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 (OSRAM) | 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 (OSRAM) |
| EP (1) | EP1395590B1 (OSRAM) |
| JP (1) | JP4279561B2 (OSRAM) |
| AT (1) | ATE340796T1 (OSRAM) |
| AU (1) | AU2002302248B2 (OSRAM) |
| CA (1) | CA2447779C (OSRAM) |
| DE (1) | DE60215000T2 (OSRAM) |
| ES (1) | ES2272712T3 (OSRAM) |
| WO (1) | WO2002094830A2 (OSRAM) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE479686T1 (de) * | 2002-10-30 | 2010-09-15 | Merck Frosst Canada Ltd | Pyridopyrrolizin- und pyridoindolizinderivate |
| EP1585511B1 (en) | 2002-12-20 | 2013-01-23 | Amgen Inc. | Asthma and allergic inflammation modulators |
| AR041089A1 (es) | 2003-05-15 | 2005-05-04 | Merck & Co Inc | Procedimiento y composiciones farmaceutiicas para tratar aterosclerosis, dislipidemias y afecciones relacionadas |
| TWI258478B (en) | 2003-10-31 | 2006-07-21 | Arena Pharm Inc | Tetrazole derivatives and methods of treatment of metabolic-related disorders thereof |
| WO2005095397A1 (en) | 2004-03-11 | 2005-10-13 | 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 |
| RU2404163C2 (ru) | 2004-12-27 | 2010-11-20 | Актелион Фармасьютиклз Лтд | Производные 2,3,4,9-тетрагидро-1h-карбазола в качестве антагонистов рецептора crth2 |
| JP2008533172A (ja) * | 2005-03-17 | 2008-08-21 | ノバルティス アクチエンゲゼルシャフト | チロシン/スレオニンキナーゼ阻害剤、特にB−RAFキナーゼ阻害剤としての、N−[3−(1−アミノ−5,6,7,8−テトラヒドロ−2,4,4b−トリアザフルオレン−9−イル)−フェニル]ベンズアミド |
| JP5072594B2 (ja) | 2005-07-22 | 2012-11-14 | 塩野義製薬株式会社 | 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 |
| JP5064219B2 (ja) | 2005-07-22 | 2012-10-31 | 塩野義製薬株式会社 | Pgd2受容体アンタゴニスト活性を有するアザインドール酸誘導体 |
| EP1915372B1 (en) * | 2005-08-12 | 2013-11-20 | Merck Canada Inc. | 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 |
| NZ574705A (en) | 2006-08-07 | 2011-12-22 | Actelion Pharmaceuticals Ltd | (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetic acid derivatives |
| CN101896178B (zh) * | 2007-10-10 | 2013-11-20 | 北京赛林泰医药技术有限公司 | 作为crth2受体拮抗剂的杂环化合物 |
| EA201001029A1 (ru) | 2007-12-19 | 2011-06-30 | Амген Инк. | Производные фенилуксусной кислоты в качестве модуляторов процесса воспаления |
| UA98839C2 (en) * | 2008-02-01 | 2012-06-25 | Панмира Фармасьютикалз, Ллк. | N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors |
| WO2009099902A1 (en) * | 2008-02-01 | 2009-08-13 | Amira Pharmaceuticals, Inc. | N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors |
| JP2011512359A (ja) * | 2008-02-14 | 2011-04-21 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体のアンタゴニストとしての環式ジアリールエーテル化合物 |
| WO2009108720A2 (en) | 2008-02-25 | 2009-09-03 | Amira Pharmaceuticals, Inc. | Antagonists of prostaglandin d2 receptors |
| JP2011518130A (ja) * | 2008-04-02 | 2011-06-23 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体のアミノアルキルフェニルアンタゴニスト |
| US20110112134A1 (en) * | 2008-05-16 | 2011-05-12 | Amira Pharmaceuticals, Inc. | Tricyclic Antagonists of Prostaglandin D2 Receptors |
| EP2300425A4 (en) * | 2008-06-24 | 2012-03-21 | Panmira Pharmaceuticals Llc | PROSTAGLANDIN D2 RECEPTOR CYCLOALCANEÝBINDLUCK ANTAGONISTS |
| MX2010014172A (es) * | 2008-07-03 | 2011-02-22 | Amira Pharmaceuticals Inc | Antagonistas de receptores de prostaglandina d2. |
| US8507473B2 (en) | 2008-09-11 | 2013-08-13 | 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 |
| US8383654B2 (en) | 2008-11-17 | 2013-02-26 | Panmira Pharmaceuticals, Llc | Heterocyclic antagonists of prostaglandin D2 receptors |
| US20100173313A1 (en) * | 2009-01-08 | 2010-07-08 | Amira Pharmaceuticals, Inc. | Biomarkers of inflammation |
| KR20120038544A (ko) | 2009-07-31 | 2012-04-23 | 판미라 파마슈티칼스, 엘엘씨 | Dp2 수용체 길항제의 안과용 약학 조성물 |
| 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 |
| AU2011203649A1 (en) | 2010-01-06 | 2012-06-14 | Brickell Biotech, Inc. | DP2 antagonist and uses thereof |
| SI2558447T1 (sl) | 2010-03-22 | 2015-01-30 | Actelion Pharmaceuticals Ltd. | Derivati 3-(heteroaril-amino)-1,2,3,4-tetrahidro-9h-karbazola in njihova uporaba kot modulatorji prostaglandinskega receptorja d2 |
| EP2590944B1 (en) | 2010-07-05 | 2015-09-30 | Actelion Pharmaceuticals Ltd. | 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators |
| US9034895B2 (en) * | 2010-08-20 | 2015-05-19 | University Of Washington Through Its Center For Commercialization | Composition and methods for treating glioblastoma |
| US9096568B2 (en) * | 2011-03-02 | 2015-08-04 | Bayer Intellectual Property Gmbh | Process for preparing aryl- and heteroarylacetic acid derivatives |
| 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 |
| EP2697223B1 (en) | 2011-04-14 | 2016-07-13 | Actelion Pharmaceuticals Ltd. | 7-(heteroaryl-amino)-6,7,8,9-tetrahydropyrido[1,2-a]indol acetic acid derivatives and their use as prostaglandin d2 receptor modulators |
| EP2794563B1 (en) | 2011-12-21 | 2017-02-22 | Actelion Pharmaceuticals Ltd | Heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators |
| WO2014006585A1 (en) | 2012-07-05 | 2014-01-09 | Actelion Pharmaceuticals Ltd | 1-phenyl-substituted heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators |
| US9797903B2 (en) | 2012-10-24 | 2017-10-24 | Winthrop-University Hospital | Non-invasive biomarker to identify subject at risk of preterm delivery |
| WO2015096651A1 (en) | 2013-12-23 | 2015-07-02 | Merck Sharp & Dohme Corp. | Pyrimidone carboxamide compounds as pde2 inhibitors |
| HRP20181555T1 (hr) | 2014-03-17 | 2018-11-30 | Idorsia Pharmaceuticals Ltd | Derivati azaindol-octene kiseline i njihova uporaba kao modulatora receptora prostaglandina d2 |
| EP3119780B1 (en) | 2014-03-18 | 2018-08-29 | Idorsia Pharmaceuticals Ltd | Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators |
| US20180021302A1 (en) | 2015-02-13 | 2018-01-25 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Ptgdr-1 and/or ptgdr-2 antagonists for preventing and/or treating systemic lupus erythematosus |
| WO2016145614A1 (en) | 2015-03-17 | 2016-09-22 | Merck Sharp & Dohme Corp. | Triazolyl pyrimidinone compounds as pde2 inhibitors |
| WO2016154081A1 (en) | 2015-03-26 | 2016-09-29 | Merck Sharp & Dohme Corp. | Pyrazolyl pyrimidinone compounds as pde2 inhibitors |
| WO2016209749A1 (en) | 2015-06-25 | 2016-12-29 | 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 |
| EA035752B1 (ru) | 2015-09-15 | 2020-08-05 | Идорсиа Фармасьютиклз Лтд | КРИСТАЛЛИЧЕСКАЯ ФОРМА (S)-2-(8-((5-ХЛОРПИРИМИДИН-2-ИЛ)(МЕТИЛ)-АМИНО)-2-ФТОР-6,7,8,9-ТЕТРАГИДРО-5Н-ПИРИДО[3,2-b]ИНДОЛ-5-ИЛ)УКСУСНОЙ КИСЛОТЫ И СОДЕРЖАЩИЕ ЕЁ ФАРМАЦЕВТИЧЕСКИЕ КОМПОЗИЦИИ |
| CN109563093B (zh) * | 2016-07-21 | 2021-09-03 | 正大天晴药业集团股份有限公司 | 作为crth2抑制剂的三并环类化合物 |
| US20200264188A1 (en) | 2017-09-13 | 2020-08-20 | Progenity, Inc. | Preeclampsia biomarkers and related 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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1241660A (en) * | 1984-06-25 | 1988-09-06 | Yvan Guindon | Indole-2-alkanoic acids |
| HUP0100156A3 (en) * | 1998-02-25 | 2002-12-28 | Genetics Inst Inc Cambridge | Indole derivatives as inhibitors of phospholipase a2 and use of them for producing pharmaceutical compositions |
| 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 EP EP02729708A patent/EP1395590B1/en not_active Expired - Lifetime
- 2002-05-22 WO PCT/CA2002/000745 patent/WO2002094830A2/en not_active Ceased
- 2002-05-22 CA CA2447779A patent/CA2447779C/en not_active Expired - Fee Related
- 2002-05-22 AU AU2002302248A patent/AU2002302248B2/en not_active Ceased
- 2002-05-22 ES ES02729708T patent/ES2272712T3/es 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 AT AT02729708T patent/ATE340796T1/de not_active IP Right Cessation
- 2002-05-22 DE DE60215000T patent/DE60215000T2/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ES2272712T3 (es) | 2007-05-01 |
| WO2002094830A8 (en) | 2003-04-10 |
| CA2447779C (en) | 2010-08-31 |
| ATE340796T1 (de) | 2006-10-15 |
| CA2447779A1 (en) | 2002-11-28 |
| AU2002302248B2 (en) | 2008-03-06 |
| EP1395590B1 (en) | 2006-09-27 |
| US20040180934A1 (en) | 2004-09-16 |
| WO2002094830A2 (en) | 2002-11-28 |
| DE60215000T2 (de) | 2007-08-09 |
| EP1395590A2 (en) | 2004-03-10 |
| WO2002094830A3 (en) | 2003-03-06 |
| US7144913B2 (en) | 2006-12-05 |
| DE60215000D1 (de) | 2006-11-09 |
| JP2004534774A (ja) | 2004-11-18 |
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