AU2014308616B2 - Certain chemical entities, compositions, and methods - Google Patents
Certain chemical entities, compositions, and methods Download PDFInfo
- Publication number
- AU2014308616B2 AU2014308616B2 AU2014308616A AU2014308616A AU2014308616B2 AU 2014308616 B2 AU2014308616 B2 AU 2014308616B2 AU 2014308616 A AU2014308616 A AU 2014308616A AU 2014308616 A AU2014308616 A AU 2014308616A AU 2014308616 B2 AU2014308616 B2 AU 2014308616B2
- Authority
- AU
- Australia
- Prior art keywords
- amino
- phenyl
- acrylamide
- quinazolin
- pyridin
- 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.)
- Active
Links
- NIFCDKHYIZNDPD-UHFFFAOYSA-N C=CC(Nc(cccc1-c2c3nc(Nc(cc4)ccc4N4CCNCC4)ncc3ccc2)c1F)=O Chemical compound C=CC(Nc(cccc1-c2c3nc(Nc(cc4)ccc4N4CCNCC4)ncc3ccc2)c1F)=O NIFCDKHYIZNDPD-UHFFFAOYSA-N 0.000 description 1
- RFYUTSSGEZINQT-UHFFFAOYSA-N C=CC(Nc1cc(-c(cccc2cn3)c2nc3Cl)ccc1)=O Chemical compound C=CC(Nc1cc(-c(cccc2cn3)c2nc3Cl)ccc1)=O RFYUTSSGEZINQT-UHFFFAOYSA-N 0.000 description 1
- ZVHNJLUGESMCBD-UHFFFAOYSA-N C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4NCCF)ncc3ccc2)ccc1)=O Chemical compound C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4NCCF)ncc3ccc2)ccc1)=O ZVHNJLUGESMCBD-UHFFFAOYSA-N 0.000 description 1
- FEFINBMHJQGFOG-UHFFFAOYSA-N C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4OCCO)ncc3ccc2)ccc1)=O Chemical compound C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4OCCO)ncc3ccc2)ccc1)=O FEFINBMHJQGFOG-UHFFFAOYSA-N 0.000 description 1
- QWIWVEQVMFPASZ-HSZRJFAPSA-N C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4O[C@H]4COCC4)ncc3ccc2)ccc1)=O Chemical compound C=CC(Nc1cc(-c2c3nc(Nc(cc4)ccc4O[C@H]4COCC4)ncc3ccc2)ccc1)=O QWIWVEQVMFPASZ-HSZRJFAPSA-N 0.000 description 1
- LMYCVCWEAHOBIY-UHFFFAOYSA-N C=CC(Nc1cccc(-c2c3nc(Nc(cc4C(N)=O)ccc4N4CCNCC4)ncc3ccc2)c1)=O Chemical compound C=CC(Nc1cccc(-c2c3nc(Nc(cc4C(N)=O)ccc4N4CCNCC4)ncc3ccc2)c1)=O LMYCVCWEAHOBIY-UHFFFAOYSA-N 0.000 description 1
- SLTCLRBFKKBLMU-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1c(cc1)ccc1Nc(ncc1ccc2)nc1c2-c(cc(cc1)OCCN2CCOCC2)c1F)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1c(cc1)ccc1Nc(ncc1ccc2)nc1c2-c(cc(cc1)OCCN2CCOCC2)c1F)=O SLTCLRBFKKBLMU-UHFFFAOYSA-N 0.000 description 1
- YAFDFECRQKNIED-UHFFFAOYSA-N CC(C)(CN(CC1)CCN1c(cc1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1)O Chemical compound CC(C)(CN(CC1)CCN1c(cc1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1)O YAFDFECRQKNIED-UHFFFAOYSA-N 0.000 description 1
- ZNCPXCWBGJGONJ-AATRIKPKSA-N CC(C)NC(/C=C/CN(C)C)=O Chemical compound CC(C)NC(/C=C/CN(C)C)=O ZNCPXCWBGJGONJ-AATRIKPKSA-N 0.000 description 1
- SDTGFHJMFNIGLA-UHFFFAOYSA-N CC(CN(C)CC1)C1Oc(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1F Chemical compound CC(CN(C)CC1)C1Oc(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1F SDTGFHJMFNIGLA-UHFFFAOYSA-N 0.000 description 1
- AGWDVXZDQIVXHX-UHFFFAOYSA-N CC(N(CC1)CCN1c(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cncc(NC(C=C)=O)c1)=O Chemical compound CC(N(CC1)CCN1c(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cncc(NC(C=C)=O)c1)=O AGWDVXZDQIVXHX-UHFFFAOYSA-N 0.000 description 1
- VLCUQGUAZIEYGU-LBPRGKRZSA-N CC(N(CC1)C[C@H]1Oc(cc1)ccc1N)=O Chemical compound CC(N(CC1)C[C@H]1Oc(cc1)ccc1N)=O VLCUQGUAZIEYGU-LBPRGKRZSA-N 0.000 description 1
- ONTFZKIERLZORE-LBPRGKRZSA-N CC(N(CC1)C[C@H]1Oc(cc1)ccc1[N+]([O-])=O)=O Chemical compound CC(N(CC1)C[C@H]1Oc(cc1)ccc1[N+]([O-])=O)=O ONTFZKIERLZORE-LBPRGKRZSA-N 0.000 description 1
- XFOIJDYHTVCKFV-UHFFFAOYSA-N CC(Nc1c(C)ccc(C(I)=N)c1)=O Chemical compound CC(Nc1c(C)ccc(C(I)=N)c1)=O XFOIJDYHTVCKFV-UHFFFAOYSA-N 0.000 description 1
- GTBJMUOALLHDHH-UHFFFAOYSA-N CCC(Nc1cc(-c2c3nc(Nc(cc4)ccc4N4CCNCC4)ncc3ccc2C)ccc1)=O Chemical compound CCC(Nc1cc(-c2c3nc(Nc(cc4)ccc4N4CCNCC4)ncc3ccc2C)ccc1)=O GTBJMUOALLHDHH-UHFFFAOYSA-N 0.000 description 1
- QSTDKFNBPBIWCH-UHFFFAOYSA-N CCCN(CC1)CCC1[IH]c(cc1)ccc1N Chemical compound CCCN(CC1)CCC1[IH]c(cc1)ccc1N QSTDKFNBPBIWCH-UHFFFAOYSA-N 0.000 description 1
- SKHBCSLXROMLQZ-UHFFFAOYSA-N CCCN(CC1)CCN1c1cc(F)ccc1N=O Chemical compound CCCN(CC1)CCN1c1cc(F)ccc1N=O SKHBCSLXROMLQZ-UHFFFAOYSA-N 0.000 description 1
- QLEIDMAURCRVCX-UHFFFAOYSA-N CCCN1CCNCC1 Chemical compound CCCN1CCNCC1 QLEIDMAURCRVCX-UHFFFAOYSA-N 0.000 description 1
- CNSYKQPBWPIWMY-UHFFFAOYSA-N CN(CC1)CCC1Nc(cc1)cc(F)c1N Chemical compound CN(CC1)CCC1Nc(cc1)cc(F)c1N CNSYKQPBWPIWMY-UHFFFAOYSA-N 0.000 description 1
- JXRRKMLMJVRYFP-UHFFFAOYSA-N CN(CC1)CCC1Nc(cc1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 Chemical compound CN(CC1)CCC1Nc(cc1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 JXRRKMLMJVRYFP-UHFFFAOYSA-N 0.000 description 1
- HPWDSOPMAATWRU-UHFFFAOYSA-N COCCN(CC1)CCN1c(c(F)c1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 Chemical compound COCCN(CC1)CCN1c(c(F)c1)cc(F)c1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 HPWDSOPMAATWRU-UHFFFAOYSA-N 0.000 description 1
- JMFASCMJSMZUEZ-UHFFFAOYSA-N COCCN(CC1)CCN1c(c(F)c1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 Chemical compound COCCN(CC1)CCN1c(c(F)c1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(NC(C=C)=O)c1 JMFASCMJSMZUEZ-UHFFFAOYSA-N 0.000 description 1
- RQWDXSWYAFKXLT-UHFFFAOYSA-N COc(cc(cc1)I)c1NC1N=C2C(C3=CC(N)=CCC3)=CC=CC2=CN1 Chemical compound COc(cc(cc1)I)c1NC1N=C2C(C3=CC(N)=CCC3)=CC=CC2=CN1 RQWDXSWYAFKXLT-UHFFFAOYSA-N 0.000 description 1
- AQRBVTDIGIVINY-UHFFFAOYSA-O COc(cc(cc1)I)c1Nc(ncc1ccc2)nc1c2-c1cccc([NH3+])c1 Chemical compound COc(cc(cc1)I)c1Nc(ncc1ccc2)nc1c2-c1cccc([NH3+])c1 AQRBVTDIGIVINY-UHFFFAOYSA-O 0.000 description 1
- 0 Cc(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(*C(C=C)=O)c1 Chemical compound Cc(cc1)ccc1Nc(ncc1ccc2)nc1c2-c1cccc(*C(C=C)=O)c1 0.000 description 1
- LOYAHFIRNLEKDC-UHFFFAOYSA-N Cc(ncc1ccc2)nc1c2Br Chemical compound Cc(ncc1ccc2)nc1c2Br LOYAHFIRNLEKDC-UHFFFAOYSA-N 0.000 description 1
- PVUYIMSIKIBVQK-UHFFFAOYSA-N Clc1ncc(ccc(CBr)c2Br)c2n1 Chemical compound Clc1ncc(ccc(CBr)c2Br)c2n1 PVUYIMSIKIBVQK-UHFFFAOYSA-N 0.000 description 1
- DLZIGNAVFWETFA-UHFFFAOYSA-N Fc(ccc(OCCN1CCOCC1)c1)c1-c1c2nc(Nc(cc3)ccc3N3CCOCC3)ncc2ccc1 Chemical compound Fc(ccc(OCCN1CCOCC1)c1)c1-c1c2nc(Nc(cc3)ccc3N3CCOCC3)ncc2ccc1 DLZIGNAVFWETFA-UHFFFAOYSA-N 0.000 description 1
- LNPWTTTUVMMYOQ-UHFFFAOYSA-N Fc(cccc1)c1-c1c2nc(Nc(cc3)ccc3N3CCOCC3)ncc2ccc1 Chemical compound Fc(cccc1)c1-c1c2nc(Nc(cc3)ccc3N3CCOCC3)ncc2ccc1 LNPWTTTUVMMYOQ-UHFFFAOYSA-N 0.000 description 1
- RJXOVESYJFXCGI-UHFFFAOYSA-N [O-][N+](c(c(F)c1)ccc1F)=O Chemical compound [O-][N+](c(c(F)c1)ccc1F)=O RJXOVESYJFXCGI-UHFFFAOYSA-N 0.000 description 1
- PFCAOHLQAYBDNR-UHFFFAOYSA-N [O-][N+](c(c(F)c1)ccc1N1CCN(CCO)CC1)=O Chemical compound [O-][N+](c(c(F)c1)ccc1N1CCN(CCO)CC1)=O PFCAOHLQAYBDNR-UHFFFAOYSA-N 0.000 description 1
- SKQNOYFXAJZTPJ-UHFFFAOYSA-N [O-][N+](c(cc1)ccc1[IH]C1CCN(CCF)CC1)=O Chemical compound [O-][N+](c(cc1)ccc1[IH]C1CCN(CCF)CC1)=O SKQNOYFXAJZTPJ-UHFFFAOYSA-N 0.000 description 1
- JMDODXMUROVURC-UHFFFAOYSA-N [O-][N+](c1cc(-c(nccc23)c2nc(Nc(cc2)ccc2N2CCOCC2)nc3Cl)ccc1)=O Chemical compound [O-][N+](c1cc(-c(nccc23)c2nc(Nc(cc2)ccc2N2CCOCC2)nc3Cl)ccc1)=O JMDODXMUROVURC-UHFFFAOYSA-N 0.000 description 1
- USLYNXZTYVVMKG-UHFFFAOYSA-N [O-][N+](c1cc(-c(nccc23)c2nc(Nc(cc2)ccc2N2CCOCC2)nc3O)ccc1)=O Chemical compound [O-][N+](c1cc(-c(nccc23)c2nc(Nc(cc2)ccc2N2CCOCC2)nc3O)ccc1)=O USLYNXZTYVVMKG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- 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
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/13—Dicarboxylic acids
