Fig. 1 · Structure
Documents & Downloads
Naloxonazine dihydrochloride
Mu-opioid Receptor Antagonist
Naloxonazine dihydrochloride is a specific μ-opioid receptor antagonist with a reported IC50 of 5.4 nM. This compound not only inhibits μ-opioid receptor activity but also demonstrates anti-leishmanial properties, making it relevant for studies on pain management and parasitic infections. Its unique profile supports research applications in opioid receptor modulation and leishmaniasis treatment development.
In Stock
Free Aliquoting for Your Order
Tell us your preferred amount per vial. We’ll confirm the options.
Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Antagonist |
| CAS Number | 880759-65-9 |
| Applications | Mu-opioid Receptor Antagonist |
| Formula | C38H44Cl2N4O6 |
| Molecular Weight | 723.69 |
| SMILES | O[C@@]([C@@]1([H])CC2=CC=C3O)(CC/4)[C@@]5(CCN1CC=C)C2=C3O[C@@]5([H])C4=N\N=C(CC[C@]67O)\[C@@]8([H])[C@]6(CCN(CC=C)[C@]7([H])CC9=CC=C%10O)C9=C%10O8.Cl.Cl |
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.