PENCICLOVIR

Penciclovir is a guanine nucleoside analogue that is phosphorylated in virus‑infected cells and inhibits viral DNA polymerase, halting DNA synthesis. It is used topically for herpes labialis. Benefits include shortened lesion duration and symptom relief. Side effects are usually mild and include local burning, numbness, erythema, and rare allergic skin reactions.

SKU: 448793f260fe Category: Tag:

Product Description


Mechanism of Action

PENCICLOVIR (ID 27043) demonstrates a multidimensional biochemical activity pattern, affecting enzyme‑regulated catalytic networks, receptor‑mediated intracellular signalling, mitochondrial respiratory pathways, oxidative‑stress regulation, ion‑channel behaviour, cytoskeletal mechanics and transcription‑factor network modulation. Structural evidence suggests potential interactions with catalytic residues, allosteric domains, transmembrane protein complexes, regulatory scaffolds and intracellular signalling intermediates. These interactions allow PENCICLOVIR to influence phosphorylation kinetics, second‑messenger signalling (Ca²⁺, cAMP, IP₃, DAG), redox‑buffering systems, ATP turnover rates and mitochondrial membrane‑potential stability.

Depending on experimental conditions, PENCICLOVIR may alter metabolic flux distribution, cytoskeletal tension, vesicular transport efficiency, chromatin‑accessibility patterns and gene‑expression networks related to stress responses, inflammation, apoptosis, autophagy and metabolic adaptation.

Benefits and Advantages

This compound is widely used across high‑resolution biochemical and pharmacological research areas, including:

  • Receptor–ligand interaction analysis and affinity‑mapping
  • Detailed enzyme‑kinetics profiling and catalytic‑pathway evaluation
  • Mitochondrial‑dynamics studies, ATP‑flux modelling and oxidative‑stress research
  • Integrated multi‑omics applications (transcriptomics, metabolomics, proteomics, phosphoproteomics)
  • Cytoskeletal and membrane‑mechanics modelling
  • Apoptosis, necroptosis, ferroptosis and autophagy signalling pathway studies
  • SAR (structure–activity relationship) and molecular‑optimisation pipelines
  • Mechanistic pharmacodynamic modelling and threshold‑activation experiments

Side Effects and Risks

Laboratory‑observed risks include:

  • Oxidative‑stress imbalance and ROS overproduction
  • Mitochondrial overload or suppression of respiratory‑chain complexes
  • Dysregulation of Na⁺/K⁺/Ca²⁺ transport and ion‑channel behaviour
  • Unintended receptor cross‑talk or inhibitory interference
  • Cytoskeletal destabilisation and membrane‑integrity compromise
  • Dose‑dependent cytotoxicity leading to apoptosis or autophagy
  • Transcriptional instability or inflammatory signalling activation (NF‑κB, JNK, MAPK)

Use exclusively under controlled laboratory conditions with strict biosafety procedures.

Datasheet


Molecular Formula

C10H15N5O3

Molecular Weight

253.26 g/mol

CAS Number

39809-25-1

Storage Condition

Store at controlled room temperature, 20-25 °C (68 -77 °F).

Solubility

1.7mg/ml

Purity

Purity information is available upon request (COA).

Synonym

penciclovir; 39809-25-1; Denavir; BRL-39123; Penciclovirum

IUPAC/Chemical Name

2-amino-9-[4-hydroxy-3-(hydroxymethyl)butyl]-1H-purin-6-one

InChl Key

JNTOCHDNEULJHD-UHFFFAOYSA-N

InChl Code

InChI=1S/C10H15N5O3/c11-10-13-8-7(9(18)14-10)12-5-15(8)2-1-6(3-16)4-17/h5-6,16-17H,1-4H2,(H3,11,13,14,18)

References

https://pubchem.ncbi.nlm.nih.gov/compound/135398748;

3D Conformer.

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