化合物KKL10
中文名稱(chēng) | 化合物KKL10 |
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中文同義詞 | 化合物KKL10;5-溴-N-(5-(對(duì)甲苯基)-1,3,4-惡二唑-2-基)噻吩-2-甲酰胺 |
英文名稱(chēng) | KKL-10 |
英文同義詞 | KKL-10;5-bromo-N-(5-(p-tolyl)-1,3,4-oxadiazol-2-yl)thiophene-2-carboxamide;KKL-10;KKL 10;KKL10;5-bromo-N-[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]thiophene-2-carboxamide;KKL10,Bacterial,Inhibitor,inhibit,KKL-10;2-Thiophenecarboxamide, 5-bromo-N-[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]- |
CAS號(hào) | 952849-76-2 |
分子式 | C14H10BrN3O2S |
分子量 | 364.22 |
EINECS號(hào) | |
相關(guān)類(lèi)別 | |
Mol文件 | 952849-76-2.mol |
結(jié)構(gòu)式 |
化合物KKL10 性質(zhì)
密度 | 1.620±0.06 g/cm3(Predicted) |
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儲(chǔ)存條件 | Store at -20°C |
溶解度 | DMSO:2.89(最大濃度 mg/mL);7.93(最大濃度 mM) |
酸度系數(shù)(pKa) | 10.04±0.70(Predicted) |
形態(tài) | 固體 |
顏色 | 白色至米白色 |
Target | Value |
ribosome rescue
() |
The ribosome rescue inhibitor KKL-10 exhibits exceptional antimicrobial activity against both attenuated and fully virulent strains of F. tularensis . The minimum inhibitory concentration (MIC) against F. tularensis strain LVS and Schu S4 are 0.12 and 0.48 μg/mL, respectively. KKL-10 arrests intracellular growth of F. tularensis during all stages of infection. KKL-10 does not affect macrophage viability or function. KKL-10 produces cytotoxic effects of less than 5% at concentrations up to 17.5 μg/mL. The combination of IFN-γ stimulation and KKL-10 activity results in a reduction of the bacterial load by >99.9%. KKL-10 is also able to inhibit growth of F. tularensis inside eukaryotic cells and show no toxicity to HepG2 cells.
安全信息
更新日期 | 產(chǎn)品編號(hào) | 產(chǎn)品名稱(chēng) | CAS號(hào) | 包裝 | 價(jià)格 |
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2024/11/08 | HY-101865 | 952849-76-2 KKL-10 | 952849-76-2 | 5mg | 1300元 |
2024/11/08 | S0147 | 952849-76-2 KKL-10 | 952849-76-2 | 5mg | 1576.46元 |