AR069083A1 - Derivados heterociclicos de 1,3-tiazol inhibidores de proteinquinasas, composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento o prevencion de trastornos proliferativos. - Google Patents
Derivados heterociclicos de 1,3-tiazol inhibidores de proteinquinasas, composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento o prevencion de trastornos proliferativos.Info
- Publication number
- AR069083A1 AR069083A1 ARP080104705A ARP080104705A AR069083A1 AR 069083 A1 AR069083 A1 AR 069083A1 AR P080104705 A ARP080104705 A AR P080104705A AR P080104705 A ARP080104705 A AR P080104705A AR 069083 A1 AR069083 A1 AR 069083A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkylene
- alkyl
- nhc
- haloalkyl
- heterocycloalkyl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 230000002265 prevention Effects 0.000 title 1
- 230000002062 proliferating effect Effects 0.000 title 1
- 125000002947 alkylene group Chemical group 0.000 abstract 50
- 125000000217 alkyl group Chemical group 0.000 abstract 21
- 125000001188 haloalkyl group Chemical group 0.000 abstract 15
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000001475 halogen functional group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 4
- 125000000732 arylene group Chemical group 0.000 abstract 3
- 125000005549 heteroarylene group Chemical group 0.000 abstract 3
- 101150009274 nhr-1 gene Proteins 0.000 abstract 2
- -1 -OH Chemical group 0.000 abstract 1
- VRNHYZLBDDWTFH-ZDUSSCGKSA-N 1-[[(1s)-1-carboxy-5-[(4-iodobenzoyl)amino]pentyl]carbamoylamino]cyclopropane-1-carboxylic acid Chemical compound C([C@@H](C(=O)O)NC(=O)NC1(CC1)C(O)=O)CCCNC(=O)C1=CC=C(I)C=C1 VRNHYZLBDDWTFH-ZDUSSCGKSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
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- 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
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- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- 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
- C07D417/14—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 three or more hetero rings
-
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Virology (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Reivindicacion 1: Un compuesto que tiene la formula (1) o una sal, solvato, éster, prodroga o estereoisomero aceptable para uso farmacéutico del mismo, donde la línea de guiones indica un enlace optativo y adicional y donde Q es como en formulas (2); M es R1, -C(O)R1, -C(S)R1, -S(O)R1, -S(O)2R1, -S(O)2NHR1, -C(O)OR1, -C(O)NHR1, -NHC(O)NH-R1, -NHC(S)NHR1, -NHC(O)OR1, -NHS(O)2R1, -N(R1)(-C(O)R1) o -N(R1)2; cada caso de R1 es independientemente H, alquilo, alquenilo, alquinilo, -(alquilen)m-arilo, -(alquilen)m-cicloalquiIo, -(alquilen)m- heteroarilo, -(alquilen)m-heterocicloalquilo o -(alquilen)m-heterocicloalquenilo, donde cualquier grupo arilo, cicloalquilo, heteroarilo, heterocicloalquilo o heterocicloalquenilo puede estar optativamente sustituido en uno o más átomos de carbono del anillo con cualquiera de lo siguientes sustituyentes, que son independientemente seleccionados, en cada caso, entre halo, alquilo, alquenilo, alquinilo, haloalquilo, hidroxialquilo, -OR6, -(alquilen)m-N(R6)2, -C(O)OR6, -NHC(O)R6, -C(O)N(R6)2, -S(O)2R7, -CN, -NO2, -(alquilen)m-arilo, -(alquilen)m-cicloalquilo, -(alquilen)m-heteroarilo, -(alquilen)m-heterocicloalquilo y -(alquilen)m-heterocicloalquenilo; donde cualquier grupo