STAVUDINE

Stavudine is a nucleoside reverse transcriptase inhibitor (NRTI) used in antiretroviral therapy. It blocks viral DNA synthesis, reducing HIV replication. Side effects include peripheral neuropathy, pancreatitis, lactic acidosis, lipodystrophy, and fatigue, requiring careful monitoring during treatment. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 920966b322c6 Category: Tag:

Product Description


Mechanism of Action

STAVUDINE exhibits a broad and highcomplexity biochemical activity spectrum, modulating hierarchical signalling cascades, deep enzymatic networks, mitochondrial functional architecture, cytoskeletal integrity, transcriptionfactor coordination and multiaxis stressresponse systems. Its molecular conformation supports interaction with catalytic pockets, allosteric microdomains, transmembrane helices, regulatory scaffolds, ionchannel architectures and redoxbuffering systems, producing wideranging effects across metabolic, genomic, structural and electrophysiological layers.

Mechanistically, STAVUDINE may alter phosphorylation topologies, reshape signallingcascade propagation (ERK, JNK, MAPK, PI3KAKT), amplify or suppress secondmessenger concentrations (Ca²⁺, cAMP, IP, DAG), modify mitochondrial membrane polarity, shift ATP/ADP cycling behaviour, regulate ROSleakage thresholds and influence global metabolic flux distribution. Its capacity to integrate signals from cytosolic, organellebound and membraneanchored proteins makes it suitable for advanced mechanistic interrogation.

HighLevel

  • Deep kinomemapping & systemslevel pathwayinterference analysis
  • Structural docking, ligandstability modelling & conformational dynamics
  • Mitochondrialstress analysis including ETC complex modelling
  • UPR, ERstress & integrated autophagy/mitophagy evaluation
  • Multiomics network reconstruction (RNAseq, phosphoproteomics, metabolomics)
  • Membranedynamics and cytoskeletal mechanotransduction studies
  • Advanced cellfate modelling across apoptosis, necroptosis & ferroptosis axes
  • Predictive SAR/QSAR pipelines using machinelearning optimisation

Toxicodynamics & Cellular Risk Spectrum

  • Rapid ROS escalation & antioxidant-system saturation
  • Mitochondrial fragmentation or ETC suppression
  • Severe ionic-flux dysregulation (Ca²⁺, Na⁺, K⁺)
  • Cytoskeletal collapse & membrane-integrity compromise
  • Inflammatory upregulation (NF-κB, STAT, IRF)
  • Activation of programmed-cell-death pathways
  • Epigenetic drift involving methylation & acetylation instability

For expert not for biological or therapeutic exposure.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C10H12N2O4

Molecular Weight

224.21 g/mol

CAS Number

3056-17-5

Storage Condition

Commercially available stavudine capsules should be stored in a tight container at a controlled room temperature of 15-30 °C. Stavudine powder for oral solution should be kept in a tight container at a controlled room temperature of 15-30 °C and protected from excessive moisture. Following reconstitution, the oral solution should be stored in a tight container at 2-8 °C.

Solubility

50 to 100 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

stavudine; 3056-17-5; sanilvudine; Zerit; 2',3'-Didehydro-3'-deoxythymidine

IUPAC/Chemical Name

1-[(2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methylpyrimidine-2,4-dione

InChl Key

XNKLLVCARDGLGL-JGVFFNPUSA-N

InChl Code

InChI=1S/C10H12N2O4/c1-6-4-12(10(15)11-9(6)14)8-3-2-7(5-13)16-8/h2-4,7-8,13H,5H2,1H3,(H,11,14,15)/t7-,8+/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/18283;

3D Conformer.

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