JP2022508953A - Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 - Google Patents
Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 Download PDFInfo
- Publication number
- JP2022508953A JP2022508953A JP2021547054A JP2021547054A JP2022508953A JP 2022508953 A JP2022508953 A JP 2022508953A JP 2021547054 A JP2021547054 A JP 2021547054A JP 2021547054 A JP2021547054 A JP 2021547054A JP 2022508953 A JP2022508953 A JP 2022508953A
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- mmol
- pyrazole
- alkyl
- amino
- 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 CC(**=C)(C=*C=C*1C2)C1=*C=C2NC Chemical compound CC(**=C)(C=*C=C*1C2)C1=*C=C2NC 0.000 description 34
- OBVGLLOYAQUDKB-JYRVWZFOSA-N CC(C)(C)OC(N(/C=C(/C(C1)CC(C2)C1CC2=O)\N)S)=O Chemical compound CC(C)(C)OC(N(/C=C(/C(C1)CC(C2)C1CC2=O)\N)S)=O OBVGLLOYAQUDKB-JYRVWZFOSA-N 0.000 description 1
- SBTMLYVNIFZHIO-UHFFFAOYSA-N CC(C)(C)OC(N(CC1C2)CC1C=C2c1n[n](C)c(N)c1C(Nc(cc1Cl)ccc1F)=O)=O Chemical compound CC(C)(C)OC(N(CC1C2)CC1C=C2c1n[n](C)c(N)c1C(Nc(cc1Cl)ccc1F)=O)=O SBTMLYVNIFZHIO-UHFFFAOYSA-N 0.000 description 1
- AVBWARCKGQCXSY-UHFFFAOYSA-N CC(C)(C)OC(Nc1c(C(Nc(cc2)cc(Cl)c2F)=O)c(C(C2)CC(C3)C2CC3(CS(C)(=O)=O)O)n[nH]1)=O Chemical compound CC(C)(C)OC(Nc1c(C(Nc(cc2)cc(Cl)c2F)=O)c(C(C2)CC(C3)C2CC3(CS(C)(=O)=O)O)n[nH]1)=O AVBWARCKGQCXSY-UHFFFAOYSA-N 0.000 description 1
- MPPHZRLGFVAUOF-UHFFFAOYSA-N CC(C)(C1(CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)O)O Chemical compound CC(C)(C1(CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)O)O MPPHZRLGFVAUOF-UHFFFAOYSA-N 0.000 description 1
- NRRZGMWSULMYOU-UHFFFAOYSA-N CC(C)(CCN1C)CS1(=O)=O Chemical compound CC(C)(CCN1C)CS1(=O)=O NRRZGMWSULMYOU-UHFFFAOYSA-N 0.000 description 1
- OOBDRRXUJGDZRJ-UHFFFAOYSA-N CC(NC1CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3Cl)ccc3F)=O)C2C1)=O Chemical compound CC(NC1CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3Cl)ccc3F)=O)C2C1)=O OOBDRRXUJGDZRJ-UHFFFAOYSA-N 0.000 description 1
- CWHCTKAJYQOXMG-UHFFFAOYSA-N CC1(C)CCN(C)CC1 Chemical compound CC1(C)CCN(C)CC1 CWHCTKAJYQOXMG-UHFFFAOYSA-N 0.000 description 1
- KHGFALRALHLMOW-UHFFFAOYSA-N CC1(C)OB(C(C2)=CC(C3)C2CC3=O)OC1(C)C Chemical compound CC1(C)OB(C(C2)=CC(C3)C2CC3=O)OC1(C)C KHGFALRALHLMOW-UHFFFAOYSA-N 0.000 description 1
- DWPQYLOKFKKZRD-AWEZNQCLSA-N CC1(C)OB(C(CC2)=C[C@H]2c(cc2)ccc2OC)OC1(C)C Chemical compound CC1(C)OB(C(CC2)=C[C@H]2c(cc2)ccc2OC)OC1(C)C DWPQYLOKFKKZRD-AWEZNQCLSA-N 0.000 description 1
- DGFSUDKBJWNNDJ-UHFFFAOYSA-N CCCN1CNC(C)(C)CC1 Chemical compound CCCN1CNC(C)(C)CC1 DGFSUDKBJWNNDJ-UHFFFAOYSA-N 0.000 description 1
- WSCGMOBBVZURIF-UHFFFAOYSA-N CCOC(C=C1CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)=O Chemical compound CCOC(C=C1CC(CC(C2)c3n[n](C)c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)=O WSCGMOBBVZURIF-UHFFFAOYSA-N 0.000 description 1
