AR066876A1 - Derivados de amida para inhibir el crecimiento de celulas cancerigenas y una composicion farmaceutica que los comprende. - Google Patents
Derivados de amida para inhibir el crecimiento de celulas cancerigenas y una composicion farmaceutica que los comprende.Info
- Publication number
- AR066876A1 AR066876A1 ARP080102395A ARP080102395A AR066876A1 AR 066876 A1 AR066876 A1 AR 066876A1 AR P080102395 A ARP080102395 A AR P080102395A AR P080102395 A ARP080102395 A AR P080102395A AR 066876 A1 AR066876 A1 AR 066876A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- substituted
- alkoxy
- aryl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
- 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Derivado de amida y una sal farmacéuticamente aceptable del mismo que inhibe el crecimiento de las células cancerígenas inducido por la sobreexpresion de un receptor del factor de crecimiento epidérmico y también evita el desarrollo de la resistencia a las drogas causado por la mutacion de la EGFR tirosina quinasa, y a una composicion farmacéutica que comprende el mismo como un ingrediente activo. Reivindicacion 1: Un derivado de amida de formula (1) o una sal farmacéuticamente aceptable del mismo: caracterizado porque: A es el grupo de formulas (2) siendo R4, R5, R6 y R7 cada uno independientemente hidrogeno, halogeno, N-alquilo C1-6 o N-hidroxi amido o C-alquilo C1-6 amido inverso(-NHCOC1-6), hidroxicarbonilo (-COOH), alquiloxicarbonilo C1-6 (-COOC1-6) alquilo C1-6, o alquilo C1-6 substituido con un grupo hidroxi, dialquilamina C1-6 o grupo heterocíclico; R1 es un grupo arilo o heterocíclico substituido con uno a cinco X, o alquilo C1-6 substituido con arilo; R2 es hidrogeno, hidroxi, alcoxi C1-6, o alcoxi C1-6 substituido con un grupo alcoxi C1-6 o heterocíclico; R3 es hidrogeno, -COOH, alquiloxicarbonilo C1-6, o amido N-no substituido o N-substituido con Y; na y nb son cada uno un entero que oscila entre 0 y 6; en donde: x es hidrogeno, halogeno, hidroxi, ciano, nitro, (mono-, di-, o trihalogeno)metilo, mercapto, alquiltio C1-6, acrilamido, alquilo C1-6, alquenilo C1-6, alquinilo C1-6, alcoxi C1-6, ariloxi, dialquilamino C1-6, o alquilo C1-6 o alcoxi C1-6 substituido con Z, con la condicion de que cuando el numero de X es dos o más, los grupos X pueden fusionarse entre sí para formar una estructura de anillo; Y es hidroxi, alquilo C1-6 o alquilo C1-6 substituido con Z, conteniendo el alquilo C1-6 una a cuatro de la parte seleccionada entre el grupo que consiste en N, O, S, SO y SO2 y Z es un grupo alquilo C1-6, arilo o heterocíclico, siendo dicho grupo arilo un grupo aromático monocíclico o bicíclico C5-12, siendo dicho grupo heterocíclico un grupo aromático o no aromático monocíclico o bicíclico C5-12 que contiene una a cuatro de la parte seleccionada entre el grupo que consiste en N, O, S, SO y SO2 y siendo dichos grupos arilo y heterocíclico no substituidos o substituidos con substituyente seleccionados entre el grupo que consiste en halogeno, hidroxilo, amino, nitro, ciano, alquilo C1-6, alquenilo C1-6, alquinilo C1-6, alcoxi C1-6, monoalquilamino C1-6 y dialquilamino C1-6.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20070054997 | 2007-06-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR066876A1 true AR066876A1 (es) | 2009-09-16 |
Family
ID=40094307
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080102395A AR066876A1 (es) | 2007-06-05 | 2008-06-05 | Derivados de amida para inhibir el crecimiento de celulas cancerigenas y una composicion farmaceutica que los comprende. |
ARP170103011A AR110003A2 (es) | 2007-06-05 | 2017-10-30 | Derivado de amida |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP170103011A AR110003A2 (es) | 2007-06-05 | 2017-10-30 | Derivado de amida |
Country Status (25)
Country | Link |
---|---|
US (1) | US8188102B2 (es) |
EP (1) | EP2167492B1 (es) |
JP (1) | JP5155391B2 (es) |
KR (1) | KR101013319B1 (es) |
CN (1) | CN101679384B (es) |
AR (2) | AR066876A1 (es) |
AU (1) | AU2008260772B2 (es) |
BR (1) | BRPI0811069B1 (es) |
CA (1) | CA2687180C (es) |
DK (1) | DK2167492T3 (es) |
ES (1) | ES2558623T3 (es) |
HK (1) | HK1142591A1 (es) |
HR (1) | HRP20160007T1 (es) |
HU (1) | HUE028243T2 (es) |
IL (1) | IL202154A (es) |
MX (1) | MX2009012772A (es) |
MY (1) | MY144972A (es) |
NZ (1) | NZ582412A (es) |
PL (1) | PL2167492T3 (es) |
PT (1) | PT2167492E (es) |
RU (1) | RU2434010C2 (es) |
TW (1) | TWI377944B (es) |
UA (1) | UA96045C2 (es) |
WO (1) | WO2008150118A2 (es) |
ZA (1) | ZA201000022B (es) |
Families Citing this family (61)
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SG174774A1 (en) | 2006-09-11 | 2011-10-28 | Curis Inc | Quinazoline based egfr inhibitors containing a zinc binding moiety |
US8119616B2 (en) | 2007-09-10 | 2012-02-21 | Curis, Inc. | Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety |
ES2659725T3 (es) | 2009-05-05 | 2018-03-19 | Dana-Farber Cancer Institute, Inc. | Inhibidores de EGFR y procedimiento de tratamiento de trastornos |
KR101217526B1 (ko) * | 2010-06-11 | 2013-01-02 | 한미사이언스 주식회사 | 아마이드 유도체 또는 이의 약학적으로 허용 가능한 염을 포함하는 약제학적 조성물 |
US8828391B2 (en) | 2011-05-17 | 2014-09-09 | Boehringer Ingelheim International Gmbh | Method for EGFR directed combination treatment of non-small cell lung cancer |
KR101317809B1 (ko) | 2011-06-07 | 2013-10-16 | 한미약품 주식회사 | 암세포의 성장을 억제하는 아마이드 유도체 및 비금속염 활택제를 포함하는 약학 조성물 |
KR101272613B1 (ko) * | 2011-10-05 | 2013-06-10 | 한미사이언스 주식회사 | 1-(4-(4-(3,4-디클로로-2-플루오로페닐아미노)-7-메톡시퀴나졸린-6-일옥시)피페리딘-1-일)프로프-2-엔-1-온 염산염의 제조 방법 및 이에 사용되는 중간체 |
US9464089B2 (en) | 2012-01-13 | 2016-10-11 | Acea Biosciences Inc. | Heterocyclic compounds and uses thereof |
US9586965B2 (en) | 2012-01-13 | 2017-03-07 | Acea Biosciences Inc. | Pyrrolo[2,3-d]pyrimidine compounds as inhibitors of protein kinases |
US9034885B2 (en) | 2012-01-13 | 2015-05-19 | Acea Biosciences Inc. | EGFR modulators and uses thereof |
CA2861010A1 (en) | 2012-01-13 | 2013-07-18 | Xiao Xu | Heterocyclic compounds and uses as anticancer agents |
CN104080774B (zh) | 2012-01-17 | 2017-02-22 | 安斯泰来制药株式会社 | 吡嗪甲酰胺化合物 |
CN102659764A (zh) * | 2012-04-16 | 2012-09-12 | 中国科学院广州生物医药与健康研究院 | 酪氨酸激酶不可逆抑制剂及其制备方法和用途 |
KR20140096571A (ko) * | 2013-01-28 | 2014-08-06 | 한미약품 주식회사 | 1-(4-(4-(3,4-디클로로-2-플루오로페닐아미노)-7-메톡시퀴나졸린-6-일옥시)피페리딘-1-일)프로프-2-엔-1-온의 제조방법 |
CA2917364C (en) | 2013-07-11 | 2020-09-29 | Acea Biosciences Inc. | Heterocyclic compounds and uses thereof |
CN104513229A (zh) * | 2013-09-28 | 2015-04-15 | 正大天晴药业集团股份有限公司 | 喹唑啉衍生物及其制备方法 |
WO2015154725A1 (zh) * | 2014-04-11 | 2015-10-15 | 四川海思科制药有限公司 | 喹唑啉衍生物及其制备方法和在医药上的应用 |
JP6769962B2 (ja) * | 2014-12-03 | 2020-10-14 | オークランド ユニサービシーズ リミティド | 癌治療のためのキナーゼ阻害剤プロドラッグ |
US10231973B2 (en) * | 2015-03-20 | 2019-03-19 | Chai Tai Tianqing Pharmaceutical Group Co., Ltd. | Salts of quinazoline derivative and method for preparing the same |
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JP7036798B2 (ja) * | 2016-08-25 | 2022-03-15 | 正大天晴▲藥▼▲業▼集▲団▼股▲フン▼有限公司 | キナゾリン誘導体の塩の結晶 |
CN108069946B (zh) * | 2016-11-08 | 2020-06-05 | 威尚(上海)生物医药有限公司 | 具有穿过血脑屏障能力的取代的喹唑啉化合物 |
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KR20210066841A (ko) * | 2018-09-21 | 2021-06-07 | 스펙트럼 파마슈티컬즈 인크 | 신규한 퀴나졸린 egfr 억제제 |
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EP4097140A4 (en) * | 2020-01-29 | 2023-10-18 | Board of Regents, The University of Texas System | USE OF QUINAZOLINE-BASED TYROSINE KINASE INHIBITORS TO TREAT CANCER WITH NRG1 FUSIONS |
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CN115894486B (zh) * | 2021-09-30 | 2024-02-09 | 北京赛特明强医药科技有限公司 | 一种氢化吡啶并喹唑啉类化合物、组合物及其应用 |
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AU2003226705B2 (en) | 2002-03-30 | 2008-11-06 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 4-(N-phenylamino)-quinazolines / quinolines as tyrosine kinase inhibitors |
GB0309009D0 (en) * | 2003-04-22 | 2003-05-28 | Astrazeneca Ab | Quinazoline derivatives |
UY28441A1 (es) * | 2003-07-29 | 2005-02-28 | Astrazeneca Ab | Derivados de quinazolina |
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BRPI0414735A (pt) | 2003-09-25 | 2006-11-21 | Astrazeneca Ab | derivado de quinazolina, composto, composição farmacêutica, uso de derivado de quinazolina, método para produzir um efeito anti-proliferativo em um animal de sangue quente, e, processo para a preparação de um derivado de quinazolina |
GB0322409D0 (en) * | 2003-09-25 | 2003-10-29 | Astrazeneca Ab | Quinazoline derivatives |
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US20100234371A1 (en) * | 2005-08-22 | 2010-09-16 | Frank Himmelsbach | Bicyclic heterocycles, pharmaceutical compositions containing these compounds, the use thereof and processes for the preparation thereof |
WO2007055513A1 (en) * | 2005-11-08 | 2007-05-18 | Hanmi Pharm. Co., Ltd. | Quinazoline derivatives as a signal transduction inhibitor and method for the preparation thereof |
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2008
- 2008-06-04 TW TW097120707A patent/TWI377944B/zh not_active IP Right Cessation
- 2008-06-05 JP JP2010511117A patent/JP5155391B2/ja active Active
- 2008-06-05 KR KR1020080052867A patent/KR101013319B1/ko active IP Right Grant
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