JP4226818B2 - ベータ−ラクタマーゼのスルフォンアミドメチルホスホン酸阻害剤 - Google Patents
ベータ−ラクタマーゼのスルフォンアミドメチルホスホン酸阻害剤 Download PDFInfo
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- JP4226818B2 JP4226818B2 JP2001507847A JP2001507847A JP4226818B2 JP 4226818 B2 JP4226818 B2 JP 4226818B2 JP 2001507847 A JP2001507847 A JP 2001507847A JP 2001507847 A JP2001507847 A JP 2001507847A JP 4226818 B2 JP4226818 B2 JP 4226818B2
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- Prior art keywords
- alkyl
- aryl
- group
- amino
- heteroaryl
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- 102000006635 beta-lactamase Human genes 0.000 title description 43
- 108090000204 Dipeptidase 1 Proteins 0.000 title description 38
- 239000003112 inhibitor Substances 0.000 title description 11
- 239000002253 acid Substances 0.000 title description 7
- 230000001580 bacterial effect Effects 0.000 claims abstract description 38
- 230000003115 biocidal effect Effects 0.000 claims abstract description 32
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 21
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 217
- 125000003118 aryl group Chemical group 0.000 claims description 157
- 150000001875 compounds Chemical class 0.000 claims description 144
- 125000001072 heteroaryl group Chemical group 0.000 claims description 130
- -1 cyano, amino, carboxy, hydroxy Chemical group 0.000 claims description 113
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 60
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 60
- 229910052739 hydrogen Inorganic materials 0.000 claims description 50
- 239000001257 hydrogen Substances 0.000 claims description 43
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 41
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 41
- 125000005843 halogen group Chemical group 0.000 claims description 37
- 125000001424 substituent group Chemical group 0.000 claims description 37
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 36
- 229940124530 sulfonamide Drugs 0.000 claims description 34
- 125000001188 haloalkyl group Chemical group 0.000 claims description 32
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 28
- 125000004442 acylamino group Chemical group 0.000 claims description 28
- 125000004423 acyloxy group Chemical group 0.000 claims description 28
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 28
- 125000005116 aryl carbamoyl group Chemical group 0.000 claims description 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 125000003545 alkoxy group Chemical group 0.000 claims description 25
- 125000004104 aryloxy group Chemical group 0.000 claims description 25
- 150000003839 salts Chemical class 0.000 claims description 25
- 150000003456 sulfonamides Chemical class 0.000 claims description 25
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 23
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 22
- 239000003242 anti bacterial agent Substances 0.000 claims description 21
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 9
- 239000003085 diluting agent Substances 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims description 9
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 9
- 125000001624 naphthyl group Chemical group 0.000 claims description 9
- 125000005493 quinolyl group Chemical group 0.000 claims description 9
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 8
- 239000003937 drug carrier Substances 0.000 claims description 8
- 125000004076 pyridyl group Chemical group 0.000 claims description 8
- 125000001544 thienyl group Chemical group 0.000 claims description 8
- 150000001408 amides Chemical class 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 7
- 125000002541 furyl group Chemical group 0.000 claims description 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 6
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 claims description 5
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000004987 dibenzofuryl group Chemical group C1(=CC=CC=2OC3=C(C21)C=CC=C3)* 0.000 claims description 5
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 3
- 125000001041 indolyl group Chemical group 0.000 claims description 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 3
- 125000002971 oxazolyl group Chemical group 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 3
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 26
- 125000004422 alkyl sulphonamide group Chemical group 0.000 claims 25
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 24
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 13
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
- 238000006467 substitution reaction Methods 0.000 claims 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 2
- 241000255925 Diptera Species 0.000 claims 1
- 235000010290 biphenyl Nutrition 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 85
- 239000003781 beta lactamase inhibitor Substances 0.000 abstract description 55
- 229940126813 beta-lactamase inhibitor Drugs 0.000 abstract description 55
- 239000000203 mixture Substances 0.000 abstract description 19
- 150000003952 β-lactams Chemical class 0.000 abstract description 5
- 229930014626 natural product Natural products 0.000 abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 60
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
- BFXHJFKKRGVUMU-UHFFFAOYSA-N 4-fluorobenzenesulfonyl chloride Chemical compound FC1=CC=C(S(Cl)(=O)=O)C=C1 BFXHJFKKRGVUMU-UHFFFAOYSA-N 0.000 description 41
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 32
- 229940126085 β‑Lactamase Inhibitor Drugs 0.000 description 32
- 239000000243 solution Substances 0.000 description 27
- 239000007787 solid Substances 0.000 description 26
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 24
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 23
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 21
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 17
- RSOPTYAZDFSMTN-UHFFFAOYSA-N 2-chloropyridin-3-ol Chemical compound OC1=CC=CN=C1Cl RSOPTYAZDFSMTN-UHFFFAOYSA-N 0.000 description 16
- 238000012360 testing method Methods 0.000 description 16
- 229940088710 antibiotic agent Drugs 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 15
- 239000003782 beta lactam antibiotic agent Substances 0.000 description 13
- 238000003818 flash chromatography Methods 0.000 description 13
- 125000000623 heterocyclic group Chemical group 0.000 description 13
- 239000002132 β-lactam antibiotic Substances 0.000 description 13
- 229940124586 β-lactam antibiotics Drugs 0.000 description 13
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 description 12
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000908 ammonium hydroxide Substances 0.000 description 12
- 229940002612 prodrug Drugs 0.000 description 12
- 239000000651 prodrug Substances 0.000 description 12
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 12
- 102000004190 Enzymes Human genes 0.000 description 11
- 108090000790 Enzymes Proteins 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 241000894006 Bacteria Species 0.000 description 10
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 8
- 238000004113 cell culture Methods 0.000 description 8
- 102000030899 Serine-Type D-Ala-D-Ala Carboxypeptidase Human genes 0.000 description 7
- 108010004832 Serine-Type D-Ala-D-Ala Carboxypeptidase Proteins 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 230000002079 cooperative effect Effects 0.000 description 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 6
- 235000019439 ethyl acetate Nutrition 0.000 description 6
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 108020004256 Beta-lactamase Proteins 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 5
- IYYIVELXUANFED-UHFFFAOYSA-N bromo(trimethyl)silane Chemical compound C[Si](C)(C)Br IYYIVELXUANFED-UHFFFAOYSA-N 0.000 description 5
- 230000000875 corresponding effect Effects 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- 150000005690 diesters Chemical class 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- VTUQHEGUXYKLIU-UHFFFAOYSA-M sodium;(2-chloropyridin-3-yl)oxy-[[(4-fluorophenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].C=1C=CN=C(Cl)C=1OP(=O)([O-])CNS(=O)(=O)C1=CC=C(F)C=C1 VTUQHEGUXYKLIU-UHFFFAOYSA-M 0.000 description 5
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 5
- 230000002195 synergetic effect Effects 0.000 description 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000007993 MOPS buffer Substances 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 229930040373 Paraformaldehyde Natural products 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- DRUIESSIVFYOMK-UHFFFAOYSA-N Trichloroacetonitrile Chemical compound ClC(Cl)(Cl)C#N DRUIESSIVFYOMK-UHFFFAOYSA-N 0.000 description 4
- 125000002877 alkyl aryl group Chemical group 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- XNTWONAICPPJDM-UHFFFAOYSA-N furan-3-sulfonamide Chemical compound NS(=O)(=O)C=1C=COC=1 XNTWONAICPPJDM-UHFFFAOYSA-N 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000002054 inoculum Substances 0.000 description 4
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 4
- 235000019341 magnesium sulphate Nutrition 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 4
- 229920002866 paraformaldehyde Polymers 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 4
- JFSCAMOLMXOBPM-REOHCLBHSA-N (2S)-3-hydroxy-2-nitramidopropanoic acid Chemical compound [N+](=O)([O-])N[C@@H](CO)C(=O)O JFSCAMOLMXOBPM-REOHCLBHSA-N 0.000 description 3
- UZMQSZBTFGHLAH-UHFFFAOYSA-N 1-benzothiophene-2-sulfonamide Chemical compound C1=CC=C2SC(S(=O)(=O)N)=CC2=C1 UZMQSZBTFGHLAH-UHFFFAOYSA-N 0.000 description 3
- KTFDYVNEGTXQCV-UHFFFAOYSA-N 2-Thiophenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CS1 KTFDYVNEGTXQCV-UHFFFAOYSA-N 0.000 description 3
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 229930186147 Cephalosporin Natural products 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 241000588697 Enterobacter cloacae Species 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- 229930182555 Penicillin Natural products 0.000 description 3
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- LDMVRAGEGIBRCJ-UHFFFAOYSA-N [NH4+].NCP([O-])(=O)Oc1ccc(cc1)[N+]([O-])=O Chemical compound [NH4+].NCP([O-])(=O)Oc1ccc(cc1)[N+]([O-])=O LDMVRAGEGIBRCJ-UHFFFAOYSA-N 0.000 description 3
- 239000002168 alkylating agent Substances 0.000 description 3
- 229940100198 alkylating agent Drugs 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- KGOJOGFECFDNOF-UHFFFAOYSA-N azane;[1-benzothiophen-2-ylsulfonyl(methyl)amino]methyl-(4-nitrophenoxy)phosphinic acid Chemical compound N.C=1C2=CC=CC=C2SC=1S(=O)(=O)N(C)CP(O)(=O)OC1=CC=C([N+]([O-])=O)C=C1 KGOJOGFECFDNOF-UHFFFAOYSA-N 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- XEYDTPFVYTVHTI-UHFFFAOYSA-N bromomethylsilane Chemical compound [SiH3]CBr XEYDTPFVYTVHTI-UHFFFAOYSA-N 0.000 description 3
- 229940124587 cephalosporin Drugs 0.000 description 3
- 150000001780 cephalosporins Chemical class 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- BJXYHBKEQFQVES-NWDGAFQWSA-N enpatoran Chemical compound N[C@H]1CN(C[C@H](C1)C(F)(F)F)C1=C2C=CC=NC2=C(C=C1)C#N BJXYHBKEQFQVES-NWDGAFQWSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 229940049954 penicillin Drugs 0.000 description 3
- 229940100595 phenylacetaldehyde Drugs 0.000 description 3
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 3
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- JQJOGAGLBDBMLU-UHFFFAOYSA-N pyridine-2-sulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=N1 JQJOGAGLBDBMLU-UHFFFAOYSA-N 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 3
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 2
- LCEWRJZMWNEILY-UHFFFAOYSA-N 1,4-dichloro-2-(2,2-diethoxyethylsulfanyl)benzene Chemical compound CCOC(OCC)CSC1=CC(Cl)=CC=C1Cl LCEWRJZMWNEILY-UHFFFAOYSA-N 0.000 description 2
- HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical compound C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 2
- UUSLLECLCKTJQF-UHFFFAOYSA-N 2-(bromomethyl)isoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(CBr)C(=O)C2=C1 UUSLLECLCKTJQF-UHFFFAOYSA-N 0.000 description 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 2
- 238000004679 31P NMR spectroscopy Methods 0.000 description 2
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- 150000002989 phenols Chemical class 0.000 description 1
- OAHKWDDSKCRNFE-UHFFFAOYSA-N phenylmethanesulfonyl chloride Chemical compound ClS(=O)(=O)CC1=CC=CC=C1 OAHKWDDSKCRNFE-UHFFFAOYSA-N 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000006308 propyl amino group Chemical group 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- JQXXHWHPUNPDRT-WLSIYKJHSA-N rifampicin Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C([O-])=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N1CC[NH+](C)CC1 JQXXHWHPUNPDRT-WLSIYKJHSA-N 0.000 description 1
- 229960001225 rifampicin Drugs 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- DIUIDFGHVYSEFY-UHFFFAOYSA-M sodium (2-chloropyridin-3-yl)oxy-[(furan-3-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[O-]P(=O)(CNS(=O)(=O)c1ccoc1)Oc1cccnc1Cl DIUIDFGHVYSEFY-UHFFFAOYSA-M 0.000 description 1
- RPHYYGNFTQXIJO-UHFFFAOYSA-M sodium (2-chloropyridin-3-yl)oxy-[(isoquinolin-5-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[O-]P(=O)(CNS(=O)(=O)c1cccc2cnccc12)Oc1cccnc1Cl RPHYYGNFTQXIJO-UHFFFAOYSA-M 0.000 description 1
- KUTOEXNESFAJAJ-UHFFFAOYSA-M sodium (2-chloropyridin-3-yl)oxy-[(pyridin-2-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].ClC1=NC=CC=C1OP([O-])(=O)CNS(=O)(=O)C1=NC=CC=C1 KUTOEXNESFAJAJ-UHFFFAOYSA-M 0.000 description 1
- BNAJTBYKCDNRSL-UHFFFAOYSA-M sodium (2-chloropyridin-3-yl)oxy-[[(4-phenylphenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].ClC1=NC=CC=C1OP([O-])(=O)CNS(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1 BNAJTBYKCDNRSL-UHFFFAOYSA-M 0.000 description 1
- VPCYPLDEXOIOMT-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[(pyridin-2-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=NC=CC=C1 VPCYPLDEXOIOMT-UHFFFAOYSA-M 0.000 description 1
- IMZHLZMTAYFYRT-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[(pyridin-3-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2cccnc2)cc1 IMZHLZMTAYFYRT-UHFFFAOYSA-M 0.000 description 1
- PNFZDKUSABFAPF-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[(thiophen-2-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2cccs2)cc1 PNFZDKUSABFAPF-UHFFFAOYSA-M 0.000 description 1
- QVSYOAOQHSLENJ-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[(thiophen-3-ylsulfonylamino)methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccsc2)cc1 QVSYOAOQHSLENJ-UHFFFAOYSA-M 0.000 description 1
- OIPMKIUVXHLBKD-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[[(2-nitrophenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccccc2[N+]([O-])=O)cc1 OIPMKIUVXHLBKD-UHFFFAOYSA-M 0.000 description 1
- PUPGONYOSLMDDS-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[[(4-nitrophenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(cc2)[N+]([O-])=O)cc1 PUPGONYOSLMDDS-UHFFFAOYSA-M 0.000 description 1
- MAECDGGUAYLMEO-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[[(4-phenylphenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(cc2)-c2ccccc2)cc1 MAECDGGUAYLMEO-UHFFFAOYSA-M 0.000 description 1
- ZBOGMIOHJYWASA-UHFFFAOYSA-M sodium (4-nitrophenoxy)-[[[4-(trifluoromethyl)phenyl]sulfonylamino]methyl]phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(cc2)C(F)(F)F)cc1 ZBOGMIOHJYWASA-UHFFFAOYSA-M 0.000 description 1
- AOUQQCVNASPOLA-UHFFFAOYSA-M sodium (benzylsulfonylamino)methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)CC1=CC=CC=C1 AOUQQCVNASPOLA-UHFFFAOYSA-M 0.000 description 1
- FDDBICRTOXBQPN-UHFFFAOYSA-M sodium (isoquinolin-5-ylsulfonylamino)methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2cccc3cnccc23)cc1 FDDBICRTOXBQPN-UHFFFAOYSA-M 0.000 description 1
- GIYAHZLRPHBAFC-UHFFFAOYSA-M sodium [(2,4-dinitrophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-] GIYAHZLRPHBAFC-UHFFFAOYSA-M 0.000 description 1
- MPAULPPUXOVXFI-UHFFFAOYSA-M sodium [(2-bromophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=C(C=CC=C1)Br MPAULPPUXOVXFI-UHFFFAOYSA-M 0.000 description 1
- UNQHVSIERJLUSW-UHFFFAOYSA-M sodium [(3,4-dichlorophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=CC(=C(C=C1)Cl)Cl UNQHVSIERJLUSW-UHFFFAOYSA-M 0.000 description 1
- WOIDIXHSJUHWNH-UHFFFAOYSA-M sodium [(4-chloro-3-nitrophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(Cl)c(c2)[N+]([O-])=O)cc1 WOIDIXHSJUHWNH-UHFFFAOYSA-M 0.000 description 1
- VZCBDHPRZXAECH-UHFFFAOYSA-M sodium [(4-chlorophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(Cl)cc2)cc1 VZCBDHPRZXAECH-UHFFFAOYSA-M 0.000 description 1
- LPXPICVHXVWKDS-UHFFFAOYSA-M sodium [(4-fluorophenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[O-][N+](=O)c1ccc(OP([O-])(=O)CNS(=O)(=O)c2ccc(F)cc2)cc1 LPXPICVHXVWKDS-UHFFFAOYSA-M 0.000 description 1
- BCLDDOQGGCRQLG-UHFFFAOYSA-M sodium [(4-fluorophenyl)sulfonylamino]methyl-quinolin-8-yloxyphosphinate Chemical compound [Na+].[O-]P(=O)(CNS(=O)(=O)c1ccc(F)cc1)Oc1cccc2cccnc12 BCLDDOQGGCRQLG-UHFFFAOYSA-M 0.000 description 1
- FFQLKNINBZPYRB-UHFFFAOYSA-M sodium [(4-methoxyphenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].COc1ccc(cc1)S(=O)(=O)NCP([O-])(=O)Oc1ccc(cc1)[N+]([O-])=O FFQLKNINBZPYRB-UHFFFAOYSA-M 0.000 description 1
- NOTJPZUZYWGBIN-UHFFFAOYSA-M sodium [(4-tert-butylphenyl)sulfonylamino]methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=CC=C(C=C1)C(C)(C)C NOTJPZUZYWGBIN-UHFFFAOYSA-M 0.000 description 1
- DHXNMGRVYPLQCU-UHFFFAOYSA-M sodium benzenesulfonamidomethyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].[N+](=O)([O-])C1=CC=C(C=C1)OP([O-])(=O)CNS(=O)(=O)C1=CC=CC=C1 DHXNMGRVYPLQCU-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- YPPQYORGOMWNMX-UHFFFAOYSA-L sodium phosphonate pentahydrate Chemical compound [Na+].[Na+].[O-]P([O-])=O YPPQYORGOMWNMX-UHFFFAOYSA-L 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- YCSXWLOMJJYNCE-UHFFFAOYSA-M sodium;(2-bromopyridin-3-yl)oxy-[[(4-fluorophenyl)sulfonylamino]methyl]phosphinate Chemical compound [Na+].C=1C=CN=C(Br)C=1OP(=O)([O-])CNS(=O)(=O)C1=CC=C(F)C=C1 YCSXWLOMJJYNCE-UHFFFAOYSA-M 0.000 description 1
- PURQRETTWIPIAF-UHFFFAOYSA-M sodium;(naphthalen-2-ylsulfonylamino)methyl-(4-nitrophenoxy)phosphinate Chemical compound [Na+].C1=CC([N+](=O)[O-])=CC=C1OP([O-])(=O)CNS(=O)(=O)C1=CC=C(C=CC=C2)C2=C1 PURQRETTWIPIAF-UHFFFAOYSA-M 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000005556 structure-activity relationship Methods 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- FKENQMMABCRJMK-RITPCOANSA-N sulbactam Chemical compound O=S1(=O)C(C)(C)[C@H](C(O)=O)N2C(=O)C[C@H]21 FKENQMMABCRJMK-RITPCOANSA-N 0.000 description 1
- 229960005256 sulbactam Drugs 0.000 description 1
- 229960005404 sulfamethoxazole Drugs 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 150000003455 sulfinic acids Chemical class 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012622 synthetic inhibitor Substances 0.000 description 1
- 238000007910 systemic administration Methods 0.000 description 1
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- VNNLHYZDXIBHKZ-UHFFFAOYSA-N thiophene-2-sulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CS1 VNNLHYZDXIBHKZ-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 125000004360 trifluorophenyl group Chemical group 0.000 description 1
- IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
- 229960001082 trimethoprim Drugs 0.000 description 1
- 150000003672 ureas Chemical group 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-O vancomycin(1+) 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)[NH2+]C)[C@H]1C[C@](C)([NH3+])[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-O 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Chemical group 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
- C07F9/655354—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
-
- 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
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- 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
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2479—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
- C07F9/2491—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1) containing the structure P(=X)n-N-N (X = O, S, Se; n = 0, 1)
-
- C—CHEMISTRY; METALLURGY
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/42—Halides thereof
- C07F9/425—Acid or estermonohalides thereof, e.g. RP(=X)(YR)(Hal) (X, Y = O, S; R = H, or hydrocarbon group)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/44—Amides thereof
- C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4407—Amides of acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
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- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
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- C07F9/65517—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
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- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
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- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
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- Bioinformatics & Cheminformatics (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14236299P | 1999-07-06 | 1999-07-06 | |
| US60/142,362 | 1999-07-06 | ||
| PCT/US2000/018344 WO2001002411A1 (en) | 1999-07-06 | 2000-07-05 | SULFONAMIDOMETHYL PHOSPHONATE INHIBITORS OF β-LACTAMASE |
Publications (3)
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| JP2003503505A JP2003503505A (ja) | 2003-01-28 |
| JP2003503505A5 JP2003503505A5 (https=) | 2008-08-14 |
| JP4226818B2 true JP4226818B2 (ja) | 2009-02-18 |
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| MX (1) | MXPA02000246A (https=) |
| WO (1) | WO2001002411A1 (https=) |
Families Citing this family (16)
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| US6884791B2 (en) * | 1999-07-06 | 2005-04-26 | Methylgene, Inc. | Inhibitors of β-lactamase |
| US6921756B2 (en) * | 1999-07-06 | 2005-07-26 | Methylgene, Inc. | Inhibitors of β-lactamase |
| ES2258980T3 (es) * | 1999-08-16 | 2006-09-16 | Revaax Pharmaceuticals Llc | Composiciones farmaceuticas que comprenden acido clavulanico o derivados del mismo para el tratamiento de trastornos del comportamiento. |
| US6426342B2 (en) * | 1999-08-16 | 2002-07-30 | Revaax Pharmaceuticals, Llc | Use of β-lactamase inhibitors as neuroprotectants |
| US20100317625A1 (en) * | 2006-05-22 | 2010-12-16 | Dininno Frank | Novel sulfonamidomethylphosphonate inhibitors of beta-lactamase |
| ES2543842T3 (es) * | 2006-05-22 | 2015-08-24 | Methylgene Inc. | Nuevos inhibidores de la beta-lactamasa |
| EP2069347A2 (en) * | 2006-09-27 | 2009-06-17 | Merck & Co., Inc. | Novel inhibitors of beta-lactamase |
| WO2009091856A2 (en) | 2008-01-18 | 2009-07-23 | Merck & Co., Inc. | Beta-lactamase inhibitors |
| US20110046101A1 (en) * | 2008-03-17 | 2011-02-24 | Dmitrienko Gary I | Bate-lactamase inhibitors |
| BRPI1013901A2 (pt) * | 2009-04-29 | 2019-09-24 | Rexahn Pharmaceuticals Inc | formulação de clavulanato para neuroproteção e tratamento de distúrbios neurodegenerativos |
| WO2015112441A1 (en) | 2014-01-22 | 2015-07-30 | Merck Sharp & Dohme Corp. | Metallo-beta-lactamase inhibitors |
| EP3139918B1 (en) | 2014-05-09 | 2019-12-25 | Merck Sharp & Dohme Corp. | Beta-tetrazolyl-propionic acids as metallo-beta-lactamase inhibitors |
| WO2016206101A1 (en) | 2015-06-26 | 2016-12-29 | Merck Sharp & Dohme Corp. | Metallo-beta-lactamase inhibitors |
| BR112018008597B1 (pt) | 2015-10-28 | 2022-03-03 | Fmc Corporation | Composto, composições herbicidas, mistura herbicida e método para o controle do crescimento de vegetação indesejada |
| WO2019018186A1 (en) | 2017-07-17 | 2019-01-24 | Merck Sharp & Dohme Corp. | Metallo-beta-lactamase inhibitors and methods of use thereof |
| CN121005742A (zh) * | 2024-05-23 | 2025-11-25 | 华东师范大学 | 作为cd73抑制剂衍生物及其应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2059923C3 (de) | 1970-12-05 | 1979-01-25 | Knoll Ag, 6700 Ludwigshafen | l-a-Isopropyl-o-[(N-methyl-N-homoveratryl)v-aminopropyl] -3,4-dimethoxyphenylacetonitril, Verfahren zu dessen Herstellung und dieses enthaltende Arzneimittel |
| US3959551A (en) | 1972-03-30 | 1976-05-25 | Hooker Chemicals & Plastics Corporation | Dialkyl alkyl and aromatic sulfonamidomethyl phosphonates |
| US3870771A (en) | 1972-03-30 | 1975-03-11 | Hooker Chemicals Plastics Corp | Dialkyl alkyl and aromatic sulfonamidomethyl phosphonates |
| DE2261081A1 (de) | 1972-12-14 | 1974-06-27 | Bayer Ag | Amidomethanphosphonsaeure-derivate |
| US4031170A (en) | 1973-08-06 | 1977-06-21 | Monsanto Company | Phosphorus compounds |
| US4032601A (en) | 1973-08-06 | 1977-06-28 | Monsanto Company | Process for the production of sulfonamide phosphonates |
| JPS5490160A (en) | 1977-12-26 | 1979-07-17 | Ihara Chem Ind Co Ltd | Alpha,alpha-disubstituted-benzylcyanide derivatives |
| JPS62126160A (ja) | 1985-11-25 | 1987-06-08 | Hokuriku Seiyaku Co Ltd | 新規なフエニルブチラルデヒド誘導体およびその製造法 |
| DE3628300A1 (de) | 1986-08-21 | 1988-02-25 | Schering Ag | Alkan- und alkoxyalkan-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende insektizide und akarizide mittel |
| EP0505122A1 (en) | 1991-03-21 | 1992-09-23 | Zeneca Limited | Alpha, alpha-dialkylbenzyl derivatives |
| GB9410721D0 (en) | 1994-05-27 | 1994-07-13 | Chiroscience Ltd | Chiral compounds and their resolution |
| US5681821A (en) | 1994-10-18 | 1997-10-28 | Georgia Tech Research Corp. | Fluorescent 1-peptidylaminoalkanephosphonate derivatives |
| GB9602516D0 (en) | 1996-02-08 | 1996-04-10 | Chiroscience Ltd | Racemisation |
| CA2204082A1 (en) | 1996-05-03 | 1997-11-03 | Michael William John Urquhart | Pharmaceutical compounds |
| WO1998056392A1 (en) * | 1997-06-13 | 1998-12-17 | Northwestern University | INHIBITORS OF β-LACTAMASES AND USES THEREFOR |
| KR100591572B1 (ko) | 1997-12-24 | 2006-06-20 | 메틸진, 인크. | 신규의 β-락타마아제 및 DD-펩티다아제 저해제 |
| ATE227295T1 (de) | 1998-07-16 | 2002-11-15 | Aventis Pharma Gmbh | Phosphin- und phosphonsäurederivate als arzneimittel |
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2000
- 2000-07-05 KR KR1020027000135A patent/KR100686988B1/ko not_active Expired - Fee Related
- 2000-07-05 ES ES00943381T patent/ES2250150T3/es not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| AU5785800A (en) | 2001-01-22 |
| DE60024455D1 (en) | 2006-01-05 |
| ATE311397T1 (de) | 2005-12-15 |
| CA2377762C (en) | 2008-09-30 |
| KR20020022084A (ko) | 2002-03-23 |
| DE60024455T2 (de) | 2006-08-03 |
| AU770599B2 (en) | 2004-02-26 |
| US6472406B1 (en) | 2002-10-29 |
| MXPA02000246A (es) | 2003-08-20 |
| EP1194436B1 (en) | 2005-11-30 |
| WO2001002411A1 (en) | 2001-01-11 |
| ES2250150T3 (es) | 2006-04-16 |
| US20040059115A1 (en) | 2004-03-25 |
| EP1194436A1 (en) | 2002-04-10 |
| JP2003503505A (ja) | 2003-01-28 |
| KR100686988B1 (ko) | 2007-02-27 |
| CA2377762A1 (en) | 2001-01-11 |
| US7030103B2 (en) | 2006-04-18 |
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| LAPS | Cancellation because of no payment of annual fees |