JP7399898B2 - PqsRインバースアゴニスト - Google Patents
PqsRインバースアゴニスト Download PDFInfo
- Publication number
- JP7399898B2 JP7399898B2 JP2020573396A JP2020573396A JP7399898B2 JP 7399898 B2 JP7399898 B2 JP 7399898B2 JP 2020573396 A JP2020573396 A JP 2020573396A JP 2020573396 A JP2020573396 A JP 2020573396A JP 7399898 B2 JP7399898 B2 JP 7399898B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- trifluoromethyl
- methyl
- pyridin
- mmol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 229940125425 inverse agonist Drugs 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims description 251
- 150000003839 salts Chemical class 0.000 claims description 56
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 229910052757 nitrogen Inorganic materials 0.000 claims description 35
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 33
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 238000002360 preparation method Methods 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 23
- 125000003342 alkenyl group Chemical group 0.000 claims description 21
- 125000000304 alkynyl group Chemical group 0.000 claims description 21
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 21
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- 201000003883 Cystic fibrosis Diseases 0.000 claims description 20
- 229910052717 sulfur Inorganic materials 0.000 claims description 20
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 125000005843 halogen group Chemical group 0.000 claims description 18
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 16
- 239000008194 pharmaceutical composition Substances 0.000 claims description 14
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 7
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 3
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 3
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 3
- 230000000241 respiratory effect Effects 0.000 claims description 3
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 2
- 230000003115 biocidal effect Effects 0.000 claims description 2
- 230000001886 ciliary effect Effects 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 230000004064 dysfunction Effects 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 134
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 132
- -1 use as a medicament Chemical class 0.000 description 97
- 238000005481 NMR spectroscopy Methods 0.000 description 86
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 69
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 52
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 51
- 238000005160 1H NMR spectroscopy Methods 0.000 description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 46
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 44
- 125000004432 carbon atom Chemical group C* 0.000 description 42
- 238000000746 purification Methods 0.000 description 37
- 239000000203 mixture Substances 0.000 description 30
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 29
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 28
- 230000014509 gene expression Effects 0.000 description 28
- YNCMLFHHXWETLD-UHFFFAOYSA-N pyocyanin Chemical compound CN1C2=CC=CC=C2N=C2C1=CC=CC2=O YNCMLFHHXWETLD-UHFFFAOYSA-N 0.000 description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 26
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 24
- 235000019439 ethyl acetate Nutrition 0.000 description 24
- 230000000694 effects Effects 0.000 description 23
- 239000000243 solution Substances 0.000 description 23
- 239000002904 solvent Substances 0.000 description 23
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 22
- 235000019341 magnesium sulphate Nutrition 0.000 description 22
- 239000012044 organic layer Substances 0.000 description 22
- 239000011541 reaction mixture Substances 0.000 description 22
- 238000000034 method Methods 0.000 description 21
- 239000003960 organic solvent Substances 0.000 description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 125000001424 substituent group Chemical group 0.000 description 18
- 239000000460 chlorine Substances 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 17
- 238000002953 preparative HPLC Methods 0.000 description 17
- 230000018612 quorum sensing Effects 0.000 description 17
- 238000012360 testing method Methods 0.000 description 17
- 229920006395 saturated elastomer Polymers 0.000 description 16
- 239000001301 oxygen Substances 0.000 description 15
- 125000004122 cyclic group Chemical group 0.000 description 14
- 239000003480 eluent Substances 0.000 description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 12
- 239000012043 crude product Substances 0.000 description 12
- UYRHHBXYXSYGHA-UHFFFAOYSA-N 2-heptyl-4-quinolone Chemical compound C1=CC=C2NC(CCCCCCC)=CC(=O)C2=C1 UYRHHBXYXSYGHA-UHFFFAOYSA-N 0.000 description 11
- 239000012267 brine Substances 0.000 description 11
- 230000002503 metabolic effect Effects 0.000 description 11
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 11
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 9
- 125000004429 atom Chemical group 0.000 description 9
- 210000004027 cell Anatomy 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 8
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
- 238000003556 assay Methods 0.000 description 8
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- 238000006467 substitution reaction Methods 0.000 description 8
- 208000035143 Bacterial infection Diseases 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 239000003242 anti bacterial agent Substances 0.000 description 7
- 229940088710 antibiotic agent Drugs 0.000 description 7
- 208000022362 bacterial infectious disease Diseases 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000011593 sulfur Substances 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
- 241000589516 Pseudomonas Species 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 6
- 239000002609 medium Substances 0.000 description 6
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 125000006413 ring segment Chemical group 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 125000004434 sulfur atom Chemical group 0.000 description 6
- 230000007923 virulence factor Effects 0.000 description 6
- 239000000304 virulence factor Substances 0.000 description 6
- CRKLMPDNKUTFGO-UHFFFAOYSA-N 6-(3-fluorophenoxy)-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound FC=1C=C(OC2=CC3=C(NC(=N3)CSC3=CC(=NC=C3)C(F)(F)F)C=C2)C=CC=1 CRKLMPDNKUTFGO-UHFFFAOYSA-N 0.000 description 5
- XMQXUOHVHBXSNG-UHFFFAOYSA-N 6-[(5,6-dichloro-1H-benzimidazol-2-yl)methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1(=NC(N)=CC(=N1)SCC=1NC2=C(N=1)C=C(Cl)C(Cl)=C2)C(F)(F)F XMQXUOHVHBXSNG-UHFFFAOYSA-N 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 5
- 206010073031 Burkholderia infection Diseases 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 5
- 208000032536 Pseudomonas Infections Diseases 0.000 description 5
- 238000002835 absorbance Methods 0.000 description 5
- 230000004913 activation Effects 0.000 description 5
- 239000008186 active pharmaceutical agent Substances 0.000 description 5
- 239000005557 antagonist Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000872 buffer Substances 0.000 description 5
- 208000024833 burkholderia infectious disease Diseases 0.000 description 5
- 238000004440 column chromatography Methods 0.000 description 5
- 230000001419 dependent effect Effects 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 125000001188 haloalkyl group Chemical group 0.000 description 5
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- QFWVAJQVYBRTCL-UHFFFAOYSA-N 4,6-dichloro-2-(trifluoromethyl)pyrimidine Chemical compound FC(F)(F)C1=NC(Cl)=CC(Cl)=N1 QFWVAJQVYBRTCL-UHFFFAOYSA-N 0.000 description 4
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 4
- PPWZDCAZQBLHBX-UHFFFAOYSA-N 6-[[6-(3-fluorophenoxy)-1H-benzimidazol-2-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound FC=1C=C(OC2=CC3=C(NC(=N3)CSC3=CC(=NC(=N3)C(F)(F)F)N)C=C2)C=CC=1 PPWZDCAZQBLHBX-UHFFFAOYSA-N 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- QWSDRNYEGNKRGV-UHFFFAOYSA-N N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3N=NC(CNC4=CC=NC(C(F)(F)F)=C4)=C3)C=C2)C=CC=C1 QWSDRNYEGNKRGV-UHFFFAOYSA-N 0.000 description 4
- GXBJUAYHTJSJOV-UHFFFAOYSA-N N-[[2-(4-phenoxyphenyl)-1,3-thiazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1SC(C2=CC=C(C=C2)OC2=CC=CC=C2)=NC=1)C(F)(F)F GXBJUAYHTJSJOV-UHFFFAOYSA-N 0.000 description 4
- RATLGXJXCCQVKO-UHFFFAOYSA-N N-[[5-(4-phenoxyphenyl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C2=CC=C(CNC3=CC(C(F)(F)F)=NC=C3)N=C2)C=CC(OC2=CC=CC=C2)=C1 RATLGXJXCCQVKO-UHFFFAOYSA-N 0.000 description 4
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 125000004414 alkyl thio group Chemical group 0.000 description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 230000032770 biofilm formation Effects 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 125000004093 cyano group Chemical group *C#N 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 210000004185 liver Anatomy 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000012279 sodium borohydride Substances 0.000 description 4
- 229910000033 sodium borohydride Inorganic materials 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 235000017550 sodium carbonate Nutrition 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 230000001018 virulence Effects 0.000 description 4
- DWNJWSPPORNJGV-UHFFFAOYSA-N (2-bromo-1,3-thiazol-5-yl)methanol Chemical compound OCC1=CN=C(Br)S1 DWNJWSPPORNJGV-UHFFFAOYSA-N 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 3
- YYHRYECWWYONCH-UHFFFAOYSA-N 2-bromo-5-(bromomethyl)-1,3-thiazole Chemical compound BrCC1=CN=C(Br)S1 YYHRYECWWYONCH-UHFFFAOYSA-N 0.000 description 3
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 3
- DAYZTDVFENRXLK-UHFFFAOYSA-N 5,6-dichloro-2-[[6-methoxy-2-(trifluoromethyl)pyrimidin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound C1(=NC(=CC(=N1)SCC=1NC2=C(N=1)C=C(Cl)C(Cl)=C2)OC)C(F)(F)F DAYZTDVFENRXLK-UHFFFAOYSA-N 0.000 description 3
- BNIGPZNUMSRVSV-UHFFFAOYSA-N 6-[(6-phenoxy-1H-benzimidazol-2-yl)methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound O(C1=CC=CC=C1)C1=CC2=C(NC(=N2)CSC2=CC(=NC(=N2)C(F)(F)F)N)C=C1 BNIGPZNUMSRVSV-UHFFFAOYSA-N 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OFHOBVBIQKEXJR-UHFFFAOYSA-N N-[(6-phenoxy-1,3-benzoxazol-2-yl)methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC1=NC2=C(O1)C=C(OC1=CC=CC=C1)C=C2)C(F)(F)F OFHOBVBIQKEXJR-UHFFFAOYSA-N 0.000 description 3
- 239000007832 Na2SO4 Substances 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 3
- 239000011668 ascorbic acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 102000005936 beta-Galactosidase Human genes 0.000 description 3
- 108010005774 beta-Galactosidase Proteins 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 230000001684 chronic effect Effects 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 229960004979 fampridine Drugs 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 125000000842 isoxazolyl group Chemical group 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 125000004043 oxo group Chemical group O=* 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 238000003571 reporter gene assay Methods 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 3
- 208000024891 symptom Diseases 0.000 description 3
- AMUCRBVIJWPJJZ-UHFFFAOYSA-N tert-butyl N-[2-(trifluoromethyl)pyridin-4-yl]carbamate Chemical compound FC(C1=NC=CC(=C1)NC(OC(C)(C)C)=O)(F)F AMUCRBVIJWPJJZ-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- 125000000335 thiazolyl group Chemical group 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- 238000013518 transcription Methods 0.000 description 3
- 230000035897 transcription Effects 0.000 description 3
- AVOWPOFIQZSVGV-UHFFFAOYSA-N (2-phenoxyphenyl)boronic acid Chemical compound OB(O)C1=CC=CC=C1OC1=CC=CC=C1 AVOWPOFIQZSVGV-UHFFFAOYSA-N 0.000 description 2
- SCRCPSNUWXMJNE-UHFFFAOYSA-N (5,6-dichloro-1H-benzimidazol-2-yl)methanethiol Chemical compound SCC1=NC2=CC(Cl)=C(Cl)C=C2N1 SCRCPSNUWXMJNE-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- JYWKEVKEKOTYEX-UHFFFAOYSA-N 2,6-dibromo-4-chloroiminocyclohexa-2,5-dien-1-one Chemical compound ClN=C1C=C(Br)C(=O)C(Br)=C1 JYWKEVKEKOTYEX-UHFFFAOYSA-N 0.000 description 2
- CPZHPTDRRJWXAA-UHFFFAOYSA-N 2,6-dichloro-N-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methyl]pyridin-4-amine Chemical compound CC(C)OC1=C(C=C(C=C1)N2C=C(N=N2)CNC3=CC(=NC(=C3)Cl)Cl)Cl CPZHPTDRRJWXAA-UHFFFAOYSA-N 0.000 description 2
- KDQFHJPYJYPAJR-UHFFFAOYSA-N 2,6-dichloro-N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]pyridin-4-amine Chemical compound C1=CC=C(C=C1)OC2=CC=C(C=C2)N3C=C(N=N3)CNC4=CC(=NC(=C4)Cl)Cl KDQFHJPYJYPAJR-UHFFFAOYSA-N 0.000 description 2
- DLJREAKDBQCNDV-UHFFFAOYSA-N 2,6-dichloro-N-[[2-(4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methyl]pyridin-4-amine Chemical compound CC(C)OC1=CC=C(C=C1)C2=NC=C(S2)CNC3=CC(=NC(=C3)Cl)Cl DLJREAKDBQCNDV-UHFFFAOYSA-N 0.000 description 2
- ZGLIJDKLZKCCIG-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1,3,4-oxadiazole Chemical compound N1=C(OC(CSC2=CC=NC(C(F)(F)F)=C2)=N1)C1=CC=C(Cl)C=C1 ZGLIJDKLZKCCIG-UHFFFAOYSA-N 0.000 description 2
- IMCVHRVFJLUONN-UHFFFAOYSA-N 2-(4-chlorophenyl)-5-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1,3-thiazole Chemical compound N1=C(C=C(C=C1)SCC=1SC(=NC=1)C1=CC=C(Cl)C=C1)C(F)(F)F IMCVHRVFJLUONN-UHFFFAOYSA-N 0.000 description 2
- YYJHYTIINUTMMZ-UHFFFAOYSA-N 2-(4-phenoxyphenyl)-5-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1,3-thiazole Chemical compound C1(OC2=CC=C(C=3SC(=CN=3)CSC3=CC(C(F)(F)F)=NC=C3)C=C2)=CC=CC=C1 YYJHYTIINUTMMZ-UHFFFAOYSA-N 0.000 description 2
- FNBAMXOFCJHISB-UHFFFAOYSA-N 2-(trifluoromethyl)-N-[[1-[4-(trifluoromethyl)phenyl]triazol-4-yl]methyl]pyridin-4-amine Chemical compound N1(C2=CC=C(C(F)(F)F)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 FNBAMXOFCJHISB-UHFFFAOYSA-N 0.000 description 2
- MEHAREFZRGNRJP-UHFFFAOYSA-N 2-(trifluoromethyl)pyrimidine-4,6-diamine Chemical compound NC1=CC(N)=NC(C(F)(F)F)=N1 MEHAREFZRGNRJP-UHFFFAOYSA-N 0.000 description 2
- KKOHDRSCZWNEPW-UHFFFAOYSA-N 2-[(2-chloropyridin-4-yl)sulfanylmethyl]-6-phenoxy-1H-benzimidazole Chemical compound ClC1=NC=CC(=C1)SCC1=NC2=C(N1)C=CC(=C2)OC1=CC=CC=C1 KKOHDRSCZWNEPW-UHFFFAOYSA-N 0.000 description 2
- RWBSXEHXELQVSS-UHFFFAOYSA-N 2-[[2-chloro-6-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-6-phenoxy-1H-benzimidazole Chemical compound C1=CC=C(C=C1)OC2=CC3=C(C=C2)N=C(N3)CSC4=CC(=NC(=C4)Cl)C(F)(F)F RWBSXEHXELQVSS-UHFFFAOYSA-N 0.000 description 2
- CDUMLCFXAIUATR-UHFFFAOYSA-N 2-[[6-methoxy-2-(trifluoromethyl)pyrimidin-4-yl]sulfanylmethyl]-6-phenoxy-1H-benzimidazole Chemical compound COC1=CC(=NC(=N1)C(F)(F)F)SCC1=NC2=C(N1)C=CC(=C2)OC1=CC=CC=C1 CDUMLCFXAIUATR-UHFFFAOYSA-N 0.000 description 2
- HMNWCUUMPVHVQI-UHFFFAOYSA-N 2-amino-5-phenoxyphenol Chemical compound C1=C(O)C(N)=CC=C1OC1=CC=CC=C1 HMNWCUUMPVHVQI-UHFFFAOYSA-N 0.000 description 2
- SPCKHVPPRJWQRZ-UHFFFAOYSA-N 2-benzhydryloxy-n,n-dimethylethanamine;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 SPCKHVPPRJWQRZ-UHFFFAOYSA-N 0.000 description 2
- DNJTXEFQXQXBSO-UHFFFAOYSA-N 2-chloro-5-[4-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]phenyl]pyridine Chemical compound C1=CC(=CC=C1CSC2=CC(=NC=C2)C(F)(F)F)C3=CN=C(C=C3)Cl DNJTXEFQXQXBSO-UHFFFAOYSA-N 0.000 description 2
- CAMBMXSMGLQFLM-UHFFFAOYSA-N 2-chloro-5-[6-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]pyridin-3-yl]pyrimidine Chemical compound C1=CC(=NC=C1C2=CN=C(N=C2)Cl)CSC3=CC(=NC=C3)C(F)(F)F CAMBMXSMGLQFLM-UHFFFAOYSA-N 0.000 description 2
- IKLDGWVKJJLXFO-UHFFFAOYSA-N 2-chloro-N-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C(OC1=C(C=C(N2N=NC(CNC3=CC(C(F)(F)F)=NC(=C3)Cl)=C2)C=C1)Cl)(C)C IKLDGWVKJJLXFO-UHFFFAOYSA-N 0.000 description 2
- AZUKNTWNXCZBFL-UHFFFAOYSA-N 2-chloro-N-[[1-(4-indazol-1-ylphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(N3C4=CC=CC=C4C=N3)C=C2)N=NC(CNC2=CC(=NC(C(F)(F)F)=C2)Cl)=C1 AZUKNTWNXCZBFL-UHFFFAOYSA-N 0.000 description 2
- JTVFJTHCHKNQOC-UHFFFAOYSA-N 2-chloro-N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3C=C(CNC4=CC(=NC(C(F)(F)F)=C4)Cl)N=N3)C=C2)C=CC=C1 JTVFJTHCHKNQOC-UHFFFAOYSA-N 0.000 description 2
- XEJYWESJDGDJIC-UHFFFAOYSA-N 2-chloro-N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]pyridin-4-amine Chemical compound C1=CC=C(C=C1)OC2=CC=C(C=C2)N3C=C(N=N3)CNC4=CC(=NC=C4)Cl XEJYWESJDGDJIC-UHFFFAOYSA-N 0.000 description 2
- BMRKLVATWZDGQO-UHFFFAOYSA-N 2-chloro-N-[[1-(4-propan-2-yloxyphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C(OC1=CC=C(N2N=NC(CNC3=CC(C(F)(F)F)=NC(=C3)Cl)=C2)C=C1)(C)C BMRKLVATWZDGQO-UHFFFAOYSA-N 0.000 description 2
- LRJFZCDAHOPEKR-UHFFFAOYSA-N 2-chloro-N-[[1-(4-pyrazolo[3,4-c]pyridin-1-ylphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C12=C(C=NN2C2=CC=C(C=C2)N2C=C(CNC3=CC(C(F)(F)F)=NC(=C3)Cl)N=N2)C=CN=C1 LRJFZCDAHOPEKR-UHFFFAOYSA-N 0.000 description 2
- BLCMKYPTOPWBHL-UHFFFAOYSA-N 2-chloro-N-[[1-(4-pyridin-3-yloxyphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3C=C(CNC4=CC(C(F)(F)F)=NC(Cl)=C4)N=N3)C=C2)C=NC=C1 BLCMKYPTOPWBHL-UHFFFAOYSA-N 0.000 description 2
- BLROWVHIQPENPV-UHFFFAOYSA-N 2-chloro-N-[[1-[4-(2-fluorophenoxy)phenyl]triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3N=NC(CNC4=CC(=NC(C(F)(F)F)=C4)Cl)=C3)C=C2)C(F)=CC=C1 BLROWVHIQPENPV-UHFFFAOYSA-N 0.000 description 2
- HCGOMSDDBIEIOD-UHFFFAOYSA-N 2-chloro-N-[[2-(3-chloro-4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1Cl)NCC1=CN=C(S1)C1=CC(Cl)=C(OC(C)C)C=C1)C(F)(F)F HCGOMSDDBIEIOD-UHFFFAOYSA-N 0.000 description 2
- QCPNUGXIPUCUSO-UHFFFAOYSA-N 2-chloro-N-[[2-(3-chloro-4-propan-2-yloxyphenyl)pyrimidin-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C(=CC=C1C1=NC=C(CNC2=CC(C(F)(F)F)=NC(Cl)=C2)C=N1)OC(C)C)Cl QCPNUGXIPUCUSO-UHFFFAOYSA-N 0.000 description 2
- QAUNBUMWXSMYAE-UHFFFAOYSA-N 2-chloro-N-[[2-(4-chloro-3-nitrophenyl)pyrimidin-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C=1(C=CC(=C(C=1)N(=O)=O)Cl)C1=NC=C(CNC2=CC(C(F)(F)F)=NC(=C2)Cl)C=N1 QAUNBUMWXSMYAE-UHFFFAOYSA-N 0.000 description 2
- ACUWXRCELXYVRN-UHFFFAOYSA-N 2-chloro-N-[[2-(4-phenoxyphenyl)-1,3-thiazol-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1Cl)NCC=1SC(C2=CC=C(C=C2)OC2=CC=CC=C2)=NC=1)C(F)(F)F ACUWXRCELXYVRN-UHFFFAOYSA-N 0.000 description 2
- VJZDLFAHBSUTHE-UHFFFAOYSA-N 2-chloro-N-[[2-(4-phenoxyphenyl)-1,3-thiazol-5-yl]methyl]pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1SC(C2=CC=C(OC3=CC=CC=C3)C=C2)=NC=1)Cl VJZDLFAHBSUTHE-UHFFFAOYSA-N 0.000 description 2
- BIFCHAFPURZTKX-UHFFFAOYSA-N 2-chloro-N-[[2-(4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound CC(C)OC1=CC=C(C=C1)C2=NC=C(S2)CNC3=CC(=NC(=C3)Cl)C(F)(F)F BIFCHAFPURZTKX-UHFFFAOYSA-N 0.000 description 2
- WHAZRRDRBMYTCU-UHFFFAOYSA-N 2-chloro-N-[[2-(4-propan-2-yloxyphenyl)pyrimidin-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1(C=2C=CC(OC(C)C)=CC=2)=NC=C(CNC2=CC(C(F)(F)F)=NC(=C2)Cl)C=N1 WHAZRRDRBMYTCU-UHFFFAOYSA-N 0.000 description 2
- CLUCNRUIXZQCHP-UHFFFAOYSA-N 2-chloro-N-[[2-[4-(2-fluorophenoxy)phenyl]pyrimidin-5-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=C(C=CC=C1)F)OC1=CC=C(C=C1)C1=NC=C(CNC2=CC(C(F)(F)F)=NC(=C2)Cl)C=N1 CLUCNRUIXZQCHP-UHFFFAOYSA-N 0.000 description 2
- ZYYNLKCPTZVIPQ-UHFFFAOYSA-N 2-heptyl-6-nitro-4-oxo-1h-quinoline-3-carboxamide Chemical group C1=C([N+]([O-])=O)C=C2C(=O)C(C(N)=O)=C(CCCCCCC)NC2=C1 ZYYNLKCPTZVIPQ-UHFFFAOYSA-N 0.000 description 2
- TVJBPWDKPCNPPL-UHFFFAOYSA-N 2-iodo-N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]-6-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3C=C(CNC4=CC(C(F)(F)F)=NC(=C4)I)N=N3)C=C2)C=CC=C1 TVJBPWDKPCNPPL-UHFFFAOYSA-N 0.000 description 2
- DYTVCSKPYOHQAE-UHFFFAOYSA-N 2-nitro-5-phenoxyaniline Chemical compound C1=C([N+]([O-])=O)C(N)=CC(OC=2C=CC=CC=2)=C1 DYTVCSKPYOHQAE-UHFFFAOYSA-N 0.000 description 2
- YUZQXQLGFJYMQC-UHFFFAOYSA-N 2-nitro-5-phenoxyphenol Chemical compound C1=C([N+]([O-])=O)C(O)=CC(OC=2C=CC=CC=2)=C1 YUZQXQLGFJYMQC-UHFFFAOYSA-N 0.000 description 2
- AZKSAVLVSZKNRD-UHFFFAOYSA-M 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide Chemical compound [Br-].S1C(C)=C(C)N=C1[N+]1=NC(C=2C=CC=CC=2)=NN1C1=CC=CC=C1 AZKSAVLVSZKNRD-UHFFFAOYSA-M 0.000 description 2
- GDYHOMLJELGQGW-UHFFFAOYSA-N 3-(4-chlorophenyl)-5-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1,2,4-oxadiazole Chemical compound C1=CC(=CC=C1C2=NOC(=N2)CSC3=CC(=NC=C3)C(F)(F)F)Cl GDYHOMLJELGQGW-UHFFFAOYSA-N 0.000 description 2
- FKMWOGFRLVFKQD-UHFFFAOYSA-N 3-chloro-2-methoxy-5-[6-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]pyridin-3-yl]pyridine Chemical compound ClC=1C=C(C=NC=1OC)C=1C=NC(=CC=1)CSC1=CC(=NC=C1)C(F)(F)F FKMWOGFRLVFKQD-UHFFFAOYSA-N 0.000 description 2
- PSPFFDXXISVKFW-UHFFFAOYSA-N 4-[(6-phenoxy-1H-benzimidazol-2-yl)methylsulfanyl]-6-(trifluoromethyl)pyridin-2-amine Chemical compound FC(C1=NC(=CC(SCC=2NC3=C(N=2)C=C(OC2=CC=CC=C2)C=C3)=C1)N)(F)F PSPFFDXXISVKFW-UHFFFAOYSA-N 0.000 description 2
- PQKXETLCUXTFTF-UHFFFAOYSA-N 4-[(6-phenoxy-1H-benzimidazol-2-yl)methylsulfanyl]pyridine-2-carbonitrile Chemical compound N#CC1=NC=CC(SCC2=NC(C=C(C=C3)OC4=CC=CC=C4)=C3N2)=C1 PQKXETLCUXTFTF-UHFFFAOYSA-N 0.000 description 2
- LCZYILKQUGVXPA-UHFFFAOYSA-N 4-[4-[[[2-(trifluoromethyl)pyridin-4-yl]amino]methyl]-1,3-thiazol-2-yl]benzonitrile Chemical compound C1=CC(=CC=C1C#N)C2=NC(=CS2)CNC3=CC(=NC=C3)C(F)(F)F LCZYILKQUGVXPA-UHFFFAOYSA-N 0.000 description 2
- BCDJEKTVXQURFC-UHFFFAOYSA-N 4-[4-[[[2-(trifluoromethyl)pyridin-4-yl]amino]methyl]triazol-1-yl]benzonitrile Chemical compound N1(C2=CC=C(C#N)C=C2)C=C(CNC2=CC=NC(C(F)(F)F)=C2)N=N1 BCDJEKTVXQURFC-UHFFFAOYSA-N 0.000 description 2
- YAFDDXTXFVRSTQ-UHFFFAOYSA-N 4-[[1-(3,4-dichlorophenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound N1(C2=CC=C(C(Cl)=C2)Cl)C=C(CSC2=CC=NC(C(F)(F)F)=C2)N=N1 YAFDDXTXFVRSTQ-UHFFFAOYSA-N 0.000 description 2
- JKMGWNPKHSSACG-UHFFFAOYSA-N 4-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methylamino]pyridine-2,6-dicarbonitrile Chemical compound C1(=CC(=C(OC(C)C)C=C1)Cl)N1C=C(CNC2=CC(C#N)=NC(C#N)=C2)N=N1 JKMGWNPKHSSACG-UHFFFAOYSA-N 0.000 description 2
- IMMZZAMFVNWJEY-UHFFFAOYSA-N 4-[[1-(3-chlorophenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound C1=CC(=CC(=C1)Cl)N2C=C(N=N2)CSC3=CC(=NC=C3)C(F)(F)F IMMZZAMFVNWJEY-UHFFFAOYSA-N 0.000 description 2
- FNEBMXWNSXQYNN-UHFFFAOYSA-N 4-[[1-(4-bromophenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound N1(C2=CC=C(Br)C=C2)N=NC(CSC2=CC=NC(C(F)(F)F)=C2)=C1 FNEBMXWNSXQYNN-UHFFFAOYSA-N 0.000 description 2
- ZVKUZBCXLOFQFM-UHFFFAOYSA-N 4-[[1-(4-chlorophenyl)pyrazol-3-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound C=1(C=CN(N=1)C1=CC=C(Cl)C=C1)CSC1=CC(C(F)(F)F)=NC=C1 ZVKUZBCXLOFQFM-UHFFFAOYSA-N 0.000 description 2
- OKAOGCCJDIBWJR-UHFFFAOYSA-N 4-[[1-(4-chlorophenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound C1=CC(=CC=C1N2C=C(N=N2)CSC3=CC(=NC=C3)C(F)(F)F)Cl OKAOGCCJDIBWJR-UHFFFAOYSA-N 0.000 description 2
- OHKPVVYGKVWOMF-UHFFFAOYSA-N 4-[[1-(4-chlorophenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidine Chemical compound N1=NN(C2=CC=C(Cl)C=C2)C=C1CSC1=NC(=NC=C1)C(F)(F)F OHKPVVYGKVWOMF-UHFFFAOYSA-N 0.000 description 2
- SJFWSLQRDSKSGW-UHFFFAOYSA-N 4-[[1-(4-methoxyphenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound N1=NN(C2=CC=C(OC)C=C2)C=C1CSC1=CC=NC(C(F)(F)F)=C1 SJFWSLQRDSKSGW-UHFFFAOYSA-N 0.000 description 2
- RCGUXDCWIIIQQU-UHFFFAOYSA-N 4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylamino]-6-(trifluoromethyl)-1H-pyridin-2-one Chemical compound N1(C2=CC=C(OC3=CC=CC=C3)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC(O)=C2)N=N1 RCGUXDCWIIIQQU-UHFFFAOYSA-N 0.000 description 2
- QSHZYVLGRCJRDU-UHFFFAOYSA-N 4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylamino]pyridine-2,6-dicarbonitrile Chemical compound N1(C2=CC=C(OC3=CC=CC=C3)C=C2)N=NC(CNC2=CC(C#N)=NC(=C2)C#N)=C1 QSHZYVLGRCJRDU-UHFFFAOYSA-N 0.000 description 2
- FDNYGGJSXYGVKW-UHFFFAOYSA-N 4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylamino]pyridine-2-carbonitrile Chemical compound C1=C(OC2=CC=C(N3C=C(CNC4=CC(C#N)=NC=C4)N=N3)C=C2)C=CC=C1 FDNYGGJSXYGVKW-UHFFFAOYSA-N 0.000 description 2
- DTFHSWZBXNIUQT-UHFFFAOYSA-N 4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound N1(C2=CC=C(OC3=CC=CC=C3)C=C2)C=C(CSC2=CC=NC(C(F)(F)F)=C2)N=N1 DTFHSWZBXNIUQT-UHFFFAOYSA-N 0.000 description 2
- CEZJOYJOPRVETI-UHFFFAOYSA-N 4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidine Chemical compound N1(C2=CC=C(OC3=CC=CC=C3)C=C2)C=C(CSC2=NC(=NC=C2)C(F)(F)F)N=N1 CEZJOYJOPRVETI-UHFFFAOYSA-N 0.000 description 2
- TUJQWQPMNYEGQT-UHFFFAOYSA-N 4-[[2-(3-chloro-4-methoxyphenyl)-1,3-thiazol-5-yl]methylamino]pyridine-2-carbonitrile Chemical compound ClC=1C=C(C=CC=1OC)C=1SC(=CN=1)CNC1=CC(=NC=C1)C#N TUJQWQPMNYEGQT-UHFFFAOYSA-N 0.000 description 2
- LJWPTPZBDRDGGJ-UHFFFAOYSA-N 4-[[2-(3-chloro-4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methylamino]-6-(trifluoromethyl)pyridine-2-carbonitrile Chemical compound C(OC1=C(C=C(C=2SC(CNC3=CC(=NC(=C3)C(F)(F)F)C#N)=CN=2)C=C1)Cl)(C)C LJWPTPZBDRDGGJ-UHFFFAOYSA-N 0.000 description 2
- XYMVIOWQRUWRTR-UHFFFAOYSA-N 4-[[2-(3-chloro-4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methylamino]pyridine-2-carbonitrile Chemical compound ClC=1C=C(C=CC=1OC(C)C)C=1SC(=CN=1)CNC1=CC(=NC=C1)C#N XYMVIOWQRUWRTR-UHFFFAOYSA-N 0.000 description 2
- ZEXPHVUZLPCTBA-UHFFFAOYSA-N 4-[[2-(4-chlorophenyl)tetrazol-5-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound N1=NN(C2=CC=C(Cl)C=C2)N=C1CSC1=CC(C(F)(F)F)=NC=C1 ZEXPHVUZLPCTBA-UHFFFAOYSA-N 0.000 description 2
- JXTNBITXSVGRRD-UHFFFAOYSA-N 4-[[2-(4-phenoxyphenyl)-1,3-thiazol-5-yl]methylamino]pyridine-2-carbonitrile Chemical compound O(C1=CC=CC=C1)C1=CC=C(C=C1)C=1SC(=CN=1)CNC1=CC(=NC=C1)C#N JXTNBITXSVGRRD-UHFFFAOYSA-N 0.000 description 2
- LHTSDPMXUFRDRS-UHFFFAOYSA-N 4-[[2-(4-propan-2-yloxyphenyl)-1,3-thiazol-5-yl]methylamino]-6-(trifluoromethyl)pyridine-2-carbonitrile Chemical compound CC(C)OC1=CC=C(C=C1)C2=NC=C(S2)CNC3=CC(=NC(=C3)C(F)(F)F)C#N LHTSDPMXUFRDRS-UHFFFAOYSA-N 0.000 description 2
- WVGHUJWYMAXUCI-UHFFFAOYSA-N 4-[[5-(4-chlorophenyl)pyridin-2-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound C1=CC(=CC=C1C2=CN=C(C=C2)CSC3=CC(=NC=C3)C(F)(F)F)Cl WVGHUJWYMAXUCI-UHFFFAOYSA-N 0.000 description 2
- RFYLRVNTOLGWGE-UHFFFAOYSA-N 4-[[5-(4-phenoxyphenyl)pyridin-2-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound O(C1=CC=CC=C1)C1=CC=C(C=C1)C=1C=CC(=NC=1)CSC1=CC(=NC=C1)C(F)(F)F RFYLRVNTOLGWGE-UHFFFAOYSA-N 0.000 description 2
- GNZKTDQOEXNZSW-UHFFFAOYSA-N 4-[[5-(6-chloropyridin-3-yl)pyridin-2-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound C1=CC(=NC=C1C2=CN=C(C=C2)Cl)CSC3=CC(=NC=C3)C(F)(F)F GNZKTDQOEXNZSW-UHFFFAOYSA-N 0.000 description 2
- NVHRMYZZBZKWPN-UHFFFAOYSA-N 4-[[5-(6-phenoxypyridin-3-yl)pyridin-2-yl]methylsulfanyl]-2-(trifluoromethyl)pyridine Chemical compound O(C1=CC=CC=C1)C1=CC=C(C=N1)C=1C=NC(=CC=1)CSC1=CC(=NC=C1)C(F)(F)F NVHRMYZZBZKWPN-UHFFFAOYSA-N 0.000 description 2
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
- URSFPJHPJSOYJA-UHFFFAOYSA-N 5,6-difluoro-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound N1=C(C=C(C=C1)SCC=1NC2=C(N=1)C=C(F)C(F)=C2)C(F)(F)F URSFPJHPJSOYJA-UHFFFAOYSA-N 0.000 description 2
- PKCHRWPMNDRVMI-UHFFFAOYSA-N 5-bromo-2-(bromomethyl)pyridine Chemical compound BrCC1=CC=C(Br)C=N1 PKCHRWPMNDRVMI-UHFFFAOYSA-N 0.000 description 2
- HVKGJEQECKQQSD-UHFFFAOYSA-N 5-chloro-6-fluoro-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound ClC=1C(=CC2=C(NC(=N2)CSC2=CC(=NC=C2)C(F)(F)F)C=1)F HVKGJEQECKQQSD-UHFFFAOYSA-N 0.000 description 2
- FWLLYQJIOKISKP-UHFFFAOYSA-N 6-(4-fluorophenoxy)-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound C(F)(C1=NC=CC(=C1)SCC=1NC2=C(N=1)C=C(OC1=CC=C(F)C=C1)C=C2)(F)F FWLLYQJIOKISKP-UHFFFAOYSA-N 0.000 description 2
- WTPHZCPTYNBQIG-UHFFFAOYSA-N 6-[(6-chloro-1H-benzimidazol-2-yl)methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1(=NC(=CC(=N1)SCC=1NC2=C(N=1)C=C(Cl)C=C2)N)C(F)(F)F WTPHZCPTYNBQIG-UHFFFAOYSA-N 0.000 description 2
- OYSJDBLLWGJMOE-UHFFFAOYSA-N 6-[(6-phenoxy-1H-benzimidazol-2-yl)methoxy]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound NC1=NC(C(F)(F)F)=NC(OCC2=NC(C=C(C=C3)OC4=CC=CC=C4)=C3N2)=C1 OYSJDBLLWGJMOE-UHFFFAOYSA-N 0.000 description 2
- WZVQXZUJSAUVHV-UHFFFAOYSA-N 6-[(6-pyridin-3-yloxy-1H-benzimidazol-2-yl)methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1=CC(=CN=C1)OC2=CC3=C(C=C2)N=C(N3)CSC4=NC(=NC(=C4)N)C(F)(F)F WZVQXZUJSAUVHV-UHFFFAOYSA-N 0.000 description 2
- UFINQDQDECURKY-UHFFFAOYSA-N 6-[[1-(4-phenoxyphenyl)triazol-4-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1=C(OC2=CC=C(N3N=NC(CSC4=NC(=NC(=C4)N)C(F)(F)F)=C3)C=C2)C=CC=C1 UFINQDQDECURKY-UHFFFAOYSA-N 0.000 description 2
- BGBWWNKCIXAXNG-UHFFFAOYSA-N 6-[[2-(3-chloro-4-methoxyphenyl)-1,3-thiazol-5-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1(=NC(N)=CC(=N1)SCC=1SC(=NC=1)C1=CC=C(C(Cl)=C1)OC)C(F)(F)F BGBWWNKCIXAXNG-UHFFFAOYSA-N 0.000 description 2
- YXXVAIXNRMSUTL-UHFFFAOYSA-N 6-[[2-(4-phenoxyphenyl)-1,3-thiazol-5-yl]methylsulfanyl]-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound C1=C(OC2=CC=C(C=3SC(=CN=3)CSC3=NC(=NC(=C3)N)C(F)(F)F)C=C2)C=CC=C1 YXXVAIXNRMSUTL-UHFFFAOYSA-N 0.000 description 2
- UQLPLJKPRIYXRJ-UHFFFAOYSA-N 6-chloro-2-(trifluoromethyl)pyrimidin-4-amine Chemical compound NC1=CC(Cl)=NC(C(F)(F)F)=N1 UQLPLJKPRIYXRJ-UHFFFAOYSA-N 0.000 description 2
- XJQZGQBSZYVVQQ-UHFFFAOYSA-N 6-chloro-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound ClC1=CC2=C(NC(=N2)CSC2=CC(=NC=C2)C(F)(F)F)C=C1 XJQZGQBSZYVVQQ-UHFFFAOYSA-N 0.000 description 2
- GWRHQZXQJJCFFT-UHFFFAOYSA-N 6-chloro-4-[[1-(4-phenoxyphenyl)triazol-4-yl]methylamino]pyridine-2-carbonitrile Chemical compound N1(C2=CC=C(OC3=CC=CC=C3)C=C2)C=C(CNC2=CC(C#N)=NC(Cl)=C2)N=N1 GWRHQZXQJJCFFT-UHFFFAOYSA-N 0.000 description 2
- HWQCJNFLRLERTQ-UHFFFAOYSA-N 6-phenoxy-2-[[2-(trifluoromethyl)pyridin-4-yl]oxymethyl]-1H-benzimidazole Chemical compound C(F)(C1=NC=CC(=C1)OCC=1NC2=C(N=1)C=C(OC1=CC=CC=C1)C=C2)(F)F HWQCJNFLRLERTQ-UHFFFAOYSA-N 0.000 description 2
- WDDYYJQQIUECAS-UHFFFAOYSA-N 6-phenoxy-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound O(C1=CC=CC=C1)C1=CC2=C(NC(=N2)CSC2=CC(=NC=C2)C(F)(F)F)C=C1 WDDYYJQQIUECAS-UHFFFAOYSA-N 0.000 description 2
- FKNMMMURHQXXGO-UHFFFAOYSA-N 6-phenylsulfanyl-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound C1=CC=C(C=C1)SC2=CC3=C(C=C2)N=C(N3)CSC4=CC(=NC=C4)C(F)(F)F FKNMMMURHQXXGO-UHFFFAOYSA-N 0.000 description 2
- KVQKLTIQLLFPKO-UHFFFAOYSA-N 6-propan-2-yl-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound C1=2NC(=NC1=CC(C(C)C)=CC=2)CSC1=CC=NC(=C1)C(F)(F)F KVQKLTIQLLFPKO-UHFFFAOYSA-N 0.000 description 2
- GXBHTIQFCBEPQI-UHFFFAOYSA-N 7-chloro-3-[2-(6-cyclopropyl-1H-indol-3-yl)-2-oxoethoxy]naphthalene-2-carboxamide Chemical compound ClC1=CC=C2C=C(C(=CC2=C1)C(=O)N)OCC(=O)C1=CNC2=CC(=CC=C12)C1CC1 GXBHTIQFCBEPQI-UHFFFAOYSA-N 0.000 description 2
- 240000002234 Allium sativum Species 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 2
- 241001453380 Burkholderia Species 0.000 description 2
- 125000006414 CCl Chemical group ClC* 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 241000282412 Homo Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 108090001090 Lectins Proteins 0.000 description 2
- 102000004856 Lectins Human genes 0.000 description 2
- 239000006137 Luria-Bertani broth Substances 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- YAAGGFLFAHBXRP-UHFFFAOYSA-N N-[(2-bromo-1,3-thiazol-5-yl)methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC1=CN=C(S1)Br)C(F)(F)F YAAGGFLFAHBXRP-UHFFFAOYSA-N 0.000 description 2
- IEQDIBFLLAGMBU-UHFFFAOYSA-N N-[(5,6-dichloro-1H-benzimidazol-2-yl)methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1NC2=C(N=1)C=C(Cl)C(Cl)=C2)C(F)(F)F IEQDIBFLLAGMBU-UHFFFAOYSA-N 0.000 description 2
- NYYWLWQFWWSZPD-UHFFFAOYSA-N N-[(6-phenoxy-1H-benzimidazol-2-yl)methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC=C(C=C1)OC2=CC3=C(C=C2)N=C(N3)CNC4=CC(=NC=C4)C(F)(F)F NYYWLWQFWWSZPD-UHFFFAOYSA-N 0.000 description 2
- NUNNPKPJQOZEAR-UHFFFAOYSA-N N-[[1-(3,4-dichlorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(C(Cl)=C2)Cl)C=C1CNC1=CC(C(F)(F)F)=NC=C1 NUNNPKPJQOZEAR-UHFFFAOYSA-N 0.000 description 2
- FGGGWOOKSZWORX-UHFFFAOYSA-N N-[[1-(3,4-difluorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(F)=C(F)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 FGGGWOOKSZWORX-UHFFFAOYSA-N 0.000 description 2
- SRTBDBHVJCXJHH-UHFFFAOYSA-N N-[[1-(3-chloro-4-cyclobutyloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(Cl)=C(OC3CCC3)C=C2)N=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1 SRTBDBHVJCXJHH-UHFFFAOYSA-N 0.000 description 2
- AHYLQXWKTIPGDX-UHFFFAOYSA-N N-[[1-(3-chloro-4-cyclopropyloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C=C1CNC1=CC=NC(C(F)(F)F)=C1)C1=CC=C(OC2CC2)C(Cl)=C1 AHYLQXWKTIPGDX-UHFFFAOYSA-N 0.000 description 2
- HVCMNCBPPOLBRI-UHFFFAOYSA-N N-[[1-(3-chloro-4-fluorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC(Cl)=C(F)C=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 HVCMNCBPPOLBRI-UHFFFAOYSA-N 0.000 description 2
- VFPRRYXALNZRBZ-UHFFFAOYSA-N N-[[1-(3-chloro-4-methoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(Cl)=C(OC)C=C2)N=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1 VFPRRYXALNZRBZ-UHFFFAOYSA-N 0.000 description 2
- YJBJDICJTHRDIA-UHFFFAOYSA-N N-[[1-(3-chloro-4-phenoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(Cl)=C(OC3=CC=CC=C3)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 YJBJDICJTHRDIA-UHFFFAOYSA-N 0.000 description 2
- SMBSNVKKVQRNSY-UHFFFAOYSA-N N-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound O(C(C)C)C1=C(C=C(N2C=C(CNC3=CC=NC(C(F)(F)F)=C3)N=N2)C=C1)Cl SMBSNVKKVQRNSY-UHFFFAOYSA-N 0.000 description 2
- FOMJNQVBPHTXGF-UHFFFAOYSA-N N-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methyl]-2-nitropyridin-4-amine Chemical compound C(OC1=C(C=C(N2N=NC(CNC3=CC(N(=O)=O)=NC=C3)=C2)C=C1)Cl)(C)C FOMJNQVBPHTXGF-UHFFFAOYSA-N 0.000 description 2
- JUQUTOKOHMVOGO-UHFFFAOYSA-N N-[[1-(3-chloro-4-pyridin-2-yloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=C(C=C(C=C2)N2N=NC(CNC3=CC(C(F)(F)F)=NC=C3)=C2)Cl)N=CC=C1 JUQUTOKOHMVOGO-UHFFFAOYSA-N 0.000 description 2
- WSSFHQJBIMXTFX-UHFFFAOYSA-N N-[[1-(3-chloro-4-pyridin-3-yloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(OC2=C(C=C(N3C=C(CNC4=CC=NC(C(F)(F)F)=C4)N=N3)C=C2)Cl)=CN=CC=C1 WSSFHQJBIMXTFX-UHFFFAOYSA-N 0.000 description 2
- ULGOFBYEJLMPJT-UHFFFAOYSA-N N-[[1-(3-chlorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(Cl)=CC=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 ULGOFBYEJLMPJT-UHFFFAOYSA-N 0.000 description 2
- LSKLJXLWMDQUAR-UHFFFAOYSA-N N-[[1-(3-fluoro-4-methoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(C(F)=C2)OC)C=C1CNC1=CC=NC(C(F)(F)F)=C1 LSKLJXLWMDQUAR-UHFFFAOYSA-N 0.000 description 2
- HGDPQDUHJQPHNM-UHFFFAOYSA-N N-[[1-(3-fluoro-4-phenoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC=CC=C1OC1=C(C=C(N2C=C(CNC3=CC(C(F)(F)F)=NC=C3)N=N2)C=C1)F HGDPQDUHJQPHNM-UHFFFAOYSA-N 0.000 description 2
- GLMBXZAACMXPLH-UHFFFAOYSA-N N-[[1-(3-fluorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=CC(F)=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 GLMBXZAACMXPLH-UHFFFAOYSA-N 0.000 description 2
- IKAJJQVUYABOAJ-UHFFFAOYSA-N N-[[1-(3-methylsulfanylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(SC)=CC=C2)N=NC(CNC2=CC=NC(C(F)(F)F)=C2)=C1 IKAJJQVUYABOAJ-UHFFFAOYSA-N 0.000 description 2
- ZHDZLMYANVUGRR-UHFFFAOYSA-N N-[[1-(4-anilinophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(NC2=CC=C(N3N=NC(CNC4=CC(C(F)(F)F)=NC=C4)=C3)C=C2)C=CC=C1 ZHDZLMYANVUGRR-UHFFFAOYSA-N 0.000 description 2
- NDVHWEYENRLJAR-UHFFFAOYSA-N N-[[1-(4-bromo-2-fluorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=C(F)C=C(Br)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 NDVHWEYENRLJAR-UHFFFAOYSA-N 0.000 description 2
- JNPDICMZLSNKAO-UHFFFAOYSA-N N-[[1-(4-bromo-3-methoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(OC)=C(Br)C=C2)C=C(CNC2=CC=NC(C(F)(F)F)=C2)N=N1 JNPDICMZLSNKAO-UHFFFAOYSA-N 0.000 description 2
- ISSNMIGGDVVAFW-UHFFFAOYSA-N N-[[1-(4-bromophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(Br)C=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 ISSNMIGGDVVAFW-UHFFFAOYSA-N 0.000 description 2
- BDLRIBNKBRDGSF-UHFFFAOYSA-N N-[[1-(4-chlorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(Cl)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 BDLRIBNKBRDGSF-UHFFFAOYSA-N 0.000 description 2
- MKPNORSVYHXHJA-UHFFFAOYSA-N N-[[1-(4-fluorophenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(F)C=C2)C=C(CNC2=CC=NC(C(F)(F)F)=C2)N=N1 MKPNORSVYHXHJA-UHFFFAOYSA-N 0.000 description 2
- HAQYMDIGNQZBME-UHFFFAOYSA-N N-[[1-(4-indazol-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(N3C4=CC=CC=C4C=N3)C=C2)C=C(CNC2=CC=NC(C(F)(F)F)=C2)N=N1 HAQYMDIGNQZBME-UHFFFAOYSA-N 0.000 description 2
- UQIYCCSKOMJFCX-UHFFFAOYSA-N N-[[1-(4-indol-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(N3C=CC4=C3C=CC=C4)C=C2)C=C1CNC1=CC=NC(C(F)(F)F)=C1 UQIYCCSKOMJFCX-UHFFFAOYSA-N 0.000 description 2
- AAMZBSMDOBIBTC-UHFFFAOYSA-N N-[[1-(4-methoxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(OC)C=C2)C=C1CNC1=CC=NC(C(F)(F)F)=C1 AAMZBSMDOBIBTC-UHFFFAOYSA-N 0.000 description 2
- ARUVANCPNKDOLY-UHFFFAOYSA-N N-[[1-(4-methylsulfanylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(C=C2)SC)N=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1 ARUVANCPNKDOLY-UHFFFAOYSA-N 0.000 description 2
- LFYPSVINGQNBCM-UHFFFAOYSA-N N-[[1-(4-phenoxyphenyl)triazol-4-yl]methyl]-5-(trifluoromethyl)pyridin-3-amine Chemical compound C1(=CC=CC=C1)OC1=CC=C(N2C=C(CNC3=CC(C(F)(F)F)=CN=C3)N=N2)C=C1 LFYPSVINGQNBCM-UHFFFAOYSA-N 0.000 description 2
- GEOSWJARIZSKOA-UHFFFAOYSA-N N-[[1-(4-propan-2-yloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C(OC1=CC=C(N2C=C(CNC3=CC(C(F)(F)F)=NC=C3)N=N2)C=C1)(C)C GEOSWJARIZSKOA-UHFFFAOYSA-N 0.000 description 2
- UNDBNELVDMFBSW-UHFFFAOYSA-N N-[[1-(4-pyrazolo[3,4-c]pyridin-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC(=CC=C1N2C=C(N=N2)CNC3=CC(=NC=C3)C(F)(F)F)N4C5=C(C=CN=C5)C=N4 UNDBNELVDMFBSW-UHFFFAOYSA-N 0.000 description 2
- KGLQXKGSYWDUCN-UHFFFAOYSA-N N-[[1-(4-pyrazolo[4,3-b]pyridin-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC2=C(C=NN2C3=CC=C(C=C3)N4C=C(N=N4)CNC5=CC(=NC=C5)C(F)(F)F)N=C1 KGLQXKGSYWDUCN-UHFFFAOYSA-N 0.000 description 2
- IDOZCHWWROCOPY-UHFFFAOYSA-N N-[[1-(4-pyrrolo[2,3-b]pyridin-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(N3C4=NC=CC=C4C=C3)C=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 IDOZCHWWROCOPY-UHFFFAOYSA-N 0.000 description 2
- DOSYMHBEWSFVIB-UHFFFAOYSA-N N-[[1-(4-pyrrolo[2,3-c]pyridin-1-ylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(N3C4=C(C=C3)C=CN=C4)C=C2)N=NC(CNC2=CC=NC(C(F)(F)F)=C2)=C1 DOSYMHBEWSFVIB-UHFFFAOYSA-N 0.000 description 2
- WTAKEFFFCHIXSV-UHFFFAOYSA-N N-[[1-[3-(morpholin-4-ylmethyl)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC(CN3CCOCC3)=CC=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 WTAKEFFFCHIXSV-UHFFFAOYSA-N 0.000 description 2
- GBYFKLSSFRTRHR-UHFFFAOYSA-N N-[[1-[3-(trifluoromethoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC(OC(F)(F)F)=CC=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 GBYFKLSSFRTRHR-UHFFFAOYSA-N 0.000 description 2
- DLFRAPXSEMTQQJ-UHFFFAOYSA-N N-[[1-[3-chloro-4-(oxetan-3-yloxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C=C1CNC1=CC(C(F)(F)F)=NC=C1)C1=CC(Cl)=C(OC2COC2)C=C1 DLFRAPXSEMTQQJ-UHFFFAOYSA-N 0.000 description 2
- GCWHJHUEVYONKQ-UHFFFAOYSA-N N-[[1-[3-chloro-4-(oxolan-3-yloxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1C(OC2=C(C=C(N3C=C(CNC4=CC=NC(C(F)(F)F)=C4)N=N3)C=C2)Cl)CCO1 GCWHJHUEVYONKQ-UHFFFAOYSA-N 0.000 description 2
- FDKMUHGDKMGPKC-UHFFFAOYSA-N N-[[1-[3-chloro-4-(trifluoromethoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC(Cl)=C(OC(F)(F)F)C=C2)C=C(CNC2=CC=NC(C(F)(F)F)=C2)N=N1 FDKMUHGDKMGPKC-UHFFFAOYSA-N 0.000 description 2
- JFNSYAIYYUVCRS-UHFFFAOYSA-N N-[[1-[4-(2-fluorophenoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC=C(C(=C1)OC2=CC=C(C=C2)N3C=C(N=N3)CNC4=CC(=NC=C4)C(F)(F)F)F JFNSYAIYYUVCRS-UHFFFAOYSA-N 0.000 description 2
- CWTUTTIODDGLTM-UHFFFAOYSA-N N-[[1-[4-(2-fluoropyridin-3-yl)oxyphenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC(=C(N=C1)F)OC2=CC=C(C=C2)N3C=C(N=N3)CNC4=CC(=NC=C4)C(F)(F)F CWTUTTIODDGLTM-UHFFFAOYSA-N 0.000 description 2
- PWVGNBCJVNPFDH-UHFFFAOYSA-N N-[[1-[4-(3-chlorophenoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(OC3=CC=CC(Cl)=C3)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 PWVGNBCJVNPFDH-UHFFFAOYSA-N 0.000 description 2
- RDBJNLVIMJVLBW-UHFFFAOYSA-N N-[[1-[4-(3-fluorophenoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(OC2=CC=C(N3C=C(CNC4=CC(C(F)(F)F)=NC=C4)N=N3)C=C2)C=C(F)C=C1 RDBJNLVIMJVLBW-UHFFFAOYSA-N 0.000 description 2
- JTNMUBKUKYHHIL-UHFFFAOYSA-N N-[[1-[4-(4-chlorophenoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(C=C2)OC2=CC=C(Cl)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 JTNMUBKUKYHHIL-UHFFFAOYSA-N 0.000 description 2
- AXEFWYDYSBKMAP-UHFFFAOYSA-N N-[[1-[4-(benzimidazol-1-yl)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(N3C=NC4=C3C=CC=C4)C=C2)N=NC(CNC2=CC=NC(C(F)(F)F)=C2)=C1 AXEFWYDYSBKMAP-UHFFFAOYSA-N 0.000 description 2
- OYHPEYWRIQJWNE-UHFFFAOYSA-N N-[[1-[4-(morpholin-4-ylmethyl)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1N(CCOC1)CC1=CC=C(N2N=NC(CNC3=CC=NC(C(F)(F)F)=C3)=C2)C=C1 OYHPEYWRIQJWNE-UHFFFAOYSA-N 0.000 description 2
- WVTMNNFNJAAIOY-UHFFFAOYSA-N N-[[1-[4-(trifluoromethoxy)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(OC(F)(F)F)C=C2)C=C(CNC2=CC(C(F)(F)F)=NC=C2)N=N1 WVTMNNFNJAAIOY-UHFFFAOYSA-N 0.000 description 2
- NHXFLIUAZPBDQP-UHFFFAOYSA-N N-[[2-(3-chloro-4-propan-2-yloxyphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1N=C(SC=1)C1=CC(=C(C=C1)OC(C)C)Cl)C(F)(F)F NHXFLIUAZPBDQP-UHFFFAOYSA-N 0.000 description 2
- FGUVKWPOHXVGKT-UHFFFAOYSA-N N-[[2-(3-chloro-4-propan-2-yloxyphenyl)pyrimidin-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(N=CC(CNC2=CC=NC(C(F)(F)F)=C2)=C1)C1=CC=C(OC(C)C)C(Cl)=C1 FGUVKWPOHXVGKT-UHFFFAOYSA-N 0.000 description 2
- ACUHHZWFFCWLJY-UHFFFAOYSA-N N-[[2-(3-phenoxyphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1N=C(C2=CC=CC(=C2)OC2=CC=CC=C2)SC=1)C(F)(F)F ACUHHZWFFCWLJY-UHFFFAOYSA-N 0.000 description 2
- HEOXXGLUMYLVQE-UHFFFAOYSA-N N-[[2-(4-chlorophenyl)-1,3-thiazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1SC(C2=CC=C(Cl)C=C2)=NC=1)C(F)(F)F HEOXXGLUMYLVQE-UHFFFAOYSA-N 0.000 description 2
- UFXFBGRWBAXCEW-UHFFFAOYSA-N N-[[2-(4-cyclopropylphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1N=C(SC=1)C1=CC=C(C2CC2)C=C1)C(F)(F)F UFXFBGRWBAXCEW-UHFFFAOYSA-N 0.000 description 2
- PKEGFARZNSUMDV-UHFFFAOYSA-N N-[[2-(4-cyclopropylphenyl)pyrimidin-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C2CC2)C=CC(=C1)C1=NC=C(CNC2=CC=NC(C(F)(F)F)=C2)C=N1 PKEGFARZNSUMDV-UHFFFAOYSA-N 0.000 description 2
- ISCHZWHWIFFZLF-UHFFFAOYSA-N N-[[2-(4-methoxy-3,5-dimethylphenyl)-1,3-thiazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1SC(=NC=1)C1=CC(C)=C(OC)C(C)=C1)C(F)(F)F ISCHZWHWIFFZLF-UHFFFAOYSA-N 0.000 description 2
- BFZGQAOSSQOELM-UHFFFAOYSA-N N-[[2-(4-methoxy-3-methylphenyl)-1,3-thiazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1SC(=NC=1)C1=CC(C)=C(OC)C=C1)C(F)(F)F BFZGQAOSSQOELM-UHFFFAOYSA-N 0.000 description 2
- WAGPTNPRNLGCJT-UHFFFAOYSA-N N-[[2-(4-methoxyphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound COC1=CC=C(C=C1)C2=NC(=CS2)CNC3=CC(=NC=C3)C(F)(F)F WAGPTNPRNLGCJT-UHFFFAOYSA-N 0.000 description 2
- RAEAGYDQAYPINN-UHFFFAOYSA-N N-[[2-(4-phenoxyphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1N=C(C2=CC=C(OC3=CC=CC=C3)C=C2)SC=1)C(F)(F)F RAEAGYDQAYPINN-UHFFFAOYSA-N 0.000 description 2
