RU2350605C2 - Аналоги хиназолина в качестве ингибиторов рецепторных тирозинкиназ - Google Patents
Аналоги хиназолина в качестве ингибиторов рецепторных тирозинкиназ Download PDFInfo
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- RU2350605C2 RU2350605C2 RU2006103493/04A RU2006103493A RU2350605C2 RU 2350605 C2 RU2350605 C2 RU 2350605C2 RU 2006103493/04 A RU2006103493/04 A RU 2006103493/04A RU 2006103493 A RU2006103493 A RU 2006103493A RU 2350605 C2 RU2350605 C2 RU 2350605C2
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- compound
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- alkyl
- compound according
- phenyl
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- 0 Clc(cc(cc1)Nc2ncnc(cc3)c2cc3NC2=NC3(CC3)CO2)c1OCC1SC=C*1 Chemical compound Clc(cc(cc1)Nc2ncnc(cc3)c2cc3NC2=NC3(CC3)CO2)c1OCC1SC=C*1 0.000 description 7
- JQCOOBLAMAGGQG-UHFFFAOYSA-N CC(C)(C)OC(N1CC2OC(Nc(cc3)cc4c3ncnc4CNc(cc3)cc(Cl)c3OCc3ccccn3)=NC2C1)=O Chemical compound CC(C)(C)OC(N1CC2OC(Nc(cc3)cc4c3ncnc4CNc(cc3)cc(Cl)c3OCc3ccccn3)=NC2C1)=O JQCOOBLAMAGGQG-UHFFFAOYSA-N 0.000 description 1
- LBWGXXAFYOQZDM-MQHWAWBQSA-N CC(C)/C=C\C(\Oc(cc1)c(C)cc1Nc(c1c2)ncnc1ccc2NC(OC1)=NC1[C@@H](C)O)=C/N Chemical compound CC(C)/C=C\C(\Oc(cc1)c(C)cc1Nc(c1c2)ncnc1ccc2NC(OC1)=NC1[C@@H](C)O)=C/N LBWGXXAFYOQZDM-MQHWAWBQSA-N 0.000 description 1
- QYTXQGUDLADZAW-UHFFFAOYSA-N CC(N1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(C)c3Oc3cnc(C)cc3)=NC2C1)=O Chemical compound CC(N1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(C)c3Oc3cnc(C)cc3)=NC2C1)=O QYTXQGUDLADZAW-UHFFFAOYSA-N 0.000 description 1
- QEYOIQPSQIZPGV-UHFFFAOYSA-N CC1(C)N=C(Nc2ccc3ncnc(CNCCCc(cc4)cc(Cl)c4OCc4ncc[s]4)c3c2)OC1 Chemical compound CC1(C)N=C(Nc2ccc3ncnc(CNCCCc(cc4)cc(Cl)c4OCc4ncc[s]4)c3c2)OC1 QEYOIQPSQIZPGV-UHFFFAOYSA-N 0.000 description 1
- QVDRXXQWRZSNSP-UHFFFAOYSA-N CC1(CO)N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ncc[s]2)OC1 Chemical compound CC1(CO)N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ncc[s]2)OC1 QVDRXXQWRZSNSP-UHFFFAOYSA-N 0.000 description 1
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- XZNJOPUUIBAHHG-UHFFFAOYSA-N CC1N=C(Nc(cc23)ccc2ncnc3Nc(cc2)cc(C)c2Oc2cnc(C)cc2)OC1 Chemical compound CC1N=C(Nc(cc23)ccc2ncnc3Nc(cc2)cc(C)c2Oc2cnc(C)cc2)OC1 XZNJOPUUIBAHHG-UHFFFAOYSA-N 0.000 description 1
- VFBVERGGWMTBDB-UHFFFAOYSA-N CC1OC(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ncc[s]2)=NC1 Chemical compound CC1OC(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ncc[s]2)=NC1 VFBVERGGWMTBDB-UHFFFAOYSA-N 0.000 description 1
- ZPHPFCOIJJJJMU-UHFFFAOYSA-N CC1OC(Nc2ccc3ncnc(CNCCCc(cc4)cc(C)c4Oc4cnc(C)cc4)c3c2)=NC1 Chemical compound CC1OC(Nc2ccc3ncnc(CNCCCc(cc4)cc(C)c4Oc4cnc(C)cc4)c3c2)=NC1 ZPHPFCOIJJJJMU-UHFFFAOYSA-N 0.000 description 1
- BKLOWMRZIXAYIC-UHFFFAOYSA-N CN(C)CCCC1N=C(Nc2ccc3ncnc(CNc(cc4)cc(Cl)c4OCc4ccccn4)c3c2)OC1 Chemical compound CN(C)CCCC1N=C(Nc2ccc3ncnc(CNc(cc4)cc(Cl)c4OCc4ccccn4)c3c2)OC1 BKLOWMRZIXAYIC-UHFFFAOYSA-N 0.000 description 1
- PKYKYZJQNRPUQR-HNNXBMFYSA-N C[C@@H]1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2Cl)ccc2OCc2cc(F)ccc2)OC1 Chemical compound C[C@@H]1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2Cl)ccc2OCc2cc(F)ccc2)OC1 PKYKYZJQNRPUQR-HNNXBMFYSA-N 0.000 description 1
- GZUOZPWXRLIDEP-JGHKVMFLSA-N C[C@H](C1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ccccn2)OC1)O Chemical compound C[C@H](C1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2ccccn2)OC1)O GZUOZPWXRLIDEP-JGHKVMFLSA-N 0.000 description 1
- PKYKYZJQNRPUQR-OAHLLOKOSA-N C[C@H]1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2cccc(F)c2)OC1 Chemical compound C[C@H]1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2cccc(F)c2)OC1 PKYKYZJQNRPUQR-OAHLLOKOSA-N 0.000 description 1
- WJYSOQZGGGHNQL-IIHBXENTSA-N Cc(cc(cc1)NCc2ncnc3c2cc(/C=N/NC(COC)=N)cc3)c1OCc1ccnc(C)c1 Chemical compound Cc(cc(cc1)NCc2ncnc3c2cc(/C=N/NC(COC)=N)cc3)c1OCc1ccnc(C)c1 WJYSOQZGGGHNQL-IIHBXENTSA-N 0.000 description 1
- PLHZDIAHMOYEAL-UHFFFAOYSA-N Cc(cc(cc1)Nc(c2c3)ncnc2ccc3NC2=NC(CCNC)CO2)c1Oc1cnc(C)cc1 Chemical compound Cc(cc(cc1)Nc(c2c3)ncnc2ccc3NC2=NC(CCNC)CO2)c1Oc1cnc(C)cc1 PLHZDIAHMOYEAL-UHFFFAOYSA-N 0.000 description 1
- VIFUXXFCXNHAER-UHFFFAOYSA-N Cc1cc(CC2(c(c3c4)ncnc3ccc4NC3=NC(COC4)C4O3)NC2)ccc1OCc1ncc[s]1 Chemical compound Cc1cc(CC2(c(c3c4)ncnc3ccc4NC3=NC(COC4)C4O3)NC2)ccc1OCc1ncc[s]1 VIFUXXFCXNHAER-UHFFFAOYSA-N 0.000 description 1
- ORSFBBZOONQXPR-UHFFFAOYSA-N Clc(cc(cc1)NCc(c2c3)ncnc2ccc3NC(OC2)=NC22CCOCC2)c1OCc1ccccn1 Chemical compound Clc(cc(cc1)NCc(c2c3)ncnc2ccc3NC(OC2)=NC22CCOCC2)c1OCc1ccccn1 ORSFBBZOONQXPR-UHFFFAOYSA-N 0.000 description 1
- WYBLAWMGYTXPAZ-UHFFFAOYSA-N NCCC1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2cccc(F)c2)OC1 Chemical compound NCCC1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2)cc(Cl)c2OCc2cccc(F)c2)OC1 WYBLAWMGYTXPAZ-UHFFFAOYSA-N 0.000 description 1
- JJVQUXGBNQOVMJ-UHFFFAOYSA-N NCCC1N=C(Nc(cc23)ccc2ncnc3Nc(cc2Cl)ccc2OCc2ccccn2)OC1 Chemical compound NCCC1N=C(Nc(cc23)ccc2ncnc3Nc(cc2Cl)ccc2OCc2ccccn2)OC1 JJVQUXGBNQOVMJ-UHFFFAOYSA-N 0.000 description 1
- NWGLCCSNDRTDGB-UHFFFAOYSA-N O=CN1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(Cl)c3OCc3ccccn3)=NC2C1 Chemical compound O=CN1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(Cl)c3OCc3ccccn3)=NC2C1 NWGLCCSNDRTDGB-UHFFFAOYSA-N 0.000 description 1
- MZRVLVVZHLHJFW-UHFFFAOYSA-N O=CN1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(Cl)c3OCc3ncc[s]3)=NC2C1 Chemical compound O=CN1CC2OC(Nc(cc3)cc4c3ncnc4Nc(cc3)cc(Cl)c3OCc3ncc[s]3)=NC2C1 MZRVLVVZHLHJFW-UHFFFAOYSA-N 0.000 description 1
- HLPAGFVYTLXLSJ-UHFFFAOYSA-N OCC1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2Cl)ccc2OCc2ncc[s]2)OC1 Chemical compound OCC1N=C(Nc(cc2)cc3c2ncnc3Nc(cc2Cl)ccc2OCc2ncc[s]2)OC1 HLPAGFVYTLXLSJ-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- 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
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- A61K31/495—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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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
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- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/642,440 US7501427B2 (en) | 2003-08-14 | 2003-08-14 | Quinazoline analogs as receptor tyrosine kinase inhibitors |
| US10/642,440 | 2003-08-14 | ||
| US55171804P | 2004-03-10 | 2004-03-10 | |
| US60/551,718 | 2004-03-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2006103493A RU2006103493A (ru) | 2007-09-20 |
| RU2350605C2 true RU2350605C2 (ru) | 2009-03-27 |
Family
ID=34198338
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006103493/04A RU2350605C2 (ru) | 2003-08-14 | 2004-08-10 | Аналоги хиназолина в качестве ингибиторов рецепторных тирозинкиназ |
Country Status (23)
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7488823B2 (en) * | 2003-11-10 | 2009-02-10 | Array Biopharma, Inc. | Cyanoguanidines and cyanoamidines as ErbB2 and EGFR inhibitors |
| RU2350605C2 (ru) * | 2003-08-14 | 2009-03-27 | Эррей Байофарма Инк. | Аналоги хиназолина в качестве ингибиторов рецепторных тирозинкиназ |
| US7501427B2 (en) | 2003-08-14 | 2009-03-10 | Array Biopharma, Inc. | Quinazoline analogs as receptor tyrosine kinase inhibitors |
| WO2007059257A2 (en) * | 2005-11-15 | 2007-05-24 | Array Biopharma Inc. | N4-phenyl-quinaz0line-4 -amine derivatives and related compounds as erbb type i receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases |
| CA2852058C (en) | 2011-10-14 | 2021-06-01 | Array Biopharma Inc. | A solid dispersion of n4-(4-([1,2,4]triazolo[1,5-a]pyridin-7-yloxy)-3-methylphenyl)-n6-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)quinazoline-4,6-diamine |
| CA2852060A1 (en) | 2011-10-14 | 2013-04-18 | Array Biopharma Inc. | Polymorphs of arry-380, a selective herb2 inhibitor and pharmaceutical compositions containing them |
| LT2827900T (lt) | 2012-03-23 | 2018-05-10 | Array Biopharma, Inc. | Amorfinė kieta dispersija, skirta panaudoti smegenų vėžio gydymui |
