AR054725A1 - Pirazolopiridinas y sales de las mismas, una composicion farmaceutica que comprende dichos compuestos, un metodo para prepararlos y su uso - Google Patents
Pirazolopiridinas y sales de las mismas, una composicion farmaceutica que comprende dichos compuestos, un metodo para prepararlos y su usoInfo
- Publication number
- AR054725A1 AR054725A1 ARP060100245A ARP060100245A AR054725A1 AR 054725 A1 AR054725 A1 AR 054725A1 AR P060100245 A ARP060100245 A AR P060100245A AR P060100245 A ARP060100245 A AR P060100245A AR 054725 A1 AR054725 A1 AR 054725A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- heterocycloalkyl
- alkyl
- aryl
- hydroxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 13
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 10
- 125000003118 aryl group Chemical group 0.000 abstract 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 8
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 239000001301 oxygen Substances 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- 239000011593 sulfur Substances 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- SINQIEAULQKUPD-UHFFFAOYSA-N 4-[4-(6-methoxy-2-naphthalenyl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine Chemical compound C1=CC2=CC(OC)=CC=C2C=C1C=1N=C(C=2C=CC(=CC=2)S(C)=O)NC=1C1=CC=NC=C1 SINQIEAULQKUPD-UHFFFAOYSA-N 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- -1 C 1- haloalkyl 6 Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000006413 ring segment Chemical group 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
- 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
- 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
- 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
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P27/00—Drugs for disorders of the senses
-
- 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
- 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
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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
-
- 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
-
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Procesos de obtencion y composiciones farmacéuticas que las comprenden. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula general (1), donde: R1 significa alquilo C1-6, alquinilo C2-6, cicloalquilo C3-10, heterocicloalquilo C3-10, arilo o heteroarilo opcionalmente sustituido una o más veces, de manera igual o diferente con K, donde heterocicloalquilo C3-10 a su vez debe estar interrumpido al menos una vez con un átomo del grupo que comprende, preferentemente consiste en, nitrogeno, oxígeno y/o azufre y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede estar interrumpido opcionalmente una o más veces, de manera igual o diferente con un grupo -C(O)-, -S(O)- o -S(O)2- y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede contener opcionalmente uno o más enlaces dobles; K significa halogeno, hidroxi o un sustituyente del grupo que comprende, preferentemente consiste en, -OR3 o -NR5R6 o para cicloalquilo C3-10, heterocicloalquilo C3-10, arilo o heteroarilo opcionalmente sustituido una o más veces, de manera igual o diferentes con L, donde heterocicloalquilo C3-10 debe a su vez estar interrumpido al menos una vez por un átomo del grupo que comprende, preferentemente consiste en, nitrogeno, oxígeno y/o azufre y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede estar interrumpido opcionalmente una o más veces, de manera igual o diferente con un grupo -C(O)-, -S(O)- o - S(O)2- y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede contener opcionalmente uno o más enlaces dobles; L significa un sustituyente del grupo que comprende, preferentemente consiste en, -C(O)R4 o -NR5R6 o para alquilo C1-6 opcionalmente sustituido una o más veces, de manera igual o diferente con halogeno, hidroxi, ciano, nitro o el grupo -NR5R6 o -C(O)R4; RA significa hidrogeno o alquilo C1-6 opcionalmente sustituido una o más veces, de manera igual o diferente con halogeno, hidroxi, ciano, nitro o el grupo -NR5R6 o -C(O)R4; R2 significa un sustituyente del grupo que comprende, preferentemente consiste en, -C(O)-NR7R7a, -S(O)2-R7, -S(O)2NR7N7a, -S(O)(NH)R7, - C(O)R7 o -C(O)OR7; R3 significa alquilo C1-6, arilo o -(CH2)n-arilo, donde alquilo C1-6, arilo o -(CH2)n-arilo pueden estar opcionalmente sustituidos una o más veces, de manera igual o diferente con alquilo C1-6, alcoxi C1-6, halogeno, hidroxi, ciano, nitro o el grupo -NR5R6 o -C(O) R4; R4 significa hidrogeno, hidroxi, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6 o el grupo -NR5R6; R5 y R6 significan en forma independiente entre sí hidrogeno, alquilo C1-6, arilo, -(CH2)n-arilo, o para un grupo -C(O)R4, donde alquilo C1-6 o arilo pueden estar opcionalmente sustituidos una o más veces, de manera igual o diferente con halogeno, hidroxi, ciano, nitro o el grupo -NR7R7a o -C(O)R4; o R5 y R6 junto con el átomo de nitrogeno al cual están unidos, forman un anillo heterocicloalquilo de entre 3 y 10 miembros, donde el anillo heterocicloalquilo debe a su vez estar interrumpido al menos una vez por un átomo del grupo que comprende, preferentemente consiste en, nitrogeno, oxígeno y/o azufre y puede estar interrumpido opcionalmente una o más veces, de manera igual o diferente con un grupo -C(O)-, -S(O)- y/o -S(O)2- y puede contener opcionalmente uno o más enlaces dobles; R7 y R7a significan en forma independiente entre sí hidrogeno, alquilo C1-6, cicloalquilo C3-10, heterocicloalquilo C3-10, arilo o heteroarilo, donde alquilo C1-6, cicloalquilo C3-10, heterocicloalquilo C3-10, arilo o heteroarilo pueden estar opcionalmente sustituidos una o más veces, de manera igual o diferente con M, donde heterocicloalquilo C3-10 debe a su vez estar interrumpido al menos una vez por un átomo del grupo que comprende, preferentemente consiste en, nitrogeno, oxígeno y/o azufre y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede estar interrumpido opcionalmente una o más veces, de manera igual o diferente con un grupo -C(O)-, -S(O)- o -S(O)2- y donde el anillo cicloalquilo C3-10 y/o heterocicloalquilo C3-10 puede contener opcionalmente uno o más enlaces dobles; o R7 y R7a junto con el átomo de nitrogeno al cual están unidos, forman un anillo heterocicloalquilo de entre 3 y 10 miembros, donde el anillo heterocicloalquilo debe a su vez estar interrumpido al menos una vez por un átomo del grupo que comprende, preferentemente consiste en, nitrogeno, oxígeno y/o azufre y puede estar interrumpido opcionalmente una o más veces, de manera igual o diferente con un grupo -C(O)-, -S(O)- o -S(O)2- y puede contener opcionalmente uno o más enlaces dobles; M significa un sustituyente del grupo que comprende, preferentemente consiste en, ciano, halogeno, hidroxi, nitro o para alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, haloalcoxi C1-6, haloalquilo C1-6, arilo, heteroarilo C3-10, -(CH2)m-fenilo o -(CH2)m-O-(CH2)qfenilo, donde alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, arilo, heteroarilo C3-10, -(CH2)m-fenilo o -(CH2)m-O-(CH2)qfenilo pueden estar opcionalmente sustituidos una o más veces, de manera igual o diferente con un sustituyente del grupo que comprende, preferentemente consiste en, amino, ciano, halogeno, hidroxi, nitro, alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, haloalquilo C1-6, -(CH2)m-fenilo o -(CH2)m-O-(CH2)qfenilo; Y1, Y2, Y3; Y4 y Y5 significan en forma independiente entre sí, -CH=, -CZ= o - N= y -N= puede aparecer 0, 1, 2, o 3 veces como un átomo del anillo; Z significa ciano, nitro, halogeno, hidroxi o un sustituyente del grupo que comprende, preferentemente consiste en, -NR5R6, -OR3, -C(O)R7, -C(O)OR7, - C(O)NR7R7a, -S(O)R7 o -S(O)2R7 o para alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-10, donde alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-10 pueden estar opcionalmente sustituidos una o más veces, de manera igual o diferente con ciano, nitro, halogeno, hidroxi, -OR3 o -NR5R6; m significa el entero 0, 1, 2, 3 o 4; n significa el entero 0, 1, 2, 3 o 4; p significa el entero 0, 1, 2, 3 o 4; y q significa el entero 0, 1, 2, 3 o 4; así como: N-oxidos, solvatos, hidratos, isomeros, diasteromeros, enantiomeros y sales de los mismos, que son inhibidores efectivos de Tie2 quinasa.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05075177A EP1683796A1 (en) | 2005-01-24 | 2005-01-24 | Pyrazolopyridines, their preparation and their medical use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR054725A1 true AR054725A1 (es) | 2007-07-11 |
Family
ID=34938008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060100245A AR054725A1 (es) | 2005-01-24 | 2006-01-24 | Pirazolopiridinas y sales de las mismas, una composicion farmaceutica que comprende dichos compuestos, un metodo para prepararlos y su uso |
Country Status (10)
| Country | Link |
|---|---|
| EP (2) | EP1683796A1 (es) |
| JP (1) | JP5203713B2 (es) |
| AR (1) | AR054725A1 (es) |
| DO (1) | DOP2006000017A (es) |
| GT (1) | GT200600025A (es) |
| PA (1) | PA8660601A1 (es) |
| PE (1) | PE20060957A1 (es) |
| TW (1) | TW200637860A (es) |
| UY (1) | UY29343A1 (es) |
| WO (1) | WO2006077168A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20061119A1 (es) * | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
| TW200815438A (en) * | 2006-06-13 | 2008-04-01 | Bayer Schering Pharma Ag | Substituted pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP1870410A1 (en) | 2006-06-13 | 2007-12-26 | Bayer Schering Pharma Aktiengesellschaft | Substituted arylpyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| FR2908409B1 (fr) | 2006-11-10 | 2009-01-09 | Sanofi Aventis Sa | Pyrazoles substituees,compositions les contenant,procede de fabrication et utilisation |
| EP1932845A1 (en) * | 2006-12-15 | 2008-06-18 | Bayer Schering Pharma Aktiengesellschaft | 3-H-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| CA2672367A1 (en) * | 2006-12-15 | 2008-06-19 | Bayer Schering Pharma Aktiengesellschaft | 3-h-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP2070929A1 (en) | 2007-12-11 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Alkynylaryl compounds and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP2671891A3 (en) | 2008-06-27 | 2014-03-05 | Amgen Inc. | Ang-2 inhibition to treat multiple sclerosis |
| EP2789614B1 (en) | 2009-08-11 | 2017-04-26 | Bristol-Myers Squibb Company | Azaindazoles as Btk kinase modulators and use thereof |
| CA2914815A1 (en) * | 2013-06-11 | 2014-12-18 | Kala Pharmaceuticals, Inc. | Urea derivatives and uses thereof |
| US20180194769A1 (en) | 2015-07-06 | 2018-07-12 | Rodin Therapeutics, Inc. | Hetero-halo inhibitors of histone deacetylase |
| US10421756B2 (en) | 2015-07-06 | 2019-09-24 | Rodin Therapeutics, Inc. | Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase |
| DK3570834T3 (en) | 2017-01-11 | 2022-02-28 | Alkermes Inc | Bicyclic inhibitors of histone deacetylase |
| AU2018313094A1 (en) | 2017-08-07 | 2020-02-20 | Rodin Therapeutics, Inc. | Bicyclic inhibitors of histone deacetylase |
| CA3241624A1 (en) * | 2021-12-22 | 2023-06-29 | Anaxis Pharma Pty Ltd | Arylsulphonamide compounds |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU7491400A (en) * | 1999-09-17 | 2001-04-17 | Abbott Gmbh & Co. Kg | Kinase inhibitors as therapeutic agents |
| PL1638941T3 (pl) * | 2003-05-22 | 2010-11-30 | Abbvie Bahamas Ltd | Indazolowe, benzizoksazolowe i benzizotiazolowe inhibitory kinaz |
-
2005
- 2005-01-24 EP EP05075177A patent/EP1683796A1/en not_active Withdrawn
-
2006
- 2006-01-20 EP EP20060701504 patent/EP1841767A1/en not_active Withdrawn
- 2006-01-20 JP JP2007551638A patent/JP5203713B2/ja not_active Expired - Fee Related
- 2006-01-20 WO PCT/EP2006/000623 patent/WO2006077168A1/en not_active Ceased
- 2006-01-23 PE PE2006000096A patent/PE20060957A1/es not_active Application Discontinuation
- 2006-01-23 GT GT200600025A patent/GT200600025A/es unknown
- 2006-01-23 DO DO2006000017A patent/DOP2006000017A/es unknown
- 2006-01-23 UY UY29343A patent/UY29343A1/es not_active Application Discontinuation
- 2006-01-24 AR ARP060100245A patent/AR054725A1/es not_active Application Discontinuation
- 2006-01-24 TW TW095102709A patent/TW200637860A/zh unknown
- 2006-01-24 PA PA20068660601A patent/PA8660601A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PE20060957A1 (es) | 2006-10-13 |
| TW200637860A (en) | 2006-11-01 |
| GT200600025A (es) | 2007-01-03 |
| PA8660601A1 (es) | 2006-08-03 |
| JP2008528458A (ja) | 2008-07-31 |
| UY29343A1 (es) | 2006-08-31 |
| JP5203713B2 (ja) | 2013-06-05 |
| DOP2006000017A (es) | 2006-08-15 |
| WO2006077168A1 (en) | 2006-07-27 |
| EP1683796A1 (en) | 2006-07-26 |
| EP1841767A1 (en) | 2007-10-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |