CN104080787B - 吡唑并吡咯烷化合物 - Google Patents
吡唑并吡咯烷化合物 Download PDFInfo
- Publication number
- CN104080787B CN104080787B CN201280068311.0A CN201280068311A CN104080787B CN 104080787 B CN104080787 B CN 104080787B CN 201280068311 A CN201280068311 A CN 201280068311A CN 104080787 B CN104080787 B CN 104080787B
- Authority
- CN
- China
- Prior art keywords
- chloro
- phenyl
- methyl
- dihydro
- isopropyl
- 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 CCOC(C(C(C=O)=C1C(C)C)=*1c(cnc(N(C)C(OC(C)(C)C)=O)n1)c1OC)=O Chemical compound CCOC(C(C(C=O)=C1C(C)C)=*1c(cnc(N(C)C(OC(C)(C)C)=O)n1)c1OC)=O 0.000 description 3
- JDFILMQFOJHLDK-UHFFFAOYSA-N CC(C)(C)OC(Nc(cc(cc1)Cl)c1O)=O Chemical compound CC(C)(C)OC(Nc(cc(cc1)Cl)c1O)=O JDFILMQFOJHLDK-UHFFFAOYSA-N 0.000 description 1
- AOQJIZISDDYGLK-UHFFFAOYSA-N CC(C)(c1c2c(C(O)=O)n[n]1-c(cnc(OC)n1)c1OC)c1cc(Cl)ccc1C2NC1=CC(Cl)=CN(C)C1=O Chemical compound CC(C)(c1c2c(C(O)=O)n[n]1-c(cnc(OC)n1)c1OC)c1cc(Cl)ccc1C2NC1=CC(Cl)=CN(C)C1=O AOQJIZISDDYGLK-UHFFFAOYSA-N 0.000 description 1
- LPWJNLQXEKVTOI-PVMDDABVSA-N CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\C(c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CNC2=O)/C1=N Chemical compound CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\C(c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CNC2=O)/C1=N LPWJNLQXEKVTOI-PVMDDABVSA-N 0.000 description 1
- QIIVTQNJIKNTON-VKLSZVPASA-N CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\C(c(cc1)ccc1Cl)N(C1=O)C(C=C2Cl)=CNC2=O)/C1=N\C Chemical compound CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\C(c(cc1)ccc1Cl)N(C1=O)C(C=C2Cl)=CNC2=O)/C1=N\C QIIVTQNJIKNTON-VKLSZVPASA-N 0.000 description 1
- DBEUCROQQJKKFN-AOUOCWBMSA-N CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\[C@@H](c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CN(C)C2=O)/C1=N Chemical compound CC(C)/C(/Nc(cnc(N(C)C)n1)c1OC)=C(\[C@@H](c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CN(C)C2=O)/C1=N DBEUCROQQJKKFN-AOUOCWBMSA-N 0.000 description 1
- YIFUVZRFHSAOMN-BBYSSXSKSA-N CC(C)/C(/Nc(cnc(OC)n1)c1OC)=C(\C(c(cc1)ccc1Cl)N(C1=O)C2=CC(Cl)=CN(Cc(cc3)ccc3OC)C2=O)/C1=N Chemical compound CC(C)/C(/Nc(cnc(OC)n1)c1OC)=C(\C(c(cc1)ccc1Cl)N(C1=O)C2=CC(Cl)=CN(Cc(cc3)ccc3OC)C2=O)/C1=N YIFUVZRFHSAOMN-BBYSSXSKSA-N 0.000 description 1
- XOJVPWIXBSSCTJ-SUHIOBAKSA-N CC(C)/C(/Nc1cnc(N(C)C)nc1OC)=C(\C(c(cc1F)ccc1C#N)NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O)/C(C(O)=O)=N Chemical compound CC(C)/C(/Nc1cnc(N(C)C)nc1OC)=C(\C(c(cc1F)ccc1C#N)NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O)/C(C(O)=O)=N XOJVPWIXBSSCTJ-SUHIOBAKSA-N 0.000 description 1
- JGCXQHSLOSLBHP-DYLBRLFTSA-N CC(C)/C(/Nc1cnc(N(C)C)nc1OC)=C(\[C@@H](c(cc1)ccc1C#N)N(C1=O)C2=CC(Cl)=CNC2=O)/C1=N Chemical compound CC(C)/C(/Nc1cnc(N(C)C)nc1OC)=C(\[C@@H](c(cc1)ccc1C#N)N(C1=O)C2=CC(Cl)=CNC2=O)/C1=N JGCXQHSLOSLBHP-DYLBRLFTSA-N 0.000 description 1
- BNNWBLWVSRAEOY-UHFFFAOYSA-N CC(C)C(C(C(c(cc1)ccc1Cl)N(C1=O)c(cccc2Cl)c2F)=C1O)=O Chemical compound CC(C)C(C(C(c(cc1)ccc1Cl)N(C1=O)c(cccc2Cl)c2F)=C1O)=O BNNWBLWVSRAEOY-UHFFFAOYSA-N 0.000 description 1
- DHHJCVYUGOVJKK-UHFFFAOYSA-N CC(C)C(C1C(c(c(C)c2)ccc2Cl)N2C(C3)=CC(NC(C)=O)=CC3Cl)N(c3ccccc3OC)N=C1C2=O Chemical compound CC(C)C(C1C(c(c(C)c2)ccc2Cl)N2C(C3)=CC(NC(C)=O)=CC3Cl)N(c3ccccc3OC)N=C1C2=O DHHJCVYUGOVJKK-UHFFFAOYSA-N 0.000 description 1
- LFUSKAAEVLYVKI-UHFFFAOYSA-N CC(C)C(C1C(c(cc2)c(C3C45)cc2Cl)N2C4=CN=CC35Cl)N(c3ccccc3OC)N=C1C2=O Chemical compound CC(C)C(C1C(c(cc2)c(C3C45)cc2Cl)N2C4=CN=CC35Cl)N(c3ccccc3OC)N=C1C2=O LFUSKAAEVLYVKI-UHFFFAOYSA-N 0.000 description 1
- HIAXIHPCDDQEJI-UHFFFAOYSA-N CC(C)C(C1C2N3c4c(C)ccc(Cl)c4-c4c2ccc(Cl)c4)N(C(N(C)C(N2C)O)=CC2=O)N=C1C3=O Chemical compound CC(C)C(C1C2N3c4c(C)ccc(Cl)c4-c4c2ccc(Cl)c4)N(C(N(C)C(N2C)O)=CC2=O)N=C1C3=O HIAXIHPCDDQEJI-UHFFFAOYSA-N 0.000 description 1
- KRRZQZAVWKPRNE-UHFFFAOYSA-O CC(C)C([NH2+]c(cnc(NC)n1)c1OC)=C(C(c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CNC2=O)C1=N Chemical compound CC(C)C([NH2+]c(cnc(NC)n1)c1OC)=C(C(c(cc1)ccc1C#N)N(C1=O)C(C=C2Cl)=CNC2=O)C1=N KRRZQZAVWKPRNE-UHFFFAOYSA-O 0.000 description 1
- HJXUIHFCSMLDBE-UHFFFAOYSA-N CC(C)C1=C(C(c(cc2)ccc2C#N)N(C2=O)C(C=C3Cl)=CNC3=O)C2=CC(C)N1c(cnc(OC)n1)c1OC Chemical compound CC(C)C1=C(C(c(cc2)ccc2C#N)N(C2=O)C(C=C3Cl)=CNC3=O)C2=CC(C)N1c(cnc(OC)n1)c1OC HJXUIHFCSMLDBE-UHFFFAOYSA-N 0.000 description 1
- FJSZGOQXFRLDML-UHFFFAOYSA-N CC(C)c1c(C(C(C=C2)=C(C)CC2Cl)N(C2=O)C(CCCC3Cl)=C3F)c2n[n]1CCOC Chemical compound CC(C)c1c(C(C(C=C2)=C(C)CC2Cl)N(C2=O)C(CCCC3Cl)=C3F)c2n[n]1CCOC FJSZGOQXFRLDML-UHFFFAOYSA-N 0.000 description 1
- YFPIZYHZFXXSNG-UHFFFAOYSA-N CC(C)c1c(C(C(CCC(Cl)=C2)=C2C2=C3Cl)N(C4=O)C2=CN(C)C3=O)c4n[n]1-c(cccc1)c1OC Chemical compound CC(C)c1c(C(C(CCC(Cl)=C2)=C2C2=C3Cl)N(C4=O)C2=CN(C)C3=O)c4n[n]1-c(cccc1)c1OC YFPIZYHZFXXSNG-UHFFFAOYSA-N 0.000 description 1
- IXSSVGZNNNVGBV-UHFFFAOYSA-N CC(C)c1c(C(C2C=C3)N(C4=O)c5c(C)ccc(Cl)c5C2C=C3Cl)c4n[n]1CC(CC1)(CCN1C(OC(C)(C)C)=O)O Chemical compound CC(C)c1c(C(C2C=C3)N(C4=O)c5c(C)ccc(Cl)c5C2C=C3Cl)c4n[n]1CC(CC1)(CCN1C(OC(C)(C)C)=O)O IXSSVGZNNNVGBV-UHFFFAOYSA-N 0.000 description 1
- PSCSHVNMQAGNHC-UHFFFAOYSA-N CC(C)c1c(C(c(c(C)c2)ccc2Cl)N(C2=O)c3c(C)ccc(Cl)c3)c2n[n]1Cc1ccccn1 Chemical compound CC(C)c1c(C(c(c(C)c2)ccc2Cl)N(C2=O)c3c(C)ccc(Cl)c3)c2n[n]1Cc1ccccn1 PSCSHVNMQAGNHC-UHFFFAOYSA-N 0.000 description 1
- VJIXYTFQQQTOIG-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2=O)c(cc(c(F)c3)Cl)c3F)c2n[n]1-c1ccccc1OC Chemical compound CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2=O)c(cc(c(F)c3)Cl)c3F)c2n[n]1-c1ccccc1OC VJIXYTFQQQTOIG-UHFFFAOYSA-N 0.000 description 1
- LHXUGFRDBNVUIT-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2=O)c(cccc3Cl)c3F)c2n[n]1-c(cccc1)c1Cl Chemical compound CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2=O)c(cccc3Cl)c3F)c2n[n]1-c(cccc1)c1Cl LHXUGFRDBNVUIT-UHFFFAOYSA-N 0.000 description 1
- GVPULNWUZWTILX-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2C=CC=C(C)C2F)C2=O)c2n[n]1Cc1ccccc1 Chemical compound CC(C)c1c(C(c(cc2)c(C)cc2Cl)N(C2C=CC=C(C)C2F)C2=O)c2n[n]1Cc1ccccc1 GVPULNWUZWTILX-UHFFFAOYSA-N 0.000 description 1
- HZPOZNUCPNEOGD-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)c-3cc2Cl)N(C2=O)c4c-3c(Cl)ccc4C)c2n[n]1-c(cnc(OC)n1)c1OC Chemical compound CC(C)c1c(C(c(cc2)c-3cc2Cl)N(C2=O)c4c-3c(Cl)ccc4C)c2n[n]1-c(cnc(OC)n1)c1OC HZPOZNUCPNEOGD-UHFFFAOYSA-N 0.000 description 1
- KKIXHOZIRLDQBW-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)c3cc2Cl)N(C2=O)C(C=C4Cl)=C3N(C)C4=O)c2n[n]1-c1cc(C#N)ncc1OC Chemical compound CC(C)c1c(C(c(cc2)c3cc2Cl)N(C2=O)C(C=C4Cl)=C3N(C)C4=O)c2n[n]1-c1cc(C#N)ncc1OC KKIXHOZIRLDQBW-UHFFFAOYSA-N 0.000 description 1
- FVKCWTDZANGKNW-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)ccc2C#N)NC(C=C2Cl)=CN(Cc(cc3)ccc3OC)C2=O)c(C(O)=O)n[n]1-c1cnc(N(C)C)nc1OC Chemical compound CC(C)c1c(C(c(cc2)ccc2C#N)NC(C=C2Cl)=CN(Cc(cc3)ccc3OC)C2=O)c(C(O)=O)n[n]1-c1cnc(N(C)C)nc1OC FVKCWTDZANGKNW-UHFFFAOYSA-N 0.000 description 1
- AQHNNAPKRZLJES-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)ccc2C#N)Nc2c(C)ccc(Cl)c2)c(C(O)=O)n[n]1-c1cc(C#N)ccc1OC Chemical compound CC(C)c1c(C(c(cc2)ccc2C#N)Nc2c(C)ccc(Cl)c2)c(C(O)=O)n[n]1-c1cc(C#N)ccc1OC AQHNNAPKRZLJES-UHFFFAOYSA-N 0.000 description 1
- SJSSRJQZFGJFOX-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)ccc2Cl)N(C2=O)C3=CC(Cl)=CNC3=O)c2n[n]1-c(cnc(N(C)C)n1)c1OC Chemical compound CC(C)c1c(C(c(cc2)ccc2Cl)N(C2=O)C3=CC(Cl)=CNC3=O)c2n[n]1-c(cnc(N(C)C)n1)c1OC SJSSRJQZFGJFOX-UHFFFAOYSA-N 0.000 description 1
- APXAMYQMZARHFC-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)ccc2Cl)N(C2=O)c(cc(cc3)Cl)c3OCC#N)c2n[n]1-c(cccc1)c1OC Chemical compound CC(C)c1c(C(c(cc2)ccc2Cl)N(C2=O)c(cc(cc3)Cl)c3OCC#N)c2n[n]1-c(cccc1)c1OC APXAMYQMZARHFC-UHFFFAOYSA-N 0.000 description 1
- UFFKTRBCKCKBRS-UHFFFAOYSA-N CC(C)c1c(C(c(cc2)ccc2F)N(C2=O)C(C=CCC3Cl)=C3F)c2n[n]1-c1ccccc1OC Chemical compound CC(C)c1c(C(c(cc2)ccc2F)N(C2=O)C(C=CCC3Cl)=C3F)c2n[n]1-c1ccccc1OC UFFKTRBCKCKBRS-UHFFFAOYSA-N 0.000 description 1
- QICJUCWQVWVZTO-UHFFFAOYSA-N CC(C)c1c(C2N(C3=O)c4c(C)ccc(Cl)c4-c4c2ccc(Cl)c4)c3n[n]1C(CC1)CN1C(OC(C)(C)C)=O Chemical compound CC(C)c1c(C2N(C3=O)c4c(C)ccc(Cl)c4-c4c2ccc(Cl)c4)c3n[n]1C(CC1)CN1C(OC(C)(C)C)=O QICJUCWQVWVZTO-UHFFFAOYSA-N 0.000 description 1
