EA200901212A1 - 3-имидазолилиндолы, предназначенные для лечения пролиферативных заболеваний - Google Patents
3-имидазолилиндолы, предназначенные для лечения пролиферативных заболеванийInfo
- Publication number
- EA200901212A1 EA200901212A1 EA200901212A EA200901212A EA200901212A1 EA 200901212 A1 EA200901212 A1 EA 200901212A1 EA 200901212 A EA200901212 A EA 200901212A EA 200901212 A EA200901212 A EA 200901212A EA 200901212 A1 EA200901212 A1 EA 200901212A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- proliferative diseases
- imidazolylindoles
- treatment
- intended
- variants
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 230000002062 proliferating effect Effects 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 abstract 2
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 abstract 2
- 102000017274 MDM4 Human genes 0.000 abstract 2
- 108050005300 MDM4 Proteins 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 208000037765 diseases and disorders Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
Classifications
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
В настоящем изобретении предлагаются соединения, относящиеся к производным 3-гетероциклилиндолила, способным ингибировать взаимодействие между р53, или его вариантами, и MDM2 и/или MDM4, или их вариантами, соответственно, и указанные соединения характеризуются формулой (I), где R, R, R, R, R, Y и Y имеют значения, определенные в описании изобретения. Благодаря их активности, соединения можно использовать для лечения различных заболеваний и нарушений, оппосредованных активностью MDM2 и/или MDM4, или их вариантами, таких как воспалительные заболевания или пролиферативные заболевания или для защиты клеток.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07105269 | 2007-03-29 | ||
PCT/EP2008/053667 WO2008119741A2 (en) | 2007-03-29 | 2008-03-27 | 3-imidazolyl-indoles for the treatment of proliferative diseases |
Publications (1)
Publication Number | Publication Date |
---|---|
EA200901212A1 true EA200901212A1 (ru) | 2010-04-30 |
Family
ID=38328915
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200901212A EA200901212A1 (ru) | 2007-03-29 | 2008-03-27 | 3-имидазолилиндолы, предназначенные для лечения пролиферативных заболеваний |
Country Status (27)
Country | Link |
---|---|
US (1) | US8053457B2 (ru) |
EP (1) | EP2142535A2 (ru) |
JP (1) | JP2010522723A (ru) |
KR (1) | KR20090122403A (ru) |
CN (1) | CN101679382A (ru) |
AR (1) | AR065860A1 (ru) |
AU (1) | AU2008234954B9 (ru) |
BR (1) | BRPI0810082A2 (ru) |
CA (1) | CA2682483A1 (ru) |
CL (1) | CL2008000899A1 (ru) |
CR (1) | CR11019A (ru) |
DO (1) | DOP2009000229A (ru) |
EA (1) | EA200901212A1 (ru) |
EC (1) | ECSP099660A (ru) |
GT (1) | GT200900256A (ru) |
IL (1) | IL200862A0 (ru) |
MA (1) | MA31260B1 (ru) |
MX (1) | MX2009010413A (ru) |
NI (1) | NI200900177A (ru) |
PA (1) | PA8774001A1 (ru) |
PE (1) | PE20081897A1 (ru) |
SM (1) | SMP200900085B (ru) |
TN (1) | TN2009000388A1 (ru) |
TW (1) | TW200843746A (ru) |
UY (1) | UY30987A1 (ru) |
WO (1) | WO2008119741A2 (ru) |
ZA (1) | ZA200906210B (ru) |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2007235578B2 (en) * | 2006-04-07 | 2011-07-14 | Janssen Pharmaceutica N.V. | Indoles and benzoimidazoles as modulators of the histamine H4 receptor |
AR070398A1 (es) * | 2008-02-22 | 2010-03-31 | Gruenenthal Chemie | Derivados sustituidos de indol |
WO2009158375A1 (en) * | 2008-06-25 | 2009-12-30 | Abbott Laboratories | Aza-cylic indole- 2 -carboxamides and methods of use thereof |
EP3269395A1 (en) | 2008-11-07 | 2018-01-17 | Massachusetts Institute Of Technology | Aminoalcohol lipidoids and uses thereof |
MX2011007598A (es) | 2009-01-16 | 2011-08-08 | Daiichi Sankyo Co Ltd | Derivados de imidazotiazol que tienen estructura de anillo de prolina. |
JP2012102017A (ja) * | 2009-03-03 | 2012-05-31 | Astellas Pharma Inc | インドール化合物 |
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CA2780547C (en) | 2009-11-12 | 2015-02-03 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
WO2011106650A2 (en) * | 2010-02-27 | 2011-09-01 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Novel p53-mdm2/p53-mdm4 antagonists to treat proliferative disease |
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US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
AU2012352177A1 (en) | 2011-12-13 | 2014-07-10 | Buck Institute For Research On Aging | Methods for improving medical therapies |
WO2013158664A2 (en) | 2012-04-17 | 2013-10-24 | Kythera Biopharmaceuticals, Inc. | Use of engineered viruses to specifically kill senescent cells |
WO2014028487A1 (en) | 2012-08-13 | 2014-02-20 | Massachusetts Institute Of Technology | Amine-containing lipidoids and uses thereof |
US9901081B2 (en) | 2012-08-23 | 2018-02-27 | Buck Institute For Research On Aging | Transgenic mouse for determining the role of senescent cells in cancer |
US9901080B2 (en) | 2012-08-23 | 2018-02-27 | Buck Institute For Research On Aging | Transgenic mouse having a transgene that converts a prodrug into a cytotoxic compound in senescent cells |
TWI586668B (zh) | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
BR112015013611A2 (pt) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | composto, e, composição farmacêutica |
WO2014179562A1 (en) | 2013-05-01 | 2014-11-06 | Massachusetts Institute Of Technology | 1,3,5-triazinane-2,4,6-trione derivatives and uses thereof |
WO2015116735A1 (en) | 2014-01-28 | 2015-08-06 | Mayo Foundation For Medical Education And Research | Methods and combinations for killing senescent cells and for treating senescence-associated diseases and disorders |
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CN109415336B (zh) | 2016-04-06 | 2023-08-29 | 密执安大学评议会 | Mdm2蛋白质降解剂 |
JP7001614B2 (ja) | 2016-04-06 | 2022-02-03 | ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン | リガンド依存性の標的タンパク質分解のための単官能性中間体 |
CN109152933B (zh) | 2016-04-21 | 2022-12-02 | 生物风险投资有限责任公司 | 诱导抗细胞凋亡bcl-2家族蛋白的降解的化合物及其用途 |
CN105906610B (zh) * | 2016-05-24 | 2018-10-23 | 绍兴文理学院 | 一种3-(4-苯基-1h-咪唑-5-基)-1h-吲哚衍生物及其制备方法和应用 |
DK3272745T3 (da) | 2016-07-21 | 2019-09-02 | Inst Farmakologii Polskiej Akademii Nauk | Imidazolylsubstituerede indolderivater, der binder 5-ht7-serotoninreceptor, og farmaceutiske sammensætninger deraf |
KR20190068544A (ko) | 2016-10-17 | 2019-06-18 | 다이이찌 산쿄 가부시키가이샤 | Mdm2 저해제와 dna 메틸트랜스페라아제 저해제의 병용 치료법 |
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JP7178357B2 (ja) | 2017-03-07 | 2022-11-25 | エフ.ホフマン-ラ ロシュ アーゲー | オキサジアゾール一過性受容器電位チャネル阻害剤 |
MX2019011945A (es) | 2017-04-05 | 2019-11-28 | Boehringer Ingelheim Int | Terapia de combinacion contra cancer. |
JOP20190245A1 (ar) | 2017-04-20 | 2019-10-15 | Novartis Ag | أنظمة توصيل إطلاق مستدام تتضمن روابط بلا أثر لنقطة الربط |
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US12084423B2 (en) | 2018-05-18 | 2024-09-10 | Bioventures, Llc | Piperlongumine analogues and uses thereof |
TW202027794A (zh) | 2018-10-03 | 2020-08-01 | 瑞士商諾華公司 | 血管生成素樣3多肽之持續遞送 |
EP3931188B1 (en) * | 2019-02-26 | 2023-08-30 | Boehringer Ingelheim International GmbH | New isoindolinone substituted indoles and derivatives as ras inhibitors |
US12186401B2 (en) | 2019-03-01 | 2025-01-07 | Ontario Institute for Cancer Research (OICR) and Sinai Health System | Amide-based proteolysis modulators of B-rapidly accelerated fibrosarcoma (BRAF) and associated uses |