- OFHFXVLNCHNQMI-UHFFFAOYSA-N N-[[2-(4-phenoxyphenyl)pyrimidin-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC=C(C=C1)OC2=CC=C(C=C2)C3=NC=C(C=N3)CNC4=CC(=NC=C4)C(F)(F)F OFHFXVLNCHNQMI-UHFFFAOYSA-N 0.000 description 2
- FNBNQEPKVWACMA-UHFFFAOYSA-N N-[[2-(4-propan-2-yloxyphenyl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound CC(C)OC1=CC=C(C=C1)C2=NC(=CS2)CNC3=CC(=NC=C3)C(F)(F)F FNBNQEPKVWACMA-UHFFFAOYSA-N 0.000 description 2
- RFYYDCJUQORCPD-UHFFFAOYSA-N N-[[2-(4-propan-2-yloxyphenyl)pyrimidin-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound CC(C)OC1=CC=C(C=C1)C2=NC=C(C=N2)CNC3=CC(=NC=C3)C(F)(F)F RFYYDCJUQORCPD-UHFFFAOYSA-N 0.000 description 2
- HRAQNLGJANWDAQ-UHFFFAOYSA-N N-[[2-(5-chloro-6-methoxypyridin-3-yl)-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound COC1=C(C=C(C=N1)C2=NC(=CS2)CNC3=CC(=NC=C3)C(F)(F)F)Cl HRAQNLGJANWDAQ-UHFFFAOYSA-N 0.000 description 2
- QFGLSDPGMJCHFP-UHFFFAOYSA-N N-[[2-(5-chloro-6-propan-2-yloxypyridin-3-yl)pyrimidin-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound ClC=1C=C(C=NC=1OC(C)C)C1=NC=C(C=N1)CNC1=CC(=NC=C1)C(F)(F)F QFGLSDPGMJCHFP-UHFFFAOYSA-N 0.000 description 2
- CSDHDCYUYAJJTN-UHFFFAOYSA-N N-[[2-(6-chloropyridin-3-yl)-1,3-thiazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1SC(=NC=1)C1=CN=C(Cl)C=C1)C(F)(F)F CSDHDCYUYAJJTN-UHFFFAOYSA-N 0.000 description 2
- LAXRFGLICGDXME-UHFFFAOYSA-N N-[[2-[4-(4-fluorophenoxy)phenyl]-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1N=C(SC=1)C1=CC=C(OC2=CC=C(F)C=C2)C=C1)C(F)(F)F LAXRFGLICGDXME-UHFFFAOYSA-N 0.000 description 2
- YPGMVGMCMRGQPE-UHFFFAOYSA-N N-[[2-[6-(4-fluorophenoxy)pyridin-3-yl]-1,3-thiazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=CC(=CC=C1OC2=NC=C(C=C2)C3=NC(=CS3)CNC4=CC(=NC=C4)C(F)(F)F)F YPGMVGMCMRGQPE-UHFFFAOYSA-N 0.000 description 2
- GAJSRAHFFMZYAX-UHFFFAOYSA-N N-[[3-(4-phenoxyphenyl)-1,2-oxazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(OC2=CC=C(C3=NOC(CNC4=CC(C(F)(F)F)=NC=C4)=C3)C=C2)=CC=CC=C1 GAJSRAHFFMZYAX-UHFFFAOYSA-N 0.000 description 2
- UYVIDVHCTZENPV-UHFFFAOYSA-N N-[[3-(4-phenoxyphenyl)-1H-1,2,4-triazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=NC=CC(=C1)NCC=1NC(C2=CC=C(C=C2)OC2=CC=CC=C2)=NN=1)C(F)(F)F UYVIDVHCTZENPV-UHFFFAOYSA-N 0.000 description 2
- OSDPGQVDZYFJBO-UHFFFAOYSA-N N-[[3-(4-phenoxyphenyl)-1H-pyrazol-5-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC1=CC(=NN1)C1=CC=C(OC2=CC=CC=C2)C=C1)C(F)(F)F OSDPGQVDZYFJBO-UHFFFAOYSA-N 0.000 description 2
- VYOIIMYHIXHKML-UHFFFAOYSA-N N-[[4-(4-phenoxyphenyl)-1,3-thiazol-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC1=NC(C2=CC=C(OC3=CC=CC=C3)C=C2)=CS1)C(F)(F)F VYOIIMYHIXHKML-UHFFFAOYSA-N 0.000 description 2
- NDSCXXMIDYTRBD-UHFFFAOYSA-N N-[[5-(3-chloro-4-methoxyphenyl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound COC1=C(C=C(C=C1)C2=CN=C(C=C2)CNC3=CC(=NC=C3)C(F)(F)F)Cl NDSCXXMIDYTRBD-UHFFFAOYSA-N 0.000 description 2
- OBIXYKYYOPABMF-UHFFFAOYSA-N N-[[5-(3-chloro-4-propan-2-yloxyphenyl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1)C1=CC=C(OC(C)C)C(Cl)=C1 OBIXYKYYOPABMF-UHFFFAOYSA-N 0.000 description 2
- AXBGJKONALDJMC-UHFFFAOYSA-N N-[[5-(3-phenoxyphenyl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(C=2C=C(OC3=CC=CC=C3)C=CC=2)=CC=C(CNC2=CC(C(F)(F)F)=NC=C2)N=C1 AXBGJKONALDJMC-UHFFFAOYSA-N 0.000 description 2
- UUNHVELVSYOGDC-UHFFFAOYSA-N N-[[5-(4-phenoxyphenyl)-1,3-thiazol-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=C(C=C(C=C1)NCC=1SC(=CN=1)C1=CC=C(OC2=CC=CC=C2)C=C1)C(F)(F)F UUNHVELVSYOGDC-UHFFFAOYSA-N 0.000 description 2
- YECOJAMXZTXPAB-UHFFFAOYSA-N N-[[5-(5,6-dichloropyridin-3-yl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C(=NC=C1C1=CC=C(CNC2=CC=NC(C(F)(F)F)=C2)N=C1)Cl)Cl YECOJAMXZTXPAB-UHFFFAOYSA-N 0.000 description 2
- NZVRIDLVUBUCBQ-UHFFFAOYSA-N N-[[5-(5-chloro-6-methoxypyridin-3-yl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound COC1=C(C=C(C=N1)C2=CN=C(C=C2)CNC3=CC(=NC=C3)C(F)(F)F)Cl NZVRIDLVUBUCBQ-UHFFFAOYSA-N 0.000 description 2
- ODAHTYHUUNJTTP-UHFFFAOYSA-N N-[[5-(6-chloropyridin-3-yl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(C=2C=CC(CNC3=CC(C(F)(F)F)=NC=C3)=NC=2)=CN=C(Cl)C=C1 ODAHTYHUUNJTTP-UHFFFAOYSA-N 0.000 description 2
- LQHZVADNPURRFW-UHFFFAOYSA-N N-[[5-(6-chloropyridin-3-yl)pyrimidin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1=C(C2=CN=C(N=C2)CNC2=CC(C(F)(F)F)=NC=C2)C=NC(Cl)=C1 LQHZVADNPURRFW-UHFFFAOYSA-N 0.000 description 2
- ZADKYFQLRZDBJW-UHFFFAOYSA-N N-[[5-(6-phenoxypyridin-3-yl)pyridin-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(C=2C=CC(CNC3=CC(C(F)(F)F)=NC=C3)=NC=2)=CN=C(OC2=CC=CC=C2)C=C1 ZADKYFQLRZDBJW-UHFFFAOYSA-N 0.000 description 2
- PPZSRPQKFNDWRG-UHFFFAOYSA-N N-[[6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound FC1=CC=C(OC2=CC3=C(NC(=N3)CNC3=CC(=NC=C3)C(F)(F)F)C=C2)C=C1 PPZSRPQKFNDWRG-UHFFFAOYSA-N 0.000 description 2
- GSYZZKKNKJYGSS-UHFFFAOYSA-N N-prop-2-ynyl-2-(trifluoromethyl)pyridin-4-amine Chemical compound FC(F)(F)c1cc(NCC#C)ccn1 GSYZZKKNKJYGSS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 241000181693 Pseudomonas aeruginosa PA14 Species 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 2
- XJLXINKUBYWONI-DQQFMEOOSA-N [[(2r,3r,4r,5r)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2s,3r,4s,5s)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemical compound NC(=O)C1=CC=C[N+]([C@@H]2[C@H]([C@@H](O)[C@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-DQQFMEOOSA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 239000000556 agonist Substances 0.000 description 2
- 125000003282 alkyl amino group Chemical group 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 229940072107 ascorbate Drugs 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzydamine Chemical compound C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 2
- 238000003573 beta galactosidase reporter gene assay Methods 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
- MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229960000520 diphenhydramine Drugs 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 210000005069 ears Anatomy 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 210000001508 eye Anatomy 0.000 description 2
- 238000003818 flash chromatography Methods 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 2
- 125000005816 fluoropropyl group Chemical group [H]C([H])(F)C([H])([H])C([H])([H])* 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 235000004611 garlic Nutrition 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 2
- 125000004969 haloethyl group Chemical group 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
- 125000001041 indolyl group Chemical group 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 2
- 125000001786 isothiazolyl group Chemical group 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000002523 lectin Substances 0.000 description 2
- 210000004072 lung Anatomy 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-VMNATFBRSA-N methanol-d1 Chemical compound [2H]OC OKKJLVBELUTLKV-VMNATFBRSA-N 0.000 description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- 229940041009 monobactams Drugs 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- REDJHBFVXFVYQM-UHFFFAOYSA-N phenyl-[4-[4-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]triazol-1-yl]phenyl]methanone Chemical compound C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)N3C=C(N=N3)CSC4=CC(=NC=C4)C(F)(F)F REDJHBFVXFVYQM-UHFFFAOYSA-N 0.000 description 2
- BWWNUIBXLSTUHM-UHFFFAOYSA-N phenyl-[4-[4-[[[2-(trifluoromethyl)pyridin-4-yl]amino]methyl]triazol-1-yl]phenyl]methanone Chemical compound C1(C(=O)C2=CC=C(N3C=C(CNC4=CC=NC(C(F)(F)F)=C4)N=N3)C=C2)=CC=CC=C1 BWWNUIBXLSTUHM-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000011321 prophylaxis Methods 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 2
- 125000002098 pyridazinyl group Chemical group 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical group C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000012453 solvate Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- 230000008685 targeting Effects 0.000 description 2
- HZMGBWWLPOVXNZ-UHFFFAOYSA-N tert-butyl N-[(5,6-dichloro-1H-benzimidazol-2-yl)methyl]-N-[2-(trifluoromethyl)pyridin-4-yl]carbamate Chemical compound CC(C)(C)OC(=O)N(CC1=NC2=CC(=C(C=C2N1)Cl)Cl)C3=CC(=NC=C3)C(F)(F)F HZMGBWWLPOVXNZ-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000003831 tetrazolyl group Chemical group 0.000 description 2
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 238000011200 topical administration Methods 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 238000004879 turbidimetry Methods 0.000 description 2
- 210000001635 urinary tract Anatomy 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- WFTRHYPZWHCURS-SQFISAMPSA-N (1Z)-N-hydroxy-4-phenoxybenzenecarboximidoyl chloride Chemical compound C1=CC(C(/Cl)=N/O)=CC=C1OC1=CC=CC=C1 WFTRHYPZWHCURS-SQFISAMPSA-N 0.000 description 1
- VHUBEHVXGDLQFO-UHFFFAOYSA-N (3-chloro-4-methoxyphenyl)boron Chemical compound [B]C1=CC=C(OC)C(Cl)=C1 VHUBEHVXGDLQFO-UHFFFAOYSA-N 0.000 description 1
- RIDRXGOBXZLKHZ-NZUANIILSA-N (3R,9S,12S,15S,18S,21S,24S,27R,30S,33S,36S,39S,42S,45S)-15,18,24,27,33-pentakis(2-aminoethyl)-30-(3-aminopropyl)-36-[(2S)-butan-2-yl]-42-[(1R)-1-hydroxyethyl]-9-(hydroxymethyl)-21,39-bis(1H-indol-3-ylmethyl)-12-methyl-1,7,10,13,16,19,22,25,28,31,34,37,40,43-tetradecazatricyclo[43.3.0.03,7]octatetracontane-2,8,11,14,17,20,23,26,29,32,35,38,41,44-tetradecone Chemical compound CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCN)NC(=O)[C@@H](CCN)NC(=O)[C@H](CCCN)NC(=O)[C@H](CCN)NC1=O)[C@@H](C)O RIDRXGOBXZLKHZ-NZUANIILSA-N 0.000 description 1
- RUCZFWMEACWFER-UHFFFAOYSA-N (5-bromopyridin-2-yl)methanol Chemical compound OCC1=CC=C(Br)C=N1 RUCZFWMEACWFER-UHFFFAOYSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 description 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 description 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 description 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 description 1
- QKDHBVNJCZBTMR-LLVKDONJSA-N (R)-temafloxacin Chemical compound C1CN[C@H](C)CN1C(C(=C1)F)=CC2=C1C(=O)C(C(O)=O)=CN2C1=CC=C(F)C=C1F QKDHBVNJCZBTMR-LLVKDONJSA-N 0.000 description 1
- XUBOMFCQGDBHNK-JTQLQIEISA-N (S)-gatifloxacin Chemical compound FC1=CC(C(C(C(O)=O)=CN2C3CC3)=O)=C2C(OC)=C1N1CCN[C@@H](C)C1 XUBOMFCQGDBHNK-JTQLQIEISA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- UWYVPFMHMJIBHE-OWOJBTEDSA-N (e)-2-hydroxybut-2-enedioic acid Chemical compound OC(=O)\C=C(\O)C(O)=O UWYVPFMHMJIBHE-OWOJBTEDSA-N 0.000 description 1
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 description 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
- KEIFWROAQVVDBN-UHFFFAOYSA-N 1,2-dihydronaphthalene Chemical compound C1=CC=C2C=CCCC2=C1 KEIFWROAQVVDBN-UHFFFAOYSA-N 0.000 description 1
- MMZYCBHLNZVROM-UHFFFAOYSA-N 1-fluoro-2-methylbenzene Chemical compound CC1=CC=CC=C1F MMZYCBHLNZVROM-UHFFFAOYSA-N 0.000 description 1
- JCAMLYAKKPJZOJ-UHFFFAOYSA-N 2,2,2-trifluoro-n-(2-nitro-4-propan-2-ylphenyl)acetamide Chemical compound CC(C)C1=CC=C(NC(=O)C(F)(F)F)C([N+]([O-])=O)=C1 JCAMLYAKKPJZOJ-UHFFFAOYSA-N 0.000 description 1
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
- IJWYNBAAUNNPKI-UHFFFAOYSA-N 2-(chloromethyl)-6-phenoxy-1,3-benzoxazole Chemical compound ClCC=1OC2=C(N=1)C=CC(=C2)OC1=CC=CC=C1 IJWYNBAAUNNPKI-UHFFFAOYSA-N 0.000 description 1
- NQEUCAFEERCRRC-UHFFFAOYSA-N 2-(trifluoromethyl)-1h-pyridine-4-thione Chemical compound FC(F)(F)C1=CC(=S)C=CN1 NQEUCAFEERCRRC-UHFFFAOYSA-N 0.000 description 1
- LYNBZRJTRHTSKI-UHFFFAOYSA-N 2-(trifluoromethyl)pyridin-4-amine Chemical compound NC1=CC=NC(C(F)(F)F)=C1 LYNBZRJTRHTSKI-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- VZAGPOQBHSQUJT-UHFFFAOYSA-N 2-[[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]sulfanylmethyl]-6-phenoxy-1H-benzimidazole Chemical compound ClC1=CC(=NC(=N1)C(F)(F)F)SCC1=NC2=C(N1)C=CC(=C2)OC1=CC=CC=C1 VZAGPOQBHSQUJT-UHFFFAOYSA-N 0.000 description 1
- CEIUIHOQDSVZJQ-UHFFFAOYSA-N 2-heptyl-3-hydroxy-4-quinolone Chemical compound C1=CC=C2C(=O)C(O)=C(CCCCCCC)NC2=C1 CEIUIHOQDSVZJQ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
- XSPQHOJEUTZTON-UHFFFAOYSA-N 2-phenoxy-1,3-benzoxazole Chemical compound N=1C2=CC=CC=C2OC=1OC1=CC=CC=C1 XSPQHOJEUTZTON-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- GACDQMDRPRGCTN-KQYNXXCUSA-N 3'-phospho-5'-adenylyl sulfate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OS(O)(=O)=O)[C@@H](OP(O)(O)=O)[C@H]1O GACDQMDRPRGCTN-KQYNXXCUSA-N 0.000 description 1
- XSJHLPIPWYOPSS-UHFFFAOYSA-N 3-(chloromethyl)-1-(4-chlorophenyl)pyrazole Chemical compound N1=C(CCl)C=CN1C1=CC=C(Cl)C=C1 XSJHLPIPWYOPSS-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
- 125000004919 3-methyl-2-pentyl group Chemical group CC(C(C)*)CC 0.000 description 1
- IWFHBRFJOHTIPU-UHFFFAOYSA-N 4,5-dichlorobenzene-1,2-diamine Chemical compound NC1=CC(Cl)=C(Cl)C=C1N IWFHBRFJOHTIPU-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- WXFBWILOVNYOSV-UHFFFAOYSA-N 4-[(2-bromo-1,3-thiazol-5-yl)methyl]-2-(trifluoromethyl)-1H-pyrimidine-4,6-diamine Chemical compound BrC=1SC(=CN=1)CC1(NC(=NC(=C1)N)C(F)(F)F)N WXFBWILOVNYOSV-UHFFFAOYSA-N 0.000 description 1
- JRCBXSNBFRNFLY-UHFFFAOYSA-N 4-[[1-(3-chloro-4-propan-2-yloxyphenyl)triazol-4-yl]methylamino]-6-(trifluoromethyl)pyridine-2-carbonitrile Chemical compound C(OC1=CC=C(C=C1Cl)N1N=NC(CNC2=CC(=NC(C(F)(F)F)=C2)C#N)=C1)(C)C JRCBXSNBFRNFLY-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 1
- FJVIHKKXPLPDSV-UHFFFAOYSA-N 4-phenoxybenzene-1,2-diamine Chemical compound C1=C(N)C(N)=CC=C1OC1=CC=CC=C1 FJVIHKKXPLPDSV-UHFFFAOYSA-N 0.000 description 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
- HWXOPDQGZZVUGG-UHFFFAOYSA-N 5,6-dichloro-2-[[2-(trifluoromethyl)pyridin-4-yl]oxymethyl]-1H-benzimidazole Chemical compound C1(=NC=CC(=C1)OCC=1NC2=C(N=1)C=C(Cl)C(Cl)=C2)C(F)(F)F HWXOPDQGZZVUGG-UHFFFAOYSA-N 0.000 description 1
- HDERLPBTBRTKQV-UHFFFAOYSA-N 5,6-dichloro-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound N1=C(C=C(C=C1)SCC=1NC2=C(N=1)C=C(Cl)C(Cl)=C2)C(F)(F)F HDERLPBTBRTKQV-UHFFFAOYSA-N 0.000 description 1
- NADICDBVRPXTIG-UHFFFAOYSA-N 5,6-dichloro-2-[[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]sulfanylmethyl]-1H-benzimidazole Chemical compound ClC1=CC2=C(NC(=N2)CSC2=NC(=NC(=C2)Cl)C(F)(F)F)C=C1Cl NADICDBVRPXTIG-UHFFFAOYSA-N 0.000 description 1
- PEDMFCHWOVJDNW-UHFFFAOYSA-N 5-fluoro-2-nitroaniline Chemical compound NC1=CC(F)=CC=C1[N+]([O-])=O PEDMFCHWOVJDNW-UHFFFAOYSA-N 0.000 description 1
- QQURWFRNETXFTN-UHFFFAOYSA-N 5-fluoro-2-nitrophenol Chemical compound OC1=CC(F)=CC=C1[N+]([O-])=O QQURWFRNETXFTN-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- KILQSRKYCWVCPP-UHFFFAOYSA-N 6-phenoxy-2-[[2-(trifluoromethyl)pyridin-4-yl]sulfanylmethyl]-1,3-benzoxazole Chemical compound O(C1=CC=CC=C1)C1=CC2=C(N=C(O2)CSC2=CC(=NC=C2)C(F)(F)F)C=C1 KILQSRKYCWVCPP-UHFFFAOYSA-N 0.000 description 1
- CJIJXIFQYOPWTF-UHFFFAOYSA-N 7-hydroxycoumarin Natural products O1C(=O)C=CC2=CC(O)=CC=C21 CJIJXIFQYOPWTF-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- GSDSWSVVBLHKDQ-UHFFFAOYSA-N 9-fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid Chemical compound FC1=CC(C(C(C(O)=O)=C2)=O)=C3N2C(C)COC3=C1N1CCN(C)CC1 GSDSWSVVBLHKDQ-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000371430 Burkholderia cenocepacia Species 0.000 description 1
- 241001136175 Burkholderia pseudomallei Species 0.000 description 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 description 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- 108010078777 Colistin Proteins 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 230000004568 DNA-binding Effects 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000620209 Escherichia coli DH5[alpha] Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 102100036250 GPI mannosyltransferase 4 Human genes 0.000 description 1
- 241000255896 Galleria mellonella Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229930182566 Gentamicin Natural products 0.000 description 1
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- AIJTTZAVMXIJGM-UHFFFAOYSA-N Grepafloxacin Chemical compound C1CNC(C)CN1C(C(=C1C)F)=CC2=C1C(=O)C(C(O)=O)=CN2C1CC1 AIJTTZAVMXIJGM-UHFFFAOYSA-N 0.000 description 1
- 101001074618 Homo sapiens GPI mannosyltransferase 4 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- GRRNUXAQVGOGFE-UHFFFAOYSA-N Hygromycin-B Natural products OC1C(NC)CC(N)C(O)C1OC1C2OC3(C(C(O)C(O)C(C(N)CO)O3)O)OC2C(O)C(CO)O1 GRRNUXAQVGOGFE-UHFFFAOYSA-N 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 108010022337 Leucine Enkephalin Proteins 0.000 description 1
- GSDSWSVVBLHKDQ-JTQLQIEISA-N Levofloxacin Chemical compound C([C@@H](N1C2=C(C(C(C(O)=O)=C1)=O)C=C1F)C)OC2=C1N1CCN(C)CC1 GSDSWSVVBLHKDQ-JTQLQIEISA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- MPIIHVQZXMMHHY-UHFFFAOYSA-N N-[(5-bromopyridin-2-yl)methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound BrC=1C=CC(=NC=1)CNC1=CC(=NC=C1)C(F)(F)F MPIIHVQZXMMHHY-UHFFFAOYSA-N 0.000 description 1
- UZUPSMNHASMPDG-UHFFFAOYSA-N N-[[1-(3-chloro-4-methylsulfanylphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1(C2=CC=C(C(Cl)=C2)SC)N=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1 UZUPSMNHASMPDG-UHFFFAOYSA-N 0.000 description 1
- BZGPOLUOOFHLKY-UHFFFAOYSA-N N-[[1-(4-pyridin-3-yloxyphenyl)triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(OC2=CC=C(N3C=C(CNC4=CC(C(F)(F)F)=NC=C4)N=N3)C=C2)=CN=CC=C1 BZGPOLUOOFHLKY-UHFFFAOYSA-N 0.000 description 1
- DVRPQZRZBAAPRG-UHFFFAOYSA-N N-[[1-[4-(N-methylanilino)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound N1=NN(C2=CC=C(N(C3=CC=CC=C3)C)C=C2)C=C1CNC1=CC(C(F)(F)F)=NC=C1 DVRPQZRZBAAPRG-UHFFFAOYSA-N 0.000 description 1
- DLVFDWVUJSRWLR-UHFFFAOYSA-N N-[[1-[4-(pyridin-4-ylmethyl)phenyl]triazol-4-yl]methyl]-2-(trifluoromethyl)pyridin-4-amine Chemical compound C1(=CC=C(C=C1)CC1=CC=NC=C1)N1N=NC(CNC2=CC(C(F)(F)F)=NC=C2)=C1 DLVFDWVUJSRWLR-UHFFFAOYSA-N 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 101150026476 PAO1 gene Proteins 0.000 description 1
- 102000016387 Pancreatic elastase Human genes 0.000 description 1
- 108010067372 Pancreatic elastase Proteins 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- UOZODPSAJZTQNH-UHFFFAOYSA-N Paromomycin II Natural products NC1C(O)C(O)C(CN)OC1OC1C(O)C(OC2C(C(N)CC(N)C2O)OC2C(C(O)C(O)C(CO)O2)N)OC1CO UOZODPSAJZTQNH-UHFFFAOYSA-N 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 101000582927 Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01) Lectin A Proteins 0.000 description 1
- 108010040201 Polymyxins Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000288906 Primates Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 101001095185 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Anthraniloyl-CoA anthraniloyltransferase Proteins 0.000 description 1
- 101100137513 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) pqsA gene Proteins 0.000 description 1
- 108700008625 Reporter Genes Proteins 0.000 description 1
- URWAJWIAIPFPJE-UHFFFAOYSA-N Rickamicin Natural products O1CC(O)(C)C(NC)C(O)C1OC1C(O)C(OC2C(CC=C(CN)O2)N)C(N)CC1N URWAJWIAIPFPJE-UHFFFAOYSA-N 0.000 description 1
- 229930192786 Sisomicin Natural products 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- HDYANYHVCAPMJV-LXQIFKJMSA-N UDP-alpha-D-glucuronic acid Chemical compound C([C@@H]1[C@H]([C@H]([C@@H](O1)N1C(NC(=O)C=C1)=O)O)O)OP(O)(=O)OP(O)(=O)O[C@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O HDYANYHVCAPMJV-LXQIFKJMSA-N 0.000 description 1
- HDYANYHVCAPMJV-UHFFFAOYSA-N Uridine diphospho-D-glucuronic acid Natural products O1C(N2C(NC(=O)C=C2)=O)C(O)C(O)C1COP(O)(=O)OP(O)(=O)OC1OC(C(O)=O)C(O)C(O)C1O HDYANYHVCAPMJV-UHFFFAOYSA-N 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 125000005354 acylalkyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 125000005041 acyloxyalkyl group Chemical group 0.000 description 1
- QBYJBZPUGVGKQQ-SJJAEHHWSA-N aldrin Chemical compound C1[C@H]2C=C[C@@H]1[C@H]1[C@@](C3(Cl)Cl)(Cl)C(Cl)=C(Cl)[C@@]3(Cl)[C@H]12 QBYJBZPUGVGKQQ-SJJAEHHWSA-N 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000000278 alkyl amino alkyl group Chemical group 0.000 description 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000004419 alkynylene group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000001668 ameliorated effect Effects 0.000 description 1
- 229960004821 amikacin Drugs 0.000 description 1
- LKCWBDHBTVXHDL-RMDFUYIESA-N amikacin Chemical compound O([C@@H]1[C@@H](N)C[C@H]([C@@H]([C@H]1O)O[C@@H]1[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O1)O)NC(=O)[C@@H](O)CCN)[C@H]1O[C@H](CN)[C@@H](O)[C@H](O)[C@H]1O LKCWBDHBTVXHDL-RMDFUYIESA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002647 aminoglycoside antibiotic agent Substances 0.000 description 1
- 229960000723 ampicillin Drugs 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical group NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000003214 anti-biofilm Effects 0.000 description 1
- 230000001775 anti-pathogenic effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 229940125715 antihistaminic agent Drugs 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000003435 antirheumatic agent Substances 0.000 description 1
- 239000003443 antiviral agent Substances 0.000 description 1
- 229940121357 antivirals Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229960005397 arbekacin Drugs 0.000 description 1
- MKKYBZZTJQGVCD-XTCKQBCOSA-N arbekacin Chemical compound O([C@@H]1[C@@H](N)C[C@H]([C@@H]([C@H]1O)O[C@@H]1[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O1)O)NC(=O)[C@@H](O)CCN)[C@H]1O[C@H](CN)CC[C@H]1N MKKYBZZTJQGVCD-XTCKQBCOSA-N 0.000 description 1
- 125000005018 aryl alkenyl group Chemical group 0.000 description 1
- 125000005015 aryl alkynyl group Chemical group 0.000 description 1
