PE20090958A1 - Compuestos heterociclicos moduladores de miosina - Google Patents
Compuestos heterociclicos moduladores de miosinaInfo
- Publication number
- PE20090958A1 PE20090958A1 PE2008001391A PE2008001391A PE20090958A1 PE 20090958 A1 PE20090958 A1 PE 20090958A1 PE 2008001391 A PE2008001391 A PE 2008001391A PE 2008001391 A PE2008001391 A PE 2008001391A PE 20090958 A1 PE20090958 A1 PE 20090958A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- members
- myosin
- carbamoyloxy
- carboxamide
- Prior art date
Links
- 102000003505 Myosin Human genes 0.000 title abstract 3
- 108060008487 Myosin Proteins 0.000 title abstract 3
- 150000002391 heterocyclic compounds Chemical class 0.000 title abstract 2
- -1 2-CHLOROPHENYL Chemical class 0.000 abstract 5
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 5
- 150000003857 carboxamides Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical class O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 2
- 208000010412 Glaucoma Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- 101150020251 NR13 gene Proteins 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 210000002460 smooth muscle Anatomy 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive 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
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/04—Drugs for genital or sexual disorders; Contraceptives for inducing labour or abortion; Uterotonics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P27/02—Ophthalmic agents
-
- 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
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen 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
- 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
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Reproductive Health (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Pulmonology (AREA)
- Endocrinology (AREA)
- Gynecology & Obstetrics (AREA)
- Ophthalmology & Optometry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Pregnancy & Childbirth (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
REFERIDA A UN COMPUESTO HETEROCICLICO DE FORMULA (I), DONDE W1 Y W2 SON CR11R12, NR13, O; W3 ES CR1R2, NR14, O; R1, R2, R11 Y R12 SON H, OH, CARBOXI, SULFANILO, SULFONILO, ENTRE OTROS; R13 Y R14 SON H, ALQUILO C1-C20, ALQUENILO C2-C20, ENTRE OTROS; Z1 ES HETEROARILO DE 5 A 7 MIEMBROS CON 1 A 3 HETEROATOMOS DE N, O Y S O HETEROCICLOALQUILO DE 3 A 7 MIEMBROS CON 1 A 3 HETEROATOMOS DE O, S Y N; Z2 ES ARILO, HETEROARILO DE 5 A 7 MIEMBROS CON 1 A 3 HETEROATOMOS DE N, O Y S O HETEROCICLOALQUILO DE 3 A 7 MIEMBROS CON 1 A 3 HETEROATOMOS DE O, S Y N; R3, R4, R5 Y R6 SON H, OH, CARBOXI, SULFONILO, ENTRE OTROS; R7 Y R10 SON H, OH, CN, HALO, ENTRE OTROS; R8 ES H, ALQUILO C1-C20, CICLOALQUILO, ENTRE OTROS; m Y p SON UN ENTERO DE 0 A 3; n ES UN ENTERO DE 0 A 4; q ES UN ENTERO DE 1 A 4. SON COMPUESTOS PREFERIDOS: N-[(2-CLOROFENIL)METIL](4-{[N-(1-ETIL(4-PIPERIDIL))CARBAMOILOXI]METIL}(2H-3,4,5,6-TETRAHIDROPIRAN-4-IL))CARBOXAMIDA, N-[(2-CLOROFENIL)METIL](4-{[N-(4-METIL-2-FENIL(1,3-TIAZOL-5-IL))CARBAMOILOXI]METIL}(2H-3,4,5,6-TETRAHIDROPIRAN-4-IL))CARBOXAMIDA, {1-(2-AMINOACETIL)-4-[(N-(2-TIENIL)CARBAMOILOXI)METIL](4-PIPERIDIL)}-N-[(2-CLOROFENIL)METIL]CARBOXAMIDA, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS MODULAN LA MIOSINA DEL MUSCULO LISO Y/O LA MIOSINA NO MUSCULAR Y SON UTILES EN EL TRATAMIENTO DE HIPERTENSION, ASMA, GLAUCOMA, APOPLEJIAS, ENTRE OTRAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96502007P | 2007-08-15 | 2007-08-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090958A1 true PE20090958A1 (es) | 2009-08-07 |
Family
ID=40350992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008001391A PE20090958A1 (es) | 2007-08-15 | 2008-08-14 | Compuestos heterociclicos moduladores de miosina |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US8088793B2 (es) |
| EP (1) | EP2195328A4 (es) |
| JP (1) | JP5670731B2 (es) |
| KR (1) | KR20100044251A (es) |
| CN (1) | CN101821279A (es) |
| AR (1) | AR069364A1 (es) |
| AU (1) | AU2008287435B2 (es) |
| CA (1) | CA2696321A1 (es) |
| CL (1) | CL2008002411A1 (es) |
| MX (1) | MX2010001692A (es) |
| NZ (1) | NZ583351A (es) |
| PE (1) | PE20090958A1 (es) |
| TW (1) | TWI426908B (es) |
| WO (1) | WO2009023193A1 (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8071625B2 (en) * | 2006-08-02 | 2011-12-06 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| US8063082B2 (en) * | 2006-08-02 | 2011-11-22 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| CN101821279A (zh) | 2007-08-15 | 2010-09-01 | 赛特凯恩蒂克公司 | 某些化学个体、组合物和方法 |
| KR20130129244A (ko) * | 2010-12-17 | 2013-11-27 | 에프. 호프만-라 로슈 아게 | 치환된 6,6-융합된 질소 헤테로환형 화합물 및 이의 용도 |
| US9725427B2 (en) | 2012-03-16 | 2017-08-08 | Biohaven Pharmaceutical Holding Company Limited | Prodrugs of riluzole and their method of use |
| JP6345645B2 (ja) * | 2012-04-02 | 2018-06-20 | サイトキネティックス, インコーポレイテッド | 横隔膜機能を向上させるための方法 |
| PL2875022T3 (pl) | 2012-07-19 | 2017-06-30 | Cayman Chemical Company, Incorporated | Związki difluorolaktamowe jako agoniści selektywni względem receptora EP4 do zastosowania w leczeniu chorób i stanów, w których pośredniczy EP4 |
| EP2970234B1 (en) * | 2013-03-15 | 2018-07-18 | Cayman Chemical Company, Inc. | Methods of synthesizing a difluorolactam analog |
| AR108326A1 (es) * | 2016-04-27 | 2018-08-08 | Samumed Llc | Isoquinolin-3-il carboxamidas y preparación y uso de las mismas |
| AR108325A1 (es) | 2016-04-27 | 2018-08-08 | Samumed Llc | Isoquinolin-3-il carboxamidas y preparación y uso de las mismas |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
| KR20190136028A (ko) | 2017-03-30 | 2019-12-09 | 에프. 호프만-라 로슈 아게 | Hpk1 억제제로서의 나프티리딘 |
| WO2018183964A1 (en) | 2017-03-30 | 2018-10-04 | Genentech, Inc. | Isoquinolines as inhibitors of hpk1 |
| CN112601584A (zh) | 2018-07-24 | 2021-04-02 | 豪夫迈·罗氏有限公司 | 异喹啉化合物及其用途 |
| TW202012405A (zh) | 2018-07-24 | 2020-04-01 | 瑞士商赫孚孟拉羅股份公司 | 萘啶化合物及其用途 |
| TW202024053A (zh) | 2018-10-02 | 2020-07-01 | 美商建南德克公司 | 異喹啉化合物及其用途 |
