JP2005525398A5 - - Google Patents
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- Publication number
- JP2005525398A5 JP2005525398A5 JP2003584046A JP2003584046A JP2005525398A5 JP 2005525398 A5 JP2005525398 A5 JP 2005525398A5 JP 2003584046 A JP2003584046 A JP 2003584046A JP 2003584046 A JP2003584046 A JP 2003584046A JP 2005525398 A5 JP2005525398 A5 JP 2005525398A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- group
- alkoxy
- atom
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 125000000217 alkyl group Chemical group 0.000 claims 217
- 125000003118 aryl group Chemical group 0.000 claims 85
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 58
- 125000003545 alkoxy group Chemical group 0.000 claims 38
- 125000002950 monocyclic group Chemical group 0.000 claims 30
- 229910052760 oxygen Inorganic materials 0.000 claims 30
- 229910052717 sulfur Inorganic materials 0.000 claims 30
- 150000001875 compounds Chemical class 0.000 claims 29
- 125000004430 oxygen atom Chemical group O* 0.000 claims 29
- 125000004434 sulfur atom Chemical group 0.000 claims 29
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 26
- 208000035475 disorder Diseases 0.000 claims 26
- 125000002877 alkyl aryl group Chemical group 0.000 claims 23
- 229910052736 halogen Inorganic materials 0.000 claims 22
- 150000002367 halogens Chemical group 0.000 claims 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims 19
- 125000003342 alkenyl group Chemical group 0.000 claims 16
- 229910052739 hydrogen Inorganic materials 0.000 claims 16
- 239000001257 hydrogen Substances 0.000 claims 16
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 16
- 125000001424 substituent group Chemical group 0.000 claims 14
- 102000010183 Bradykinin receptor Human genes 0.000 claims 13
- 108050001736 Bradykinin receptor Proteins 0.000 claims 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 13
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 12
- 125000000623 heterocyclic group Chemical group 0.000 claims 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 12
- 229910052799 carbon Inorganic materials 0.000 claims 11
- 229920006395 saturated elastomer Polymers 0.000 claims 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 8
- 125000004414 alkyl thio group Chemical group 0.000 claims 8
- 125000000304 alkynyl group Chemical group 0.000 claims 8
- 125000004104 aryloxy group Chemical group 0.000 claims 8
- 125000004001 thioalkyl group Chemical group 0.000 claims 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 7
- 230000001225 therapeutic effect Effects 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- 238000009472 formulation Methods 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- -1 methylenedioxy Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000005551 pyridylene group Chemical group 0.000 claims 4
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims 3
- 125000004450 alkenylene group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
- 125000003386 piperidinyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000005556 thienylene group Chemical group 0.000 claims 2
- 125000005001 aminoaryl group Chemical group 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37135002P | 2002-04-10 | 2002-04-10 | |
| PCT/US2003/009974 WO2003087090A2 (en) | 2002-04-10 | 2003-03-31 | Novel heteroaryl alkylamide derivatives useful as bradykinin receptor modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005525398A JP2005525398A (ja) | 2005-08-25 |
| JP2005525398A5 true JP2005525398A5 (https=) | 2006-05-25 |
Family
ID=29250669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003584046A Withdrawn JP2005525398A (ja) | 2002-04-10 | 2003-03-31 | ブラジキニン受容体モジュレーターとして有用な新規なヘテロアリールアルキルアミド誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US6958349B2 (https=) |
| EP (1) | EP1495017A2 (https=) |
| JP (1) | JP2005525398A (https=) |
| AU (1) | AU2003226188A1 (https=) |
| CA (1) | CA2481855A1 (https=) |
| WO (1) | WO2003087090A2 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003299757A1 (en) * | 2002-12-19 | 2004-07-14 | Elan Pharmaceuticals Inc. | Substituted n-phenyl sulfonamide bradykinin antagonists |
| EP2359833A1 (en) | 2003-04-25 | 2011-08-24 | Gilead Sciences, Inc. | Antiviral phosphonate analogs |
| ME03423B (me) * | 2004-07-27 | 2020-01-20 | Gilead Sciences Inc | Fosfonatni analozi jedinjenja hiv inhibitora |
| WO2008026018A1 (en) * | 2006-09-01 | 2008-03-06 | Topotarget Switzerland Sa | New method for the treatment of inflammatory diseases |
| TWI407960B (zh) | 2007-03-23 | 2013-09-11 | Jerini Ag | 小分子緩激肽ｂ２受體調節劑 |
| US7807629B1 (en) | 2007-06-05 | 2010-10-05 | Alcon Research, Ltd. | Use of bradykinin and related B2R agonists to treat ocular hypertension and glaucoma |
| US8173668B1 (en) | 2007-06-05 | 2012-05-08 | Alcon Research, Ltd. | Use of non-peptidic bradykinin receptor agonists to treat ocular hypertension and glaucoma |
| UA103329C2 (ru) | 2008-07-08 | 2013-10-10 | Гилиад Сайенсиз, Инк. | Соли соединений-ингибиторов вич |
| WO2013144113A1 (en) | 2012-03-26 | 2013-10-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for prevention or treatment of ischemia related organ damage |
| CA2904052A1 (en) * | 2013-03-14 | 2014-10-02 | Shire Human Genetic Therapies, Inc. | Methods of treating b2-bradykinin receptor mediated angioedema |
| SG11201610476VA (en) * | 2014-07-01 | 2017-01-27 | Millennium Pharm Inc | Heteroaryl compounds useful as inhibitors of sumo activating enzyme |
| SI3661937T1 (sl) | 2017-08-01 | 2021-11-30 | Gilead Sciences, Inc. | Kristalinične oblike etil((S)-((((2R,5R)-5-(6-amino-9H-purin-9-IL)-4- fluoro-2,5-dihidrofuran-2-IL)oksi)metil)(fenoksi)fosforil)-L-alaninata (GS-9131) za zdravljenje virusnih okužb |
| WO2019101906A1 (en) | 2017-11-24 | 2019-05-31 | Pharvaris B.V. | Novel bradykinin b2 receptor antagonists |
| UY38707A (es) | 2019-05-23 | 2020-12-31 | Pharvaris Gmbh | Nuevos antagonistas cíclicos del receptor b2 de bradiquinina |
| UY38706A (es) | 2019-05-23 | 2020-12-31 | Pharvaris Gmbh | Antagonistas cíclicos del receptor b2 de bradiquinina |
| EP4499100A1 (en) | 2022-03-25 | 2025-02-05 | Pharvaris GmbH | Therapeutic uses of bradykinin b2-receptor antagonists |
| TW202345810A (zh) | 2022-03-25 | 2023-12-01 | 瑞士商帕法瑞斯有限責任公司 | 包含緩激肽ｂ２受體拮抗劑之固態延長釋放組成物 |
| IL315699A (en) | 2022-03-25 | 2024-11-01 | Pharvaris Gmbh | A solid composition comprising dissolved bradykinin B2 receptor antagonists |
| CN117342963B (zh) * | 2023-09-28 | 2025-06-17 | 上海予君生物科技发展有限公司 | 一种1,4-二羰基化合物、及其制备方法和应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5574042A (en) * | 1992-11-02 | 1996-11-12 | Fujisawa Pharmaceutical Co., Ltd | Imidazo [1,2-a] pyridines and their pharmaceutical use |
| AU686115B2 (en) | 1992-11-02 | 1998-02-05 | Fujisawa Pharmaceutical Co., Ltd. | Imidazo (I,2-a) pyridine derivatives as bradykinin antagonists, pharmaceuticals and processes for their preparation |
| AU680870B2 (en) * | 1993-04-28 | 1997-08-14 | Astellas Pharma Inc. | New heterocyclic compounds |
| GB9519077D0 (en) | 1995-09-18 | 1995-11-15 | Fujisawa Pharmaceutical Co | New heterocyclic compounds |
| DE19610784A1 (de) * | 1996-03-19 | 1997-09-25 | Hoechst Ag | Fluoralkyl- und Fluoralkoxysubstituierte heterocyclische Bradykinin-Antagonisten, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19712960A1 (de) * | 1997-03-27 | 1998-10-01 | Hoechst Ag | Benzyloxy-substituierte, anellierte N-Heterocyclen, Verfahren zu ihrer Herstellung und ihre Verwendung als Bradykininrezeptorantagonisten |
| ATE233104T1 (de) * | 1997-09-18 | 2003-03-15 | Janssen Pharmaceutica Nv | Kondensierte imidazolderivate zur erhöhung der oralen bioverfügbarkeit von pharmazeutika |
| AU2985399A (en) * | 1998-04-03 | 1999-10-25 | Alcon Laboratories, Inc. | Non-peptide bradykinin receptor antagonists for use in controlling intraocular pressure and treating glaucoma |
| CA2347001A1 (en) * | 1998-10-21 | 2000-04-27 | Fujisawa Pharmaceutical Co., Ltd. | Vitreous form of known bradykinin antagonist |
-
2003
- 2003-03-31 WO PCT/US2003/009974 patent/WO2003087090A2/en not_active Ceased
- 2003-03-31 US US10/403,186 patent/US6958349B2/en not_active Expired - Lifetime
- 2003-03-31 JP JP2003584046A patent/JP2005525398A/ja not_active Withdrawn
- 2003-03-31 CA CA002481855A patent/CA2481855A1/en not_active Abandoned
- 2003-03-31 AU AU2003226188A patent/AU2003226188A1/en not_active Abandoned
- 2003-03-31 EP EP03746573A patent/EP1495017A2/en not_active Withdrawn
-
2004
- 2004-12-16 US US11/014,471 patent/US7358261B2/en not_active Expired - Lifetime
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