CN101679425B - 6-(吡咯并吡啶基)嘧啶-2-基胺及其治疗癌症和艾滋病的用途 - Google Patents
6-(吡咯并吡啶基)嘧啶-2-基胺及其治疗癌症和艾滋病的用途 Download PDFInfo
- Publication number
- CN101679425B CN101679425B CN2008800197101A CN200880019710A CN101679425B CN 101679425 B CN101679425 B CN 101679425B CN 2008800197101 A CN2008800197101 A CN 2008800197101A CN 200880019710 A CN200880019710 A CN 200880019710A CN 101679425 B CN101679425 B CN 101679425B
- Authority
- CN
- China
- Prior art keywords
- compound
- compounds
- tumour
- purposes
- cancer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- DHXRPEZNWUMWIN-ISTTXYCBSA-N C/C(/N(C)/C=C\C=C)=C/N Chemical compound C/C(/N(C)/C=C\C=C)=C/N DHXRPEZNWUMWIN-ISTTXYCBSA-N 0.000 description 1
- CHTFWVDBUXUMCE-UHFFFAOYSA-N CC(C)(C)OC(N1CCC(CC#C)CC1)=O Chemical compound CC(C)(C)OC(N1CCC(CC#C)CC1)=O CHTFWVDBUXUMCE-UHFFFAOYSA-N 0.000 description 1
- HVMCMFDCPBNMCE-UHFFFAOYSA-N CN1CCC(Cc2cc(-c3c[nH]c4ncccc34)nc(N)n2)CC1 Chemical compound CN1CCC(Cc2cc(-c3c[nH]c4ncccc34)nc(N)n2)CC1 HVMCMFDCPBNMCE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007028515A DE102007028515A1 (de) | 2007-06-21 | 2007-06-21 | 6-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
| DE102007028515.0 | 2007-06-21 | ||
| PCT/EP2008/004151 WO2008155000A1 (de) | 2007-06-21 | 2008-05-23 | 6-(pyrrolopyridinyl)- pyrimidin-2-yl-amin-derivate und ihre verwendung zur behandlung von krebs und aids |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101679425A CN101679425A (zh) | 2010-03-24 |
| CN101679425B true CN101679425B (zh) | 2013-11-06 |
Family
ID=39916277
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008800197101A Expired - Fee Related CN101679425B (zh) | 2007-06-21 | 2008-05-23 | 6-(吡咯并吡啶基)嘧啶-2-基胺及其治疗癌症和艾滋病的用途 |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8546390B2 (enExample) |
| EP (1) | EP2155745B1 (enExample) |
| JP (1) | JP5411849B2 (enExample) |
| KR (1) | KR20100040862A (enExample) |
| CN (1) | CN101679425B (enExample) |
| AR (1) | AR067081A1 (enExample) |
| AU (1) | AU2008266584B2 (enExample) |
| BR (1) | BRPI0812944A2 (enExample) |
| CA (1) | CA2691223C (enExample) |
| DE (1) | DE102007028515A1 (enExample) |
| EA (1) | EA016160B1 (enExample) |
| ES (1) | ES2533873T3 (enExample) |
| IL (1) | IL202828A0 (enExample) |
| MX (1) | MX2009013341A (enExample) |
| WO (1) | WO2008155000A1 (enExample) |
| ZA (1) | ZA201000432B (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2009010984A (es) * | 2007-04-10 | 2010-01-15 | Sgx Pharmaceuticals Inc | Moduladores de heterociclo cinasa de anillo fusionado. |
| DE102008031517A1 (de) * | 2008-07-03 | 2010-01-07 | Merck Patent Gmbh | Pyrrolopyridinyl-pyrimidin-2-yl-amin-derivate |
| DE102009019962A1 (de) * | 2009-05-05 | 2010-11-11 | Merck Patent Gmbh | 3-([1,2,3]Triazol-4-yl)-pyrrolo[2,3-b]pyridinderivate |
| DE102009060175A1 (de) | 2009-12-23 | 2011-06-30 | Merck Patent GmbH, 64293 | Pyrrolo[2,3-d] pyrazin-7-yl-pyrimidin-Verbindungen |
| DE102009060174A1 (de) * | 2009-12-23 | 2011-06-30 | Merck Patent GmbH, 64293 | Pyrrolopyridinyl-pyrimidin-2-yl-amin-derivate |
| DE102010050558A1 (de) * | 2010-11-05 | 2012-05-10 | Merck Patent Gmbh | 1H-Pyrrolo[2,3-b]pyridinderivate |
| DE102010053347A1 (de) | 2010-12-03 | 2012-06-06 | Merck Patent Gmbh | 3-Hetaryl-substituierte Pyrrolo[2,3-b] pyridin-derivative als PDK1-Inhibitoren |
| DE102011009961A1 (de) | 2011-02-01 | 2012-08-02 | Merck Patent Gmbh | 7-Azaindolderivate |
| EP2867236B1 (en) | 2012-06-29 | 2017-06-14 | Pfizer Inc | Novel 4-(substituted-amino)-7h-pyrrolo[2,3-d]pyrimidines as lrrk2 inhibitors |
| BR112015016395A2 (pt) | 2013-01-18 | 2017-07-11 | Hoffmann La Roche | pirazóis 3-substituídos e uso como inibidores de dlk |
| DK2970265T3 (en) * | 2013-03-15 | 2018-10-01 | Plexxikon Inc | HETEROCYCLIC COMPOUNDS AND APPLICATIONS THEREOF |
| US20140303121A1 (en) | 2013-03-15 | 2014-10-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| WO2015092592A1 (en) | 2013-12-17 | 2015-06-25 | Pfizer Inc. | Novel 3,4-disubstituted-1h-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7h-pyrrolo[2,3-c]pyridazines as lrrk2 inhibitors |
| KR102161364B1 (ko) | 2015-09-14 | 2020-09-29 | 화이자 인코포레이티드 | LRRK2 억제제로서 이미다조[4,5-c]퀴놀린 및 이미다조[4,5-c][1,5]나프티리딘 유도체 |
| WO2017161004A1 (en) * | 2016-03-15 | 2017-09-21 | University Of South Florida | PKCδ INHIBITOR FORMULATIONS AND USES THEREOF CROSS-REFERENCE TO RELATED APPLICATIONS |
| RU2738646C2 (ru) | 2016-04-01 | 2020-12-15 | РЕКЬЮРИУМ АйПи ХОЛДИНГС, ЛЛС | Модуляторы эстрогеновых рецепторов |
| EP3694855A1 (en) | 2017-10-13 | 2020-08-19 | Plexxikon Inc. | Solid forms of a compound for modulating kinases |
| TW202104221A (zh) * | 2019-04-09 | 2021-02-01 | 美商普雷辛肯公司 | 用於ep300或cbp調節及其適應症之化合物及方法 |
| AU2020326691A1 (en) | 2019-08-06 | 2022-03-03 | Recurium Ip Holdings, Llc | Estrogen receptor modulators for treating mutants |
| CN118772140A (zh) * | 2023-04-07 | 2024-10-15 | 四川大学 | 一类化合物及其在治疗hDHODH介导的疾病中的用途 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005095400A1 (en) * | 2004-03-30 | 2005-10-13 | Vertex Pharmaceuticals Incorporated | Azaindoles useful as inhibitors of jak and other protein kinases |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5747469A (en) | 1991-03-06 | 1998-05-05 | Board Of Regents, The University Of Texas System | Methods and compositions comprising DNA damaging agents and p53 |
| GB9904387D0 (en) | 1999-02-25 | 1999-04-21 | Pharmacia & Upjohn Spa | Antitumour synergistic composition |
| US6265434B1 (en) | 1999-04-06 | 2001-07-24 | Merck & Co., Inc. | Pyrrolidine modulators of chemokine receptor activity |
| GB0308466D0 (en) | 2003-04-11 | 2003-05-21 | Novartis Ag | Organic compounds |
| WO2005123672A2 (en) * | 2004-06-14 | 2005-12-29 | Takeda San Diego, Inc. | Kinase inhibitors |
| MX2007001127A (es) * | 2004-07-27 | 2007-07-11 | Sgx Pharmaceuticals Inc | Moduladores de pirrolo-piridina cinasa. |
| US20090233955A1 (en) * | 2004-12-08 | 2009-09-17 | Frazee James S | 1H-Pyrrolo[2,3-B]Pyridnes |
| US20080300267A1 (en) | 2005-05-16 | 2008-12-04 | Barun Okram | Compounds and Compositions as Protein Kinase Inhibitors |
| DE102006012617A1 (de) | 2006-03-20 | 2007-09-27 | Merck Patent Gmbh | 4-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
-
2007
- 2007-06-21 DE DE102007028515A patent/DE102007028515A1/de not_active Withdrawn
-
2008
- 2008-05-23 JP JP2010512544A patent/JP5411849B2/ja not_active Expired - Fee Related
- 2008-05-23 ES ES08758743.2T patent/ES2533873T3/es active Active
- 2008-05-23 KR KR1020107001385A patent/KR20100040862A/ko not_active Withdrawn
- 2008-05-23 CA CA2691223A patent/CA2691223C/en not_active Expired - Fee Related
- 2008-05-23 WO PCT/EP2008/004151 patent/WO2008155000A1/de not_active Ceased
- 2008-05-23 EP EP08758743.2A patent/EP2155745B1/de not_active Not-in-force
- 2008-05-23 AU AU2008266584A patent/AU2008266584B2/en not_active Ceased
- 2008-05-23 BR BRPI0812944-4A2A patent/BRPI0812944A2/pt not_active IP Right Cessation
- 2008-05-23 MX MX2009013341A patent/MX2009013341A/es not_active Application Discontinuation
- 2008-05-23 US US12/664,791 patent/US8546390B2/en not_active Expired - Fee Related
- 2008-05-23 EA EA201000004A patent/EA016160B1/ru not_active IP Right Cessation
- 2008-05-23 CN CN2008800197101A patent/CN101679425B/zh not_active Expired - Fee Related
- 2008-06-20 AR ARP080102634A patent/AR067081A1/es unknown
-
2009
- 2009-12-17 IL IL202828A patent/IL202828A0/en unknown
-
2010
- 2010-01-20 ZA ZA201000432A patent/ZA201000432B/xx unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005095400A1 (en) * | 2004-03-30 | 2005-10-13 | Vertex Pharmaceuticals Incorporated | Azaindoles useful as inhibitors of jak and other protein kinases |
Non-Patent Citations (1)
| Title |
|---|
| FRESNEDA ETAL.Synthesis of the indole alkaloids meridianins from the tunicate aplidium meridianum.《tetrahedron》.2001,第57卷(第2001期),2355-2363. * |
Also Published As
| Publication number | Publication date |
|---|---|
| EA201000004A1 (ru) | 2010-06-30 |
| IL202828A0 (en) | 2010-06-30 |
| CN101679425A (zh) | 2010-03-24 |
| CA2691223A1 (en) | 2008-12-24 |
| MX2009013341A (es) | 2010-01-18 |
| EP2155745B1 (de) | 2015-01-28 |
| JP2010530376A (ja) | 2010-09-09 |
| KR20100040862A (ko) | 2010-04-21 |
| EP2155745A1 (de) | 2010-02-24 |
| DE102007028515A1 (de) | 2008-12-24 |
| US20110082140A1 (en) | 2011-04-07 |
| EA016160B1 (ru) | 2012-02-28 |
| WO2008155000A1 (de) | 2008-12-24 |
| US8546390B2 (en) | 2013-10-01 |
| AU2008266584B2 (en) | 2013-04-04 |
| AU2008266584A1 (en) | 2008-12-24 |
| CA2691223C (en) | 2015-12-01 |
| AR067081A1 (es) | 2009-09-30 |
| ZA201000432B (en) | 2010-10-27 |
| JP5411849B2 (ja) | 2014-02-12 |
| BRPI0812944A2 (pt) | 2014-12-16 |
| ES2533873T3 (es) | 2015-04-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101679425B (zh) | 6-(吡咯并吡啶基)嘧啶-2-基胺及其治疗癌症和艾滋病的用途 | |
| JP5587874B2 (ja) | ピロロピリジニルピリミジン−2−イルアミン誘導体 | |
| CN103502247B (zh) | 7-氮杂吲哚衍生物 | |
| ES2436445T3 (es) | Derivados de 3-([1,2,3]triazol-4-il)-pirrolo[2,3-b]piridina | |
| JP5891233B2 (ja) | 7−([1,2,3]トリアゾール−4−イル)−ピロロ[2,3−b]ピラジン誘導体 | |
| JP5524864B2 (ja) | 4−(ピロロ[2,3−c]ピリジン−3−イル)ピリミジン−2−アミン誘導体 | |
| CN103403005B (zh) | 5-([1,2,3]-三唑-4-基)-7H-吡咯并[2,3-d]嘧啶衍生物 | |
| CN102666544B (zh) | 吡咯并[2,3-d]吡嗪-7-基嘧啶化合物 | |
| JP2013544264A (ja) | PDK1阻害剤としての3−ヘタリール置換ピロロ[2,3−b]ピリジン誘導体 | |
| CN101616918A (zh) | 4-(吡咯并吡啶基)嘧啶-2-基胺衍生物 | |
| CN103764651B (zh) | 适合治疗癌症疾病的7-氮杂吲哚衍生物 | |
| HK1142332A (en) | 6-(pyrrolopyridinyl)pyrimidin-2-ylamine derivatives and the use thereof for the treatment of cancer and aids | |
| HK1140203A (en) | 4-(pyrrolopyridinyl)pyrimidin-2-ylamine derivatives | |
| HK1157766A (en) | Pyrrolopyridinylpyrimidin-2-ylamine derivatives | |
| HK1169118A (en) | 3-([1,2,3]triazol-4-yl)-pyrrolo[2,3-b]pyridine derivatives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1142332 Country of ref document: HK |
|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: WD Ref document number: 1142332 Country of ref document: HK |
|
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20131106 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |