Fig. 1 · Structure
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Bisfentidine
H2 Receptor Antagonist
Bisfentidine is an H2 receptor antagonist that effectively inhibits the H2 receptors located on gastric parietal cells, leading to a reduction in gastric acid secretion. Additionally, Bisfentidine interacts with cytochrome P-450 in liver microsomes, influencing drug metabolism. This compound is valuable for research applications related to drug metabolic processes, lipid peroxidation, and the investigation of peptic ulcer disease.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Antagonist |
| CAS Number | 96153-56-9 |
| Applications | H2 Receptor Antagonist |
| Formula | C14H18N4 |
| Molecular Weight | 242.32 |
| Synonyms | DA-5047 |
| SMILES | CC(C)N/C=N/C1=CC=C(C2=CN=C(C)N2)C=C1 |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
Preparing Stock Solutions
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.