Fig. 1 · Structure

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Norvancomycin monohydrochloride

Anti-Infection Agent

Norvancomycin monohydrochloride is an anti-infection agent that acts as a cell wall synthesis inhibitor. It targets peptidoglycan precursors in Gram-positive bacteria, irreversibly inhibiting bacterial cell wall synthesis and demonstrating significant antibacterial activity. This reagent is primarily utilized in the study of Gram-positive bacterial infections, particularly those caused by methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant Staphylococcus epidermidis (MRSE). Additionally, Norvancomycin monohydrochloride can be integrated into bionic calcium phosphate coatings on titanium implants to enhance antibacterial properties and mitigate postoperative orthopedic infections.

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 213997-73-0
Applications Anti-Infection Agent
Formula C65H74Cl3N9O24
Molecular Weight 1471.69
Synonyms N-Demethylvancomycin monohydrochloride; NVCM monohydrochloride
SMILES
O[C@@H]1[C@@H](O[C@@](O[C@@H](C)[C@H]2O)([H])C[C@@]2(N)C)[C@@H](O[C@H](CO)[C@H]1O)OC3=C(OC4=CC=C([C@H]([C@H]5NC([C@H](N)CC(C)C)=O)O)C=C4Cl)C=C([C@](NC([C@@H](NC5=O)CC(N)=O)=O)([H])C(N[C@](C6=O)([H])C7=CC8=C(O)C=C7)=O)C=C3OC9=CC=C([C@H]([C@](C(N[C@@](C(O)=O)([H])C%10=C8C(O)=CC(O)=C%10)=O)([H])N6)O)C=C9Cl.Cl

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

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.

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