JP4279561B2 - プロスタグランジンD2受容体拮抗薬としてのジヒドロピロロ[1,2−a]インドールおよびテトラヒドロピリド[1,2−a]−インドール誘導体 - Google Patents
プロスタグランジンD2受容体拮抗薬としてのジヒドロピロロ[1,2−a]インドールおよびテトラヒドロピリド[1,2−a]−インドール誘導体 Download PDFInfo
- Publication number
- JP4279561B2 JP4279561B2 JP2002591503A JP2002591503A JP4279561B2 JP 4279561 B2 JP4279561 B2 JP 4279561B2 JP 2002591503 A JP2002591503 A JP 2002591503A JP 2002591503 A JP2002591503 A JP 2002591503A JP 4279561 B2 JP4279561 B2 JP 4279561B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- halogen
- dihydro
- pyrrolo
- indol
- 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.)
- Expired - Fee Related
Links
- 0 C[n]1nccc1-c1c2c(Sc3ccc(*)cc3)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 Chemical compound C[n]1nccc1-c1c2c(Sc3ccc(*)cc3)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 0.000 description 3
- ZWPWAUHSOCPTSI-UHFFFAOYSA-N CC(C)c1c2c(C(c(ccc(Cl)c3)c3I)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 Chemical compound CC(C)c1c2c(C(c(ccc(Cl)c3)c3I)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 ZWPWAUHSOCPTSI-UHFFFAOYSA-N 0.000 description 1
- UQOAGPJNTPXLQM-UHFFFAOYSA-N CC(C)c1c2c(C(c3cc4ccccc4cc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 Chemical compound CC(C)c1c2c(C(c3cc4ccccc4cc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1 UQOAGPJNTPXLQM-UHFFFAOYSA-N 0.000 description 1
- UMBMGVCHMAHCQA-UHFFFAOYSA-N CC(C)c1cc(OC)cc2c1c(Sc(cc1)ccc1Cl)c1[n]2CCC1CC(O)=O Chemical compound CC(C)c1cc(OC)cc2c1c(Sc(cc1)ccc1Cl)c1[n]2CCC1CC(O)=O UMBMGVCHMAHCQA-UHFFFAOYSA-N 0.000 description 1
- PBVIMYGWTDRABZ-UHFFFAOYSA-N CCC(c1c2c(Sc(cc3)ccc3Cl)c(C(CC(O)=O)CC3)[n]3c2cc(-c2n[n](C)nn2)c1)OC Chemical compound CCC(c1c2c(Sc(cc3)ccc3Cl)c(C(CC(O)=O)CC3)[n]3c2cc(-c2n[n](C)nn2)c1)OC PBVIMYGWTDRABZ-UHFFFAOYSA-N 0.000 description 1
- GLLZYNSWLKZZQV-UHFFFAOYSA-N CCOC(C(CC[n](c1c2c(Br)cc(F)c1)c1c2Sc(cc2)ccc2Cl)C1=O)=O Chemical compound CCOC(C(CC[n](c1c2c(Br)cc(F)c1)c1c2Sc(cc2)ccc2Cl)C1=O)=O GLLZYNSWLKZZQV-UHFFFAOYSA-N 0.000 description 1
- PWGMBUQHILNMAW-UHFFFAOYSA-N CS(c1c2c(C(c(cc3)ccc3-c3ccccc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1)(=O)=O Chemical compound CS(c1c2c(C(c(cc3)ccc3-c3ccccc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1)(=O)=O PWGMBUQHILNMAW-UHFFFAOYSA-N 0.000 description 1
- VCZASWFGPQFOFT-UHFFFAOYSA-N CS(c1c2c(C(c(cc3)ccc3Cl)=O)c(C(CC(O)=O)CCC3)[n]3c2cc(F)c1)(=O)=O Chemical compound CS(c1c2c(C(c(cc3)ccc3Cl)=O)c(C(CC(O)=O)CCC3)[n]3c2cc(F)c1)(=O)=O VCZASWFGPQFOFT-UHFFFAOYSA-N 0.000 description 1
- WWGXFHBBGBWISU-UHFFFAOYSA-N CS(c1c2c(C(c3cc4ccccc4cc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1)(=O)=O Chemical compound CS(c1c2c(C(c3cc4ccccc4cc3)=O)c(C(CC(O)=O)CC3)[n]3c2cc(F)c1)(=O)=O WWGXFHBBGBWISU-UHFFFAOYSA-N 0.000 description 1
- CQBAYBAJTSDOCP-UHFFFAOYSA-N C[n]1c(-c(c2c3[n](CCC4CC(O)=O)c4c2Sc(cc2)ccc2Cl)cc(F)c3F)ccc1 Chemical compound C[n]1c(-c(c2c3[n](CCC4CC(O)=O)c4c2Sc(cc2)ccc2Cl)cc(F)c3F)ccc1 CQBAYBAJTSDOCP-UHFFFAOYSA-N 0.000 description 1
- YJZBQDCGDUEUOZ-UHFFFAOYSA-N C[n]1c(-c2cccc3c2c(Sc(cc2)ccc2Cl)c2[n]3CCC2CC(O)=O)ccc1 Chemical compound C[n]1c(-c2cccc3c2c(Sc(cc2)ccc2Cl)c2[n]3CCC2CC(O)=O)ccc1 YJZBQDCGDUEUOZ-UHFFFAOYSA-N 0.000 description 1