- PGJNDFGKSIQLID-UHFFFAOYSA-N CC(C)c1c(C2N(C3=O)c4cc(Cl)ncc4-c4c2ccc(Cl)c4)c3n[n]1-c(cccc1)c1OC Chemical compound CC(C)c1c(C2N(C3=O)c4cc(Cl)ncc4-c4c2ccc(Cl)c4)c3n[n]1-c(cccc1)c1OC PGJNDFGKSIQLID-UHFFFAOYSA-N 0.000 description 1
- IZZZCTYUBDCVRG-UHFFFAOYSA-N CC(c1c2c(C(O)=O)n[n]1-c(cnc(N(C)C(OC(C)(C)C)=O)n1)c1OC)c1cc(C#N)ccc1C2NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O Chemical compound CC(c1c2c(C(O)=O)n[n]1-c(cnc(N(C)C(OC(C)(C)C)=O)n1)c1OC)c1cc(C#N)ccc1C2NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O IZZZCTYUBDCVRG-UHFFFAOYSA-N 0.000 description 1
- FOZGPHQBYVLAHW-UHFFFAOYSA-N CCN(C=C(C=C1Cl)N)C1=O Chemical compound CCN(C=C(C=C1Cl)N)C1=O FOZGPHQBYVLAHW-UHFFFAOYSA-N 0.000 description 1
- HLBTUFRSPSKYBO-UHFFFAOYSA-O CCOC(C(C(C(c(cc1)c(C2C)cc1Cl)O)=C2[NH2+]c(cnc(N(C)C)n1)c1OC)=N)=O Chemical compound CCOC(C(C(C(c(cc1)c(C2C)cc1Cl)O)=C2[NH2+]c(cnc(N(C)C)n1)c1OC)=N)=O HLBTUFRSPSKYBO-UHFFFAOYSA-O 0.000 description 1
- FYPJIXPDESURNP-UHFFFAOYSA-N CCOC(C[n](c(C(C)C)c1C(C2C=CC(Cl)=CC2C)N2C(C3)=C(C)C=CC3Cl)nc1C2=O)=O Chemical compound CCOC(C[n](c(C(C)C)c1C(C2C=CC(Cl)=CC2C)N2C(C3)=C(C)C=CC3Cl)nc1C2=O)=O FYPJIXPDESURNP-UHFFFAOYSA-N 0.000 description 1
- YTJFFUVFYLPEEQ-UHFFFAOYSA-N CCOC(c(c(Br)c1C(C)C)n[n]1-c(cc(C#N)nc1)c1OC)=O Chemical compound CCOC(c(c(Br)c1C(C)C)n[n]1-c(cc(C#N)nc1)c1OC)=O YTJFFUVFYLPEEQ-UHFFFAOYSA-N 0.000 description 1
- DSZVFTWNFCQROS-UHFFFAOYSA-N CCOC(c(c(Br)c1C(C)C)n[n]1-c(cnc(NC)n1)c1OC)=O Chemical compound CCOC(c(c(Br)c1C(C)C)n[n]1-c(cnc(NC)n1)c1OC)=O DSZVFTWNFCQROS-UHFFFAOYSA-N 0.000 description 1
- CYQXTLOBUUQIDQ-UHFFFAOYSA-N CCOC(c(c(C(c(cc1)ccc1Cl)NC(C=C1Cl)=CN(C)C1=O)c1C(C)C)n[n]1-c(cnc(N(C)C)n1)c1OC)=O Chemical compound CCOC(c(c(C(c(cc1)ccc1Cl)NC(C=C1Cl)=CN(C)C1=O)c1C(C)C)n[n]1-c(cnc(N(C)C)n1)c1OC)=O CYQXTLOBUUQIDQ-UHFFFAOYSA-N 0.000 description 1
- FFNUZZJACGBPDB-UHFFFAOYSA-N CCOC(c(c(C(c(cc1)ccc1Cl)O)c1C(C)C)n[n]1-c(c(NC)n1)cnc1OC)=O Chemical compound CCOC(c(c(C(c(cc1)ccc1Cl)O)c1C(C)C)n[n]1-c(c(NC)n1)cnc1OC)=O FFNUZZJACGBPDB-UHFFFAOYSA-N 0.000 description 1
- YQEVXEDOCRTDQP-UHFFFAOYSA-N CCOC(c(c(C(c(cc1F)ccc1C#N)NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O)c1C(C)C)n[n]1-c1cnc(N(C)C)nc1OC)=O Chemical compound CCOC(c(c(C(c(cc1F)ccc1C#N)NC(C=C1Cl)=CN(Cc(cc2)ccc2OC)C1=O)c1C(C)C)n[n]1-c1cnc(N(C)C)nc1OC)=O YQEVXEDOCRTDQP-UHFFFAOYSA-N 0.000 description 1
- LTOYROGUBUOZNI-UHFFFAOYSA-N CCOC(c(cc1C(C)C)n[n]1-c(cnc(SC)n1)c1OC)=O Chemical compound CCOC(c(cc1C(C)C)n[n]1-c(cnc(SC)n1)c1OC)=O LTOYROGUBUOZNI-UHFFFAOYSA-N 0.000 description 1
- GIBXTRGSDNQKFO-UHFFFAOYSA-N COc(ccc(C#N)c1)c1NN Chemical compound COc(ccc(C#N)c1)c1NN GIBXTRGSDNQKFO-UHFFFAOYSA-N 0.000 description 1
- GCSMEDXFNCPNGA-UHFFFAOYSA-N Cc1ccc(-c2c(C(C(C(C3CCC3)=O)=C3O)N4C3=O)ccc(Cl)c2)c4c1F Chemical compound Cc1ccc(-c2c(C(C(C(C3CCC3)=O)=C3O)N4C3=O)ccc(Cl)c2)c4c1F GCSMEDXFNCPNGA-UHFFFAOYSA-N 0.000 description 1
- CXHOJLOLUDOQIT-UHFFFAOYSA-N Oc(c(I)c1)cnc1Cl Chemical compound Oc(c(I)c1)cnc1Cl CXHOJLOLUDOQIT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/4709—Non-condensed quinolines and containing further 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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further 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
- A61K31/495—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
- 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
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161564591P | 2011-11-29 | 2011-11-29 | |
| US61/564,591 | 2011-11-29 | ||
| PCT/IB2012/056796 WO2013080141A1 (en) | 2011-11-29 | 2012-11-28 | Pyrazolopyrrolidine compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104080787A CN104080787A (zh) | 2014-10-01 |
| CN104080787B true CN104080787B (zh) | 2016-09-14 |
Family
ID=47428784
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280068311.0A Expired - Fee Related CN104080787B (zh) | 2011-11-29 | 2012-11-28 | 吡唑并吡咯烷化合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8969341B2 (OSRAM) |
| EP (1) | EP2785717B1 (OSRAM) |
| JP (1) | JP5992054B2 (OSRAM) |
| CN (1) | CN104080787B (OSRAM) |
| WO (1) | WO2013080141A1 (OSRAM) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone 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 |
| BR112015013611A2 (pt) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | composto, e, composição farmacêutica |
| EP2948453B1 (en) | 2013-01-22 | 2017-08-02 | Novartis AG | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the p53/mdm2 interaction |
| WO2014115077A1 (en) | 2013-01-22 | 2014-07-31 | Novartis Ag | Substituted purinone compounds |
| 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 |
| 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 |
| MX2015016425A (es) * | 2013-05-28 | 2016-03-03 | Novartis Ag | Derivados de pirazolo-pirrolidin-4-ona y su uso en el tratamiento de enfermedades. |
| WO2015004610A1 (en) * | 2013-07-11 | 2015-01-15 | Adamed Sp. Z O.O. | 1,5-dihydropyrrol-2-one derivatives as inhibitors of p53-mdm2/mdm4 protein-protein interaction |
| RS63733B1 (sr) | 2013-10-18 | 2022-12-30 | Celgene Quanticel Research Inc | Inhibitori bromodomena |
| CA2931249A1 (en) * | 2013-11-21 | 2015-05-28 | Novartis Ag | Pyrrolopyrrolone derivatives and their use as bet inhibitors |
| CN105130995B (zh) * | 2015-09-09 | 2017-08-11 | 杭州成邦医药科技有限公司 | 吡咯酮类化合物及其制备方法和应用 |
| 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 |
| GB201617758D0 (en) * | 2016-10-20 | 2016-12-07 | Almac Discovery Limited | Pharmaceutical compounds |
| PH12020550995A1 (en) * | 2017-12-29 | 2021-04-19 | Gan & Lee Pharmaceuticals | Compound capable of being used as tumor inhibitor, preparation method therefor, and application thereof |
| EP3511334A1 (en) * | 2018-01-16 | 2019-07-17 | Adamed sp. z o.o. | 1,2,3',5'-tetrahydro-2'h-spiro[indole-3,1'-pyrrolo[3,4-c]pyrrole]-2,3'-dione compounds as therapeutic agents activating tp53 |
| CN117157296A (zh) * | 2021-01-21 | 2023-12-01 | 首都医科大学附属北京天坛医院 | Fpr1的调节剂及其使用方法 |
| WO2022155860A1 (en) * | 2021-01-21 | 2022-07-28 | Biofront Therapeutics (Beijing) Co., Ltd. | Modulators of fpr1 and methods of using the same |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| US12251372B2 (en) | 2022-05-25 | 2025-03-18 | Trustees Of Boston University | Antileishmanial compounds, compositions and use thereof |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007068637A1 (en) * | 2005-12-12 | 2007-06-21 | Nerviano Medical Sciences S.R.L. | Substituted pyrrolo-pyrazole derivatives active as kinase inhibitors |
| CN101605798A (zh) * | 2006-12-14 | 2009-12-16 | 第一三共株式会社 | 咪唑并噻唑衍生物 |
| US20100210632A1 (en) * | 2007-03-30 | 2010-08-19 | Hiroyuki Kai | Novel pyrrolinone derivative and pharmaceutical composition comprising the same |
| WO2010141738A2 (en) * | 2009-06-03 | 2010-12-09 | President And Fellows Of Harvard College | Compositions and method for inhibiting tumor growth |
| WO2011076786A1 (en) * | 2009-12-22 | 2011-06-30 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
Family Cites Families (68)
| 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 |
| DE1931193A1 (de) | 1968-06-20 | 1970-01-02 | Geigy Ag J R | Verfahren zur Herstellung von neuen Imidazolidinonderivaten |
| GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
| 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 |
| US5093330A (en) | 1987-06-15 | 1992-03-03 | Ciba-Geigy Corporation | Staurosporine derivatives substituted at methylamino nitrogen |
| 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 |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| TW225528B (OSRAM) | 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 |
| 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 |
| 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 |
| 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 |
| UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
| GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
| 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 |
| 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 |
| AU2003235504A1 (en) | 2002-05-13 | 2003-11-11 | 3-Dimensional Pharmaceuticals, Inc. | Method for cytoprotection through mdm2 and hdm2 inhibition |
| 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 |
| 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 |
| 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 |
| WO2007096334A1 (en) | 2006-02-24 | 2007-08-30 | Pfizer Italia Srl | Pyrrolopyrrolones active as kinase inhibitors |
| ES2548002T3 (es) | 2006-03-22 | 2015-10-13 | F. Hoffmann-La Roche Ag | Pirazoles como 11beta-SD1 |
| US8367699B2 (en) | 2006-09-15 | 2013-02-05 | Nexuspharma, Inc. | Tetrahydro-isoquinolines |
| 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 |
| 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 |
| 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 |
| 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 |
-
2012
- 2012-11-28 WO PCT/IB2012/056796 patent/WO2013080141A1/en not_active Ceased
- 2012-11-28 CN CN201280068311.0A patent/CN104080787B/zh not_active Expired - Fee Related
- 2012-11-28 JP JP2014544018A patent/JP5992054B2/ja not_active Expired - Fee Related
- 2012-11-28 EP EP12805775.9A patent/EP2785717B1/en not_active Not-in-force
- 2012-11-28 US US14/361,068 patent/US8969341B2/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007068637A1 (en) * | 2005-12-12 | 2007-06-21 | Nerviano Medical Sciences S.R.L. | Substituted pyrrolo-pyrazole derivatives active as kinase inhibitors |
| CN101605798A (zh) * | 2006-12-14 | 2009-12-16 | 第一三共株式会社 | 咪唑并噻唑衍生物 |
| US20100210632A1 (en) * | 2007-03-30 | 2010-08-19 | Hiroyuki Kai | Novel pyrrolinone derivative and pharmaceutical composition comprising the same |
| WO2010141738A2 (en) * | 2009-06-03 | 2010-12-09 | President And Fellows Of Harvard College | Compositions and method for inhibiting tumor growth |
| WO2011076786A1 (en) * | 2009-12-22 | 2011-06-30 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
Non-Patent Citations (1)
| Title |
|---|
| Fragment-Based Discovery of Bromodomain Inhibitors Part 1:Inhibitor Binding Modes and Implications for Lead Discovery;Chun-wa Chung, et al.,;《Journal of Medicinal Chemistry》;20111205;第55卷(第2期);第576-578页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2785717B1 (en) | 2016-01-13 |
| US8969341B2 (en) | 2015-03-03 |
| CN104080787A (zh) | 2014-10-01 |
| WO2013080141A1 (en) | 2013-06-06 |
| EP2785717A1 (en) | 2014-10-08 |
| JP5992054B2 (ja) | 2016-09-14 |
| JP2014533745A (ja) | 2014-12-15 |
| US20140350010A1 (en) | 2014-11-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104080787B (zh) | 吡唑并吡咯烷化合物 | |
| CN104321325B (zh) | 吡咯并吡咯烷酮化合物 | |
| KR101694383B1 (ko) | 이미다조피롤리디논 화합물 | |
| US9556180B2 (en) | Pyrazolo[3,4-d]pyrimidinone compounds as inhibitors of the P53/MDM2 interaction | |
| CN102574785A (zh) | 四取代的杂芳基化合物和它们作为mdm2和/或mdm4调节剂的用途 | |
| CN103459396B (zh) | 作为c-Met酪氨酸激酶抑制剂的[1,2,4]三唑并[4,3-b]哒嗪化合物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160914 |