TESTOSTERONE UNDECANOATE

Testosterone undecanoate is a very longacting ester used in both oral and injectable forms for stable androgen replacement. Side effects include cough postinjection, elevated hematocrit, edema, and potential cardiovascular risk. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 01edb6bfd382 Category: Tag:

Product Description


Mechanism of Action

TESTOSTERONE UNDECANOATE 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 TESTOSTERONE UNDECANOATE to influence metabolic, structural, genomic, electrophysiological and stressadaptive systems simultaneously.

TESTOSTERONE UNDECANOATE 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

C30H48O3

Molecular Weight

456.7 g/mol

CAS Number

5949-44-0

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

<1 mg/mL

Purity

Purity information is available upon request (COA).

Synonym

Testosterone undecanoate; 5949-44-0; Pantestone; Restandol; Aveed

IUPAC/Chemical Name

[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] undecanoate

InChl Key

UDSFVOAUHKGBEK-CNQKSJKFSA-N

InChl Code

InChI=1S/C30H48O3/c1-4-5-6-7-8-9-10-11-12-28(32)33-27-16-15-25-24-14-13-22-21-23(31)17-19-29(22,2)26(24)18-20-30(25,27)3/h21,24-27H,4-20H2,1-3H3/t24-,25-,26-,27-,29-,30-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/65157;

3D Conformer.

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