JP6762299B2 - 免疫調節剤 - Google Patents
免疫調節剤 Download PDFInfo
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- JP6762299B2 JP6762299B2 JP2017524423A JP2017524423A JP6762299B2 JP 6762299 B2 JP6762299 B2 JP 6762299B2 JP 2017524423 A JP2017524423 A JP 2017524423A JP 2017524423 A JP2017524423 A JP 2017524423A JP 6762299 B2 JP6762299 B2 JP 6762299B2
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- Prior art keywords
- cyclohexyl
- fluoroquinoline
- ethyl
- benzamide
- mmol
- Prior art date
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- 0 CC(CC#CCN(C)CN)*(C)=C Chemical compound CC(CC#CCN(C)CN)*(C)=C 0.000 description 4
- JCIHTLANYGNMGL-UHFFFAOYSA-N C1C2C=CC=CC12 Chemical compound C1C2C=CC=CC12 JCIHTLANYGNMGL-UHFFFAOYSA-N 0.000 description 2
- HKNTWJMEJZJDGW-UHFFFAOYSA-N COc(cc1)ccc1NC(C1CCC(Cc2ccccc2)CC1)=O Chemical compound COc(cc1)ccc1NC(C1CCC(Cc2ccccc2)CC1)=O HKNTWJMEJZJDGW-UHFFFAOYSA-N 0.000 description 2
- MKBRAZBSNHKNFV-UHFFFAOYSA-N CC(CCNC)=O Chemical compound CC(CCNC)=O MKBRAZBSNHKNFV-UHFFFAOYSA-N 0.000 description 1
- JCHWHOHZZYWUMP-UHFFFAOYSA-N CC1(C)OB(C(CC2)=CCC22OCCO2)OC1(C)C Chemical compound CC1(C)OB(C(CC2)=CCC22OCCO2)OC1(C)C JCHWHOHZZYWUMP-UHFFFAOYSA-N 0.000 description 1
- QAMLQBKWDBAMJO-FCDKUWBWSA-N CCC([C@H](CC1)CC[C@@H]1Oc1ccnc2c1cccc2)NC(c(cc1)ccc1Cl)=O Chemical compound CCC([C@H](CC1)CC[C@@H]1Oc1ccnc2c1cccc2)NC(c(cc1)ccc1Cl)=O QAMLQBKWDBAMJO-FCDKUWBWSA-N 0.000 description 1
- SZMXHLLOPWHWSP-BEYSDYMESA-N CC[C@H]([C@H](CC1)CC[C@H]1c1cc2ccccc2nc1)NC(c(cc1)ccc1-c1ccccc1)=O Chemical compound CC[C@H]([C@H](CC1)CC[C@H]1c1cc2ccccc2nc1)NC(c(cc1)ccc1-c1ccccc1)=O SZMXHLLOPWHWSP-BEYSDYMESA-N 0.000 description 1
- RBNWKOWQBDCJNI-UHFFFAOYSA-N COc1ccc(C2CCC(CC(NCc3ccccc3)=O)CC2)cc1 Chemical compound COc1ccc(C2CCC(CC(NCc3ccccc3)=O)CC2)cc1 RBNWKOWQBDCJNI-UHFFFAOYSA-N 0.000 description 1
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- VFAKILSPWSMVSP-IZAXUBKRSA-N N#Cc(cc1)ccc1C(NC[C@H](CC1)CC[C@H]1c1ccccc1)=O Chemical compound N#Cc(cc1)ccc1C(NC[C@H](CC1)CC[C@H]1c1ccccc1)=O VFAKILSPWSMVSP-IZAXUBKRSA-N 0.000 description 1
- YPCHPGLGWGZWCT-RHGYRFJNSA-N O=C(C[C@H](CC1)CC[C@H]1c1c(cc(cc2)F)c2ncc1)N([C@@H](CO1)c2ccccc2)C1=O Chemical compound O=C(C[C@H](CC1)CC[C@H]1c1c(cc(cc2)F)c2ncc1)N([C@@H](CO1)c2ccccc2)C1=O YPCHPGLGWGZWCT-RHGYRFJNSA-N 0.000 description 1
- HCTBXXSKSHOTFM-UHFFFAOYSA-N O=C(Cc(cc1)ccc1Cl)NC(CC1)CCC1c1ccccc1 Chemical compound O=C(Cc(cc1)ccc1Cl)NC(CC1)CCC1c1ccccc1 HCTBXXSKSHOTFM-UHFFFAOYSA-N 0.000 description 1
- GKFAKZJLWUKPGM-UAPYVXQJSA-N O=C(Cc(cc1)ccc1Cl)N[C@H](CC1)CC[C@@H]1c1c(cccc2)c2ncc1 Chemical compound O=C(Cc(cc1)ccc1Cl)N[C@H](CC1)CC[C@@H]1c1c(cccc2)c2ncc1 GKFAKZJLWUKPGM-UAPYVXQJSA-N 0.000 description 1
- IEBIWDLFUTUSGF-UHFFFAOYSA-N O=C(NC(CC1)CCN1c1c(cc(cc2)F)c2ncc1)Nc(cc1)ccc1F Chemical compound O=C(NC(CC1)CCN1c1c(cc(cc2)F)c2ncc1)Nc(cc1)ccc1F IEBIWDLFUTUSGF-UHFFFAOYSA-N 0.000 description 1
- NMEUHEOYGLUDKZ-WOVMCDHWSA-N O=C(N[C@H](CC1)CC[C@H]1c1ccccc1)Nc1cc(Cl)ccc1 Chemical compound O=C(N[C@H](CC1)CC[C@H]1c1ccccc1)Nc1cc(Cl)ccc1 NMEUHEOYGLUDKZ-WOVMCDHWSA-N 0.000 description 1
- KLRLEPJKIXCIFM-CALCHBBNSA-N O=C([C@H]1CC[C@@H](Cc2ccccc2)CC1)Nc(cc1)ccc1F Chemical compound O=C([C@H]1CC[C@@H](Cc2ccccc2)CC1)Nc(cc1)ccc1F KLRLEPJKIXCIFM-CALCHBBNSA-N 0.000 description 1
- KLRLEPJKIXCIFM-QAQDUYKDSA-N O=C([C@H]1CC[C@H](Cc2ccccc2)CC1)Nc(cc1)ccc1F Chemical compound O=C([C@H]1CC[C@H](Cc2ccccc2)CC1)Nc(cc1)ccc1F KLRLEPJKIXCIFM-QAQDUYKDSA-N 0.000 description 1
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- C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
- C07C255/60—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton at least one of the singly-bound nitrogen atoms being acylated
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