CL2009000429A1 - Compuestos derivados de carbamoil-heterociclos fusionados, en especial pirrolo[3,2-c]piridin-2-carboxamidas, inhibidores de smo; composicion farmaceutica que comprende dichos compuestos; y uso en la profilaxis o tratamiento del cancer. - Google Patents
Compuestos derivados de carbamoil-heterociclos fusionados, en especial pirrolo[3,2-c]piridin-2-carboxamidas, inhibidores de smo; composicion farmaceutica que comprende dichos compuestos; y uso en la profilaxis o tratamiento del cancer.Info
- Publication number
- CL2009000429A1 CL2009000429A1 CL2009000429A CL2009000429A CL2009000429A1 CL 2009000429 A1 CL2009000429 A1 CL 2009000429A1 CL 2009000429 A CL2009000429 A CL 2009000429A CL 2009000429 A CL2009000429 A CL 2009000429A CL 2009000429 A1 CL2009000429 A1 CL 2009000429A1
- Authority
- CL
- Chile
- Prior art keywords
- compounds
- carbamoyl
- cancer
- treatment
- carboxamides
- Prior art date
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Classifications
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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
-
- 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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-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
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
COMPUESTO QUE TIENE UNA ACTIVIDAD INHIBIDORA DE SMO SUPERIOR Y BAJA TOXICIDAD, QUE ES SUFICIENTEMENTE SATISFACTORIA COMO PRODUCTO FARMACÉUTICO, REPRESENTADO POR LA FAMILIA. EN EL CUAL ANILLO A ES ANILLO DE 5 A 7 MIEMBROS QUE TIENE SUSTITUYENTE(S) EN FORMA OPCIONAL, DONDE LOS SUSTITUYENTES ESTÁN UNIDOS EN FORMA OPCIONAL ENTRE SI PARA FORMAR UN ANILLO; X ES O, S O NR1 (R1 ES UN ÁTOMO DE HIDRÓGENO O UN GRUPO HIDROCARBURO QUE TIENE SUSTITUYENTE{S) EN FORMA OPCIONAL); R3 ES CARBAMOILO QUE TIENE SUSTITUYENTES) EN FORMA OPCIONAL; Y R3 ES HIDROXI QUE TIENE SUSTITUYENTE(S) EN FORMA OPCIONAL, O UNA DE SUS SALES, SUS COMPOSICIONES FARMACÉUTICAS Y SU USO EN EL TRATAMIENTO DEL CÁNCER.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008045134 | 2008-02-26 | ||
JP2008256755 | 2008-10-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2009000429A1 true CL2009000429A1 (es) | 2009-09-25 |
Family
ID=40905094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2009000429A CL2009000429A1 (es) | 2008-02-26 | 2009-02-25 | Compuestos derivados de carbamoil-heterociclos fusionados, en especial pirrolo[3,2-c]piridin-2-carboxamidas, inhibidores de smo; composicion farmaceutica que comprende dichos compuestos; y uso en la profilaxis o tratamiento del cancer. |
Country Status (28)
Country | Link |
---|---|
US (2) | US8399449B2 (es) |
EP (1) | EP2247588B1 (es) |
JP (2) | JP4719317B2 (es) |
KR (1) | KR101569949B1 (es) |
CN (1) | CN102015705B (es) |
AR (1) | AR070479A1 (es) |
AU (1) | AU2009217982B2 (es) |
BR (1) | BRPI0908417B1 (es) |
CA (1) | CA2716773C (es) |
CL (1) | CL2009000429A1 (es) |
CO (1) | CO6321277A2 (es) |
CR (1) | CR11661A (es) |
DO (1) | DOP2010000260A (es) |
EA (1) | EA020144B1 (es) |
EC (1) | ECSP10010496A (es) |
ES (1) | ES2586252T3 (es) |
GE (1) | GEP20125664B (es) |
HK (1) | HK1150274A1 (es) |
IL (1) | IL207735A (es) |
JO (1) | JO3259B1 (es) |
MA (1) | MA32164B1 (es) |
MX (1) | MX2010009372A (es) |
MY (1) | MY150379A (es) |
NZ (1) | NZ587719A (es) |
PE (1) | PE20091556A1 (es) |
TW (1) | TWI480282B (es) |
WO (1) | WO2009107850A2 (es) |
ZA (1) | ZA201006063B (es) |
Families Citing this family (26)
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CL2009000429A1 (es) * | 2008-02-26 | 2009-09-25 | Takeda Pharmaceuticals Co | Compuestos derivados de carbamoil-heterociclos fusionados, en especial pirrolo[3,2-c]piridin-2-carboxamidas, inhibidores de smo; composicion farmaceutica que comprende dichos compuestos; y uso en la profilaxis o tratamiento del cancer. |
WO2011013752A1 (ja) * | 2009-07-31 | 2011-02-03 | 塩野義製薬株式会社 | 縮合へテロ環誘導体を含有する医薬組成物 |
US9169279B2 (en) | 2009-07-31 | 2015-10-27 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
ES2650665T3 (es) | 2009-07-31 | 2018-01-19 | Grünenthal GmbH | Método de cristalización y biodisponibilidad |
US20160016982A1 (en) | 2009-07-31 | 2016-01-21 | Thar Pharmaceuticals, Inc. | Crystallization method and bioavailability |
GEP20146075B (en) | 2009-08-26 | 2014-04-10 | Takeda Pharmaceuticals Co | Fused heterocyclic ring derivative and usage thereof |
WO2011024869A1 (ja) * | 2009-08-26 | 2011-03-03 | 武田薬品工業株式会社 | 縮合複素環誘導体およびその用途 |
US8614208B2 (en) | 2009-08-26 | 2013-12-24 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
EP2471791B1 (en) | 2009-08-26 | 2014-11-12 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
WO2012071517A2 (en) | 2010-11-24 | 2012-05-31 | Thar Pharmaceuticals, Inc. | Novel crystalline forms |
WO2012154731A1 (en) * | 2011-05-08 | 2012-11-15 | Vanderbilt University | Substituted 1h-pyrrolo[3,2-c]quinolin-4(5h)-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m4 |
CN104583194A (zh) | 2012-05-11 | 2015-04-29 | 艾伯维公司 | 作为nampt抑制剂的哒嗪和吡啶衍生物 |
PT3077544T (pt) * | 2013-12-03 | 2019-08-01 | Celestra Life Science Llc | Projeto baseado em fundamentos de uma terapia alvo para 0 cancro |
WO2015140964A1 (ja) | 2014-03-19 | 2015-09-24 | 株式会社 東芝 | 電池用電極材料、非水電解質電池及び電池パック |
US20170015677A1 (en) * | 2014-03-31 | 2017-01-19 | Boston Biomedical, Inc. | New tricyclic quinone derivative |
WO2016198691A1 (en) | 2015-06-11 | 2016-12-15 | Basilea Pharmaceutica Ag | Efflux-pump inhibitors and therapeutic uses thereof |
US9962378B2 (en) * | 2015-09-17 | 2018-05-08 | Macau University Of Science And Technology | ROS1 inhibitor and its use |
EP3412667B1 (en) | 2016-02-01 | 2021-11-03 | Takeda Pharmaceutical Company Limited | Cocrystal |
WO2017208070A1 (en) | 2016-05-31 | 2017-12-07 | Grünenthal GmbH | Bisphosphonic acid and coformers with lysin, glycin, nicotinamide for treating psoriatic arthritis |
US11299469B2 (en) | 2016-11-29 | 2022-04-12 | Sumitomo Dainippon Pharma Oncology, Inc. | Naphthofuran derivatives, preparation, and methods of use thereof |
JP7091201B2 (ja) | 2018-09-14 | 2022-06-27 | 株式会社東芝 | 活物質、電極、二次電池、電池パック、及び車両 |
RU2711968C1 (ru) * | 2018-11-22 | 2020-01-24 | федеральное государственное бюджетное образовательное учреждение высшего образования "Пермский национальный исследовательский политехнический университет" | Анальгезирующее средство |
CN110172068A (zh) * | 2019-06-05 | 2019-08-27 | 河南龙湖生物技术有限公司 | 具有抗肿瘤活性的苯并噻唑类化合物及其制备方法和应用 |
CN115997122A (zh) | 2020-06-26 | 2023-04-21 | 拉夸里亚创药株式会社 | 类维生素a与癌治疗剂的组合疗法有效的癌患者的选择方法、及类维生素a与癌治疗剂的组合药物 |
CN113292477B (zh) * | 2021-06-01 | 2023-06-02 | 四川大学 | 一种铱催化的碳氢活化反应合成异吲哚-1-酮类化合物的方法 |
CN113429422B (zh) * | 2021-07-26 | 2022-05-10 | 中国人民解放军军事科学院军事医学研究院 | 一种噻吩并喹诺酮类化合物及其制备方法和应用 |
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EP1181296A1 (en) | 1999-06-03 | 2002-02-27 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
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EP1698335A4 (en) | 2003-12-26 | 2007-08-01 | Ono Pharmaceutical Co | AGENT FOR PREVENTING AND / OR TREATING DISEASES INVOLVING A MITOCHONDRIAL BENZODIAZEPINE RECEPTOR |
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BRPI0614578A2 (pt) * | 2005-08-16 | 2011-04-05 | Irm Llc | composto, composição farmacêutica como inibidores de proteìna cinases, bem como seu método e uso |
AR056560A1 (es) * | 2005-10-06 | 2007-10-10 | Astrazeneca Ab | Pirrolopiridinonas como moduladores cb1 |
WO2007085188A1 (en) * | 2006-01-27 | 2007-08-02 | Shanghai Hengrui Pharmaceutical Co. Ltd. | Pyrrolo [3,2-c] pyridine-4-one 2-indolinone protein kinase inhibitors |
KR20090006089A (ko) * | 2006-04-14 | 2009-01-14 | 노파르티스 아게 | 헤지호그 경로 관련 질환의 치료에서의 바이아릴카르복스아미드의 용도 |
BRPI0808772A2 (pt) * | 2007-03-14 | 2014-08-12 | Exelixis Inc | Inibidores da via de hedgehog |
PE20090188A1 (es) * | 2007-03-15 | 2009-03-20 | Novartis Ag | Compuestos heterociclicos como moduladores de la senda de hedgehog |
CL2009000429A1 (es) * | 2008-02-26 | 2009-09-25 | Takeda Pharmaceuticals Co | Compuestos derivados de carbamoil-heterociclos fusionados, en especial pirrolo[3,2-c]piridin-2-carboxamidas, inhibidores de smo; composicion farmaceutica que comprende dichos compuestos; y uso en la profilaxis o tratamiento del cancer. |
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2009
- 2009-02-25 CL CL2009000429A patent/CL2009000429A1/es unknown
- 2009-02-25 PE PE2009000279A patent/PE20091556A1/es active IP Right Grant
- 2009-02-25 AR ARP090100644A patent/AR070479A1/es active IP Right Grant
- 2009-02-25 TW TW098105923A patent/TWI480282B/zh active
- 2009-02-25 JP JP2010533355A patent/JP4719317B2/ja active Active
- 2009-02-25 BR BRPI0908417-7A patent/BRPI0908417B1/pt active IP Right Grant
- 2009-02-25 CN CN2009801148111A patent/CN102015705B/zh active Active
- 2009-02-25 US US12/919,413 patent/US8399449B2/en active Active
- 2009-02-25 JO JOP/2009/0079A patent/JO3259B1/ar active
- 2009-02-25 AU AU2009217982A patent/AU2009217982B2/en active Active
- 2009-02-25 EA EA201070994A patent/EA020144B1/ru unknown
- 2009-02-25 NZ NZ587719A patent/NZ587719A/en unknown
- 2009-02-25 CA CA2716773A patent/CA2716773C/en active Active
- 2009-02-25 US US12/392,640 patent/US8217176B2/en active Active
- 2009-02-25 MX MX2010009372A patent/MX2010009372A/es active IP Right Grant
- 2009-02-25 KR KR1020107021331A patent/KR101569949B1/ko active IP Right Grant
- 2009-02-25 EP EP09714922.3A patent/EP2247588B1/en active Active
- 2009-02-25 GE GEAP200911952A patent/GEP20125664B/en unknown
- 2009-02-25 WO PCT/JP2009/054007 patent/WO2009107850A2/en active Application Filing
- 2009-02-25 ES ES09714922.3T patent/ES2586252T3/es active Active
- 2009-02-25 MY MYPI2010004006A patent/MY150379A/en unknown
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2010
- 2010-08-22 IL IL207735A patent/IL207735A/en active IP Right Grant
- 2010-08-25 ZA ZA2010/06063A patent/ZA201006063B/en unknown
- 2010-08-26 DO DO2010000260A patent/DOP2010000260A/es unknown
- 2010-08-31 CR CR11661A patent/CR11661A/es unknown
- 2010-09-21 MA MA33195A patent/MA32164B1/fr unknown
- 2010-09-23 CO CO10117653A patent/CO6321277A2/es active IP Right Grant
- 2010-09-23 EC EC2010010496A patent/ECSP10010496A/es unknown
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2011
- 2011-02-03 JP JP2011022188A patent/JP5490030B2/ja active Active
- 2011-04-29 HK HK11104328.2A patent/HK1150274A1/zh unknown
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