| US11612606B2 (en) | 2018-10-03 | 2023-03-28 | Genentech, Inc. | 8-aminoisoquinoline compounds and uses thereof |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3227709A (en) | 1961-11-28 | 1966-01-04 | Merck & Co Inc | Derivatives of cephalosporin c and process |
| GB1339764A (en) * | 1971-03-29 | 1973-12-05 | Ici Ltd | Pyridine derivatives |
| DE2851953A1 (de) * | 1978-12-01 | 1980-06-19 | Thomae Gmbh Dr K | Neue spectinomycylamine, verfahren zu ihrer herstellung und diese enthaltenden arzneimittel |
| JP2838148B2 (ja) | 1991-08-15 | 1998-12-16 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
| JPH07247274A (ja) | 1994-03-10 | 1995-09-26 | Wakamoto Pharmaceut Co Ltd | ピバル酸 テトラゾリルフェニルエステル誘導体、それらを有効成分として含有するエラスターゼ阻害剤及び肺障害治療剤 |
| EP1195372A1 (en) | 1994-04-18 | 2002-04-10 | Mitsubishi Pharma Corporation | N-heterocyclic substituted benzamide derivatives with antihypertensive activity |
| WO1998041510A1 (en) | 1997-03-14 | 1998-09-24 | Shionogi & Co., Ltd. | Novel benzolactam derivatives and medicinal compositions comprising the same |
| CN1279668A (zh) | 1997-11-18 | 2001-01-10 | 帝人株式会社 | 环胺衍生物及其作为药物的用途 |
| US6107291A (en) * | 1997-12-19 | 2000-08-22 | Amgen Inc. | Azepine or larger medium ring derivatives and methods of use |
| GB9807833D0 (en) * | 1998-04-09 | 1998-06-10 | Boc Group Plc | Separation of air |
| US6420364B1 (en) * | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
| US6410566B1 (en) | 2000-05-16 | 2002-06-25 | Teijin Limited | Cyclic amine derivatives and their use as drugs |
| CA2321348A1 (en) | 2000-09-27 | 2002-03-27 | Blaise Magloire N'zemba | Aromatic derivatives with hiv integrase inhibitory properties |
| DE10063008A1 (de) | 2000-12-16 | 2002-06-20 | Merck Patent Gmbh | Carbonsäureamidderivate |
| CN103288815A (zh) * | 2001-10-12 | 2013-09-11 | 阿泽范药品公司 | β-内酰胺后叶加压素V1a拮抗剂 |
| AR038368A1 (es) | 2002-02-01 | 2005-01-12 | Novartis Ag | Compuestos n-pirimidin-2-il-aminas sustituidas como inhibidores de ige, una composicion farmaceutica y el uso de dichos compuestos para la preparacion de un medicamento |
| EP1534693A2 (en) * | 2002-09-06 | 2005-06-01 | Elan Pharmaceuticals, Inc. | 1, 3-diamino-2-hydroxypropane prodrug derivatives |
| ES2387909T3 (es) * | 2003-01-14 | 2012-10-03 | Cytokinetics, Inc. | Compuestos, composiciones y procedimientos de tratamiento de la insuficiencia cardiaca |
| US7223788B2 (en) | 2003-02-14 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Substituted N-aryl heterocycles, process for their preparation and their use as medicaments |
| WO2004081005A1 (en) * | 2003-03-07 | 2004-09-23 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| GB0319124D0 (en) | 2003-08-14 | 2003-09-17 | Smithkline Beecham Corp | Chemical compounds |
| WO2005016883A2 (en) * | 2003-08-14 | 2005-02-24 | Icos Corporation | Acrylamide derivatives as vla-1 integrin antagonists and uses thereof |
| JP4380508B2 (ja) * | 2003-11-28 | 2009-12-09 | 田辺三菱製薬株式会社 | 医薬組成物 |
| EP1711175A1 (en) * | 2004-02-04 | 2006-10-18 | Active Biotech AB | Diurea derivatives |
