Date published: 2026-4-24

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Terpendole E (CAS 167427-23-8)

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Alternate Names:
1′α-Hydroxy-paspaline; FO 2546L
Application:
Terpendole E is a ACAT and Eg5 inhibitor
CAS Number:
167427-23-8
Molecular Weight:
437.6
Molecular Formula:
C28H39NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Terpendole E is a ACAT (Acyl-CoA:cholesterol acyltransferase) and Eg5 (Mitotic Kinesin Spindle Protein) inhibitor. Also a specific inhibitor of M phase.


Terpendole E (CAS 167427-23-8) References

  1. A novel action of terpendole E on the motor activity of mitotic Kinesin Eg5.  |  Nakazawa, J., et al. 2003. Chem Biol. 10: 131-7. PMID: 12618185
  2. Development and application of bioprobes for Mammalian cell cycle analyses.  |  Osada, H. 2003. Curr Med Chem. 10: 727-32. PMID: 12678775
  3. A novel approach to indoloditerpenes by Nazarov photocyclization: synthesis and biological investigations of terpendole E analogues.  |  Churruca, F., et al. 2010. Org Lett. 12: 2096-9. PMID: 20387880
  4. Kinesin spindle protein (KSP) inhibitors with 2,3-fused indole scaffolds.  |  Oishi, S., et al. 2010. J Med Chem. 53: 5054-8. PMID: 20521839
  5. Terpendole E, a kinesin Eg5 inhibitor, is a key biosynthetic intermediate of indole-diterpenes in the producing fungus Chaunopycnis alba.  |  Motoyama, T., et al. 2012. Chem Biol. 19: 1611-9. PMID: 23261604
  6. Terpendole E and its derivative inhibit STLC- and GSK-1-resistant Eg5.  |  Tarui, Y., et al. 2014. Chembiochem. 15: 934-8. PMID: 24648249
  7. Detection of oxygen addition peaks for terpendole E and related indole-diterpene alkaloids in a positive-mode ESI-MS.  |  Hongo, Y., et al. 2014. J Mass Spectrom. 49: 537-42. PMID: 24913406
  8. Synthesis of (±)-terpendole E.  |  Teranishi, T., et al. 2015. Biosci Biotechnol Biochem. 79: 11-5. PMID: 25184606
  9. Biosynthetic approaches to creating bioactive fungal metabolites: Pathway engineering and activation of secondary metabolism.  |  Motoyama, T. and Osada, H. 2016. Bioorg Med Chem Lett. 26: 5843-5850. PMID: 27865702
  10. Novel Allosteric Pathway of Eg5 Regulation Identified through Multivariate Statistical Analysis of Hydrogen-Exchange Mass Spectrometry (HX-MS) Ligand Screening Data.  |  Sheff, JG., et al. 2017. Mol Cell Proteomics. 16: 428-437. PMID: 28062800
  11. Identification of Indole Diterpenes in Ipomoea asarifolia and Ipomoea muelleri, Plants Tremorgenic to Livestock.  |  Lee, ST., et al. 2017. J Agric Food Chem. 65: 5266-5277. PMID: 28571312
  12. Detection of the tremorgenic mycotoxin paxilline and its desoxy analog in ergot of rye and barley: a new class of mycotoxins added to an old problem.  |  Bauer, JI., et al. 2017. Anal Bioanal Chem. 409: 5101-5112. PMID: 28674820
  13. The Known Antimammalian and Insecticidal Alkaloids Are Not Responsible for the Antifungal Activity of Epichloë Endophytes.  |  Fernando, K., et al. 2021. Plants (Basel). 10: PMID: 34834850
  14. Identification, Characterization, and Evaluation of Nematophagous Fungal Species of Arthrobotrys and Tolypocladium for the Management of Meloidogyne incognita.  |  Kassam, R., et al. 2021. Front Microbiol. 12: 790223. PMID: 34956156

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Terpendole E, 1 mg

sc-391039
1 mg
$240.00