JP6774562B2 - 置換ピロリジン化合物およびその使用 - Google Patents
置換ピロリジン化合物およびその使用 Download PDFInfo
- Publication number
- JP6774562B2 JP6774562B2 JP2019510869A JP2019510869A JP6774562B2 JP 6774562 B2 JP6774562 B2 JP 6774562B2 JP 2019510869 A JP2019510869 A JP 2019510869A JP 2019510869 A JP2019510869 A JP 2019510869A JP 6774562 B2 JP6774562 B2 JP 6774562B2
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- pharmaceutically acceptable
- alkyl
- inhibitors
- acceptable salt
- 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.)
- Active
Links
- 0 *c1c(C(N*)=O)[n](CCCCCCC2)c2c1C(C(N*)=O)=O Chemical compound *c1c(C(N*)=O)[n](CCCCCCC2)c2c1C(C(N*)=O)=O 0.000 description 6
- BOOOFYIGDHEYMP-HXUWFJFHSA-N C[C@](C(F)(F)F)(C(N)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O Chemical compound C[C@](C(F)(F)F)(C(N)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O BOOOFYIGDHEYMP-HXUWFJFHSA-N 0.000 description 2
- KYQJFMXGDILKQG-UHFFFAOYSA-N Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O KYQJFMXGDILKQG-UHFFFAOYSA-N 0.000 description 2
- HXJQSAQAQAPTAI-UHFFFAOYSA-N Cc1c(C(Nc2cc(C(F)F)ncc2)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc2cc(C(F)F)ncc2)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O HXJQSAQAQAPTAI-UHFFFAOYSA-N 0.000 description 2
- ISBDYYOLPRINPR-UHFFFAOYSA-N CC(C)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(C(F)F)c2F)=O)c1C)=O)=O Chemical compound CC(C)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(C(F)F)c2F)=O)c1C)=O)=O ISBDYYOLPRINPR-UHFFFAOYSA-N 0.000 description 1
- JDCAEUCJNXMESQ-UHFFFAOYSA-N CC(C)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2Cl)ccc2F)=O)c1C)=O)=O Chemical compound CC(C)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2Cl)ccc2F)=O)c1C)=O)=O JDCAEUCJNXMESQ-UHFFFAOYSA-N 0.000 description 1
- AKFLHODMFPIXAH-UHFFFAOYSA-N CC(C)(C)OC(NC1(CC1)c1c[nH]nn1)=O Chemical compound CC(C)(C)OC(NC1(CC1)c1c[nH]nn1)=O AKFLHODMFPIXAH-UHFFFAOYSA-N 0.000 description 1
- WYKVCZXBXSNIQV-UHFFFAOYSA-N CC(C)C1(COC1)C(N)(N)N Chemical compound CC(C)C1(COC1)C(N)(N)N WYKVCZXBXSNIQV-UHFFFAOYSA-N 0.000 description 1
- HIXLPXCVOTTYCF-UHFFFAOYSA-N CC(C1)(CS1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O Chemical compound CC(C1)(CS1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O HIXLPXCVOTTYCF-UHFFFAOYSA-N 0.000 description 1
- GJHZZRVGCDRGBR-UHFFFAOYSA-N CCC(C(CCF)(CCF)NC(OCc1ccccc1)=O)=O Chemical compound CCC(C(CCF)(CCF)NC(OCc1ccccc1)=O)=O GJHZZRVGCDRGBR-UHFFFAOYSA-N 0.000 description 1
- GXWYXULRLAFDFE-UHFFFAOYSA-N CCOC(C(c1c(CCC2)[n]2c(C(OC)=O)c1C)=O)=O Chemical compound CCOC(C(c1c(CCC2)[n]2c(C(OC)=O)c1C)=O)=O GXWYXULRLAFDFE-UHFFFAOYSA-N 0.000 description 1
- BOOOFYIGDHEYMP-FQEVSTJZSA-N C[C@@](C(F)(F)F)(C(N)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O Chemical compound C[C@@](C(F)(F)F)(C(N)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O BOOOFYIGDHEYMP-FQEVSTJZSA-N 0.000 description 1
- GFFVOEVMSGLFDI-NRFANRHFSA-N C[C@@](C(F)(F)F)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O Chemical compound C[C@@](C(F)(F)F)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O GFFVOEVMSGLFDI-NRFANRHFSA-N 0.000 description 1
- GFFVOEVMSGLFDI-OAQYLSRUSA-N C[C@](C(F)(F)F)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O Chemical compound C[C@](C(F)(F)F)(C(NC)=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O GFFVOEVMSGLFDI-OAQYLSRUSA-N 0.000 description 1
- HIXLPXCVOTTYCF-NEWFWRPPSA-N C[C@](C1)(C[S@@]1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O Chemical compound C[C@](C1)(C[S@@]1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2)cc(F)c2F)=O)c1C)=O)=O HIXLPXCVOTTYCF-NEWFWRPPSA-N 0.000 description 1
- HIXLPXCVOTTYCF-JUKHWHIISA-N C[C@](C1)(C[S@]1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O Chemical compound C[C@](C1)(C[S@]1=O)NC(C(c1c(CCC2)[n]2c(C(Nc(cc2F)ccc2F)=O)c1C)=O)=O HIXLPXCVOTTYCF-JUKHWHIISA-N 0.000 description 1
- KGRFDNOJYUWCRH-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(C#N)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(C#N)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O KGRFDNOJYUWCRH-UHFFFAOYSA-N 0.000 description 1
- ZMZJBUWFGAOAHT-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=N)=N)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=N)=N)=O)=O ZMZJBUWFGAOAHT-UHFFFAOYSA-N 0.000 description 1
- AMRLYSSGANCGGU-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C#C)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C#C)=O)=O AMRLYSSGANCGGU-UHFFFAOYSA-N 0.000 description 1
- NNIPCTNJBVAMCQ-BOPFTXTBSA-N Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)/C(/N)=C/N(C)N)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)/C(/N)=C/N(C)N)=O)=O NNIPCTNJBVAMCQ-BOPFTXTBSA-N 0.000 description 1
- LRUHUPVDHZBOIV-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1ccccc1)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1ccccc1)=O)=O LRUHUPVDHZBOIV-UHFFFAOYSA-N 0.000 description 1
- FKUYEFIBLJWFHG-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[o]1)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[o]1)=O)=O FKUYEFIBLJWFHG-UHFFFAOYSA-N 0.000 description 1
- JHZWOBJZFZOGNA-UHFFFAOYSA-O Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=[NH2+])=N)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=[NH2+])=N)=O)=O JHZWOBJZFZOGNA-UHFFFAOYSA-O 0.000 description 1
- HOLWVMYHUMMPKG-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(C2)CC12C#N)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(C2)CC12C#N)=O)=O HOLWVMYHUMMPKG-UHFFFAOYSA-N 0.000 description 1
- RSYSXPQRXLXDQX-UHFFFAOYSA-N Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O RSYSXPQRXLXDQX-UHFFFAOYSA-N 0.000 description 1
- RCFHZLKULPMUMS-WPZCJLIBSA-N Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)C2C2)c2c1C(C(NC(C1)(CC1(F)F)c1cnn[nH]1)=O)=O Chemical compound Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)C2C2)c2c1C(C(NC(C1)(CC1(F)F)c1cnn[nH]1)=O)=O RCFHZLKULPMUMS-WPZCJLIBSA-N 0.000 description 1
- GARXGXIMSVEZHA-IUODEOHRSA-N Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O GARXGXIMSVEZHA-IUODEOHRSA-N 0.000 description 1
- HNQOBZHSSXFFIS-IUODEOHRSA-N Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1cnn[nH]1)=O)=O Chemical compound Cc1c(C(Nc(cc2)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1cnn[nH]1)=O)=O HNQOBZHSSXFFIS-IUODEOHRSA-N 0.000 description 1
- ARYFPUZRBRDBJD-UHFFFAOYSA-N Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC(C1)(C2)CC12C(N)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC(C1)(C2)CC12C(N)=O)=O)=O ARYFPUZRBRDBJD-UHFFFAOYSA-N 0.000 description 1
- VODUOCVTPPLDOX-UHFFFAOYSA-N Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NC)=O)=O)=O VODUOCVTPPLDOX-UHFFFAOYSA-N 0.000 description 1
- YWVFDVWCGWUNEE-UHFFFAOYSA-N Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[nH]1)=O)=O Chemical compound Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[nH]1)=O)=O YWVFDVWCGWUNEE-UHFFFAOYSA-N 0.000 description 1
- VBOBNVOCPFMYPA-IAQYHMDHSA-N Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc(cc2Cl)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O VBOBNVOCPFMYPA-IAQYHMDHSA-N 0.000 description 1
- SLPYPUIPQODCTG-UHFFFAOYSA-N Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=N)=N)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C(SC=N)=N)=O)=O SLPYPUIPQODCTG-UHFFFAOYSA-N 0.000 description 1