- C07C57/145—Maleic acid
-
- 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
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero 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
- C07D413/02—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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57484—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Zoology (AREA)
- Cell Biology (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- Wood Science & Technology (AREA)
- Hospice & Palliative Care (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biophysics (AREA)
- Food Science & Technology (AREA)
- General Physics & Mathematics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2019201461A AU2019201461B2 (en) | 2013-08-23 | 2019-03-04 | Certain chemical entities, compositions, and methods |
| AU2021200372A AU2021200372B2 (en) | 2013-08-23 | 2021-01-20 | Certain chemical entities, compositions, and methods |
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361869596P | 2013-08-23 | 2013-08-23 | |
| US61/869,596 | 2013-08-23 | ||
| US201361900283P | 2013-11-05 | 2013-11-05 | |
| US61/900,283 | 2013-11-05 | ||
| US201462000946P | 2014-05-20 | 2014-05-20 | |
| US62/000,946 | 2014-05-20 | ||
| PCT/US2014/052409 WO2015027222A2 (en) | 2013-08-23 | 2014-08-22 | Certain chemical entities, compositions, and methods |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2019201461A Division AU2019201461B2 (en) | 2013-08-23 | 2019-03-04 | Certain chemical entities, compositions, and methods |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2014308616A1 AU2014308616A1 (en) | 2016-03-10 |
| AU2014308616B2 true AU2014308616B2 (en) | 2018-12-06 |
Family
ID=52484273
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2014308616A Active AU2014308616B2 (en) | 2013-08-23 | 2014-08-22 | Certain chemical entities, compositions, and methods |
| AU2019201461A Active AU2019201461B2 (en) | 2013-08-23 | 2019-03-04 | Certain chemical entities, compositions, and methods |
| AU2021200372A Active AU2021200372B2 (en) | 2013-08-23 | 2021-01-20 | Certain chemical entities, compositions, and methods |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2019201461A Active AU2019201461B2 (en) | 2013-08-23 | 2019-03-04 | Certain chemical entities, compositions, and methods |
| AU2021200372A Active AU2021200372B2 (en) | 2013-08-23 | 2021-01-20 | Certain chemical entities, compositions, and methods |
Country Status (20)
| Country | Link |
|---|---|
| US (8) | US9550770B2 (enExample) |
| EP (2) | EP3508204A1 (enExample) |
| JP (1) | JP6559132B2 (enExample) |
| KR (1) | KR102339228B1 (enExample) |
| CN (3) | CN111285813A (enExample) |
| AU (3) | AU2014308616B2 (enExample) |
| BR (1) | BR112016005199B1 (enExample) |
| CA (1) | CA2921410C (enExample) |
| DK (1) | DK3035936T3 (enExample) |
| ES (1) | ES2729381T3 (enExample) |
| HU (1) | HUE043465T2 (enExample) |
| IL (2) | IL244189B (enExample) |
| MX (1) | MX369863B (enExample) |
| NZ (1) | NZ718190A (enExample) |
| PH (2) | PH12019500143B1 (enExample) |
| PL (1) | PL3035936T3 (enExample) |
| PT (1) | PT3035936T (enExample) |
| RU (1) | RU2718876C2 (enExample) |
| SG (2) | SG10201908045VA (enExample) |
| WO (1) | WO2015027222A2 (enExample) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9227978B2 (en) | 2013-03-15 | 2016-01-05 | Araxes Pharma Llc | Covalent inhibitors of Kras G12C |
| AU2014308616B2 (en) | 2013-08-23 | 2018-12-06 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| JO3805B1 (ar) | 2013-10-10 | 2021-01-31 | Araxes Pharma Llc | مثبطات كراس جي12سي |
| US10947201B2 (en) | 2015-02-17 | 2021-03-16 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| SG11201706869XA (en) | 2015-03-24 | 2017-09-28 | Shanghai Yingli Pharm Co Ltd | Condensed ring derivative, and preparation method, intermediate, pharmaceutical composition and use thereof |
