MX2009006397A - Derivados de imidazotiazol. - Google Patents
Derivados de imidazotiazol.Info
- Publication number
- MX2009006397A MX2009006397A MX2009006397A MX2009006397A MX2009006397A MX 2009006397 A MX2009006397 A MX 2009006397A MX 2009006397 A MX2009006397 A MX 2009006397A MX 2009006397 A MX2009006397 A MX 2009006397A MX 2009006397 A MX2009006397 A MX 2009006397A
- Authority
- MX
- Mexico
- Prior art keywords
- protein
- inhibit
- interaction
- show
- mdm2
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
-
- 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
- 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
- C07D513/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Abstract
Se pretende proveer compuestos novedosos que inhiben la interacción entre la proteína Mdm2 (dobles di-minutos murinos) y la proteína p53 y muestra una actividad antitumoral; están provistos los derivados de 'midazotiazol que tienen varios sustituyentes como se representa por la siguiente fórmula general (1), la cual inhibe la interacción entre la proteína Md2 y la proteína p53 y muestra una actividad antitumoral, en donde R1, R2, R3, R4 y R5 en la fórmula general (1) cada uno son como se definen en la descripción. (ver fórmula (1)).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006336662 | 2006-12-14 | ||
PCT/JP2007/073930 WO2008072655A1 (ja) | 2006-12-14 | 2007-12-12 | イミダゾチアゾール誘導体 |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009006397A true MX2009006397A (es) | 2009-08-13 |
Family
ID=39511672
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009006397A MX2009006397A (es) | 2006-12-14 | 2007-12-12 | Derivados de imidazotiazol. |
Country Status (11)
Country | Link |
---|---|
US (1) | US20090312310A1 (es) |
EP (1) | EP2103619A4 (es) |
JP (1) | JPWO2008072655A1 (es) |
KR (1) | KR20090090383A (es) |
CN (1) | CN101605798A (es) |
AU (1) | AU2007332493A1 (es) |
BR (1) | BRPI0720546A2 (es) |
CA (1) | CA2672565A1 (es) |
MX (1) | MX2009006397A (es) |
TW (1) | TW200831518A (es) |
WO (1) | WO2008072655A1 (es) |
Families Citing this family (40)
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US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
WO2009151069A1 (ja) * | 2008-06-12 | 2009-12-17 | 第一三共株式会社 | 4,7-ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
JP2011037819A (ja) * | 2008-11-21 | 2011-02-24 | Tosoh Corp | ヒドロキシアルキルトリエチレンジアミン類の製造方法 |
DK2380892T3 (da) * | 2009-01-16 | 2014-06-30 | Daiichi Sankyo Co Ltd | Imidazothiazolderivat med prolinringstruktur |
NZ600430A (en) | 2009-11-12 | 2014-06-27 | Univ Michigan | Spiro-oxindole mdm2 antagonists |
WO2012064973A2 (en) | 2010-11-10 | 2012-05-18 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
EA201390682A1 (ru) | 2010-11-12 | 2014-01-30 | Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган | Спирооксиндольные антагонисты mdm2 |
CN103648499B (zh) | 2011-01-10 | 2017-02-15 | 无限药品股份有限公司 | 用于制备异喹啉酮的方法及异喹啉酮的固体形式 |
JP2014513699A (ja) | 2011-05-11 | 2014-06-05 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | スピロ−オキシインドールmdm2アンタゴニスト |
CA2842190A1 (en) | 2011-07-19 | 2013-01-24 | Infinity Pharmaceuticals Inc. | Heterocyclic compounds and uses thereof |
EP2734520B1 (en) | 2011-07-19 | 2016-09-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2013032591A1 (en) | 2011-08-29 | 2013-03-07 | Infinity Pharmaceuticals Inc. | Heterocyclic compounds and uses thereof |
US9630979B2 (en) | 2011-09-29 | 2017-04-25 | Infinity Pharmaceuticals, Inc. | Inhibitors of monoacylglycerol lipase and methods of their use |
US8969341B2 (en) * | 2011-11-29 | 2015-03-03 | Novartis Ag | Pyrazolopyrrolidine compounds |
