JP5309021B2 - 抗菌組成物 - Google Patents

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Publication number

JP5309021B2

JP5309021B2 JP2009515958A JP2009515958A JP5309021B2 JP 5309021 B2 JP5309021 B2 JP 5309021B2 JP 2009515958 A JP2009515958 A JP 2009515958A JP 2009515958 A JP2009515958 A JP 2009515958A JP 5309021 B2 JP5309021 B2 JP 5309021B2

Authority

JP

Japan

Prior art keywords

mmol

pyridin

optionally substituted

ethyl

group

Prior art date

2006-06-22

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.)

Expired - Fee Related

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• 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 8
• 239000000203 mixture Substances 0.000 title description 69
• 150000001875 compounds Chemical class 0.000 claims abstract description 86
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 61
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 29
• 239000001257 hydrogen Substances 0.000 claims abstract description 29
• 125000006413 ring segment Chemical group 0.000 claims abstract description 28
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 27
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 15
• 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims abstract description 9
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 6
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 6
• 150000003568 thioethers Chemical class 0.000 claims abstract description 6
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 5
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 5
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 4
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 4
• 125000004450 alkenylene group Chemical group 0.000 claims abstract description 4
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 49
• 229910052757 nitrogen Inorganic materials 0.000 claims description 27
• 125000001424 substituent group Chemical group 0.000 claims description 21
• 230000001580 bacterial effect Effects 0.000 claims description 19
• 150000003839 salts Chemical class 0.000 claims description 12
• 125000004432 carbon atom Chemical group C* 0.000 claims description 11
• 125000001620 monocyclic carbocycle group Chemical group 0.000 claims description 9
• JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 9
• 238000011109 contamination Methods 0.000 claims description 8
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
• 239000003242 anti bacterial agent Substances 0.000 claims description 7
• 125000002837 carbocyclic group Chemical group 0.000 claims description 7
• 125000002527 bicyclic carbocyclic group Chemical group 0.000 claims description 6
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
• 239000012453 solvate Substances 0.000 claims description 5
• UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims description 4
• 150000001204 N-oxides Chemical class 0.000 claims description 3
• KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical class C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 3
• CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 3
• 125000004419 alkynylene group Chemical group 0.000 claims description 3
• 229910052799 carbon Chemical group 0.000 claims description 3
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
• 150000003222 pyridines Chemical class 0.000 claims description 3
• HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical class C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 2
• 125000002947 alkylene group Chemical group 0.000 claims description 2
• 150000003216 pyrazines Chemical group 0.000 claims description 2
• 239000000758 substrate Substances 0.000 claims description 2
• KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical class C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
• SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical class N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
• AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical class C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 2
• SRSKXJVMVSSSHB-UHFFFAOYSA-N 1h-pyrrolo[3,2-c]pyridine Chemical class N1=CC=C2NC=CC2=C1 SRSKXJVMVSSSHB-UHFFFAOYSA-N 0.000 claims 1
• PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Chemical class C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 1
• FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical class C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
• 125000003545 alkoxy group Chemical group 0.000 claims 1
• 239000003937 drug carrier Substances 0.000 claims 1
• 239000008194 pharmaceutical composition Substances 0.000 claims 1
• 150000003230 pyrimidines Chemical group 0.000 claims 1
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 187
• 239000011541 reaction mixture Substances 0.000 description 112
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 92
• 239000007787 solid Substances 0.000 description 82
• 239000000243 solution Substances 0.000 description 81
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 78
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 65
• 235000019439 ethyl acetate Nutrition 0.000 description 64
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 63
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 61
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 60
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 56
• 238000005481 NMR spectroscopy Methods 0.000 description 48
• -1 2-methyl-2-propynyl Chemical group 0.000 description 43
• 239000002904 solvent Substances 0.000 description 43
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 40
• 238000006243 chemical reaction Methods 0.000 description 35
• 238000001816 cooling Methods 0.000 description 35
• 239000012299 nitrogen atmosphere Substances 0.000 description 32
• 239000011734 sodium Substances 0.000 description 32
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 30
• 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 29
• BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 24
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
• 239000012044 organic layer Substances 0.000 description 22
• 238000005160 1H NMR spectroscopy Methods 0.000 description 21
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
• 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 21
• 238000000746 purification Methods 0.000 description 21
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 19
• 239000000377 silicon dioxide Substances 0.000 description 18
• 239000000047 product Substances 0.000 description 17
• 238000003756 stirring Methods 0.000 description 17
• 239000000725 suspension Substances 0.000 description 17
• LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 16
• 239000000741 silica gel Substances 0.000 description 15
• 229910002027 silica gel Inorganic materials 0.000 description 15
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 14
• OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 14
• 238000004128 high performance liquid chromatography Methods 0.000 description 14
• 239000012258 stirred mixture Substances 0.000 description 14
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 13
• 239000012267 brine Substances 0.000 description 13
• 235000019441 ethanol Nutrition 0.000 description 13
• 238000002953 preparative HPLC Methods 0.000 description 13
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 13
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 12
• 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 12
• 101710183280 Topoisomerase Proteins 0.000 description 12
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
• NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 12
• 230000000694 effects Effects 0.000 description 12
• 235000019253 formic acid Nutrition 0.000 description 12
• 238000000034 method Methods 0.000 description 12
• SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 12
• IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 11
• 238000004587 chromatography analysis Methods 0.000 description 11
• 125000002950 monocyclic group Chemical group 0.000 description 11
• HFLVEWBPLLPPMX-UHFFFAOYSA-N 1-(7-bromo-5-pyridin-3-yl-1,3-benzothiazol-2-yl)-3-ethylurea Chemical compound C=1C(Br)=C2SC(NC(=O)NCC)=NC2=CC=1C1=CC=CN=C1 HFLVEWBPLLPPMX-UHFFFAOYSA-N 0.000 description 10
• 239000003208 petroleum Substances 0.000 description 10
• LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 10
• 239000002585 base Substances 0.000 description 9
• YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].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 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 9
• 239000000706 filtrate Substances 0.000 description 9
• 235000017557 sodium bicarbonate Nutrition 0.000 description 9
• 229910000030 sodium bicarbonate Inorganic materials 0.000 description 9
• 125000003118 aryl group Chemical group 0.000 description 8
• WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 8
• PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 8
• ABMYEXAYWZJVOV-UHFFFAOYSA-N pyridin-3-ylboronic acid Chemical compound OB(O)C1=CC=CN=C1 ABMYEXAYWZJVOV-UHFFFAOYSA-N 0.000 description 8
• 235000011121 sodium hydroxide Nutrition 0.000 description 8
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
• 239000004202 carbamide Substances 0.000 description 7
• 238000001914 filtration Methods 0.000 description 7
• 150000002431 hydrogen Chemical class 0.000 description 7
• KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 6
• OXJWGXOCTDLNRC-UHFFFAOYSA-N 1-(5-bromo-7-pyridin-3-yl-1,3-benzothiazol-2-yl)-3-ethylurea Chemical compound C=12SC(NC(=O)NCC)=NC2=CC(Br)=CC=1C1=CC=CN=C1 OXJWGXOCTDLNRC-UHFFFAOYSA-N 0.000 description 6
• NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
• VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 6
• 241000894006 Bacteria Species 0.000 description 6
• 208000035143 Bacterial infection Diseases 0.000 description 6
• 108020004414 DNA Proteins 0.000 description 6
• AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 6
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
• 229960000583 acetic acid Drugs 0.000 description 6
• QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
• 235000011114 ammonium hydroxide Nutrition 0.000 description 6
• 208000022362 bacterial infectious disease Diseases 0.000 description 6
• 239000003054 catalyst Substances 0.000 description 6
• 125000001072 heteroaryl group Chemical group 0.000 description 6
• 125000000842 isoxazolyl group Chemical group 0.000 description 6
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
• 235000011056 potassium acetate Nutrition 0.000 description 6
• 125000000714 pyrimidinyl group Chemical group 0.000 description 6
• 238000010992 reflux Methods 0.000 description 6
• 229920006395 saturated elastomer Polymers 0.000 description 6
• FUCJAPOSIFKDLA-UHFFFAOYSA-N 1-(5-bromo-7-pyridin-2-yl-1,3-benzothiazol-2-yl)-3-ethylurea Chemical compound C=12SC(NC(=O)NCC)=NC2=CC(Br)=CC=1C1=CC=CC=N1 FUCJAPOSIFKDLA-UHFFFAOYSA-N 0.000 description 5
• 0 C*c1nc(cc(cc2-c3cnccc3)Br)c2[s]1 Chemical compound C*c1nc(cc(cc2-c3cnccc3)Br)c2[s]1 0.000 description 5
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
• ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 5
• 230000000845 anti-microbial effect Effects 0.000 description 5
• 229940088710 antibiotic agent Drugs 0.000 description 5
• 238000003556 assay Methods 0.000 description 5
• 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 5
• FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 5
• 229910000024 caesium carbonate Inorganic materials 0.000 description 5
• 239000012043 crude product Substances 0.000 description 5
• 239000003814 drug Substances 0.000 description 5
• 229940079593 drug Drugs 0.000 description 5
• 238000003818 flash chromatography Methods 0.000 description 5
• FSAFVTMBEIXIOA-UHFFFAOYSA-N methyl 2-(ethylcarbamoylamino)-5-pyridin-3-yl-1,3-benzothiazole-7-carboxylate Chemical compound C=1C(C(=O)OC)=C2SC(NC(=O)NCC)=NC2=CC=1C1=CC=CN=C1 FSAFVTMBEIXIOA-UHFFFAOYSA-N 0.000 description 5
• 238000012544 monitoring process Methods 0.000 description 5
• 125000003386 piperidinyl group Chemical group 0.000 description 5
• 125000003226 pyrazolyl group Chemical group 0.000 description 5
• 125000004076 pyridyl group Chemical group 0.000 description 5
• 125000000168 pyrrolyl group Chemical group 0.000 description 5
• 235000010288 sodium nitrite Nutrition 0.000 description 5
• 125000000335 thiazolyl group Chemical group 0.000 description 5
• DEOAPUTWHUSPEQ-UHFFFAOYSA-N 1-(5,7-dibromo-1,3-benzothiazol-2-yl)-3-ethylurea Chemical compound BrC1=CC(Br)=C2SC(NC(=O)NCC)=NC2=C1 DEOAPUTWHUSPEQ-UHFFFAOYSA-N 0.000 description 4
• WXMMYNLMFRCZJR-UHFFFAOYSA-N 1-ethyl-3-(7-iodo-5-pyridin-3-yl-1,3-benzothiazol-2-yl)urea Chemical compound C=1C(I)=C2SC(NC(=O)NCC)=NC2=CC=1C1=CC=CN=C1 WXMMYNLMFRCZJR-UHFFFAOYSA-N 0.000 description 4
• 108091006112 ATPases Proteins 0.000 description 4
• 102000057290 Adenosine Triphosphatases Human genes 0.000 description 4
• XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
• IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 4
• 108090000790 Enzymes Proteins 0.000 description 4
• 102000004190 Enzymes Human genes 0.000 description 4
• 239000005909 Kieselgur Substances 0.000 description 4
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
• HABVCDVEINHWTR-UHFFFAOYSA-N [B].[B].C(CO)(=O)OCC(C)(C)C Chemical compound [B].[B].C(CO)(=O)OCC(C)(C)C HABVCDVEINHWTR-UHFFFAOYSA-N 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• 230000002378 acidificating effect Effects 0.000 description 4
• 125000000217 alkyl group Chemical group 0.000 description 4
• 239000007864 aqueous solution Substances 0.000 description 4
• 125000002619 bicyclic group Chemical group 0.000 description 4
• 230000015572 biosynthetic process Effects 0.000 description 4
• OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 4
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
• 125000002541 furyl group Chemical group 0.000 description 4
• 239000012362 glacial acetic acid Substances 0.000 description 4
• 150000002430 hydrocarbons Chemical group 0.000 description 4
• 125000001041 indolyl group Chemical group 0.000 description 4
• 208000015181 infectious disease Diseases 0.000 description 4
• 239000003112 inhibitor Substances 0.000 description 4
• 125000001786 isothiazolyl group Chemical group 0.000 description 4
• 125000002757 morpholinyl group Chemical group 0.000 description 4
• 125000002971 oxazolyl group Chemical group 0.000 description 4
• 125000004193 piperazinyl group Chemical group 0.000 description 4
• 229910000160 potassium phosphate Inorganic materials 0.000 description 4
• 235000011009 potassium phosphates Nutrition 0.000 description 4
• 238000003786 synthesis reaction Methods 0.000 description 4
• 239000006188 syrup Substances 0.000 description 4
• 235000020357 syrup Nutrition 0.000 description 4
• 125000001113 thiadiazolyl group Chemical group 0.000 description 4
• 125000001544 thienyl group Chemical group 0.000 description 4
• UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 4
• 230000000699 topical effect Effects 0.000 description 4
• 229910000404 tripotassium phosphate Inorganic materials 0.000 description 4
• 235000019798 tripotassium phosphate Nutrition 0.000 description 4
• KUMKXVOROOAIRR-UHFFFAOYSA-N 1-(7-amino-5-pyridin-3-yl-1,3-benzothiazol-2-yl)-3-ethylurea Chemical compound C=1C(N)=C2SC(NC(=O)NCC)=NC2=CC=1C1=CC=CN=C1 KUMKXVOROOAIRR-UHFFFAOYSA-N 0.000 description 3
• BAEARKULMMURTJ-UHFFFAOYSA-N 1-[7-(5-cyanopyridin-2-yl)-5-hydroxy-1,3-benzothiazol-2-yl]-3-ethylurea Chemical compound C=12SC(NC(=O)NCC)=NC2=CC(O)=CC=1C1=CC=C(C#N)C=N1 BAEARKULMMURTJ-UHFFFAOYSA-N 0.000 description 3
• NISGIWQRZXIHFR-UHFFFAOYSA-N 1-ethyl-3-(7-nitro-5-pyridin-3-yl-1,3-benzothiazol-2-yl)urea Chemical compound C=1C([N+]([O-])=O)=C2SC(NC(=O)NCC)=NC2=CC=1C1=CC=CN=C1 NISGIWQRZXIHFR-UHFFFAOYSA-N 0.000 description 3
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