JP5452925B2 - Ｐｇｄｓ阻害剤としてのピリミジンアミド化合物 - Google Patents
Ｐｇｄｓ阻害剤としてのピリミジンアミド化合物 Download PDFInfo
- Publication number
- JP5452925B2 JP5452925B2 JP2008534664A JP2008534664A JP5452925B2 JP 5452925 B2 JP5452925 B2 JP 5452925B2 JP 2008534664 A JP2008534664 A JP 2008534664A JP 2008534664 A JP2008534664 A JP 2008534664A JP 5452925 B2 JP5452925 B2 JP 5452925B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- pyrimidine
- carboxylic acid
- benzylamide
- fluoro
- 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.)
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Links
- 0 *NS(c1cc(CNC(c2cnc(-c3cccnc3)nc2)=O)ccc1)(=O)=O Chemical compound *NS(c1cc(CNC(c2cnc(-c3cccnc3)nc2)=O)ccc1)(=O)=O 0.000 description 1
- VHEQYTMTTNZDND-UHFFFAOYSA-N CC(C)N(CCNS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O)C(C)C Chemical compound CC(C)N(CCNS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O)C(C)C VHEQYTMTTNZDND-UHFFFAOYSA-N 0.000 description 1
- AJHRVJDBJZHLOT-UHFFFAOYSA-N CC(CNS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O)O Chemical compound CC(CNS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O)O AJHRVJDBJZHLOT-UHFFFAOYSA-N 0.000 description 1
- QKSHKCHXEZVFAP-UHFFFAOYSA-N CC1C(c(nc2)ncc2C(NCc2cccc(S(NCCOC)=O)c2)=O)=CC=CC1F Chemical compound CC1C(c(nc2)ncc2C(NCc2cccc(S(NCCOC)=O)c2)=O)=CC=CC1F QKSHKCHXEZVFAP-UHFFFAOYSA-N 0.000 description 1
- SFAHHTFDPMQXKE-UHFFFAOYSA-N CCOC(Cc1c[s]c(NC(c2cnc(C3C=CC=CC3C)nc2)=O)n1)=O Chemical compound CCOC(Cc1c[s]c(NC(c2cnc(C3C=CC=CC3C)nc2)=O)n1)=O SFAHHTFDPMQXKE-UHFFFAOYSA-N 0.000 description 1
- VAECNHCIFKAKQZ-UHFFFAOYSA-N COc(ccc(CNC(c1cnc(-c2ccccc2)nc1)=O)c1)c1OC Chemical compound COc(ccc(CNC(c1cnc(-c2ccccc2)nc1)=O)c1)c1OC VAECNHCIFKAKQZ-UHFFFAOYSA-N 0.000 description 1
- AIRAVOKVLAAGRU-UHFFFAOYSA-N NS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O Chemical compound NS(c1cccc(CNC(c2cnc(-c3cc(F)ccc3)nc2)=O)c1)(=O)=O AIRAVOKVLAAGRU-UHFFFAOYSA-N 0.000 description 1
- BTPMPSXYHSQPTQ-UHFFFAOYSA-N O=C(c1cnc(-c2cc(F)ccc2)nc1)NCc1cc(S(NCCCN2CCCC2)(=O)=O)ccc1 Chemical compound O=C(c1cnc(-c2cc(F)ccc2)nc1)NCc1cc(S(NCCCN2CCCC2)(=O)=O)ccc1 BTPMPSXYHSQPTQ-UHFFFAOYSA-N 0.000 description 1
- ZSWOWJFYKHDETJ-UHFFFAOYSA-N O=C(c1cnc(-c2ccccc2)nc1)NCCc(cc1)cc2c1OCCCO2 Chemical compound O=C(c1cnc(-c2ccccc2)nc1)NCCc(cc1)cc2c1OCCCO2 ZSWOWJFYKHDETJ-UHFFFAOYSA-N 0.000 description 1
- MDNQTLWWKALWJG-UHFFFAOYSA-N O=C(c1cnc(-c2ccccc2)nc1)Nc1ccn[nH]1 Chemical compound O=C(c1cnc(-c2ccccc2)nc1)Nc1ccn[nH]1 MDNQTLWWKALWJG-UHFFFAOYSA-N 0.000 description 1
- JLMZQOWMYYLDAN-UHFFFAOYSA-N O=C(c1cnc(-c2ccccc2)nc1)Nc1ncc[s]1 Chemical compound O=C(c1cnc(-c2ccccc2)nc1)Nc1ncc[s]1 JLMZQOWMYYLDAN-UHFFFAOYSA-N 0.000 description 1