| US10259816B2 (en) | 2015-04-24 | 2019-04-16 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | Condensed-ring pyrimidylamino derivative, preparation method therefor, and intermediate, pharmaceutical composition and applications thereof |
| CN113999180B (zh) * | 2015-07-03 | 2024-03-26 | 上海医药集团股份有限公司 | 喹唑啉类化合物、其中间体、制备方法、药物组合物和应用 |
| CN106366093B (zh) * | 2015-07-21 | 2020-08-18 | 广州再极医药科技有限公司 | 稠环嘧啶类化合物、中间体、其制备方法、组合物和应用 |
| EP3889145B1 (en) | 2015-12-17 | 2024-02-21 | Merck Patent GmbH | 8-cyano-5-piperidino-quinolines as tlr7/8 antagonists and their uses for treating immune disorders |
| CN106243044A (zh) * | 2016-06-30 | 2016-12-21 | 浙江大学 | 含卤代丙烯酰胺侧链的嘧啶类衍生物及制备和应用 |
| CN106279027A (zh) * | 2016-07-26 | 2017-01-04 | 沈阳药科大学 | (1‑芳基‑1h‑吡唑‑4‑基)(3,4,5‑三甲氧基苯基)甲酮、甲酮肟类化合物及其用途 |
| CN106187923A (zh) * | 2016-08-01 | 2016-12-07 | 沈阳药科大学 | 2‑芳基‑4‑芳酰基‑三氮唑类化合物及其用途 |
| US10947214B2 (en) * | 2016-08-08 | 2021-03-16 | Merck Patent Gmbh | TLR7/8 antagonists and uses thereof |
| EP4006035B1 (en) * | 2016-08-15 | 2023-11-22 | Neupharma, Inc. | Quinazoline derivatives as tyrosine kinase inhibitors for the treatment of cancer |
| ES2852123T3 (es) | 2016-11-28 | 2021-09-13 | Teijin Pharma Ltd | Derivados de ((piridin-2-il)-amino)pirido[3,4-d]pirimidina y ((piridazin-3-il)-amino)pirido[3,4-d]pirimidina como inhibidores de CDK4/6 para tratar p. ej. artritis reumatoide, arteriosclerosis, fibrosis pulmonar, infarto cerebral o cáncer |
| RS63004B1 (sr) * | 2016-11-28 | 2022-03-31 | Teijin Pharma Ltd | Kristal pirido[3, 4-d]pirimidin derivata ili njegov solvat |
| EP3573966A1 (en) * | 2017-01-26 | 2019-12-04 | Araxes Pharma LLC | Fused n-heterocyclic compounds and methods of use thereof |
| WO2018140599A1 (en) | 2017-01-26 | 2018-08-02 | Araxes Pharma Llc | Benzothiophene and benzothiazole compounds and methods of use thereof |
| FR3066761B1 (fr) * | 2017-05-23 | 2020-10-30 | Centre Nat Rech Scient | Nouveaux composes inhibiteurs des canaux ioniques |
| JP2020521740A (ja) | 2017-05-25 | 2020-07-27 | アラクセス ファーマ エルエルシー | 変異体kras、hrasまたはnrasの調節因子としてのキナゾリン誘導体 |
| CN111032655B (zh) * | 2017-08-31 | 2022-09-02 | 达纳-法伯癌症研究所股份有限公司 | Egfr和/或her2抑制剂和使用方法 |
| KR102613433B1 (ko) | 2017-10-11 | 2023-12-13 | 주식회사 대웅제약 | 신규한 페닐피리딘 유도체 및 이를 포함하는 약학 조성물 |
| US11465975B2 (en) | 2018-02-08 | 2022-10-11 | Neupharma, Inc | Certain chemical entities, compositions, and methods |
| CN108690389A (zh) * | 2018-04-23 | 2018-10-23 | 河北晨阳工贸集团有限公司 | 一种led光固化水性木器漆及其制备方法 |
| US12134620B2 (en) | 2018-08-01 | 2024-11-05 | Araxes Pharma Llc | Heterocyclic spiro compounds and methods of use thereof for the treatment of cancer |
| EP3898626A1 (en) * | 2018-12-19 | 2021-10-27 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| JP2022515197A (ja) | 2018-12-19 | 2022-02-17 | アレイ バイオファーマ インコーポレイテッド | がんを治療するためのfgfr阻害剤としての7-((3,5-ジメトキシフェニル)アミノ)キノキサリン誘導体 |
| US20210161897A1 (en) | 2019-11-12 | 2021-06-03 | Astrazeneca Ab | Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer |
| WO2021138391A1 (en) | 2019-12-30 | 2021-07-08 | Tyra Biosciences, Inc. | Indazole compounds |
| AU2021211871A1 (en) | 2020-01-20 | 2022-09-08 | Astrazeneca Ab | Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer |
| EP4116305A4 (en) * | 2020-03-06 | 2024-07-17 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | THIENOPYRIMIDINE DERIVATIVE AND PREPARATION METHOD THEREFOR |
| WO2021180032A1 (en) * | 2020-03-13 | 2021-09-16 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | Novel Therapeutic Methods |
| US20210369709A1 (en) | 2020-05-27 | 2021-12-02 | Astrazeneca Ab | EGFR TKIs FOR USE IN THE TREATMENT OF NON-SMALL CELL LUNG CANCER |
| CN115942937B (zh) * | 2020-08-17 | 2025-07-25 | 浙江扬厉医药技术有限公司 | 嘧啶并环类化合物 |
| WO2022061224A1 (en) | 2020-09-21 | 2022-03-24 | Landos Biopharma, Inc. | Nlrx1 ligands |
| WO2022271749A1 (en) * | 2021-06-22 | 2022-12-29 | Blueprint Medicines Corporation | Heterocyclic egfr inhibitors for use in the treatment of cancer |
| CN117940424A (zh) * | 2021-06-22 | 2024-04-26 | 缆图药品公司 | Egfr抑制剂 |
| WO2022271612A1 (en) * | 2021-06-22 | 2022-12-29 | Blueprint Medicines Corporation | Heterocyclic egfr inhibitors for use in the treatment of cancer |
| WO2022271613A1 (en) * | 2021-06-22 | 2022-12-29 | Blueprint Medicines Corporation | Heterocyclic egfr inhibitors for use in the treatment of cancer |
| CN115583946A (zh) * | 2021-07-06 | 2023-01-10 | 赛诺哈勃药业(成都)有限公司 | 杂环化合物及其作为cdk抑制剂的用途 |
| WO2023010354A1 (zh) * | 2021-08-04 | 2023-02-09 | 四川大学华西医院 | 一种具有egfr抑制活性的小分子化合物及其制备方法与应用 |
| WO2023071998A1 (zh) * | 2021-10-26 | 2023-05-04 | 杭州德睿智药科技有限公司 | 新型嘧啶或三嗪取代吡啶并杂环化合物 |
| IL315848A (en) | 2022-03-31 | 2024-11-01 | Astrazeneca Ab | Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors in combination with an AKT inhibitor for cancer treatment |
| CA3249080A1 (en) | 2022-04-28 | 2023-11-02 | Astrazeneca Ab | Condensed bicyclic heteroaromatic compounds and their use in the treatment of cancer |
| WO2023209090A1 (en) | 2022-04-28 | 2023-11-02 | Astrazeneca Ab | Bicyclic heteroaromatic compounds and their application in the treatment of cancer |
| US20240116926A1 (en) | 2022-04-28 | 2024-04-11 | Astrazeneca Ab | Heteroaromatic compounds |
| WO2023209088A1 (en) | 2022-04-28 | 2023-11-02 | Astrazeneca Ab | Bicyclic heteroaromatic compounds and their use in the treatment of cancer |
| KR20250029133A (ko) | 2022-06-27 | 2025-03-04 | 아스트라제네카 아베 | 암 치료를 위한 표피성장인자 수용체 티로신 키나제 억제제를 포함하는 조합물 |
| CN119654152A (zh) | 2022-07-08 | 2025-03-18 | 阿斯利康(瑞典)有限公司 | 与hgf-受体抑制剂组合用于治疗癌症的表皮生长因子受体酪氨酸激酶抑制剂 |
| WO2025010279A2 (en) * | 2023-07-03 | 2025-01-09 | Resero Therapeutics, Llc. | Polo-like kinase 1 inhibitors |
| WO2025235874A1 (en) * | 2024-05-10 | 2025-11-13 | Schrödinger, Inc. | Heterocyclics as egfr inhibitors |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001021598A1 (en) * | 1999-09-23 | 2001-03-29 | Astrazeneca Ab | Therapeutic quinazoline compounds |
| WO2007117607A2 (en) * | 2006-04-06 | 2007-10-18 | Novartis Ag | Quinazolines for pdk1 inhibition |
| WO2013013031A1 (en) * | 2011-07-19 | 2013-01-24 | Abbvie Inc. | Pyridazino [4, 5 -d] pyrimidin- (6h) -one inhibitors of wee - 1 kinase |
| WO2013130660A1 (en) * | 2012-02-28 | 2013-09-06 | Amgen Inc. | Amides as pim inhibitors |
| WO2014037750A1 (en) * | 2012-09-07 | 2014-03-13 | Cancer Research Technology Limited | Inhibitor compounds |
Family Cites Families (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB587936A (en) | 1944-09-05 | 1947-05-09 | Francis Henry Swinden Curd | New quinazoline derivatives |
| GB8515934D0 (en) | 1985-06-24 | 1985-07-24 | Janssen Pharmaceutica Nv | (4-piperidinomethyl and-hetero)purines |
| US5052558A (en) | 1987-12-23 | 1991-10-01 | Entravision, Inc. | Packaged pharmaceutical product |
| US5033252A (en) | 1987-12-23 | 1991-07-23 | Entravision, Inc. | Method of packaging and sterilizing a pharmaceutical product |
| US5323907A (en) | 1992-06-23 | 1994-06-28 | Multi-Comp, Inc. | Child resistant package assembly for dispensing pharmaceutical medications |
| US6334997B1 (en) | 1994-03-25 | 2002-01-01 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| JP3696884B2 (ja) | 1994-03-25 | 2005-09-21 | アイソテクニカ、インコーポレーテッド | ジュウテリウム化による薬物の効能の増強 |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| BR9707425A (pt) | 1996-02-12 | 1999-07-20 | Univ Rutgers | Composto processo terapêutico para inibir o crescimento de células cancerosas e processo para utilizar o composto |
