
Secnidazole
CAS No. 3366-95-8
Secnidazole ( PM 185184 | RP 14539 )
产品货号. M14142 CAS No. 3366-95-8
Secnidazole (RP-14539) 是一种唑类抗生素和黏质沙雷菌毒力的咪唑缓释剂,具有口服活性。Secnidazole 作为一种类似于酰基高丝氨酸内酯,能有效抑制 QS 导致铜绿假单胞菌的发病衰减。Secnidazole 在体外对多种厌氧革兰氏阴性和革兰氏阳性细菌均有抗菌活性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥275 | 有现货 |
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10MG | ¥405 | 有现货 |
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25MG | ¥470 | 有现货 |
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50MG | ¥729 | 有现货 |
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100MG | ¥875 | 有现货 |
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200MG | ¥1045 | 有现货 |
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500MG | ¥1264 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Secnidazole
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Secnidazole (RP-14539) 是一种唑类抗生素和黏质沙雷菌毒力的咪唑缓释剂,具有口服活性。Secnidazole 作为一种类似于酰基高丝氨酸内酯,能有效抑制 QS 导致铜绿假单胞菌的发病衰减。Secnidazole 在体外对多种厌氧革兰氏阴性和革兰氏阳性细菌均有抗菌活性。
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产品描述Secnidazole (trade names Flagentyl, Sindose, Secnil) is a nitroimidazole anti-infective. Effectiveness in the treatment of dientamoebiasis has been reported. Secnidazole is structurally related to the commonly used 5-nitroimidazoles metronidazole and tinidazole. (In Vitro):Secnidazole (RP-14539) (0-5000 μM; 5 or 10 min) inhibits CYP2C19 and CYP3A4, with IC50 values of 3873 μM and 3722 μM, respectively.Secnidazole (0-5000 μM; 5 or 10 min) does not exhibit time-dependent inhibition.Secnidazole (0-5000 μM; 5 or 10 min) has an apparent IC50 value of 503 μM for direct inhibition of human ALDH2.Secnidazole (0-5000 μM; 5 or 10 min) has concentration-dependent inhibition at higher concentration with some of the CYP isoforms notably CYP2A6, CYP2B6, and CYP2D6.Secnidazole (10 μL; 20 h; the secnidazole solution was two-fold serially diluted using Mueller–Hinton broth to obtain dilutions ranging from 80 to 0.3125 mg/mL) inhibits S.marcescens growth with a MIC50 value of 10 mg/mL.(In Vivo):Secnidazole (100 μL; ip.; for 5 days) has protective activity against S.marcescens pathogenesis and can diminish its pathogenesis in mice.
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体外实验Secnidazole (RP-14539) (0-5000 μM; 5 or 10 min) inhibits CYP2C19 and CYP3A4, with IC50 values of 3873 μM and 3722 μM, respectively.Secnidazole (0-5000 μM; 5 or 10 min) does not exhibit time-dependent inhibition. Secnidazole (0-5000 μM; 5 or 10 min) has an apparent IC50 value of 503 μM for direct inhibition of human ALDH2.Secnidazole (0-5000 μM; 5 or 10 min) has concentration-dependent inhibition at higher concentration with some of the CYP isoforms notably CYP2A6, CYP2B6, and CYP2D6.Secnidazole (10 μL; 20 h; the secnidazole solution was two-fold serially diluted using Mueller–Hinton broth to obtain dilutions ranging from 80 to 0.3125 mg/mL) inhibits S.marcescens growth with a MIC50 value of 10 mg/mL. Cell Viability Assay Cell Line:S.marcescens Concentration:10 μL (the secnidazole solution was two-fold serially diluted using Mueller–Hinton broth to obtain dilutions ranging from 80 to 0.3125 mg/mL)Incubation Time:20 hResult:Had no inhibitory effect on S.marcescens growth at 2 mg/mL (equivalent to 1/5 MIC).
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体内实验Secnidazole (100 μL; ip.; for 5 days) has protective activity against S.marcescens pathogenesis and can diminish its pathogenesis in mice. Animal Model:Female healthy albino mice Dosage:100 μL Administration:100 μL; ip.; for 5 days Result:Significantly diminished the bacteria s capacity to kill mice.
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同义词PM 185184 | RP 14539
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通路Others
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靶点Other Targets
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受体Others
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研究领域Infection
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适应症——
化学信息
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CAS Number3366-95-8
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分子量185.18
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分子式C7H11N3O3
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纯度>98% (HPLC)
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溶解度Ethanol: 37 mg/mL (199.8 mM); Water: 37 mg/mL (199.8 mM); DMSO: 37 mg/mL (199.8 mM)
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SMILES(2RS)-(2-methyl-5-nitro-1H-imidazol-1-yl)propan-2-ol
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化学全称1-(2-methyl-5-nitro-1H-imidazol-1-yl)propan-2-ol
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. De Backer, et al. Clinical Microbiology and Infection 16 (5): 470–472.
产品手册




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