Fig. 1 · Structure
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Cephalosporin C zinc salt
SAMHD1 Inhibitor
Cephalosporin C zinc salt is a potent inhibitor of the HIV-induced SAMHD1 enzyme, exhibiting an IC50 value of 1.1 μM. This compound has demonstrated moderate anti-orthopoxvirus activity, making it an important tool in the study of viral replication and resistance mechanisms. Its multifaceted biological activity supports research in virology and therapeutic development for viral infections.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Inhibitor |
| CAS Number | 59143-60-1 |
| Applications | SAMHD1 Inhibitor |
| Formula | C16H19N3O8SZn |
| Molecular Weight | 478.78 |
| SMILES | CC(OCC1=C(C([O-])=O)N(C([C@H]2NC(CCC[C@@H](N)C([O-])=O)=O)=O)[C@]2([H])SC1)=O.[Zn+2] |
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.