- NQNSGOIFUIMYBZ-UHFFFAOYSA-O Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C1=[N+]=CS1)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)C1=[N+]=CS1)=O)=O NQNSGOIFUIMYBZ-UHFFFAOYSA-O 0.000 description 1
- WRMTULCTQIDTJD-UHFFFAOYSA-N Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(N)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(N)=O)=O)=O WRMTULCTQIDTJD-UHFFFAOYSA-N 0.000 description 1
- JSRZDJNDLPMVHE-UHFFFAOYSA-N Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O JSRZDJNDLPMVHE-UHFFFAOYSA-N 0.000 description 1
- JQWCEYRILZTJJD-UHFFFAOYSA-N Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1ccccc1)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1ccccc1)=O)=O JQWCEYRILZTJJD-UHFFFAOYSA-N 0.000 description 1
- NYRULGHTEHZRQN-UHFFFAOYSA-N Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[o]1)=O)=O Chemical compound Cc1c(C(Nc(cc2F)cc(F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1nnc(C)[o]1)=O)=O NYRULGHTEHZRQN-UHFFFAOYSA-N 0.000 description 1
- QWRDHKUPHMFQQN-IAQYHMDHSA-N Cc1c(C(Nc(cc2F)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc(cc2F)ccc2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O QWRDHKUPHMFQQN-IAQYHMDHSA-N 0.000 description 1
- GMQLGJJXMDVYBI-UHFFFAOYSA-O Cc1c(C(Nc(ccc(F)c2F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C([NH3+])=CN[NH2+2])=O)=O Chemical compound Cc1c(C(Nc(ccc(F)c2F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C([NH3+])=CN[NH2+2])=O)=O GMQLGJJXMDVYBI-UHFFFAOYSA-O 0.000 description 1
- QMHZTQOYPKXGJC-UHFFFAOYSA-N Cc1c(C(Nc(ccc(F)c2F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc(ccc(F)c2F)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O QMHZTQOYPKXGJC-UHFFFAOYSA-N 0.000 description 1
- LXETZQNHIIREER-GDNBJRDFSA-N Cc1c(C(Nc(cccc2Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)/C(/N)=C/NN)=O)=O Chemical compound Cc1c(C(Nc(cccc2Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)/C(/N)=C/NN)=O)=O LXETZQNHIIREER-GDNBJRDFSA-N 0.000 description 1
- YPSAWSLQXCVOFK-UHFFFAOYSA-O Cc1c(C(Nc(cccc2Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NN)=C[NH3+])=O)=O Chemical compound Cc1c(C(Nc(cccc2Cl)c2F)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NN)=C[NH3+])=O)=O YPSAWSLQXCVOFK-UHFFFAOYSA-O 0.000 description 1
- BTBUESRCBXWRFW-UHFFFAOYSA-N Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O Chemical compound Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O BTBUESRCBXWRFW-UHFFFAOYSA-N 0.000 description 1
- ZTETUIHLYHMGBX-UHFFFAOYSA-N Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)c1c[nH]nn1)=O)=O ZTETUIHLYHMGBX-UHFFFAOYSA-N 0.000 description 1
- ACXVSWWSVCRTBR-SECBINFHSA-N Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](C[C@@H](C2)F)c2c1C(C(NC1(COC1)C(F)(F)F)=O)=O Chemical compound Cc1c(C(Nc(ccnc2C(F)F)c2F)=O)[n](C[C@@H](C2)F)c2c1C(C(NC1(COC1)C(F)(F)F)=O)=O ACXVSWWSVCRTBR-SECBINFHSA-N 0.000 description 1
- UFNFDIKXQQEPRA-UHFFFAOYSA-N Cc1c(C(Nc2cc(C#N)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C1=CNNN1)=O)=O Chemical compound Cc1c(C(Nc2cc(C#N)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C1=CNNN1)=O)=O UFNFDIKXQQEPRA-UHFFFAOYSA-N 0.000 description 1
- MVCRBBSVTDUREK-UHFFFAOYSA-N Cc1c(C(Nc2cc(C(F)F)ccc2)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O Chemical compound Cc1c(C(Nc2cc(C(F)F)ccc2)=O)[n](CCC2)c2c1C(C(NC(C1)(CC1(F)F)C(NC)=O)=O)=O MVCRBBSVTDUREK-UHFFFAOYSA-N 0.000 description 1
- MADCJRUEHZZXGR-UHFFFAOYSA-N Cc1c(C(Nc2cc(C(F)F)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc2cc(C(F)F)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O MADCJRUEHZZXGR-UHFFFAOYSA-N 0.000 description 1
- XZYJIPIVMNKWNI-UHFFFAOYSA-N Cc1c(C(Nc2cc(C(F)F)ncc2)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O Chemical compound Cc1c(C(Nc2cc(C(F)F)ncc2)=O)[n](C(C2)C2C2)c2c1C(C(NC1(CC1)c1nnc[s]1)=O)=O XZYJIPIVMNKWNI-UHFFFAOYSA-N 0.000 description 1
- SCPXCDRTCXNZCL-UHFFFAOYSA-N Cc1c(C(Nc2cc(Cl)cc(Cl)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc2cc(Cl)cc(Cl)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O SCPXCDRTCXNZCL-UHFFFAOYSA-N 0.000 description 1
- HQTZBWCPEHWQPZ-UHFFFAOYSA-N Cc1c(C(Nc2cc(F)cc(Cl)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C1=CNNN1)=O)=O Chemical compound Cc1c(C(Nc2cc(F)cc(Cl)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C1=CNNN1)=O)=O HQTZBWCPEHWQPZ-UHFFFAOYSA-N 0.000 description 1
- XDLVLSYVZBRROH-UHFFFAOYSA-N Cc1c(C(Nc2cc(F)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C#C)=O)=O Chemical compound Cc1c(C(Nc2cc(F)ccc2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C#C)=O)=O XDLVLSYVZBRROH-UHFFFAOYSA-N 0.000 description 1
- XQDKBKGJSNEZTF-UHFFFAOYSA-O Cc1c(C(Nc2cccc(F)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NC)=CN[NH3+])=O)=O Chemical compound Cc1c(C(Nc2cccc(F)c2)=O)[n](CCC2)c2c1C(C(NC1(CC1)C(NC)=CN[NH3+])=O)=O XQDKBKGJSNEZTF-UHFFFAOYSA-O 0.000 description 1
- CMPCXXBMUXKBFA-IUODEOHRSA-N Cc1c(C(Nc2ccnc(C(F)F)c2)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)C1=CNN(C)N1)=O)=O Chemical compound Cc1c(C(Nc2ccnc(C(F)F)c2)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)C1=CNN(C)N1)=O)=O CMPCXXBMUXKBFA-IUODEOHRSA-N 0.000 description 1
- OQBSLJGLWRTTND-ZYHUDNBSSA-N Cc1c(C(Nc2ccnc(C(F)F)c2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O Chemical compound Cc1c(C(Nc2ccnc(C(F)F)c2F)=O)[n]([C@H](C2)[C@H]2C2)c2c1C(C(NC1(CC1)c1c[nH]nn1)=O)=O OQBSLJGLWRTTND-ZYHUDNBSSA-N 0.000 description 1
- QWJBPWJXMJVPDN-UHFFFAOYSA-N Cc1c(C(O)=O)[n](CCC2)c2c1C(C(O)=O)=O Chemical compound Cc1c(C(O)=O)[n](CCC2)c2c1C(C(O)=O)=O QWJBPWJXMJVPDN-UHFFFAOYSA-N 0.000 description 1
- HGGSDAHVIQBNFG-UHFFFAOYSA-N Cc1c(C(O[n]2nnc3c2nccc3)=O)[n](CCC2)c2c1C(C(NC1(CC1)C#C)=O)=O Chemical compound Cc1c(C(O[n]2nnc3c2nccc3)=O)[n](CCC2)c2c1C(C(NC1(CC1)C#C)=O)=O HGGSDAHVIQBNFG-UHFFFAOYSA-N 0.000 description 1
- KSCVQJSNYDFHOT-UHFFFAOYSA-N NC(C1)(CC1(F)F)C(O)=O Chemical compound NC(C1)(CC1(F)F)C(O)=O KSCVQJSNYDFHOT-UHFFFAOYSA-N 0.000 description 1
- NYYPFTITHJCRHQ-UHFFFAOYSA-N NC1(CC1)C1=CNCN1 Chemical compound NC1(CC1)C1=CNCN1 NYYPFTITHJCRHQ-UHFFFAOYSA-N 0.000 description 1
- SEONRICTAYAILT-UHFFFAOYSA-N OC(C(C1)(CC1(F)F)NC(OCc1ccccc1)=O)=O Chemical compound OC(C(C1)(CC1(F)F)NC(OCc1ccccc1)=O)=O SEONRICTAYAILT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/40—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
- 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
-
- 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
- A61K31/02—Halogenated hydrocarbons
- A61K31/025—Halogenated hydrocarbons carbocyclic
- A61K31/03—Halogenated hydrocarbons carbocyclic aromatic
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
-
- 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
- A61K31/40—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
- A61K31/407—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 other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- 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
- A61K31/4192—1,2,3-Triazoles
-
- 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
- A61K31/4196—1,2,4-Triazoles
-
- 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
- A61K31/4245—Oxadiazoles
-
- 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
- A61K31/433—Thidiazoles
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
-
- 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)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Biotechnology (AREA)
- Gastroenterology & Hepatology (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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2020167860A JP6983296B2 (ja) | 2016-08-26 | 2020-10-02 | 置換ピロリジン化合物およびその使用 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662380063P | 2016-08-26 | 2016-08-26 | |
| US62/380,063 | 2016-08-26 | ||
| US201662416020P | 2016-11-01 | 2016-11-01 | |
| US62/416,020 | 2016-11-01 | ||
| PCT/US2017/048565 WO2018039531A1 (en) | 2016-08-26 | 2017-08-25 | Substituted pyrrolizine compounds and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020167860A Division JP6983296B2 (ja) | 2016-08-26 | 2020-10-02 | 置換ピロリジン化合物およびその使用 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2019530652A JP2019530652A (ja) | 2019-10-24 |
| JP6774562B2 true JP6774562B2 (ja) | 2020-10-28 |
Family
ID=59772819
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019510869A Active JP6774562B2 (ja) | 2016-08-26 | 2017-08-25 | 置換ピロリジン化合物およびその使用 |
| JP2020167860A Active JP6983296B2 (ja) | 2016-08-26 | 2020-10-02 | 置換ピロリジン化合物およびその使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020167860A Active JP6983296B2 (ja) | 2016-08-26 | 2020-10-02 | 置換ピロリジン化合物およびその使用 |
Country Status (31)
| Country | Link |
|---|---|
| US (4) | US10328053B2 (https=) |
| EP (2) | EP3504212B1 (https=) |
| JP (2) | JP6774562B2 (https=) |
| KR (2) | KR102224081B1 (https=) |
| CN (2) | CN109790168B (https=) |
| AU (3) | AU2017315863C1 (https=) |
| BR (1) | BR112019003415A2 (https=) |
| CA (1) | CA3033681C (https=) |
| CL (2) | CL2019000473A1 (https=) |
| CO (1) | CO2019001634A2 (https=) |
| CR (1) | CR20190100A (https=) |
| DO (2) | DOP2019000040A (https=) |
| EC (1) | ECSP19012917A (https=) |
| ES (2) | ES2967453T3 (https=) |
| IL (2) | IL264800B (https=) |
| JO (1) | JOP20190024A1 (https=) |
| MX (1) | MX394010B (https=) |
| MY (1) | MY192450A (https=) |
| NZ (1) | NZ750757A (https=) |
| PE (1) | PE20190631A1 (https=) |
| PH (1) | PH12019500393A1 (https=) |
| PL (2) | PL3922634T3 (https=) |
| PT (1) | PT3504212T (https=) |
| SA (1) | SA519401180B1 (https=) |
| SG (1) | SG11201901131VA (https=) |
| SI (1) | SI3504212T1 (https=) |
| TW (1) | TWI765906B (https=) |
| UA (1) | UA124673C2 (https=) |
| UY (1) | UY37374A (https=) |
| WO (1) | WO2018039531A1 (https=) |
| ZA (1) | ZA201901431B (https=) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT3154989T (pt) | 2014-06-11 | 2021-05-18 | Venatorx Pharmaceuticals Inc | Inibidores de beta-lactamase |
| JOP20190024A1 (ar) * | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
| KR20200083552A (ko) | 2017-11-02 | 2020-07-08 | 아이쿠리스 게엠베하 운트 코. 카게 | B형 간염 바이러스 (hbv)에 활성인 신규 고활성 피라졸로-피페리딘 치환된 인돌-2-카르복스아미드 |
| EA202091113A1 (ru) | 2017-11-02 | 2020-08-28 | Айкурис Гмбх Унд Ко. Кг | Новые высокоактивные аминотиазолзамещенные индол-2-карбоксамиды, активные в отношении вируса гепатита b (hbv) |
| WO2019118358A1 (en) | 2017-12-11 | 2019-06-20 | VenatoRx Pharmaceuticals, Inc. | Hepatitis b capsid assembly modulators |
| JP7050165B2 (ja) | 2018-02-26 | 2022-04-07 | ギリアード サイエンシーズ, インコーポレイテッド | Hbv複製阻害剤としての置換ピロリジン化合物 |
| WO2019185016A1 (zh) | 2018-03-30 | 2019-10-03 | 正大天晴药业集团股份有限公司 | 含有n杂五元环的衣壳蛋白装配抑制剂、其药物组合物和用途 |
| CN110437232B (zh) * | 2018-05-04 | 2022-04-12 | 上海长森药业有限公司 | 双并环脲类核衣壳抑制剂及其药物用途 |
| CN113549079A (zh) * | 2018-05-25 | 2021-10-26 | 正大天晴药业集团股份有限公司 | 2,3-二氢-1h-吡咯嗪-7-甲酰胺类衍生物及其应用 |
| JP2021527638A (ja) * | 2018-06-11 | 2021-10-14 | ベナトルクス ファーマシューティカルズ,インク. | B型肝炎カプシドアセンブリモジュレーター |
| TWI826492B (zh) * | 2018-07-27 | 2023-12-21 | 加拿大商愛彼特生物製藥公司 | 經取代四氫環戊[c]吡咯、經取代二氫吡咯,其類似物及使用其之方法 |
| US20230056135A1 (en) * | 2018-10-05 | 2023-02-23 | Emory University | Monomer and multimeric anti-hbv agents |
| US12331320B2 (en) | 2018-10-10 | 2025-06-17 | The Research Foundation For The State University Of New York | Genome edited cancer cell vaccines |
| EP3873464B1 (en) * | 2018-11-01 | 2025-07-30 | Merck Sharp & Dohme LLC | Novel substituted pyrazole compounds as indoleamine 2,3-dioxygenase inhibitors |
| UY38437A (es) | 2018-11-02 | 2020-05-29 | Aicuris Gmbh & Co Kg | Nuevas urea 6,7-dihidro-4h-pirazolo[1,5-a]pirazinas activas contra el virus de la hepatitis b (hbv) |
| PY1991603A (es) | 2018-11-02 | 2020-09-17 | Aicuris Gmbh & Co Kg | Nueva 6,7-dihidro-4h-pirazolo [1,5-a] pirazina indole -2-carboxamidas activas contra el virus de la hepatitis b (vhb) |
| AR117189A1 (es) | 2018-11-02 | 2021-07-21 | Aicuris Gmbh & Co Kg | Derivados de 6,7-dihidro-4h-pirazolo[1,5-a]pirazin indol-2-carboxamidas activos contra el virus de la hepatitis b (vhb) |
| AR116946A1 (es) | 2018-11-02 | 2021-06-30 | Aicuris Gmbh & Co Kg | Derivados de urea 6,7-dihidro-4h-pirazolo[4,3-c]piridinas activas contra el virus de la hepatitis b (vhb) |
| WO2020089460A1 (en) | 2018-11-02 | 2020-05-07 | Aicuris Gmbh & Co. Kg | Novel urea 6,7-dihydro-4h-thiazolo[5,4-c]pyridines active against the hepatitis b virus (hbv) |
| EA202092159A1 (ru) * | 2019-01-25 | 2020-12-15 | Чиа Тай Тянцин Фармасьютикал Груп Ко., Лтд. | Содержащий n-гетероциклическое пятичленное кольцо ингибитор сборки капсидного белка, его фармацевтическая композиция и их применение |
| CN113365999B (zh) * | 2019-01-31 | 2023-04-14 | 正大天晴药业集团股份有限公司 | 含有吡咯并杂环的衣壳蛋白装配抑制剂 |
| WO2020169784A1 (en) | 2019-02-22 | 2020-08-27 | Janssen Sciences Ireland Unlimited Company | Amide derivatives useful in the treatment of hbv infection or hbv-induced diseases |
| MX2021012105A (es) * | 2019-04-03 | 2021-11-03 | Aligos Therapeutics Inc | Compuestos de pirrol. |
| WO2020221824A1 (en) | 2019-04-30 | 2020-11-05 | Aicuris Gmbh & Co. Kg | Novel indolizine-2-carboxamides active against the hepatitis b virus (hbv) |
| BR112021021564A2 (pt) | 2019-04-30 | 2022-01-04 | Aicuris Gmbh & Co Kg | Indol-2-carboxamidas inovadoras ativas contra o vírus da hepatite b (hbv) |
| JP2022533008A (ja) | 2019-04-30 | 2022-07-21 | アイクリス ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト | B型肝炎ウイルス(hbv)に対し活性な新規のオキサリルピペラジン |
| US20220227785A1 (en) | 2019-04-30 | 2022-07-21 | Aicuris Gmbh & Co. Kg | Novel phenyl and pyridyl ureas active against the hepatitis b virus (hbv) |
| WO2020255013A1 (en) | 2019-06-18 | 2020-12-24 | Janssen Sciences Ireland Unlimited Company | Combination of hepatitis b virus (hbv) vaccines and capsid assembly modulators being amide derivatives |
| US12384745B2 (en) | 2019-09-29 | 2025-08-12 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Crystal form of five-membered n heterocyclic compound, and application thereof |
| AU2020355384B2 (en) | 2019-09-29 | 2025-12-18 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Crystalline form of capsid protein assembly inhibitor containing N hetero five-membered ring, and application thereof |
| DK4037708T3 (da) | 2019-09-30 | 2024-09-30 | Gilead Sciences Inc | HBV-vacciner og fremgangsmåder til at behandle HBV |
| EP4245372A3 (en) | 2019-11-13 | 2023-11-22 | Xi'An Xintong Pharmaceutical Research Co., Ltd. | Hbv inhibitor and use thereof |
| CN114728973B (zh) * | 2019-11-22 | 2024-06-28 | 正大天晴药业集团股份有限公司 | 一种核蛋白抑制剂的晶型及其应用 |
| WO2021188959A1 (en) | 2020-03-20 | 2021-09-23 | Gilead Sciences, Inc. | Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same |
| CN113493441B (zh) * | 2020-04-03 | 2024-07-09 | 广东东阳光药业股份有限公司 | 新型螺环类化合物及其在药物中的应用 |
| WO2022095950A1 (zh) * | 2020-11-05 | 2022-05-12 | 正大天晴药业集团股份有限公司 | 包含衣壳蛋白抑制剂和核苷类似物的药物组合 |
| CN114685514A (zh) * | 2020-12-29 | 2022-07-01 | 广东东阳光药业有限公司 | 新型酰胺吡咯类化合物及其在药物中的应用 |
| WO2022241134A1 (en) | 2021-05-13 | 2022-11-17 | Gilead Sciences, Inc. | COMBINATION OF A TLR8 MODULATING COMPOUND AND ANTI-HBV siRNA THERAPEUTICS |
| WO2025240243A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies with bulevirtide and an inhibitory nucleic acid targeting hepatitis b virus |
| WO2025240242A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies with ribavirin |
| WO2025240244A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies comprising bulevirtide and lonafarnib for use in the treatment of hepatitis d virus infection |
| WO2025240246A1 (en) | 2024-05-13 | 2025-11-20 | Gilead Sciences, Inc. | Combination therapies with ribavirin |
Family Cites Families (249)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1032805A (en) | 1903-03-11 | 1912-07-16 | Miller O A Treeing Machine Co | Shoe-form. |
| US4851423A (en) | 1986-12-10 | 1989-07-25 | Schering Corporation | Pharmaceutically active compounds |
| MX9200299A (es) | 1991-02-07 | 1992-12-01 | Roussel Uclaf | Nuevos derivados biciclicos nitrogenados, su procedimiento de preparacion los nuevos compuestos intermedios obtenidos su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen. |
| JP4373497B2 (ja) | 1996-06-19 | 2009-11-25 | ローン−プーラン・ロレ・リミテツド | 置換されたアザビシクロ化合物、ならびにtnfおよびサイクリックampホスホジエステラーゼ産生の阻害剤としてのそれらの使用 |
| US5733912A (en) | 1997-02-19 | 1998-03-31 | Abbott Laboratories | 7A-heterocycle substituted hexahydro-1H-pyrrolizine compounds useful in controlling chemical synaptic transmission |
| AU735366B2 (en) | 1997-09-29 | 2001-07-05 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
| US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| AU4231299A (en) | 1998-06-04 | 1999-12-20 | Abbott Laboratories | Cell adhesion-inhibiting antinflammatory compounds |
| WO2000075145A1 (en) | 1999-06-03 | 2000-12-14 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| EP1202970A1 (en) | 1999-07-30 | 2002-05-08 | Vertex Pharmaceuticals Incorporated | Cyclic amine derivatives for the treatment of neurological diseases |
| WO2001014336A1 (en) | 1999-08-20 | 2001-03-01 | Nippon Kayaku Kabushiki Kaisha | Benzene derivatives substituted by aromatic ring and process for producing the same |
| WO2001098301A1 (en) | 2000-06-20 | 2001-12-27 | Japan Tobacco Inc. | Pyrazolopyridine compounds and use thereof as drugs |
| GB0021885D0 (en) | 2000-09-06 | 2000-10-18 | Fujisawa Pharmaceutical Co | New use |
| DE10046029A1 (de) | 2000-09-18 | 2002-03-28 | Bayer Ag | Indazole |
| EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| NZ526883A (en) | 2001-02-20 | 2005-11-25 | Chugai Pharmaceutical Co Ltd | Azoles as malonyl-coa decarboxylase inhibitors useful as metabolic modulators |
| JP4176477B2 (ja) | 2001-03-01 | 2008-11-05 | 塩野義製薬株式会社 | Hivインテグラーゼ阻害活性を有する含窒素芳香族複素環誘導体 |
| WO2002083628A1 (en) | 2001-04-13 | 2002-10-24 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1,4-disubstituted benzo-fused compounds |
| CA2447475A1 (en) | 2001-05-25 | 2002-12-05 | Chu-Biao Xue | Hydantion derivatives as inhibitors of matrix metalloproteinases |
| WO2003007888A2 (en) | 2001-07-20 | 2003-01-30 | Adipogenix, Inc. | Fat accumulation-modulating compounds |
| WO2003053941A2 (en) | 2001-12-20 | 2003-07-03 | Bristol-Myers Squibb Company | Barbituric acid derivatives as inhibitors of tnf-alpha converting enzyme (tace) and/or matrix metalloproteinases |
| US20030236277A1 (en) * | 2002-02-14 | 2003-12-25 | Kadow John F. | Indole, azaindole and related heterocyclic pyrrolidine derivatives |
| US6995144B2 (en) | 2002-03-14 | 2006-02-07 | Eisai Co., Ltd. | Nitrogen containing heterocyclic compounds and medicines containing the same |
| NZ536728A (en) | 2002-04-25 | 2006-07-28 | Ono Pharmaceutical Co | Diketohydrazine derivative compounds and drugs containing the compounds as the active ingredient |
| WO2004024705A1 (ja) | 2002-09-10 | 2004-03-25 | Takeda Pharmaceutical Company Limited | 5員複素環化合物 |
| AU2003267071A1 (en) | 2002-09-13 | 2004-04-30 | Synta Pharmaceuticals Corp. | Synthesis of indolizines |
| CA2497903A1 (en) | 2002-09-18 | 2004-04-01 | Ono Pharmaceutical Co., Ltd. | Triazaspiro[5.5]undecane derivatives and drugs comprising the same as the active ingredient |
| EP1553098A1 (en) | 2002-10-18 | 2005-07-13 | Ono Pharmaceutical Co., Ltd. | Spiroheterocyclic derivative compounds and drugs comprising the compounds as the active ingredient |
| EP1581496A4 (en) | 2002-12-02 | 2008-04-23 | Gilead Sciences Inc | 2-SUBSTITUTED 3-PROPENAMIDE DERIVATIVES AND PROCESS FOR THEIR PREPARATION |
| US7320989B2 (en) | 2003-02-28 | 2008-01-22 | Encysive Pharmaceuticals, Inc. | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists |
| WO2004082606A2 (en) | 2003-03-13 | 2004-09-30 | Synta Pharmaceuticals Corp. | Fused pyrrole compounds |
| EP1479676A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Benzimidazole-derivatives as factor xa inhibitors |
| WO2005023761A2 (en) | 2003-09-11 | 2005-03-17 | Kemia, Inc. | Cytokine inhibitors |
| JP2007507529A (ja) | 2003-09-30 | 2007-03-29 | サイオス・インコーポレーテツド | 複素環式アミドおよびスルホンアミド |
| EP1678146A1 (en) | 2003-10-23 | 2006-07-12 | Pharmacia Corporation | Pyrimidine compounds for the treatment of inflammation |
| WO2005039506A2 (en) | 2003-10-24 | 2005-05-06 | Exelixis, Inc. | P70s6 kinase modulators and method of use |
| US7071182B2 (en) | 2003-12-23 | 2006-07-04 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| US20050137243A1 (en) | 2003-12-23 | 2005-06-23 | Souers Andrew J. | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| US20050137187A1 (en) | 2003-12-23 | 2005-06-23 | Souers Andrew J. | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| US7049307B2 (en) | 2003-12-23 | 2006-05-23 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| CN102911161A (zh) * | 2004-02-20 | 2013-02-06 | 贝林格尔.英格海姆国际有限公司 | 病毒聚合酶抑制剂 |
| CN1946691A (zh) | 2004-02-27 | 2007-04-11 | 先灵公司 | 作为丙型肝炎病毒ns3丝氨酸蛋白酶抑制剂的化合物 |
| PT1725544E (pt) | 2004-03-09 | 2009-07-02 | Boehringer Ingelheim Pharma | 3-[4-heterociclil-1,2,3-triazol-1-il]-n-aril-benzamidas como inibidores da produção de citocinas para o tratamento de doenças inflamatórias crónicas |
| WO2005099824A1 (en) | 2004-03-30 | 2005-10-27 | Synta Pharmaceuticals, Corp. | 1-glyoxylamide indolizines for treating lung and ovarian cancer |
| WO2005102381A1 (ja) | 2004-04-26 | 2005-11-03 | Ono Pharmaceutical Co., Ltd. | カテプシンk阻害薬およびpth類を併用することを特徴とする骨密度増加剤 |
| CN101437524B (zh) * | 2004-09-14 | 2012-01-11 | 法莫赛特股份有限公司 | 2'-氟-2'-烷基-取代的或其它任选取代的呋喃核糖基嘧啶和嘌呤及其衍生物的制备 |
| US8492539B2 (en) | 2004-09-14 | 2013-07-23 | Gilead Pharmasset Llc | Preparation of 2′-fluoro-2′-alkyl-substituted or other optionally substituted ribofuranosyl pyrimidines and purines and their derivatives |
| US7531560B2 (en) | 2004-11-10 | 2009-05-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Anti-cytokine heterocyclic compounds |
| GB0426661D0 (en) | 2004-12-06 | 2005-01-05 | Isis Innovation | Pyrrolidine compounds |
| EP1841766A1 (en) | 2005-01-19 | 2007-10-10 | Biolipox AB | Pyrrolopyridines useful in the treatment of inflammation |
| GB0503054D0 (en) | 2005-02-14 | 2005-03-23 | Smithkline Beecham Corp | Chemical compounds |
| WO2006091862A2 (en) | 2005-02-24 | 2006-08-31 | Kemia, Inc. | Cytokine inhibitors and their use in therapy |
| US20080214527A1 (en) | 2005-08-04 | 2008-09-04 | Takashi Kawasuji | Hiv Integrase Inhibitors |
| TWI382019B (zh) | 2005-08-19 | 2013-01-11 | Array Biopharma Inc | 作為類鐸受體(toll-like receptor)調節劑之胺基二氮雜呯 |
| TW201402124A (zh) | 2005-08-19 | 2014-01-16 | Array Biopharma Inc | 作為類鐸受體(toll-like receptor)調節劑之8-經取代苯并氮雜呯 |
| EP1940786B1 (en) | 2005-09-16 | 2010-08-18 | Arrow Therapeutics Limited | Biphenyl derivatives and their use in treating hepatitis c |
| WO2007058990A2 (en) | 2005-11-14 | 2007-05-24 | Kemia, Inc. | Therapy using cytokine inhibitors |
| SG10202003901UA (en) | 2005-12-13 | 2020-05-28 | Incyte Holdings Corp | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors |
| CN101007798B (zh) | 2006-01-24 | 2011-01-26 | 中国人民解放军军事医学科学院毒物药物研究所 | 苯并间二氧杂环戊烯衍生物及其制备方法和医药用途 |
| US8222423B2 (en) | 2006-02-14 | 2012-07-17 | Dana-Farber Cancer Institute, Inc. | Bifunctional histone deacetylase inhibitors |
| US8017612B2 (en) | 2006-04-18 | 2011-09-13 | Japan Tobacco Inc. | Piperazine compound and use thereof as a HCV polymerase inhibitor |
| TW200815438A (en) | 2006-06-13 | 2008-04-01 | Bayer Schering Pharma Ag | Substituted pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| TW200815437A (en) | 2006-06-13 | 2008-04-01 | Bayer Schering Pharma Ag | Substituted aminopyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP1870410A1 (en) | 2006-06-13 | 2007-12-26 | Bayer Schering Pharma Aktiengesellschaft | Substituted arylpyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP1867648A1 (en) | 2006-06-13 | 2007-12-19 | Bayer Schering Pharma Aktiengesellschaft | Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them. |
| KR101130380B1 (ko) | 2006-06-13 | 2012-04-23 | 상하이 인스티튜트 오브 마테리아 메디카 차이니즈 아카데미 오브 싸이언시즈 | 헤테로시클릭 비뉴클레오시드 화합물, 그의 제조방법, 약학적 조성물 및 항바이러스성 약제로서의 용도 |
| EP1867647A1 (en) | 2006-06-13 | 2007-12-19 | Bayer Schering Pharma Aktiengesellschaft | Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them. |
| US8158810B2 (en) | 2006-07-27 | 2012-04-17 | Gilead Sciences, Inc. | ALDH-2 inhibitors in the treatment of addiction |
| EP1900739A1 (en) | 2006-08-30 | 2008-03-19 | Cellzome Ag | Diazolodiazine derivatives as kinase inhibitors |
| EP1932845A1 (en) | 2006-12-15 | 2008-06-18 | Bayer Schering Pharma Aktiengesellschaft | 3-H-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| EP2125808A2 (en) | 2006-12-15 | 2009-12-02 | Bayer Schering Pharma Aktiengesellschaft | 3-h-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| WO2008091681A2 (en) | 2007-01-23 | 2008-07-31 | Housey Gerard M | Theramutein modulators |
| EP2727909A1 (en) | 2007-03-16 | 2014-05-07 | The Scripps Research Institute | Inhibitors of focal adhesion kinase |
| CN101679440A (zh) | 2007-04-02 | 2010-03-24 | 帕劳制药股份有限公司 | 作为jak3抑制剂的吡咯并嘧啶衍生物 |
| MX2009010984A (es) | 2007-04-10 | 2010-01-15 | Sgx Pharmaceuticals Inc | Moduladores de heterociclo cinasa de anillo fusionado. |
| CA2691444C (en) | 2007-06-29 | 2016-06-14 | Gilead Sciences, Inc. | Purine derivatives and their use as modulators of toll-like receptor 7 |
| AU2008279447A1 (en) | 2007-07-19 | 2009-01-29 | Metabolex, Inc. | N-azacyclic substituted pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives as agonists of the RUP3 or GPR119 receptor for the treatment of diabetes and metabolic disorders |
| EP2188272B1 (en) | 2007-08-06 | 2016-02-24 | reMynd NV | Phenyl- and benzylthiazolylpiperazine derivatives for the treatment of neurodegenerative diseases |
| WO2009034433A2 (en) | 2007-09-10 | 2009-03-19 | Glenmark Pharmaceuticals, S.A. | 3-azabicyclo [3.1.0] hexane derivatives as vanilloid receptor ligands |
| CN101861151B (zh) | 2007-09-14 | 2014-08-13 | 梅特希尔基因公司 | 使用组蛋白脱乙酰基酶hdac1、hdac2和/或hdac3的选择性抑制剂和微管稳定剂的癌症组合治疗 |
| AU2008316895A1 (en) | 2007-10-22 | 2009-04-30 | Memory Pharmaceuticals Corporation | (1,4-diaza-bicyclo[3.2.2]non-6-en-4-yl)-heterocyclyl-methanone ligands for nicotinic acetylcholine receptors, useful for the treatment of disease |
| MX2010004995A (es) | 2007-11-29 | 2010-05-20 | Boehringer Ingelheim Int | Derivados de amidas del acido 6,7-dihidro-5h-imidazo[1,2-a]imidazo l-3-carboxilico. |
| EP2070929A1 (en) | 2007-12-11 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Alkynylaryl compounds and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
| RU2544856C2 (ru) | 2008-01-25 | 2015-03-20 | Сергей Олегович Бачурин | НОВЫЕ ПРОИЗВОДНЫЕ 2,3,4,5-ТЕТРАГИДРО-1-ПИРИДО[4,3-b]ИНДОЛА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
| US8673970B2 (en) | 2008-02-21 | 2014-03-18 | Sequoia Pharmaceuticals, Inc. | HIV protease inhibitor and cytochrome p450 inhibitor combinations |
| CA2721060A1 (en) | 2008-04-09 | 2009-10-15 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| WO2009133834A1 (ja) | 2008-04-28 | 2009-11-05 | 塩野義製薬株式会社 | 血管内皮リパーゼ阻害活性を有するケトアミド誘導体 |
| US20090298834A1 (en) | 2008-06-02 | 2009-12-03 | Hassan Pajouhesh | 4-(aminomethyl)cyclohexanamine derivatives as calcium channel blockers |
| US20090326019A1 (en) | 2008-06-11 | 2009-12-31 | Yat Sun Or | 3,4-bicyclic pyrrolidine antivirals |
| CA2727174A1 (en) | 2008-06-20 | 2010-01-21 | Jiangao Song | Aryl gpr119 agonists and uses thereof |
| JP5465720B2 (ja) | 2008-07-08 | 2014-04-09 | インサイト・コーポレイション | インドールアミン2,3−ジオキシゲナーゼの阻害剤としての1,2,5−オキサジアゾール |
| JO3041B1 (ar) | 2008-07-25 | 2016-09-05 | Galapagos Nv | مركبات جديدة مفيدة لمعالجة الأمراض التنكسية والالتهابية |
| FR2934593B1 (fr) | 2008-07-29 | 2010-09-10 | Pf Medicament | Derives dimeriques d'artemisinine et application en therapie anticancereuse |
| WO2010014913A1 (en) | 2008-08-01 | 2010-02-04 | Ventirx Pharmaceuticals, Inc. | Toll-like receptor agonist formulations and their use |
| US20110190347A1 (en) | 2008-08-21 | 2011-08-04 | Richter Gedeon Nyrt. | Methods for treating neuropathic pain |
| WO2010029299A1 (en) | 2008-09-12 | 2010-03-18 | Biolipox Ab | Pyrimidinone derivaties for use as medicaments |
| TW201024298A (en) | 2008-09-23 | 2010-07-01 | Palau Pharma Sa | (R)-3-(N,N-dimethylamino)pyrrolidine derivatives |
| EP2358720B1 (en) | 2008-10-16 | 2016-03-02 | The Regents of The University of California | Fused ring heteroaryl kinase inhibitors |
| WO2010053998A1 (en) | 2008-11-05 | 2010-05-14 | Xenon Pharmaceuticals, Inc. | Spiro-condensed indole derivatives as sodium channel inhibitors |
| RS53347B (sr) | 2008-12-09 | 2014-10-31 | Gilead Sciences, Inc. | Modulatori toll-sličnih receptora |
| US20110237633A1 (en) | 2008-12-11 | 2011-09-29 | Bijoy Panicker | Small molecule modulators of hepatocyte growth factor (scatter factor) activity |
| TW201038569A (en) | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
| TW201035102A (en) | 2009-03-04 | 2010-10-01 | Gruenethal Gmbh | Sulfonylated tetrahydroazolopyrazines and their use as medicinal products |
| MX2011010218A (es) | 2009-04-02 | 2011-10-10 | Merck Patent Gmbh | Inhibidores de autotaxina. |
| CN102369186B (zh) | 2009-04-02 | 2014-07-09 | 默克专利有限公司 | 作为自分泌运动因子抑制剂的哌啶和哌嗪衍生物 |
| WO2011003418A1 (en) | 2009-07-08 | 2011-01-13 | Leo Pharma A/S | Heterocyclic compounds as jak receptor and protein tyrosine kinase inhibitors |
| RU2016108987A (ru) | 2009-08-18 | 2018-11-26 | Вентиркс Фармасьютикалз, Инк. | Замещенные бензоазепины в качестве модуляторов toll-подобного рецептора |
| CN105669553A (zh) | 2009-08-18 | 2016-06-15 | 文蒂雷克斯药品公司 | 作为toll样受体调节剂的取代的苯并氮杂* |
| CN102596958A (zh) | 2009-09-21 | 2012-07-18 | 吉里德科学公司 | 用于抗病毒治疗的2’-氟代carba-核苷类似物 |
| WO2011048611A1 (en) | 2009-10-07 | 2011-04-28 | Torrent Pharmaceuticals Limited | Novel fused pyridazine derivatives |
| JP5694345B2 (ja) | 2009-10-22 | 2015-04-01 | ギリアード サイエンシーズ, インコーポレイテッド | Toll様受容体の調節因子 |
| US20110178104A1 (en) | 2010-01-07 | 2011-07-21 | Polymedix Inc. | Anti-Heparin Compounds |
| WO2011087051A1 (ja) | 2010-01-14 | 2011-07-21 | 国立大学法人金沢大学 | S1p2受容体アンタゴニストを含む粥状動脈硬化治療薬 |
| WO2011106106A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae |
| CA2793086C (en) | 2010-03-18 | 2018-08-21 | Institut Pasteur Korea | Substituted imidazo[1,2-a]pyridine compounds and their use in the treatment of bacterial infections |
| WO2011133707A2 (en) | 2010-04-23 | 2011-10-27 | Kineta, Inc. | Anti-viral compounds |
| KR20130069640A (ko) | 2010-04-23 | 2013-06-26 | 키네타, 인크. | 항-바이러스 화합물 |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| US20110312996A1 (en) | 2010-05-17 | 2011-12-22 | Intermune, Inc. | Novel inhibitors of hepatitis c virus replication |
| WO2011145669A1 (ja) | 2010-05-19 | 2011-11-24 | 大日本住友製薬株式会社 | アミド誘導体 |
| TWI500617B (zh) | 2010-05-31 | 2015-09-21 | Ono Pharmaceutical Co | Purine ketone derivatives |
| US8975232B2 (en) | 2010-07-29 | 2015-03-10 | President And Fellows Of Harvard College | Macrocyclic kinase inhibitors and uses thereof |
| MX2013001240A (es) | 2010-07-30 | 2013-08-27 | Ranbaxy Lab Ltd | Inhibidores de metaloproteinas de matriz. |
| WO2012020567A1 (en) | 2010-08-09 | 2012-02-16 | Raqualia Pharma Inc. | Acyl piperazine derivatives as ttx-s blockers |
| JP6039559B2 (ja) | 2010-09-02 | 2016-12-07 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Lpa受容体アンタゴニストとしてのピラゾロピリジノン誘導体 |
| WO2012038942A1 (en) | 2010-09-24 | 2012-03-29 | Ranbaxy Laboratories Limited | Matrix metalloproteinase inhibitors |
| WO2012050868A1 (en) | 2010-09-28 | 2012-04-19 | Georgia Tech Research Corporation | Histone deacetylase (hdac) inhibitors targeting prostate tumors and methods of making and using thereof |
| EP3195868A3 (en) | 2010-10-01 | 2017-08-02 | VentiRx Pharmaceuticals, Inc. | Therapeutic use of a tlr agonist and combination therapy |
| CN103237549A (zh) | 2010-10-01 | 2013-08-07 | 帆德制药股份有限公司 | 过敏性疾病的治疗方法 |
| WO2012058645A1 (en) | 2010-10-29 | 2012-05-03 | Biogen Idec Ma Inc. | Heterocyclic tyrosine kinase inhibitors |
| PY1153144A (es) | 2010-12-10 | 2015-01-01 | Gilead Sciences Inc | Inhibidores macrocíclicos de virus flaviviridae |
| TWI574687B (zh) | 2011-01-03 | 2017-03-21 | 古利斯股份有限公司 | 具有鋅結合部份之刺蝟拮抗劑 |
| EP3208263A1 (en) | 2011-01-12 | 2017-08-23 | VentiRx Pharmaceuticals, Inc. | Substituted benzoazepines as toll-like receptor modulators |
| DK2663555T3 (en) | 2011-01-12 | 2017-03-27 | Ventirx Pharmaceuticals Inc | SUBSTITUTED BENZOAZEPINS AS MODULATORS OF TOLL-LIKE RECEPTORS |
| US20120184572A1 (en) | 2011-01-13 | 2012-07-19 | Metabolex, Inc. | Aryl gpr119 agonists and uses thereof |
| MX2013009393A (es) | 2011-02-18 | 2013-08-29 | Vertex Pharma | Piperidinamidas cromano-espirociclicas como moduladores de canales de iones. |
| EP2678050B1 (en) | 2011-02-24 | 2020-10-14 | Emory University | Noggin blocking compositions for ossification and methods related thereto |
| US20140086839A1 (en) | 2011-03-17 | 2014-03-27 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Quinolone analogs for treating autoimmune diseases |
| US9464065B2 (en) | 2011-03-24 | 2016-10-11 | The Scripps Research Institute | Compounds and methods for inducing chondrogenesis |
| PT3590928T (pt) | 2011-04-08 | 2021-08-19 | Janssen Sciences Ireland Unlimited Co | Derivados de pirimidina para o tratamento de infeções virais |
| DK2709619T3 (en) | 2011-05-16 | 2018-01-15 | Cellceutix Corp | RELATIONSHIPS FOR USING THE TREATMENT OF MUCOSITIS |
| JP6130827B2 (ja) | 2011-05-17 | 2017-05-17 | 塩野義製薬株式会社 | ヘテロ環化合物 |
| AU2012258220B2 (en) | 2011-05-18 | 2017-01-19 | Janssen Sciences Ireland Uc | Quinazoline derivatives for the treatment of viral infections and further diseases |
| TWI635093B (zh) | 2011-05-19 | 2018-09-11 | 基利科學股份有限公司 | 用於製備抗hiv藥劑的方法與中間物 |
| CN103748087A (zh) | 2011-06-07 | 2014-04-23 | 大日本住友制药株式会社 | 吲唑和吡咯并吡啶衍生物和其药学用途 |
| JP5977347B2 (ja) * | 2011-07-01 | 2016-08-24 | バルーク エス.ブルームバーグ インスティテュート | Hbv感染に対する抗ウイルス剤としてのスルファモイルベンズアミド誘導体 |
| TWI454466B (zh) | 2011-07-22 | 2014-10-01 | Ken Tsung Wong | 可用於有機薄膜太陽能電池之化合物及有機薄膜太陽能電池 |
| KR102088637B1 (ko) | 2011-07-29 | 2020-03-13 | 메르크 파텐트 게엠베하 | 전자 소자용 화합물 |
| WO2013042139A1 (en) | 2011-09-23 | 2013-03-28 | Advinus Therapeutics Limited | Amide compounds, compositions and applications thereof |
| WO2013059278A2 (en) | 2011-10-17 | 2013-04-25 | Enanta Pharmaceuticals, Inc. | Hepatitis c virus inhibitors |
| US9199997B2 (en) | 2011-11-29 | 2015-12-01 | Ono Pharmaceutical Co., Ltd. | Purinone derivative hydrochloride |
| CA2857964A1 (en) | 2011-12-05 | 2013-06-13 | Brandeis University | Treatment of amyloidosis by compounds that regulate retromer stabilization |
| DE102011121022A1 (de) | 2011-12-13 | 2013-06-13 | Merck Patent Gmbh | Organische Sensibilisatoren für Up- Conversion |
| BR112014015197A8 (pt) | 2011-12-21 | 2017-06-13 | Novira Therapeutics Inc | agentes antivirais de hepatite b |
| TWI573792B (zh) | 2012-02-01 | 2017-03-11 | 歐陸斯迪公司 | 新穎治療劑 |
| SG11201404743TA (en) | 2012-02-08 | 2014-09-26 | Janssen R & D Ireland | Piperidino-pyrimidine derivatives for the treatment of viral infections |
| WO2013144228A1 (en) | 2012-03-29 | 2013-10-03 | Basf Se | Pesticidal methods using heterocyclic compounds and derivatives for combating animal pests |
| US20130267517A1 (en) | 2012-03-31 | 2013-10-10 | Hoffmann-La Roche Inc. | Novel 4-methyl-dihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection |
| ES2575398T3 (es) | 2012-03-31 | 2016-06-28 | F. Hoffmann-La Roche Ag | 4-Metil-dihidropirimidinas novedosas para el tratamiento y la profilaxis de la infección por el virus de la hepatitis B |
| JPWO2013161871A1 (ja) | 2012-04-25 | 2015-12-24 | 興和株式会社 | Tlr阻害作用を有するチオフェン誘導体 |
| AR091279A1 (es) | 2012-06-08 | 2015-01-21 | Gilead Sciences Inc | Inhibidores macrociclicos de virus flaviviridae |
| BR112014030649A2 (pt) | 2012-06-08 | 2017-06-27 | Gilead Sciences Inc | inibidores macrocíclicos da flaviviridae vírus |
| PT2861604T (pt) | 2012-06-08 | 2017-05-05 | Gilead Sciences Inc | Inibidores macrocíclicos de vírus flaviridae |
| MX369417B (es) | 2012-08-10 | 2019-11-07 | Janssen Sciences Ireland Uc | Derivados de alquilpirimidina para el tratamiento de infecciones víricas y otras enfermedades. |
| WO2014031872A2 (en) | 2012-08-23 | 2014-02-27 | The Broad Institute, Inc. | Small molecule inhibitors for treating parasitic infections |
| EA026957B1 (ru) | 2012-08-28 | 2017-06-30 | Янссен Сайенсиз Айрлэнд Юси | Конденсированные бициклические производные сульфамоила и их применение в качестве лекарственных препаратов для лечения гепатита b |
| KR102271574B1 (ko) | 2012-08-28 | 2021-07-01 | 얀센 사이언시즈 아일랜드 언리미티드 컴퍼니 | 설파모일-아릴아미드 및 b형 간염 치료제로서의 그 용도 |
| EP2892899B1 (en) | 2012-09-06 | 2018-03-21 | Bristol-Myers Squibb Company | Imidazopyridazine jak3 inhibitors and their use for the treatment of inflammatory and autoimmune diseases |
| CA2881322A1 (en) | 2012-09-10 | 2014-03-13 | F. Hoffmann-La Roche Ag | 6-amino acid heteroaryldihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection |
| US9593115B2 (en) | 2012-09-21 | 2017-03-14 | Advinus Therapeutics Ltd. | Substituted fused tricyclic compounds, compositions, and medicinal applications thereof |
| DK2903968T3 (en) | 2012-10-02 | 2017-01-30 | Gilead Sciences Inc | INHIBITORS OF HISTON DEMETHYLASES |
| DK2906563T3 (en) | 2012-10-10 | 2018-06-06 | Janssen Sciences Ireland Uc | PYRROLO [3,2-D] PYRIMIDINE DERIVATIVES FOR TREATING VIRUS INFECTIONS AND OTHER DISEASES |
| EA035431B1 (ru) | 2012-11-16 | 2020-06-15 | Янссен Сайенсиз Айрлэнд Юси | Гетероциклические замещенные производные 2-амино-хиназолина в качестве модуляторов tlr7 и/или tlr8 для лечения вирусных инфекций |
| WO2014089296A2 (en) | 2012-12-06 | 2014-06-12 | Institute For Hepatitis And Virus Research | Functionalized benzamide derivatives as antiviral agents against hbv infection |
| CA2894399A1 (en) | 2012-12-06 | 2014-06-12 | Quanticel Pharmaceuticals, Inc. | Histone demethylase inhibitors |
| JP2014133739A (ja) | 2012-12-12 | 2014-07-24 | Dainippon Sumitomo Pharma Co Ltd | インダゾール誘導体またはピロロピリジン誘導体からなる医薬 |
| SMT201800070T1 (it) | 2012-12-19 | 2018-03-08 | Celgene Quanticel Res Inc | Inibiorti di istone demetilasi |
| JP2016507496A (ja) | 2012-12-21 | 2016-03-10 | ゼニス・エピジェネティクス・コーポレイションZenith Epigenetics Corp. | ブロモドメイン阻害剤としての新規複素環式化合物 |
| BR112015014968A2 (pt) | 2012-12-21 | 2017-07-11 | Quanticel Pharmaceuticals Inc | inibidores de histona-desmetilase |
| JO3781B1 (ar) | 2012-12-24 | 2021-01-31 | Cadila Healthcare Ltd | مشتقات الكينولون |
| BR112015015584A2 (pt) | 2012-12-27 | 2017-12-12 | Baruch S Blumberg Inst | novos agentes antivirais contra infecção por hbv |
| EP2943204B1 (en) | 2013-01-10 | 2019-03-13 | Venatorx Pharmaceuticals Inc | Beta-lactamase inhibitors |
| SMT201700317T1 (it) | 2013-01-29 | 2017-09-07 | Redx Pharma Plc | Derivati piridinici in qualità di inibitori rock teneri |
| SG11201506639XA (en) | 2013-02-21 | 2015-09-29 | Janssen Sciences Ireland Uc | 2-aminopyrimidine derivatives for the treatment of viral infections |
| GB201303109D0 (en) | 2013-02-21 | 2013-04-10 | Domainex Ltd | Novel pyrimidine compounds |
| PE20151667A1 (es) | 2013-02-27 | 2015-11-27 | Epitherapeutics Aps | Inhibidores de histona desmetilasas |
| WO2014131847A1 (en) | 2013-02-28 | 2014-09-04 | Janssen R&D Ireland | Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b |
| US9738637B2 (en) | 2013-03-12 | 2017-08-22 | Celgene Quantical Research, Inc. | Histone demethylase inhibitors |
| US8993771B2 (en) | 2013-03-12 | 2015-03-31 | Novira Therapeutics, Inc. | Hepatitis B antiviral agents |
| KR20150130491A (ko) | 2013-03-13 | 2015-11-23 | 제넨테크, 인크. | 피라졸로 화합물 및 그것의 용도 |
| WO2014151958A1 (en) | 2013-03-14 | 2014-09-25 | VenatoRx Pharmaceuticals, Inc. | Beta-lactamase inhibitors |
| EP2969007B1 (en) | 2013-03-14 | 2019-05-08 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| CA2903465A1 (en) | 2013-03-15 | 2014-09-25 | Quanticel Pharmaceuticals, Inc. | Histone demethylase inhibitors |
| MX353412B (es) | 2013-04-03 | 2018-01-10 | Janssen Sciences Ireland Uc | Derivados de n-fenil-carboxamida y su uso como medicamentos para el tratamiento de la hepatitis b. |
| WO2014179144A1 (en) | 2013-04-29 | 2014-11-06 | E. I. Du Pont De Nemours And Company | Fungicidal heterocyclic compounds |
| DK2997019T3 (en) | 2013-05-17 | 2018-12-03 | Janssen Sciences Ireland Uc | SULFAMOYLTHIOPHENAMIDE DERIVATIVES AND USE THEREOF AS MEDICINES FOR TREATING HEPATITIS B |
| BR112015028873A2 (pt) | 2013-05-17 | 2017-07-25 | Hoffmann La Roche | heteroaril-diidro-pirimidinas interligados na posição 6, para o tratamento e profilaxia de infecção pelo vírus da hepatite b |
| TWI733288B (zh) | 2013-05-17 | 2021-07-11 | 愛爾蘭商健生科學愛爾蘭無限公司 | 胺磺醯基吡咯醯胺衍生物及其作為用於治療b型肝炎藥物的用途 |
| EP3013797B1 (en) | 2013-06-28 | 2018-01-03 | BeiGene, Ltd. | Fused tricyclic amide compounds as multiple kinase inhibitors |
| WO2015002894A1 (en) | 2013-07-02 | 2015-01-08 | Pharmacyclics, Inc. | Purinone compounds as kinase inhibitors |
| HRP20180791T1 (hr) * | 2013-07-25 | 2018-09-07 | Janssen Sciences Ireland Uc | Glioksamid supstituirani derivati pirolamida i njihova uporaba kao lijekova za liječenje hepatitisa b |
| EP3035924A4 (en) | 2013-08-20 | 2017-04-19 | City of Hope | Hdac8 inhibitors for treating cancer |
| KR101715090B1 (ko) | 2013-08-28 | 2017-03-13 | 한국화학연구원 | 신규한 화합물 또는 이의 약학적으로 허용가능한 염, 및 이를 유효성분으로 함유하는 인플루엔자 바이러스 감염으로 인한 질환의 예방 또는 치료용 약학적 조성물 |
| US9920073B2 (en) | 2013-10-04 | 2018-03-20 | Drexel University | Compositions useful for inhibiting HIV-1 infection and methods using same |
| WO2015057945A1 (en) | 2013-10-18 | 2015-04-23 | Indiana University Research And Technology Corporation | Hepatitis b viral assembly effectors |
| EP3057956B1 (en) | 2013-10-18 | 2021-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
| CA2923712C (en) | 2013-10-23 | 2021-11-02 | Janssen Sciences Ireland Uc | Carboxamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| WO2015073774A1 (en) | 2013-11-14 | 2015-05-21 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis b infections |
| WO2015085238A1 (en) | 2013-12-05 | 2015-06-11 | The Regents Of The University Of California, A California Corporation | Inhibitors of lpxc |
| US9181288B2 (en) | 2014-01-16 | 2015-11-10 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US9169212B2 (en) | 2014-01-16 | 2015-10-27 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| EA201691261A1 (ru) | 2014-01-30 | 2016-11-30 | Ф. Хоффманн-Ля Рош Аг | Новые дигидрохинолизиноны для лечения и профилактики инфекции, вызванной вирусом гепатита b |
| CA2936947A1 (en) | 2014-02-05 | 2015-08-13 | Novira Therapeutics, Inc. | Combination therapy for treatment of hbv infections |
| TW201620893A (zh) | 2014-02-06 | 2016-06-16 | 健生科學愛爾蘭無限公司 | 磺醯胺基吡咯醯胺衍生物及其用作治療b型肝炎之醫藥品的用途 |
| US9400280B2 (en) | 2014-03-27 | 2016-07-26 | Novira Therapeutics, Inc. | Piperidine derivatives and methods of treating hepatitis B infections |
| CN106456602B (zh) | 2014-03-27 | 2020-11-24 | 范德比尔特大学 | 取代的吲哚mcl-1抑制剂 |
| KR20160148715A (ko) | 2014-05-13 | 2016-12-26 | 에프. 호프만-라 로슈 아게 | B형 간염 바이러스 감염의 치료 또는 예방을 위한 신규한 다이하이드로퀴놀리진온 |
| CN106459061B (zh) | 2014-05-30 | 2020-01-21 | 齐鲁制药有限公司 | 作为hbv抑制剂的二氢嘧啶并环衍生物 |
| US20170152226A1 (en) | 2014-07-16 | 2017-06-01 | Novogen Ltd. | Functionalised and substituted indoles as anti-cancer agents |
| BR112017002970B1 (pt) | 2014-08-14 | 2023-04-11 | F. Hoffmann-La Roche Ag | Novas piridazonas e triazinonas para o tratamento e profilaxia da infecção pelo vírus da hepatite b |
| HRP20210927T1 (hr) | 2014-08-15 | 2021-09-03 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Spojevi pirolopirimidina koje se koriste kao agonist tlr7 |
| SG11201701182VA (en) | 2014-08-27 | 2017-03-30 | Gilead Sciences Inc | Compounds and methods for inhibiting histone demethylases |
| CN107912040B (zh) | 2014-10-10 | 2021-04-06 | 基因泰克公司 | 作为组蛋白脱甲基酶抑制剂的吡咯烷酰胺化合物 |
| US9637485B2 (en) | 2014-11-03 | 2017-05-02 | Hoffmann-La Roche Inc. | 6,7-dihydrobenzo[a]quinolizin-2-one derivatives for the treatment and prophylaxis of hepatitis B virus infection |
| WO2016110821A1 (en) | 2015-01-08 | 2016-07-14 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
| MA41338B1 (fr) | 2015-01-16 | 2019-07-31 | Hoffmann La Roche | Composés de pyrazine pour le traitement de maladies infectieuses |
| WO2016128908A1 (en) | 2015-02-12 | 2016-08-18 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
| JP6948952B2 (ja) | 2015-05-28 | 2021-10-13 | ビーエイエスエフ・ソシエタス・エウロパエアBasf Se | 均一系触媒によるカルボニル化合物の還元的アミノ化法 |
| WO2016201370A1 (en) | 2015-06-12 | 2016-12-15 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| US11174267B2 (en) | 2015-06-12 | 2021-11-16 | The Regents Of The University Of California | Spiroindolinones and therapeutic uses thereof |
| US10875876B2 (en) | 2015-07-02 | 2020-12-29 | Janssen Sciences Ireland Uc | Cyclized sulfamoylarylamide derivatives and the use thereof as medicaments for the treatment of hepatitis B |
| US10500577B2 (en) | 2015-07-20 | 2019-12-10 | CE Pharm CO., LTD | Oxalic amide ligands, and uses thereof in copper-catalyzed coupling reaction of aryl halides |
| WO2017015451A1 (en) | 2015-07-22 | 2017-01-26 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| AR105911A1 (es) | 2015-09-03 | 2017-11-22 | Forma Therapeutics Inc | Inhibidores de hdac8 bicíclicos fusionados [6,6] |
| GB201516614D0 (en) | 2015-09-18 | 2015-11-04 | Redx Pharma Plc | Antibacterial compounds |
| UA121345C2 (uk) | 2015-11-05 | 2020-05-12 | Чіа Тай Тяньцин Фармасьютікал Груп Ко., Лтд. | 7-(тіазол-5-іл)піролопіримідин як агоніст рецептора tlr7 |
| WO2017083304A1 (en) | 2015-11-09 | 2017-05-18 | Gilead Sciences, Inc. | Therapeutic compositions for treatment of human immunodeficiency virus |
| CN106928219B (zh) | 2015-12-31 | 2021-08-20 | 上海医药集团股份有限公司 | 含氮稠杂环化合物、制备方法、中间体、组合物和应用 |
| CO2018009382A2 (es) * | 2016-03-09 | 2018-09-20 | Univ Emory | Eliminación del virus de la hepatitis b con agentes antivirales |
| PL3429591T3 (pl) | 2016-03-16 | 2023-07-17 | Kura Oncology, Inc. | Podstawione pochodne tieno[2,3-d]pirymidyny jako inhibitory meniny-mll i metody ich zastosowania |
| WO2017161524A1 (zh) | 2016-03-23 | 2017-09-28 | 华东理工大学 | 丙酮酸脱氢酶激酶抑制剂及其应用 |
| CN107226805A (zh) | 2016-03-24 | 2017-10-03 | 北京天诚医药科技有限公司 | 芳香族酰胺类衍生物、其制备方法及其在医药上的应用 |
| ES2946970T3 (es) | 2016-03-31 | 2023-07-28 | Vertex Pharma | Regulador de conductancia transmembrana de moduladores de fibrosis quística |
| TW201808888A (zh) | 2016-05-05 | 2018-03-16 | 嘉來克生命科學有限責任公司 | 整合應激途徑之調節劑 |
| WO2017209265A1 (ja) | 2016-06-03 | 2017-12-07 | 塩野義製薬株式会社 | 二環性複素環誘導体およびそれらを含有する医薬組成物 |
| CA3028228A1 (en) | 2016-06-10 | 2017-12-14 | Enanta Pharmaceuticals, Inc. | Hepatitis b antiviral agents |
| CN107537157B (zh) | 2016-06-29 | 2022-05-17 | 无敌媒体有限公司 | 用于减少具有虚拟货币的电子游戏中的欺诈的系统和方法 |
| JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
| JP7050165B2 (ja) | 2018-02-26 | 2022-04-07 | ギリアード サイエンシーズ, インコーポレイテッド | Hbv複製阻害剤としての置換ピロリジン化合物 |
-
2017
- 2017-06-16 JO JOP/2019/0024A patent/JOP20190024A1/ar unknown
- 2017-08-24 UY UY0001037374A patent/UY37374A/es not_active Application Discontinuation
- 2017-08-25 SI SI201730822T patent/SI3504212T1/sl unknown
- 2017-08-25 CN CN201780059448.2A patent/CN109790168B/zh active Active
- 2017-08-25 WO PCT/US2017/048565 patent/WO2018039531A1/en not_active Ceased
- 2017-08-25 PE PE2019000413A patent/PE20190631A1/es unknown
- 2017-08-25 BR BR112019003415-3A patent/BR112019003415A2/pt not_active Application Discontinuation
- 2017-08-25 UA UAA201901737A patent/UA124673C2/uk unknown
- 2017-08-25 CA CA3033681A patent/CA3033681C/en active Active
- 2017-08-25 KR KR1020197008165A patent/KR102224081B1/ko active Active
- 2017-08-25 EP EP17761755.2A patent/EP3504212B1/en active Active
- 2017-08-25 US US15/686,499 patent/US10328053B2/en active Active
- 2017-08-25 SG SG11201901131VA patent/SG11201901131VA/en unknown
- 2017-08-25 CR CR20190100A patent/CR20190100A/es unknown
- 2017-08-25 ES ES21173731T patent/ES2967453T3/es active Active
- 2017-08-25 PL PL21173731.7T patent/PL3922634T3/pl unknown
- 2017-08-25 PT PT177617552T patent/PT3504212T/pt unknown
- 2017-08-25 MX MX2019002049A patent/MX394010B/es unknown
- 2017-08-25 CN CN202110955764.6A patent/CN113620960A/zh active Pending
- 2017-08-25 EP EP21173731.7A patent/EP3922634B1/en active Active
- 2017-08-25 JP JP2019510869A patent/JP6774562B2/ja active Active
- 2017-08-25 KR KR1020217006241A patent/KR102343747B1/ko active Active
- 2017-08-25 AU AU2017315863A patent/AU2017315863C1/en active Active
- 2017-08-25 ES ES17761755T patent/ES2879674T3/es active Active
- 2017-08-25 TW TW106128937A patent/TWI765906B/zh active
- 2017-08-25 PL PL17761755T patent/PL3504212T3/pl unknown
- 2017-08-25 NZ NZ750757A patent/NZ750757A/en unknown
- 2017-08-25 MY MYPI2019000980A patent/MY192450A/en unknown
-
2019
- 2019-02-12 IL IL264800A patent/IL264800B/en active IP Right Grant
- 2019-02-22 PH PH12019500393A patent/PH12019500393A1/en unknown
- 2019-02-22 CO CONC2019/0001634A patent/CO2019001634A2/es unknown
- 2019-02-22 EC ECSENADI201912917A patent/ECSP19012917A/es unknown
- 2019-02-22 DO DO2019000040A patent/DOP2019000040A/es unknown
- 2019-02-22 CL CL2019000473A patent/CL2019000473A1/es unknown
- 2019-02-25 SA SA519401180A patent/SA519401180B1/ar unknown
- 2019-03-07 ZA ZA2019/01431A patent/ZA201901431B/en unknown
- 2019-05-03 US US16/403,247 patent/US10874640B2/en active Active
- 2019-07-12 CL CL2019001976A patent/CL2019001976A1/es unknown
-
2020
- 2020-05-28 AU AU2020203499A patent/AU2020203499B2/en active Active
- 2020-10-02 JP JP2020167860A patent/JP6983296B2/ja active Active
- 2020-11-04 US US17/089,030 patent/US20210251957A1/en not_active Abandoned
-
2021
- 2021-02-09 IL IL280747A patent/IL280747B/en unknown
- 2021-06-10 DO DO2021000112A patent/DOP2021000112A/es unknown
- 2021-09-27 AU AU2021240103A patent/AU2021240103B2/en active Active
-
2022
- 2022-11-29 US US18/059,806 patent/US12161625B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6983296B2 (ja) | 置換ピロリジン化合物およびその使用 | |
| JP7050165B2 (ja) | Hbv複製阻害剤としての置換ピロリジン化合物 | |
| HK40064069B (en) | Substituted pyrrolizine compounds and uses thereof | |
| HK40064069A (en) | Substituted pyrrolizine compounds and uses thereof | |
| HK40009562B (en) | Substituted pyrrolizine compounds and uses thereof | |
| HK40009562A (en) | Substituted pyrrolizine compounds and uses thereof | |
| HK40032660B (en) | Substituted pyrrolizine compounds as hbv replication inhibitors | |
| HK40042757B (en) | Substituted pyrrolizine compounds as hbv replication inhibitors | |
| HK40042757A (en) | Substituted pyrrolizine compounds as hbv replication inhibitors | |
| EA038135B1 (ru) | Замещенные пирролизины и их применение |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20190417 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20190417 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20200213 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20200304 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200604 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20200904 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20201002 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6774562 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |