CN102036561A - 蛋白激酶调节剂 - Google Patents
蛋白激酶调节剂 Download PDFInfo
- Publication number
- CN102036561A CN102036561A CN2009801155149A CN200980115514A CN102036561A CN 102036561 A CN102036561 A CN 102036561A CN 2009801155149 A CN2009801155149 A CN 2009801155149A CN 200980115514 A CN200980115514 A CN 200980115514A CN 102036561 A CN102036561 A CN 102036561A
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- 0 *C1NC(****2)=C2c2c1c(*)c(*)[s]2 Chemical compound *C1NC(****2)=C2c2c1c(*)c(*)[s]2 0.000 description 7
- MXSXPCDVADEKHZ-UHFFFAOYSA-N N#Cc(cc1)cc2c1c([s]cc1)c1c(Cl)n2 Chemical compound N#Cc(cc1)cc2c1c([s]cc1)c1c(Cl)n2 MXSXPCDVADEKHZ-UHFFFAOYSA-N 0.000 description 3
- YAVSHDIJXOTQSY-UHFFFAOYSA-N N#Cc1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1 Chemical compound N#Cc1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1 YAVSHDIJXOTQSY-UHFFFAOYSA-N 0.000 description 3
- AQMWJXTWTOCLPY-UHFFFAOYSA-N CNc1ncc(-c(ccc(C(OC)=O)c2)c2NC2=O)c2n1 Chemical compound CNc1ncc(-c(ccc(C(OC)=O)c2)c2NC2=O)c2n1 AQMWJXTWTOCLPY-UHFFFAOYSA-N 0.000 description 2
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- FFYFVQIUCOSRPH-UHFFFAOYSA-N Clc1c(cc[s]2)c2c(cccc2)c2n1 Chemical compound Clc1c(cc[s]2)c2c(cccc2)c2n1 FFYFVQIUCOSRPH-UHFFFAOYSA-N 0.000 description 2
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- KVQYHOITLPMKDW-UHFFFAOYSA-N OC(c1ccc(c2cnccc2c(Nc2ccccc2)n2)c2c1)=O Chemical compound OC(c1ccc(c2cnccc2c(Nc2ccccc2)n2)c2c1)=O KVQYHOITLPMKDW-UHFFFAOYSA-N 0.000 description 2
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- CPQGDSMLYPDIFV-UHFFFAOYSA-N Bc(c(C(O)=O)n1)cnc1SC Chemical compound Bc(c(C(O)=O)n1)cnc1SC CPQGDSMLYPDIFV-UHFFFAOYSA-N 0.000 description 1
- DAUPXNKUCWHZBK-UHFFFAOYSA-N C#Cc1cccc(Nc2c3ncncc3c(ccc(C(N)=O)c3)c3n2)c1 Chemical compound C#Cc1cccc(Nc2c3ncncc3c(ccc(C(N)=O)c3)c3n2)c1 DAUPXNKUCWHZBK-UHFFFAOYSA-N 0.000 description 1
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- QDMVBYNNBWKOHH-UHFFFAOYSA-N CN(C)CCNc1c(cc[s]2)c2c(cccc2)c2n1 Chemical compound CN(C)CCNc1c(cc[s]2)c2c(cccc2)c2n1 QDMVBYNNBWKOHH-UHFFFAOYSA-N 0.000 description 1
- XEOSVNIBLFBARW-UHFFFAOYSA-N CN(C)CCOc(cc1Cl)ccc1N Chemical compound CN(C)CCOc(cc1Cl)ccc1N XEOSVNIBLFBARW-UHFFFAOYSA-N 0.000 description 1
- XZEUIRORHFCWOQ-UHFFFAOYSA-N CN(C)CCOc(cc1Cl)ccc1[N+]([O-])=O Chemical compound CN(C)CCOc(cc1Cl)ccc1[N+]([O-])=O XZEUIRORHFCWOQ-UHFFFAOYSA-N 0.000 description 1
- SPAHRPKPEPZZFG-UHFFFAOYSA-N CNc(nc1)nc(C(OC)=O)c1Br Chemical compound CNc(nc1)nc(C(OC)=O)c1Br SPAHRPKPEPZZFG-UHFFFAOYSA-N 0.000 description 1
- JQUYQUASWUHALF-UHFFFAOYSA-N CNc(ncc1c(ccc(C(OC)=O)c2)c2n2)nc1c2Cl Chemical compound CNc(ncc1c(ccc(C(OC)=O)c2)c2n2)nc1c2Cl JQUYQUASWUHALF-UHFFFAOYSA-N 0.000 description 1
- KWIKUKWCLKBUMA-UHFFFAOYSA-N CNc1nc2c(Nc3ccccc3)nc(cc(cc3)C(O)=O)c3c2cn1 Chemical compound CNc1nc2c(Nc3ccccc3)nc(cc(cc3)C(O)=O)c3c2cn1 KWIKUKWCLKBUMA-UHFFFAOYSA-N 0.000 description 1
- ITJWQMCGDKDXHO-UHFFFAOYSA-N COC(c(c1n2)cccc1c(cncc1)c1c2Cl)=O Chemical compound COC(c(c1n2)cccc1c(cncc1)c1c2Cl)=O ITJWQMCGDKDXHO-UHFFFAOYSA-N 0.000 description 1
- HHCMPCGFJHHCBQ-UHFFFAOYSA-N COC(c(cccc1c2cnccc22)c1nc2Nc1cccc(Cl)c1)=O Chemical compound COC(c(cccc1c2cnccc22)c1nc2Nc1cccc(Cl)c1)=O HHCMPCGFJHHCBQ-UHFFFAOYSA-N 0.000 description 1
- MYZJIEWTRJTWCD-UHFFFAOYSA-N COC(c(nc(nc1)SC)c1Br)=O Chemical compound COC(c(nc(nc1)SC)c1Br)=O MYZJIEWTRJTWCD-UHFFFAOYSA-N 0.000 description 1
- YWDVLONOSCLOSE-UHFFFAOYSA-N COC(c1cc2nc(Nc3cc(C(O)=O)ccc3)c(cc[s]3)c3c2cc1)=O Chemical compound COC(c1cc2nc(Nc3cc(C(O)=O)ccc3)c(cc[s]3)c3c2cc1)=O YWDVLONOSCLOSE-UHFFFAOYSA-N 0.000 description 1
- MSZVVEWLFFTCCE-UHFFFAOYSA-N COC(c1ccc(-c([s]c(Br)c2)c2C(N2)=O)c2c1)=O Chemical compound COC(c1ccc(-c([s]c(Br)c2)c2C(N2)=O)c2c1)=O MSZVVEWLFFTCCE-UHFFFAOYSA-N 0.000 description 1
- IYFALRRQRHZZMJ-UHFFFAOYSA-N COCCOc(cc1F)ccc1N Chemical compound COCCOc(cc1F)ccc1N IYFALRRQRHZZMJ-UHFFFAOYSA-N 0.000 description 1
- MLZMWVQSLFCPIF-UHFFFAOYSA-N CS(NC(c1ccc(c([s]cc2)c2c(Nc2ccccc2)n2)c2c1)=O)(=O)=O Chemical compound CS(NC(c1ccc(c([s]cc2)c2c(Nc2ccccc2)n2)c2c1)=O)(=O)=O MLZMWVQSLFCPIF-UHFFFAOYSA-N 0.000 description 1
- OOYSDWIQEOMJTE-UHFFFAOYSA-N C[NH+](c(c(Cl)c1)ccc1OCCN1CCOCC1)[O-] Chemical compound C[NH+](c(c(Cl)c1)ccc1OCCN1CCOCC1)[O-] OOYSDWIQEOMJTE-UHFFFAOYSA-N 0.000 description 1
- NXAAETHXJFMCHK-UHFFFAOYSA-N N#CC(C1)C=Cc(c2c3ccnc2)c1nc3Cl Chemical compound N#CC(C1)C=Cc(c2c3ccnc2)c1nc3Cl NXAAETHXJFMCHK-UHFFFAOYSA-N 0.000 description 1
- FYSSSWKZHVZAFL-UHFFFAOYSA-N N#Cc(cc1)cc(N2)c1-c([s]cc1)c1C2=O Chemical compound N#Cc(cc1)cc(N2)c1-c([s]cc1)c1C2=O FYSSSWKZHVZAFL-UHFFFAOYSA-N 0.000 description 1
- QYMARLQEROXMRP-UHFFFAOYSA-N N#Cc1cc2nc(Nc3ccccc3)c(ccnc3)c3c2cc1 Chemical compound N#Cc1cc2nc(Nc3ccccc3)c(ccnc3)c3c2cc1 QYMARLQEROXMRP-UHFFFAOYSA-N 0.000 description 1
- DUPUQAYQFXVOCR-UHFFFAOYSA-N NC(c1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1)=O Chemical compound NC(c1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1)=O DUPUQAYQFXVOCR-UHFFFAOYSA-N 0.000 description 1
- LGIAFOUFIPEPGA-UHFFFAOYSA-N NNC(c1cccc(c2cnccc22)c1nc2Nc1cc(Cl)ccc1)=O Chemical compound NNC(c1cccc(c2cnccc22)c1nc2Nc1cc(Cl)ccc1)=O LGIAFOUFIPEPGA-UHFFFAOYSA-N 0.000 description 1
- JQIQAPGNEHFIGB-UHFFFAOYSA-N Nc(c(Cl)c1)ccc1OCCN1CCOCC1 Chemical compound Nc(c(Cl)c1)ccc1OCCN1CCOCC1 JQIQAPGNEHFIGB-UHFFFAOYSA-N 0.000 description 1
- CUMTUBVTKOYYOU-UHFFFAOYSA-N Nc(c(F)c1)ccc1I Chemical compound Nc(c(F)c1)ccc1I CUMTUBVTKOYYOU-UHFFFAOYSA-N 0.000 description 1
- MPSKSPVONPVFPQ-UHFFFAOYSA-N O=C(c1ccc(-c([s]cc2)c2C(N2)=O)c2c1)NCc1cnccc1 Chemical compound O=C(c1ccc(-c([s]cc2)c2C(N2)=O)c2c1)NCc1cnccc1 MPSKSPVONPVFPQ-UHFFFAOYSA-N 0.000 description 1
- YJUQRWQHQNUAKY-UHFFFAOYSA-N O=C(c1ccc(-c([s]cc2)c2C(N2)=O)c2c1)Nc1ccc(CN(CC2)CCS2=O)cc1 Chemical compound O=C(c1ccc(-c([s]cc2)c2C(N2)=O)c2c1)Nc1ccc(CN(CC2)CCS2=O)cc1 YJUQRWQHQNUAKY-UHFFFAOYSA-N 0.000 description 1
- DSNJDLWXDIHPKN-UHFFFAOYSA-N O=C1Nc2ccccc2-c2c1cc[s]2 Chemical compound O=C1Nc2ccccc2-c2c1cc[s]2 DSNJDLWXDIHPKN-UHFFFAOYSA-N 0.000 description 1
- ZJWIJPRRJBELMF-UHFFFAOYSA-N OC(c1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1)=O Chemical compound OC(c1cc2nc(Nc3ccccc3)c(cc[s]3)c3c2cc1)=O ZJWIJPRRJBELMF-UHFFFAOYSA-N 0.000 description 1
- PXPHNDRTHCIMIA-UHFFFAOYSA-N OCc1ccc(-c([s]cc2)c2C(N2)=O)c2c1 Chemical compound OCc1ccc(-c([s]cc2)c2C(N2)=O)c2c1 PXPHNDRTHCIMIA-UHFFFAOYSA-N 0.000 description 1
- YOZNUAQXXJHWQZ-UHFFFAOYSA-N c(cc1)ccc1Nc1c(ccnc2)c2c(ccc(-c2nnn[nH]2)c2)c2n1 Chemical compound c(cc1)ccc1Nc1c(ccnc2)c2c(ccc(-c2nnn[nH]2)c2)c2n1 YOZNUAQXXJHWQZ-UHFFFAOYSA-N 0.000 description 1
- GRGMICYYBLNCCB-UHFFFAOYSA-N c1c[s]c2c(ccc(C3=NNNN3)c3)c3nc(Nc3ccccc3)c12 Chemical compound c1c[s]c2c(ccc(C3=NNNN3)c3)c3nc(Nc3ccccc3)c12 GRGMICYYBLNCCB-UHFFFAOYSA-N 0.000 description 1
Images
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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6784508P | 2008-02-29 | 2008-02-29 | |
| US61/067,845 | 2008-02-29 | ||
| US10390808P | 2008-10-08 | 2008-10-08 | |
| US61/103,908 | 2008-10-08 | ||
| PCT/US2009/035609 WO2009108912A1 (en) | 2008-02-29 | 2009-02-28 | Protein kinase modulators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102036561A true CN102036561A (zh) | 2011-04-27 |
Family
ID=41016490
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801155149A Pending CN102036561A (zh) | 2008-02-29 | 2009-02-28 | 蛋白激酶调节剂 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US8168651B2 (https=) |
| EP (1) | EP2259678A4 (https=) |
| JP (1) | JP2011515337A (https=) |
| CN (1) | CN102036561A (https=) |
| AU (1) | AU2009219154A1 (https=) |
| CA (1) | CA2716755A1 (https=) |
| MX (1) | MX2010009445A (https=) |
| WO (1) | WO2009108912A1 (https=) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102731431A (zh) * | 2012-06-20 | 2012-10-17 | 盛世泰科生物医药技术(苏州)有限公司 | 一种5-溴噻唑-4-甲酸的制备方法 |
| CN109369526A (zh) * | 2018-12-19 | 2019-02-22 | 桂林理工大学 | 一种两面针碱衍生物的合成方法及其抗肿瘤应用 |
| WO2019191896A1 (en) * | 2018-04-03 | 2019-10-10 | 3Sm Biotron Inc. | Fms-like tyrosine kinase inhibitors |
| CN111320605A (zh) * | 2020-03-09 | 2020-06-23 | 吉林工程技术师范学院 | 一种银催化的含氟菲啶衍生物的制备方法 |
| CN113302184A (zh) * | 2018-11-15 | 2021-08-24 | 日本新药株式会社 | 1,3,4-噁二唑啉酮化合物和药物 |
| CN113444085A (zh) * | 2020-03-26 | 2021-09-28 | 东南大学 | 一种具有克服顺铂耐药的抗肿瘤化合物及其制备与应用 |
| CN113444084A (zh) * | 2020-03-26 | 2021-09-28 | 东南大学 | 一类抗肿瘤化合物及其制备与用途 |
| CN114369096A (zh) * | 2020-10-16 | 2022-04-19 | 上海迪诺医药科技有限公司 | 三杂环衍生物、其药物组合物及应用 |
| CN117295736A (zh) * | 2021-03-01 | 2023-12-26 | 剑桥实业有限公司 | 苯并[c][2,6]萘啶衍生物、其组合物及其治疗用途 |
| CN114369096B (zh) * | 2020-10-16 | 2026-05-01 | 上海迪诺医药科技有限公司 | 三杂环衍生物、其药物组合物及应用 |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7956064B2 (en) * | 2006-09-01 | 2011-06-07 | Cylene Pharmaceuticals, Inc. | Fused tricyclic compounds as serine-threonine protein kinase and PARP modulators |
| PT2268618E (pt) | 2008-03-03 | 2015-10-12 | Novartis Ag | Compostos e composições moduladores da actividade tlr |
| US20100173013A1 (en) * | 2009-01-08 | 2010-07-08 | Denis Drygin | Treatment of neoplastic disorders using combination therapies |
| BRPI1016185A2 (pt) * | 2009-04-17 | 2016-04-19 | Cylene Pharmaceuticals Inc | processo para o tratamento de distúrbios associados à atividade da proteína quinase ck2 |
| US9968574B2 (en) * | 2009-05-15 | 2018-05-15 | The University Of Kentucky Research Foundation | Treatment of MCI and Alzheimer's disease |
| CN102596969A (zh) * | 2009-08-26 | 2012-07-18 | 赛林药物股份有限公司 | 用作蛋白激酶调节剂的稠合喹啉类化合物 |
| JP5567137B2 (ja) * | 2009-09-03 | 2014-08-06 | ブリストル−マイヤーズ スクイブ カンパニー | Jak2阻害剤、ならびに骨髄増殖性疾患および癌の治療のためのそれらの使用 |
| MX2012003316A (es) * | 2009-09-16 | 2012-07-23 | Cylene Pharmaceuticals Inc | Compuestos triciclicos y usos farmaceuticos de los mismos. |
| WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
| PH12012500901A1 (en) | 2009-11-05 | 2016-08-05 | Rhizen Pharmaceuticals Sa | Novel benzopyran kinase modulators |
| WO2011063398A1 (en) * | 2009-11-23 | 2011-05-26 | Cylene Pharamaceuticals, Inc. | Polymorphs and salts of a kinase inhibitor |
| US9109227B2 (en) | 2010-01-05 | 2015-08-18 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | FLT3 receptor antagonists for the treatment or the prevention of pain disorders |
| US10106798B2 (en) | 2010-01-05 | 2018-10-23 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | FLT3 receptor antagonists for the treatment or the prevention of pain disorders |
| TWI503323B (zh) * | 2010-03-29 | 2015-10-11 | Oncotherapy Science Inc | 三環化合物以及含此化合物之pbk抑制劑 |
| HRP20190128T1 (hr) | 2011-05-04 | 2019-03-08 | Rhizen Pharmaceuticals S.A. | Novi spojevi kao modulatori protein kinaza |
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| CN110945001B (zh) * | 2018-04-03 | 2022-11-25 | 硕英生医股份有限公司 | Fms样酪氨酸激酶抑制剂 |
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| CN113302184A (zh) * | 2018-11-15 | 2021-08-24 | 日本新药株式会社 | 1,3,4-噁二唑啉酮化合物和药物 |
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| CN113444085A (zh) * | 2020-03-26 | 2021-09-28 | 东南大学 | 一种具有克服顺铂耐药的抗肿瘤化合物及其制备与应用 |
| WO2021190142A1 (zh) * | 2020-03-26 | 2021-09-30 | 东南大学 | 一类抗肿瘤化合物及其制备与用途 |
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| CN113444084A (zh) * | 2020-03-26 | 2021-09-28 | 东南大学 | 一类抗肿瘤化合物及其制备与用途 |
| CN114369096A (zh) * | 2020-10-16 | 2022-04-19 | 上海迪诺医药科技有限公司 | 三杂环衍生物、其药物组合物及应用 |
| WO2022078480A1 (zh) * | 2020-10-16 | 2022-04-21 | 上海迪诺医药科技有限公司 | 三杂环衍生物、其药物组合物及应用 |
| CN114369096B (zh) * | 2020-10-16 | 2026-05-01 | 上海迪诺医药科技有限公司 | 三杂环衍生物、其药物组合物及应用 |
| CN117295736A (zh) * | 2021-03-01 | 2023-12-26 | 剑桥实业有限公司 | 苯并[c][2,6]萘啶衍生物、其组合物及其治疗用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009108912A1 (en) | 2009-09-03 |
| JP2011515337A (ja) | 2011-05-19 |
| US20090239859A1 (en) | 2009-09-24 |
| EP2259678A4 (en) | 2011-07-27 |
| AU2009219154A1 (en) | 2009-09-03 |
| US8168651B2 (en) | 2012-05-01 |
| US20120208792A1 (en) | 2012-08-16 |
| EP2259678A1 (en) | 2010-12-15 |
| CA2716755A1 (en) | 2009-09-03 |
| MX2010009445A (es) | 2011-05-25 |
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