JP2015500824A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015500824A5 JP2015500824A5 JP2014545346A JP2014545346A JP2015500824A5 JP 2015500824 A5 JP2015500824 A5 JP 2015500824A5 JP 2014545346 A JP2014545346 A JP 2014545346A JP 2014545346 A JP2014545346 A JP 2014545346A JP 2015500824 A5 JP2015500824 A5 JP 2015500824A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrrole
- dihydroxy
- methoxyphenyl
- alkyl
- carboxylate
- 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
- 150000001875 compounds Chemical class 0.000 claims 51
- 229910052739 hydrogen Inorganic materials 0.000 claims 33
- 239000001257 hydrogen Substances 0.000 claims 33
- -1 3,4-dibutoxy-1,2,5-triphenyl-1H-pyrrole Chemical compound 0.000 claims 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 22
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 14
- 125000001072 heteroaryl group Chemical group 0.000 claims 12
- 125000005843 halogen group Chemical group 0.000 claims 10
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 8
- 239000000651 prodrug Substances 0.000 claims 8
- 229940002612 prodrug Drugs 0.000 claims 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- LCEDQNDDFOCWGG-UHFFFAOYSA-N morpholine-4-carbaldehyde Chemical compound O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 claims 7
- 239000012453 solvate Substances 0.000 claims 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 4
- 239000004480 active ingredient Substances 0.000 claims 4
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 4
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 3
- 208000035143 Bacterial infection Diseases 0.000 claims 3
- 208000022362 bacterial infectious disease Diseases 0.000 claims 3
- 230000003115 biocidal effect Effects 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- RFIOZSIHFNEKFF-UHFFFAOYSA-M piperazine-1-carboxylate Chemical compound [O-]C(=O)N1CCNCC1 RFIOZSIHFNEKFF-UHFFFAOYSA-M 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 2
- 241000193738 Bacillus anthracis Species 0.000 claims 2
- 241000894006 Bacteria Species 0.000 claims 2
- 241000186781 Listeria Species 0.000 claims 2
- 241000193998 Streptococcus pneumoniae Species 0.000 claims 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 2
- 150000001241 acetals Chemical class 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims 2
- FMQVJAPGSVCECP-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1 FMQVJAPGSVCECP-UHFFFAOYSA-N 0.000 claims 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 2
- VGNWOFPNOVAHOE-UHFFFAOYSA-N ethyl 3-diethoxyphosphoryloxy-5-(dimethylcarbamoyl)-4-hydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(OP(=O)(OCC)OCC)c(O)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 VGNWOFPNOVAHOE-UHFFFAOYSA-N 0.000 claims 2
- DSGYDCBOQWWSEA-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 DSGYDCBOQWWSEA-UHFFFAOYSA-N 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229940031000 streptococcus pneumoniae Drugs 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 150000003952 β-lactams Chemical class 0.000 claims 2
- PIZVVTVJCRYWKC-UHFFFAOYSA-N (2,6-dimethylcyclohexyl) 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)OC1C(C)CCCC1C PIZVVTVJCRYWKC-UHFFFAOYSA-N 0.000 claims 1
- GGWXJENHOMSQKF-UHFFFAOYSA-N 1-(2-methoxyphenyl)-2-n,2-n,5-n,5-n-tetramethyl-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound COC1=CC=CC=C1N1C(C(=O)N(C)C)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C GGWXJENHOMSQKF-UHFFFAOYSA-N 0.000 claims 1
- GBHQRRAPCIPUGZ-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-2-n,2-n,5-n,5-n-tetraethyl-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C1=CC(OCC)=CC=C1N1C(C(=O)N(CC)CC)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(CC)CC GBHQRRAPCIPUGZ-UHFFFAOYSA-N 0.000 claims 1
- BUROUEYQJNZHGV-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-2-n,2-n,5-n,5-n-tetraethyl-3,4-dihydroxypyrrole-2,5-dicarboxamide Chemical compound C1=CC(OCC)=CC=C1N1C(C(=O)N(CC)CC)=C(O)C(O)=C1C(=O)N(CC)CC BUROUEYQJNZHGV-UHFFFAOYSA-N 0.000 claims 1
- HJTQFKHMMYPOFT-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-2-n,2-n,5-n,5-n-tetramethyl-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C1=CC(OCC)=CC=C1N1C(C(=O)N(C)C)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C HJTQFKHMMYPOFT-UHFFFAOYSA-N 0.000 claims 1
- JXQFJDCZOCJXPJ-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-2-n,5-n-diethyl-3,4-dihydroxypyrrole-2,5-dicarboxamide Chemical compound CCNC(=O)C1=C(O)C(O)=C(C(=O)NCC)N1C1=CC=C(OCC)C=C1 JXQFJDCZOCJXPJ-UHFFFAOYSA-N 0.000 claims 1
- NJIUTCOWMDMOBP-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-3,4-dihydroxy-2-n,2-n,5-n,5-n-tetramethylpyrrole-2,5-dicarboxamide Chemical compound C1=CC(OCC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)N(C)C NJIUTCOWMDMOBP-UHFFFAOYSA-N 0.000 claims 1
- XUDHEDLJBBQCQI-UHFFFAOYSA-N 1-(4-ethoxyphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxamide Chemical compound C1=CC(OCC)=CC=C1N1C(C(N)=O)=C(O)C(O)=C1C(N)=O XUDHEDLJBBQCQI-UHFFFAOYSA-N 0.000 claims 1
- ZZDUTDMZQXGMCG-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1COC1=C(C(N)=O)N(C=2C=CC(F)=CC=2)C(C(=O)N)=C1OCC1=CC=CC=C1 ZZDUTDMZQXGMCG-UHFFFAOYSA-N 0.000 claims 1
- YVOWDUCUGHQQJJ-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-dihydroxy-2-n,2-n,5-n,5-n-tetra(propan-2-yl)pyrrole-2,5-dicarboxamide Chemical compound CC(C)N(C(C)C)C(=O)C1=C(O)C(O)=C(C(=O)N(C(C)C)C(C)C)N1C1=CC=C(F)C=C1 YVOWDUCUGHQQJJ-UHFFFAOYSA-N 0.000 claims 1
- ZBJUSVVQRJDSGX-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-dihydroxy-2-n,2-n,5-n,5-n-tetramethylpyrrole-2,5-dicarboxamide Chemical compound CN(C)C(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(F)C=C1 ZBJUSVVQRJDSGX-UHFFFAOYSA-N 0.000 claims 1
- QZTZTGCDGKRSDH-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-dihydroxy-2-n,5-n-dimethyl-2-n,5-n-di(propan-2-yl)pyrrole-2,5-dicarboxamide Chemical compound CC(C)N(C)C(=O)C1=C(O)C(O)=C(C(=O)N(C)C(C)C)N1C1=CC=C(F)C=C1 QZTZTGCDGKRSDH-UHFFFAOYSA-N 0.000 claims 1
- QMBAYVKQWUOPLP-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-dihydroxy-2-n,5-n-dimethyl-2-n,5-n-diphenylpyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1N(C)C(=O)C(N1C=2C=CC(F)=CC=2)=C(O)C(O)=C1C(=O)N(C)C1=CC=CC=C1 QMBAYVKQWUOPLP-UHFFFAOYSA-N 0.000 claims 1
- ONCYLCLHYYNRTG-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxamide Chemical compound NC(=O)C1=C(O)C(O)=C(C(N)=O)N1C1=CC=C(F)C=C1 ONCYLCLHYYNRTG-UHFFFAOYSA-N 0.000 claims 1
- KWUBPEPBIOWVDV-UHFFFAOYSA-N 1-(4-methoxyphenyl)-2-n,2-n,5-n,5-n-tetramethyl-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C KWUBPEPBIOWVDV-UHFFFAOYSA-N 0.000 claims 1
