AR054047A1 - Derivados de fenilquinazolina - Google Patents
Derivados de fenilquinazolinaInfo
- Publication number
- AR054047A1 AR054047A1 ARP060102035A ARP060102035A AR054047A1 AR 054047 A1 AR054047 A1 AR 054047A1 AR P060102035 A ARP060102035 A AR P060102035A AR P060102035 A ARP060102035 A AR P060102035A AR 054047 A1 AR054047 A1 AR 054047A1
- Authority
- AR
- Argentina
- Prior art keywords
- hal
- atoms
- nhcoa
- mono
- so2naa
- Prior art date
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- 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
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- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- 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
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
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- 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
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Abstract
Nuevos derivados de fenilquinazolinas de la formula (1) en donde R1 es Hal, OH; OA, SH, SA, H o A, R2 y R3 son en cada caso, de modo independiente entre sí, -O-(X)s-Q,-S-(X)s-Q, -NHCO- (X) s -Q, -CONH- (X)s -Q, -CONA-(X)s-Q, NH(CO)NH-(X)s-Q, - NH(CO)O-(X)s-Q, -NHSO2-(X)s-Q, -SO2NH-(X)s-Q, -SO2NA-(X)s-Q, NHCOA, Hal, Het o H, en donde, en el caso de que R2 = H, entonces R3 es distinto H, o en caso de que R3 = H, entonces R2 es distinto de H, R4, R5 son en cada caso, de modo independiente entre sí, H, Hal, CN, NO2, A, OH, OA, SH, SA, (CH2)nCOOH, (CH2)nCOOA, O(CH2)0CONH2, CONHA, CONNA', NH2, NHA, NAA', NHCOOA, NHCO(CH2)nNH2, NHCONHA, SOA, SO2A; SO2NH2, SO2NHA, SO2NAA' u O(CH2)0Het1, dos radicales adyacentes, seleccionados del grupo R1, R2, R3, también son juntos metilendioxi o etilendioxi, A, A' son en cada caso, de modo independiente entre sí alquilo no ramificado o ramificado con 1-10 átomos de C, en donde 1-5 átomos de H pueden estar reemplazados por F, Cl y/o Br, Alk o alquilo cíclico con 3-7 átomos de C, A y A' también son juntos una cadena alquileno con 2, 3, 4, 5 o 6 átomos de C, en donde uno o dos grupos CH2, pueden estar reemplazados por O, S, SO, SO2; NH, NA y/o N-COOA, Alk es alquenilo con 2-6 átomos de C, X es alquileno C1-10 o alquenileno C2-C10 no ramificado o ramificado no sustituido o mono-, di-, tri - tetrasustituido con A, OA, OH, SH, SA, Hal, NO2, CN, Ar, O ar, COOH, COOA, CHO, C(=O)A, C(=O)Ar, SO2A, CONH2, SO2NH2, CONHA, XONNA', SO2NHA, SO2NAA?,NH2, NHA, NAA'OCONH2, OCONHA, OCONAA', NHCOA, NHCOOA, NACOOA, NHSO2OA, NASO2OA, NHCONH2, NACONH2, NHCONH2, NHCONHA, NACONHA; NHCONAA', NACONAA', y/u =O, en donde también uno, dos o tres grupos C pueden estar reemplazados por O, S, SO, SO2, NCO, NACO, CONH, CONA, SO2NH, SO2NA, NHSO2, NASO2 y/o por grupos NH, Q es H, Carb, Ar o Het, Carb es cicloalquilo con 3-7 átomos de C o cicloalquenilo con 3-7 átomos de C no sustituido o mono-, di, tri-, tetra- o pentasustituido con