JP2022510736A - 大環状化合物とその使用 - Google Patents
大環状化合物とその使用 Download PDFInfo
- Publication number
- JP2022510736A JP2022510736A JP2021554804A JP2021554804A JP2022510736A JP 2022510736 A JP2022510736 A JP 2022510736A JP 2021554804 A JP2021554804 A JP 2021554804A JP 2021554804 A JP2021554804 A JP 2021554804A JP 2022510736 A JP2022510736 A JP 2022510736A
- Authority
- JP
- Japan
- Prior art keywords
- group
- disease
- methyl
- mixture
- ring
- 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.)
- Pending
Links
- 0 CCCc1ccc(C(C(C)(C)C(OC=C)=O)c2c(C)c(C=C=*C3CCCCCOCc4ccc5cc4)c3cc2)cc1CCC5=* Chemical compound CCCc1ccc(C(C(C)(C)C(OC=C)=O)c2c(C)c(C=C=*C3CCCCCOCc4ccc5cc4)c3cc2)cc1CCC5=* 0.000 description 28
- WLFSLGSFEIRGLX-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c3ccc(CCCCC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c3ccc(CCCCC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O WLFSLGSFEIRGLX-UHFFFAOYSA-N 0.000 description 2
- WGHKKFZNQHTOQB-UHFFFAOYSA-N CCOC(CC(c1ccc(CCN(C2)C(c3ccc(CCCCC4)cc3)=O)c2c1)c1ccc2[n]4nnc2c1C)=O Chemical compound CCOC(CC(c1ccc(CCN(C2)C(c3ccc(CCCCC4)cc3)=O)c2c1)c1ccc2[n]4nnc2c1C)=O WGHKKFZNQHTOQB-UHFFFAOYSA-N 0.000 description 2
- DIFIATYJHKKAFN-UHFFFAOYSA-N Cc(cc1)c(C)c(nn2)c1[n]2I Chemical compound Cc(cc1)c(C)c(nn2)c1[n]2I DIFIATYJHKKAFN-UHFFFAOYSA-N 0.000 description 2
- CXWGWMWDZHBBCS-UHFFFAOYSA-N C=CCCc(cc1)c(CCO2)c2c1C(O)=O Chemical compound C=CCCc(cc1)c(CCO2)c2c1C(O)=O CXWGWMWDZHBBCS-UHFFFAOYSA-N 0.000 description 1
- JOCRMLDCZZERNB-UHFFFAOYSA-N C=CCCc1ccc(C(O)=O)c2c1OCC2 Chemical compound C=CCCc1ccc(C(O)=O)c2c1OCC2 JOCRMLDCZZERNB-UHFFFAOYSA-N 0.000 description 1
- TZRBLWJXXOCOSI-UHFFFAOYSA-N CC(C(C(CC(O)=O)c1cc(CN(CC2)C(c3ccc(CCCC4)cc3)=O)c2cc1)C=C1)c2c1[n]4nn2 Chemical compound CC(C(C(CC(O)=O)c1cc(CN(CC2)C(c3ccc(CCCC4)cc3)=O)c2cc1)C=C1)c2c1[n]4nn2 TZRBLWJXXOCOSI-UHFFFAOYSA-N 0.000 description 1
- WMBSAFNIYWYALX-XHPQRKPJSA-N CC(C)(C(c1cc(C/C(/CCC2)=C\C(c3c(C)cc(COCCCC4C5C4C=N4)cc3C)=O)c2cc1)c1c(C)c4c5cc1)C(O)=O Chemical compound CC(C)(C(c1cc(C/C(/CCC2)=C\C(c3c(C)cc(COCCCC4C5C4C=N4)cc3C)=O)c2cc1)c1c(C)c4c5cc1)C(O)=O WMBSAFNIYWYALX-XHPQRKPJSA-N 0.000 description 1
- ZORGODMSMYBMGT-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(CCCCC3)c4)c4Cl)=O)c2cc1)c1ccc2[n]3nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(CCCCC3)c4)c4Cl)=O)c2cc1)c1ccc2[n]3nnc2c1C)C(O)=O ZORGODMSMYBMGT-UHFFFAOYSA-N 0.000 description 1
- ZTOKWKBIWAFLOH-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(COCCC3)c4)c4Cl)=O)c2c(C)c1)c1ccc2[n]3nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(COCCC3)c4)c4Cl)=O)c2c(C)c1)c1ccc2[n]3nnc2c1C)C(O)=O ZTOKWKBIWAFLOH-UHFFFAOYSA-N 0.000 description 1
- HUEBLGCGYHTQAB-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(COCCC3)c4)c4Cl)=O)c2cc1)c1cc(OC)c2[n]3nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c(c(Cl)cc(COCCC3)c4)c4Cl)=O)c2cc1)c1cc(OC)c2[n]3nnc2c1C)C(O)=O HUEBLGCGYHTQAB-UHFFFAOYSA-N 0.000 description 1
- OAVXPIYGLYMUSA-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c3c(C)cc(COCCC4)cc3C)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c3c(C)cc(COCCC4)cc3C)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O OAVXPIYGLYMUSA-UHFFFAOYSA-N 0.000 description 1
- DWEOJCOWUYVGKM-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c(cc1)c(C)c2c1[NH+]4[N-]2)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c(cc1)c(C)c2c1[NH+]4[N-]2)C(O)=O DWEOJCOWUYVGKM-UHFFFAOYSA-N 0.000 description 1
- FWWWKCOFTUKSGQ-UHFFFAOYSA-N CC(C)(C(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O Chemical compound CC(C)(C(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)C(O)=O FWWWKCOFTUKSGQ-UHFFFAOYSA-N 0.000 description 1
- PJIQPVWEYQBGBM-UHFFFAOYSA-N CC(C)(C(c1cc(CNCC2)c2cc1)c(c(C)c1NN)ccc1NCCCCCc(cc1)ccc1C(O)=O)C(OC)=O Chemical compound CC(C)(C(c1cc(CNCC2)c2cc1)c(c(C)c1NN)ccc1NCCCCCc(cc1)ccc1C(O)=O)C(OC)=O PJIQPVWEYQBGBM-UHFFFAOYSA-N 0.000 description 1
- FEBJOZLLYAOUMF-UHFFFAOYSA-N CC(C)(C(c1ccc(CCN(C2)C(c3c(C)cc(COCCC4)cc3C)=O)c2c1)c1ccc2[n]4nnc2c1C)C(OC)=O Chemical compound CC(C)(C(c1ccc(CCN(C2)C(c3c(C)cc(COCCC4)cc3C)=O)c2c1)c1ccc2[n]4nnc2c1C)C(OC)=O FEBJOZLLYAOUMF-UHFFFAOYSA-N 0.000 description 1
- REHWUKOVRIFSKZ-UHFFFAOYSA-N CC(C)(C(c1ccc(CCN(C2)C(c3ccc(COCCC4)cc3)=O)c2c1)c1ccc2[n]4nnc2c1C)C(OC)=O Chemical compound CC(C)(C(c1ccc(CCN(C2)C(c3ccc(COCCC4)cc3)=O)c2c1)c1ccc2[n]4nnc2c1C)C(OC)=O REHWUKOVRIFSKZ-UHFFFAOYSA-N 0.000 description 1
- RYWOYVPKCVIQAU-UHFFFAOYSA-N CC(C)(C(c1ccc(CCNC2)c2c1)c(cc1)c(C)c2c1[n](CCCOCc1cc(C)c(C(O)=O)c(C)c1)nn2)C(OC)=O Chemical compound CC(C)(C(c1ccc(CCNC2)c2c1)c(cc1)c(C)c2c1[n](CCCOCc1cc(C)c(C(O)=O)c(C)c1)nn2)C(OC)=O RYWOYVPKCVIQAU-UHFFFAOYSA-N 0.000 description 1
- IASOWTXUUUGAQF-UHFFFAOYSA-N CC(C)(C(c1ccc(CCNC2)c2c1)c(cc1)c(C)c2c1[n](CCCOCc1cc(Cl)c(C(O)=O)c(Cl)c1)nn2)C(OC)=O Chemical compound CC(C)(C(c1ccc(CCNC2)c2c1)c(cc1)c(C)c2c1[n](CCCOCc1cc(Cl)c(C(O)=O)c(Cl)c1)nn2)C(OC)=O IASOWTXUUUGAQF-UHFFFAOYSA-N 0.000 description 1
- DVNRNHNPMDFWJU-UHFFFAOYSA-N CC(C)(C)OC(C(CC1)Cc2c1ccc([B+]OC(C)(C)C(C)(C)O)c2)=O Chemical compound CC(C)(C)OC(C(CC1)Cc2c1ccc([B+]OC(C)(C)C(C)(C)O)c2)=O DVNRNHNPMDFWJU-UHFFFAOYSA-N 0.000 description 1
- PWPKRLMPHNRWHK-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)Cc2c1ccc(Br)c2)=O Chemical compound CC(C)(C)OC(N(CC1)Cc2c1ccc(Br)c2)=O PWPKRLMPHNRWHK-UHFFFAOYSA-N 0.000 description 1
- USQDGQDWUOLBHX-UHFFFAOYSA-N CC(C)(C)OC(c(c(C)c1)c(C)cc1Br)=O Chemical compound CC(C)(C)OC(c(c(C)c1)c(C)cc1Br)=O USQDGQDWUOLBHX-UHFFFAOYSA-N 0.000 description 1
- LJPLYMMGVKSQJP-UHFFFAOYSA-N CC(C)(C)OC(c(c(Cl)cc(OCCCC[n]1ncc2c1ccc(C=O)c2C)c1)c1Cl)=O Chemical compound CC(C)(C)OC(c(c(Cl)cc(OCCCC[n]1ncc2c1ccc(C=O)c2C)c1)c1Cl)=O LJPLYMMGVKSQJP-UHFFFAOYSA-N 0.000 description 1
- LDJMYWKCAUMAES-UHFFFAOYSA-N CC(C)(C)OC(c1c(C)cc(COCCC[n]2nnc3c2ccc(Br)c3C)cc1C)=O Chemical compound CC(C)(C)OC(c1c(C)cc(COCCC[n]2nnc3c2ccc(Br)c3C)cc1C)=O LDJMYWKCAUMAES-UHFFFAOYSA-N 0.000 description 1
- ALGLVOAVJRGBKO-UHFFFAOYSA-N CC(C)(C)OC(c1c(C)cc(COCCC[n]2nnc3c2ccc(C#N)c3C)cc1C)=O Chemical compound CC(C)(C)OC(c1c(C)cc(COCCC[n]2nnc3c2ccc(C#N)c3C)cc1C)=O ALGLVOAVJRGBKO-UHFFFAOYSA-N 0.000 description 1
- QYFDMIZMPAMGHX-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(CCCCCCC2NC2c(c(C(CC=O)=O)c2C)ccc2Br)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(CCCCCCC2NC2c(c(C(CC=O)=O)c2C)ccc2Br)cc1)=O QYFDMIZMPAMGHX-UHFFFAOYSA-N 0.000 description 1
- DNVZKFRFYFVLAC-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(CCCCCOC(C(C=O)c2ccc(C)cc2)C=O)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(CCCCCOC(C(C=O)c2ccc(C)cc2)C=O)cc1)=O DNVZKFRFYFVLAC-UHFFFAOYSA-N 0.000 description 1
- CFLUPKJMKOWPFU-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(CCCCC[NH+]2[N-]c3c2ccc(C=C)c3C)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(CCCCC[NH+]2[N-]c3c2ccc(C=C)c3C)cc1)=O CFLUPKJMKOWPFU-UHFFFAOYSA-N 0.000 description 1
- UIYYECFMMDMBJD-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(CCOCCOS(c2ccc(C)cc2)(=O)=O)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(CCOCCOS(c2ccc(C)cc2)(=O)=O)cc1)=O UIYYECFMMDMBJD-UHFFFAOYSA-N 0.000 description 1
- KSKPFDMZTLVXIY-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(COCCCNc2ccc(C(c3cc(CN(CC4)C(OC(C)(C)C)=O)c4cc3)O)c(C)c2N=C)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(COCCCNc2ccc(C(c3cc(CN(CC4)C(OC(C)(C)C)=O)c4cc3)O)c(C)c2N=C)cc1)=O KSKPFDMZTLVXIY-UHFFFAOYSA-N 0.000 description 1
- CXXSKIFGRDTVEY-UHFFFAOYSA-N CC(C)(C)OC(c1ccc(COCCC[n]2nnc3c(C)c(Br)ccc23)cc1)=O Chemical compound CC(C)(C)OC(c1ccc(COCCC[n]2nnc3c(C)c(Br)ccc23)cc1)=O CXXSKIFGRDTVEY-UHFFFAOYSA-N 0.000 description 1
- CJQODVICEJAJPY-UHFFFAOYSA-N CC(C)(C1)Oc2c1c(C(O)=O)ccc2OCC=C Chemical compound CC(C)(C1)Oc2c1c(C(O)=O)ccc2OCC=C CJQODVICEJAJPY-UHFFFAOYSA-N 0.000 description 1
- NHKQDHOBQIEZIT-UHFFFAOYSA-N CC(C)(Cc1c(CCC=C)cc2)Oc1c2C(O)=O Chemical compound CC(C)(Cc1c(CCC=C)cc2)Oc1c2C(O)=O NHKQDHOBQIEZIT-UHFFFAOYSA-N 0.000 description 1
- ADVHJSVEPMXSTL-UHFFFAOYSA-N CC(C)(Cc1c(CCCCC[n]2nnc3c(C)c(C(CC(O)=O)c4ccc(CCN5C6)c6c4)ccc23)cc2)Oc1c2C5=O Chemical compound CC(C)(Cc1c(CCCCC[n]2nnc3c(C)c(C(CC(O)=O)c4ccc(CCN5C6)c6c4)ccc23)cc2)Oc1c2C5=O ADVHJSVEPMXSTL-UHFFFAOYSA-N 0.000 description 1
- JEMDPRMHWJNHIR-UHFFFAOYSA-N CC(C)(Cc1c(cc2)I)Oc1c2C(OC)=O Chemical compound CC(C)(Cc1c(cc2)I)Oc1c2C(OC)=O JEMDPRMHWJNHIR-UHFFFAOYSA-N 0.000 description 1
- PGLFDIQKRBOPLG-UHFFFAOYSA-N CC(COc1cc(I)ccc1C(OC)=O)=C Chemical compound CC(COc1cc(I)ccc1C(OC)=O)=C PGLFDIQKRBOPLG-UHFFFAOYSA-N 0.000 description 1
- RURTVAJMRTWQQN-UHFFFAOYSA-N CC(Cc(c(O)c(cc1)C(OC)=O)c1I)=C Chemical compound CC(Cc(c(O)c(cc1)C(OC)=O)c1I)=C RURTVAJMRTWQQN-UHFFFAOYSA-N 0.000 description 1
- ONEODKYPDFYZSI-UHFFFAOYSA-N CC(O1)=C(COC(CC(c2ccc(CCN(C3)C(c4ccc(COCCC5)cc4)=O)c3c2)c2ccc3[n]5nnc3c2C)=O)OC1=O Chemical compound CC(O1)=C(COC(CC(c2ccc(CCN(C3)C(c4ccc(COCCC5)cc4)=O)c3c2)c2ccc3[n]5nnc3c2C)=O)OC1=O ONEODKYPDFYZSI-UHFFFAOYSA-N 0.000 description 1
- MOIVLYFQVGMGRT-UHFFFAOYSA-N CC1c2c(C)c(C(CC(O)=O)c3cc(CN(CC4)C(c5ccc(COCCCCC6)cc5C)=O)c4cc3)ccc2C6N=CC1 Chemical compound CC1c2c(C)c(C(CC(O)=O)c3cc(CN(CC4)C(c5ccc(COCCCCC6)cc5C)=O)c4cc3)ccc2C6N=CC1 MOIVLYFQVGMGRT-UHFFFAOYSA-N 0.000 description 1
- PTJGHOVDOPUVCK-UHFFFAOYSA-N CCCCCC1c(ccc(C=O)c2)c2N=C1 Chemical compound CCCCCC1c(ccc(C=O)c2)c2N=C1 PTJGHOVDOPUVCK-UHFFFAOYSA-N 0.000 description 1
- WJXCYJOQOXOFGE-UHFFFAOYSA-N CCOC(C)CC(c1ccc(CCN(C2)C(OC(C)(C)C)=O)c2c1)c(cc1)c(C)c2c1N(CCCOCc1cc(C)c(C(OC(C)(C)C)=O)c(C)c1)N=CC2 Chemical compound CCOC(C)CC(c1ccc(CCN(C2)C(OC(C)(C)C)=O)c2c1)c(cc1)c(C)c2c1N(CCCOCc1cc(C)c(C(OC(C)(C)C)=O)c(C)c1)N=CC2 WJXCYJOQOXOFGE-UHFFFAOYSA-N 0.000 description 1
- RZJSUYPWFRPLBW-PLNGDYQASA-N CCOC(CC(c1cc(CN(CC2)C(c3ccc(CC/C=C\CC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)=O Chemical compound CCOC(CC(c1cc(CN(CC2)C(c3ccc(CC/C=C\CC4)cc3)=O)c2cc1)c1ccc2[n]4nnc2c1C)=O RZJSUYPWFRPLBW-PLNGDYQASA-N 0.000 description 1
- CHKMSYBZBMLDDY-UHFFFAOYSA-N CCOC(CC(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c1ccc2[N]4(C3)C3C=Nc2c1C)=O Chemical compound CCOC(CC(c1cc(CN(CC2)C(c3ccc(COCCC4)cc3)=O)c2cc1)c1ccc2[N]4(C3)C3C=Nc2c1C)=O CHKMSYBZBMLDDY-UHFFFAOYSA-N 0.000 description 1
- WDPARRIZBQXPSL-UHFFFAOYSA-N CCOC(c(cc1)cc(O)c1I)=O Chemical compound CCOC(c(cc1)cc(O)c1I)=O WDPARRIZBQXPSL-UHFFFAOYSA-N 0.000 description 1
- OSDRWHGRJUZAHM-UHFFFAOYSA-N CCc(cc(cc1)C#CCO)c1C(OC)=O Chemical compound CCc(cc(cc1)C#CCO)c1C(OC)=O OSDRWHGRJUZAHM-UHFFFAOYSA-N 0.000 description 1
- FFVNCXKOXIRVHQ-UHFFFAOYSA-N CCc1cc(Br)ccc1C(OC)=O Chemical compound CCc1cc(Br)ccc1C(OC)=O FFVNCXKOXIRVHQ-UHFFFAOYSA-N 0.000 description 1
- IBCMXUIUIPAGDZ-UHFFFAOYSA-N CCc1cc(C=O)ccc1C(OC(C)(C)C)=O Chemical compound CCc1cc(C=O)ccc1C(OC(C)(C)C)=O IBCMXUIUIPAGDZ-UHFFFAOYSA-N 0.000 description 1
- DFDZXDKDAYHROI-UHFFFAOYSA-N CCc1cc(CCC=O)ccc1C(OC)=O Chemical compound CCc1cc(CCC=O)ccc1C(OC)=O DFDZXDKDAYHROI-UHFFFAOYSA-N 0.000 description 1
- ZQOGNMUFTXAOKE-UHFFFAOYSA-N CCc1cc(CCCCC[n]2nnc3c(C)c(C(CC(O)=O)c4cc(CN5CC6)c6cc4)ccc23)ccc1C5=O Chemical compound CCc1cc(CCCCC[n]2nnc3c(C)c(C(CC(O)=O)c4cc(CN5CC6)c6cc4)ccc23)ccc1C5=O ZQOGNMUFTXAOKE-UHFFFAOYSA-N 0.000 description 1
- XUQBKIYVBQSGCS-UHFFFAOYSA-N CCc1cc(CCCO)ccc1C(OC)=O Chemical compound CCc1cc(CCCO)ccc1C(OC)=O XUQBKIYVBQSGCS-UHFFFAOYSA-N 0.000 description 1
- GAOMLXNKCBLNHY-UHFFFAOYSA-N COC(c(cc1)c(CCO2)c2c1Br)=O Chemical compound COC(c(cc1)c(CCO2)c2c1Br)=O GAOMLXNKCBLNHY-UHFFFAOYSA-N 0.000 description 1
- SBTMDPNYHPDEIZ-UHFFFAOYSA-N COC(c(cc1OCC=C)ccc1Br)=O Chemical compound COC(c(cc1OCC=C)ccc1Br)=O SBTMDPNYHPDEIZ-UHFFFAOYSA-N 0.000 description 1
- DQXAGKKXBBRASQ-UHFFFAOYSA-N Cc(c(N=O)c(cc1)NCCCO)c1[Br]=C Chemical compound Cc(c(N=O)c(cc1)NCCCO)c1[Br]=C DQXAGKKXBBRASQ-UHFFFAOYSA-N 0.000 description 1
- AIBRJIYOSLKVFL-UHFFFAOYSA-N Cc(c([N+]([O-])=O)c(cc1)F)c1Br Chemical compound Cc(c([N+]([O-])=O)c(cc1)F)c1Br AIBRJIYOSLKVFL-UHFFFAOYSA-N 0.000 description 1
- CBEIBQXPHYMJMF-UHFFFAOYSA-N Cc(cc1)cc(nn2)c1[n]2I Chemical compound Cc(cc1)cc(nn2)c1[n]2I CBEIBQXPHYMJMF-UHFFFAOYSA-N 0.000 description 1
- XAWSXQQAXHTYSE-UHFFFAOYSA-N Cc1c(C=C)ccc2c1CC=NN2CCCO Chemical compound Cc1c(C=C)ccc2c1CC=NN2CCCO XAWSXQQAXHTYSE-UHFFFAOYSA-N 0.000 description 1
- IJMGWTRKZJAKHL-UHFFFAOYSA-N Cc1c(C=C=CCN2CCCOCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(ON=C)=O)c1cc4c3cc1 Chemical compound Cc1c(C=C=CCN2CCCOCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(ON=C)=O)c1cc4c3cc1 IJMGWTRKZJAKHL-UHFFFAOYSA-N 0.000 description 1
- ANDHSWIIAURJOL-UHFFFAOYSA-N Cc1c2nn[n](CCCCCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 Chemical compound Cc1c2nn[n](CCCCCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 ANDHSWIIAURJOL-UHFFFAOYSA-N 0.000 description 1
- SQPPUZPRNDXOGU-UHFFFAOYSA-N Cc1c2nn[n](CCCCCc(cc3)c(CCO4)c4c3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1ccc3c4c1 Chemical compound Cc1c2nn[n](CCCCCc(cc3)c(CCO4)c4c3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1ccc3c4c1 SQPPUZPRNDXOGU-UHFFFAOYSA-N 0.000 description 1
- LSVULQHPICKQFS-UHFFFAOYSA-N Cc1c2nn[n](CCCCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 Chemical compound Cc1c2nn[n](CCCCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 LSVULQHPICKQFS-UHFFFAOYSA-N 0.000 description 1
- BKVRKYBTVXEOAT-UHFFFAOYSA-N Cc1c2nn[n](CCCCCc(cc3F)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 Chemical compound Cc1c2nn[n](CCCCCc(cc3F)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 BKVRKYBTVXEOAT-UHFFFAOYSA-N 0.000 description 1
- WCOIZFZXZBJKTQ-UHFFFAOYSA-N Cc1c2nn[n](CCCOCc(cc3OC(F)(F)F)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 Chemical compound Cc1c2nn[n](CCCOCc(cc3OC(F)(F)F)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 WCOIZFZXZBJKTQ-UHFFFAOYSA-N 0.000 description 1
- VINGHLJSZCAXNO-UHFFFAOYSA-N Cc1c2nn[n](CCOCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 Chemical compound Cc1c2nn[n](CCOCCc(cc3)ccc3C(N(CC3)C4)=O)c2ccc1C(CC(O)=O)c1cc4c3cc1 VINGHLJSZCAXNO-UHFFFAOYSA-N 0.000 description 1
- QUVYQXFRHJEXPW-UHFFFAOYSA-N Cc1cc(COCCC[n]2nnc3c(C)c(C(CC(O)=O)c4ccc(CCN5C6)c6c4)ccc23)cc(C)c1C5=O Chemical compound Cc1cc(COCCC[n]2nnc3c(C)c(C(CC(O)=O)c4ccc(CCN5C6)c6c4)ccc23)cc(C)c1C5=O QUVYQXFRHJEXPW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/18—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- 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
- A61K31/4748—Quinolines; Isoquinolines forming part of bridged 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
- A61K31/535—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
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/16—Peri-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Gastroenterology & Hepatology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2024102161A JP2024123202A (ja) | 2018-12-05 | 2024-06-25 | 大環状化合物とその使用 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2018228234 | 2018-12-05 | ||
| JP2018228234 | 2018-12-05 | ||
| PCT/JP2019/048593 WO2020116660A1 (en) | 2018-12-05 | 2019-12-04 | Macrocyclic compound and use thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024102161A Division JP2024123202A (ja) | 2018-12-05 | 2024-06-25 | 大環状化合物とその使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022510736A true JP2022510736A (ja) | 2022-01-27 |
| JP2022510736A5 JP2022510736A5 (https=) | 2022-11-30 |
| JPWO2020116660A5 JPWO2020116660A5 (https=) | 2022-11-30 |
Family
ID=70975488
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021554804A Pending JP2022510736A (ja) | 2018-12-05 | 2019-12-04 | 大環状化合物とその使用 |
| JP2024102161A Pending JP2024123202A (ja) | 2018-12-05 | 2024-06-25 | 大環状化合物とその使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2024102161A Pending JP2024123202A (ja) | 2018-12-05 | 2024-06-25 | 大環状化合物とその使用 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US11518763B2 (https=) |
| EP (1) | EP3890738A4 (https=) |
| JP (2) | JP2022510736A (https=) |
| KR (1) | KR102919982B1 (https=) |
| CN (1) | CN113164468A (https=) |
| AR (1) | AR117251A1 (https=) |
| AU (1) | AU2019391942B2 (https=) |
| BR (1) | BR112021010704A2 (https=) |
| CA (1) | CA3121952C (https=) |
| CL (1) | CL2021001451A1 (https=) |
| CO (1) | CO2021007304A2 (https=) |
| MX (1) | MX2021006527A (https=) |
| NZ (1) | NZ776102A (https=) |
| PH (1) | PH12021551262A1 (https=) |
| SG (1) | SG11202105125XA (https=) |
| TW (1) | TWI820266B (https=) |
| UA (1) | UA127872C2 (https=) |
| WO (1) | WO2020116660A1 (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3833662B1 (en) | 2018-08-20 | 2024-01-17 | Janssen Pharmaceutica NV | Inhibitors of keap1-nrf2 protein-protein interaction |
| AU2020283361B2 (en) | 2019-05-31 | 2025-11-27 | Ube Corporation | Benzotriazole derivative |
| CN116406364A (zh) * | 2020-09-14 | 2023-07-07 | 赛诺菲公司 | 用于治疗红细胞障碍和炎性疾病的四氢异喹啉衍生物 |
| KR20260005897A (ko) * | 2023-04-03 | 2026-01-12 | 에이스링크 테라퓨틱스, 인코포레이티드 | 신규 화합물 및 이의 용도 |
| CN119707895B (zh) * | 2023-12-18 | 2026-03-31 | 江苏苏中药业研究院有限公司 | 一种7-甲酰基-2,3-二氢苯并呋喃-4-碳腈的制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015092713A1 (en) * | 2013-12-18 | 2015-06-25 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 regulators |
| WO2018140876A1 (en) * | 2017-01-30 | 2018-08-02 | Biogen Ma Inc. | Nrf2 activator |
| WO2018181345A1 (ja) * | 2017-03-28 | 2018-10-04 | 武田薬品工業株式会社 | 複素環化合物 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012028959A1 (en) | 2010-08-31 | 2012-03-08 | Pablo Villoslada | Agonists of neurotrophin receptors and their use as medicaments |
| DK3492455T3 (da) | 2013-06-21 | 2023-08-14 | Karyopharm Therapeutics Inc | 1,2,4-triazoler som nukleare transportmodulatorer og anvendelse til behandling af specifikke former for cancer |
| LT3307739T (lt) | 2015-06-15 | 2021-03-10 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 reguliatoriai |
| WO2016203401A1 (en) | 2015-06-15 | 2016-12-22 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 regulators |
| CA2988373A1 (en) | 2015-06-15 | 2016-12-22 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 regulators |
| US10201531B2 (en) | 2015-08-12 | 2019-02-12 | Mochida Pharmaceutical Co., Ltd. | Indazolyl-oxo-isothiazole compounds |
| US10364256B2 (en) | 2015-10-06 | 2019-07-30 | Glaxosmithkline Intellectual Property Development Limited | Biaryl pyrazoles as NRF2 regulators |
| US10351530B2 (en) | 2015-10-06 | 2019-07-16 | Glaxosmithkline Intellectual Property Development Limited | Arylcyclohexyl pyrazoles as NRF2 regulators |
| JP2020500919A (ja) | 2016-12-12 | 2020-01-16 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Nrf2レギュレーターとしての3−カルボン酸ピロール |
| JP2020500918A (ja) | 2016-12-12 | 2020-01-16 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Nrf2レギュレーターとしてのn−アリールピラゾール |
| EP3555068B1 (en) | 2016-12-14 | 2020-12-02 | GlaxoSmithKline Intellectual Property Development Limited | 3-oxo-1,4-diazepinyle compounds as nrf2 activators |
| ES2901617T3 (es) | 2016-12-14 | 2022-03-23 | Glaxosmithkline Ip Dev Ltd | Bisarilamidas como reguladores de NRF2 |
| US11117905B2 (en) | 2016-12-14 | 2021-09-14 | Glaxosmithkline Intellectual Property Development Limited | Bisaryl heterocycles as NRF2 activators |
| CA3044773A1 (en) | 2016-12-15 | 2018-06-21 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 activators |
| JP2020502152A (ja) | 2016-12-15 | 2020-01-23 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Nrf2アクチベーターとしてのエーテル結合トリアゾール |
| UY37551A (es) | 2016-12-27 | 2018-07-31 | Biogen Ma Inc | Activador de nrf2 |
| US20190389830A1 (en) | 2017-01-30 | 2019-12-26 | Biogen Ma Inc. | Nrf2 activator |
-
2019
- 2019-12-04 MX MX2021006527A patent/MX2021006527A/es unknown
- 2019-12-04 AU AU2019391942A patent/AU2019391942B2/en active Active
- 2019-12-04 UA UAA202102856A patent/UA127872C2/uk unknown
- 2019-12-04 NZ NZ776102A patent/NZ776102A/en unknown
- 2019-12-04 BR BR112021010704-5A patent/BR112021010704A2/pt unknown
- 2019-12-04 EP EP19892751.9A patent/EP3890738A4/en active Pending
- 2019-12-04 SG SG11202105125XA patent/SG11202105125XA/en unknown
- 2019-12-04 JP JP2021554804A patent/JP2022510736A/ja active Pending
- 2019-12-04 CN CN201980080214.5A patent/CN113164468A/zh active Pending
- 2019-12-04 US US17/299,659 patent/US11518763B2/en active Active
- 2019-12-04 TW TW108144324A patent/TWI820266B/zh active
- 2019-12-04 AR ARP190103549A patent/AR117251A1/es unknown
- 2019-12-04 CA CA3121952A patent/CA3121952C/en active Active
- 2019-12-04 WO PCT/JP2019/048593 patent/WO2020116660A1/en not_active Ceased
- 2019-12-04 KR KR1020217020790A patent/KR102919982B1/ko active Active
-
2021
- 2021-05-31 PH PH12021551262A patent/PH12021551262A1/en unknown
- 2021-06-02 CL CL2021001451A patent/CL2021001451A1/es unknown
- 2021-06-03 CO CONC2021/0007304A patent/CO2021007304A2/es unknown
-
2024
- 2024-06-25 JP JP2024102161A patent/JP2024123202A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015092713A1 (en) * | 2013-12-18 | 2015-06-25 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 regulators |
| WO2018140876A1 (en) * | 2017-01-30 | 2018-08-02 | Biogen Ma Inc. | Nrf2 activator |
| WO2018181345A1 (ja) * | 2017-03-28 | 2018-10-04 | 武田薬品工業株式会社 | 複素環化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3890738A4 (en) | 2022-08-17 |
| SG11202105125XA (en) | 2021-06-29 |
| US20220119391A1 (en) | 2022-04-21 |
| PH12021551262A1 (en) | 2021-10-25 |
| CA3121952C (en) | 2025-05-13 |
| TWI820266B (zh) | 2023-11-01 |
| WO2020116660A1 (en) | 2020-06-11 |
| AU2019391942A1 (en) | 2021-06-03 |
| CO2021007304A2 (es) | 2021-06-21 |
| TW202039494A (zh) | 2020-11-01 |
| JP2024123202A (ja) | 2024-09-10 |
| NZ776102A (en) | 2024-12-20 |
| CN113164468A (zh) | 2021-07-23 |
| MX2021006527A (es) | 2021-07-21 |
| AR117251A1 (es) | 2021-07-21 |
| AU2019391942B2 (en) | 2024-03-21 |
| CL2021001451A1 (es) | 2021-12-24 |
| UA127872C2 (uk) | 2024-01-31 |
| BR112021010704A2 (pt) | 2021-08-24 |
| KR20210099622A (ko) | 2021-08-12 |
| KR102919982B1 (ko) | 2026-02-02 |
| CA3121952A1 (en) | 2020-06-11 |
| US11518763B2 (en) | 2022-12-06 |
| EP3890738A1 (en) | 2021-10-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7253640B2 (ja) | 複素環化合物およびその用途 | |
| US12595265B2 (en) | Inhibitors of activin receptor-like kinase | |
| JP7152369B2 (ja) | 複素環化合物およびその用途 | |
| US11518763B2 (en) | Macrocyclic compound and use thereof | |
| JP7034941B2 (ja) | Lsd1/hdac二重阻害剤としてのシクロプロピル-アミド化合物 | |
| KR102050150B1 (ko) | 융합-고리 화합물, 약학 조성물 및 이들의 용도 | |
| WO2018181345A1 (ja) | 複素環化合物 | |
| CA3133753A1 (en) | Novel small molecule inhibitors of tead transcription factors | |
| JP7548814B2 (ja) | Ido阻害剤および/またはido-hdac二重阻害剤としての多環式化合物 | |
| TW201702226A (zh) | 尿素衍生物或其醫藥上可接受鹽 | |
| CA3180387A1 (en) | Macrocyclic 2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1 | |
| CA3018358A1 (en) | Pyridyl derivatives as bromodomain inhibitors | |
| JP2022510874A (ja) | ヒストンアセチラーゼp300阻害剤及びその用途 | |
| JP2025512098A (ja) | 複素環化合物 | |
| CA3018275A1 (en) | Benzo[b]furans as bromodomain inhibitors | |
| JP2025539434A (ja) | 複素環化合物及びその用途 | |
| CN117321042A (zh) | 用于治疗炎症性疾病或癌症的氧代二氢吲哚化合物 | |
| JP2021183587A (ja) | 複素環化合物 | |
| RU2798235C9 (ru) | Макроциклическое соединение и его применение | |
| RU2798235C2 (ru) | Макроциклическое соединение и его применение | |
| TW202440081A (zh) | σ-1受體拮抗劑及其應用 | |
| JP2026509885A (ja) | マクロ環状複素環化合物及びその用途 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20221121 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20221121 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20231226 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20240507 |