| CA2601709C (en) * | 2005-03-22 | 2017-02-14 | Azevan Pharmaceuticals, Inc. | Beta-lactamylalkanoic acids |
| JPWO2006137350A1 (ja) * | 2005-06-22 | 2009-01-15 | キッセイ薬品工業株式会社 | 新規なフロピリジン誘導体、それを含有する医薬組成物およびそれらの用途 |
| JP2009514866A (ja) | 2005-11-02 | 2009-04-09 | サイトキネティクス・インコーポレーテッド | ある種の化学物質、組成物、および方法 |
| WO2007109615A2 (en) * | 2006-03-21 | 2007-09-27 | Azevan Pharmaceuticals, Inc. | β -LACTAMYL VASOPRESSIN V2 ANTAGONISTS |
| MX2008012482A (es) * | 2006-03-31 | 2008-10-10 | Abbott Lab | Compuestos de indazol. |
| US8017612B2 (en) * | 2006-04-18 | 2011-09-13 | Japan Tobacco Inc. | Piperazine compound and use thereof as a HCV polymerase inhibitor |
| WO2007143822A1 (en) | 2006-06-14 | 2007-12-21 | Methylgene Inc. | Sulfamide and sulfamate derivatives as histone deacetylase inhibitors |
| WO2008016676A2 (en) | 2006-08-02 | 2008-02-07 | Cytokinetics, Incorporated | Certain chemical entities, compositions, and methods |
| US8063082B2 (en) | 2006-08-02 | 2011-11-22 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| US8071625B2 (en) | 2006-08-02 | 2011-12-06 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| CN101821279A (zh) | 2007-08-15 | 2010-09-01 | 赛特凯恩蒂克公司 | 某些化学个体、组合物和方法 |
-
2008
- 2008-08-11 CN CN200880111558A patent/CN101821279A/zh active Pending
- 2008-08-11 MX MX2010001692A patent/MX2010001692A/es active IP Right Grant
- 2008-08-11 US US12/228,421 patent/US8088793B2/en not_active Expired - Fee Related
- 2008-08-11 JP JP2010521009A patent/JP5670731B2/ja not_active Expired - Fee Related
- 2008-08-11 KR KR1020107005370A patent/KR20100044251A/ko not_active Ceased
- 2008-08-11 NZ NZ583351A patent/NZ583351A/xx not_active IP Right Cessation
- 2008-08-11 CA CA2696321A patent/CA2696321A1/en not_active Abandoned
- 2008-08-11 WO PCT/US2008/009636 patent/WO2009023193A1/en not_active Ceased
- 2008-08-11 EP EP08795242A patent/EP2195328A4/en not_active Withdrawn
- 2008-08-11 AU AU2008287435A patent/AU2008287435B2/en not_active Ceased
- 2008-08-14 AR ARP080103556A patent/AR069364A1/es unknown
- 2008-08-14 PE PE2008001391A patent/PE20090958A1/es not_active Application Discontinuation
- 2008-08-14 CL CL2008002411A patent/CL2008002411A1/es unknown
- 2008-08-14 TW TW097130926A patent/TWI426908B/zh not_active IP Right Cessation
-
2011
- 2011-11-30 US US13/308,287 patent/US8759374B2/en active Active
-
2012
- 2012-09-12 US US13/612,713 patent/US8895582B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| KR20100044251A (ko) | 2010-04-29 |
| US20120135964A1 (en) | 2012-05-31 |
| AU2008287435B2 (en) | 2013-05-16 |
| TWI426908B (zh) | 2014-02-21 |
| US8088793B2 (en) | 2012-01-03 |
| AR069364A1 (es) | 2010-01-20 |
| CL2008002411A1 (es) | 2009-07-17 |
| AU2008287435A1 (en) | 2009-02-19 |
| US20090275537A1 (en) | 2009-11-05 |
| TW200922583A (en) | 2009-06-01 |
| US8895582B2 (en) | 2014-11-25 |
| JP5670731B2 (ja) | 2015-02-18 |
| EP2195328A4 (en) | 2011-06-15 |
| US8759374B2 (en) | 2014-06-24 |
| MX2010001692A (es) | 2010-04-22 |
| US20130053348A1 (en) | 2013-02-28 |
| NZ583351A (en) | 2012-05-25 |
| JP2010536752A (ja) | 2010-12-02 |
| EP2195328A1 (en) | 2010-06-16 |
| WO2009023193A1 (en) | 2009-02-19 |
| CA2696321A1 (en) | 2009-02-19 |
| CN101821279A (zh) | 2010-09-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20090958A1 (es) | Compuestos heterociclicos moduladores de miosina | |
| PE20110367A1 (es) | DERIVADOS DE 4-CIANO-4-FENIL-PIRROLIDIN-2-CARBOXAMIDAS SUSTITUIDAS COMO INHIBIDORES DE LA INTERACCION p53-MDM2 | |
| PE20060186A1 (es) | Antagonistas de cgrp seleccionados, procedimientos para su preparacion asi como su uso como medicamento | |
| PE20080418A1 (es) | Compuestos y composiciones como moduladores de la via de hedgehog | |
| EA200870462A1 (ru) | Производные бифениламидлактама в качестве ингибиторов 11-бета-гидроксистероиддегидрогеназы 1 | |
| EA200870358A1 (ru) | 2-(циклический амино) пиримидоновые производные в качестве ингибиторов tpk1 | |
| PE20080830A1 (es) | Compuestos derivados de sulfonilo que modulan el receptor cb2 | |
| ATE473210T1 (de) | Substituierte pyrrolidinone als hemmer von 11- beta-hydroxysteroiddehydrogenase 1 | |
| EA200870461A1 (ru) | Производные лактама циклогексилимидазола в качестве ингибиторов 11-бета-гидроксистероид-дегидрогеназы 1 | |
| ATE542811T1 (de) | Piperidinylsubstituierte pyrrolidinone als inhibitoren von 11-beta- hydroxysteroiddehydrogenase 1 | |
| IS8058A (is) | Sýklísk súlfónamíð til að hamla gamma seytiasa | |
| PE20090423A1 (es) | Compuestos moduladores de sirtuina | |
| EA200601660A1 (ru) | Ингибирующие mtp арилпиперидины или пиперазины, замещенные 5-членными гетероциклами | |
| RU2389722C2 (ru) | Варианты имидазола в качестве модуляторов рецептора гамма-аминомасляной кислоты (gaba) для лечения желудочно-кишечных (жк) расстройств | |
| PE20091656A1 (es) | Compuestos heterociclicos como inhibidores de la cinasa raf | |
| AR048652A1 (es) | 4-fenilamino-quinazolin-6-il-amidas | |
| SI2049475T1 (sl) | Pirolidinoni substituirani s cikloheksilom kot inhibitorji 11-betahidroksisteroid dehidrogenaze 1 | |
| UY31986A (es) | Derivados n- sustituídos de la 2-metil-propionamida;{1-[5-sustiuido-4-sustituido-tiazol-2-il-carbamoil]-1-metil-etil} amidas de ácidos carboxílicos sustituidos, derivados farmacéuticamente aceptables de los mismos, composiciones y aplicaciones. | |
| PE20090813A1 (es) | Inhibidores de la 11b-hidroxiesteroide-deshidrogenasa | |
| BRPI0410445A (pt) | inibidores de amida de ácido pirrolopiridina-2-carboxìlico de glicogênio fosforilase | |
| PE20090620A1 (es) | Derivados de 1,2,4,5-tetrahidro-3h-benzazepinas, su procedimiento de preparacion y las composiciones farmaceuticas que las contienen | |
| PE20080409A1 (es) | Compuestos que modulan en el receptor cb2 | |
| EA200870196A1 (ru) | Индолсульфонамидные модуляторы рецепторов прогестерона | |
| PE20080404A1 (es) | Derivados bencil-amino-piperidina como inhibidores de cetp | |
| CR9384A (es) | Derivados del acido 5-fenil-pentanoico como inhibidores de la metaloproeinasa de la matriz para el tratamiento de asma y otras enfermedades |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |