KR20180132629A - 글리코시다제 저해제 - Google Patents
글리코시다제 저해제 Download PDFInfo
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- KR20180132629A KR20180132629A KR1020187025792A KR20187025792A KR20180132629A KR 20180132629 A KR20180132629 A KR 20180132629A KR 1020187025792 A KR1020187025792 A KR 1020187025792A KR 20187025792 A KR20187025792 A KR 20187025792A KR 20180132629 A KR20180132629 A KR 20180132629A
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- 0 CCN(*)C(C)CN(CC)C(*)* Chemical compound CCN(*)C(C)CN(CC)C(*)* 0.000 description 7
- HBEISXKDRDAGOU-UHFFFAOYSA-N CC(C)(C)OC(N(CCc1n2)Cc1cnc2Cl)=O Chemical compound CC(C)(C)OC(N(CCc1n2)Cc1cnc2Cl)=O HBEISXKDRDAGOU-UHFFFAOYSA-N 0.000 description 1
- AYBZOZAOPVHROI-UHFFFAOYSA-N CC(C)C(c(cc1)cnc1N(CC1)CCN1C(C)c1cc(OCC2)c2cc1)O Chemical compound CC(C)C(c(cc1)cnc1N(CC1)CCN1C(C)c1cc(OCC2)c2cc1)O AYBZOZAOPVHROI-UHFFFAOYSA-N 0.000 description 1
- DWWCWYRGVAHKIL-UHFFFAOYSA-N CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c(cc1)ncc1C(OC)=O Chemical compound CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c(cc1)ncc1C(OC)=O DWWCWYRGVAHKIL-UHFFFAOYSA-N 0.000 description 1
- XUYJIPKVQOXQJP-UHFFFAOYSA-N CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c(nc1)ncc1C1=CCCC1 Chemical compound CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c(nc1)ncc1C1=CCCC1 XUYJIPKVQOXQJP-UHFFFAOYSA-N 0.000 description 1
- MUKHJBZWOIVIJT-UHFFFAOYSA-N CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c1ncc(C(C)O)cc1 Chemical compound CC(c(cc1)cc2c1nccn2)N(CC1)CCN1c1ncc(C(C)O)cc1 MUKHJBZWOIVIJT-UHFFFAOYSA-N 0.000 description 1
- HDQRMDLGIIPLLC-UHFFFAOYSA-N CC(c1cc(OCC2)c2cc1)N(CC1)CCC1c1nnc(C)[o]1 Chemical compound CC(c1cc(OCC2)c2cc1)N(CC1)CCC1c1nnc(C)[o]1 HDQRMDLGIIPLLC-UHFFFAOYSA-N 0.000 description 1
- MLMJBZRGNNRXIW-UHFFFAOYSA-N CC(c1cc(OCC2)c2cc1)N(CC1)CCN1c(cc1)c[n]2c1cnc2C Chemical compound CC(c1cc(OCC2)c2cc1)N(CC1)CCN1c(cc1)c[n]2c1cnc2C MLMJBZRGNNRXIW-UHFFFAOYSA-N 0.000 description 1
- RJKCTCJUOLSAEW-UHFFFAOYSA-N CC(c1cc(OCC2)c2cc1)N(CC1)CCN1c(cc1)ncc1C(N(C)C)=O Chemical compound CC(c1cc(OCC2)c2cc1)N(CC1)CCN1c(cc1)ncc1C(N(C)C)=O RJKCTCJUOLSAEW-UHFFFAOYSA-N 0.000 description 1
- BYWMKFNBBKYACE-UHFFFAOYSA-N CC(c1cc(OCC2)c2cc1)N1CCNCC1 Chemical compound CC(c1cc(OCC2)c2cc1)N1CCNCC1 BYWMKFNBBKYACE-UHFFFAOYSA-N 0.000 description 1
- FCONYVAYFJDBDI-UHFFFAOYSA-N CC(c1cc2nccnc2cc1)Cl Chemical compound CC(c1cc2nccnc2cc1)Cl FCONYVAYFJDBDI-UHFFFAOYSA-N 0.000 description 1
- ZNSFDCIIHLSDKI-UHFFFAOYSA-N CC(c1cc2nccnc2cc1)N(CC1)CCN1C(S1)=NNC1=O Chemical compound CC(c1cc2nccnc2cc1)N(CC1)CCN1C(S1)=NNC1=O ZNSFDCIIHLSDKI-UHFFFAOYSA-N 0.000 description 1
- YUNACVOBOJKTSI-UHFFFAOYSA-N CC(c1nnc(N(CC2)CCN2C(C)c(cc2)cc3c2nccn3)[s]1)O Chemical compound CC(c1nnc(N(CC2)CCN2C(C)c(cc2)cc3c2nccn3)[s]1)O YUNACVOBOJKTSI-UHFFFAOYSA-N 0.000 description 1
- YMIMKEQSIPJDIE-UHFFFAOYSA-N CCOC(c1c[n](C(CC2)CCN2C(C)c2cc(OCC3)c3cc2)nc1)=O Chemical compound CCOC(c1c[n](C(CC2)CCN2C(C)c2cc(OCC3)c3cc2)nc1)=O YMIMKEQSIPJDIE-UHFFFAOYSA-N 0.000 description 1
- CGSWTRTYXLGAFI-UHFFFAOYSA-N Cc1nc2ncccc2[s]1 Chemical compound Cc1nc2ncccc2[s]1 CGSWTRTYXLGAFI-UHFFFAOYSA-N 0.000 description 1
- ZPWVMEBCBJNTNY-UHFFFAOYSA-N OC1(CCCC1)c(cc1)cnc1Cl Chemical compound OC1(CCCC1)c(cc1)cnc1Cl ZPWVMEBCBJNTNY-UHFFFAOYSA-N 0.000 description 1
- CSNIZNHTOVFARY-UHFFFAOYSA-N c1n[s]c2c1cccc2 Chemical compound c1n[s]c2c1cccc2 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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| US12016852B2 (en) | 2018-08-22 | 2024-06-25 | Asceneuron Sa | Pyrrolidine glycosidase inhibitors |
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| US20220143042A1 (en) | 2019-02-22 | 2022-05-12 | Asceneuron Sa | Fused glycosidase inhibitors |
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| US20210186958A1 (en) | 2021-06-24 |
| EA201991697A1 (ru) | 2020-03-04 |
| JP7082446B2 (ja) | 2022-06-08 |
| JP2020509003A (ja) | 2020-03-26 |
| EP3419971A1 (en) | 2019-01-02 |
| EP3419971B1 (en) | 2022-04-20 |
| CN110770226B (zh) | 2023-11-10 |
| MA43677A (fr) | 2018-11-28 |
| US11612599B2 (en) | 2023-03-28 |
| MX2018010192A (es) | 2019-01-31 |
| WO2017144633A1 (en) | 2017-08-31 |
| CA3012560A1 (en) | 2017-08-31 |
| ZA201905405B (en) | 2021-08-25 |
| CN108884077A (zh) | 2018-11-23 |
| AU2017222958B2 (en) | 2019-07-18 |
| AU2017222958A1 (en) | 2018-08-02 |
| JP2019510006A (ja) | 2019-04-11 |
| CN110770226A (zh) | 2020-02-07 |
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