heterocicloalquilo o heterocicloalquenilo puede estar optativamente sustituido en uno o más átomos de nitrogeno del anillo con cualquiera de lo siguientes sustituyentes, cada uno de los cuales es independientemente seleccionado entre alquilo, alquenilo, alquinilo, haloalquilo, hidroxialquilo, -(alquilen)m-N(R6)2, -C(O)OR6, -C(O)N(R6)2, -S(O)2R7, -(alquilen)m-arilo, -(alquilen)m-cicloalquilo, -(alquilen)m-heteroarilo, -(alquilen)m-heterocicloalquilo y -(alquilen)m-heterocicloalquenilo y donde cualquier grupo sustituyente arilo o heteroarilo puede estar optativamente sustituido con hasta 5 sustituyentes, que pueden ser iguales diferentes, y son seleccionados entre halo, -OH, alquilo, -C(O)OR6, -N(R6)2, -NHC(O)R6, -C(O)N(R6)2, -S(O)2R7, -CN, -OH, -NO2, y -O-alquilo, y donde cualquier grupo arilo, cicloalquilo, heteroarilo, heterocicloalquilo o heterocicloalquenilo puede estar optativamente fusionado a un grupo arilo, cicloalquilo, heteroarilo, heterocicloalquilo o heterocicloalquenilo, cada vez que aparece, es independientemente H, alquilo, haloalquilo, hidroxialquilo, -(alquilen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)R6 o -(alquilen)m-N(R6)2, o R2 y el átomo de carbono del anillo al cual está acoplado, se combinan para formar un grupo carbonilo; R3 es H, alquilo, haloalquilo, hidroxialquilo, -(alquilen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)-R6 o -(alquilen)m-N(R6)2, o bien R3 y R3a, junto con el átomo de carbono comun al cual cada uno de ellos está unido, se unen para formar un grupo carbonilo o un grupo espirocíclico cicloalquiIo o heterocicloalquilo; R3a es H, alquilo, haloalquilo, hidroxialquilo, -(alquilen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)-R6 o -(alquilen)m-N(R6)2; cada vez que aparece, R5 es independientemente H, alquilo, -(alquilen)m-arilo, -(alquilen)m-heteroarilo, -(alquiIen)m-heterocicloalquilo, -(alquilen)m-N(R6)2, -(alquilen)m-OH, -(alquilen)m--NHC(O)R6, hidroxialquilo, haloalquilo, -C(O)R6, -C(O)OR6, -C(O)-(alquilen)-N(R6)2, -(alquilen)m-NHC(O)R6, -NHC(O)OR6 o - NHS(O)2R7; cada vez que aparece, R6 es independientemente H, alquilo, haloalquilo, cicloalquilo, arilo, heterocicloalquilo o heteroarilo; cada vez que aparece R7, es independientemente H, alquilo, arilo, cicloalquilo o haloalquilo; R8 es H, alquilo, -OH, -O-alquilo o haloalquilo; R10 es H, alquilo, haloalquilo, hidroxialquilo, -(alquilen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)R6 o -(alquilen)m-N(R6)2,o R10 y R10a, junto con el átomo de carbono comun al cual cada uno de ellos está unido, se unen para formar un grupo carbonilo o un grupo espirocíclico cicloalquilo o heterocicloalquilo; R10a es H, alquilo, haloalquilo, hidroxialquilo, -(alquiIen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)-R6 o -(alquilen)m-N(R6)2; cada vez que aparece, R11 es independientemente H, alquilo, haloalquilo, hidroxialquilo, -(alquilen)m-C(O)N(R6)2, -(alquilen)m-NHC(O)-R6 o -(alquilen)m-N(R6)2, o bien R11 y el átomo de carbono del anillo al cual está acoplado, se combinan para formar un grupo carbonilo; cada vez que aparece, R12 es independientemente H, alquilo, -(alquilen)m-arilo, -(alquilen)m-heteroarilo, -(alquilen)m-heterocicloalquilo, -S(O)2R7, haloalquilo, hidroxialquilo, -C(O)R6 o -C(O)OR6; Ar es arileno o heteroarileno, donde el arileno o heteroarileno está unido por medio de 2 cualesquiera de sus átomo de carbono adyacentes, y donde el grupo arileno o