SOLANESOL

Solanesol is a terpene alcohol used as a precursor in ubiquinone (CoQ10) and vitamin K synthesis. It is not used therapeutically itself. Exposure may cause mild irritation or headache.

SKU: ef0016bcd69f Category: Tag:

Product Description


Mechanism of Action

SOLANESOL (ID 27458) exhibits a broad and high‑complexity biochemical activity spectrum, modulating hierarchical signalling cascades, deep enzymatic networks, mitochondrial functional architecture, cytoskeletal integrity, transcription‑factor coordination and multi‑axis stress‑response systems. Its molecular conformation supports interaction with catalytic pockets, allosteric microdomains, transmembrane helices, regulatory scaffolds, ion‑channel architectures and redox‑buffering systems, producing wide‑ranging effects across metabolic, genomic, structural and electrophysiological layers.

Mechanistically, SOLANESOL may alter phosphorylation topologies, reshape signalling‑cascade propagation (ERK, JNK, MAPK, PI3K–AKT), amplify or suppress second‑messenger concentrations (Ca²⁺, cAMP, IP₃, DAG), modify mitochondrial membrane polarity, shift ATP/ADP cycling behaviour, regulate ROS‑leakage thresholds and influence global metabolic flux distribution. Its capacity to integrate signals from cytosolic, organelle‑bound and membrane‑anchored proteins makes it suitable for advanced mechanistic interrogation.

High‑Level Research Applications

  • Deep kinome‑mapping & systems‑level pathway‑interference analysis
  • Structural docking, ligand‑stability modelling & conformational dynamics
  • Mitochondrial‑stress analysis including ETC complex modelling
  • UPR, ER‑stress & integrated autophagy/mitophagy evaluation
  • Multi‑omics network reconstruction (RNA‑seq, phosphoproteomics, metabolomics)
  • Membrane‑dynamics and cytoskeletal mechanotransduction studies
  • Advanced cell‑fate modelling across apoptosis, necroptosis & ferroptosis axes
  • Predictive SAR/QSAR pipelines using machine‑learning 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 laboratory use only — not for biological or therapeutic exposure.

Datasheet


Molecular Formula

C45H74O

Molecular Weight

631.1 g/mol

CAS Number

13190-97-1

Storage Condition

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

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Solanesol; 13190-97-1; Nonaisoprenol; Betulanonaprenol; 2,6,10,14,18,22,26,30,34-Hexatriacontanonaen-1-ol, 3,7,11,15,19,23,27,31,35-nonamethyl-, (2E,6E,10E,14E,18E,22E,26E,30E)-

IUPAC/Chemical Name

(2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol

InChl Key

AFPLNGZPBSKHHQ-MEGGAXOGSA-N

InChl Code

InChI=1S/C45H74O/c1-37(2)19-11-20-38(3)21-12-22-39(4)23-13-24-40(5)25-14-26-41(6)27-15-28-42(7)29-16-30-43(8)31-17-32-44(9)33-18-34-45(10)35-36-46/h19,21,23,25,27,29,31,33,35,46H,11-18,20,22,24,26,28,30,32,34,36H2,1-10H3/b38-21+,39-23+,40-25+,41-27+,42-29+,43-31+,44-33+,45-35+

References

https://pubchem.ncbi.nlm.nih.gov/compound/5477212;

3D Conformer.

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