KR101473068B1 - 치환된 이소퀴놀리논 및 퀴나졸리논 - Google Patents
치환된 이소퀴놀리논 및 퀴나졸리논 Download PDFInfo
- Publication number
- KR101473068B1 KR101473068B1 KR1020127019166A KR20127019166A KR101473068B1 KR 101473068 B1 KR101473068 B1 KR 101473068B1 KR 1020127019166 A KR1020127019166 A KR 1020127019166A KR 20127019166 A KR20127019166 A KR 20127019166A KR 101473068 B1 KR101473068 B1 KR 101473068B1
- Authority
- KR
- South Korea
- Prior art keywords
- phenyl
- alkyl
- methoxy
- isoquinolin
- dihydro
- 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
- 0 *c1ccc(C(c2cc(*)c(*)cc2*2)N(*)C2=O)cc1 Chemical compound *c1ccc(C(c2cc(*)c(*)cc2*2)N(*)C2=O)cc1 0.000 description 12
- DPXHMEWNPSYFDF-UHFFFAOYSA-N CC(C)(C)OC(N(C)CCN(CC(OC)=O)C1CCC(CN(C)c(cc2)nc(F)c2Br)CC1)=O Chemical compound CC(C)(C)OC(N(C)CCN(CC(OC)=O)C1CCC(CN(C)c(cc2)nc(F)c2Br)CC1)=O DPXHMEWNPSYFDF-UHFFFAOYSA-N 0.000 description 1
- XBYCTDUSWHFZMF-KESTWPANSA-N CC(C)(C)OC(N(C)CCN(CC(OC)=O)[C@H]1CC[C@H](CN(C)c(cc2)ncc2I)CC1)=O Chemical compound CC(C)(C)OC(N(C)CCN(CC(OC)=O)[C@H]1CC[C@H](CN(C)c(cc2)ncc2I)CC1)=O XBYCTDUSWHFZMF-KESTWPANSA-N 0.000 description 1
- UNZLFEPRQSYMMN-UHFFFAOYSA-N CC(C)(C)OC(NC1CCC(CNc(cc2)nc(F)c2Br)CC1)=O Chemical compound CC(C)(C)OC(NC1CCC(CNc(cc2)nc(F)c2Br)CC1)=O UNZLFEPRQSYMMN-UHFFFAOYSA-N 0.000 description 1
- PCLOGHHCVDXJJD-UHFFFAOYSA-N CC(C)Nc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)Cc3ccncc3)c2cc1 Chemical compound CC(C)Nc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)Cc3ccncc3)c2cc1 PCLOGHHCVDXJJD-UHFFFAOYSA-N 0.000 description 1
- CMXOSMMTNMNWDM-CZCVHRGNSA-N CC(C)Oc(cc([C@H](c(cc1)ccc1Cl)N(C(C1)=O)c(cc2)ncc2N(C)C[C@H](CC2)CC[C@]22C3(C4)[C@@H]2C3CN(C)C4=O)c1c1)c1OC Chemical compound CC(C)Oc(cc([C@H](c(cc1)ccc1Cl)N(C(C1)=O)c(cc2)ncc2N(C)C[C@H](CC2)CC[C@]22C3(C4)[C@@H]2C3CN(C)C4=O)c1c1)c1OC CMXOSMMTNMNWDM-CZCVHRGNSA-N 0.000 description 1
- TZTVTMGZQVEMTM-XXCFHSPASA-N CC(C)Oc(cc([C@H](c(cc1)ccc1Cl)N(C(C1)=O)c2ccc([C@H](C)N(CCC3)C3C(OC)=O)cc2)c1c1)c1OC Chemical compound CC(C)Oc(cc([C@H](c(cc1)ccc1Cl)N(C(C1)=O)c2ccc([C@H](C)N(CCC3)C3C(OC)=O)cc2)c1c1)c1OC TZTVTMGZQVEMTM-XXCFHSPASA-N 0.000 description 1
- CLRSLRWKONPSRQ-UHFFFAOYSA-N CC(C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)CC(CC3)CCC3N(CCN3C)CC3=O)c2cc1OC Chemical compound CC(C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)CC(CC3)CCC3N(CCN3C)CC3=O)c2cc1OC CLRSLRWKONPSRQ-UHFFFAOYSA-N 0.000 description 1
- OPUVUYZSZHKNRJ-UHFFFAOYSA-N CC(C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(ccc(C(OC)=O)c3)c3O[Si+](C)(C)C(C)(C)C)c2cc1OC Chemical compound CC(C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(ccc(C(OC)=O)c3)c3O[Si+](C)(C)C(C)(C)C)c2cc1OC OPUVUYZSZHKNRJ-UHFFFAOYSA-N 0.000 description 1
- RTXBFXPWNNENIR-HJHNVZRJSA-N CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)CC(CC3)CCC3NS(C)(=O)=O)c2cc1OC Chemical compound CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)CC(CC3)CCC3NS(C)(=O)=O)c2cc1OC RTXBFXPWNNENIR-HJHNVZRJSA-N 0.000 description 1
- IPXCNZMRGCEREM-NYRHXDHDSA-N CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ncc3N(C)C[C@H](CC3)CC[C@@H]3NC(OC(C)(C)C)=O)c2cc1OC Chemical compound CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ncc3N(C)C[C@H](CC3)CC[C@@H]3NC(OC(C)(C)C)=O)c2cc1OC IPXCNZMRGCEREM-NYRHXDHDSA-N 0.000 description 1
- DQUQYOGFVHTURI-IBGZPJMESA-N CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)NC(C2)=O)c2cc1OC Chemical compound CC(C)Oc1cc([C@H](c(cc2)ccc2Cl)NC(C2)=O)c2cc1OC DQUQYOGFVHTURI-IBGZPJMESA-N 0.000 description 1
- OULQWIAPTHWKSL-UHFFFAOYSA-N CC(COc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC)OC Chemical compound CC(COc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC)OC OULQWIAPTHWKSL-UHFFFAOYSA-N 0.000 description 1
- CAGZMCSXFPQMPM-UHFFFAOYSA-N CCCN(C(C)C)c1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)Cc3ccncc3)c2cc1 Chemical compound CCCN(C(C)C)c1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)Cc3ccncc3)c2cc1 CAGZMCSXFPQMPM-UHFFFAOYSA-N 0.000 description 1
- UFKCCNWBDYXJMD-UHFFFAOYSA-N CCOC(Cc(cc1)cc(OC)c1OCc(cc1)ccc1OC)=O Chemical compound CCOC(Cc(cc1)cc(OC)c1OCc(cc1)ccc1OC)=O UFKCCNWBDYXJMD-UHFFFAOYSA-N 0.000 description 1
- GIUFMFBEWZVERI-UHFFFAOYSA-N CCOC(Cc(cc1OC)ccc1OC(C)C)=O Chemical compound CCOC(Cc(cc1OC)ccc1OC(C)C)=O GIUFMFBEWZVERI-UHFFFAOYSA-N 0.000 description 1
- UMKRVSUXBNWXEF-UHFFFAOYSA-N CCOc1cc(CC(N(C2c(cc3)ccc3Cl)c(ccc(C)c3)c3OCC(OC)=O)=O)c2cc1OCC Chemical compound CCOc1cc(CC(N(C2c(cc3)ccc3Cl)c(ccc(C)c3)c3OCC(OC)=O)=O)c2cc1OCC UMKRVSUXBNWXEF-UHFFFAOYSA-N 0.000 description 1
- YEVDXGQZCAZIOY-UHFFFAOYSA-N CCOc1ccc(CC(Cl)=O)cc1OCC Chemical compound CCOc1ccc(CC(Cl)=O)cc1OCC YEVDXGQZCAZIOY-UHFFFAOYSA-N 0.000 description 1
- YRLLFVUXQAFARK-LLVKDONJSA-N CC[C@@H](C)Oc(c(OC)c1)cc(C(c(cc2)ccc2Cl)=O)c1[N+]([O-])=O Chemical compound CC[C@@H](C)Oc(c(OC)c1)cc(C(c(cc2)ccc2Cl)=O)c1[N+]([O-])=O YRLLFVUXQAFARK-LLVKDONJSA-N 0.000 description 1
- XPWWFZVWBXLCPB-MOJDWNGGSA-N CC[C@@H](C)Oc(cc(C(c(cc1)ccc1Cl)N(C(C1)=O)c(cc2)ccc2C(OC)=O)c1c1)c1OC Chemical compound CC[C@@H](C)Oc(cc(C(c(cc1)ccc1Cl)N(C(C1)=O)c(cc2)ccc2C(OC)=O)c1c1)c1OC XPWWFZVWBXLCPB-MOJDWNGGSA-N 0.000 description 1
- ZDRUXXFMVAAUQM-QHSQBYJISA-N CC[C@@H](C)Oc1cc(C(c(c(CN)c2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(c(CN)c2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC ZDRUXXFMVAAUQM-QHSQBYJISA-N 0.000 description 1
- MEMPXHHRCPTSPQ-QHSQBYJISA-N CC[C@@H](C)Oc1cc(C(c(c(NC(NC)=O)c2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(c(NC(NC)=O)c2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(C)C)c2cc1OC MEMPXHHRCPTSPQ-QHSQBYJISA-N 0.000 description 1
- DERUQPZTBLGCOC-HZRSZRRBSA-N CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(CCC3)C3=O)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3N(CCC3)C3=O)c2cc1OC DERUQPZTBLGCOC-HZRSZRRBSA-N 0.000 description 1
- IVPOKBWGTNYQOK-LFDVRYLKSA-N CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3NCC3CCCC3)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c(cc3)ccc3NCC3CCCC3)c2cc1OC IVPOKBWGTNYQOK-LFDVRYLKSA-N 0.000 description 1
- WKPFGADMDMLPOJ-XFBJNOSPSA-N CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c3ccc(C(C)N(CC4)CCC4NC(C)=O)cc3)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c3ccc(C(C)N(CC4)CCC4NC(C)=O)cc3)c2cc1OC WKPFGADMDMLPOJ-XFBJNOSPSA-N 0.000 description 1
- DMFLDGGXDGDWDL-XOBGVXBPSA-N CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c3ccc(C(C)N4CCNCC4)cc3)c2cc1OC Chemical compound CC[C@@H](C)Oc1cc(C(c(cc2)ccc2Cl)N(C(C2)=O)c3ccc(C(C)N4CCNCC4)cc3)c2cc1OC DMFLDGGXDGDWDL-XOBGVXBPSA-N 0.000 description 1
- WJJSRGLHHXPJFD-UFFVCSGVSA-N CN(C(C(F)(F)F)=O)c(cc1)ccc1/N=C/c(cc1)ccc1Cl Chemical compound CN(C(C(F)(F)F)=O)c(cc1)ccc1/N=C/c(cc1)ccc1Cl WJJSRGLHHXPJFD-UFFVCSGVSA-N 0.000 description 1
- XWPOIDVLCGXMCS-UHFFFAOYSA-N CN(C)CC(CC1)CCC1N(CCC1)C1=O Chemical compound CN(C)CC(CC1)CCC1N(CCC1)C1=O XWPOIDVLCGXMCS-UHFFFAOYSA-N 0.000 description 1
- QTFGBHVLLJESHQ-UHFFFAOYSA-N CN(C)CC(CC1)CCC1N(CCCC1)C1=O Chemical compound CN(C)CC(CC1)CCC1N(CCCC1)C1=O QTFGBHVLLJESHQ-UHFFFAOYSA-N 0.000 description 1
- GSTLLKPMOMAOIQ-UHFFFAOYSA-N CN(C)c(cc1)ccc1N(C(c(cc1)ccc1Cl)c(cc1OCCOC)c(C2)cc1OC)C2=O Chemical compound CN(C)c(cc1)ccc1N(C(c(cc1)ccc1Cl)c(cc1OCCOC)c(C2)cc1OC)C2=O GSTLLKPMOMAOIQ-UHFFFAOYSA-N 0.000 description 1
- BBOXRFHFPGWQCA-UHFFFAOYSA-N CN(CC(CC1)CCC1N(CCN1C)CC1=O)I Chemical compound CN(CC(CC1)CCC1N(CCN1C)CC1=O)I BBOXRFHFPGWQCA-UHFFFAOYSA-N 0.000 description 1
- JIFRZQKERCKZLF-UHFFFAOYSA-N CN(CC(CC1)CCC1N(CCOC1)C1=O)I Chemical compound CN(CC(CC1)CCC1N(CCOC1)C1=O)I JIFRZQKERCKZLF-UHFFFAOYSA-N 0.000 description 1
- OTANBXYOAQXXBJ-UHFFFAOYSA-N CN(CC(CC1)CCC1N)C(C=C1)=NN(C)C1Br Chemical compound CN(CC(CC1)CCC1N)C(C=C1)=NN(C)C1Br OTANBXYOAQXXBJ-UHFFFAOYSA-N 0.000 description 1
- KWDXLSIINCZBOI-UHFFFAOYSA-N CN(CC(CC1)CCC1NCC(OC)=O)c(cn1)cnc1Br Chemical compound CN(CC(CC1)CCC1NCC(OC)=O)c(cn1)cnc1Br KWDXLSIINCZBOI-UHFFFAOYSA-N 0.000 description 1
- BYZQYAUITWOTEI-UHFFFAOYSA-N CN(CC(CC1)CCC1NCCN)c(nc1)ccc1I Chemical compound CN(CC(CC1)CCC1NCCN)c(nc1)ccc1I BYZQYAUITWOTEI-UHFFFAOYSA-N 0.000 description 1
- UXMFFRFGEASXKL-UHFFFAOYSA-N COc(cc1)ccc1N(C(c(cc1)ccc1Cl)c(cc(c(OC)c1)OC)c1N1)C1=O Chemical compound COc(cc1)ccc1N(C(c(cc1)ccc1Cl)c(cc(c(OC)c1)OC)c1N1)C1=O UXMFFRFGEASXKL-UHFFFAOYSA-N 0.000 description 1
- VKVGAVMRFMGWMB-YFKPBYRVSA-N C[C@@H](c(cc1)ncc1Br)N Chemical compound C[C@@H](c(cc1)ncc1Br)N VKVGAVMRFMGWMB-YFKPBYRVSA-N 0.000 description 1
- WZKZRSOWLZKJCL-UHFFFAOYSA-N Ic1ccc(C[n]2cncc2)cc1 Chemical compound Ic1ccc(C[n]2cncc2)cc1 WZKZRSOWLZKJCL-UHFFFAOYSA-N 0.000 description 1
- GAKAGTKSDDUOMU-UHFFFAOYSA-N NCC(C1)CC1OC(c(cc1)ccc1[NH+]([O-])O)=O Chemical compound NCC(C1)CC1OC(c(cc1)ccc1[NH+]([O-])O)=O GAKAGTKSDDUOMU-UHFFFAOYSA-N 0.000 description 1
- JAQPHLXOWXJMOW-UHFFFAOYSA-N [O-][N+](c1cc(C(c(cc2)ccc2Cl)=O)c(CC(O)=O)cc1)=O Chemical compound [O-][N+](c1cc(C(c(cc2)ccc2Cl)=O)c(CC(O)=O)cc1)=O JAQPHLXOWXJMOW-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- C07D239/80—Oxygen atoms
- C07D239/82—Oxygen atoms with an aryl radical attached in position 4
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- C07D405/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- 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
- C07D413/10—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 carbon chain containing aromatic 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
-
- 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
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US28899209P | 2009-12-22 | 2009-12-22 | |
| US61/288,992 | 2009-12-22 | ||
| CN2010078927 | 2010-11-19 | ||
| CNPCT/CN2010/078927 | 2010-11-19 | ||
| PCT/EP2010/070364 WO2011076786A1 (en) | 2009-12-22 | 2010-12-21 | Substituted isoquinolinones and quinazolinones |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR20147029863A Division KR20140140602A (ko) | 2009-12-22 | 2010-12-21 | 치환된 이소퀴놀리논 및 퀴나졸리논 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20120112618A KR20120112618A (ko) | 2012-10-11 |
| KR101473068B1 true KR101473068B1 (ko) | 2014-12-15 |
Family
ID=43530866
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127019166A Expired - Fee Related KR101473068B1 (ko) | 2009-12-22 | 2010-12-21 | 치환된 이소퀴놀리논 및 퀴나졸리논 |
| KR20147029863A Withdrawn KR20140140602A (ko) | 2009-12-22 | 2010-12-21 | 치환된 이소퀴놀리논 및 퀴나졸리논 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR20147029863A Withdrawn KR20140140602A (ko) | 2009-12-22 | 2010-12-21 | 치환된 이소퀴놀리논 및 퀴나졸리논 |
Country Status (41)
Families Citing this family (122)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2118123T3 (pl) | 2007-01-31 | 2016-06-30 | Dana Farber Cancer Inst Inc | Stabilizowane peptydy p53 i ich zastosowania |
| KR101525754B1 (ko) | 2007-03-28 | 2015-06-09 | 프레지던트 앤드 펠로우즈 오브 하바드 칼리지 | 스티칭된 폴리펩티드 |
| GB0811643D0 (en) | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
| US20100317593A1 (en) * | 2009-06-12 | 2010-12-16 | Astrazeneca Ab | 2,3-dihydro-1h-indene compounds |
| US8440693B2 (en) * | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
| SG10201500639TA (en) | 2010-01-27 | 2015-03-30 | Arena Pharm Inc | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| CA2807685C (en) | 2010-08-13 | 2020-10-06 | Aileron Therapeutics, Inc. | P53 derived peptidomimetic macrocycle |
| AU2011305525B2 (en) | 2010-09-22 | 2016-08-18 | Arena Pharmaceuticals, Inc. | Modulators of the GPR119 receptor and the treatment of disorders related thereto |
| PH12013501840A1 (en) | 2011-03-16 | 2016-06-17 | Mitsubishi Tanabe Pharma Corp | Nitrogen-containing saturated heterocyclic compound |
| US20140066369A1 (en) * | 2011-04-19 | 2014-03-06 | Arena Pharmaceuticals, Inc. | Modulators Of The GPR119 Receptor And The Treatment Of Disorders Related Thereto |
| US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone compounds |
| WO2012175520A1 (en) * | 2011-06-20 | 2012-12-27 | Novartis Ag | Hydroxy substituted isoquinolinone derivatives |
| WO2013049250A1 (en) * | 2011-09-27 | 2013-04-04 | Amgen Inc. | Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer |
| TW201806968A (zh) | 2011-10-18 | 2018-03-01 | 艾利倫治療公司 | 擬肽巨環化合物 |
| WO2013080141A1 (en) | 2011-11-29 | 2013-06-06 | Novartis Ag | Pyrazolopyrrolidine compounds |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| US8815926B2 (en) * | 2012-01-26 | 2014-08-26 | Novartis Ag | Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases |
| BR112014020103A2 (pt) | 2012-02-15 | 2018-10-09 | Aileron Therapeutics, Inc. | macrociclos peptidomiméticos |
| CA2864120A1 (en) | 2012-02-15 | 2013-08-22 | Aileron Therapeutics, Inc. | Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles |
| JP6171003B2 (ja) * | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
| DK2880447T3 (da) * | 2012-07-31 | 2019-08-12 | Novartis Ag | Markører forbundet med følsomhed for hæmmere af human double minute 2 (MDM2) |
| JP5764628B2 (ja) * | 2012-09-14 | 2015-08-19 | 田辺三菱製薬株式会社 | 医薬組成物 |
| KR20150082307A (ko) | 2012-11-01 | 2015-07-15 | 에일러론 테라퓨틱스 인코포레이티드 | 이치환 아미노산 및 이의 제조 및 사용 방법 |
| BR112015013611A2 (pt) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | composto, e, composição farmacêutica |
| BG111378A (bg) | 2013-01-14 | 2015-01-30 | Николай Цветков | Субституирани индазолови производни като in-vitro mao-b инхибитори |
| WO2014115077A1 (en) | 2013-01-22 | 2014-07-31 | Novartis Ag | Substituted purinone compounds |
| EP2948453B1 (en) | 2013-01-22 | 2017-08-02 | Novartis AG | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| AU2014223547B2 (en) | 2013-02-28 | 2017-11-16 | Amgen Inc. | A benzoic acid derivative MDM2 inhibitor for the treatment of cancer |
| EP2970237B1 (en) | 2013-03-14 | 2017-09-27 | Amgen Inc. | Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer |
| CN103232400B (zh) * | 2013-04-26 | 2015-01-21 | 苏州大学 | 一种制备喹唑啉-2-硫酮的方法 |
| EP3004109A1 (en) | 2013-05-27 | 2016-04-13 | Novartis AG | Imidazopyrrolidinone derivatives and their use in the treatment of disease |
| US8975417B2 (en) | 2013-05-27 | 2015-03-10 | Novartis Ag | Pyrazolopyrrolidine derivatives and their use in the treatment of disease |
| MX2015016425A (es) | 2013-05-28 | 2016-03-03 | Novartis Ag | Derivados de pirazolo-pirrolidin-4-ona y su uso en el tratamiento de enfermedades. |
| JP2016520118A (ja) | 2013-05-28 | 2016-07-11 | ノバルティス アーゲー | Bet阻害剤としてのピラゾロ−ピロリジン−4−オン誘導体および疾患の処置におけるその使用 |
| JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
| EP3049442A4 (en) | 2013-09-26 | 2017-06-28 | Costim Pharmaceuticals Inc. | Methods for treating hematologic cancers |
| CA2931249A1 (en) | 2013-11-21 | 2015-05-28 | Novartis Ag | Pyrrolopyrrolone derivatives and their use as bet inhibitors |
| WO2015084804A1 (en) | 2013-12-03 | 2015-06-11 | Novartis Ag | Combination of mdm2 inhibitor and braf inhibitor and their use |
| AU2014372166B2 (en) | 2013-12-23 | 2017-10-26 | Novartis Ag | Pharmaceutical combinations |
| MX2016008363A (es) | 2013-12-23 | 2016-09-08 | Novartis Ag | Combinaciones farmaceuticas. |
| JOP20200094A1 (ar) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | جزيئات جسم مضاد لـ pd-1 واستخداماتها |
| JOP20200096A1 (ar) | 2014-01-31 | 2017-06-16 | Children’S Medical Center Corp | جزيئات جسم مضاد لـ tim-3 واستخداماتها |
| CA2936962C (en) | 2014-03-14 | 2024-03-05 | Novartis Ag | Antibody molecules to lag-3 and uses thereof |
| PE20161552A1 (es) * | 2014-06-17 | 2017-01-11 | Pfizer | Compuestos de dihidroisoquinolinona sustituida |
| TW201613576A (en) * | 2014-06-26 | 2016-04-16 | Novartis Ag | Intermittent dosing of MDM2 inhibitor |
| WO2016035023A1 (en) | 2014-09-03 | 2016-03-10 | Novartis Ag | Pharmaceutical combinations and their use |
| CA2960824A1 (en) | 2014-09-13 | 2016-03-17 | Novartis Ag | Combination therapies of alk inhibitors |
| MX2017003797A (es) | 2014-09-24 | 2017-06-15 | Aileron Therapeutics Inc | Macrociclos peptidomimeticos y usos de los mismos. |
| SG10201902598VA (en) | 2014-09-24 | 2019-04-29 | Aileron Therapeutics Inc | Peptidomimetic macrocycles and formulations thereof |
| EP3662903A3 (en) | 2014-10-03 | 2020-10-14 | Novartis AG | Combination therapies |
| WO2016057322A1 (en) | 2014-10-08 | 2016-04-14 | Salk Institute For Biological Studies | Ppar agonists and methods of use thereof |
| MA41044A (fr) | 2014-10-08 | 2017-08-15 | Novartis Ag | Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer |
| CA2964367C (en) | 2014-10-14 | 2024-01-30 | Novartis Ag | Antibody molecules to pd-l1 and uses thereof |
| CN116850181A (zh) | 2015-01-06 | 2023-10-10 | 艾尼纳制药公司 | 治疗与s1p1受体有关的病症的方法 |
| HK1247089A1 (zh) | 2015-03-10 | 2018-09-21 | Aduro Biotech, Inc. | 用於活化“干扰素基因刺激物”依赖性信号传导的组合物和方法 |
| US10253067B2 (en) | 2015-03-20 | 2019-04-09 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
| AU2016284162A1 (en) | 2015-06-22 | 2018-02-01 | Arena Pharmaceuticals, Inc. | Crystalline L-arginine salt of (R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta[b]indol-3-yl)acetic acid(Compound1) for use in SIP1 receptor-associated disorders |
| US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
| DK3317301T3 (da) | 2015-07-29 | 2021-06-28 | Immutep Sas | Kombinationsterapier omfattende antistofmolekyler mod lag-3 |
| WO2017019896A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to pd-1 |
| TWI750129B (zh) | 2015-08-03 | 2021-12-21 | 瑞士商諾華公司 | 作為血液學毒性生物標記之gdf-15 |
| JP2018522936A (ja) | 2015-08-14 | 2018-08-16 | ノバルティス アーゲー | ぶどう膜黒色腫の処置のためのmdm2阻害剤 |
| CA2992221C (en) | 2015-08-28 | 2023-06-27 | Novartis Ag | Mdm2 inhibitors and combinations thereof |
| JP2018528949A (ja) | 2015-08-28 | 2018-10-04 | ノバルティス アーゲー | Pi3k阻害剤およびmdm2阻害剤を使用する組み合わせ療法 |
| CN108368161A (zh) | 2015-09-10 | 2018-08-03 | 艾瑞朗医疗公司 | 作为mcl-1调节剂的拟肽大环化合物 |
| GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
| GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
| BR112018008891A8 (pt) | 2015-11-03 | 2019-02-26 | Janssen Biotech Inc | anticorpos que se ligam especificamente a pd-1 e tim-3 e seus usos |
| WO2017106656A1 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Antibody molecules to pd-1 and uses thereof |
| WO2017156398A1 (en) * | 2016-03-10 | 2017-09-14 | Assia Chemical Industries Ltd. | Solid state forms of venetoclax and processes for preparation of venetoclax |
| PE20181446A1 (es) | 2016-03-17 | 2018-09-12 | Hoffmann La Roche | Derivados de 5-etil-4-metil-pirazol-3-carboxamida con actividad como de taar |
| CN109152843A (zh) | 2016-05-20 | 2019-01-04 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| US11098077B2 (en) | 2016-07-05 | 2021-08-24 | Chinook Therapeutics, Inc. | Locked nucleic acid cyclic dinucleotide compounds and uses thereof |
| WO2018092020A1 (en) * | 2016-11-15 | 2018-05-24 | Novartis Ag | Dose and regimen for hdm2-p53 interaction inhibitors |
| WO2018092064A1 (en) | 2016-11-18 | 2018-05-24 | Novartis Ag | Combinations of mdm2 inhibitors and bcl-xl inhibitors |
| PL3689868T3 (pl) | 2016-12-01 | 2024-03-11 | Arvinas Operations, Inc. | Pochodne tetrahydronaftalenu i tetrahydroizochinoliny jako degradery receptorów estrogenowych |
| US11173211B2 (en) | 2016-12-23 | 2021-11-16 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of rapidly accelerated Fibrosarcoma polypeptides |
| AU2018220521A1 (en) | 2017-02-16 | 2019-09-05 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| GB201704966D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| US20200101079A1 (en) | 2017-04-05 | 2020-04-02 | Boehringer Ingelheim International Gmbh | Anticancer combination therapy |
| UY37695A (es) | 2017-04-28 | 2018-11-30 | Novartis Ag | Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo |
| US20200172628A1 (en) | 2017-06-22 | 2020-06-04 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
| WO2019053595A1 (en) | 2017-09-12 | 2019-03-21 | Novartis Ag | INHIBITORS OF PROTEIN KINASE C FOR THE TREATMENT OF CHOROIDAL MELLANOMA |
| EP3694518A1 (en) | 2017-10-12 | 2020-08-19 | Novartis AG | Combinations of mdm2 inhibitors with inhibitors of erk for treating cancers |
| CA3081602A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
| US12398209B2 (en) | 2018-01-22 | 2025-08-26 | Janssen Biotech, Inc. | Methods of treating cancers with antagonistic anti-PD-1 antibodies |
| TWI869346B (zh) | 2018-05-30 | 2025-01-11 | 瑞士商諾華公司 | Entpd2抗體、組合療法、及使用該等抗體和組合療法之方法 |
| WO2019236757A1 (en) | 2018-06-06 | 2019-12-12 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the s1p1 receptor |
| AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
| CN112912376A (zh) | 2018-08-20 | 2021-06-04 | 阿尔维纳斯运营股份有限公司 | 用于治疗神经变性疾病的具有E3泛素连接酶结合活性并靶向α-突触核蛋白的蛋白水解靶向嵌合(PROTAC)化合物 |
| KR20210106437A (ko) | 2018-12-20 | 2021-08-30 | 노파르티스 아게 | 3-(1-옥소이소인돌린-2-일)피페리딘-2,6-디온 유도체를 포함하는 투약 요법 및 약학적 조합물 |
| US12479817B2 (en) | 2019-02-15 | 2025-11-25 | Novartis Ag | Substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| AU2020222345B2 (en) | 2019-02-15 | 2022-11-17 | Novartis Ag | 3-(1-oxo-5-(piperidin-4-yl)isoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| US20230092679A1 (en) | 2019-05-20 | 2023-03-23 | Novartis Ag | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
| MX2022002415A (es) | 2019-08-26 | 2022-03-22 | Arvinas Operations Inc | Metodos de tratamiento del cancer de mama con derivados de tetrahidronaftaleno como degradadores del receptor de estrogenos. |
| US20220331318A1 (en) | 2019-09-16 | 2022-10-20 | Novartis Ag | Use of an mdm2 inhibitor for the treatment of myelofibrosis |
| US20220348651A1 (en) | 2019-09-18 | 2022-11-03 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
| JP2023506958A (ja) | 2019-12-20 | 2023-02-20 | ノバルティス アーゲー | 骨髄線維症および骨髄異形成症候群を処置するための、デシタビンまたは抗pd-1抗体スパルタリズマブを伴うかまたは伴わない抗tim-3抗体mbg453および抗tgf-ベータ抗体nis793の組合せ |
| GB201919219D0 (en) | 2019-12-23 | 2020-02-05 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| WO2021260528A1 (en) | 2020-06-23 | 2021-12-30 | Novartis Ag | Dosing regimen comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| US20230313313A1 (en) | 2020-08-27 | 2023-10-05 | Otsuka Pharmaceutical Co., Ltd. | Biomarkers for cancer therapy using mdm2 antagonists |
| JP2023539663A (ja) | 2020-08-28 | 2023-09-15 | アルビナス・オペレーションズ・インコーポレイテッド | 急速進行性線維肉腫タンパク質分解化合物及び関連する使用方法 |
| BR112023004656A2 (pt) | 2020-09-14 | 2023-05-09 | Arvinas Operations Inc | Formas cristalinas e amorfas de um composto para a degradação direcionada do receptor de estrogênio |
| US20240042051A1 (en) | 2020-11-24 | 2024-02-08 | Francesca Rocchetti | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
| EP4251648A2 (en) | 2020-11-24 | 2023-10-04 | Novartis AG | Anti-cd48 antibodies, antibody drug conjugates, and uses thereof |
| CN117794929A (zh) | 2021-02-02 | 2024-03-29 | 法国施维雅药厂 | 选择性bcl-xl protac化合物及使用方法 |
| GB202103080D0 (en) | 2021-03-04 | 2021-04-21 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| KR20250027281A (ko) | 2022-05-20 | 2025-02-25 | 노파르티스 아게 | Epha2 bcl-xl 억제제 항체-약물 접합체 및 그의 사용 방법 |
| AU2023273734A1 (en) | 2022-05-20 | 2024-12-12 | Les Laboratoires Servier | Met bcl-xl inhibitor antibody-drug conjugates and methods of use thereof |
| WO2024054591A1 (en) | 2022-09-07 | 2024-03-14 | Arvinas Operations, Inc. | Rapidly accelerated fibrosarcoma (raf) degrading compounds and associated methods of use |
| WO2024126453A1 (en) | 2022-12-15 | 2024-06-20 | Boehringer Ingelheim International Gmbh | New substituted indole-2-carboxamides as phgdh inhibitors |
| IL322700A (en) | 2023-03-10 | 2025-10-01 | Novartis Ag | Antibody-drug conjugates that inhibit fennerase and methods of using them |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
| WO2025111450A1 (en) | 2023-11-22 | 2025-05-30 | Les Laboratoires Servier | Anti-cd74 antibody-drug conjugates and methods of use thereof |
| WO2025215536A1 (en) | 2024-04-10 | 2025-10-16 | Novartis Ag | Macrocyclic panras inhibitors for the treatment of cancer |
Family Cites Families (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR901228A (fr) | 1943-01-16 | 1945-07-20 | Deutsche Edelstahlwerke Ag | Système d'aimant à entrefer annulaire |
| US3829420A (en) | 1970-07-13 | 1974-08-13 | Sumitomo Chemical Co | 3,4-dihydro-2(1h)-quinazolinones and preparation thereof |
| US4099002A (en) | 1970-12-23 | 1978-07-04 | Sumitomo Chemical Company, Limited | Quinazolinone derivatives and a process for production thereof |
| JPS4822715B1 (enExample) | 1970-12-28 | 1973-07-07 | ||
| JPS5427356B2 (enExample) | 1972-03-31 | 1979-09-10 | ||
| GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
| US4258187A (en) | 1977-06-16 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Process for preparing quinazolinone oxides |
| US4335127A (en) | 1979-01-08 | 1982-06-15 | Janssen Pharmaceutica, N.V. | Piperidinylalkyl quinazoline compounds, composition and method of use |
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| EP0100172B1 (en) | 1982-07-23 | 1987-08-12 | Imperial Chemical Industries Plc | Amide derivatives |
| GB8327256D0 (en) | 1983-10-12 | 1983-11-16 | Ici Plc | Steroid derivatives |
| DE3420799A1 (de) | 1984-06-04 | 1985-12-05 | Bayer Ag, 5090 Leverkusen | Chromogene 4,4-diaryl-dihydrochinazolone, ihre herstellung und verwendung |
| US5010099A (en) | 1989-08-11 | 1991-04-23 | Harbor Branch Oceanographic Institution, Inc. | Discodermolide compounds, compositions containing same and method of preparation and use |
| US5395855A (en) | 1990-05-07 | 1995-03-07 | Ciba-Geigy Corporation | Hydrazones |
| NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
| WO1993004047A1 (en) | 1991-08-16 | 1993-03-04 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| TW225528B (enExample) | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
