JP6495822B2 - Hcv感染用の2’−クロロヌクレオシド類似体 - Google Patents
Hcv感染用の2’−クロロヌクレオシド類似体 Download PDFInfo
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- JP6495822B2 JP6495822B2 JP2015535875A JP2015535875A JP6495822B2 JP 6495822 B2 JP6495822 B2 JP 6495822B2 JP 2015535875 A JP2015535875 A JP 2015535875A JP 2015535875 A JP2015535875 A JP 2015535875A JP 6495822 B2 JP6495822 B2 JP 6495822B2
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- 0 CC(C)N1C=C(*)C(*)=NC2OC12 Chemical compound CC(C)N1C=C(*)C(*)=NC2OC12 0.000 description 9
- BQAKSPCSQAEBDZ-ILJSZOFFSA-N CC(C)(C)C(SCCOP(OC1)(O[C@@H](CC2)[C@@H]1O[C@H]2N(C=CC(N1)=O)C1=O)=O)=O Chemical compound CC(C)(C)C(SCCOP(OC1)(O[C@@H](CC2)[C@@H]1O[C@H]2N(C=CC(N1)=O)C1=O)=O)=O BQAKSPCSQAEBDZ-ILJSZOFFSA-N 0.000 description 1
- YZIZBHYZZKWMEG-PZJWPPBQSA-N CC(C)OP(O)(OC[C@H](CCCC1)O[C@H]1N(C=CC(N1COCc2ccccc2)=O)C1=O)=O Chemical compound CC(C)OP(O)(OC[C@H](CCCC1)O[C@H]1N(C=CC(N1COCc2ccccc2)=O)C1=O)=O YZIZBHYZZKWMEG-PZJWPPBQSA-N 0.000 description 1
- PCELAPFXIYEDAA-FOCIZLCUSA-N CC(CCC[C@H](N(C=CC(N)=N1)C1=O)O[C@@H]1COP(O)(OP(O)(OP(O)(OC)=O)=O)=O)[C@@H]1O Chemical compound CC(CCC[C@H](N(C=CC(N)=N1)C1=O)O[C@@H]1COP(O)(OP(O)(OP(O)(OC)=O)=O)=O)[C@@H]1O PCELAPFXIYEDAA-FOCIZLCUSA-N 0.000 description 1
- FIUKKNASPSRAPX-UHFFFAOYSA-N CC1C(N(C=CC(N2)=O)C2=O)OC(CCOP(Oc2ccccc2)=O)C1O Chemical compound CC1C(N(C=CC(N2)=O)C2=O)OC(CCOP(Oc2ccccc2)=O)C1O FIUKKNASPSRAPX-UHFFFAOYSA-N 0.000 description 1
- OCHJBQXIFVGXJF-OVXNBMDESA-N CCCCOC(C(C)NP(OC[C@@]1([C@H](C)[C@H](N(C=CC(N2)=O)C2=O)OC1)O)(Oc1ccccc1)=O)=O Chemical compound CCCCOC(C(C)NP(OC[C@@]1([C@H](C)[C@H](N(C=CC(N2)=O)C2=O)OC1)O)(Oc1ccccc1)=O)=O OCHJBQXIFVGXJF-OVXNBMDESA-N 0.000 description 1
- TVWGOOSIKRBHPH-UNGBFZJXSA-N CCCCOC([C@@H](C)NP(OC[C@H]([C@H]([C@@]1(C)Cl)O)O[C@H]1N(C=CC(N1)=O)C1=O)(Oc1ccccc1)=O)=O Chemical compound CCCCOC([C@@H](C)NP(OC[C@H]([C@H]([C@@]1(C)Cl)O)O[C@H]1N(C=CC(N1)=O)C1=O)(Oc1ccccc1)=O)=O TVWGOOSIKRBHPH-UNGBFZJXSA-N 0.000 description 1
- AYMUBHQASLPVPJ-QSYHIEBSSA-N CCCCOC([C@H](C)NP(OC[C@H]([C@H]([C@@H]1C)O)O[C@H]1N(C=CC(N1)=O)C1=O)(Oc1ccccc1)=O)=O Chemical compound CCCCOC([C@H](C)NP(OC[C@H]([C@H]([C@@H]1C)O)O[C@H]1N(C=CC(N1)=O)C1=O)(Oc1ccccc1)=O)=O AYMUBHQASLPVPJ-QSYHIEBSSA-N 0.000 description 1
- UTWLHSVZVBQLPI-SFLUZMGESA-N C[C@@H](C(OCC(C)(C)C)=O)NP(OC[C@H](C[C@@H]1C)O[C@H]1N(C=CC(N1COCc2ccccc2)=O)C1=O)(Oc1ccccc1)=O Chemical compound C[C@@H](C(OCC(C)(C)C)=O)NP(OC[C@H](C[C@@H]1C)O[C@H]1N(C=CC(N1COCc2ccccc2)=O)C1=O)(Oc1ccccc1)=O UTWLHSVZVBQLPI-SFLUZMGESA-N 0.000 description 1
- HDWCVDLNZJDFDM-GLFKHWCOSA-N C[C@@H]1C(c2ccc3[n]2ncnc3N)O[C@H](COC(c2ccccc2)=O)[C@H]1OC(c1ccccc1)=O Chemical compound C[C@@H]1C(c2ccc3[n]2ncnc3N)O[C@H](COC(c2ccccc2)=O)[C@H]1OC(c1ccccc1)=O HDWCVDLNZJDFDM-GLFKHWCOSA-N 0.000 description 1
- DWPKKGWQVXDJQR-IXERZQKFSA-N C[C@@H]1[C@H](N(C=CC(N2)=O)C2=O)O[C@H](CO2)[C@H]1O[P@]2(OCCSC(C(C)(C)C)=O)=O Chemical compound C[C@@H]1[C@H](N(C=CC(N2)=O)C2=O)O[C@H](CO2)[C@H]1O[P@]2(OCCSC(C(C)(C)C)=O)=O DWPKKGWQVXDJQR-IXERZQKFSA-N 0.000 description 1
- RJIDLWHDWOMTOO-MCOSLZNDSA-N C[C@@H]1[C@H]([n]2c3ncnc(N)c3nc2)O[C@H](CO)[C@H]1O Chemical compound C[C@@H]1[C@H]([n]2c3ncnc(N)c3nc2)O[C@H](CO)[C@H]1O RJIDLWHDWOMTOO-MCOSLZNDSA-N 0.000 description 1
- IAIFRGSJIJCVCO-GAJNKVMBSA-N C[C@@]1([C@H]([n]2c3ncnc(N)c3cc2)O[C@H](CO)[C@H]1O)Cl Chemical compound C[C@@]1([C@H]([n]2c3ncnc(N)c3cc2)O[C@H](CO)[C@H]1O)Cl IAIFRGSJIJCVCO-GAJNKVMBSA-N 0.000 description 1
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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