 | 深圳信立泰药业股份有限公司 | 一种手性3-(4-环丙基-2,5-二氧杂咪唑啉-4-基)丙酸的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6163661A (ja) * | 1984-09-05 | 1986-04-01 | Microbial Chem Res Found | ヒスタジン関連化合物 |
| US5993815A (en) * | 1996-11-08 | 1999-11-30 | University Of Vermont | Methods and compositions for inhibiting the activation of thrombin-activatable fibrinolysis inhibitor (TAFI) |
| SE9901572D0 (sv) * | 1999-05-03 | 1999-05-03 | Astra Ab | New compounds |
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2001
- 2001-08-08 HR HR20030103A patent/HRP20030103A2/hr not_active Application Discontinuation
- 2001-08-08 CN CN01813131A patent/CN1443173A/zh active Pending
- 2001-08-08 DE DE60140368T patent/DE60140368D1/de not_active Expired - Lifetime
- 2001-08-08 KR KR10-2003-7002279A patent/KR20030022412A/ko not_active Ceased
- 2001-08-08 BR BR0113289-0A patent/BR0113289A/pt not_active Application Discontinuation
- 2001-08-08 SI SI200130950T patent/SI1311488T1/sl unknown
- 2001-08-08 HU HU0303763A patent/HUP0303763A3/hu unknown
- 2001-08-08 IL IL15322501A patent/IL153225A0/xx unknown
- 2001-08-08 AT AT01954264T patent/ATE447557T1/de active
- 2001-08-08 AU AU2001276605A patent/AU2001276605A1/en not_active Abandoned
- 2001-08-08 SK SK173-2003A patent/SK1732003A3/sk unknown
- 2001-08-08 ES ES01954264T patent/ES2334101T3/es not_active Expired - Lifetime
- 2001-08-08 EA EA200201239A patent/EA005532B1/ru not_active IP Right Cessation
- 2001-08-08 OA OA1200300039A patent/OA12362A/fr unknown
- 2001-08-08 EE EEP200300070A patent/EE200300070A/xx unknown
- 2001-08-08 EP EP01954264A patent/EP1311488B1/en not_active Expired - Lifetime
- 2001-08-08 MX MXPA03001425A patent/MXPA03001425A/es active IP Right Grant
- 2001-08-08 CA CA2419633A patent/CA2419633C/en not_active Expired - Fee Related
- 2001-08-08 PT PT01954264T patent/PT1311488E/pt unknown
- 2001-08-08 PL PL36105401A patent/PL361054A1/xx not_active Application Discontinuation
- 2001-08-08 DK DK01954264T patent/DK1311488T3/da active
- 2001-08-08 WO PCT/IB2001/001425 patent/WO2002014285A1/en not_active Ceased
- 2001-08-08 CZ CZ2003388A patent/CZ2003388A3/cs unknown
- 2001-08-08 NZ NZ522823A patent/NZ522823A/en unknown
- 2001-08-08 JP JP2002519428A patent/JP4119746B2/ja not_active Expired - Fee Related
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- 2001-08-15 UY UY26889A patent/UY26889A1/es not_active Application Discontinuation
- 2001-08-15 PE PE2001000815A patent/PE20020352A1/es not_active Application Discontinuation
- 2001-08-16 TN TNTNSN01126A patent/TNSN01126A1/fr unknown
- 2001-08-16 AP APAP/P/2001/002250A patent/AP1375A/en active
- 2001-08-16 SV SV2001000602A patent/SV2002000602A/es unknown
- 2001-11-14 DO DO2001000233A patent/DOP2001000233A/es unknown
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2002
- 2002-11-28 IS IS6638A patent/IS6638A/is unknown
- 2002-11-28 BG BG107330A patent/BG107330A/xx unknown
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2003
- 2003-02-04 MA MA27025A patent/MA26940A1/fr unknown
- 2003-02-14 NO NO20030706A patent/NO20030706L/no not_active Application Discontinuation
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2008
- 2008-02-27 JP JP2008045382A patent/JP4778531B2/ja not_active Expired - Fee Related
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2009
- 2009-12-30 CY CY20091101349T patent/CY1109693T1/el unknown
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