heteroarileno puede estar optativamente sustituido con hasta 4 sustituyentes, que pueden ser iguales o diferentes, y son independientemente seleccionados entre halo, alquilo, alcoxi, ariloxi, -NH2, -NH-alquilo, -N(alquil)2, -SR6, -S(O)R7, -S(O)2R7, -C(O)R6, -C(O)OR6, -C(O)N(R6)2, -NHC(O)R6, haloalquilo, -CN y NO2, de manera tal que: cuando Ar es tetrahidronaftileno, cada uno de R2 y R3 es diferente de hidrogeno; W es N(R12)2-, -S-, -O- o -C(R5)2-, donde, cuando W es -C(R5)2-, tanto los grupos R5 como el átomo de carbono comun al cual están unidos, se pueden combinar para formar un grupo espirocíclico cicloalquilo o heterocicloalquilo, donde dicho grupo espirocíclico puede estar optativamente sustituido con hasta 4 grupos, que pueden ser iguales o diferentes y que son seleccionados entre halo, alquilo, alquenilo, alquinilo, haloalquilo, hidroxialquilo, -OR6, -(alquilen)m-N(R6)2, -C(O)OR6, -NHC(O)R6, -C(O)N(R6)2, -S(O)2R7, -CN, -OH, -NO2, -(alquilen)m-arilo, -(alquilen)m-cicloalquilo, -(alquilen)m-heteroarilo, -(alquilen)m-heterocicloalquilo y -(alquilen)m-heterocicloalquenilo; Y es H, halo, alquilo o -CN; Z es -C(R8)- o -N- cuando el enlace optativo y adicional está ausente y Z es -C- cuando el enlace optativo y adicional está presente; cada vez que aparece, m es independientemente 0 o 1; n es un entero en el rango de 0 a 2; y p es 0 o 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98332707P | 2007-10-29 | 2007-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR069083A1 true AR069083A1 (es) | 2009-12-30 |
Family
ID=40251710
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080104705A AR069083A1 (es) | 2007-10-29 | 2008-10-28 | Derivados heterociclicos de 1,3-tiazol inhibidores de proteinquinasas, composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento o prevencion de trastornos proliferativos. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8476278B2 (es) |
| EP (1) | EP2212318B1 (es) |
| JP (1) | JP5230035B2 (es) |
| CN (1) | CN101910165A (es) |
| AR (1) | AR069083A1 (es) |
| CA (1) | CA2703978A1 (es) |
| CL (1) | CL2008003200A1 (es) |
| MX (1) | MX2010004875A (es) |
| PE (1) | PE20091347A1 (es) |
| TW (1) | TW200930715A (es) |
| WO (1) | WO2009058728A1 (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2078002B1 (en) * | 2006-10-31 | 2013-08-28 | Merck Sharp & Dohme Corp. | 2-aminothiazole-4-carboxylic amides as protein kinase inhibitors |
| WO2009058729A2 (en) * | 2007-10-29 | 2009-05-07 | Schering Corporation | Thiazole carboxamide derivatives and their to treat cancer |
| US20110129440A1 (en) * | 2007-10-29 | 2011-06-02 | Schering Corporation | Heterocyclic Urea and Thiourea Derivatives and Methods of Use Thereof |
| EP2470183B1 (en) * | 2009-08-26 | 2015-09-16 | Merck Sharp & Dohme Corp. | Heterocyclic amide compounds as protein kinase inhibitors |
| WO2011029802A1 (en) * | 2009-09-08 | 2011-03-17 | F. Hoffmann-La Roche Ag | 4-substituted pyridin-3-yl-carboxamide compounds and methods of use |
| US8435976B2 (en) * | 2009-09-08 | 2013-05-07 | F. Hoffmann-La Roche | 4-substituted pyridin-3-yl-carboxamide compounds and methods of use |
| CN102153538B (zh) * | 2010-02-11 | 2013-12-11 | 山东轩竹医药科技有限公司 | 苯并环衍生物 |
| PE20130405A1 (es) | 2010-04-07 | 2013-04-10 | Hoffmann La Roche | Compuestos de pirazol-4-il-heterociclil-carboxamida y metodos de uso |
| KR101871436B1 (ko) | 2010-05-17 | 2018-06-27 | 인코젠 쎄라퓨틱스 프라이빗 리미티드 | 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물 |
| EP2590968A1 (en) * | 2010-07-06 | 2013-05-15 | Novartis AG | Cyclic ether compounds useful as kinase inhibitors |
| CN102924445B (zh) * | 2011-08-11 | 2015-07-08 | 上海吉铠医药科技有限公司 | Pim激酶抑制剂及其制备方法与在制药中的应用 |
| CN104321322A (zh) | 2012-03-30 | 2015-01-28 | 理森制药股份公司 | 作为c-met蛋白激酶调节剂的新型3,5-二取代-3h-咪唑并[4,5-b]吡啶和3,5-二取代-3h-[1,2,3]三唑并[4,5-b]吡啶化合物 |
| TW202146393A (zh) | 2020-03-03 | 2021-12-16 | 美商皮克醫療公司 | Eif4e抑制劑及其用途 |
| WO2021237111A1 (en) * | 2020-05-21 | 2021-11-25 | Stemsynergy Therapeutics, Inc. | Notch inhibitors and uses thereof |
| BR112023015210A2 (pt) * | 2021-01-29 | 2023-11-07 | Cedilla Therapeutics Inc | Inibidores de cdk2 e métodos de uso dos mesmos |
| CN113069451B (zh) * | 2021-04-02 | 2022-08-09 | 苏州大学 | 一种吡咯-2-磺酰胺化合物的制备方法及其在制备抗肿瘤药物中的应用 |
| JP2024532276A (ja) | 2021-08-25 | 2024-09-05 | ピク セラピューティクス, インコーポレイテッド | eIF4E阻害剤及びその使用 |
| US12234231B2 (en) | 2021-08-25 | 2025-02-25 | PIC Therapeutics, Inc. | EIF4E inhibitors and uses thereof |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA200301696B (en) | 2000-09-15 | 2004-04-28 | Vertex Pharma | Isoxazoles and their use as inhibitors of erk. |
| FR2856685B1 (fr) * | 2003-06-25 | 2005-09-23 | Merck Sante Sas | Derives de thiazolylpiperidine, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent |
| TWI372050B (en) * | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| EP2009005A4 (en) * | 2006-04-19 | 2010-06-02 | Astellas Pharma Inc | AZOLECARBOXAMIDE DERIVATIVE |
| EP2078002B1 (en) * | 2006-10-31 | 2013-08-28 | Merck Sharp & Dohme Corp. | 2-aminothiazole-4-carboxylic amides as protein kinase inhibitors |
| CA2668210C (en) * | 2006-10-31 | 2013-03-12 | Schering Corporation | Anilinopiperazine derivatives and methods of use thereof |
| JP4968860B2 (ja) * | 2006-10-31 | 2012-07-04 | シェーリング コーポレイション | アニリノピペラジン誘導体およびアニリノピペラジン誘導体を使用する方法 |
| CN101910164A (zh) * | 2007-10-29 | 2010-12-08 | 先灵公司 | 作为蛋白质激酶抑制剂的二酰氨基噻唑衍生物 |
| US20110129440A1 (en) * | 2007-10-29 | 2011-06-02 | Schering Corporation | Heterocyclic Urea and Thiourea Derivatives and Methods of Use Thereof |
-
2008
- 2008-10-27 MX MX2010004875A patent/MX2010004875A/es unknown
- 2008-10-27 WO PCT/US2008/081316 patent/WO2009058728A1/en not_active Ceased
- 2008-10-27 JP JP2010532171A patent/JP5230035B2/ja not_active Expired - Fee Related
- 2008-10-27 CN CN200880123470XA patent/CN101910165A/zh active Pending
- 2008-10-27 CA CA2703978A patent/CA2703978A1/en not_active Abandoned
- 2008-10-27 EP EP08845572.0A patent/EP2212318B1/en active Active
- 2008-10-27 US US12/738,487 patent/US8476278B2/en active Active
- 2008-10-28 AR ARP080104705A patent/AR069083A1/es not_active Application Discontinuation
- 2008-10-28 PE PE2008001843A patent/PE20091347A1/es not_active Application Discontinuation
- 2008-10-28 CL CL2008003200A patent/CL2008003200A1/es unknown
- 2008-10-28 TW TW097141426A patent/TW200930715A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2010004875A (es) | 2010-05-19 |
| JP2011502156A (ja) | 2011-01-20 |
| CL2008003200A1 (es) | 2009-11-27 |
| CN101910165A (zh) | 2010-12-08 |
| CA2703978A1 (en) | 2009-05-07 |
| PE20091347A1 (es) | 2009-09-18 |
| EP2212318A1 (en) | 2010-08-04 |
| US20100331313A1 (en) | 2010-12-30 |
| TW200930715A (en) | 2009-07-16 |
| US8476278B2 (en) | 2013-07-02 |
| JP5230035B2 (ja) | 2013-07-10 |
| WO2009058728A1 (en) | 2009-05-07 |
| EP2212318B1 (en) | 2013-07-24 |
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