Valacyclovir hydrochloride

SKU: orb1309816

Description

Valacyclovir hydrochloride

Research Area

Cell Biology, Infectious Disease & Virology, Molecular Biology

Key Properties

• CAS Number: 124832-27-5
• MW: 360.80
• Purity: ≥95% (May vary between batches)
• Formula: C₁₃H₂₀N₆O₄·HCl
• SMILES: Cl.CC(C)[C@H](N)C(=O)OCCOCn1cnc2c1nc(N)[nH]c2=O
• Target: HSV,DNA/RNA Synthesis,Antibiotic,Antibacterial
• Solubility: DMSO:20.4 mg/mL (56.54 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (5.54 mM)

Bioactivity

• Target IC50:
  HSV1:2.9 μg/mL (IC50)
• In Vivo:
  Valaciclovir is the L-valine ester of aciclovir, the absorption of which occurs in the intestinal lumen and is converted to the L-valine ester of aciclovir.Valaciclovir inhibits the uptake of dipeptide transporter protein substrates, e.g., cephalosporin.
  Read more...
• In Vitro:
  In male CD rats, Valaciclovir was absorbed orally, efficiently metabolized and rapidly distributed.

Storage & Handling

• Storage: -20°C
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

RNA Synthesis, RNASynthesis, Valaciclovir, Valaciclovir HCl, Valaciclovir hydrochloride, Valaciclovir Hydrochloride, Valacyclovir, Valacyclovir hydrochloride, Valacyclovir Hydrochloride, DNA Synthesis, DNA polymerase, DNASynthesis, Antibiotic, Herpes simplex virus, Inhibitor, HSV, inhibit

Compound Identifiers

PubChem CID

135398741