- RWMORAFKNKQOES-UHFFFAOYSA-N OC(Cc1c[s]c(NC(c2cnc(-c3ccccc3)nc2)=O)n1)=O Chemical compound OC(Cc1c[s]c(NC(c2cnc(-c3ccccc3)nc2)=O)n1)=O RWMORAFKNKQOES-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/12—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 chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Otolaryngology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72357005P | 2005-10-04 | 2005-10-04 | |
| US60/723,570 | 2005-10-04 | ||
| PCT/US2006/038841 WO2007041634A1 (en) | 2005-10-04 | 2006-10-04 | Pyrimidine amide compounds as pgds inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009510170A JP2009510170A (ja) | 2009-03-12 |
| JP2009510170A5 JP2009510170A5 (https=) | 2009-11-19 |
| JP5452925B2 true JP5452925B2 (ja) | 2014-03-26 |
Family
ID=37635758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008534664A Active JP5452925B2 (ja) | 2005-10-04 | 2006-10-04 | Ｐｇｄｓ阻害剤としてのピリミジンアミド化合物 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8202863B2 (https=) |
| EP (1) | EP1937652B1 (https=) |
| JP (1) | JP5452925B2 (https=) |
| KR (1) | KR101457966B1 (https=) |
| CN (2) | CN101538246B (https=) |
| AR (1) | AR056871A1 (https=) |
| AU (1) | AU2006299428B2 (https=) |
| BR (1) | BRPI0616815A2 (https=) |
| CA (1) | CA2624749C (https=) |
| CR (1) | CR9832A (https=) |
| DO (1) | DOP2006000210A (https=) |
| EC (1) | ECSP088335A (https=) |
| ES (1) | ES2514471T3 (https=) |
| IL (1) | IL190411A (https=) |
| MA (1) | MA29925B1 (https=) |
| MY (1) | MY151172A (https=) |
| NO (1) | NO20082000L (https=) |
| NZ (1) | NZ567208A (https=) |
| PE (2) | PE20070589A1 (https=) |
| RU (1) | RU2420519C2 (https=) |
| SG (1) | SG166121A1 (https=) |
| TN (1) | TNSN08104A1 (https=) |
| TW (1) | TWI415839B (https=) |
| UA (1) | UA93213C2 (https=) |
| UY (1) | UY29840A1 (https=) |
| WO (1) | WO2007041634A1 (https=) |
| ZA (1) | ZA200802222B (https=) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7759350B2 (en) * | 2005-09-15 | 2010-07-20 | Orchid Research Laboratories Ltd. | Pyrimidine carboxamides |
| DOP2006000210A (es) | 2005-10-04 | 2007-06-15 | Aventis Pharma Inc | Compuestos de pirimidina amida como inhibidores de pgds |
| EP2004596A2 (en) | 2006-04-11 | 2008-12-24 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of voltage-gated sodium channels |
| CA2672373C (en) | 2006-12-19 | 2011-08-30 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
| EP2132196A1 (en) | 2007-02-26 | 2009-12-16 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
| KR101669432B1 (ko) | 2007-08-27 | 2016-10-26 | 다트 뉴로사이언스 (케이만) 엘티디. | 치료적 이속사졸 화합물 |
| AU2008310660A1 (en) * | 2007-10-11 | 2009-04-16 | Vertex Pharmaceuticals Incorporated | Heteroaryl amides useful as inhibitors of voltage-gated sodium channels |
| KR20100075631A (ko) | 2007-10-11 | 2010-07-02 | 버텍스 파마슈티칼스 인코포레이티드 | 전압개폐 나트륨 채널의 억제제로서 유용한 아릴 아미드 |
| WO2009049181A1 (en) | 2007-10-11 | 2009-04-16 | Vertex Pharmaceuticals Incorporated | Amides useful as inhibitors of voltage-gated sodium channels |
| WO2009064449A1 (en) * | 2007-11-13 | 2009-05-22 | Renovis, Inc. | Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same |
| EP2261210B1 (en) * | 2008-02-06 | 2014-10-22 | Msd K.K. | 3-substituted sulfonyl piperazine derivative |
| WO2009140364A2 (en) * | 2008-05-13 | 2009-11-19 | Cayman Chemical Company | Methods for assaying compounds or agents for ability to displace potent ligands of hematopoietic prostaglandin d synthase |
| CA2725481A1 (en) | 2008-06-18 | 2009-12-23 | Pfizer Limited | Nicotinamide derivatives |
| TW201010997A (en) | 2008-06-18 | 2010-03-16 | Pfizer Ltd | Nicotinamide derivatives |
| US8536185B2 (en) | 2008-09-22 | 2013-09-17 | Cayman Chemical Company, Incorporated | Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases |
| WO2010056044A2 (ko) * | 2008-11-11 | 2010-05-20 | (주)아모레퍼시픽 | 바닐로이드 수용체 길항제로 작용하는 신규 화합물, 이의 이성질체 또는 이의 약제학적으로 허용 가능한 염 및 이를 포함하는 약학 조성물 |
| KR101367057B1 (ko) | 2009-03-17 | 2014-02-25 | (주)아모레퍼시픽 | 피부 자극 완화용 조성물 |
| KR101252335B1 (ko) | 2009-07-16 | 2013-04-08 | (주)아모레퍼시픽 | 피부 노화 방지용 조성물 |
| ES2564454T3 (es) | 2009-03-09 | 2016-03-22 | Taiho Pharmaceutical Co., Ltd. | Compuesto de piperazina que puede inhibir la prostaglandina D sintasa |
| NZ599099A (en) * | 2009-10-08 | 2013-05-31 | Sanofi Sa | Phenyloxadiazole derivatives as pgds inhibitors |
| WO2011090062A1 (ja) | 2010-01-22 | 2011-07-28 | 大鵬薬品工業株式会社 | Pgds阻害作用を有するピペラジン化合物 |
| US9320723B2 (en) * | 2010-05-03 | 2016-04-26 | University Of Rochester | Methods of treating thyroid eye disease |
| AU2011261164A1 (en) * | 2010-06-01 | 2012-12-13 | The University Of Queensland | Haematopoietic-prostaglandin D2 synthase inhibitors |
| WO2012033069A1 (ja) | 2010-09-07 | 2012-03-15 | 大鵬薬品工業株式会社 | プロスタグランジンd合成酵素を阻害するピペリジン化合物 |
| KR101271223B1 (ko) | 2011-01-27 | 2013-06-07 | 한국과학기술연구원 | 아미노피리미딘 유도체 및 이를 포함하는 세포외 신호조절 키나제의 제해제 |
| CN104159587A (zh) * | 2012-01-06 | 2014-11-19 | 南佛罗里达大学 | 组合物、使用方法、以及治疗方法 |
| CN104926808B (zh) * | 2012-08-24 | 2018-09-14 | 广东东阳光药业有限公司 | 二氢嘧啶类化合物及其在药物中的应用 |
| CN108430992A (zh) | 2015-12-17 | 2018-08-21 | 阿斯特克斯医疗公司 | 作为h-pgds抑制剂的喹啉-3-甲酰胺 |
| WO2017160832A1 (en) * | 2016-03-14 | 2017-09-21 | Emory University | Amide-sulfamide derivatives, compositions, and uses related to cxcr4 inhibition |
| JOP20190072A1 (ar) | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | مشتقات 1، 3 سيكلوبوتان ثنائي الاستبدال أو آزيتيدين كمثبطات للإنزيم المخلق للبروستاجلاندين d المكون للدم |
| TW201908311A (zh) | 2017-06-13 | 2019-03-01 | 英商葛蘭素史克智慧財產發展有限公司 | 化合物 |
| WO2019084529A1 (en) * | 2017-10-29 | 2019-05-02 | China Medical University | ADAM9 INHIBITORS AND USES THEREOF |
| JP2021506811A (ja) | 2017-12-13 | 2021-02-22 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドＧｌａｘｏｓｍｉｔｈｋｌｉｎｅ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ Ｄｅｖｅｌｏｐｍｅｎｔ Ｌｉｍｉｔｅｄ | Ｈ−ｐｇｄｓの阻害剤として作用する縮合ピリジン |
| MX2020009887A (es) * | 2018-03-23 | 2020-10-12 | Step Pharma S A S | Derivados de aminopiridina como inhibidores de ctps1. |
| CN112969698A (zh) | 2018-11-08 | 2021-06-15 | 葛兰素史密斯克莱知识产权发展有限公司 | 化学化合物 |
| BR112022023025A2 (pt) * | 2020-05-13 | 2023-03-28 | Chdi Foundation Inc | Moduladores de htt para tratar doença de huntington |
| CN115667259B (zh) | 2020-06-19 | 2025-06-17 | 佐藤制药株式会社 | 抑制h-pgds的稠环化合物 |
| US12331046B2 (en) * | 2020-10-23 | 2025-06-17 | Nimbus Clotho, Inc. | CTPS1 inhibitors and uses thereof |
| CN113004208A (zh) * | 2021-03-08 | 2021-06-22 | 沈阳药科大学 | 一种抑制黄嘌呤氧化酶活性的化合物及制备方法和应用 |
| US12281116B2 (en) | 2021-11-17 | 2025-04-22 | Chdi Foundation, Inc. | HTT modulators for treating Huntington's disease |
| WO2023113023A1 (ja) | 2021-12-17 | 2023-06-22 | 佐藤製薬株式会社 | Ｈ－ｐｇｄｓを阻害するアザインドール誘導体 |
| CA3245288A1 (en) * | 2022-02-28 | 2025-06-13 | Shionogi & Co., Ltd. | INDAZOLE COMPOUND AND ITS PHARMACEUTICAL USE |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2934543A1 (de) * | 1979-08-27 | 1981-04-02 | Basf Ag, 6700 Ludwigshafen | Substituierte n-benzoylanthranilsaeurederivate und deren anydroverbindungen, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
| JPH03112985A (ja) * | 1989-09-28 | 1991-05-14 | Morishita Pharmaceut Co Ltd | Ｎ―（１ｈ―テトラゾール―５―イル）―２―フェニル―５―ピリミジンカルボキシアミド類及びその合成用中間体 |
| GB9405347D0 (en) * | 1994-03-18 | 1994-05-04 | Agrevo Uk Ltd | Fungicides |
| JP2000226372A (ja) * | 1999-02-01 | 2000-08-15 | Nippon Soda Co Ltd | アミド化合物、その製造方法及び農園芸用殺虫剤 |
| JP2002003370A (ja) * | 1999-09-20 | 2002-01-09 | Takeda Chem Ind Ltd | メラニン凝集ホルモン拮抗剤 |
| EP1218336A2 (en) * | 1999-09-20 | 2002-07-03 | Takeda Chemical Industries, Ltd. | Melanin concentrating hormone antagonist |
| MY138097A (en) * | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| JP2003112985A (ja) | 2001-10-01 | 2003-04-18 | Nre Happiness Kk | 食品残渣肥、飼料原料化システムおよびそれに使用する破砕貯留処理ユニット並びに乾燥冷却処理ユニット |
| JPWO2004011430A1 (ja) * | 2002-07-25 | 2005-11-24 | アステラス製薬株式会社 | ナトリウムチャネル阻害剤 |
| JP4595542B2 (ja) * | 2002-07-30 | 2010-12-08 | 萬有製薬株式会社 | ベンズイミダゾール誘導体を有効成分とするメラニン凝集ホルモン受容体拮抗剤 |
| EP1606289B1 (en) * | 2003-02-14 | 2009-12-02 | Glaxo Group Limited | Carboxamide derivatives |
| PT1471057E (pt) * | 2003-04-25 | 2006-05-31 | Actimis Pharmaceuticals Inc | Derivados de acido pirimidinilacetico uteis para o tratamento de doencas mediadas por crth2 |
| MXPA06003949A (es) * | 2003-10-07 | 2006-06-27 | Renovis Inc | Compuestos amida como ligandos del canal de ion y su uso. |
| CA2553968A1 (en) * | 2004-01-23 | 2005-08-11 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments of inflammatory and neuropathic pain |
| DOP2006000210A (es) | 2005-10-04 | 2007-06-15 | Aventis Pharma Inc | Compuestos de pirimidina amida como inhibidores de pgds |
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