| CN108135901A (zh) | 2015-09-04 | 2018-06-08 | 亚狮康私人有限公司 | 胆管癌的治疗 |
| JP2019514864A (ja) * | 2016-04-21 | 2019-06-06 | アスラン ファーマシューティカルズ ピーティーイー リミテッド | 肝癌の治療方法 |
| GB201611580D0 (en) * | 2016-07-01 | 2016-08-17 | Aslan Pharmaceuticals Pte Ltd | Method |
| CN106349231A (zh) * | 2016-08-09 | 2017-01-25 | 浙江医药高等专科学校 | 一类含卤代噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂 |
| CN106317039A (zh) * | 2016-08-09 | 2017-01-11 | 浙江医药高等专科学校 | 一种含噻吩磺酰胺结构的乙氧苯并喹唑啉类酪氨酸激酶抑制剂、制备方法及用途 |
| CN106279135A (zh) * | 2016-08-09 | 2017-01-04 | 浙江医药高等专科学校 | 一种噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂 |
| CN106349230A (zh) * | 2016-08-09 | 2017-01-25 | 浙江医药高等专科学校 | 一种含硝基噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂及用途 |
| CN106317040A (zh) * | 2016-08-09 | 2017-01-11 | 浙江医药高等专科学校 | 含噻吩磺酰胺结构的苯并喹唑啉类酪氨酸激酶抑制剂、制备方法及用途 |
| US11225515B2 (en) | 2016-08-26 | 2022-01-18 | Agency For Science, Technology And Research | Macrophage stimulating protein receptor (or RON—recepteur d'Origine Nantais) antibodies and uses thereof |
| WO2018160138A1 (en) | 2017-03-02 | 2018-09-07 | Aslan Pharmaceuticals Pte Ltd | Dhodh inhibitor for treating haematological cancer |
| EA201992573A1 (ru) | 2017-04-28 | 2020-04-06 | Сиэтл Дженетикс, Инк. | Лечение her2-положительных злокачественных новообразований |
| WO2018222135A1 (en) | 2017-06-02 | 2018-12-06 | Aslan Pharmaceuticals Pte Ltd | Cancer therapy |
| WO2018222134A1 (en) | 2017-06-02 | 2018-12-06 | Aslan Pharmaceuticals Pte Ltd | Cancer therapy |
| CN112654612A (zh) | 2018-09-18 | 2021-04-13 | 苏州赞荣医药科技有限公司 | 作为抗肿瘤剂的喹唑啉衍生物 |
| AU2019359036A1 (en) * | 2018-10-09 | 2021-06-03 | Aslan Pharmaceuticals Pte Ltd | Malonate salt of varlitinib |
| CN111499622B (zh) * | 2019-07-08 | 2023-06-06 | 山东省科学院菏泽分院 | 一种治疗胆管癌的药物的制备方法 |
| TW202214641A (zh) | 2020-06-30 | 2022-04-16 | 美商艾瑞生藥股份有限公司 | Her2突變抑制劑 |
| MX2023015139A (es) | 2021-06-26 | 2024-01-22 | Array Biopharma Inc | Inhibidores de mutacion de her2. |
| WO2023081637A1 (en) * | 2021-11-02 | 2023-05-11 | Enliven Therapeutics, Inc. | Fused tetracyclic quinazoline derivatives as inhibitors of erbb2 |
| EP4501925A4 (en) * | 2022-03-28 | 2025-08-27 | Jiangsu Hengrui Pharmaceuticals Co Ltd | NITROGEN-CONTAINING HETEROCYCLIC COMPOUND, PREPARATION METHOD AND PHARMACEUTICAL USE THEREOF |
| TW202530231A (zh) * | 2023-09-27 | 2025-08-01 | 大陸商江蘇恒瑞醫藥股份有限公司 | 喹唑啉衍生物的可藥用鹽、其結晶形式及用途 |
Citations (4)
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|---|---|---|---|---|
| WO1996015118A1 (en) * | 1994-11-12 | 1996-05-23 | Zeneca Limited | Aniline derivatives |
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