- COLVCKWALHUMBA-UHFFFAOYSA-N CCOC(c1c(N)[n](C)nc1C(C1)CC1c1ccccc1)=O Chemical compound CCOC(c1c(N)[n](C)nc1C(C1)CC1c1ccccc1)=O COLVCKWALHUMBA-UHFFFAOYSA-N 0.000 description 1
- XHHNUNRKWKYVOM-UHFFFAOYSA-N CN(C1N)N=C(C(C2)CC(C3)C2CC3N(CCN2)C2=O)C1C(Nc(cc1)cc(Cl)c1F)=O Chemical compound CN(C1N)N=C(C(C2)CC(C3)C2CC3N(CCN2)C2=O)C1C(Nc(cc1)cc(Cl)c1F)=O XHHNUNRKWKYVOM-UHFFFAOYSA-N 0.000 description 1
- ILKMLMGHMJETTB-UHFFFAOYSA-N CN(C1N)N=C(C(C2)CC3C2CNC3)C1C(Nc(cc1Cl)ccc1F)=O Chemical compound CN(C1N)N=C(C(C2)CC3C2CNC3)C1C(Nc(cc1Cl)ccc1F)=O ILKMLMGHMJETTB-UHFFFAOYSA-N 0.000 description 1
- AYVDQORKOKQUSK-UHFFFAOYSA-N CN1NC(C(C2)CC2c2ccccc2)C(C(Cl)=O)=C1N Chemical compound CN1NC(C(C2)CC2c2ccccc2)C(C(Cl)=O)=C1N AYVDQORKOKQUSK-UHFFFAOYSA-N 0.000 description 1
- AUJWQTVWPIPRMJ-UHFFFAOYSA-N CNc1c(C(Nc(cc2)cc(Cl)c2F)=O)c(C(C2)CC(C3)C2CC3O)n[n]1C Chemical compound CNc1c(C(Nc(cc2)cc(Cl)c2F)=O)c(C(C2)CC(C3)C2CC3O)n[n]1C AUJWQTVWPIPRMJ-UHFFFAOYSA-N 0.000 description 1
- JRRNVFZDCOUHFB-UHFFFAOYSA-N COC(C(CC1)CC1c1ccccc1)=O Chemical compound COC(C(CC1)CC1c1ccccc1)=O JRRNVFZDCOUHFB-UHFFFAOYSA-N 0.000 description 1
- BJIAMLQBICRMII-UHFFFAOYSA-N COC(c1ccc(C(CC2)=CC2=O)c(OC)c1)=O Chemical compound COC(c1ccc(C(CC2)=CC2=O)c(OC)c1)=O BJIAMLQBICRMII-UHFFFAOYSA-N 0.000 description 1
- BCWXCAWSARGLMK-UHFFFAOYSA-N CS(CC1(CC(CC(C2)c3n[nH]c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)O)(=O)=O Chemical compound CS(CC1(CC(CC(C2)c3n[nH]c(N)c3C(Nc(cc3)cc(Cl)c3F)=O)C2C1)O)(=O)=O BCWXCAWSARGLMK-UHFFFAOYSA-N 0.000 description 1
- PBIBIRGMZPIFSW-UHFFFAOYSA-N C[n]1nc(C(C2)=CC3C2CSC3)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)=CC3C2CSC3)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N PBIBIRGMZPIFSW-UHFFFAOYSA-N 0.000 description 1
- CMIXVSTZFATZGJ-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(C(NC2CC2)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(C(NC2CC2)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1N CMIXVSTZFATZGJ-UHFFFAOYSA-N 0.000 description 1
- LNUVJOAWLZQOPC-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(C2)CNC2=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(C2)CNC2=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N LNUVJOAWLZQOPC-UHFFFAOYSA-N 0.000 description 1
- KNTAYHIDJXRORR-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(CN2)OC2=O)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(CN2)OC2=O)c(C(Nc(cc2Cl)ccc2F)=O)c1N KNTAYHIDJXRORR-UHFFFAOYSA-N 0.000 description 1
- ZQOCHUGDQKQKQU-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(CS(C)(=O)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1 Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(CS(C)(=O)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1 ZQOCHUGDQKQKQU-UHFFFAOYSA-N 0.000 description 1