- KVEYBWAPJPSMPE-UHFFFAOYSA-N C[n]1nnc(-c2cc([n](CCC3CC(O)=O)c3c3Sc(cc4)ccc4Cl)c3c(-c3ccccc3)c2)n1 Chemical compound C[n]1nnc(-c2cc([n](CCC3CC(O)=O)c3c3Sc(cc4)ccc4Cl)c3c(-c3ccccc3)c2)n1 KVEYBWAPJPSMPE-UHFFFAOYSA-N 0.000 description 1
- DAYKZJBLSJNFHN-LWKPJOBUSA-N O=C(CC1c2cc(c(Br)cc([FH+])c3)c3[n]2CC1)N([C@@H](Cc1ccccc1)CO1)C1=O Chemical compound O=C(CC1c2cc(c(Br)cc([FH+])c3)c3[n]2CC1)N([C@@H](Cc1ccccc1)CO1)C1=O DAYKZJBLSJNFHN-LWKPJOBUSA-N 0.000 description 1
- PSGVTLWKHBXAKG-UHFFFAOYSA-N OC(CC(CC[n]1c2c3c(-c4c[s]c5c4cccc5)cc(F)c2)c1c3Sc(cc1)ccc1Cl)=O Chemical compound OC(CC(CC[n]1c2c3c(-c4c[s]c5c4cccc5)cc(F)c2)c1c3Sc(cc1)ccc1Cl)=O PSGVTLWKHBXAKG-UHFFFAOYSA-N 0.000 description 1
- IGXILIUGQKSYDH-UHFFFAOYSA-N OC(CC(CC[n]1c2c3c(-c4cc(cccc5)c5cc4)cc(F)c2)c1c3Sc(cc1)ccc1Cl)=O Chemical compound OC(CC(CC[n]1c2c3c(-c4cc(cccc5)c5cc4)cc(F)c2)c1c3Sc(cc1)ccc1Cl)=O IGXILIUGQKSYDH-UHFFFAOYSA-N 0.000 description 1
- RJXYASAESKAMFJ-UHFFFAOYSA-N OC(CC(CC[n]1c2c3c(Sc(cc4)ccc4Cl)cc(F)c2F)c1c3Sc(cc1)ccc1Cl)=O Chemical compound OC(CC(CC[n]1c2c3c(Sc(cc4)ccc4Cl)cc(F)c2F)c1c3Sc(cc1)ccc1Cl)=O RJXYASAESKAMFJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- 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
-
- 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
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29307701P | 2001-05-23 | 2001-05-23 | |
| PCT/CA2002/000745 WO2002094830A2 (en) | 2001-05-23 | 2002-05-22 | DIHYDROPYRROLO[1,2-A]INDOLE AND TETRAHYDROPYRIDO[1,2-a]-INDOLE DERIVATIVES AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004534774A JP2004534774A (ja) | 2004-11-18 |
| JP2004534774A5 JP2004534774A5 (enExample) | 2005-12-22 |
| JP4279561B2 true JP4279561B2 (ja) | 2009-06-17 |
Family
ID=23127559
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002591503A Expired - Fee Related JP4279561B2 (ja) | 2001-05-23 | 2002-05-22 | プロスタグランジンD2受容体拮抗薬としてのジヒドロピロロ[1,2−a]インドールおよびテトラヒドロピリド[1,2−a]−インドール誘導体 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7144913B2 (enExample) |
| EP (1) | EP1395590B1 (enExample) |
| JP (1) | JP4279561B2 (enExample) |
| AT (1) | ATE340796T1 (enExample) |
| AU (1) | AU2002302248B2 (enExample) |
| CA (1) | CA2447779C (enExample) |
| DE (1) | DE60215000T2 (enExample) |
| ES (1) | ES2272712T3 (enExample) |
| WO (1) | WO2002094830A2 (enExample) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
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| BR0315681A (pt) * | 2002-10-30 | 2005-09-06 | Merck Frosst Canada Inc | Composto e seus sais e hidratos farmaceuticamente aceitáveis, composição farmacêutica, métodos para o tratamento de doenças mediadas pela prostaglandina d2, para o tratamento de congestão nasal, para o tratamento de asma alérgica, e para o tratamento de rinite alérgica, composto ou um seu sal ou solvato farmaceuticamente aceitável, sal ou hidrato do composto, e, uso de um composto ou de um seu sal ou solvato farmaceuticamente aceitável |
| ES2401079T3 (es) | 2002-12-20 | 2013-04-16 | Amgen Inc. | Moduladores del asma y de la inflamación alérgica |
| AR041089A1 (es) * | 2003-05-15 | 2005-05-04 | Merck & Co Inc | Procedimiento y composiciones farmaceutiicas para tratar aterosclerosis, dislipidemias y afecciones relacionadas |
| PE20050483A1 (es) | 2003-10-31 | 2005-08-25 | Arena Pharm Inc | Derivados de tetrazol de formula (i), sus composiciones farmaceuticas y procesos para producir composiciones farmaceuticas |
| US7714132B2 (en) | 2004-03-11 | 2010-05-11 | Actelion Pharmaceuticals, Ltd. | Tetrahydropyridoindole derivatives |
| ITMI20040874A1 (it) * | 2004-04-30 | 2004-07-30 | Ist Naz Stud Cura Dei Tumori | Derivati indolici ed azaindolici con azione antitumorale |
| WO2006052798A2 (en) * | 2004-11-08 | 2006-05-18 | Merck & Co., Inc. | Method of treating pathological blushing |
| PE20060949A1 (es) | 2004-12-23 | 2006-10-11 | Arena Pharm Inc | Derivados fusionados de pirazol como agonistas del receptor de niacina |
| DK1833791T3 (da) | 2004-12-27 | 2011-10-24 | Actelion Pharmaceuticals Ltd | 2,3,4,9-tetrahydor-1H-carbazolderivater som CRTH2 receptorantagonister |
| MX2007011435A (es) * | 2005-03-17 | 2007-12-05 | Novartis Ag | N-[3-(1-amino-5,6,7,8-tetrahidro-2,4,4b-triazafluoren-9-il)-fenil ]-benzamidas como inhibidores de cinasa de tirosina/treonina, en particular de cinasa b-raf. |
| WO2007010964A1 (ja) | 2005-07-22 | 2007-01-25 | Shionogi & Co., Ltd. | Pgd2受容体アンタゴニスト活性を有するインドール誘導体 |
| US7842692B2 (en) | 2005-07-22 | 2010-11-30 | Shionogi & Co., Ltd. | Azaindole derivative having PGD2 receptor antagonistic activity |
| CA2618550C (en) * | 2005-08-12 | 2013-12-17 | Merck Frosst Canada Ltd. | Indole derivatives as crth2 receptor antagonists |
| EP1932839A4 (en) | 2005-09-06 | 2014-09-10 | Shionogi & Co | INDOLECARBOXYLATE ACID DERIVATIVE HAVING ANTAGONIST EFFECT OF THE PGD2 RECEPTOR |
| RU2448092C2 (ru) | 2006-08-07 | 2012-04-20 | Актелион Фармасьютиклз Лтд | Производные (3-амино-1,2,3,4-тетрагидро-9н-карбазол-9-ил)уксусной кислоты |
| US8772312B2 (en) * | 2007-10-10 | 2014-07-08 | Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. | Heterocyclic compounds as CRTH2 receptor antagonists |
| ES2471919T3 (es) | 2007-12-19 | 2014-06-27 | Amgen, Inc | Derivados de ácido fenilac�tico como moduladores de inflamación |
| NZ587709A (en) * | 2008-02-01 | 2012-06-29 | Panmira Pharmaceuticals Llc | N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors |
| UA98839C2 (en) * | 2008-02-01 | 2012-06-25 | Панмира Фармасьютикалз, Ллк. | N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors |
| WO2009102893A2 (en) * | 2008-02-14 | 2009-08-20 | Amira Pharmaceuticals, Inc. | CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 receptors |
| EP2245022A4 (en) | 2008-02-25 | 2012-02-22 | Panmira Pharmaceuticals Llc | ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS |
| US8426449B2 (en) * | 2008-04-02 | 2013-04-23 | Panmira Pharmaceuticals, Llc | Aminoalkylphenyl antagonists of prostaglandin D2 receptors |
| US20110112134A1 (en) * | 2008-05-16 | 2011-05-12 | Amira Pharmaceuticals, Inc. | Tricyclic Antagonists of Prostaglandin D2 Receptors |
| WO2010008864A2 (en) * | 2008-06-24 | 2010-01-21 | Amira Pharmaceuticals, Inc. | Cycloalkane[b]indole angtagonists of prostaglandin d2 receptors |
| EP2307362A4 (en) * | 2008-07-03 | 2012-05-09 | Panmira Pharmaceuticals Llc | ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS |
| WO2010030360A1 (en) | 2008-09-11 | 2010-03-18 | Arena Pharmaceuticals, Inc. | 3H-IMIDAZO[4,5-b]PYRIDIN-5-OL DERIVATIVES USEFUL IN THE TREATMENT OF GPR81 RECEPTOR DISORDERS |
| GB2463788B (en) * | 2008-09-29 | 2010-12-15 | Amira Pharmaceuticals Inc | Heteroaryl antagonists of prostaglandin D2 receptors |
| WO2010042652A2 (en) | 2008-10-08 | 2010-04-15 | Amira Pharmaceuticals, Inc. | Heteroalkyl biphenyl antagonists of prostaglandin d2 receptors |
| GB2465062B (en) * | 2008-11-06 | 2011-04-13 | Amira Pharmaceuticals Inc | Cycloalkane(B)azaindole antagonists of prostaglandin D2 receptors |
| WO2010057118A2 (en) * | 2008-11-17 | 2010-05-20 | Amira Pharmaceuticals, Inc. | Heterocyclic antagonists of prostaglandin d2 receptors |
| US20100173313A1 (en) * | 2009-01-08 | 2010-07-08 | Amira Pharmaceuticals, Inc. | Biomarkers of inflammation |
| WO2011014587A2 (en) | 2009-07-31 | 2011-02-03 | Amira Pharmaceuticals, Inc. | Ophthalmic pharmaceutical compositions of dp2 receptor antagonists |
| SG10201404662YA (en) * | 2009-08-05 | 2014-10-30 | Panmira Pharmaceuticals Llc | Dp2 antagonist and uses thereof |
| WO2011035417A1 (en) * | 2009-09-25 | 2011-03-31 | Aegera Therapeutics Inc. | Hsp-90 binding compounds, compositions thereof, and their use fn the treatment of autoimmune and inflammatory diseases |
| EP2521713A4 (en) | 2010-01-06 | 2013-10-02 | Panmira Pharmaceuticals Llc | ANTAGONIST OF DP2 AND ITS USES |
| US8697869B2 (en) | 2010-03-22 | 2014-04-15 | Actelion Pharmaceuticals Ltd. | 3-(heteroaryl-amino)-1,2,3,4-tetrahydro-9H-carbazole derivatives and their use as prostaglandin D2 receptor modulators |
| MX2012015082A (es) | 2010-07-05 | 2013-02-21 | Actelion Pharmaceuticals Ltd | Derivados heterociclico 1-fenil-sustituidos y sus uso como moduladores del receptor d2 de prostaglandina. |
| PL2606032T3 (pl) * | 2010-08-20 | 2015-07-31 | Univ Washington Through Its Center For Commercialization | Kompozycja i sposoby terapii glejakaep |
| BR112013022282B1 (pt) * | 2011-03-02 | 2019-03-26 | Bayer Intellectual Property Gmbh | Processo para a preparação de derivados de ácidos aril- e heteroaril acético |
| WO2012126084A1 (en) * | 2011-03-24 | 2012-09-27 | Pharmascience Inc. | Hsp-90 binding compounds, compositions thereof, and their use iν the treatment and prevention of fungal infections |
| MX338516B (es) | 2011-04-14 | 2016-04-20 | Actelion Pharmaceuticals Ltd | Derivados de acido 7- (heteroaril-amino) -6, 7, 8, 9- tetrahidropirido[1,2-a] indol acetico y sus usos como modulador del receptor de prostaglandina. |
| US9255090B2 (en) | 2011-12-21 | 2016-02-09 | Actelion Pharmaceuticals Ltd. | Heterocyclyl derivatives and their use as prostaglandin D2 receptor modulators |
| US9169270B2 (en) | 2012-07-05 | 2015-10-27 | Actelion Pharmaceuticals Ltd. | 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin D2 receptor modulators |
| EP2912458B1 (en) | 2012-10-24 | 2018-07-18 | NYU Winthrop Hospital | Non-invasive biomarker to identify subjects at risk of preterm delivery |
| WO2015096651A1 (en) | 2013-12-23 | 2015-07-02 | Merck Sharp & Dohme Corp. | Pyrimidone carboxamide compounds as pde2 inhibitors |
| MX384987B (es) | 2014-03-17 | 2025-03-14 | Idorsia Pharmaceuticals Ltd | Derivados del ácido acético azaindol y su uso como moduladores de receptor de prostaglandina d2. |
| BR112016021443A8 (pt) | 2014-03-18 | 2017-12-26 | Actelion Pharmaceuticals Ltd | Derivados de ácido acético azaindol e seu uso como moduladores de receptor de prostaglandina d2 |
| ES2991300T3 (es) | 2015-02-13 | 2024-12-03 | Inserm Institut Nat De La Sante Et De Larecherche Medicale | Antagonistas de PTGDR-1 y/o PTGDR-2 para prevenir y/o tratar lupus eritematoso sistémico |
| WO2016145614A1 (en) | 2015-03-17 | 2016-09-22 | Merck Sharp & Dohme Corp. | Triazolyl pyrimidinone compounds as pde2 inhibitors |
| US10287269B2 (en) | 2015-03-26 | 2019-05-14 | Merck Sharp & Dohme Corp. | Pyrazolyl pyrimidinone compounds as PDE2 inhibitors |
| US10647727B2 (en) | 2015-06-25 | 2020-05-12 | Merck Sharp & Dohme Corp. | Substituted pyrazolo/imidazolo bicyclic compounds as PDE2 inhibitors |
| WO2017000277A1 (en) | 2015-07-01 | 2017-01-05 | Merck Sharp & Dohme Corp. | Substituted triazolo bicycliccompounds as pde2 inhibitors |
| US10351560B2 (en) | 2015-09-15 | 2019-07-16 | Idorsia Pharmaceuticals Ltd | Crystalline forms |
| EP3489235A4 (en) * | 2016-07-21 | 2020-01-08 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Tricyclic compound as crth2 inhibitor |
| WO2019055661A1 (en) | 2017-09-13 | 2019-03-21 | Progenity, Inc. | PRE-ÉCLAMPSIE BIOMARKERS AND ASSOCIATED SYSTEMS AND METHODS |
| EP4070113A4 (en) | 2019-12-04 | 2023-12-20 | Biora Therapeutics, Inc. | ASSESSMENT OF PREECAMPSIA USING FREE AND DISSOCIATE PLACENTAL GROWTH FACTOR ASSAYS |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1241660A (en) * | 1984-06-25 | 1988-09-06 | Yvan Guindon | Indole-2-alkanoic acids |
| EA200000873A1 (ru) * | 1998-02-25 | 2001-04-23 | Дженетикс Инститьют, Инк. | Ингибиторы фосфолипазы a |
| AR041089A1 (es) * | 2003-05-15 | 2005-05-04 | Merck & Co Inc | Procedimiento y composiciones farmaceutiicas para tratar aterosclerosis, dislipidemias y afecciones relacionadas |
-
2002
- 2002-05-22 CA CA2447779A patent/CA2447779C/en not_active Expired - Fee Related
- 2002-05-22 WO PCT/CA2002/000745 patent/WO2002094830A2/en not_active Ceased
- 2002-05-22 AU AU2002302248A patent/AU2002302248B2/en not_active Ceased
- 2002-05-22 DE DE60215000T patent/DE60215000T2/de not_active Expired - Lifetime
- 2002-05-22 AT AT02729708T patent/ATE340796T1/de not_active IP Right Cessation
- 2002-05-22 EP EP02729708A patent/EP1395590B1/en not_active Expired - Lifetime
- 2002-05-22 JP JP2002591503A patent/JP4279561B2/ja not_active Expired - Fee Related
- 2002-05-22 US US10/474,929 patent/US7144913B2/en not_active Expired - Fee Related
- 2002-05-22 ES ES02729708T patent/ES2272712T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| WO2002094830A2 (en) | 2002-11-28 |
| AU2002302248B2 (en) | 2008-03-06 |
| ATE340796T1 (de) | 2006-10-15 |
| CA2447779C (en) | 2010-08-31 |
| ES2272712T3 (es) | 2007-05-01 |
| WO2002094830A8 (en) | 2003-04-10 |
| WO2002094830A3 (en) | 2003-03-06 |
| US20040180934A1 (en) | 2004-09-16 |
| US7144913B2 (en) | 2006-12-05 |
| EP1395590A2 (en) | 2004-03-10 |
| DE60215000T2 (de) | 2007-08-09 |
| CA2447779A1 (en) | 2002-11-28 |
| EP1395590B1 (en) | 2006-09-27 |
| DE60215000D1 (de) | 2006-11-09 |
| JP2004534774A (ja) | 2004-11-18 |
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