| WO1994010202A1 (en) | 1992-10-28 | 1994-05-11 | Genentech, Inc. | Vascular endothelial cell growth factor antagonists |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| US5508300A (en) | 1994-01-14 | 1996-04-16 | Pfizer Inc. | Dihydro pyrazolopyrroles, compositions and use |
| CA2216796C (en) | 1995-03-30 | 2003-09-02 | Pfizer Inc. | Quinazoline derivatives |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| US5843901A (en) | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| KR100437582B1 (ko) | 1995-07-06 | 2004-12-17 | 노파르티스 아게 | 피롤로피리미딘및그들의제조방법 |
| US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| EA001595B1 (ru) | 1996-04-12 | 2001-06-25 | Варнер-Ламберт Компани | Необратимые ингибиторы тирозинкиназ |
| EP0907642B1 (en) | 1996-06-24 | 2005-11-02 | Pfizer Inc. | Phenylamino-substituted tricyclic derivatives for treatment of hyperproliferative diseases |
| WO1998001467A2 (en) | 1996-07-05 | 1998-01-15 | Novartis Ag | Inhibitors of the interaction between p53 and mdm2 |
| JP2001500851A (ja) | 1996-08-30 | 2001-01-23 | ノバルティス アクチエンゲゼルシャフト | エポシロンの製造法および製造過程中に得られる中間生産物 |
| DE69724269T2 (de) | 1996-09-06 | 2004-06-09 | Obducat Ab | Verfahren für das anisotrope ätzen von strukturen in leitende materialien |
| DE19638745C2 (de) | 1996-09-11 | 2001-05-10 | Schering Ag | Monoklonale Antikörper gegen die extrazelluläre Domäne des menschlichen VEGF - Rezeptorproteins (KDR) |
| AU4342997A (en) | 1996-09-13 | 1998-04-02 | Sugen, Inc. | Use of quinazoline derivatives for the manufacture of a medicament in the reatment of hyperproliferative skin disorders |
| EP0837063A1 (en) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | 4-Aminoquinazoline derivatives |
| WO1998019362A1 (en) | 1996-10-28 | 1998-05-07 | Abb Power System Ab | Sea electrode for a high voltage direct current transmission system |
| AU753546B2 (en) | 1996-11-18 | 2002-10-24 | Helmholtz-Zentrum Fuer Infektionsforschung Gmbh | Epothilone C, D, E and F, production process, and their use as cytostatic as well as phytosanitary agents |
| US6441186B1 (en) | 1996-12-13 | 2002-08-27 | The Scripps Research Institute | Epothilone analogs |
| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| HRP980143A2 (en) | 1997-04-09 | 1999-02-28 | Soo Sung Ko | 4,4-disubstituted-3,4-dihydro-2 (1h)-quinazolinones useful as hiv reverse transcriptase inhibitors |
| CO4940418A1 (es) | 1997-07-18 | 2000-07-24 | Novartis Ag | Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso |
| GB9721069D0 (en) | 1997-10-03 | 1997-12-03 | Pharmacia & Upjohn Spa | Polymeric derivatives of camptothecin |
| US6194181B1 (en) | 1998-02-19 | 2001-02-27 | Novartis Ag | Fermentative preparation process for and crystal forms of cytostatics |
| NZ506742A (en) | 1998-02-25 | 2003-09-26 | Sloan Kettering Inst Cancer | Synthesis of desoxyepothilones and hydroxy acid derivative intermediates |
| JP4516690B2 (ja) | 1998-08-11 | 2010-08-04 | ノバルティス アーゲー | 血管形成阻害活性を有するイソキノリン誘導体 |
| GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
| UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
| IL143069A0 (en) | 1998-11-20 | 2002-04-21 | Kosan Biosciences Inc | Recombinant methods and materials for producing epothilone and epothilone derivatives |
| ATE300957T1 (de) | 1998-12-22 | 2005-08-15 | Genentech Inc | Antagonisten von vaskular-endothelialen zellwachstumsfaktoren und ihre anwendung |
| AU766081B2 (en) | 1999-03-30 | 2003-10-09 | Novartis Ag | Phthalazine derivatives for treating inflammatory diseases |
| WO2000066560A1 (en) | 1999-05-04 | 2000-11-09 | American Home Products Corporation | Quinazolinone and benzoxazine derivatives as progesterone receptor modulators |
| JP2001302515A (ja) | 2000-04-18 | 2001-10-31 | Sumitomo Pharmaceut Co Ltd | ポリ(adp−リボース)ポリメラーゼ阻害剤 |
| US6479499B1 (en) | 2000-06-28 | 2002-11-12 | National Science Council | 2-phenyl-4-quinazolinone compounds, 2-phenyl-4-alkoxy-quinazoline compounds and their pharmaceutical compositions |
| MXPA03001169A (es) | 2000-08-10 | 2003-06-30 | Pharmacia Italia Spa | Biciclo-pirazoles activos como inhibidores de quinasa, proceso para su preparacion y composiciones farmaceuticas que comprenden los mismos. |
| PE20020354A1 (es) | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
| TWI238824B (en) | 2001-05-14 | 2005-09-01 | Novartis Ag | 4-amino-5-phenyl-7-cyclobutyl-pyrrolo[2,3-d]pyrimidine derivatives |
| GB0119249D0 (en) | 2001-08-07 | 2001-10-03 | Novartis Ag | Organic compounds |
| RU2305095C2 (ru) | 2001-12-18 | 2007-08-27 | Ф.Хоффманн-Ля Рош Аг | Цис-2,4,5-трифенилимидазолины и фармацевтическая композиция на их основе |
| CA2473740A1 (en) | 2002-01-18 | 2003-07-31 | David Solow-Cordero | Methods of treating conditions associated with an edg receptor |
| AU2003235504A1 (en) | 2002-05-13 | 2003-11-11 | 3-Dimensional Pharmaceuticals, Inc. | Method for cytoprotection through mdm2 and hdm2 inhibition |
| US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
| JP2007524596A (ja) | 2003-02-28 | 2007-08-30 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | 共結晶医薬組成物 |
| US20040213264A1 (en) | 2003-04-25 | 2004-10-28 | Nortel Networks Limited | Service class and destination dominance traffic management |
| EP1657238A4 (en) | 2003-08-22 | 2008-12-03 | Takeda Pharmaceutical | CONDENSATE PYRIMIDINE DERIVATIVE AND ITS USE |
| DE602004018338D1 (de) | 2003-09-22 | 2009-01-22 | Onepharm Res And Dev Gmbh | Prävention und behandlung von durch entzündung ausgelöstem und/oder immunvermitteltem knochenschwund |
| KR20060127413A (ko) | 2003-11-25 | 2006-12-12 | 카이론 코포레이션 | 항암제로서의 퀴나졸리논 화합물 |
| CN1953965B (zh) | 2004-05-18 | 2012-07-04 | 霍夫曼-拉罗奇有限公司 | 新型顺式咪唑啉类化合物 |
| EP1750706B1 (en) | 2004-06-01 | 2016-10-05 | University Of Virginia Patent Foundation | Dual small molecule inhibitors of cancer and angiogenesis |
| GB0419481D0 (en) | 2004-09-02 | 2004-10-06 | Cancer Rec Tech Ltd | Isoindolin-1-one derivatives |
| US20060069085A1 (en) | 2004-09-28 | 2006-03-30 | Rulin Zhao | Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones |
| WO2006074262A1 (en) | 2005-01-05 | 2006-07-13 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase inhibitors |
| WO2006097337A2 (en) | 2005-03-18 | 2006-09-21 | Onepharm Gmbh | 11β-HYDROXYSTEROID DEHYDROGENASES |
| US7576082B2 (en) | 2005-06-24 | 2009-08-18 | Hoffman-La Roche Inc. | Oxindole derivatives |
| CA2631907A1 (en) | 2005-12-12 | 2007-06-21 | Nerviano Medical Sciences S.R.L. | Substituted pyrrolo-pyrazole derivatives active as kinase inhibitors |
| WO2007096334A1 (en) | 2006-02-24 | 2007-08-30 | Pfizer Italia Srl | Pyrrolopyrrolones active as kinase inhibitors |
| DE102006016426A1 (de) | 2006-04-07 | 2007-10-11 | Merck Patent Gmbh | Neuartige Cyclobutyl-Verbindungen als Kinase-Inhibitoren |
| US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| US8367699B2 (en) | 2006-09-15 | 2013-02-05 | Nexuspharma, Inc. | Tetrahydro-isoquinolines |
| US8101644B2 (en) | 2007-03-30 | 2012-01-24 | Shionogi & Co., Ltd. | Pyrrolinone derivative and pharmaceutical composition comprising the same |
| WO2008130614A2 (en) | 2007-04-20 | 2008-10-30 | University Of Pittsburg-Of The Commonwealth System Of Higher Education | Selective and dual-action p53/mdm2/mdm4 antagonists |
| JP2011507910A (ja) | 2007-12-21 | 2011-03-10 | ユニバーシティー オブ ロチェスター | 真核生物の寿命を変更するための方法 |
| UY31982A (es) | 2008-07-16 | 2010-02-26 | Boehringer Ingelheim Int | Derivados de 1,2-dihidropiridin-3-carboxamidas n-sustituidas |
| WO2010035727A1 (ja) | 2008-09-25 | 2010-04-01 | 塩野義製薬株式会社 | 新規ピロリノン誘導体およびそれを含有する医薬組成物 |
| MX2011006108A (es) | 2008-12-08 | 2011-11-18 | Vm Pharma Llc | Composiciones de inhibidores de los receptores tirosina quinasa. |
| WO2010141738A2 (en) | 2009-06-03 | 2010-12-09 | President And Fellows Of Harvard College | Compositions and method for inhibiting tumor growth |
| US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
| WO2011161031A1 (en) | 2010-06-22 | 2011-12-29 | Glaxosmithkline Llc | Benzotriazolodiazepine compounds inhibitors of bromodomains |
| US20120065210A1 (en) | 2010-09-15 | 2012-03-15 | Xin-Jie Chu | Substituted hexahydropyrrolo[1,2-c]imidazolones |
| GB201016880D0 (en) | 2010-10-07 | 2010-11-17 | Riotech Pharmaceuticals Ltd | Phosphodiesterase inhibitors |
| TWI535723B (zh) | 2010-11-12 | 2016-06-01 | 密西根大學董事會 | 螺-吲哚酮mdm2拮抗劑 |
| WO2012151512A2 (en) | 2011-05-04 | 2012-11-08 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| WO2012174487A2 (en) | 2011-06-17 | 2012-12-20 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| WO2012175520A1 (en) | 2011-06-20 | 2012-12-27 | Novartis Ag | Hydroxy substituted isoquinolinone derivatives |
| US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone compounds |
| WO2013033268A2 (en) | 2011-08-29 | 2013-03-07 | Coferon, Inc. | Bivalent bromodomain ligands, and methods of using same |
| WO2013080141A1 (en) | 2011-11-29 | 2013-06-06 | Novartis Ag | Pyrazolopyrrolidine compounds |
| US8815926B2 (en) | 2012-01-26 | 2014-08-26 | Novartis Ag | Substituted pyrrolo[3,4-D]imidazoles for the treatment of MDM2/4 mediated diseases |
| JP6171003B2 (ja) | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
-
2010
- 2010-12-20 US US12/973,474 patent/US8440693B2/en not_active Expired - Fee Related
- 2010-12-21 RS RS20140667A patent/RS53676B1/sr unknown
- 2010-12-21 AR ARP100104820A patent/AR079663A1/es active IP Right Grant
- 2010-12-21 JO JO2010470A patent/JO2974B1/en active
- 2010-12-21 PE PE2012000866A patent/PE20121510A1/es active IP Right Grant
- 2010-12-21 AU AU2010334890A patent/AU2010334890B2/en not_active Ceased
- 2010-12-21 PT PT107929440T patent/PT2516009E/pt unknown
- 2010-12-21 WO PCT/EP2010/070364 patent/WO2011076786A1/en not_active Ceased
- 2010-12-21 MX MX2012007336A patent/MX2012007336A/es active IP Right Grant
- 2010-12-21 NZ NZ600716A patent/NZ600716A/xx not_active IP Right Cessation
- 2010-12-21 BR BR112012018412-1A patent/BR112012018412B1/pt not_active IP Right Cessation
- 2010-12-21 SI SI201030821T patent/SI2516009T1/sl unknown
- 2010-12-21 EA EA201200920A patent/EA021126B1/ru not_active IP Right Cessation
- 2010-12-21 GE GEAP201012760A patent/GEP20146042B/en unknown
- 2010-12-21 JP JP2012545293A patent/JP5542962B2/ja not_active Expired - Fee Related
- 2010-12-21 IN IN5467DEN2012 patent/IN2012DN05467A/en unknown
- 2010-12-21 CA CA2785340A patent/CA2785340C/en active Active
- 2010-12-21 KR KR1020127019166A patent/KR101473068B1/ko not_active Expired - Fee Related
- 2010-12-21 SG SG2012044244A patent/SG181734A1/en unknown
- 2010-12-21 DK DK10792944.0T patent/DK2516009T3/en active
- 2010-12-21 ES ES10792944T patent/ES2527001T3/es active Active
- 2010-12-21 EP EP10792944.0A patent/EP2516009B1/en active Active
- 2010-12-21 PH PH1/2012/501291A patent/PH12012501291A1/en unknown
- 2010-12-21 HR HRP20141259AT patent/HRP20141259T1/hr unknown
- 2010-12-21 PL PL10792944T patent/PL2516009T3/pl unknown
- 2010-12-21 TW TW099145068A patent/TWI629264B/zh not_active IP Right Cessation
- 2010-12-21 MY MYPI2012002732A patent/MY156438A/en unknown
- 2010-12-21 KR KR20147029863A patent/KR20140140602A/ko not_active Withdrawn
- 2010-12-22 UY UY33131A patent/UY33131A/xx not_active Application Discontinuation
-
2012
- 2012-06-15 MA MA34976A patent/MA33832B1/fr unknown
- 2012-06-18 ZA ZA2012/04467A patent/ZA201204467B/en unknown
- 2012-06-18 IL IL220492A patent/IL220492A/en active IP Right Grant
- 2012-06-19 DO DO2012000172A patent/DOP2012000172A/es unknown
- 2012-06-19 CR CR20120333A patent/CR20120333A/es unknown
- 2012-06-20 TN TNP2012000309A patent/TN2012000309A1/en unknown
- 2012-06-20 EC ECSP12011990 patent/ECSP12011990A/es unknown
- 2012-06-21 CL CL2012001688A patent/CL2012001688A1/es unknown
- 2012-06-21 NI NI201200111A patent/NI201200111A/es unknown
- 2012-06-22 GT GT201200208A patent/GT201200208A/es unknown
- 2012-06-22 HN HN2012001332A patent/HN2012001332A/es unknown
- 2012-06-22 CO CO12105263A patent/CO6561772A2/es unknown
-
2013
- 2013-02-27 US US13/778,910 patent/US9051279B2/en active Active
-
2014
- 2014-12-22 SM SM201400193T patent/SMT201400193B/xx unknown
Non-Patent Citations (2)
| Title |
|---|
| Mollov et al., Acta Chimica Academiae Scientiarum Hungaricae, Vol. 98(3), pages 315-319 (1978년 공개) * |
| Zhang et al., Synthesis, Vol.11, pages 1775-1780(2006년 공개) * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101473068B1 (ko) | 치환된 이소퀴놀리논 및 퀴나졸리논 | |
| KR101257158B1 (ko) | 단백질 티로신 키나제 억제제로서의 퀴놀린 및 퀴녹살린의 유도체 | |
| KR101694383B1 (ko) | 이미다조피롤리디논 화합물 | |
| EP2855483B1 (en) | Pyrrolopyrrolidinone compounds | |
| AU2014249192B2 (en) | BET bromodomain inhibitors and therapeutic methods using the same | |
| EP2640467B1 (en) | Crystalline form of an inhibitor of mdm2/4 and p53 interaction | |
| JP2010526120A (ja) | Pi3k脂質キナーゼ阻害剤としての置換イミダゾピリダジン | |
| JP2010504933A (ja) | Pi3k脂質キナーゼ阻害剤としてのピラゾロピリミジン | |
| JP2010522723A (ja) | 増殖性疾患の処置のための3−イミダゾリル−インドール | |
| JP2010503629A (ja) | ヤヌスキナーゼ阻害剤として有用なベンゾオキサゾールおよびオキサゾロピリジン | |
| WO2012176123A1 (en) | 3 - imidazolyl- indoles for the treatment of proliferative diseases | |
| CN102770182B (zh) | 被取代的异喹啉酮类和喹唑酮类 | |
| HK1170972B (en) | Substituted isoquinolinones and quinazolinones |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A201 | Request for examination | ||
| AMND | Amendment | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| AMND | Amendment | ||
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
St.27 status event code: N-2-6-B10-B15-exm-PE0601 |
|
| A107 | Divisional application of patent | ||
| AMND | Amendment | ||
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0104 | Divisional application for international application |
St.27 status event code: A-0-1-A10-A18-div-PA0104 St.27 status event code: A-0-1-A10-A16-div-PA0104 |
|
| PX0901 | Re-examination |
St.27 status event code: A-2-3-E10-E12-rex-PX0901 |
|
| R17-X000 | Change to representative recorded |
St.27 status event code: A-3-3-R10-R17-oth-X000 |
|
| PX0701 | Decision of registration after re-examination |
St.27 status event code: A-3-4-F10-F13-rex-PX0701 |
|
| X701 | Decision to grant (after re-examination) | ||
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
St.27 status event code: A-2-4-F10-F11-exm-PR0701 |
|
| PR1002 | Payment of registration fee |
St.27 status event code: A-2-2-U10-U12-oth-PR1002 Fee payment year number: 1 |
|
| PG1601 | Publication of registration |
St.27 status event code: A-4-4-Q10-Q13-nap-PG1601 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 4 |
|
| R18-X000 | Changes to party contact information recorded |
St.27 status event code: A-5-5-R10-R18-oth-X000 |
|
| FPAY | Annual fee payment |
Payment date: 20181129 Year of fee payment: 5 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 5 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 6 |
|
| R18-X000 | Changes to party contact information recorded |
St.27 status event code: A-5-5-R10-R18-oth-X000 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 7 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 8 |
|
| PR1001 | Payment of annual fee |
St.27 status event code: A-4-4-U10-U11-oth-PR1001 Fee payment year number: 9 |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: A-4-4-U10-U13-oth-PC1903 Not in force date: 20231210 Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: N-4-6-H10-H13-oth-PC1903 Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE Not in force date: 20231210 |