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Secnidazole
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Secnidazole图片
CAS NO:3366-95-8
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
10mg电议
50mg电议
100mg电议
500mg电议
1 g电议
5 g电议

产品名称
塞克硝唑
RP-14539
PM-185184
产品介绍
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。Secnidazole 可用于各种疾病的研究,如阿米巴病和贾第虫病,以及细菌性阴道炎。
生物活性

Secnidazole (RP-14539) is an orally active azoleantibioticand a imidazole mitigator ofSerratia marcescensvirulence. Secnidazole, as an analog of acylhomoserine lactones, effectively inhibits QS resulting in the attenuation ofPseudomonas aeruginosapathogenesis. Secnidazole has antimicrobial activity against many anaerobic Gram-negative and Gram-positivebacterialspecies in vitro. Secnidazole can be used for the research of various diseases, such as amoebiasis and giardiasis, andbacterialvaginitis[1][2][3].

IC50& Target

Amebae

 

体外研究
(In Vitro)

Secnidazole (RP-14539) (0-5000 μM; 5 or 10 min) inhibits CYP2C19 and CYP3A4, with IC50values of 3873 μM and 3722 μM, respectively[2].
Secnidazole (0-5000 μM; 5 or 10 min) does not exhibit time-dependent inhibition[2].
Secnidazole (0-5000 μM; 5 or 10 min) has an apparent IC50value of 503 μM for direct inhibition of human ALDH2[2].
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[2].
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) inhibitsS.marcescensgrowth with a MIC50value of 10 mg/mL[3].

Cell Viability Assay[3]

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 h
Result:Had no inhibitory effect onS.marcescensgrowth at 2 mg/mL (equivalent to 1/5 MIC).
体内研究
(In Vivo)

Secnidazole (100 μL; ip.; for 5 days) has protective activity againstS.marcescenspathogenesis and can diminish its pathogenesis in mice[3].

Animal Model:Female healthy albino mice[3]
Dosage:100 μL
Administration:100 μL; ip.; for 5 days
Result:Significantly diminished the bacteria s capacity to kill mice.
Clinical Trial
分子量

185.18

性状

Solid

Formula

C7H11N3O3

CAS 号

3366-95-8

中文名称

塞克硝唑

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : ≥ 30 mg/mL(162.00 mM)

H2O : 25 mg/mL(135.00 mM;Need ultrasonic)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM5.4002 mL27.0008 mL54.0015 mL
5 mM1.0800 mL5.4002 mL10.8003 mL
10 mM0.5400 mL2.7001 mL5.4002 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 50 mg/mL (270.01 mM); Clear solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。