- VPXNJGQRXSIRFI-UHFFFAOYSA-N 1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(N)=O)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(N)=O VPXNJGQRXSIRFI-UHFFFAOYSA-N 0.000 claims 1
- VOKBSFHJZWOGJQ-UHFFFAOYSA-N 1-(4-methoxyphenyl)-n,n-dimethyl-3,4-bis(phenylmethoxy)-5-(piperidine-1-carbonyl)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCCCC2)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C VOKBSFHJZWOGJQ-UHFFFAOYSA-N 0.000 claims 1
- PLDJSFMGOQBRDF-UHFFFAOYSA-N 1-(4-methoxyphenyl)-n,n-dimethyl-5-(4-methylpiperazine-1-carbonyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCN(C)CC2)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C PLDJSFMGOQBRDF-UHFFFAOYSA-N 0.000 claims 1
- MSSYTIJSIYAKOP-UHFFFAOYSA-N 1-(4-methoxyphenyl)-n,n-dimethyl-5-(morpholine-4-carbonyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCOCC2)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N(C)C MSSYTIJSIYAKOP-UHFFFAOYSA-N 0.000 claims 1
- QRVFJNBUWPNVII-UHFFFAOYSA-N 1-[4-(dimethylcarbamoyl)phenyl]-3,4-dihydroxy-2-n,2-n,5-n,5-n-tetramethylpyrrole-2,5-dicarboxamide Chemical compound CN(C)C(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(C(=O)N(C)C)C=C1 QRVFJNBUWPNVII-UHFFFAOYSA-N 0.000 claims 1
- XSFBYONTFLQODU-UHFFFAOYSA-N 2,2-dimethylpropyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound COc1ccc(cc1)-n1c(C(=O)OCC(C)(C)C)c(O)c(O)c1C(=O)N(C)C XSFBYONTFLQODU-UHFFFAOYSA-N 0.000 claims 1
- PMLRKSWISJJURS-UHFFFAOYSA-N 2-[4-(2-carboxypropan-2-yl)-2,5-bis(dimethylcarbamoyl)-1-(4-methoxyphenyl)pyrrol-3-yl]-2-methylpropanoic acid Chemical compound CC(C)(C1=C(N(C(=C1C(C)(C)C(=O)O)C(=O)N(C)C)C2=CC=C(C=C2)OC)C(=O)N(C)C)C(=O)O PMLRKSWISJJURS-UHFFFAOYSA-N 0.000 claims 1
- SPXXQEAGOZGEBY-UHFFFAOYSA-N 2-n,2-n,5-n,5-n-tetraethyl-1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1COC1=C(C(=O)N(CC)CC)N(C=2C=CC(OC)=CC=2)C(C(=O)N(CC)CC)=C1OCC1=CC=CC=C1 SPXXQEAGOZGEBY-UHFFFAOYSA-N 0.000 claims 1
- KMQCPIGRQAFTNW-UHFFFAOYSA-N 2-n,2-n,5-n,5-n-tetraethyl-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxamide Chemical compound CCN(CC)C(=O)C1=C(O)C(O)=C(C(=O)N(CC)CC)N1C1=CC=C(OC)C=C1 KMQCPIGRQAFTNW-UHFFFAOYSA-N 0.000 claims 1
- SHQHPAYCEWSFGW-UHFFFAOYSA-N 2-n,2-n,5-n,5-n-tetramethyl-3,4-bis(phenylmethoxy)-1-[4-(trifluoromethyl)phenyl]pyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1COC1=C(C(=O)N(C)C)N(C=2C=CC(=CC=2)C(F)(F)F)C(C(=O)N(C)C)=C1OCC1=CC=CC=C1 SHQHPAYCEWSFGW-UHFFFAOYSA-N 0.000 claims 1
- GVOURTQHNRLYBW-UHFFFAOYSA-N 2-n,5-n-diethyl-1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1COC1=C(C(=O)NCC)N(C=2C=CC(OC)=CC=2)C(C(=O)NCC)=C1OCC1=CC=CC=C1 GVOURTQHNRLYBW-UHFFFAOYSA-N 0.000 claims 1
- DVQAQRWAGJBXOP-UHFFFAOYSA-N 3,4-dihydroxy-1-(2-methoxyphenyl)-2-n,2-n,5-n,5-n-tetramethylpyrrole-2,5-dicarboxamide Chemical compound COC1=CC=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)N(C)C DVQAQRWAGJBXOP-UHFFFAOYSA-N 0.000 claims 1
- JOECWWZBDPISPH-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)-2-n,2-n,5-n,5-n-tetramethylpyrrole-2,5-dicarboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)N(C)C JOECWWZBDPISPH-UHFFFAOYSA-N 0.000 claims 1
- WEDPCOCBPAHNRA-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethyl-5-(4-methylpiperazine-1-carbonyl)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCN(C)CC2)=C(O)C(O)=C1C(=O)N(C)C WEDPCOCBPAHNRA-UHFFFAOYSA-N 0.000 claims 1
- UOQOGHVYPSKNFX-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethyl-5-(morpholine-4-carbonyl)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCOCC2)=C(O)C(O)=C1C(=O)N(C)C UOQOGHVYPSKNFX-UHFFFAOYSA-N 0.000 claims 1
- WVDRGZSXXNAHIM-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethyl-5-(piperidine-1-carbonyl)pyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCCCC2)=C(O)C(O)=C1C(=O)N(C)C WVDRGZSXXNAHIM-UHFFFAOYSA-N 0.000 claims 1
- VTOUAFDEQWTHCP-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarbonitrile Chemical compound C1=CC(OC)=CC=C1N1C(C#N)=C(O)C(O)=C1C#N VTOUAFDEQWTHCP-UHFFFAOYSA-N 0.000 claims 1
- XGGQBWAPZNKQDN-UHFFFAOYSA-N 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(N)=O)=C(O)C(O)=C1C(N)=O XGGQBWAPZNKQDN-UHFFFAOYSA-N 0.000 claims 1
- UMFMGHXREKZXGB-UHFFFAOYSA-N 3,4-dihydroxy-2-n,2-n,5-n,5-n-tetramethyl-1-[4-(trifluoromethyl)phenyl]pyrrole-2,5-dicarboxamide Chemical compound CN(C)C(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(C(F)(F)F)C=C1 UMFMGHXREKZXGB-UHFFFAOYSA-N 0.000 claims 1
- LMGVWCVJXZBBFO-UHFFFAOYSA-N 3,4-dimethoxy-1-(4-methylphenyl)-2,5-diphenylpyrrole Chemical compound C=1C=C(C)C=CC=1N1C(C=2C=CC=CC=2)=C(OC)C(OC)=C1C1=CC=CC=C1 LMGVWCVJXZBBFO-UHFFFAOYSA-N 0.000 claims 1
- SMBKTARVADHYBC-UHFFFAOYSA-N 3-[4-(2-carboxy-2-methylpropyl)-2-(dimethylcarbamoyl)-5-ethoxycarbonyl-1-(4-methoxyphenyl)pyrrol-3-yl]-2,2-dimethylpropanoic acid Chemical compound CCOC(=O)C1=C(CC(C)(C)C(O)=O)C(CC(C)(C)C(O)=O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 SMBKTARVADHYBC-UHFFFAOYSA-N 0.000 claims 1
- AAZUGUANVDRRFV-UHFFFAOYSA-N 3-[4-[2-(dimethylcarbamoyl)-5-ethoxycarbonyl-3,4-dihydroxypyrrol-1-yl]phenoxy]propylphosphonic acid Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OCCCP(O)(O)=O)cc1 AAZUGUANVDRRFV-UHFFFAOYSA-N 0.000 claims 1
- KWNLCFHVCZWDEY-UHFFFAOYSA-N 4-[2-[4-[1-(1-carboxypiperidin-4-yl)piperidin-2-yl]-2-(dimethylcarbamoyl)-5-ethoxycarbonyl-1-(4-methoxyphenyl)pyrrol-3-yl]piperidin-1-yl]piperidine-1-carboxylic acid Chemical compound CCOC(=O)C1=C(C(=C(N1C2=CC=C(C=C2)OC)C(=O)N(C)C)C3CCCCN3C4CCN(CC4)C(=O)O)C5CCCCN5C6CCN(CC6)C(=O)O KWNLCFHVCZWDEY-UHFFFAOYSA-N 0.000 claims 1
- FWPMOWFCZPJQLC-UHFFFAOYSA-N 5-N,2-dibenzyl-1-(4-fluorophenyl)-3,4-dihydroxy-2-N,5-N-dimethyl-3H-pyrrole-2,5-dicarboxamide Chemical compound C(C1=CC=CC=C1)C1(N(C(=C(C1O)O)C(=O)N(C)CC1=CC=CC=C1)C1=CC=C(C=C1)F)C(=O)NC FWPMOWFCZPJQLC-UHFFFAOYSA-N 0.000 claims 1
- VYUKIORTVYLDDL-UHFFFAOYSA-N 5-acetyl-3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethylpyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(C)=O VYUKIORTVYLDDL-UHFFFAOYSA-N 0.000 claims 1
- ZQZQKHRCANHASA-UHFFFAOYSA-N 5-cyano-1-(4-fluorophenyl)-n,n-dimethyl-3,4-bis(phenylmethoxy)pyrrole-2-carboxamide Chemical compound C=1C=CC=CC=1COC1=C(C#N)N(C=2C=CC(F)=CC=2)C(C(=O)N(C)C)=C1OCC1=CC=CC=C1 ZQZQKHRCANHASA-UHFFFAOYSA-N 0.000 claims 1
- MPSINJQOYWDDEJ-UHFFFAOYSA-N 5-cyano-3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethylpyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C#N MPSINJQOYWDDEJ-UHFFFAOYSA-N 0.000 claims 1
- RMYIXOSZJDCDLS-UHFFFAOYSA-N 5-dimethylphosphoryl-3,4-dihydroxy-1-(4-methoxyphenyl)-n,n-dimethylpyrrole-2-carboxamide Chemical compound C1=CC(OC)=CC=C1N1C(P(C)(C)=O)=C(O)C(O)=C1C(=O)N(C)C RMYIXOSZJDCDLS-UHFFFAOYSA-N 0.000 claims 1
- CVOAEQJGMAMECS-UHFFFAOYSA-N 5-n-ethyl-1-(4-methoxyphenyl)-2-n,2-n-dimethyl-3,4-bis(phenylmethoxy)pyrrole-2,5-dicarboxamide Chemical compound C=1C=CC=CC=1COC1=C(C(=O)N(C)C)N(C=2C=CC(OC)=CC=2)C(C(=O)NCC)=C1OCC1=CC=CC=C1 CVOAEQJGMAMECS-UHFFFAOYSA-N 0.000 claims 1
- NBIUCXJUHBIBGD-UHFFFAOYSA-N 5-n-ethyl-3,4-dihydroxy-1-(4-methoxyphenyl)-2-n,2-n-dimethylpyrrole-2,5-dicarboxamide Chemical compound CCNC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 NBIUCXJUHBIBGD-UHFFFAOYSA-N 0.000 claims 1
- KUQBCMASKDMQBT-UHFFFAOYSA-N 5-o-ethyl 2-o-propan-2-yl 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OC(C)C)N1C1=CC=C(OC)C=C1 KUQBCMASKDMQBT-UHFFFAOYSA-N 0.000 claims 1
- 241000193830 Bacillus <bacterium> Species 0.000 claims 1
- 208000031729 Bacteremia Diseases 0.000 claims 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 1
- FDMXOYHNUBMUJP-UHFFFAOYSA-N CCOC(=O)c1c(C(COCCOC)C(O)=O)c(C(COCCOC)C(O)=O)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 Chemical compound CCOC(=O)c1c(C(COCCOC)C(O)=O)c(C(COCCOC)C(O)=O)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 FDMXOYHNUBMUJP-UHFFFAOYSA-N 0.000 claims 1
- GFODNOFYFLHTJG-UHFFFAOYSA-N CCOC(=O)c1c(C(OCCOCCOC)C(C)(C)C(O)=O)c(C(OCCOCCOC)C(C)(C)C(O)=O)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 Chemical compound CCOC(=O)c1c(C(OCCOCCOC)C(C)(C)C(O)=O)c(C(OCCOCCOC)C(C)(C)C(O)=O)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 GFODNOFYFLHTJG-UHFFFAOYSA-N 0.000 claims 1
- CIAGBXIVXTZDPZ-UHFFFAOYSA-N CCOC(=O)c1c(c(c(C(=O)N(C)C)n1-c1ccc(OC)cc1)C(C)(C)C(O)=O)C(C)(C)C(O)=O Chemical compound CCOC(=O)c1c(c(c(C(=O)N(C)C)n1-c1ccc(OC)cc1)C(C)(C)C(O)=O)C(C)(C)C(O)=O CIAGBXIVXTZDPZ-UHFFFAOYSA-N 0.000 claims 1
- PUOJGKPDOMVYDA-UHFFFAOYSA-N CCOC(=O)c1c(c(c(C(=O)N(C)C)n1-c1ccc(OCCOCCOCCOC)cc1)C(C)(C)C(O)=O)C(C)(C)C(O)=O Chemical compound CCOC(=O)c1c(c(c(C(=O)N(C)C)n1-c1ccc(OCCOCCOCCOC)cc1)C(C)(C)C(O)=O)C(C)(C)C(O)=O PUOJGKPDOMVYDA-UHFFFAOYSA-N 0.000 claims 1
- 229930186147 Cephalosporin Natural products 0.000 claims 1
- 241000193403 Clostridium Species 0.000 claims 1
- 241000193468 Clostridium perfringens Species 0.000 claims 1
- 201000000628 Gas Gangrene Diseases 0.000 claims 1
- 108010028921 Lipopeptides Proteins 0.000 claims 1
- 201000009906 Meningitis Diseases 0.000 claims 1
- 206010027253 Meningitis pneumococcal Diseases 0.000 claims 1
- 206010033078 Otitis media Diseases 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 208000009362 Pneumococcal Pneumonia Diseases 0.000 claims 1
- 206010058859 Pneumococcal bacteraemia Diseases 0.000 claims 1
- 206010054047 Pneumococcal sepsis Diseases 0.000 claims 1
- 206010035664 Pneumonia Diseases 0.000 claims 1
- 206010035728 Pneumonia pneumococcal Diseases 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 229930189077 Rifamycin Natural products 0.000 claims 1
- 206010040047 Sepsis Diseases 0.000 claims 1
- 241001505901 Streptococcus sp. 'group A' Species 0.000 claims 1
- 239000004098 Tetracycline Substances 0.000 claims 1
- NONQGAHZSKKFGF-UHFFFAOYSA-N [1-(4-fluorophenyl)-3,4-dihydroxy-5-(piperidine-1-carbonyl)pyrrol-2-yl]-piperidin-1-ylmethanone Chemical compound C=1C=C(F)C=CC=1N1C(C(=O)N2CCCCC2)=C(O)C(O)=C1C(=O)N1CCCCC1 NONQGAHZSKKFGF-UHFFFAOYSA-N 0.000 claims 1
- TUPWUSQOJXTMJM-UHFFFAOYSA-N [1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)-5-(piperidine-1-carbonyl)pyrrol-2-yl]-piperidin-1-ylmethanone Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCCCC2)=C(OCC=2C=CC=CC=2)C(OCC=2C=CC=CC=2)=C1C(=O)N1CCCCC1 TUPWUSQOJXTMJM-UHFFFAOYSA-N 0.000 claims 1
- ZIHTVEMYSZHRKF-UHFFFAOYSA-N [2,5-bis(dimethylcarbamoyl)-1-(4-methoxyphenyl)-4-[4-(phosphonooxymethyl)benzoyl]oxypyrrol-3-yl] 4-(phosphonooxymethyl)benzoate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(OC(=O)C=2C=CC(COP(O)(O)=O)=CC=2)C(OC(=O)C=2C=CC(COP(O)(O)=O)=CC=2)=C1C(=O)N(C)C ZIHTVEMYSZHRKF-UHFFFAOYSA-N 0.000 claims 1
- WLERKEJZDRANGE-UHFFFAOYSA-N [2,5-bis(dimethylcarbamoyl)-4-[2,2-dimethyl-3-[2-(2-phosphonooxyethoxy)ethoxy]propanoyl]oxy-1-(4-methoxyphenyl)pyrrol-3-yl] 2,2-dimethyl-3-[2-(2-phosphonooxyethoxy)ethoxy]propanoate Chemical compound CC(C(=O)OC1=C(N(C(=C1OC(C(COCCOCCOP(=O)(O)O)(C)C)=O)C(N(C)C)=O)C1=CC=C(C=C1)OC)C(N(C)C)=O)(COCCOCCOP(=O)(O)O)C WLERKEJZDRANGE-UHFFFAOYSA-N 0.000 claims 1
- IDWNSSHICILHSW-UHFFFAOYSA-N [2-(dimethylcarbamoyl)-5-ethoxycarbonyl-4-hydroxy-1-(4-methoxyphenyl)pyrrol-3-yl] 4-piperidin-1-ylpiperidine-1-carboxylate Chemical compound CN(C)C(=O)C=1N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C(O)C=1OC(=O)N(CC1)CCC1N1CCCCC1 IDWNSSHICILHSW-UHFFFAOYSA-N 0.000 claims 1
- IWSAESASYDFBKK-UHFFFAOYSA-N [3,4-dihydroxy-1-(4-methoxyphenyl)-5-(piperazine-1-carbonyl)pyrrol-2-yl]-piperazin-1-ylmethanone Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCNCC2)=C(O)C(O)=C1C(=O)N1CCNCC1 IWSAESASYDFBKK-UHFFFAOYSA-N 0.000 claims 1
- SNBQPOXNWPKFCL-UHFFFAOYSA-N [3,4-dihydroxy-1-(4-methoxyphenyl)-5-(piperidine-1-carbonyl)pyrrol-2-yl]-piperidin-1-ylmethanone Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N2CCCCC2)=C(O)C(O)=C1C(=O)N1CCCCC1 SNBQPOXNWPKFCL-UHFFFAOYSA-N 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 229940126574 aminoglycoside antibiotic Drugs 0.000 claims 1
- 239000002647 aminoglycoside antibiotic agent Substances 0.000 claims 1
- 230000001548 androgenic effect Effects 0.000 claims 1
- 239000004599 antimicrobial Substances 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229940065181 bacillus anthracis Drugs 0.000 claims 1
- 239000003781 beta lactamase inhibitor Substances 0.000 claims 1
- 229940126813 beta-lactamase inhibitor Drugs 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 229940124587 cephalosporin Drugs 0.000 claims 1
- 150000001780 cephalosporins Chemical class 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 235000012000 cholesterol Nutrition 0.000 claims 1
- ICCBRSCLOYNJLW-UHFFFAOYSA-N cyclopentyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound COc1ccc(cc1)-n1c(C(=O)OC2CCCC2)c(O)c(O)c1C(=O)N(C)C ICCBRSCLOYNJLW-UHFFFAOYSA-N 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- AFWPVDHYWTZDDB-UHFFFAOYSA-N diethyl 1-(1,3-benzodioxol-5-yl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OCO2)C2=C1 AFWPVDHYWTZDDB-UHFFFAOYSA-N 0.000 claims 1
- FKGQSTMYMSJOMM-UHFFFAOYSA-N diethyl 1-(2,4-dimethoxyphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1OC FKGQSTMYMSJOMM-UHFFFAOYSA-N 0.000 claims 1
- BPGYXYMYDDHRGB-UHFFFAOYSA-N diethyl 1-(3,4-dimethoxyphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC)C(OC)=C1 BPGYXYMYDDHRGB-UHFFFAOYSA-N 0.000 claims 1
- VTKHQSFRNBCTGI-UHFFFAOYSA-N diethyl 1-(4-chlorophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(Cl)C=C1 VTKHQSFRNBCTGI-UHFFFAOYSA-N 0.000 claims 1
- BDLXFDWTAXUKQO-UHFFFAOYSA-N diethyl 1-(4-cyanophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(C#N)C=C1 BDLXFDWTAXUKQO-UHFFFAOYSA-N 0.000 claims 1
- QSEURUFOGPQQAA-UHFFFAOYSA-N diethyl 1-(4-ethoxy-3,5-difluorophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC(F)=C(OCC)C(F)=C1 QSEURUFOGPQQAA-UHFFFAOYSA-N 0.000 claims 1
- NADRSOGIKIHLLP-UHFFFAOYSA-N diethyl 1-(4-ethoxyphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OCC)C=C1 NADRSOGIKIHLLP-UHFFFAOYSA-N 0.000 claims 1
- RJSXCHDROYNGIK-UHFFFAOYSA-N diethyl 1-(4-ethylphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(CC)C=C1 RJSXCHDROYNGIK-UHFFFAOYSA-N 0.000 claims 1
- HYCKAEBEBFWGES-UHFFFAOYSA-N diethyl 1-(4-fluorophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(F)C=C1 HYCKAEBEBFWGES-UHFFFAOYSA-N 0.000 claims 1
- OIIZSHYBNMIPCA-UHFFFAOYSA-N diethyl 1-(4-fluorophenyl)-3-hydroxy-4-(2-hydroxyethoxy)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCCO)=C(C(=O)OCC)N1C1=CC=C(F)C=C1 OIIZSHYBNMIPCA-UHFFFAOYSA-N 0.000 claims 1
- RAYOYPGFNQGWHY-UHFFFAOYSA-N diethyl 1-(4-fluorophenyl)-3-hydroxy-4-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCC(=O)OC(C)(C)C)=C(C(=O)OCC)N1C1=CC=C(F)C=C1 RAYOYPGFNQGWHY-UHFFFAOYSA-N 0.000 claims 1
- LUTHIGWPFWTSAT-UHFFFAOYSA-N diethyl 1-(4-methoxyphenyl)-3-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]-4-phenylmethoxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C=1N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C(OCC(=O)OC(C)(C)C)C=1OCC1=CC=CC=C1 LUTHIGWPFWTSAT-UHFFFAOYSA-N 0.000 claims 1
- FUFNVNMNYLYAJY-UHFFFAOYSA-N diethyl 1-(4-tert-butylphenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(C(C)(C)C)C=C1 FUFNVNMNYLYAJY-UHFFFAOYSA-N 0.000 claims 1
- OXQRBJZZBRCHFR-UHFFFAOYSA-N diethyl 3,4-diacetyloxy-1-phenylpyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(OC(C)=O)C(OC(C)=O)=C(C(=O)OCC)N1C1=CC=CC=C1 OXQRBJZZBRCHFR-UHFFFAOYSA-N 0.000 claims 1
- MJPDWBFTQCXEQI-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(2-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=CC=C1OC MJPDWBFTQCXEQI-UHFFFAOYSA-N 0.000 claims 1
- GRXHDPCQALQSNC-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(3,4,5-trimethoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC(OC)=C(OC)C(OC)=C1 GRXHDPCQALQSNC-UHFFFAOYSA-N 0.000 claims 1
- GUGRRUPBUNBGJB-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(3-iodo-4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC)C(I)=C1 GUGRRUPBUNBGJB-UHFFFAOYSA-N 0.000 claims 1
- BIEFFZUJBNSISK-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(3-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=CC(OC)=C1 BIEFFZUJBNSISK-UHFFFAOYSA-N 0.000 claims 1
- LCIRRIRDAUTABX-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(3-phenoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=CC(OC=2C=CC=CC=2)=C1 LCIRRIRDAUTABX-UHFFFAOYSA-N 0.000 claims 1
- YWLCOURCGBQXSR-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(4-methylphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(C)C=C1 YWLCOURCGBQXSR-UHFFFAOYSA-N 0.000 claims 1
- QBMPMRKNPUVXME-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(4-phenoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C(C=C1)=CC=C1OC1=CC=CC=C1 QBMPMRKNPUVXME-UHFFFAOYSA-N 0.000 claims 1
- AGYOKYMHTFCXLO-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(4-propan-2-ylphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(C(C)C)C=C1 AGYOKYMHTFCXLO-UHFFFAOYSA-N 0.000 claims 1
- IZMBFZIVHJBXHE-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-(4-propoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound C1=CC(OCCC)=CC=C1N1C(C(=O)OCC)=C(O)C(O)=C1C(=O)OCC IZMBFZIVHJBXHE-UHFFFAOYSA-N 0.000 claims 1
- NZWBGMKAKSVLFP-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-(2-methoxyethoxy)phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)OCC)n1-c1ccc(OCCOC)cc1 NZWBGMKAKSVLFP-UHFFFAOYSA-N 0.000 claims 1
- QEZABXRONZJNRB-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-(3-morpholin-4-ylpropoxy)phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)OCC)n1-c1ccc(OCCCN2CCOCC2)cc1 QEZABXRONZJNRB-UHFFFAOYSA-N 0.000 claims 1
- AHKKBQJIPCFRFF-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-(trifluoromethoxy)phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC(F)(F)F)C=C1 AHKKBQJIPCFRFF-UHFFFAOYSA-N 0.000 claims 1
- PJYDQLXVXPVSII-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-(trifluoromethyl)phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(C(F)(F)F)C=C1 PJYDQLXVXPVSII-UHFFFAOYSA-N 0.000 claims 1
- VLWXWEMBNAEBGB-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-[(4-methoxyphenyl)methoxy]phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)OCC)n1-c1ccc(OCc2ccc(OC)cc2)cc1 VLWXWEMBNAEBGB-UHFFFAOYSA-N 0.000 claims 1
- PZGOYGOWYYHBNB-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)OCC)n1-c1ccc(OCCOCCOCCOC)cc1 PZGOYGOWYYHBNB-UHFFFAOYSA-N 0.000 claims 1
- DGSCHZZUSXHEJX-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-[4-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]phenyl]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)OCC)n1-c1ccc(OCCOCCOCCOCCOC)cc1 DGSCHZZUSXHEJX-UHFFFAOYSA-N 0.000 claims 1
- QTDVZSVRYIDDQL-UHFFFAOYSA-N diethyl 3,4-dihydroxy-1-phenylpyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=CC=C1 QTDVZSVRYIDDQL-UHFFFAOYSA-N 0.000 claims 1
- JPOVKZGFGMEKSS-UHFFFAOYSA-N diethyl 3-(2-amino-2-oxoethoxy)-1-(4-fluorophenyl)-4-hydroxypyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCC(N)=O)=C(C(=O)OCC)N1C1=CC=C(F)C=C1 JPOVKZGFGMEKSS-UHFFFAOYSA-N 0.000 claims 1
- JKQPJSGPOALDJN-UHFFFAOYSA-N diethyl 3-(2-amino-2-oxoethoxy)-4-hydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCC(N)=O)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1 JKQPJSGPOALDJN-UHFFFAOYSA-N 0.000 claims 1
- NOVUYIUZVOKHOW-UHFFFAOYSA-N diethyl 3-hydroxy-1-(4-methoxyphenyl)-4-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCC(=O)OC(C)(C)C)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1 NOVUYIUZVOKHOW-UHFFFAOYSA-N 0.000 claims 1
- JOISYQDUZKRXJO-UHFFFAOYSA-N diethyl 3-hydroxy-4-(2-hydroxyethoxy)-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound CCOC(=O)C1=C(O)C(OCCO)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1 JOISYQDUZKRXJO-UHFFFAOYSA-N 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- ZSZOLFFCCWPVAM-UHFFFAOYSA-N dimethyl 1-(4-bromophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound COC(=O)C1=C(O)C(O)=C(C(=O)OC)N1C1=CC=C(Br)C=C1 ZSZOLFFCCWPVAM-UHFFFAOYSA-N 0.000 claims 1
- PYEZJBAZPLJKTL-UHFFFAOYSA-N dimethyl 1-(4-chlorophenyl)-3,4-dihydroxypyrrole-2,5-dicarboxylate Chemical compound COC(=O)C1=C(O)C(O)=C(C(=O)OC)N1C1=CC=C(Cl)C=C1 PYEZJBAZPLJKTL-UHFFFAOYSA-N 0.000 claims 1
- AEBJWQDZDSQJOU-UHFFFAOYSA-N dimethyl 3,4-diacetyloxy-1-phenylpyrrole-2,5-dicarboxylate Chemical compound COC(=O)C1=C(OC(C)=O)C(OC(C)=O)=C(C(=O)OC)N1C1=CC=CC=C1 AEBJWQDZDSQJOU-UHFFFAOYSA-N 0.000 claims 1
- RLNHHFPBDYGLLN-UHFFFAOYSA-N dimethyl 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound COC(=O)C1=C(O)C(O)=C(C(=O)OC)N1C1=CC=C(OC)C=C1 RLNHHFPBDYGLLN-UHFFFAOYSA-N 0.000 claims 1
- FOGCUJWGZKTTCJ-UHFFFAOYSA-N dimethyl 3,4-dihydroxy-1-phenylpyrrole-2,5-dicarboxylate Chemical compound COC(=O)C1=C(O)C(O)=C(C(=O)OC)N1C1=CC=CC=C1 FOGCUJWGZKTTCJ-UHFFFAOYSA-N 0.000 claims 1
- HKLFPQMNKYONQX-UHFFFAOYSA-N dipropan-2-yl 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)OC(C)C)=C(O)C(O)=C1C(=O)OC(C)C HKLFPQMNKYONQX-UHFFFAOYSA-N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- YMQJWPSLYXOGMN-UHFFFAOYSA-N ditert-butyl 3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2,5-dicarboxylate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)OC(C)(C)C)=C(O)C(O)=C1C(=O)OC(C)(C)C YMQJWPSLYXOGMN-UHFFFAOYSA-N 0.000 claims 1
- LBZUTQSXPRDNKJ-UHFFFAOYSA-N ditert-butyl 3,4-dihydroxy-1-(4-nitrophenyl)pyrrole-2,5-dicarboxylate Chemical compound CC(C)(C)OC(=O)C1=C(O)C(O)=C(C(=O)OC(C)(C)C)N1C1=CC=C([N+]([O-])=O)C=C1 LBZUTQSXPRDNKJ-UHFFFAOYSA-N 0.000 claims 1
- 206010014599 encephalitis Diseases 0.000 claims 1
- BAMAEFPMBWZISW-UHFFFAOYSA-N ethyl 1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)-5-(2h-tetrazol-5-yl)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C2=NNN=N2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 BAMAEFPMBWZISW-UHFFFAOYSA-N 0.000 claims 1
- ZVELVOLBNZLUNJ-UHFFFAOYSA-N ethyl 1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)-5-pyridin-2-ylpyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2N=CC=CC=2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 ZVELVOLBNZLUNJ-UHFFFAOYSA-N 0.000 claims 1
- AWZXSCQLJRVKJX-UHFFFAOYSA-N ethyl 1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)-5-pyridin-3-ylpyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2C=NC=CC=2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 AWZXSCQLJRVKJX-UHFFFAOYSA-N 0.000 claims 1
- CEDPAGLENFJWMQ-UHFFFAOYSA-N ethyl 1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)-5-pyridin-4-ylpyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2C=CN=CC=2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 CEDPAGLENFJWMQ-UHFFFAOYSA-N 0.000 claims 1
- FLBFZCDJGLIQIQ-UHFFFAOYSA-N ethyl 1-(4-methoxyphenyl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2OC(C)=NN=2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 FLBFZCDJGLIQIQ-UHFFFAOYSA-N 0.000 claims 1
- XBXWSVWOBHMTPX-UHFFFAOYSA-N ethyl 1-[4-(3-diethoxyphosphorylpropoxy)phenyl]-5-(dimethylcarbamoyl)-3,4-dihydroxypyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OCCCP(=O)(OCC)OCC)cc1 XBXWSVWOBHMTPX-UHFFFAOYSA-N 0.000 claims 1
- WYTXKMSTRYUIHN-UHFFFAOYSA-N ethyl 3,4-bis(diethoxyphosphoryloxy)-5-(dimethylcarbamoyl)-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(OP(=O)(OCC)OCC)C(OP(=O)(OCC)OCC)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 WYTXKMSTRYUIHN-UHFFFAOYSA-N 0.000 claims 1
- DHBJGQVXIDDTTC-UHFFFAOYSA-N ethyl 3,4-diacetyloxy-5-(dimethylcarbamoyl)-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(OC(C)=O)C(OC(C)=O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 DHBJGQVXIDDTTC-UHFFFAOYSA-N 0.000 claims 1
- TVFBWRFTZRYEQM-UHFFFAOYSA-N ethyl 3,4-dihydroxy-1-(4-methoxyphenyl)-5-(2H-tetrazol-5-yl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(-c2nn[nH]n2)n1-c1ccc(OC)cc1 TVFBWRFTZRYEQM-UHFFFAOYSA-N 0.000 claims 1
- KRTAVIQVPAFLND-UHFFFAOYSA-N ethyl 3,4-dihydroxy-1-(4-methoxyphenyl)-5-(4-methylpiperazine-1-carbonyl)pyrrole-2-carboxylate Chemical compound C=1C=C(OC)C=CC=1N1C(C(=O)OCC)=C(O)C(O)=C1C(=O)N1CCN(C)CC1 KRTAVIQVPAFLND-UHFFFAOYSA-N 0.000 claims 1
- RLADPQONVGGUPG-UHFFFAOYSA-N ethyl 3,4-dihydroxy-1-(4-methoxyphenyl)-5-(methylcarbamoyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)NC)n1-c1ccc(OC)cc1 RLADPQONVGGUPG-UHFFFAOYSA-N 0.000 claims 1
- LFWMRWQGJVHFLJ-UHFFFAOYSA-N ethyl 3,4-dihydroxy-1-(4-methoxyphenyl)-5-(morpholine-4-carbonyl)pyrrole-2-carboxylate Chemical compound C=1C=C(OC)C=CC=1N1C(C(=O)OCC)=C(O)C(O)=C1C(=O)N1CCOCC1 LFWMRWQGJVHFLJ-UHFFFAOYSA-N 0.000 claims 1
- DWTBDNSKLIKOGT-UHFFFAOYSA-N ethyl 3,4-dihydroxy-1-(4-methoxyphenyl)-5-pyridin-2-ylpyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(-c2ccccn2)n1-c1ccc(OC)cc1 DWTBDNSKLIKOGT-UHFFFAOYSA-N 0.000 claims 1
- QTGUERDQURTWMP-UHFFFAOYSA-N ethyl 4-diethoxyphosphoryloxy-5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(OP(=O)(OCC)OCC)c(C(=O)N(C)C)n1-c1ccc(OC)cc1 QTGUERDQURTWMP-UHFFFAOYSA-N 0.000 claims 1
- FBQNZCXZZJCGNG-UHFFFAOYSA-N ethyl 5-(2-methoxyphenyl)-1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2C(=CC=CC=2)OC)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 FBQNZCXZZJCGNG-UHFFFAOYSA-N 0.000 claims 1
- ZIGYJWNJTXPBAM-UHFFFAOYSA-N ethyl 5-(4-ethyl-1,3-thiazol-2-yl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(-c2nc(CC)cs2)n1-c1ccc(OC)cc1 ZIGYJWNJTXPBAM-UHFFFAOYSA-N 0.000 claims 1
- NWCPQDVYWMQRSY-UHFFFAOYSA-N ethyl 5-(5-ethyl-1,3,4-oxadiazol-2-yl)-1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C=2OC(CC)=NN=2)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 NWCPQDVYWMQRSY-UHFFFAOYSA-N 0.000 claims 1
- KWESGDQFDJCDBF-UHFFFAOYSA-N ethyl 5-(dibutylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCCCN(CCCC)C(=O)C1=C(O)C(O)=C(C(=O)OCC)N1C1=CC=C(OC)C=C1 KWESGDQFDJCDBF-UHFFFAOYSA-N 0.000 claims 1
- PXYDLKSLNDQICJ-UHFFFAOYSA-N ethyl 5-(diethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(CC)CC)N1C1=CC=C(OC)C=C1 PXYDLKSLNDQICJ-UHFFFAOYSA-N 0.000 claims 1
- FUYBAWSWHFMXED-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-1-(4-fluorophenyl)-3,4-dihydroxypyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(F)C=C1 FUYBAWSWHFMXED-UHFFFAOYSA-N 0.000 claims 1
- KBTPQRHAFMOINT-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-1-(4-iodophenyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C(=O)N(C)C)N(C=2C=CC(I)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 KBTPQRHAFMOINT-UHFFFAOYSA-N 0.000 claims 1
- WTPPJTBHISKRRV-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-1-(4-methoxyphenyl)-3,4-bis(3-methoxypropanoyloxy)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(OC(=O)CCOC)C(OC(=O)CCOC)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 WTPPJTBHISKRRV-UHFFFAOYSA-N 0.000 claims 1
- YIYFEFGMARTRTD-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-bis(dimethylcarbamoyloxy)-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(OC(=O)N(C)C)C(OC(=O)N(C)C)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 YIYFEFGMARTRTD-UHFFFAOYSA-N 0.000 claims 1
- UBNUVMDEYUQRDW-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-bis[[2,2-dimethyl-3-(3-phosphonooxypropoxy)propanoyl]oxy]-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CC(C(=O)OC1=C(N(C(=C1OC(C(COCCCOP(=O)(O)O)(C)C)=O)C(=O)OCC)C1=CC=C(C=C1)OC)C(N(C)C)=O)(COCCCOP(=O)(O)O)C UBNUVMDEYUQRDW-UHFFFAOYSA-N 0.000 claims 1
- FDRUWMHNOCQLSN-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(3-iodo-4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C(I)=C1 FDRUWMHNOCQLSN-UHFFFAOYSA-N 0.000 claims 1
- SXTHRUMZWXQKSI-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-hydroxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(O)C=C1 SXTHRUMZWXQKSI-UHFFFAOYSA-N 0.000 claims 1
- VVTRQWNRKFXCCB-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-iodophenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(I)C=C1 VVTRQWNRKFXCCB-UHFFFAOYSA-N 0.000 claims 1
- MOSAQCXHHZZOMF-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-phosphonooxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OP(O)(O)=O)cc1 MOSAQCXHHZZOMF-UHFFFAOYSA-N 0.000 claims 1
- XDNMCQWHGILEGI-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-[4-(2-methoxyethoxy)phenyl]pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OCCOC)cc1 XDNMCQWHGILEGI-UHFFFAOYSA-N 0.000 claims 1
- SYQUQBUMLAZDPR-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-[4-(3-methylsulfonylpropoxy)phenyl]pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(OCCCS(C)(=O)=O)C=C1 SYQUQBUMLAZDPR-UHFFFAOYSA-N 0.000 claims 1
- KAPYLRABHREAJJ-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-[4-(3-morpholin-4-ylpropoxy)phenyl]pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(=O)N(C)C)N1C(C=C1)=CC=C1OCCCN1CCOCC1 KAPYLRABHREAJJ-UHFFFAOYSA-N 0.000 claims 1
- XIOXEIHKKDYPFP-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-[4-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]phenyl]pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OCCOCCOCCOCCOC)cc1 XIOXEIHKKDYPFP-UHFFFAOYSA-N 0.000 claims 1
- ZYKOLZDCPSZCFS-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-[4-[3-(4-methylpiperazin-1-yl)propoxy]phenyl]pyrrole-2-carboxylate Chemical compound CCOC(=O)c1c(O)c(O)c(C(=O)N(C)C)n1-c1ccc(OCCCN2CCN(C)CC2)cc1 ZYKOLZDCPSZCFS-UHFFFAOYSA-N 0.000 claims 1
- KXXHOAMJQSAVMQ-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-(phosphonooxymethoxy)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(OCOP(O)(O)=O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 KXXHOAMJQSAVMQ-UHFFFAOYSA-N 0.000 claims 1
- INZHJFDYYHFGFH-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-phosphonooxypyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(OP(O)(O)=O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 INZHJFDYYHFGFH-UHFFFAOYSA-N 0.000 claims 1
- BUDGCJRRYHDWOU-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-sulfamoyloxypyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(OS(N)(=O)=O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 BUDGCJRRYHDWOU-UHFFFAOYSA-N 0.000 claims 1
- QDUHUECQPWUOSR-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-4-(dimethylcarbamoyloxy)-3-hydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(OC(=O)N(C)C)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 QDUHUECQPWUOSR-UHFFFAOYSA-N 0.000 claims 1
- ZAJQHLQGSJYLOQ-UHFFFAOYSA-N ethyl 5-(dimethylcarbamoyl)-4-hydroxy-1-(4-methoxyphenyl)-3-(phosphonooxymethoxy)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(OCOP(O)(O)=O)C(O)=C(C(=O)N(C)C)N1C1=CC=C(OC)C=C1 ZAJQHLQGSJYLOQ-UHFFFAOYSA-N 0.000 claims 1
- FUJUFBVUSIOUKZ-UHFFFAOYSA-N ethyl 5-carbamoyl-1-(4-methoxyphenyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C(N)=O)N(C=2C=CC(OC)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 FUJUFBVUSIOUKZ-UHFFFAOYSA-N 0.000 claims 1
- KFQKIYLCAGDAIB-UHFFFAOYSA-N ethyl 5-carbamoyl-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C(N)=O)N1C1=CC=C(OC)C=C1 KFQKIYLCAGDAIB-UHFFFAOYSA-N 0.000 claims 1
- FKQFUBBNLJKLAX-UHFFFAOYSA-N ethyl 5-cyano-1-(4-fluorophenyl)-3,4-bis(phenylmethoxy)pyrrole-2-carboxylate Chemical compound C=1C=CC=CC=1COC1=C(C#N)N(C=2C=CC(F)=CC=2)C(C(=O)OCC)=C1OCC1=CC=CC=C1 FKQFUBBNLJKLAX-UHFFFAOYSA-N 0.000 claims 1
- IZDPPEMUXYQXPI-UHFFFAOYSA-N ethyl 5-cyano-1-(4-fluorophenyl)-3,4-dihydroxypyrrole-2-carboxylate Chemical compound CCOC(=O)C1=C(O)C(O)=C(C#N)N1C1=CC=C(F)C=C1 IZDPPEMUXYQXPI-UHFFFAOYSA-N 0.000 claims 1
- 229940124307 fluoroquinolone Drugs 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 206010017931 gastrointestinal anthrax Diseases 0.000 claims 1
- 239000002955 immunomodulating agent Substances 0.000 claims 1
- 229940121354 immunomodulator Drugs 0.000 claims 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 claims 1
- 206010023332 keratitis Diseases 0.000 claims 1
- 239000003120 macrolide antibiotic agent Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 208000004593 pneumococcal meningitis Diseases 0.000 claims 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 claims 1
- RJERKPDKXSHLMF-UHFFFAOYSA-N propan-2-yl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)OC(C)C RJERKPDKXSHLMF-UHFFFAOYSA-N 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 229960003292 rifamycin Drugs 0.000 claims 1
- HJYYPODYNSCCOU-ODRIEIDWSA-N rifamycin SV Chemical compound OC1=C(C(O)=C2C)C3=C(O)C=C1NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@H](C)[C@@H](OC)\C=C\O[C@@]1(C)OC2=C3C1=O HJYYPODYNSCCOU-ODRIEIDWSA-N 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
- 208000022218 streptococcal pneumonia Diseases 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- JXOOHNNNIWTSPG-UHFFFAOYSA-N tert-butyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrole-2-carboxylate Chemical compound C1=CC(OC)=CC=C1N1C(C(=O)N(C)C)=C(O)C(O)=C1C(=O)OC(C)(C)C JXOOHNNNIWTSPG-UHFFFAOYSA-N 0.000 claims 1
- KTJUHIFIPKDQRT-UHFFFAOYSA-N tert-butyl n-[5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)pyrrol-2-yl]sulfonylcarbamate Chemical compound C1=CC(OC)=CC=C1N1C(S(=O)(=O)NC(=O)OC(C)(C)C)=C(O)C(O)=C1C(=O)N(C)C KTJUHIFIPKDQRT-UHFFFAOYSA-N 0.000 claims 1
- 229960002180 tetracycline Drugs 0.000 claims 1
- 229930101283 tetracycline Natural products 0.000 claims 1
- 235000019364 tetracycline Nutrition 0.000 claims 1
- 150000003522 tetracyclines Chemical class 0.000 claims 1
- 239000003053 toxin Substances 0.000 claims 1
- 231100000765 toxin Toxicity 0.000 claims 1
- 108700012359 toxins Proteins 0.000 claims 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 claims 1
- 229940126085 β‑Lactamase Inhibitor Drugs 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11191986.6A EP2602248A1 (en) | 2011-12-05 | 2011-12-05 | Novel pyrrole compounds |
| EP11191986.6 | 2011-12-05 | ||
| PCT/GB2012/053022 WO2013083975A2 (en) | 2011-12-05 | 2012-12-05 | Novel pyrrole derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015500824A JP2015500824A (ja) | 2015-01-08 |
| JP2015500824A5 true JP2015500824A5 (https=) | 2016-01-28 |
Family
ID=47846072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014545346A Pending JP2015500824A (ja) | 2011-12-05 | 2012-12-05 | 新規ピロール誘導体 |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US9221756B2 (https=) |
| EP (2) | EP2602248A1 (https=) |
| JP (1) | JP2015500824A (https=) |
| CN (1) | CN104011019B (https=) |
| AU (1) | AU2012349829A1 (https=) |
| BR (1) | BR112014012983A2 (https=) |
| CA (1) | CA2855351A1 (https=) |
| HK (1) | HK1201836A1 (https=) |
| IL (1) | IL232502A0 (https=) |
| MX (1) | MX2014006686A (https=) |
| SG (1) | SG11201402097XA (https=) |
| WO (1) | WO2013083975A2 (https=) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2602248A1 (en) | 2011-12-05 | 2013-06-12 | University Of Leicester | Novel pyrrole compounds |
| GB201309932D0 (en) * | 2013-06-04 | 2013-07-17 | Univ Leicester | Novel pyrrole derivative |
| GB201309960D0 (en) * | 2013-06-04 | 2013-07-17 | Univ Leicester | Novel pyrrole derivatives |
| GB201309934D0 (en) * | 2013-06-04 | 2013-07-17 | Univ Leicester | Novel pyrrole derivatives |
| GB201309935D0 (en) * | 2013-06-04 | 2013-07-17 | Univ Leicester | Novel pyrrole derivatives |
| GB201310126D0 (en) * | 2013-06-06 | 2013-07-24 | Univ Leicester | Novel pyrrole derivatives |
| CN108129476A (zh) * | 2017-11-27 | 2018-06-08 | 华中农业大学 | 一种杂环内酰胺衍生物及其用于作物病原菌杀菌剂的用途 |
| GB201905721D0 (en) | 2019-04-24 | 2019-06-05 | Univ Dundee | Compounds |
| CN114736201B (zh) * | 2022-06-13 | 2022-09-02 | 奥锐特药业(天津)有限公司 | 芜地溴铵中间体的制备方法 |
Family Cites Families (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3224939A (en) * | 1963-03-21 | 1965-12-21 | Lilly Co Eli | Method for treating helminthic infections |
| US3427305A (en) * | 1966-11-01 | 1969-02-11 | Searle & Co | 5 - ((halo/alkoxy)phenyl) - 1 - (p - sulfonamido(phenyl/benzyl)) - 2 - pyrrolepropionic acids |
| GB1311336A (en) * | 1970-09-07 | 1973-03-28 | Ici Ltd | Quaternary salts of pyrolylpyridine derivatives |
| US4637829A (en) | 1984-04-27 | 1987-01-20 | Ciba-Geigy Corporation | Sulfonylureas |
| US5019130A (en) | 1989-11-03 | 1991-05-28 | Clairol Incorporated | Substituted N-aryl pyrroles in oxidative hair dye compositions |
| US5175180A (en) | 1990-12-20 | 1992-12-29 | G. D. Searle & Co. | N-substituted n-(alpha-triazolyl-toluyl)pyrrole compounds and use for treatment of circulatory disorders |
| JP3374922B2 (ja) | 1991-05-09 | 2003-02-10 | 日産化学工業株式会社 | 複素環式第3級アミンの製造方法 |
| CA2119155C (en) | 1991-10-18 | 1999-06-15 | Dennis Paul Phillion | Fungicides for the control of take-all disease of plants |
| US5484937A (en) | 1992-08-04 | 1996-01-16 | G.D. Searle & Co. | N-substituted N-(α-triazolyl-toluyl)pyrrole compounds for treatment of circulatory disorders |
| DE4217952A1 (de) | 1992-05-30 | 1993-12-02 | Basf Ag | Chinoxalin-2,3(1H,4H)-dione |
| US5324747A (en) | 1992-07-15 | 1994-06-28 | Hoffmann-La Roche Inc. | N-substituted anilines, inhibitors of phospholipases A2 |
| AU5891494A (en) | 1993-01-29 | 1994-08-15 | Nippon Soda Co., Ltd. | Heterocyclic derivative |
| US5451597A (en) | 1993-05-27 | 1995-09-19 | G.D. Searle & Co. | Treatment of circulatory disorders using n-substituted (α-imidazolyl-toluyl) pyrrole angiotensin II antagonists |
| DE4412334A1 (de) | 1994-04-11 | 1995-10-19 | Hoechst Ag | Substituierte N-Heteroaroylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| DE4445088A1 (de) | 1994-12-16 | 1996-06-20 | Ibv Ind Bioverfahren | Mehrkomponentenbleichsystem aus Oxidoreductasen, Oxidationsmitteln, Mediatoren und Mediator-verstärkenden oder recyclierenden Verbindungen zur Verwendung mit waschaktiven Substanzen |
| EP0717143A1 (de) | 1994-12-16 | 1996-06-19 | Lignozym GmbH | Mehrkomponentensystem zum Verändern, Abbau oder Bleichen von Lignin, ligninhaltigen Materialien oder ähnlichen Stoffen sowie Verfahren zu seiner Anwendung |
| DK0807112T3 (da) | 1995-02-03 | 2001-12-17 | Upjohn Co | Antimikrobiel heteroaromatisk ringsubstitueret phenyloxazolidinon |
| WO1996033994A1 (en) | 1995-04-28 | 1996-10-31 | Nippon Soda Co., Ltd. | Amino-substituted derivatives, process for the preparation thereof, and herbicide |
| WO1997047299A1 (en) * | 1996-06-12 | 1997-12-18 | 3-Dimensional Pharmaceuticals, Inc. | Amidino and guanidino heterocyclic protease inhibitors |
| AU6357896A (en) | 1996-06-19 | 1998-01-07 | Hans-Peter Call | Multicomponent system for use with detergent substances |
| JPH10181212A (ja) | 1996-10-22 | 1998-07-07 | Fuji Photo Film Co Ltd | 光学的情報記録媒体 |
| JP3399756B2 (ja) | 1996-10-22 | 2003-04-21 | 三菱製紙株式会社 | 平版印刷版の処理方法 |
| DE19718742A1 (de) | 1997-05-02 | 1998-11-05 | Hoechst Ag | Verfahren zur Herstellung von aromatischen Aldehyden durch katalytische Gasphasenhydrierung der Carbonsäuren |
| DE69842143D1 (de) | 1997-10-24 | 2011-04-07 | Nissan Chemical Ind Ltd | Sulfamoyl-verbindungen und bakterizide für landwirtschaft oder gartenbau |
| US6069141A (en) | 1998-02-13 | 2000-05-30 | Pharmacia & Upjohn Company | Substituted aminophenyl isoxazoline derivatives useful as antimicrobials |
| JP2000131839A (ja) * | 1998-08-19 | 2000-05-12 | Mitsubishi Chemicals Corp | 光重合性組成物及び光重合性画像形成材料 |
| JP2000086713A (ja) | 1998-09-14 | 2000-03-28 | Toyo Ink Mfg Co Ltd | 硬化性組成物、それを用いた硬化皮膜の形成方法および硬化物 |
| JP2000280621A (ja) | 1999-03-30 | 2000-10-10 | Mitsui Chemicals Inc | 光記録媒体 |
| US6350761B1 (en) * | 1999-07-30 | 2002-02-26 | Berlex Laboratories, Inc. | Benzenamine derivatives as anti-coagulants |
| IT1313601B1 (it) | 1999-08-05 | 2002-09-09 | Isagro Ricerca Srl | Fenilpirazoli ad attivita' erbicida |
| EP1379522B1 (en) | 2001-04-12 | 2005-01-26 | F. Hoffmann-La Roche Ag | DIHYDRO-BENZO(b)(1,4)DIAZEPIN-2-ONE DERIVATIVES AS MGLUR2 ANTAGONISTS I |
| GB0119172D0 (en) | 2001-08-06 | 2001-09-26 | Melacure Therapeutics Ab | Phenyl pyrrole derivatives |
| US7064218B2 (en) | 2001-12-26 | 2006-06-20 | Genelabs Technologies, Inc. | Aromatic compounds and poly(oxyalkylene) containing aromatic compounds possessing antibacterial, antifungal or antitumor activity |
| KR20040091720A (ko) | 2002-03-12 | 2004-10-28 | 와이어쓰 | N1-(2'-피리딜)-1,2-프로판디아민 설팜산의 제조방법 및생물학적 활성 피페라진 합성시의 이의 용도 |
| US6803379B2 (en) | 2002-06-04 | 2004-10-12 | Jose A. Fernandez-Pol | Pharmacological agents and methods of treatment that inactivate pathogenic prokaryotic and eukaryotic cells and viruses by attacking highly conserved domains in structural metalloprotein and metalloenzyme targets |
| KR100482276B1 (ko) * | 2002-08-12 | 2005-04-13 | 한국과학기술연구원 | 피롤계 화합물, 그 중합체 및 이들을 이용한 el 소자 |
| FR2844797B1 (fr) | 2002-09-24 | 2004-10-22 | Servier Lab | Nouveau procede de synthese industriel des tetraesters de l'acide 5-[bis (carboxymethyl)]-3-carboxymethyl-4-cyano-2- thiophenecarboxylique, et application a la synthese des sels bivalents de l'acide ranelique et de leurs hydrates |
| WO2004101531A1 (en) | 2003-04-29 | 2004-11-25 | Dr. Reddy's Laboratories Ltd. | Antiinfective 1,2,3-triazole derivatives, process for their preparation and pharmaceutical compositions containing them |
| JP2005215443A (ja) * | 2004-01-30 | 2005-08-11 | Fuji Photo Film Co Ltd | 重合性組成物及びそれを用いた画像形成材料 |
| JP4606749B2 (ja) * | 2004-02-16 | 2011-01-05 | 富士フイルム株式会社 | 平版印刷方法及びそれに用いる平版印刷版原版 |
| JP2008506776A (ja) * | 2004-07-19 | 2008-03-06 | メルク エンド カムパニー インコーポレーテッド | ヒストン脱アセチル化酵素阻害剤 |
| ES2534605T3 (es) | 2004-08-23 | 2015-04-24 | Eli Lilly And Company | Agentes receptores de la histamina H3, preparación y usos terapéuticos |
| CN100355748C (zh) | 2004-09-20 | 2007-12-19 | 中国人民解放军军事医学科学院毒物药物研究所 | 芳酰肼类化合物及其用于制备免疫抑制剂的用途 |
| JP4755829B2 (ja) | 2005-01-11 | 2011-08-24 | 花王株式会社 | ピロリジン誘導体の製造方法 |
| CN100562514C (zh) | 2005-07-22 | 2009-11-25 | 中国科学院上海药物研究所 | 一类取代丙酰胺衍生物、其制备方法和用途 |
| WO2007027878A2 (en) | 2005-08-31 | 2007-03-08 | Emergent Product Development Gaithersburg Inc. | 4-substituted 2-aryloxyphenol derivatives as antibacterial agents |
| CA2649861A1 (en) * | 2006-04-26 | 2007-11-08 | Merck & Co., Inc. | Disubstituted aniline compounds |
| CL2007002097A1 (es) | 2006-07-20 | 2008-01-18 | Smithkline Beecham Corp | Compuestos derivados de pirrolidina o morfolina antagonistas de urotensina ii; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar insuficiencia cardiaca congestiva, insuficiencia cardiaca isquemica, angina, isquemia del miocardio, vejiga hiperactiva, asma y/o copd, entre otras. |
| ES2614931T3 (es) | 2006-08-04 | 2017-06-02 | Beth Israel Deaconess Medical Center | Inhibidores de la piruvato cinasa y métodos de tratamiento de enfermedad |
| PT2079678E (pt) * | 2006-10-31 | 2013-03-05 | Cadila Healthcare Ltd | Agonista seletivo do rt-beta 1 |
| US7776877B2 (en) | 2007-06-22 | 2010-08-17 | Chemocentryx, Inc. | N-(2-(hetaryl)aryl) arylsulfonamides and N-(2-(hetaryl) hetaryl arylsulfonamides |
| US8552208B2 (en) | 2007-09-11 | 2013-10-08 | University of Tennesseee Research Foundation | Analogs of tetramic acid |
| WO2009073973A1 (en) | 2007-12-11 | 2009-06-18 | Merck Frosst Canada Ltd. | Novel heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| JP2010059293A (ja) * | 2008-09-03 | 2010-03-18 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用材料ならびに有機エレクトロルミネッセンス素子 |
| JP5620365B2 (ja) | 2008-03-21 | 2014-11-05 | エンソン インコーポレイテッド | 多官能分子システムを用いた積層体への金属の接着促進 |
| NZ592603A (en) | 2008-10-21 | 2013-02-22 | Metabolex Inc | Aryl gpr120 receptor agonists and uses thereof |
| WO2010103473A1 (en) | 2009-03-10 | 2010-09-16 | Chu De Brest | Method of treatment of polycystic diseases and chronic lymphocytic leukemia |
| FR2943058B1 (fr) | 2009-03-11 | 2011-06-03 | Centre Nat Rech Scient | Derives de pyrazolo°1,5-a!-1,3,5-triazines, leur preparation et leur application en therapeutique. |
| CN101853963A (zh) | 2009-03-30 | 2010-10-06 | 张家港市国泰华荣化工新材料有限公司 | 防过充的锂离子电池电解液及由其制备的锂离子电池 |
| UA118080C2 (uk) * | 2009-06-11 | 2018-11-26 | Еббві Айрленд Анлімітед Компані | Противірусні сполуки |
| WO2011043479A1 (ja) | 2009-10-09 | 2011-04-14 | 田辺三菱製薬株式会社 | 脳梗塞治療薬 |
| WO2011043480A1 (ja) * | 2009-10-09 | 2011-04-14 | 田辺三菱製薬株式会社 | ホモシステイン合成酵素阻害薬 |
| KR20140085437A (ko) | 2011-08-29 | 2014-07-07 | 피티씨 테라퓨틱스, 인크. | 항균 화합물 및 이의 사용 방법 |
| EP2602248A1 (en) | 2011-12-05 | 2013-06-12 | University Of Leicester | Novel pyrrole compounds |
| GB201309935D0 (en) * | 2013-06-04 | 2013-07-17 | Univ Leicester | Novel pyrrole derivatives |
-
2011
- 2011-12-05 EP EP11191986.6A patent/EP2602248A1/en not_active Ceased
-
2012
- 2012-12-05 MX MX2014006686A patent/MX2014006686A/es unknown
- 2012-12-05 HK HK15102414.7A patent/HK1201836A1/xx unknown
- 2012-12-05 JP JP2014545346A patent/JP2015500824A/ja active Pending
- 2012-12-05 AU AU2012349829A patent/AU2012349829A1/en not_active Abandoned
- 2012-12-05 CA CA2855351A patent/CA2855351A1/en not_active Abandoned
- 2012-12-05 SG SG11201402097XA patent/SG11201402097XA/en unknown
- 2012-12-05 WO PCT/GB2012/053022 patent/WO2013083975A2/en not_active Ceased
- 2012-12-05 EP EP12830899.6A patent/EP2788324A2/en not_active Withdrawn
- 2012-12-05 CN CN201280060023.0A patent/CN104011019B/zh not_active Expired - Fee Related
- 2012-12-05 US US14/360,365 patent/US9221756B2/en not_active Expired - Fee Related
- 2012-12-05 BR BR112014012983A patent/BR112014012983A2/pt not_active IP Right Cessation
-
2014
- 2014-05-08 IL IL232502A patent/IL232502A0/en unknown
-
2015
- 2015-10-30 US US14/928,461 patent/US20160046576A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015500824A5 (https=) | ||
| KR100882377B1 (ko) | 치환된 이속사졸 및 항생제로서의 이들의 용도 | |
| Tanitame et al. | Synthesis and antibacterial activity of novel and potent DNA gyrase inhibitors with azole ring | |
| AU2004304717B2 (en) | Substituted arylpyrazoles as parasiticidal agents | |
| DE60210654T2 (de) | Aryl substituierte oxazolidinone mit antibacterieller activität | |
| AU2006257647A1 (en) | Substituted arylpyrazoles for use against parasites | |
| CN104011019B (zh) | 吡咯衍生物 | |
| ES2533095T3 (es) | Agonistas de receptores de esfingosina-1-fosfato | |
| EP2379546A1 (en) | Monocarbams | |
| EP1646629A2 (en) | Cyclopropyl group substituted oxazolidinone antibiotics and derivatives thereof | |
| RU2468023C1 (ru) | Новые производные оксазолидинона с циклическим амидоксимом или циклическим амидразоном и содержащие их фармацевтические композиции | |
| KR20110094305A (ko) | 박테리아 감염에 대항하는 2-(피페리딘-1-일)-4-아졸릴-티아졸-5-카르복실산 유도체 | |
| KR20110051266A (ko) | 살진균제로서의 헤테로사이클 치환된 아닐리노피리미딘 | |
| KR100652470B1 (ko) | 사이클로알킬 치환 아미노메틸피롤리딘 유도체 | |
| WO1998052939A1 (en) | Cis-disubstituted aminocycloalkyl-pyrrolidine derivatives | |
| WO2000053594A1 (en) | Aminomethylpyrrolidine derivatives having aromatic substituents | |
| JPS6056989A (ja) | β−ラクタム抗バクテリア剤 | |
| EP3347343B1 (en) | Azetidinimines as carbapenemases inhibitors | |
| CA2997851C (en) | Azetidinimines as carbapenemases inhibitors | |
| WO2007040326A1 (en) | A novel oxazolidinone formamide derivative and preparation method therof | |
| EP4467539A1 (en) | Oxazole derivative compound having antibacterial activity and medical use thereof | |
| RU2021104896A (ru) | Пестицидно-активные бициклические гетероароматические соединения | |
| HK40023323A (en) | Compound having cyclic structure | |
| HK1096824B (en) | Substituted arylpyrazoles as parasiticidal agents | |
| WO2008010070A3 (en) | Novel oxazolidinone derivatives |