- ZTRPGPYXFHQPIS-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(CS(CCCBr)(=O)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(CS(CCCBr)(=O)=O)O)c(C(Nc(cc2Cl)ccc2F)=O)c1N ZTRPGPYXFHQPIS-UHFFFAOYSA-N 0.000 description 1
- SWDCFNKYTMGWFP-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3(CS(CCCN2CCOCC2)(=O)=O)O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3(CS(CCCN2CCOCC2)(=O)=O)O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N SWDCFNKYTMGWFP-UHFFFAOYSA-N 0.000 description 1
- KLLAERVJKZKTTM-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3=C2SCCCS2)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3=C2SCCCS2)c(C(Nc(cc2Cl)ccc2F)=O)c1N KLLAERVJKZKTTM-UHFFFAOYSA-N 0.000 description 1
- UHBJCJOHKSEBFJ-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3=O)c(C(Nc(cc2Cl)ccc2F)=O)c1 Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3=O)c(C(Nc(cc2Cl)ccc2F)=O)c1 UHBJCJOHKSEBFJ-UHFFFAOYSA-N 0.000 description 1
- FIXWGHBFMZBQME-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3=O)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3=O)c(C(Nc(cc2Cl)ccc2F)=O)c1N FIXWGHBFMZBQME-UHFFFAOYSA-N 0.000 description 1
- XSSPNRVZOJARHK-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N XSSPNRVZOJARHK-UHFFFAOYSA-N 0.000 description 1
- JPJHMZRSRITBIH-UHFFFAOYSA-N C[n]1nc(C(C2)CC(C3)C2CC3OS(C)(=O)=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(C3)C2CC3OS(C)(=O)=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N JPJHMZRSRITBIH-UHFFFAOYSA-N 0.000 description 1
- SNAZWPXKTJPHAC-UHFFFAOYSA-N C[n]1nc(C(C2)CC(CN3)C2CC3=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC(CN3)C2CC3=O)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N SNAZWPXKTJPHAC-UHFFFAOYSA-N 0.000 description 1
- GFCZRWULMZZAJI-UHFFFAOYSA-N C[n]1nc(C(C2)CC3C2CSC3)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C(C2)CC3C2CSC3)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N GFCZRWULMZZAJI-UHFFFAOYSA-N 0.000 description 1
- GMQQHFDMSAKCED-AWEZNQCLSA-N C[n]1nc(C(CC2)=C[C@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C(CC2)=C[C@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N GMQQHFDMSAKCED-AWEZNQCLSA-N 0.000 description 1
- HRHZYWLKXOKRPU-UHFFFAOYSA-N C[n]1nc(C2CC(CC(C3)C(N)=O)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C2CC(CC(C3)C(N)=O)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N HRHZYWLKXOKRPU-UHFFFAOYSA-N 0.000 description 1
- DQJXAAXRXPAMBP-UHFFFAOYSA-N C[n]1nc(C2CC(CC(C3)C(OC)=O)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C2CC(CC(C3)C(OC)=O)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N DQJXAAXRXPAMBP-UHFFFAOYSA-N 0.000 description 1
- FIXRVHRRTKVHMK-UHFFFAOYSA-N C[n]1nc(C2CC(CC(C3)c4c[nH]cn4)C3C2)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc(C2CC(CC(C3)c4c[nH]cn4)C3C2)c(C(Nc(cc2Cl)ccc2F)=O)c1N FIXRVHRRTKVHMK-UHFFFAOYSA-N 0.000 description 1
- IOWPNBPOZLLEQS-UHFFFAOYSA-N C[n]1nc(C2CC(CCC3)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc(C2CC(CCC3)C3C2)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N IOWPNBPOZLLEQS-UHFFFAOYSA-N 0.000 description 1
- FSWKAXVBQRIOOG-HNNXBMFYSA-N C[n]1nc([C@@H](CC2)C=C2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc([C@@H](CC2)C=C2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N FSWKAXVBQRIOOG-HNNXBMFYSA-N 0.000 description 1
- YHWOUVBPHBWWHH-CABCVRRESA-N C[n]1nc([C@@H](CC2)C[C@@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc([C@@H](CC2)C[C@@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N YHWOUVBPHBWWHH-CABCVRRESA-N 0.000 description 1
- YHWOUVBPHBWWHH-HUUCEWRRSA-N C[n]1nc([C@H](CC2)C[C@@H]2c(cc2)ccc2OC)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N Chemical compound C[n]1nc([C@H](CC2)C[C@@H]2c(cc2)ccc2OC)c(C(Nc(cc2)cc(Cl)c2F)=O)c1N YHWOUVBPHBWWHH-HUUCEWRRSA-N 0.000 description 1
- YHWOUVBPHBWWHH-LSDHHAIUSA-N C[n]1nc([C@H](CC2)C[C@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N Chemical compound C[n]1nc([C@H](CC2)C[C@H]2c(cc2)ccc2OC)c(C(Nc(cc2Cl)ccc2F)=O)c1N YHWOUVBPHBWWHH-LSDHHAIUSA-N 0.000 description 1
- KWQJCDUICGUVNQ-UHFFFAOYSA-N C[n]1ncc(C(CC2)CC2c2n[n](C)c(N)c2C(Nc(cc2Cl)ccc2F)=O)c1 Chemical compound C[n]1ncc(C(CC2)CC2c2n[n](C)c(N)c2C(Nc(cc2Cl)ccc2F)=O)c1 KWQJCDUICGUVNQ-UHFFFAOYSA-N 0.000 description 1
- IKNQPNLSEBWZKX-UHFFFAOYSA-N Cc(cc1)cc(Cl)c1F Chemical compound Cc(cc1)cc(Cl)c1F IKNQPNLSEBWZKX-UHFFFAOYSA-N 0.000 description 1
- IMCULDWFDHJIPO-UHFFFAOYSA-N Cc1nc2cc(NC(c(cc3)ccc3S(N(C)Cc3ccccc3)(=O)=O)=O)ccc2[s]1 Chemical compound Cc1nc2cc(NC(c(cc3)ccc3S(N(C)Cc3ccccc3)(=O)=O)=O)ccc2[s]1 IMCULDWFDHJIPO-UHFFFAOYSA-N 0.000 description 1
- ZRYKHZXSPWBXAO-UHFFFAOYSA-N Nc1c(C(NC(CC=C2F)C=C2Cl)=O)c(C2=CC(CC(C3)=O)C3C2)n[nH]1 Chemical compound Nc1c(C(NC(CC=C2F)C=C2Cl)=O)c(C2=CC(CC(C3)=O)C3C2)n[nH]1 ZRYKHZXSPWBXAO-UHFFFAOYSA-N 0.000 description 1
- FZKYKKMDZZRBFS-UHFFFAOYSA-N O=C(CC1)C=C1c1ccncc1 Chemical compound O=C(CC1)C=C1c1ccncc1 FZKYKKMDZZRBFS-UHFFFAOYSA-N 0.000 description 1
- MDVFUPOJJJSPOY-UHFFFAOYSA-N O=C(CC1)CC1c1ccccc1Cl Chemical compound O=C(CC1)CC1c1ccccc1Cl MDVFUPOJJJSPOY-UHFFFAOYSA-N 0.000 description 1
- JKZSHWDPOQYSJW-UHFFFAOYSA-N O=C(CN(c(cc(C(F)(F)F)cc1)c1Cl)S(c1ccccc1)(=O)=O)NCc1ccncc1 Chemical compound O=C(CN(c(cc(C(F)(F)F)cc1)c1Cl)S(c1ccccc1)(=O)=O)NCc1ccncc1 JKZSHWDPOQYSJW-UHFFFAOYSA-N 0.000 description 1
- HBIRLKKYXKFKMI-UHFFFAOYSA-N OC(C1)=CC2C1CNC2 Chemical compound OC(C1)=CC2C1CNC2 HBIRLKKYXKFKMI-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/08—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
-
- 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
- A61K31/415—1,2-Diazoles
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
-
- 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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/08—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 carbon chain containing alicyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/08—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing alicyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/08—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing alicyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862748906P | 2018-10-22 | 2018-10-22 | |
| US62/748,906 | 2018-10-22 | ||
| US201962858790P | 2019-06-07 | 2019-06-07 | |
| US62/858,790 | 2019-06-07 | ||
| PCT/US2019/057362 WO2020086533A1 (en) | 2018-10-22 | 2019-10-22 | 5-membered heteroaryl carboxamide compounds for treatment of hbv |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022508953A true JP2022508953A (ja) | 2022-01-19 |
| JPWO2020086533A5 JPWO2020086533A5 (https=) | 2023-06-22 |
| JP2022508953A5 JP2022508953A5 (https=) | 2023-06-22 |
Family
ID=68610300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021547054A Pending JP2022508953A (ja) | 2018-10-22 | 2019-10-22 | Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US11560370B1 (https=) |
| EP (1) | EP3870296A1 (https=) |
| JP (1) | JP2022508953A (https=) |
| KR (1) | KR20210095143A (https=) |
| CN (1) | CN113195055A (https=) |
| AU (1) | AU2019364352A1 (https=) |
| BR (1) | BR112021007602A2 (https=) |
| CA (1) | CA3117449A1 (https=) |
| IL (1) | IL282433A (https=) |
| MA (1) | MA53983A (https=) |
| MX (1) | MX2021004580A (https=) |
| PH (1) | PH12021550887A1 (https=) |
| SG (1) | SG11202104086PA (https=) |
| TW (1) | TW202028190A (https=) |
| WO (1) | WO2020086533A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023523241A (ja) * | 2020-04-22 | 2023-06-02 | アッセンブリー バイオサイエンシズ,インコーポレイテッド | Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111205264A (zh) * | 2020-02-25 | 2020-05-29 | 成都睿智化学研究有限公司 | 一种合成同位羟基和甲磺酰甲基化合物的新方法 |
| US20230295096A1 (en) * | 2020-04-22 | 2023-09-21 | Assembly Biosciences, Inc. | Pyrazole carboxamide compounds for treatment of hbv |
| JP2023551474A (ja) * | 2020-11-25 | 2023-12-08 | エフ. ホフマン-ラ ロシュ アーゲー | B型肝炎ウイルス感染症の処置および予防のための芳香族架橋環アミド誘導体 |
| WO2023069547A1 (en) * | 2021-10-20 | 2023-04-27 | Assembly Biosciences, Inc. | 5-membered heteroaryl carboxamide compounds for treatment of hbv |
| CN118339163A (zh) * | 2021-10-20 | 2024-07-12 | 组装生物科学股份有限公司 | 新的晶型 |
| WO2023105481A1 (en) * | 2021-12-10 | 2023-06-15 | Assembly Biosciences, Inc. | Pharmaceutical compositions for the treatment of hbv |