- 125000004350 aryl cycloalkyl group Chemical group 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- BIDUPMYXGFNAEJ-APGVDKLISA-N astromicin Chemical compound O[C@@H]1[C@H](N(C)C(=O)CN)[C@@H](OC)[C@@H](O)[C@H](N)[C@H]1O[C@@H]1[C@H](N)CC[C@@H]([C@H](C)N)O1 BIDUPMYXGFNAEJ-APGVDKLISA-N 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000003725 azepanyl group Chemical group 0.000 description 1
- 125000002785 azepinyl group Chemical group 0.000 description 1
- 125000002393 azetidinyl group Chemical group 0.000 description 1
- 125000004069 aziridinyl group Chemical group 0.000 description 1
- 125000003943 azolyl group Chemical group 0.000 description 1
- 230000007921 bacterial pathogenicity Effects 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 229960001192 bekanamycin Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 229960000333 benzydamine Drugs 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 239000003782 beta lactam antibiotic agent Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000001851 biosynthetic effect Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- 239000007975 buffered saline Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- HUSUHZRVLBSGBO-UHFFFAOYSA-L calcium;dihydrogen phosphate;hydroxide Chemical compound O.[Ca+2].OP([O-])([O-])=O HUSUHZRVLBSGBO-UHFFFAOYSA-L 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 229940041011 carbapenems Drugs 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000003833 cell viability Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 150000001782 cephems Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 238000004296 chiral HPLC Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 229960003405 ciprofloxacin Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229960003346 colistin Drugs 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 229940097362 cyclodextrins Drugs 0.000 description 1
- 125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000003678 cyclohexadienyl group Chemical group C1(=CC=CCC1)* 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 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 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000298 cyclopropenyl group Chemical group [H]C1=C([H])C1([H])* 0.000 description 1
- 239000000824 cytostatic agent Substances 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 229960003807 dibekacin Drugs 0.000 description 1
- JJCQSGDBDPYCEO-XVZSLQNASA-N dibekacin Chemical compound O1[C@H](CN)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N JJCQSGDBDPYCEO-XVZSLQNASA-N 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 description 1
- 125000005051 dihydropyrazinyl group Chemical group N1(CC=NC=C1)* 0.000 description 1
- 125000005052 dihydropyrazolyl group Chemical group N1(NCC=C1)* 0.000 description 1
- 125000004655 dihydropyridinyl group Chemical group N1(CC=CC=C1)* 0.000 description 1
- 125000005054 dihydropyrrolyl group Chemical group [H]C1=C([H])C([H])([H])C([H])([H])N1* 0.000 description 1
- 125000005072 dihydrothiopyranyl group Chemical group S1C(CCC=C1)* 0.000 description 1
- 125000006202 diisopropylaminoethyl group Chemical group [H]C([H])([H])C([H])(N(C([H])([H])C([H])([H])*)C([H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000005879 dioxolanyl group Chemical group 0.000 description 1
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
- 239000002988 disease modifying antirheumatic drug Substances 0.000 description 1
- 125000005411 dithiolanyl group Chemical group S1SC(CC1)* 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000000890 drug combination Substances 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- 229960002549 enoxacin Drugs 0.000 description 1
- IDYZIJYBMGIQMJ-UHFFFAOYSA-N enoxacin Chemical compound N1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 IDYZIJYBMGIQMJ-UHFFFAOYSA-N 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- AFAXGSQYZLGZPG-UHFFFAOYSA-N ethanedisulfonic acid Chemical compound OS(=O)(=O)CCS(O)(=O)=O AFAXGSQYZLGZPG-UHFFFAOYSA-N 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- 125000006534 ethyl amino methyl group Chemical group [H]N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000003889 eye drop Substances 0.000 description 1
- 229940012356 eye drops Drugs 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 238000001917 fluorescence detection Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229960003704 framycetin Drugs 0.000 description 1
- PGBHMTALBVVCIT-VCIWKGPPSA-N framycetin Chemical compound N[C@@H]1[C@@H](O)[C@H](O)[C@H](CN)O[C@@H]1O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](N)C[C@@H](N)[C@@H]2O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CN)O2)N)O[C@@H]1CO PGBHMTALBVVCIT-VCIWKGPPSA-N 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 229960003923 gatifloxacin Drugs 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003168 generic drug Substances 0.000 description 1
- 229960002518 gentamicin Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- 229960000642 grepafloxacin Drugs 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 125000004447 heteroarylalkenyl group Chemical group 0.000 description 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 description 1
- 125000005312 heteroarylalkynyl group Chemical group 0.000 description 1
- 125000005349 heteroarylcycloalkyl group Chemical group 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000000589 high-performance liquid chromatography-mass spectrometry Methods 0.000 description 1
- 210000005260 human cell Anatomy 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- GRRNUXAQVGOGFE-NZSRVPFOSA-N hygromycin B Chemical compound O[C@@H]1[C@@H](NC)C[C@@H](N)[C@H](O)[C@H]1O[C@H]1[C@H]2O[C@@]3([C@@H]([C@@H](O)[C@@H](O)[C@@H](C(N)CO)O3)O)O[C@H]2[C@@H](O)[C@@H](CO)O1 GRRNUXAQVGOGFE-NZSRVPFOSA-N 0.000 description 1
- 229940097277 hygromycin b Drugs 0.000 description 1
- CFUQBFQTFMOZBK-QUCCMNQESA-N ibazocine Chemical compound C12=CC(O)=CC=C2C[C@H]2N(CC=C(C)C)CC[C@]1(C)C2(C)C CFUQBFQTFMOZBK-QUCCMNQESA-N 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical group O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 150000003949 imides Chemical group 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000000099 in vitro assay Methods 0.000 description 1
- 238000005462 in vivo assay Methods 0.000 description 1
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000035992 intercellular communication Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000007917 intracranial administration Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000007913 intrathecal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002527 isonitriles Chemical class 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000004628 isothiazolidinyl group Chemical group S1N(CCC1)* 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 125000003965 isoxazolidinyl group Chemical group 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 229960000318 kanamycin Drugs 0.000 description 1
- 229930027917 kanamycin Natural products 0.000 description 1
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 1
- 229930182823 kanamycin A Natural products 0.000 description 1
- 229930182824 kanamycin B Natural products 0.000 description 1
- SKKLOUVUUNMCJE-FQSMHNGLSA-N kanamycin B Chemical compound N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SKKLOUVUUNMCJE-FQSMHNGLSA-N 0.000 description 1
- SKKLOUVUUNMCJE-UHFFFAOYSA-N kanendomycin Natural products NC1C(O)C(O)C(CN)OC1OC1C(O)C(OC2C(C(N)C(O)C(CO)O2)O)C(N)CC1N SKKLOUVUUNMCJE-UHFFFAOYSA-N 0.000 description 1
- 101150066555 lacZ gene Proteins 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- URLZCHNOLZSCCA-UHFFFAOYSA-N leu-enkephalin Chemical compound C=1C=C(O)C=CC=1CC(N)C(=O)NCC(=O)NCC(=O)NC(C(=O)NC(CC(C)C)C(O)=O)CC1=CC=CC=C1 URLZCHNOLZSCCA-UHFFFAOYSA-N 0.000 description 1
- 229960003376 levofloxacin Drugs 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 238000001294 liquid chromatography-tandem mass spectrometry Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical class [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 1
- 210000001853 liver microsome Anatomy 0.000 description 1
- 229960002422 lomefloxacin Drugs 0.000 description 1
- ZEKZLJVOYLTDKK-UHFFFAOYSA-N lomefloxacin Chemical compound FC1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNC(C)C1 ZEKZLJVOYLTDKK-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000004199 lung function Effects 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- CKJNUZNMWOVDFN-UHFFFAOYSA-N methanone Chemical compound O=[CH-] CKJNUZNMWOVDFN-UHFFFAOYSA-N 0.000 description 1
- 229940102398 methyl anthranilate Drugs 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 238000010172 mouse model Methods 0.000 description 1
- 229960003702 moxifloxacin Drugs 0.000 description 1
- FABPRXSRWADJSP-MEDUHNTESA-N moxifloxacin Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 FABPRXSRWADJSP-MEDUHNTESA-N 0.000 description 1
- 108010036341 murepavadin Proteins 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- JORAUNFTUVJTNG-BSTBCYLQSA-N n-[(2s)-4-amino-1-[[(2s,3r)-1-[[(2s)-4-amino-1-oxo-1-[[(3s,6s,9s,12s,15r,18s,21s)-6,9,18-tris(2-aminoethyl)-3-[(1r)-1-hydroxyethyl]-12,15-bis(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]amino]butan-2-yl]amino]-3-h Chemical compound CC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O.CCC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@H]([C@@H](C)O)CN[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O JORAUNFTUVJTNG-BSTBCYLQSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MHWLWQUZZRMNGJ-UHFFFAOYSA-N nalidixic acid Chemical compound C1=C(C)N=C2N(CC)C=C(C(O)=O)C(=O)C2=C1 MHWLWQUZZRMNGJ-UHFFFAOYSA-N 0.000 description 1
- 229960000210 nalidixic acid Drugs 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 229960000808 netilmicin Drugs 0.000 description 1
- ZBGPYVZLYBDXKO-HILBYHGXSA-N netilmycin Chemical compound O([C@@H]1[C@@H](N)C[C@H]([C@@H]([C@H]1O)O[C@@H]1[C@]([C@H](NC)[C@@H](O)CO1)(C)O)NCC)[C@H]1OC(CN)=CC[C@H]1N ZBGPYVZLYBDXKO-HILBYHGXSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 229960001180 norfloxacin Drugs 0.000 description 1
- OGJPXUAPXNRGGI-UHFFFAOYSA-N norfloxacin Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC(F)=C1N1CCNCC1 OGJPXUAPXNRGGI-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 229960001699 ofloxacin Drugs 0.000 description 1
- 244000039328 opportunistic pathogen Species 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 125000003566 oxetanyl group Chemical group 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- LRTFPLFDLJYEKT-UHFFFAOYSA-N para-isopropylaniline Chemical compound CC(C)C1=CC=C(N)C=C1 LRTFPLFDLJYEKT-UHFFFAOYSA-N 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 229960001914 paromomycin Drugs 0.000 description 1
- UOZODPSAJZTQNH-LSWIJEOBSA-N paromomycin Chemical compound N[C@@H]1[C@@H](O)[C@H](O)[C@H](CN)O[C@@H]1O[C@H]1[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](N)C[C@@H](N)[C@@H]2O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)O[C@@H]1CO UOZODPSAJZTQNH-LSWIJEOBSA-N 0.000 description 1
- 229960005065 paromomycin sulfate Drugs 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 150000002959 penams Chemical class 0.000 description 1
- 150000002961 penems Chemical class 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 239000013612 plasmid Substances 0.000 description 1
- XDJYMJULXQKGMM-UHFFFAOYSA-N polymyxin E1 Natural products CCC(C)CCCCC(=O)NC(CCN)C(=O)NC(C(C)O)C(=O)NC(CCN)C(=O)NC1CCNC(=O)C(C(C)O)NC(=O)C(CCN)NC(=O)C(CCN)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CCN)NC1=O XDJYMJULXQKGMM-UHFFFAOYSA-N 0.000 description 1
- KNIWPHSUTGNZST-UHFFFAOYSA-N polymyxin E2 Natural products CC(C)CCCCC(=O)NC(CCN)C(=O)NC(C(C)O)C(=O)NC(CCN)C(=O)NC1CCNC(=O)C(C(C)O)NC(=O)C(CCN)NC(=O)C(CCN)NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)C(CCN)NC1=O KNIWPHSUTGNZST-UHFFFAOYSA-N 0.000 description 1
- 229940041153 polymyxins Drugs 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 239000003910 polypeptide antibiotic agent Substances 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 230000001124 posttranscriptional effect Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- XJMOSONTPMZWPB-UHFFFAOYSA-M propidium iodide Chemical compound [I-].[I-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CCC[N+](C)(CC)CC)=C1C1=CC=CC=C1 XJMOSONTPMZWPB-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 229960003485 ribostamycin Drugs 0.000 description 1
- 229930190553 ribostamycin Natural products 0.000 description 1
- NSKGQURZWSPSBC-NLZFXWNVSA-N ribostamycin Chemical compound N[C@H]1[C@H](O)[C@@H](O)[C@H](CN)O[C@@H]1O[C@@H]1[C@@H](O[C@H]2[C@@H]([C@@H](O)[C@H](CO)O2)O)[C@H](O)[C@@H](N)C[C@H]1N NSKGQURZWSPSBC-NLZFXWNVSA-N 0.000 description 1
- NSKGQURZWSPSBC-UHFFFAOYSA-N ribostamycin A Natural products NC1C(O)C(O)C(CN)OC1OC1C(OC2C(C(O)C(CO)O2)O)C(O)C(N)CC1N NSKGQURZWSPSBC-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 229960005456 sisomicin Drugs 0.000 description 1
- URWAJWIAIPFPJE-YFMIWBNJSA-N sisomycin Chemical compound O1C[C@@](O)(C)[C@H](NC)[C@@H](O)[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](CC=C(CN)O2)N)[C@@H](N)C[C@H]1N URWAJWIAIPFPJE-YFMIWBNJSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910001467 sodium calcium phosphate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000012439 solid excipient Substances 0.000 description 1
- 239000002047 solid lipid nanoparticle Substances 0.000 description 1
- 229960004954 sparfloxacin Drugs 0.000 description 1
- DZZWHBIBMUVIIW-DTORHVGOSA-N sparfloxacin Chemical compound C1[C@@H](C)N[C@@H](C)CN1C1=C(F)C(N)=C2C(=O)C(C(O)=O)=CN(C3CC3)C2=C1F DZZWHBIBMUVIIW-DTORHVGOSA-N 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229960000268 spectinomycin Drugs 0.000 description 1
- UNFWWIHTNXNPBV-WXKVUWSESA-N spectinomycin Chemical compound O([C@@H]1[C@@H](NC)[C@@H](O)[C@H]([C@@H]([C@H]1O1)O)NC)[C@]2(O)[C@H]1O[C@H](C)CC2=O UNFWWIHTNXNPBV-WXKVUWSESA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- LZCVVMQABORALM-UHFFFAOYSA-N spiro[2.5]octyl Chemical group [CH]1CC11CCCCC1 LZCVVMQABORALM-UHFFFAOYSA-N 0.000 description 1
- LMUMMJCCZMWLEN-UHFFFAOYSA-N spiro[3.3]heptyl Chemical group [CH]1CCC11CCC1 LMUMMJCCZMWLEN-UHFFFAOYSA-N 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000002636 symptomatic treatment Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960004576 temafloxacin Drugs 0.000 description 1
- VXKIWRUDWDSIFX-UHFFFAOYSA-N tert-butyl N-[(6-phenoxy-1,3-benzoxazol-2-yl)methyl]-N-[2-(trifluoromethyl)pyridin-4-yl]carbamate Chemical compound O(C1=CC=CC=C1)C1=CC2=C(N=C(O2)CN(C(OC(C)(C)C)=O)C2=CC(=NC=C2)C(F)(F)F)C=C1 VXKIWRUDWDSIFX-UHFFFAOYSA-N 0.000 description 1
- 229960003604 testosterone Drugs 0.000 description 1
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002053 thietanyl group Chemical group 0.000 description 1
- 125000001730 thiiranyl group Chemical group 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- 125000001166 thiolanyl group Chemical group 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 230000000451 tissue damage Effects 0.000 description 1
- 231100000827 tissue damage Toxicity 0.000 description 1
- 229960000707 tobramycin Drugs 0.000 description 1
- NLVFBUXFDBBNBW-PBSUHMDJSA-N tobramycin Chemical compound N[C@@H]1C[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N NLVFBUXFDBBNBW-PBSUHMDJSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- ODLHGICHYURWBS-LKONHMLTSA-N trappsol cyclo Chemical compound CC(O)COC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)COCC(O)C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1COCC(C)O ODLHGICHYURWBS-LKONHMLTSA-N 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 229960000497 trovafloxacin Drugs 0.000 description 1
- WVPSKSLAZQPAKQ-CDMJZVDBSA-N trovafloxacin Chemical compound C([C@H]1[C@@H]([C@H]1C1)N)N1C(C(=CC=1C(=O)C(C(O)=O)=C2)F)=NC=1N2C1=CC=C(F)C=C1F WVPSKSLAZQPAKQ-CDMJZVDBSA-N 0.000 description 1
- 239000012137 tryptone Substances 0.000 description 1
- ORHBXUUXSCNDEV-UHFFFAOYSA-N umbelliferone Chemical compound C1=CC(=O)OC2=CC(O)=CC=C21 ORHBXUUXSCNDEV-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
- 239000002132 β-lactam antibiotic Substances 0.000 description 1
- 229940124586 β-lactam antibiotics Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP18181475 | 2018-07-03 | ||
| EP18181475.7 | 2018-07-03 | ||
| PCT/EP2019/067899 WO2020007938A1 (en) | 2018-07-03 | 2019-07-03 | PqsR INVERSE AGONISTS |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| JP2021529203A JP2021529203A (ja) | 2021-10-28 |
| JP2021529203A5 JP2021529203A5 (https=) | 2022-07-04 |
| JPWO2020007938A5 JPWO2020007938A5 (https=) | 2022-07-04 |
| JP7399898B2 true JP7399898B2 (ja) | 2023-12-18 |
Family
ID=62846069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020573396A Active JP7399898B2 (ja) | 2018-07-03 | 2019-07-03 | PqsRインバースアゴニスト |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US11883387B2 (https=) |
| EP (1) | EP3818045A1 (https=) |
| JP (1) | JP7399898B2 (https=) |
| AU (1) | AU2019297409B2 (https=) |
| CA (1) | CA3103351A1 (https=) |
| WO (1) | WO2020007938A1 (https=) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3164264A1 (en) * | 2020-01-02 | 2021-07-08 | Helmholtz-Zentrum Fur Infektionsforschung Gmbh | Novel pqsr inverse agonists |
| US12528783B2 (en) | 2020-01-02 | 2026-01-20 | Helmholtz-Zentrum Fur Infektionsforschung Gmbh | PqsR inverse agonists |
| WO2024186827A2 (en) * | 2023-03-06 | 2024-09-12 | The Regents Of The University Of California | Novel host-directed therapeutic agent for the treatment of infectious diseases |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017139428A1 (en) | 2016-02-10 | 2017-08-17 | Janssen Pharmaceutica Nv | Substituted 1,2,3-triazoles as nr2b-selective nmda modulators |
| CN108003151A (zh) | 2016-10-27 | 2018-05-08 | 湖南化工研究院有限公司 | N-杂芳基甲基嘧啶胺类化合物及其制备方法与应用 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8877940B2 (en) | 2011-02-22 | 2014-11-04 | Institut National De La Recherche Scientifique | Antibiotic tolerance inhibitors |
| US9643933B2 (en) | 2013-04-23 | 2017-05-09 | The General Hospital Corporation | Compounds useful as antibiotic tolerance inhibitors |
| WO2016007837A1 (en) | 2014-07-11 | 2016-01-14 | Spero Therapeutics, Inc. | Carbonyl linked bicyclic heteroaryl antibiotic tolerance inhibitors |
| WO2016040764A1 (en) | 2014-09-12 | 2016-03-17 | Spero Therapeutics, Inc. | Carbonyl linked bicyclic heteroaryl n-benzimidazoles and analogs as antibiotic tolerance inhibitors |
| WO2016112088A1 (en) | 2015-01-06 | 2016-07-14 | Spero Therapeutics, Inc. | Aryloxyacetylindoles and analogs as antibiotic tolerance inhibitors |
-
2019
- 2019-07-03 US US17/257,804 patent/US11883387B2/en active Active
- 2019-07-03 EP EP19741977.3A patent/EP3818045A1/en active Pending
- 2019-07-03 JP JP2020573396A patent/JP7399898B2/ja active Active
- 2019-07-03 AU AU2019297409A patent/AU2019297409B2/en active Active
- 2019-07-03 WO PCT/EP2019/067899 patent/WO2020007938A1/en not_active Ceased
- 2019-07-03 CA CA3103351A patent/CA3103351A1/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017139428A1 (en) | 2016-02-10 | 2017-08-17 | Janssen Pharmaceutica Nv | Substituted 1,2,3-triazoles as nr2b-selective nmda modulators |
| CN108003151A (zh) | 2016-10-27 | 2018-05-08 | 湖南化工研究院有限公司 | N-杂芳基甲基嘧啶胺类化合物及其制备方法与应用 |
Non-Patent Citations (1)
| Title |
|---|
| DATABASE REGISTRY on STN,RN 1546402-30-5 REGISTRY Entered STN: 17 Feb 2014 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA3103351A1 (en) | 2020-01-09 |
| AU2019297409B2 (en) | 2022-12-01 |
| WO2020007938A1 (en) | 2020-01-09 |
| EP3818045A1 (en) | 2021-05-12 |
| JP2021529203A (ja) | 2021-10-28 |
| US11883387B2 (en) | 2024-01-30 |
| AU2019297409A1 (en) | 2021-01-07 |
| US20210353606A1 (en) | 2021-11-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2702647C (en) | Thiopyrimidine-based compounds and uses thereof | |
| EP1562911B1 (en) | Compositions useful as inhibitors of jak and other protein kinases | |
| US9242977B2 (en) | Trk-inhibiting compound | |
| JP4688498B2 (ja) | Jakインヒビターとしてのヘテロアリール−ピリミジン誘導体 | |
| KR20090125779A (ko) | 브라디키닌 b2 수용체 조절제로서 8-옥시-퀴놀린 유도체 | |
| JP2008503492A (ja) | Rho−キナーゼの新規阻害剤 | |
| JP2010537967A (ja) | 癌及び乾癬の治療に有用な複素環式アミド | |
| JP7399898B2 (ja) | PqsRインバースアゴニスト | |
| JP2014509616A (ja) | 治療用イミダゾ[1,2−a]ピリジン化合物 | |
| CA3144506A1 (en) | Substituted amino heteroaryl derivatives and compositions thereof usefule as antifibrotic compounds | |
| US11548900B2 (en) | Oxazino-quinazoline and oxazino-quinoline type compound, preparation method and uses thereof | |
| KR20180105801A (ko) | TGase 2 억제제로서의 퀴놀린-5,8-디온 유도체 및 이를 포함하는 약제학적 조성물 | |
| US20180305331A1 (en) | Pyridone derivatives and their use as kinase inhibitors | |
| WO2020046975A1 (en) | Methods of treating neurodegenerative diseases | |
| WO2011057892A1 (en) | 2,3-dihydrobenzoxazine and 2,3-dihydrobenzothiazine derivates as hif-inhibitors for the treatment of cancer and inflammatory diseases | |
| JP7421655B2 (ja) | 新規なPqsRインバースアゴニスト | |
| US7119109B2 (en) | Heteroarylheteroalkylamine derivatives and their use as inhibitors of nitric oxide synthase | |
| EP4085054B1 (en) | New pqsr inverse agonists | |
| US10472326B2 (en) | PQSR modulators | |
| EP1572686A1 (en) | Anthranilic acid amide derivatives and their pharmaceutical use | |
| MXPA06008833A (en) | Heteroarylaminopyrazole derivatives useful for the treatment of diabetes |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20220624 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20220624 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20230615 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20230628 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230912 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20231129 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20231206 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 7399898 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |