CAS No. 298708-79-9

Batch: Purity:99.03
Bay 41-4109 racemate Chemical Structure
Chemical Structure
Check the Bay 41-4109 racemate product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name methyl 4-(2-chloro-4-fluorophenyl)-2-(3,5-difluoro-2-pyridinyl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate
CAS Number 298708-79-9
Molecular Formula

C18H13ClF3N3O2

Molecular Weight (MW) 395.76
SMILES CC1=C(C(N=C(N1)C2=C(C=C(C=N2)F)F)C3=C(C=C(C=C3)F)Cl)C(=O)OC
InChIKey FVNJBPMQWSIGJK-UHFFFAOYSA-N

Ordering Information

Biological Activity

Bay 41-4109 racemate is a heteroaryldihydropyrimidine antiviral agent that inhibits human hepatitis B virus (HBV) with an IC50 of. It acts as a capsid assembly modulator by targeting the HBV core protein, which destabilizes proper viral capsids and accelerates core protein degradation. This mechanism blocks pregenomic RNA packaging, ultimately preventing viral DNA synthesis and HBV replication in host cells. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 79 mg/mL (199.61 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 11 mg/mL
Water ˂1 mg/mL
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).
Note: Technical data last updated: Sep 1, 2026.