| EP4665330A1 (en) * | 2023-02-17 | 2025-12-24 | Merck Sharp & Dohme LLC | Plasma kallikrein inhibitors |
| KR102827002B1 (ko) * | 2023-06-28 | 2025-06-30 | 국립순천대학교산학협력단 | 신규한 마리노바자난 화합물 및 이를 포함하는 암 전이 및 침윤 억제, 또는 암 치료용 조성물 |
| WO2025029961A1 (en) * | 2023-07-31 | 2025-02-06 | Makscientific, Llc | Pharmaceutical compositions, and preparation and methods of use thereof |
| CN117603089A (zh) * | 2023-11-29 | 2024-02-27 | 南通瑞合达医药科技有限公司 | 一种环戊腈的合成方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005501073A (ja) * | 2001-08-06 | 2005-01-13 | フアルマシア・イタリア・エツセ・ピー・アー | キナーゼ阻害薬活性を有するアミノイソオキサゾール誘導体 |
| JP2006510627A (ja) * | 2002-12-05 | 2006-03-30 | ヴァーナリス(ケンブリッジ)リミテッド | 癌治療用のhsp90阻害剤としての3−(2−ヒドロキシ−フェニル)−1h−ピラゾール−4−カルボン酸アミド誘導体 |
| JP2012526820A (ja) * | 2009-05-12 | 2012-11-01 | ロマーク ラボラトリーズ エル.シー. | ハロアルキルヘテロアリールベンズアミド化合物 |
| CN105503730A (zh) * | 2015-12-25 | 2016-04-20 | 山东大学 | 吡唑类衍生物及其制备方法与应用 |
| JP2016518437A (ja) * | 2013-05-17 | 2016-06-23 | ヤンセン・サイエンシズ・アイルランド・ユーシー | スルファモイルチオフェンアミド誘導体およびb型肝炎を治療するための医薬品としてのその使用 |
| CN108250112A (zh) * | 2018-01-30 | 2018-07-06 | 西北大学 | 一种1-烷基-1-芳硫基-2-(1h)-萘酮衍生物及其制备方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008130584A1 (en) | 2007-04-20 | 2008-10-30 | Schering Corporation | Pyrimidinone derivatives and methods of use thereof |
| EP3085368A1 (en) | 2011-07-01 | 2016-10-26 | Baruch S. Blumberg Institute | Sulfamoylbenzamide derivatives as antiviral agents against hbv infection |
| WO2013010069A1 (en) | 2011-07-13 | 2013-01-17 | Indiana University Research And Technology Corporation | Modified viral structural protein with antiviral activity |
| EA026977B1 (ru) | 2012-01-06 | 2017-06-30 | Янссен Сайенсиз Айрлэнд Юси | 4,4-дизамещенные 1,4-дигидропиримидины и их применение в качестве лекарственных препаратов для лечения гепатита b |
| 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 |
| EA038942B1 (ru) | 2012-08-28 | 2021-11-12 | Янссен Сайенсиз Айрлэнд Юси | Сульфамоил-ариламиды и их применение в качестве лекарственных препаратов для лечения гепатита b |
| MX2015002954A (es) | 2012-09-10 | 2015-06-05 | Hoffmann La Roche | Nuevas 6-aminoacido-heteroarilhidropirimidinas para el tratamiento y profilaxis de la infeccion del virus de la hepatitis b. |
| CA2889892A1 (en) | 2012-11-09 | 2014-05-15 | Indiana University Research And Technology Corporation | Alternative uses for hbv assembly effectors |
| CA2892606A1 (en) | 2012-12-06 | 2014-06-12 | Baruch S. Blumberg Institute | Functionalized benzamide derivatives as antiviral agents against hbv infection |
| CN105209031A (zh) | 2012-12-27 | 2015-12-30 | 德雷克塞尔大学 | 针对hbv感染的新型抗病毒剂 |
| HUE034820T2 (en) | 2013-02-28 | 2018-02-28 | Janssen Sciences Ireland Uc | Sulphamoyl arylamides and their use as medicaments for the treatment of hepatitis B |
| EA027068B1 (ru) | 2013-04-03 | 2017-06-30 | Янссен Сайенсиз Айрлэнд Юси | Производные n-фенилкарбоксамида и их применение в качестве лекарственных препаратов для лечения гепатита b |
| TWI651300B (zh) | 2013-05-17 | 2019-02-21 | 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 |
| CN105209470B (zh) | 2013-05-17 | 2018-02-06 | 豪夫迈·罗氏有限公司 | 用于治疗和预防乙型肝炎病毒感染的6‑桥连的杂芳基二氢嘧啶 |
| DK3024819T3 (en) | 2013-07-25 | 2018-06-06 | Janssen Sciences Ireland Uc | GLYOXAMIDE-SUBSTITUTED PYRROLAMIDE DERIVATIVES AND THE USE THEREOF AS MEDICINES FOR TREATING HEPATITIS B |
| AU2014348518B2 (en) * | 2013-11-14 | 2019-01-03 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| WO2015118057A1 (en) | 2014-02-06 | 2015-08-13 | Janssen Sciences Ireland Uc | Sulphamoylpyrrolamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| EP3271019A1 (en) * | 2015-03-19 | 2018-01-24 | Novira Therapeutics Inc. | Azocane and azonane derivatives and methods of treating hepatitis b infections |
| UY37581A (es) * | 2017-02-02 | 2018-08-31 | Gilead Sciences Inc | Compuestos para el tratamiento de la infección por virus de la hepatitis b |
-
2019
- 2019-10-22 TW TW108138129A patent/TW202028190A/zh unknown
- 2019-10-22 MX MX2021004580A patent/MX2021004580A/es unknown
- 2019-10-22 US US17/287,681 patent/US11560370B1/en active Active
- 2019-10-22 CA CA3117449A patent/CA3117449A1/en active Pending
- 2019-10-22 JP JP2021547054A patent/JP2022508953A/ja active Pending
- 2019-10-22 BR BR112021007602-6A patent/BR112021007602A2/pt not_active IP Right Cessation
- 2019-10-22 MA MA053983A patent/MA53983A/fr unknown
- 2019-10-22 WO PCT/US2019/057362 patent/WO2020086533A1/en not_active Ceased
- 2019-10-22 CN CN201980082985.8A patent/CN113195055A/zh active Pending
- 2019-10-22 EP EP19805797.8A patent/EP3870296A1/en not_active Withdrawn
- 2019-10-22 KR KR1020217015135A patent/KR20210095143A/ko not_active Withdrawn
- 2019-10-22 AU AU2019364352A patent/AU2019364352A1/en not_active Abandoned
- 2019-10-22 SG SG11202104086PA patent/SG11202104086PA/en unknown
-
2021
- 2021-04-19 IL IL282433A patent/IL282433A/en unknown
- 2021-04-21 PH PH12021550887A patent/PH12021550887A1/en unknown
-
2022
- 2022-11-17 US US17/989,237 patent/US12030869B2/en active Active
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005501073A (ja) * | 2001-08-06 | 2005-01-13 | フアルマシア・イタリア・エツセ・ピー・アー | キナーゼ阻害薬活性を有するアミノイソオキサゾール誘導体 |
| JP2006510627A (ja) * | 2002-12-05 | 2006-03-30 | ヴァーナリス(ケンブリッジ)リミテッド | 癌治療用のhsp90阻害剤としての3−(2−ヒドロキシ−フェニル)−1h−ピラゾール−4−カルボン酸アミド誘導体 |
| JP2012526820A (ja) * | 2009-05-12 | 2012-11-01 | ロマーク ラボラトリーズ エル.シー. | ハロアルキルヘテロアリールベンズアミド化合物 |
| JP2016518437A (ja) * | 2013-05-17 | 2016-06-23 | ヤンセン・サイエンシズ・アイルランド・ユーシー | スルファモイルチオフェンアミド誘導体およびb型肝炎を治療するための医薬品としてのその使用 |
| CN105503730A (zh) * | 2015-12-25 | 2016-04-20 | 山东大学 | 吡唑类衍生物及其制备方法与应用 |
| CN108250112A (zh) * | 2018-01-30 | 2018-07-06 | 西北大学 | 一种1-烷基-1-芳硫基-2-(1h)-萘酮衍生物及其制备方法 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023523241A (ja) * | 2020-04-22 | 2023-06-02 | アッセンブリー バイオサイエンシズ,インコーポレイテッド | Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 |
| JP7830347B2 (ja) | 2020-04-22 | 2026-03-16 | アッセンブリー バイオサイエンシズ,インコーポレイテッド | Hbvの処置のための5員のヘテロアリールカルボキサミド化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2019364352A1 (en) | 2021-06-03 |
| US12030869B2 (en) | 2024-07-09 |
| KR20210095143A (ko) | 2021-07-30 |
| EP3870296A1 (en) | 2021-09-01 |
| BR112021007602A2 (pt) | 2021-07-27 |
| WO2020086533A1 (en) | 2020-04-30 |
| SG11202104086PA (en) | 2021-05-28 |
| US20240150324A1 (en) | 2024-05-09 |
| CN113195055A (zh) | 2021-07-30 |
| MA53983A (fr) | 2021-12-15 |
| PH12021550887A1 (en) | 2022-02-21 |
| MX2021004580A (es) | 2021-09-08 |
| CA3117449A1 (en) | 2020-04-30 |
| IL282433A (en) | 2021-06-30 |
| TW202028190A (zh) | 2020-08-01 |
| US11560370B1 (en) | 2023-01-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12030869B2 (en) | 5-membered heteroaryl carboxamide compounds for treatment of HBV | |
| JP7150903B2 (ja) | B型肝炎ウイルスコアタンパク質モジュレーター | |
| US9512122B2 (en) | Spirocyclic compounds as tryptophan hydroxylase inhibitors | |
| JP7759877B2 (ja) | 治療用化合物 | |
| CN115843294B (zh) | 用于治疗hbv的5元杂芳基甲酰胺化合物 | |
| MX2012006667A (es) | Compuesto de oxadiazol novedosos. | |
| WO2020051319A1 (en) | Cyclic sulfamide compounds for treatment of hbv | |
| WO2020051320A1 (en) | Cyclic sulfamide compounds for treatment of hbv | |
| US20230295096A1 (en) | Pyrazole carboxamide compounds for treatment of hbv | |
| US20250276966A1 (en) | Nitrogen-Linked Benzisoxazole Sulfonamide Derivatives | |
| EA053034B1 (ru) | 5-членные гетероарилкарбоксамидные соединения для лечения гепатита b | |
| WO2023069547A1 (en) | 5-membered heteroaryl carboxamide compounds for treatment of hbv | |
| WO2021216661A1 (en) | Pyrazole carboxamide compounds for treatment of hbv | |
| HK40090691A (zh) | 用於治疗hbv的5元杂芳基甲酰胺化合物 | |
| WO2023069545A1 (en) | 5-membered heteroaryl carboxamide compounds for treatment of hbv | |
| TW202409010A (zh) | 人類呼吸道融合病毒及人類間質肺炎病毒之抑制劑 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20221021 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20221021 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20221219 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230614 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20231026 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20231101 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20240126 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20240620 |