A, OA, OH, SH, SA, Hal, NO2; CN, (CH2)nAr', (CH2)nCOOH, (CH2)nCOOA, CHO, COA, SO2A, CONH2, SO2NH2, CONHA, CONAA', SO2NHA, SO2NAA', NH2, NHA, NAA', OCONH2, OCONHA, OCONAA', NHCOA, NHCOOA, NACOOA, NHSO2OA, NASO2OA, NHCONH, NACONH2, NHCONHA, NACONHA, NHCONAA' y/o NACONAA', Ar es fenilo, naftilo o bifenilo no sustituido o mono-, di-, tri-, tetra- o pentasustituido con A, OA, OH, SH, SA, Hal, NO2, CN (CH2)nAr', (CH2)nCOOA, CHO, COA, SO2A, CONH2, SO2NH2, CONHA, CONAA', SO2NHA, SO2NAA', NH2, NHA, NAA', OCoN2; OCONHA, OCONAA', NHCOA, NHCOA, NHCOOA, NACOOA, NHSO2OA, NASO2OA, NHCONH2, NACONH2, NHCONHA; NACONHA, NHCONAA', NACONAA', y/o tetraazol, Ar' es fenilo, naftilo o bifenilo no sustituido o mono-, di- o trisustituido con A, OA, OH, SH, SA, Hal, NO2, CH, (CH2)n fenilo, (CH2)nCOOH, (CH2)nCOOA, CHO, COA, SO2A, CONH2, SO2NH2, CONHA, CONAA', SO2NHA, SO2NAA', NH2, NHA, NAA', OCONH2, OCONHA, OCONAA', NHCOA, NACOOA, NHSO2OA, NASO2OA, NHCONH2, NACONH2, NHCONHA, NACONHA, NHCONAA' y/o NACONAA', Het es un heterociclo mono-, o bicíclico saturado, insaturado o aromático con 1 a 4 átomos de N, O y/o S, que puede estar mono-, di o trisustituido con A, OA, OH, SH,SA, Hal, NO2, CN, (CH2)nAr', (CH2)nCOOH, (CH2)nCOOA, CHO, COA, SO2A, CONH2, SO2nH2, CONHA, CONNA', SO2NHA, SO2NAA', NH2, NHA, NAA', OCONH2, OCONHA, OCONAA, NHCOA, NHCOOA, NACOOA, NHSO2OA, NASO2OA, NHCONH2, NACONH2, NHCONHA, NACONHA, NHCONAA', NACONAA', SO2A, =S, =NH, =NA y/u =O (oxígeno del carbonilo),,Het1 un heterociclo monocíclico saturado, insaturado o aromático con 1 a 2 átomos de N y/u O, que puede estar mono- o disustituido con A, OA, OH, Hal y/u =O (oxígeno el carbonilo), Hal es F Cl, Br, o I, n es 0, 1, 2, 3, o 4, o es 1, 2, o 3, s es 0, 1 o 2, así como sus derivados, sales, ,solvatos, tautomeros y estereoisomeros de utilidad farmacéutica, incluyendo sus mezclas en todas las proporciones. Son inhibidores de HSP90 y pueden ser utilizados para preparar un medicamento para el tratamiento de enfermedades en las que la inhibicion, la regulacion y/o la modulacion de la HSP90 desempana un papel importante
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005022977A DE102005022977A1 (de) | 2005-05-19 | 2005-05-19 | Phenylchinazolinderivate |
Publications (1)
Publication Number | Publication Date |
---|---|
AR054047A1 true AR054047A1 (es) | 2007-05-30 |
Family
ID=36763987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060102035A AR054047A1 (es) | 2005-05-19 | 2006-05-19 | Derivados de fenilquinazolina |
Country Status (15)
Country | Link |
---|---|
US (1) | US7947696B2 (es) |
EP (1) | EP1881965A1 (es) |
JP (1) | JP5075117B2 (es) |
KR (1) | KR20080016651A (es) |
CN (1) | CN101180278B (es) |
AR (1) | AR054047A1 (es) |
AU (1) | AU2006246744B2 (es) |
BR (1) | BRPI0610134A2 (es) |
CA (1) | CA2608766A1 (es) |
DE (1) | DE102005022977A1 (es) |
HK (1) | HK1119690A1 (es) |
MX (1) | MX2007014264A (es) |
RU (1) | RU2421449C2 (es) |
WO (1) | WO2006122631A1 (es) |
ZA (1) | ZA200710966B (es) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE541844T1 (de) * | 2005-12-21 | 2012-02-15 | Abbott Lab | Antivirale verbindungen |
AR061185A1 (es) * | 2006-05-26 | 2008-08-13 | Chugai Pharmaceutical Co Ltd | Compuestos heterociclicos como inhibidores de hsp90. composiciones farmaceuticas. |
EP2109612B1 (en) | 2007-02-01 | 2010-11-10 | AstraZeneca AB | 5,6,7,8-tetrahydropteridine derivatives as hsp90 inhibitors |
CL2008000629A1 (es) * | 2007-03-01 | 2008-08-29 | Chugai Pharmaceutical Co Ltd | Compuestos macrociclicos derivados de 6-aril-4-mercapto-[1.3.5]triazina/[1.3]pirimidin-2-amina; composicion farmaceutica, utiles en el tratamiento del cancer. |
ES2395114T3 (es) * | 2007-03-27 | 2013-02-08 | Synta Pharmaceuticals Corporation | Derivados de triazinona y de diazinona útiles como inhibidores de Hsp90 |
AU2008242983B2 (en) * | 2007-04-16 | 2013-07-11 | Abbvie Inc. | 7-substituted indole Mcl-1 inhibitors |
GB2449293A (en) * | 2007-05-17 | 2008-11-19 | Evotec | Compounds having Hsp90 inhibitory activity |
DE102007032739A1 (de) * | 2007-07-13 | 2009-01-15 | Merck Patent Gmbh | Chinazolinamidderivate |
GB0722680D0 (en) * | 2007-11-19 | 2007-12-27 | Topotarget As | Therapeutic compounds and their use |
US20110281908A1 (en) * | 2008-10-06 | 2011-11-17 | Emory University | Aminoquinoline Derived Heat Shock Protein 90 Inhibitors, Methods Of Preparing Same, And Methods For Their Use |
DE102008061214A1 (de) | 2008-12-09 | 2010-06-10 | Merck Patent Gmbh | Chinazolinamidderivate |
RU2015144653A (ru) | 2009-03-25 | 2018-12-29 | Эббви Инк. | Противовирусные соединения и их применения |
AR077405A1 (es) | 2009-07-10 | 2011-08-24 | Sanofi Aventis | Derivados del indol inhibidores de hsp90, composiciones que los contienen y utilizacion de los mismos para el tratamiento del cancer |
FR2949467B1 (fr) | 2009-09-03 | 2011-11-25 | Sanofi Aventis | Nouveaux derives de 5,6,7,8-tetrahydroindolizine inhibiteurs d'hsp90, compositions les contenant et utilisation |
DE102010046837A1 (de) * | 2010-09-29 | 2012-03-29 | Merck Patent Gmbh | Phenylchinazolinderivate |
MX2013007938A (es) * | 2011-01-07 | 2013-11-01 | Taiho Pharmaceutical Co Ltd | Compuesto biciclico novedoso o sal del mismo. |
AR091858A1 (es) | 2012-07-25 | 2015-03-04 | Sova Pharmaceuticals Inc | INHIBIDORES DE CISTATIONIN-g-LIASA (CSE) |
CA2952230C (en) * | 2014-06-13 | 2023-03-21 | Yuma Therapeutics, Inc. | Pyrimidine compounds and methods using the same |
CA3015417A1 (en) | 2016-03-01 | 2017-09-08 | Propellon Therapeutics Inc. | Inhibitors of wdr5 protein-protein binding |
EP3423451B1 (en) | 2016-03-01 | 2022-08-17 | Propellon Therapeutics Inc. | Inhibitors of wdr5 protein-protein binding |
KR101990669B1 (ko) * | 2016-05-31 | 2019-06-19 | 전남대학교산학협력단 | 퀴나졸린 유도체, 이의 제조방법 및 이를 함유하는 인플루엔자 바이러스 치료용 약학적 조성물 |
CN113286785A (zh) * | 2019-01-04 | 2021-08-20 | 贝尔布鲁克实验室有限责任公司 | 作为治疗剂的cGAS活性的抑制剂 |
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Publication number | Priority date | Publication date | Assignee | Title |
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JPH06192099A (ja) * | 1992-10-07 | 1994-07-12 | Sumitomo Pharmaceut Co Ltd | 腫瘍壊死因子産生阻害剤 |
US5646154A (en) | 1992-10-07 | 1997-07-08 | Sumitomo Pharmaceuticals Co., Ltd. | Pharmaceutical compositions for inhibiting the formation of tumor necrosis factor |
JPH11209350A (ja) * | 1998-01-26 | 1999-08-03 | Eisai Co Ltd | 含窒素複素環誘導体およびその医薬 |
AU2001293826A1 (en) * | 2000-09-25 | 2002-04-02 | Janssen Pharmaceutica N.V. | Farnesyl transferase inhibiting quinoline and quinazoline derivatives as farnesyl transferase inhibitors |
AR038658A1 (es) | 2001-06-15 | 2005-01-26 | Novartis Ag | Derivados de 4-aril-2(1h) quinazolinona y 4-aril-quinazolina 2-sustituidas, un proceso para su preparacion, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de un medicamento |
DE10163991A1 (de) * | 2001-12-24 | 2003-07-03 | Merck Patent Gmbh | Pyrrolo-pyrimidine |
KR101139314B1 (ko) | 2003-08-29 | 2012-04-26 | 베르날리스(캠브리지)리미티드 | 피리미도티오펜 화합물 |
EP1685115A1 (en) * | 2003-11-03 | 2006-08-02 | Warner-Lambert Company LLC | Novel norepinephrine reuptake inhibitors for the treatment of central nervous system disorders |
-
2005
- 2005-05-19 DE DE102005022977A patent/DE102005022977A1/de not_active Withdrawn
-
2006
- 2006-04-24 KR KR1020077029415A patent/KR20080016651A/ko not_active Application Discontinuation
- 2006-04-24 JP JP2008511580A patent/JP5075117B2/ja not_active Expired - Fee Related
- 2006-04-24 CA CA002608766A patent/CA2608766A1/en not_active Abandoned
- 2006-04-24 EP EP06724519A patent/EP1881965A1/de not_active Withdrawn
- 2006-04-24 MX MX2007014264A patent/MX2007014264A/es active IP Right Grant
- 2006-04-24 AU AU2006246744A patent/AU2006246744B2/en not_active Ceased
- 2006-04-24 BR BRPI0610134-8A patent/BRPI0610134A2/pt not_active IP Right Cessation
- 2006-04-24 US US11/914,604 patent/US7947696B2/en not_active Expired - Fee Related
- 2006-04-24 CN CN2006800174191A patent/CN101180278B/zh not_active Expired - Fee Related
- 2006-04-24 RU RU2007146388/04A patent/RU2421449C2/ru not_active IP Right Cessation
- 2006-04-24 WO PCT/EP2006/003734 patent/WO2006122631A1/de active Application Filing
- 2006-05-19 AR ARP060102035A patent/AR054047A1/es not_active Application Discontinuation
-
2007
- 2007-12-18 ZA ZA200710966A patent/ZA200710966B/xx unknown
-
2008
- 2008-10-28 HK HK08111820.5A patent/HK1119690A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO2006122631A1 (de) | 2006-11-23 |
CA2608766A1 (en) | 2006-11-23 |
RU2421449C2 (ru) | 2011-06-20 |
JP2008540587A (ja) | 2008-11-20 |
DE102005022977A1 (de) | 2006-12-07 |
JP5075117B2 (ja) | 2012-11-14 |
BRPI0610134A2 (pt) | 2010-06-01 |
ZA200710966B (en) | 2008-12-31 |
CN101180278B (zh) | 2011-05-04 |
HK1119690A1 (es) | 2009-03-13 |
CN101180278A (zh) | 2008-05-14 |
US20080214586A1 (en) | 2008-09-04 |
AU2006246744A1 (en) | 2006-11-23 |
MX2007014264A (es) | 2008-01-22 |
AU2006246744B2 (en) | 2011-11-03 |
EP1881965A1 (de) | 2008-01-30 |
KR20080016651A (ko) | 2008-02-21 |
RU2007146388A (ru) | 2009-06-27 |
US7947696B2 (en) | 2011-05-24 |
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