CU24282B1 - Derivados de benzamidas empleados en el tratamiento de enfermedades proliferativas - Google Patents
Derivados de benzamidas empleados en el tratamiento de enfermedades proliferativasInfo
- Publication number
- CU24282B1 CU24282B1 CUP2015000029A CU20150029A CU24282B1 CU 24282 B1 CU24282 B1 CU 24282B1 CU P2015000029 A CUP2015000029 A CU P2015000029A CU 20150029 A CU20150029 A CU 20150029A CU 24282 B1 CU24282 B1 CU 24282B1
- Authority
- CU
- Cuba
- Prior art keywords
- group
- pyrimidinyl
- formula
- pyridyl
- benzamids
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 230000002062 proliferating effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 4-methylpiperazinyl group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000005551 pyridylene group Chemical group 0.000 abstract 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 abstract 1
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 abstract 1
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epidemiology (AREA)
Abstract
<p>La presente invención se relaciona a un compuesto de la fórmula (I):</p> <p>ESPACIO PARA FÓRMULA</p> <p>en donde A y A´ representan independientemente un grupo fenileno o un grupo piridileno; R2 es un átomo de hidrógeno o un grupo alquilo (C1-C4), R3 es un grupo 2-piridilo, grupo 3-piridilo, un grupo 4-piridilo, un grupo 2-pirimidinilo, un grupo 4-pirimidinilo, o un grupo 5-pirimidinilo; R4 es un grupo carbonilo o un grupo sulfonilo, y R5 es un grupo –NH-(CH2)a-NR6R7 o un grupo 4-metilpiperazinilo, con a que es un entero de 1 a 4, R6 y R7 representan independientemente un grupo alquilo de (C1-C4), o R6 y R7 junto con el átomo de nitrógeno al cual se enlazan que forman un grupo heterociclo el cual es elegido entre un grupo 4-metilpiperazinilo, un grupo morfolino, un grupo pirrolidinilo y un grupo piperidino, o cualquiera de sus sales aceptables farmacéuticamente. La invención se relaciona además a composiciones farmacéuticas que contienen un compuesto de la fórmula (I) o cualesquiera de sus sales aceptables farmacéuticamente y un proceso de preparación para obtenerlos. Los compuestos (I) son útiles para tratamiento de cáncer.</p>
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12186684.2A EP2712862A1 (en) | 2012-09-28 | 2012-09-28 | New anti-invasive compounds |
| PCT/IB2013/058992 WO2014049578A1 (en) | 2012-09-28 | 2013-09-30 | New anti-invasive compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CU20150029A7 CU20150029A7 (es) | 2015-09-29 |
| CU24282B1 true CU24282B1 (es) | 2017-11-07 |
Family
ID=47018046
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CUP2015000029A CU24282B1 (es) | 2012-09-28 | 2013-09-30 | Derivados de benzamidas empleados en el tratamiento de enfermedades proliferativas |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US9969715B2 (es) |
| EP (2) | EP2712862A1 (es) |
| JP (1) | JP6209215B2 (es) |
| KR (1) | KR102175775B1 (es) |
| CN (1) | CN104903293B (es) |
| AU (1) | AU2013322131B2 (es) |
| BR (1) | BR112015006979B1 (es) |
| CA (1) | CA2886804C (es) |
| CU (1) | CU24282B1 (es) |
| DK (1) | DK2900635T3 (es) |
| ES (1) | ES2598056T3 (es) |
| HR (1) | HRP20161286T1 (es) |
| MX (1) | MX366633B (es) |
| PL (1) | PL2900635T3 (es) |
| PT (1) | PT2900635T (es) |
| RU (1) | RU2641650C2 (es) |
| WO (1) | WO2014049578A1 (es) |
| ZA (1) | ZA201502126B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2926297B1 (fr) * | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
| EP2505198A1 (en) * | 2011-04-01 | 2012-10-03 | Société Splicos | Compounds for use as therapeutic agents affecting p53 expression and/or activity |
| EP2712862A1 (en) * | 2012-09-28 | 2014-04-02 | Splicos | New anti-invasive compounds |
| JP2016535755A (ja) * | 2013-11-06 | 2016-11-17 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | Ｇｓｋ−３阻害剤 |
| AU2014369926B2 (en) | 2013-12-24 | 2019-07-18 | Oncotartis, Inc. | Benzamide and nicotinamide compounds and methods of using same |
| EP3594205A1 (en) * | 2018-07-09 | 2020-01-15 | Abivax | Phenyl-n-aryl derivatives for treating a rna virus infection |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4423065A (en) | 1982-05-04 | 1983-12-27 | Eli Lilly And Company | Naphthalenamine insecticides |
| IL68500A (en) | 1982-05-04 | 1986-07-31 | Lilly Co Eli | N-(2,4-dinitro-6-trifluoromethylphenyl)-1-naphthylamines,their preparation and anti coccidial compositions containing them |
| KR860001567A (ko) * | 1984-08-30 | 1986-03-20 | 김순영 | 상의용 무가봉 입체 재단법 |
| BR0210191A (pt) * | 2001-06-06 | 2004-04-06 | Agouron Pharma | Agentes não peptìdicos da gnrh, composições farmacêuticas e métodos para o seu uso, e processos para os preparar e aos seus intermediários |
| EP1655295A1 (en) * | 2004-11-03 | 2006-05-10 | Schering Aktiengesellschaft | Anthranilamide pyridinureas as VEGF receptor kinase inhibitors |
| US8030487B2 (en) * | 2006-07-07 | 2011-10-04 | Targegen, Inc. | 2-amino—5-substituted pyrimidine inhibitors |
| FR2926297B1 (fr) | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
| WO2010007756A1 (ja) * | 2008-07-14 | 2010-01-21 | 塩野義製薬株式会社 | Ｔｔｋ阻害作用を有するピリジン誘導体 |
| EP2361902A4 (en) * | 2008-11-21 | 2012-04-25 | Astellas Pharma Inc | 4,6-DIAMINONICOTINSÄUREAMIDVERBINDUNG |
| FR2943669B1 (fr) * | 2009-03-24 | 2011-05-06 | Sanofi Aventis | Derives de nicotinamide,leur preparation et leur application en therapeutique |
| US8703768B2 (en) * | 2010-06-09 | 2014-04-22 | Hoffmann-La Roche Inc. | Nitrogen containing heteroaryl compounds |
| EP2712862A1 (en) * | 2012-09-28 | 2014-04-02 | Splicos | New anti-invasive compounds |
-
2012
- 2012-09-28 EP EP12186684.2A patent/EP2712862A1/en not_active Withdrawn
-
2013
- 2013-09-30 DK DK13812086.0T patent/DK2900635T3/en active
- 2013-09-30 KR KR1020157010969A patent/KR102175775B1/ko active Active
- 2013-09-30 CN CN201380060496.5A patent/CN104903293B/zh active Active
- 2013-09-30 EP EP13812086.0A patent/EP2900635B1/en active Active
- 2013-09-30 JP JP2015533750A patent/JP6209215B2/ja active Active
- 2013-09-30 HR HRP20161286TT patent/HRP20161286T1/hr unknown
- 2013-09-30 MX MX2015003706A patent/MX366633B/es active IP Right Grant
- 2013-09-30 PL PL13812086T patent/PL2900635T3/pl unknown
- 2013-09-30 WO PCT/IB2013/058992 patent/WO2014049578A1/en not_active Ceased
- 2013-09-30 CU CUP2015000029A patent/CU24282B1/es unknown
- 2013-09-30 AU AU2013322131A patent/AU2013322131B2/en active Active
- 2013-09-30 CA CA2886804A patent/CA2886804C/en active Active
- 2013-09-30 RU RU2015115360A patent/RU2641650C2/ru active
- 2013-09-30 ES ES13812086.0T patent/ES2598056T3/es active Active
- 2013-09-30 BR BR112015006979-7A patent/BR112015006979B1/pt active IP Right Grant
- 2013-09-30 US US14/432,328 patent/US9969715B2/en active Active
- 2013-09-30 PT PT138120860T patent/PT2900635T/pt unknown
-
2015
- 2015-03-27 ZA ZA2015/02126A patent/ZA201502126B/en unknown
-
2018
- 2018-04-05 US US15/946,120 patent/US10717724B2/en active Active
-
2020
- 2020-04-15 US US16/848,916 patent/US11427566B2/en active Active
Also Published As
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