WO2022137085A1 (en) * | 2020-12-22 | 2022-06-30 | Novartis Ag | Indole derivatives useful in treating conditions associated with cgas |
US20220306609A1 (en) * | 2021-03-23 | 2022-09-29 | Nido Biosciences, Inc. | Bicyclic compounds as androgen receptor modulators |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19948417A1 (de) * | 1999-10-07 | 2001-04-19 | Morphochem Ag | Imidazol-Derivate und ihre Verwendung als Arzneimittel |
JP2002114780A (ja) * | 2000-10-11 | 2002-04-16 | Taisho Pharmaceut Co Ltd | 4−(3−インドリル)イミダゾール誘導体 |
EP1856123B1 (en) | 2005-02-22 | 2016-02-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of mdm2 and uses thereof |
US7576082B2 (en) | 2005-06-24 | 2009-08-18 | Hoffman-La Roche Inc. | Oxindole derivatives |
-
2008
- 2008-03-27 AU AU2008234954A patent/AU2008234954B9/en not_active Ceased
- 2008-03-27 PE PE2008000554A patent/PE20081897A1/es not_active Application Discontinuation
- 2008-03-27 US US12/593,721 patent/US8053457B2/en not_active Expired - Fee Related
- 2008-03-27 EP EP08735532A patent/EP2142535A2/en not_active Withdrawn
- 2008-03-27 MX MX2009010413A patent/MX2009010413A/es not_active Application Discontinuation
- 2008-03-27 KR KR1020097022526A patent/KR20090122403A/ko not_active Withdrawn
- 2008-03-27 WO PCT/EP2008/053667 patent/WO2008119741A2/en active Application Filing
- 2008-03-27 EA EA200901212A patent/EA200901212A1/ru unknown
- 2008-03-27 JP JP2010500280A patent/JP2010522723A/ja active Pending
- 2008-03-27 AR ARP080101262A patent/AR065860A1/es unknown
- 2008-03-27 CA CA002682483A patent/CA2682483A1/en not_active Abandoned
- 2008-03-27 BR BRPI0810082-9A2A patent/BRPI0810082A2/pt not_active IP Right Cessation
- 2008-03-27 CN CN200880017611A patent/CN101679382A/zh active Pending
- 2008-03-28 UY UY30987A patent/UY30987A1/es not_active Application Discontinuation
- 2008-03-28 PA PA20088774001A patent/PA8774001A1/es unknown
- 2008-03-28 TW TW097111568A patent/TW200843746A/zh unknown
- 2008-03-28 CL CL2008000899A patent/CL2008000899A1/es unknown
-
2009
- 2009-09-08 ZA ZA200906210A patent/ZA200906210B/xx unknown
- 2009-09-09 CR CR11019A patent/CR11019A/es unknown
- 2009-09-10 IL IL200862A patent/IL200862A0/en unknown
- 2009-09-24 TN TNP2009000388A patent/TN2009000388A1/fr unknown
- 2009-09-24 MA MA32230A patent/MA31260B1/fr unknown
- 2009-09-28 DO DO2009000229A patent/DOP2009000229A/es unknown
- 2009-09-28 NI NI200900177A patent/NI200900177A/es unknown
- 2009-09-28 GT GT200900256A patent/GT200900256A/es unknown
- 2009-09-29 EC EC2009009660A patent/ECSP099660A/es unknown
- 2009-10-28 SM SM200900085T patent/SMP200900085B/it unknown
Also Published As
Publication number | Publication date |
---|---|
PA8774001A1 (es) | 2008-11-19 |
GT200900256A (es) | 2010-03-15 |
ZA200906210B (en) | 2010-05-26 |
ECSP099660A (es) | 2009-10-30 |
IL200862A0 (en) | 2010-05-17 |
CL2008000899A1 (es) | 2009-02-20 |
WO2008119741A3 (en) | 2008-12-04 |
SMAP200900085A (it) | 2010-01-19 |
JP2010522723A (ja) | 2010-07-08 |
MX2009010413A (es) | 2009-10-20 |
KR20090122403A (ko) | 2009-11-27 |
SMP200900085B (it) | 2010-11-12 |
PE20081897A1 (es) | 2009-02-09 |
CA2682483A1 (en) | 2008-10-09 |
AU2008234954B2 (en) | 2011-10-27 |
MA31260B1 (fr) | 2010-03-01 |
CN101679382A (zh) | 2010-03-24 |
BRPI0810082A2 (pt) | 2014-10-21 |
NI200900177A (es) | 2010-09-09 |
TW200843746A (en) | 2008-11-16 |
EP2142535A2 (en) | 2010-01-13 |
UY30987A1 (es) | 2008-10-31 |
US8053457B2 (en) | 2011-11-08 |
CR11019A (es) | 2009-10-20 |
WO2008119741A2 (en) | 2008-10-09 |
TN2009000388A1 (en) | 2010-12-31 |
AU2008234954B9 (en) | 2012-02-02 |
US20100125064A1 (en) | 2010-05-20 |
AR065860A1 (es) | 2009-07-08 |
AU2008234954A1 (en) | 2008-10-09 |
DOP2009000229A (es) | 2009-10-31 |
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