1245732-48-2
- Product Name:Zoliflodacin
- Molecular Formula:C66H100N6O27
- Purity:99%
- Molecular Weight:1409.53
Product Details:
CasNo: 1245732-48-2
Molecular Formula: C66H100N6O27
Appearance: Off‑white to pale yellow
Packing: Aluminium bag
Throughput: 100KG/Month
Purity: 99%
Physical‑Chemical Properties
Appearance: Off‑white to pale yellow solid / powder Sparingly soluble in water, soluble in certain organic solvents.
Mechanism of Action
Zoliflodacin is a bactericidal type‑II topoisomerase inhibitor. It targets bacterial DNA gyrase (GyrB subunit) and topoisomerase IV via a novel binding site distinct from fluoroquinolones, blocking bacterial DNA replication and cell division. It exhibits no cross‑resistance with existing antibiotic classes and retains activity against multi‑drug‑resistant Neisseria gonorrhoeae strains.
Indications
For the treatment of uncomplicated urogenital gonorrhea caused by Neisseria gonorrhoeae, in adults and paediatric patients aged 12 years and older with body weight ≥35 kg. It is administered as single‑dose oral therapy, approved by US‑FDA in December 2025 (brand name Nuzolvence)U.S. Food ....
Clinical feature: Single oral dose replaces traditional injectable ceftriaxone‑based regimen, suitable for fluoroquinolone‑resistant and cephalosporin‑resistant gonorrhea isolates.
API Quality Profile
- HPLC Purity: NLT 98.0%
- Related Substances: Total impurities ≤1.0%, individual unknown impurity ≤0.15%
- Loss on drying: ≤0.5%
- COA, HPLC, NMR, MS available for R&D and formulation development. Note: Pharmacopoeia monograph (EP/USP) not yet officially published.
Storage & Packing
Store sealed under dry, cool conditions, avoid direct light. Standard packing: 1 g, 5 g, 100 g, 1 kg / aluminium foil bag or drum for R&D & pilot manufacture.
Disclaimer
This material description is for pharmaceutical raw‑material reference only, not clinical medication guidance.
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