THALIDOMIDE

Thalidomide is an immunomodulatory and antiangiogenic agent used for multiple myeloma and erythema nodosum leprosum. It reduces TNF and modulates Tcell responses. Side effects include severe teratogenicity, neuropathy, sedation, constipation, thrombosis, and rash, requiring strict monitoring. Only GMP materials will be supplied, logistics all according to GDP.

SKU: b49a359d99da Category: Tag:

Product Description


Mechanism of Action

THALIDOMIDE demonstrates a broad and highly integrated biochemical activity architecture involving multiaxis signalling interference, mitochondrial-network recalibration, catalyticdomain modulation, cytoskeletal restructuring, redoxequilibrium shaping, ionflux redistribution and transcriptionfactor pathway realignment. Its molecular geometry allows docking to catalytic residues, allosteric regulators, hydrophobic transmembrane helices, nucleotidebinding pockets, structural scaffolds and polymeric cytoskeletal networks. This enables THALIDOMIDE to influence metabolic, structural, genomic, electrophysiological and stressadaptive systems simultaneously.

THALIDOMIDE may modulate phosphorylation gradients, modify ERK/JNK/MAPK propagation speeds, influence PI3KAKT survival bias, shift Gprotein signalling states, control Ca²⁺ microdomain behaviour, alter IP/DAG cascades, and recalibrate cAMPPKA pathway amplitude. Mitochondrial impacts include ETCcomplex redistribution, ATP/ADP cycle reshaping, ROSthreshold displacement, membranepotential polarity changes and organellestress crosssignalling.

HighPrecision

  • Ultrascale kinome disruption & catalyticcascade modelling
  • Molecular docking & conformationalflow prediction
  • UPR/ERstress and mitophagy/autophagy integration research
  • Fullspectrum multiomics reconstruction (RNAseq, metabolomics, phosphoproteomics)
  • Advanced cytoskeletal forcedistribution & polymerturnover analysis
  • Cellfate simulation across apoptosis, ferroptosis, necroptosis & parthanatos
  • AIenhanced SAR/QSAR simulation for molecular optimisation

Toxicodynamics & Hazard Spectrum

  • Rapid ROS escalation & antioxidantbuffer collapse
  • Mitochondrial fragmentation or ETC suppression
  • Severe Ca²⁺/Na⁺/K⁺ ionflux destabilisation
  • Cytoskeletal polymer breakdown & structuralintegrity failure
  • Membrane rupture & lipidbilayer thinning
  • Overactivation of inflammatory cascades (NF-κB, STAT, IRF)
  • Activation of multiple programmed-cell-death pathways
  • Epigenetic drift including methylation instability

For expert not intended for biological exposure.

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

Datasheet


Molecular Formula

C13H10N2O4

Molecular Weight

258.23 g/mol

CAS Number

50-35-1

Storage Condition

Commercially available thalidomide capsules should be stored at 15-30 °C and protected from light.

Solubility

less than 1 mg/mL at 72 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

thalidomide; 50-35-1; Thalomid; Contergan; Pantosediv

IUPAC/Chemical Name

2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione

InChl Key

UEJJHQNACJXSKW-UHFFFAOYSA-N

InChl Code

InChI=1S/C13H10N2O4/c16-10-6-5-9(11(17)14-10)15-12(18)7-3-1-2-4-8(7)13(15)19/h1-4,9H,5-6H2,(H,14,16,17)

References

https://pubchem.ncbi.nlm.nih.gov/compound/5426;

3D Conformer.

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