1. Anti-infection
  2. Bacterial
  3. FtsZ-IN-4

FtsZ-IN-4 是一种口服有效的细胞分裂蛋白丝状温度敏感突变体 Z (FtsZ) 抑制剂,具有良好的抑菌活性。FtsZ-IN-4 具有良好的活性分子性能,对健康细胞低毒 (CC50 >20 μg/mL)。

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FtsZ-IN-4 Chemical Structure

FtsZ-IN-4 Chemical Structure

CAS No. : 2882904-64-3

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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

FtsZ-IN-4 is an orally active FtsZ (filamenting temperature-sensitive mutant Z) inhibitor, exhibits excellent antibacterial activity. FtsZ-IN-4 shows good pharmaceutical properties with low cytotoxicity (CC50 >20 μg/mL)[1].

IC50 & Target

Target: Filamenting temperature-sensitive mutant Z (FtsZ)[1]

体外研究
(In Vitro)

MIC: Minimum inhibition concentration; MBC: Minimum bactericidal concentration.
FtsZ-IN-4 (compound 30) shows potent antibacterial activity to B. subtilis and S. aureus with MICs of 0.008-0.25 μg/mL, respectively[1].
FtsZ-IN-4 (0.064 μg/mL or 0.5 μg/mL; 0-24 h) shows rapid bactericidal properties within 3 h, and the MBC/MIC ratios are ≤4, satisfying CLSI standards[1].
FtsZ-IN-4 (>20 μg/mL; 72 h) exerts low cytotoxicity towards Vero cells [1].
FtsZ-IN-4 (0.016 μg/mL; 3 h) increases the length of the B. subtilis ATCC9372, causes abnormal bacterial cell division and lead to bacterial cell death[1].
FtsZ-IN-4 (10 μg/mL; 0-15 min) induces SaFtsZ polymerization and (0-35 μg/mL; 30 min) inhibits the GTPase activity of SaFtsZ in a dose-dependent manner[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: Vero cells (African green monkey kidney cells)
Concentration: >20 μg/mL
Incubation Time: 72 hours
Result: Exhibited the 50% cytotoxic concentration (CC50) >20 μg/mL, much more than the inhibition of B. subtilis ATCC9372 (MIC =0.016 μg/mL).

Cell Proliferation Assay[1]

Cell Line: S. aureus ATCC25923 and Bacillus ATCC9372
Concentration: 1×, 2×, 4×, 8× MIC; MIC =0.125 μg/mL (S. aureus); 0.016 μg/mL (Bacillus)
Incubation Time: 3, 6, 12, 24 hours
Result: Reduced B. subtilis ATCC9372 and S. aureus ATCC25923 cells below the lowest detectable limit (103 CFU/ mL) in 3 h.
体内研究
(In Vivo)

FtsZ-IN-4 (compound 30) (5 mg/kg; p.o.) exhibits moderate exposure (AUC(0-t) =544.2 h*ng/mL) and an oral bioavailability (F) of 61.2% in mice[1].
FtsZ-IN-4 (25 mg/kg; i.v.) exerts good in vivo efficacy in mice. Murine pharmacokinetic profiles of FtsZ-IN-4[1]

Route Dose (mg/kg) T1/2 (h) Tmax (h) Cmax (ng/mL) AUC(0-t) (h•ng/mL) AUC(0-∞) (h•ng/mL) Vss (ng/mL) CL (mL/h/kg) F (%)
i.v. 1 0.28 0.083 480.5 177.8 178.7 1545.5 5682.8 /
5 2.26 0.5 429.3 544.2 559.3 / / 61.2

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male ICR mice (infected with S. aureus ATCC25923)[1]
Dosage: 25 mg/kg
Administration: Intraperitoneal injection; 0.5 mL
Result: Significantly reduced the bacteria burden and showed comparable in vivo efficacy with vancomycin.
分子量

387.81

Formula

C21H16ClF2NO2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献

FtsZ-IN-4 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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