BENZNIDAZOLE

Benznidazole is a research-grade compound used in advanced pharmaceutical and biochemical studies. Chemical & Pharmacological Characteristics The compound is a small nitroheterocycle with moderate lipophilicity and limited aqueous solubility, often requiring co-solvents for in vitro dosing. Nitro groups introduce redox-reactive behavior and can drive bioactivation-dependent efficacy and toxicity. Exposure-response can differ substantially between host cells and parasite stages. It is primarily applied to investigate compound-specific mechanisms, physicochemical behavior, and analytical or formulation-relevant characteristics under controlled laboratory conditions.

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Product Description


Chemical & Pharmacological Characteristics

The compound is a small nitroheterocycle with moderate lipophilicity and limited aqueous solubility, often requiring co-solvents for in vitro dosing. Nitro groups introduce redox-reactive behavior and can drive bioactivation-dependent efficacy and toxicity. Exposure-response can differ substantially between host cells and parasite stages.

Mechanism of Action

Benznidazole is bioactivated by parasite and host nitroreductase systems to generate reactive intermediates that damage macromolecules, including DNA and proteins. This leads to impaired parasite replication and cell death in susceptible organisms.

Because activity depends on enzymatic activation and redox environment, experimental outcomes are influenced by oxygen tension, metabolic state, and antioxidant capacity. Resistance can arise through altered nitroreductase activity, enhanced detoxification, or repair pathways, so mechanistic studies should include genotyped strains and orthogonal damage markers.

Advanced Research Applications

  • Protozoal infection models and comparative efficacy benchmarking
  • Nitroheterocycle bioactivation and redox metabolism studies
  • Resistance mechanism mapping (nitroreductase and detox pathway profiling)
  • Host-parasite selectivity studies with DNA damage and stress biomarkers
  • Analytical stability and impurity profiling for nitroheterocycle APIs

Toxicodynamics & Cellular Hazard Spectrum

  • Reactive metabolite formation may drive host cytotoxicity signatures at high exposure
  • Genotoxic stress markers may appear in sensitive assays; interpret carefully
  • Redox-sensitive assay interference; use orthogonal endpoints
  • Solvent and solubility artifacts in vitro; validate dosing and precipitation
  • Follow hazardous handling guidance for nitro-containing organics

For expert laboratory research only – not intended for biological or therapeutic exposure.

Datasheet


Molecular Formula

C12H12N4O3

Molecular Weight

260.25 g/mol

CAS Number

22994-85-0

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

>39 [ug/mL] (The mean of the results at pH 7.4)

Purity

Purity information is available upon request (COA).

Synonym

BENZNIDAZOLE; 22994-85-0; Radanil; Benznidazol; Benzonidazole

IUPAC/Chemical Name

N-benzyl-2-(2-nitroimidazol-1-yl)acetamide

InChl Key

CULUWZNBISUWAS-UHFFFAOYSA-N

InChl Code

InChI=1S/C12H12N4O3/c17-11(14-8-10-4-2-1-3-5-10)9-15-7-6-13-12(15)16(18)19/h1-7H,8-9H2,(H,14,17)

References

https://pubchem.ncbi.nlm.nih.gov/compound/31593; small-molecule

3D Conformer.

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