| WO1997030035A1 (en) | 1996-02-13 | 1997-08-21 | Zeneca Limited | Quinazoline derivatives as vegf inhibitors |
| PT885198E (pt) | 1996-03-05 | 2002-06-28 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| EP1054012B1 (en) | 1998-01-05 | 2003-06-11 | Eisai Co., Ltd. | Purine derivatives and adenosine a2 receptor antagonists serving as preventives/remedies for diabetes |
| JP3990061B2 (ja) | 1998-01-05 | 2007-10-10 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | プリン誘導体および糖尿病の予防・治療剤としてのアデノシンa2受容体拮抗剤 |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| BRPI0017548B8 (pt) | 1999-02-10 | 2023-05-02 | Astrazeneca Ab | Composto |
| CA2376835C (en) | 1999-07-02 | 2009-09-15 | Eisai Co., Ltd. | Condensed imidazole compounds and a therapeutic agent for diabetes mellitus |
| AU2001258628A1 (en) | 2000-05-31 | 2001-12-11 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| UA73993C2 (uk) | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
| MXPA02012905A (es) | 2000-07-07 | 2004-07-30 | Angiogene Pharm Ltd | Derivados de colquinol como agentes de dano vascular.. |
| BR0112225A (pt) | 2000-07-07 | 2003-05-06 | Angiogene Pharm Ltd | Composto, composição farmacêutica, uso de um composto, e, processo papa preparar um composto |
| UA80295C2 (en) | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
| AU2004222387A1 (en) | 2003-03-13 | 2004-09-30 | Synta Pharmaceuticals Corp. | Fused pyrrole compounds |
| WO2005032481A2 (en) | 2003-09-30 | 2005-04-14 | Scios Inc. | Quinazoline derivatives as medicaments |
| CA2577588C (en) | 2004-10-29 | 2013-09-10 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting bicyclic pyrimidine derivatives |
| CR9465A (es) | 2005-03-25 | 2008-06-19 | Surface Logix Inc | Compuestos mejorados farmacocineticamente |
| GB0526246D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
| TWI389893B (zh) | 2007-07-06 | 2013-03-21 | Astellas Pharma Inc | 二(芳胺基)芳基化合物 |
| SI2215094T1 (sl) | 2007-11-15 | 2016-05-31 | Ym Biosciences Australia Pty Ltd | N vsebujoče heterociklične spojine |
| EP2269993B1 (en) * | 2008-04-23 | 2013-02-27 | Kyowa Hakko Kirin Co., Ltd. | 2-aminoquinazoline derivative |
| WO2010019762A1 (en) | 2008-08-13 | 2010-02-18 | Jenrin Discovery | Purine compounds as cannabinoid receptor blockers |
| WO2010056758A1 (en) | 2008-11-12 | 2010-05-20 | Yangbo Feng | Quinazoline derivatives as kinase inhibitors |
| JP5918693B2 (ja) | 2009-05-05 | 2016-05-18 | ダナ ファーバー キャンサー インスティテュート インコーポレイテッド | Egfr阻害剤及び疾患の治療方法 |
| BR112012008019A2 (pt) | 2009-10-07 | 2016-03-01 | Sloan Kettering Inst Cancer | derivados de purina úteis como inibidores de hsp90 |
| US7741330B1 (en) | 2009-10-12 | 2010-06-22 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase |
| WO2011079231A1 (en) * | 2009-12-23 | 2011-06-30 | Gatekeeper Pharmaceutical, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
| WO2011106168A1 (en) | 2010-02-24 | 2011-09-01 | Dcam Pharma Inc | Purine compounds for treating autoimmune and demyelinating diseases |
| FR2959510B1 (fr) * | 2010-04-28 | 2013-04-26 | Centre Nat Rech Scient | Derives de pyrido[3,2-d]pyrimidine, leurs procedes de preparation et leurs utilisations therapeutiques |
| CN102260263A (zh) | 2010-05-26 | 2011-11-30 | 四川大学 | 一类二苯胺基嘌呤衍生物及制备方法和医药用途 |
| CN103889962B (zh) | 2011-04-01 | 2017-05-03 | 犹他大学研究基金会 | 作为受体酪氨酸激酶btk抑制剂的取代的n‑(3‑(嘧啶‑4‑基)苯基)丙烯酰胺类似物 |
| WO2013005157A1 (en) | 2011-07-05 | 2013-01-10 | Lupin Limited | Sulfone derivatives and their use as pkm2 modulators for the treatment of cancer |
| PT3009431T (pt) | 2011-07-27 | 2017-12-26 | Astrazeneca Ab | Compostos de 2-(2,4,5-anilino-substituídos)pirimidina como moduladores úteis do egfr para o tratamento do cancro |
| ES2725790T3 (es) | 2011-08-26 | 2019-09-27 | Neupharma Inc | Algunas entidades químicas, composiciones, y métodos |
| WO2013040515A1 (en) | 2011-09-14 | 2013-03-21 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| EP2785184B1 (en) | 2011-11-30 | 2020-06-10 | Emory University | Compositions comprising jak inhibitors and haart drugs for use in the prevention or treatment of hiv |
| WO2013106792A1 (en) | 2012-01-13 | 2013-07-18 | Acea Biosciences Inc. | Heterocyclic compounds and uses as anticancer agents. |
| TW201336847A (zh) | 2012-02-07 | 2013-09-16 | Taiho Pharmaceutical Co Ltd | 喹啉基吡咯并嘧啶化合物或其鹽 |
| US8802697B2 (en) | 2012-07-11 | 2014-08-12 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
| TW201427958A (zh) | 2012-09-14 | 2014-07-16 | Univ Nat Yang Ming | 芳基胺取代之嘧啶及喹唑啉及其作為抗癌藥物之用途 |
| NZ706857A (en) | 2012-09-28 | 2018-05-25 | Ignyta Inc | Azaquinazoline inhibitors of atypical protein kinase c |
| CN103864792B (zh) | 2012-12-12 | 2017-01-18 | 山东亨利医药科技有限责任公司 | 作为酪氨酸激酶抑制剂的含氮并环类化合物 |
| CN103936742B (zh) | 2013-01-17 | 2017-05-03 | 程鹏 | 含嘌呤基的新型pi3k抑制剂及其制备方法和应用 |
| WO2014130693A1 (en) | 2013-02-25 | 2014-08-28 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
| WO2014135245A1 (en) | 2013-03-05 | 2014-09-12 | Merck Patent Gmbh | 9-(aryl or heteroaryl)-2-(pyrazolyl, pyrrolidinyl or cyclopentyl)aminopurine derivatives as anticancer agents |
| EP3342770B1 (en) | 2013-03-06 | 2022-03-30 | AstraZeneca AB | Quinazoline inhibitors of activating mutant forms of epidermal growth factor receptor |
| WO2014180524A1 (en) | 2013-05-06 | 2014-11-13 | Merck Patent Gmbh | Macrocycles as kinase inhibitors |
| CN103554038B (zh) | 2013-06-19 | 2015-10-14 | 云南大学 | 多卤代苯腈喹唑啉酮化合物及其制备方法和用途 |
| AU2014287016B2 (en) | 2013-07-11 | 2018-11-01 | Acea Biosciences Inc. | Pyrimidine derivatives as kinase inhibitors |
| CN105452257B (zh) | 2013-08-12 | 2017-09-05 | 大鹏药品工业株式会社 | 新型稠合嘧啶化合物或其盐 |
| AU2014308616B2 (en) | 2013-08-23 | 2018-12-06 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US20160272645A1 (en) | 2013-10-18 | 2016-09-22 | Medivation Technologies, Inc. | Heterocyclic Compounds and Methods of Use |
| GB201404987D0 (en) | 2014-03-20 | 2014-05-07 | Redx Pharma Ltd | Compounds |
| WO2015151006A1 (en) | 2014-03-29 | 2015-10-08 | Lupin Limited | Substituted purine compounds as btk inhibitors |
| KR20170003688A (ko) | 2014-05-14 | 2017-01-09 | 더 리젠츠 오브 더 유니버시티 오브 콜로라도, 어 바디 코포레이트 | 단백질 탈아세틸화효소 억제제 및 이중 단백질 탈아세틸화효소-단백질 키나제 억제제로서의 헤테로사이클릭 하이드록삼산 및 그 이용 방법 |
| CN104086551B (zh) | 2014-06-06 | 2016-09-21 | 人福医药集团股份公司 | 化合物及其制备方法和用途 |
| TW201613644A (en) | 2014-06-17 | 2016-04-16 | Acerta Pharma Bv | Therapeutic combinations of a BTK inhibitor, a PI3K inhibitor, and/or a JAK-2 inhibitor |
| CN105315283A (zh) | 2014-07-22 | 2016-02-10 | 成都贝斯凯瑞生物科技有限公司 | 一种Bruton酪氨酸激酶抑制剂 |
| CA2959602A1 (en) | 2014-08-01 | 2016-02-04 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
| EP3242878B1 (en) | 2015-01-08 | 2020-10-14 | Impetis Biosciences Ltd. | Bicyclic compounds, compositions and medicinal applications thereof |
| CN105837576B (zh) | 2015-01-14 | 2019-03-26 | 湖北生物医药产业技术研究院有限公司 | Btk抑制剂 |
| US10947201B2 (en) | 2015-02-17 | 2021-03-16 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| CN105777759B (zh) | 2016-04-29 | 2018-01-26 | 杭州和正医药有限公司 | 一种布鲁顿酪氨酸激酶抑制剂 |
| EP4006035B1 (en) | 2016-08-15 | 2023-11-22 | Neupharma, Inc. | Quinazoline derivatives as tyrosine kinase inhibitors for the treatment of cancer |
-
2014
- 2014-08-22 AU AU2014308616A patent/AU2014308616B2/en active Active
- 2014-08-22 EP EP19157227.0A patent/EP3508204A1/en active Pending
- 2014-08-22 BR BR112016005199-8A patent/BR112016005199B1/pt active IP Right Grant
- 2014-08-22 NZ NZ718190A patent/NZ718190A/en unknown
- 2014-08-22 SG SG10201908045V patent/SG10201908045VA/en unknown
- 2014-08-22 ES ES14838403T patent/ES2729381T3/es active Active
- 2014-08-22 US US14/466,896 patent/US9550770B2/en active Active
- 2014-08-22 KR KR1020167007174A patent/KR102339228B1/ko active Active
- 2014-08-22 WO PCT/US2014/052409 patent/WO2015027222A2/en not_active Ceased
- 2014-08-22 CN CN202010143416.4A patent/CN111285813A/zh active Pending
- 2014-08-22 CA CA2921410A patent/CA2921410C/en active Active
- 2014-08-22 SG SG11201601138PA patent/SG11201601138PA/en unknown
- 2014-08-22 CN CN201910197492.0A patent/CN109851617B/zh active Active
- 2014-08-22 PT PT14838403T patent/PT3035936T/pt unknown
- 2014-08-22 PH PH1/2019/500143A patent/PH12019500143B1/en unknown
- 2014-08-22 DK DK14838403.5T patent/DK3035936T3/da active
- 2014-08-22 US US14/913,336 patent/US20170050936A1/en not_active Abandoned
- 2014-08-22 PL PL14838403T patent/PL3035936T3/pl unknown
- 2014-08-22 EP EP14838403.5A patent/EP3035936B1/en active Active
- 2014-08-22 JP JP2016536501A patent/JP6559132B2/ja active Active
- 2014-08-22 HU HUE14838403A patent/HUE043465T2/hu unknown
- 2014-08-22 CN CN201480058610.5A patent/CN105682661B/zh active Active
- 2014-08-22 RU RU2016110412A patent/RU2718876C2/ru active
- 2014-08-22 MX MX2016002137A patent/MX369863B/es active IP Right Grant
-
2016
- 2016-02-18 PH PH12016500330A patent/PH12016500330A1/en unknown
- 2016-02-18 IL IL244189A patent/IL244189B/en active IP Right Grant
- 2016-11-22 US US15/359,370 patent/US9849139B2/en active Active
-
2017
- 2017-11-07 US US15/806,165 patent/US10172868B2/en active Active
-
2018
- 2018-11-13 US US16/188,852 patent/US10653701B2/en active Active
-
2019
- 2019-03-04 AU AU2019201461A patent/AU2019201461B2/en active Active
- 2019-07-16 IL IL268094A patent/IL268094B/en active IP Right Grant
-
2020
- 2020-04-08 US US16/843,610 patent/US11304957B2/en active Active
-
2021
- 2021-01-20 AU AU2021200372A patent/AU2021200372B2/en active Active
-
2022
- 2022-02-25 US US17/681,387 patent/US11865120B2/en active Active
-
2023
- 2023-11-27 US US18/519,150 patent/US12403145B2/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001021598A1 (en) * | 1999-09-23 | 2001-03-29 | Astrazeneca Ab | Therapeutic quinazoline compounds |
| WO2007117607A2 (en) * | 2006-04-06 | 2007-10-18 | Novartis Ag | Quinazolines for pdk1 inhibition |
| WO2013013031A1 (en) * | 2011-07-19 | 2013-01-24 | Abbvie Inc. | Pyridazino [4, 5 -d] pyrimidin- (6h) -one inhibitors of wee - 1 kinase |
| WO2013130660A1 (en) * | 2012-02-28 | 2013-09-06 | Amgen Inc. | Amides as pim inhibitors |
| WO2014037750A1 (en) * | 2012-09-07 | 2014-03-13 | Cancer Research Technology Limited | Inhibitor compounds |
Non-Patent Citations (3)
| Title |
|---|
| CAS RN 1026642-77-2; STN entry date: 8 June 2008N-(3-Chloro-4-fluorophenyl)-8-[4-[(diethylamino)methyl]-1-piperidinyl]-pyrimido[5,4-d]pyrimidin-2-amine * |
| CAS RN 1082700-91-1; STN entry date: 10 December 2008N,4,6,8-Tetrakis(4-methoxyphenyl)-pyrimido[5,4-d]pyrimidin-2-amine * |
| HE, Y. et al, "Synthesis and SAR of novel quinazolines as potent and brainpenetrant c-jun N-terminal kinase (JNK) Inhibitors", Bioorganic & Medicinal Chemistry Letters, 2011, vol. 21, pp. 1719-1723 * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2021200372B2 (en) | Certain chemical entities, compositions, and methods | |
| AU2017218983B2 (en) | Certain chemical entities, compositions, and methods | |
| EP2916838A1 (en) | Certain chemical entities, compositions, and methods | |
| HK1226939B (en) | Certain chemical entities, compositions, and methods | |
| HK40009359A (en) | Chemical entities, compositions, and methods | |
| HK40009359B (en) | Chemical entities, compositions, and methods |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) |