US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
ES2691742T5 (es) | 2012-11-01 | 2022-03-18 | Infinity Pharmaceuticals Inc | Tratamiento de cánceres utilizando moduladores de isoformas de PI3 cinasa |
CA2895504A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
NZ629037A (en) | 2013-03-15 | 2017-04-28 | Infinity Pharmaceuticals Inc | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
US20160113932A1 (en) | 2013-05-30 | 2016-04-28 | Infinity Pharmaceuticals, Inc. | Treatment of cancers using pi3 kinase isoform modulators |
CA2925944C (en) | 2013-10-04 | 2023-01-10 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2015051241A1 (en) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2015061204A1 (en) | 2013-10-21 | 2015-04-30 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
EP4066834A1 (en) | 2014-03-19 | 2022-10-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds for use in the treatment of pi3k-gamma mediated disorders |
WO2015160975A2 (en) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Combination therapies |
US20150320754A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
WO2015168079A1 (en) | 2014-04-29 | 2015-11-05 | Infinity Pharmaceuticals, Inc. | Pyrimidine or pyridine derivatives useful as pi3k inhibitors |
BR112016029662B1 (pt) | 2014-06-19 | 2023-10-24 | Takeda Pharmaceutical Company Limited | COMPOSTO DE FÓRMULA Bf OU UMA FORMA FARMACEUTICAMENTE ACEITÁVEL DO MESMO, COMPOSIÇÃO FARMACÊUTICA COMPREENDENDO O MESMO E SEU USO |
WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US11192898B2 (en) | 2016-04-06 | 2021-12-07 | The Regents Of The University Of Michigan | MDM2 protein degraders |
CA3020281A1 (en) | 2016-04-06 | 2017-10-12 | The Regents Of The University Of Michigan | Monofunctional intermediates for ligand-dependent target protein degradation |
PL3458101T3 (pl) | 2016-05-20 | 2021-05-31 | F. Hoffmann-La Roche Ag | Koniugaty PROTAC-przeciwciało i sposoby ich stosowania |
US10919914B2 (en) | 2016-06-08 | 2021-02-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
WO2017223422A1 (en) | 2016-06-24 | 2017-12-28 | Infinity Pharmaceuticals, Inc. | Combination therapies |
KR101948805B1 (ko) * | 2016-07-05 | 2019-02-15 | 한국과학기술연구원 | 항종양 효과를 갖는 이미다조옥사졸 유도체 및 이를 포함하는 약학적 조성물 |
US11332479B2 (en) | 2016-07-05 | 2022-05-17 | Korea Institute Of Science And Technology | Imidazooxazole derivative having antitumor effect, and pharmaceutical composition including same |
JP2022504541A (ja) | 2018-10-08 | 2022-01-13 | ザ リージェンツ オブ ザ ユニバーシティー オブ ミシガン | 低分子mdm2タンパク質デグレーダー |
EP4121043A1 (en) | 2020-03-19 | 2023-01-25 | Kymera Therapeutics, Inc. | Mdm2 degraders and uses thereof |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
US11548866B1 (en) | 2021-11-22 | 2023-01-10 | Ligature Therapeutics Pte. Ltd. | Therapeutic compounds and methods of use thereof |
US11504381B1 (en) * | 2021-11-22 | 2022-11-22 | Ligature Therapeutics Pte. Ltd. | Therapeutic compounds and methods of use thereof |
Family Cites Families (26)
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CA1271480A (en) * | 1985-04-22 | 1990-07-10 | Toyo Jozo Co., Ltd. | 5,6-dihydroimidazo[2,1-b]thiazole-2-carboxamide derivatives or salts thereof |
JP3670309B2 (ja) * | 1993-04-01 | 2005-07-13 | 第一製薬株式会社 | 二環性複素環化合物 |
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GB9819860D0 (en) | 1998-09-12 | 1998-11-04 | Zeneca Ltd | Chemical compounds |
CA2360671A1 (en) * | 1999-01-29 | 2000-08-03 | The Board Of Trustees Of The University Of Illinois | P53 inhibitors and therapeutic use of the same |
US6740495B1 (en) | 2000-04-03 | 2004-05-25 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase assay |
US6979551B2 (en) | 2000-04-03 | 2005-12-27 | Rigel Pharmaceuticals, Inc. | Assays for identifying ubiquitin agents and for identifying agents that modify the activity of ubiquitin agents |
JP2002105085A (ja) * | 2000-09-28 | 2002-04-10 | Yamanouchi Pharmaceut Co Ltd | 新規イミダゾチアゾール誘導体 |
JP4497921B2 (ja) | 2001-11-13 | 2010-07-07 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換1,4−ベンゾジアゼピンおよび癌の処置のためのその使用 |
JP4477351B2 (ja) | 2001-12-18 | 2010-06-09 | エフ.ホフマン−ラ ロシュ アーゲー | シス−2,4,5−トリフェニル−イミダゾリン類及び腫瘍の処理へのそれらの使用 |
EP1463501B1 (en) | 2001-12-18 | 2008-06-11 | F. Hoffmann-La Roche AG | Cis-imidazolines as mdm2 inhibitors |
WO2003095625A2 (en) | 2002-05-13 | 2003-11-20 | 3-Dimensional Pharmaceuticals, Inc. | Method for cytoprotection through mdm2 and hdm2 inhibition |
GB0215650D0 (en) * | 2002-07-05 | 2002-08-14 | Cyclacel Ltd | Bisarylsufonamide compounds |
US20040197893A1 (en) | 2002-10-16 | 2004-10-07 | Carsten Schubert | HDM2-inhibitor complexes and uses thereof |
US6916833B2 (en) | 2003-03-13 | 2005-07-12 | Hoffmann-La Roche Inc. | Substituted piperidines |
EA200501513A1 (ru) | 2003-04-25 | 2006-06-30 | Орто-Макнейл Фармасьютикал, Инк. | Замещённые 1, 4 - диазепины и их применения |
US20040213264A1 (en) | 2003-04-25 | 2004-10-28 | Nortel Networks Limited | Service class and destination dominance traffic management |
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US7425638B2 (en) | 2003-06-17 | 2008-09-16 | Hoffmann-La Roche Inc. | Cis-imidazolines |
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EP1643989B1 (en) | 2003-06-17 | 2010-04-28 | F. Hoffmann-La Roche Ag | Cis-imidazolines as mdm2 inhibitors |
ATE414693T1 (de) | 2004-05-18 | 2008-12-15 | Hoffmann La Roche | Neuartige cis-imidazoline |
US7893278B2 (en) | 2004-06-17 | 2011-02-22 | Hoffman-La Roche Inc. | CIS-imidazolines |
GB0419481D0 (en) | 2004-09-02 | 2004-10-06 | Cancer Rec Tech Ltd | Isoindolin-1-one derivatives |
EA019566B1 (ru) | 2005-02-22 | 2014-04-30 | Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган | Низкомолекулярные ингибиторы mdm2 |
MX2007011151A (es) | 2005-03-16 | 2007-10-17 | Hoffmann La Roche | Cis-2,4,5-triaril-imidazolinas y su uso como medicamentos anticancer. |
-
2007
- 2007-12-12 KR KR1020097014594A patent/KR20090090383A/ko not_active Application Discontinuation
- 2007-12-12 MX MX2009006397A patent/MX2009006397A/es not_active Application Discontinuation
- 2007-12-12 AU AU2007332493A patent/AU2007332493A1/en not_active Abandoned
- 2007-12-12 CA CA002672565A patent/CA2672565A1/en not_active Abandoned
- 2007-12-12 WO PCT/JP2007/073930 patent/WO2008072655A1/ja active Application Filing
- 2007-12-12 CN CNA2007800513481A patent/CN101605798A/zh active Pending
- 2007-12-12 JP JP2008549331A patent/JPWO2008072655A1/ja active Pending
- 2007-12-12 BR BRPI0720546-5A patent/BRPI0720546A2/pt not_active IP Right Cessation
- 2007-12-12 EP EP07850481A patent/EP2103619A4/en not_active Withdrawn
- 2007-12-14 TW TW096147802A patent/TW200831518A/zh unknown
-
2009
- 2009-06-11 US US12/456,131 patent/US20090312310A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CA2672565A1 (en) | 2008-06-19 |
KR20090090383A (ko) | 2009-08-25 |
CN101605798A (zh) | 2009-12-16 |
TW200831518A (en) | 2008-08-01 |
JPWO2008072655A1 (ja) | 2010-04-02 |
BRPI0720546A2 (pt) | 2015-06-23 |
EP2103619A1 (en) | 2009-09-23 |
AU2007332493A1 (en) | 2008-06-19 |
WO2008072655A1 (ja) | 2008-06-19 |
EP2103619A4 (en) | 2011-11-23 |
US20090312310A1 (en) | 2009-12-17 |
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Legal Events
Date | Code | Title | Description |
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FA | Abandonment or withdrawal |