AR064246A1 - Derivados de 5h-pirimido[5,4-d][2]benzazepinas inhibidores de la progresion mitotica,composiciones farmaceuticas que los contienen y usos como agentes anticancer. - Google Patents
Derivados de 5h-pirimido[5,4-d][2]benzazepinas inhibidores de la progresion mitotica,composiciones farmaceuticas que los contienen y usos como agentes anticancer.Info
- Publication number
- AR064246A1 AR064246A1 ARP070105104A ARP070105104A AR064246A1 AR 064246 A1 AR064246 A1 AR 064246A1 AR P070105104 A ARP070105104 A AR P070105104A AR P070105104 A ARP070105104 A AR P070105104A AR 064246 A1 AR064246 A1 AR 064246A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- optionally substituted
- heteroaryl
- aryl
- aliphatic
- Prior art date
Links
- 239000002246 antineoplastic agent Substances 0.000 title 1
- 150000008038 benzoazepines Chemical class 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- -1 -OCH2CH3 Chemical group 0.000 abstract 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000006162 fluoroaliphatic group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Enzymes And Modification Thereof (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Un compuesto de la formula (I) o una de sus sales farmacéuticamente aceptables, en la que Ra se selecciona del grupo que consiste en grupo alifático C1-3 grupo fluoroalifático C1-3, -R1 , -R2, y T-R2, T es una cadena alquileno C1-3 opcionalmente sustituida con fluoro; R1 es un grupo arilo, heteroarilo, o heterociclilo, opcionalmente sustituido; R2 se selecciona del grupo que consiste en halo; -C:::C-R3; -N(R4)2; y -OR5; R3 es hidrogeno o un grupo alifático, arilo, heteroarilo, o heterociclilo, opcionalmente sustituido; cada R4 es independientemente hidrogeno o un grupo alifático, arilo, heteroarilo, o heterociclilo opcionalmente sustituido con dos R4 sobre el mismo átomo de nitrogeno, considerados junto con el átomo de nitrogeno forman un heteroarilo de 5 a 8 miembros o un anillo heterocíclilo de 4 a 8 miembros opcionalmente sustituido que tienen, en adicion al átomo de nitrogeno, 0,2 heteroátomos en el anillo seleccionados entre N, O y S; R5 es hidrogeno o un grupo alifático, arilo, heteroarilo o heterociclilo, opcionalmente sustituido; y Rb se selecciona del grupo que consiste en fluoro, cloro, -CH3, -CF3. -OH, OCH2, -OCF3, -OCH2CH3, y OCH2CF3.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85934006P | 2006-11-16 | 2006-11-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR064246A1 true AR064246A1 (es) | 2009-03-25 |
Family
ID=39315133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070105104A AR064246A1 (es) | 2006-11-16 | 2007-11-16 | Derivados de 5h-pirimido[5,4-d][2]benzazepinas inhibidores de la progresion mitotica,composiciones farmaceuticas que los contienen y usos como agentes anticancer. |
Country Status (34)
| Country | Link |
|---|---|
| US (7) | US8026246B2 (es) |
| EP (4) | EP2497773B1 (es) |
| JP (3) | JP5102839B2 (es) |
| KR (2) | KR101342014B1 (es) |
| CN (2) | CN103483343B (es) |
| AR (1) | AR064246A1 (es) |
| AT (1) | ATE556076T1 (es) |
| AU (1) | AU2007322046B2 (es) |
| BR (1) | BRPI0718803B8 (es) |
| CA (1) | CA2669680C (es) |
| CL (1) | CL2007003244A1 (es) |
| CR (3) | CR10782A (es) |
| CY (1) | CY1112828T1 (es) |
| DK (2) | DK2497772T3 (es) |
| EA (1) | EA015779B1 (es) |
| ES (3) | ES2384123T3 (es) |
| GE (1) | GEP20125459B (es) |
| HR (2) | HRP20120490T1 (es) |
| IL (1) | IL198690A0 (es) |
| MA (1) | MA30988B1 (es) |
| MX (3) | MX348568B (es) |
| MY (1) | MY153243A (es) |
| NO (1) | NO343338B1 (es) |
| NZ (3) | NZ577042A (es) |
| PH (1) | PH12012502057B1 (es) |
| PL (2) | PL2086981T3 (es) |
| PT (2) | PT2086981E (es) |
| RS (2) | RS52313B (es) |
| SG (2) | SG10201503350TA (es) |
| SI (2) | SI2086981T1 (es) |
| TW (1) | TWI401255B (es) |
| UA (1) | UA94129C2 (es) |
| WO (1) | WO2008063525A1 (es) |
| ZA (1) | ZA200903279B (es) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ551370A (en) | 2004-05-14 | 2009-08-28 | Millennium Pharm Inc | Compounds and methods for inhibiting mitotic progression by inhibiting of aurora kinase |
| CL2007003244A1 (es) | 2006-11-16 | 2008-04-04 | Millennium Pharm Inc | Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer. |
| AR074487A1 (es) * | 2008-12-05 | 2011-01-19 | Millennium Pharm Inc | Tiolactamas inhibidoras de proteinquinasas plk, composiciones farmaceuticas que las contienen y usos de las mismas para el tratamiento de trastornos proliferativos e inflamatorios, en particular cancer. |
| CA2747326C (en) * | 2008-12-22 | 2017-05-16 | Millennium Pharmaceuticals, Inc. | Combination of aurora kinase inhibitors and anti-cd20 antibodies |
| JO3635B1 (ar) * | 2009-05-18 | 2020-08-27 | Millennium Pharm Inc | مركبات صيدلانية صلبة وطرق لانتاجها |
| JO3434B1 (ar) | 2009-07-31 | 2019-10-20 | Millennium Pharm Inc | مركبات صيدلانية لمعالجة السرطان وامراض واضطرابات اخري |
| BR112012020557A8 (pt) * | 2010-02-19 | 2018-01-02 | Millennium Pharm Inc | formas cristalinas de 4-{[9-cloro-7-(2-flúor-6-metoifenil)-5h-pirimido[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoato de sódio |
| US20120107304A1 (en) | 2010-04-27 | 2012-05-03 | Boehringer Ingelheim International Gmbh | Combination therapy in treatment of oncological and fibrotic diseases |
| ES2526671T3 (es) * | 2010-06-22 | 2015-01-14 | Glaxosmithkline Llc | Compuestos de benzotriazoldiazepina inhibidores de bromodominios |
| AR086656A1 (es) * | 2011-06-03 | 2014-01-15 | Millennium Pharm Inc | Combinacion de inhibidores de mek e inhibidores selectivos de la quinasa aurora a |
| US20130303519A1 (en) * | 2012-03-20 | 2013-11-14 | Millennium Pharmaceuticals, Inc. | Methods of treating cancer using aurora kinase inhibitors |
| CN103772391A (zh) * | 2012-10-23 | 2014-05-07 | 杨子娇 | 一类治疗房角狭窄的化合物及其用途 |
| CA2907726A1 (en) * | 2013-03-22 | 2014-09-25 | Millennium Pharmaceuticals, Inc. | Combination of catalytic mtorc1/2 inhibitors and selective inhibitors of aurora a kinase |
| US10335494B2 (en) | 2013-12-06 | 2019-07-02 | Millennium Pharmaceuticals, Inc. | Combination of aurora kinase inhibitors and anti-CD30 antibodies |
| US20180263979A1 (en) * | 2014-12-23 | 2018-09-20 | Millennium Pharmaceuticals, Inc. | Combination of raf inhibitors and aurora kinase inhibitors |
| US20180207173A1 (en) | 2015-07-21 | 2018-07-26 | Millennium Pharmaceuticals, Inc. | Administration of aurora kinase inhibitor and chemotherapeutic agents |
| WO2017044567A1 (en) | 2015-09-09 | 2017-03-16 | Icahn School Of Medicine At Mount Sinai | Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents |
| CA2997784A1 (en) | 2015-09-09 | 2017-03-16 | Icahn School Of Medicine At Mount Sinai | Heterocyclic constrained tricyclic sulfonamides as anti-cancer agents |
| WO2017146253A1 (ja) | 2016-02-26 | 2017-08-31 | 公益財団法人がん研究会 | Hp1の機能に着目した抗癌剤のスクリーニング方法及び評価系 |
| EP3429571B1 (en) | 2016-03-15 | 2025-10-08 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors for use in the treatment of neoplastic diseases |
| JP6188986B1 (ja) * | 2017-03-23 | 2017-08-30 | 株式会社ノエビア | 時計遺伝子発現量調整剤及びエラスチン産生促進剤 |
| WO2019195658A1 (en) | 2018-04-05 | 2019-10-10 | Dana-Farber Cancer Institute, Inc. | Sting levels as a biomarker for cancer immunotherapy |
| WO2020049208A1 (es) | 2018-09-09 | 2020-03-12 | Fundacio Privada Institut De Recerca De La Sida - Caixa | Aurora cinasa como diana para tratar, prevenir o curar una infección por vih o sida |
| US20220305048A1 (en) | 2019-08-26 | 2022-09-29 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
| EP4504710A1 (en) | 2022-04-07 | 2025-02-12 | Eli Lilly and Company | Process for making a kras g12c inhibitor |
| US20250249019A1 (en) | 2022-04-08 | 2025-08-07 | Eli Lilly And Company | Method of treatment including kras g12c inhibitors and aurora a inhibitors |
| AU2023297941A1 (en) | 2022-06-30 | 2025-01-16 | Eli Lilly And Company | Kras g12c inhibitor for treating cancer |
| WO2025075211A1 (en) | 2023-10-03 | 2025-04-10 | Takeda Pharmaceutical Company Limited | Alisertib and paclitaxel for treating small cell lung cancer |
| WO2025245045A1 (en) | 2024-05-21 | 2025-11-27 | The Regents Of The University Of California | Methods of treating lung cancer |
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| NZ551370A (en) | 2004-05-14 | 2009-08-28 | Millennium Pharm Inc | Compounds and methods for inhibiting mitotic progression by inhibiting of aurora kinase |
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| JP2008526723A (ja) | 2004-12-30 | 2008-07-24 | アステックス、セラピューティックス、リミテッド | Cdk、gsk及びオーロラキナーゼの活性を調節するピラゾール誘導体 |
| DK1962830T3 (da) | 2005-12-23 | 2013-06-24 | Glaxosmithkline Llc | Azaindolhæmmere af aurorakinaser. |
| EP2054413A2 (en) | 2006-08-09 | 2009-05-06 | Millennium Pharmaceuticals, Inc. | Pyridobenzazepine compounds and methods for inhibiting mitotic progression |
| CL2007003244A1 (es) | 2006-11-16 | 2008-04-04 | Millennium Pharm Inc | Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer. |
| JO3635B1 (ar) | 2009-05-18 | 2020-08-27 | Millennium Pharm Inc | مركبات صيدلانية صلبة وطرق لانتاجها |
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2007
- 2007-11-09 CL CL200703244A patent/CL2007003244A1/es unknown
- 2007-11-14 BR BRPI0718803A patent/BRPI0718803B8/pt active IP Right Grant
- 2007-11-14 MX MX2012011396A patent/MX348568B/es unknown
- 2007-11-14 TW TW096143087A patent/TWI401255B/zh active
- 2007-11-14 SI SI200730975T patent/SI2086981T1/sl unknown
- 2007-11-14 ES ES07867449T patent/ES2384123T3/es active Active
- 2007-11-14 ZA ZA200903279A patent/ZA200903279B/xx unknown
- 2007-11-14 JP JP2009537199A patent/JP5102839B2/ja active Active
- 2007-11-14 ES ES12153134.7T patent/ES2537451T3/es active Active
- 2007-11-14 GE GEAP200711309A patent/GEP20125459B/en unknown
- 2007-11-14 RS RS20120247A patent/RS52313B/sr unknown
- 2007-11-14 MY MYPI20091846A patent/MY153243A/en unknown
- 2007-11-14 EP EP12153134.7A patent/EP2497773B1/en active Active
- 2007-11-14 RS RS20150047A patent/RS53788B1/sr unknown
- 2007-11-14 NZ NZ577042A patent/NZ577042A/en unknown
- 2007-11-14 EA EA200970486A patent/EA015779B1/ru unknown
- 2007-11-14 CN CN201310367332.9A patent/CN103483343B/zh active Active
- 2007-11-14 DK DK12153131.3T patent/DK2497772T3/en active
- 2007-11-14 SI SI200731591T patent/SI2497772T1/sl unknown
- 2007-11-14 EP EP07867449A patent/EP2086981B1/en active Active
- 2007-11-14 HR HRP20120490TT patent/HRP20120490T1/hr unknown
- 2007-11-14 PT PT07867449T patent/PT2086981E/pt unknown
- 2007-11-14 WO PCT/US2007/023948 patent/WO2008063525A1/en not_active Ceased
- 2007-11-14 KR KR1020117022355A patent/KR101342014B1/ko active Active
- 2007-11-14 AU AU2007322046A patent/AU2007322046B2/en active Active
- 2007-11-14 MX MX2009004670A patent/MX2009004670A/es active IP Right Grant
- 2007-11-14 KR KR1020097012501A patent/KR101110458B1/ko active Active
- 2007-11-14 AT AT07867449T patent/ATE556076T1/de active
- 2007-11-14 UA UAA200906211A patent/UA94129C2/ru unknown
- 2007-11-14 PT PT121531313T patent/PT2497772E/pt unknown
- 2007-11-14 SG SG10201503350TA patent/SG10201503350TA/en unknown
- 2007-11-14 CN CN2007800423837A patent/CN101547924B/zh active Active
- 2007-11-14 NZ NZ597252A patent/NZ597252A/xx unknown
- 2007-11-14 NZ NZ611898A patent/NZ611898A/en not_active IP Right Cessation
- 2007-11-14 PL PL07867449T patent/PL2086981T3/pl unknown
- 2007-11-14 SG SG2011080652A patent/SG176443A1/en unknown
- 2007-11-14 EP EP12153131.3A patent/EP2497772B1/en active Active
- 2007-11-14 CA CA2669680A patent/CA2669680C/en active Active
- 2007-11-14 US US11/985,277 patent/US8026246B2/en active Active
- 2007-11-14 PL PL12153131T patent/PL2497772T3/pl unknown
- 2007-11-14 ES ES12153131.3T patent/ES2528793T3/es active Active
- 2007-11-14 DK DK07867449.6T patent/DK2086981T3/da active
- 2007-11-14 MX MX2012011398A patent/MX343391B/es unknown
- 2007-11-14 EP EP15155821.0A patent/EP2944639B1/en active Active
- 2007-11-16 AR ARP070105104A patent/AR064246A1/es unknown
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2009
- 2009-05-08 CR CR10782A patent/CR10782A/es unknown
- 2009-05-11 IL IL198690A patent/IL198690A0/en active IP Right Grant
- 2009-05-13 NO NO20091864A patent/NO343338B1/no unknown
- 2009-06-12 MA MA31985A patent/MA30988B1/fr unknown
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2011
- 2011-08-25 US US13/217,729 patent/US9988384B2/en active Active
- 2011-08-25 US US13/217,659 patent/US20110312942A1/en not_active Abandoned
- 2011-08-30 JP JP2011187930A patent/JP5452811B2/ja active Active
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2012
- 2012-06-06 CY CY20121100518T patent/CY1112828T1/el unknown
- 2012-10-12 PH PH12012502057A patent/PH12012502057B1/en unknown
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2013
- 2013-11-15 JP JP2013236439A patent/JP2014055166A/ja active Pending
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2014
- 2014-04-04 CR CR20140154A patent/CR20140154A/es unknown
- 2014-10-15 US US14/514,687 patent/US9765076B2/en active Active
- 2014-11-27 CR CR20140544A patent/CR20140544A/es unknown
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2015
- 2015-01-13 HR HRP20150047TT patent/HRP20150047T1/hr unknown
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2018
- 2018-06-01 US US15/996,166 patent/US10836766B2/en active Active
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2020
- 2020-11-16 US US17/099,266 patent/US11958855B2/en active Active
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2024
- 2024-03-07 US US18/598,629 patent/US20240400567A1/en active Pending
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