Date published: 2025-12-18

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Aconitine (CAS 302-27-2)

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Alternate Names:
Aconitine is also known as Acetylbenzoylaconine.
Application:
Aconitine is a lipid-soluble and potent neurotoxin that activates voltage gated, tetrodotoxin-sensitive sodium channels.
CAS Number:
302-27-2
Purity:
≥98%
Molecular Weight:
645.73
Molecular Formula:
C34H47NO11
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Aconitine is a lipid-soluble and potent neurotoxin that activates voltage gated sodium channels. Aconitine can inhibit non-quantal acetylcholine release and can induce neuromuscular blockage, specifically blocking the nerve compound action potential. Studies show that Aconitine is toxic to neuron cells at a concentration of 2%. Aconitine can block tetrodotoxin-sensitive Na+ channels. Aconitine is also known as Acetylbenzoylaconine, and (1α,3α,6α,14α,15α,16β)-20-Ethyl-1,6,16-trimethoxy-4-(methoxymethyl)aconitane-3,8,13,14,15-pentol 8-acetate 14-benzoate.


Aconitine (CAS 302-27-2) References

  1. Study of neurotoxic effects and underlying mechanisms of aconitine on cerebral cortex neuron cells.  |  Peng, C., et al. 2009. Arch Pharm Res. 32: 1533-43. PMID: 20091266
  2. Pharmacokinetics of aconitine as the targeted marker of Fuzi (Aconitum carmichaeli) following single and multiple oral administrations of Fuzi extracts in rat by UPLC/MS/MS.  |  Tang, L., et al. 2012. J Ethnopharmacol. 141: 736-41. PMID: 21924342
  3. Pharmacokinetics of aconitine in rat skin after oral and transdermal gel administrations.  |  Zhang, QL., et al. 2012. Biomed Chromatogr. 26: 622-6. PMID: 22139640
  4. Non-quantal acetylcholine release at mouse neuromuscular junction: effects of elevated quantal release and aconitine.  |  Yu, SP. and Van der Kloot, W. 1990. Neurosci Lett. 117: 111-6. PMID: 2290606
  5. Cladosporium cladosporioides XJ-AC03, an aconitine-producing endophytic fungus isolated from Aconitum leucostomum.  |  Yang, K., et al. 2013. World J Microbiol Biotechnol. 29: 933-8. PMID: 23269506
  6. Observation on effects of aconitine via acupoint injection in rabbits.  |  Ni, F., et al. 2013. Chin J Integr Med. 19: 36-41. PMID: 23275014
  7. Blocking effects of hypaconitine and aconitine on nerve action potentials in phrenic nerve-diaphragm muscles of mice.  |  Muroi, M., et al. 1990. Neuropharmacology. 29: 567-72. PMID: 2385329
  8. Gram-scale purification of aconitine and identification of lappaconitine in Aconitum karacolicum.  |  Tarbe, M., et al. 2017. Fitoterapia. 120: 85-92. PMID: 28552596
  9. Quantitative analysis of aconitine in body fluids in a case of aconitine poisoning.  |  Cho, YS., et al. 2020. Forensic Sci Med Pathol. 16: 330-334. PMID: 31802365
  10. Pharmacokinetic effects of ginsenoside Rg1 on aconitine, benzoylaconine and aconine by UHPLC-MS/MS.  |  Xu, Y., et al. 2020. Biomed Chromatogr. 34: e4793. PMID: 31919877
  11. Clinical relationship between blood concentration and clinical symptoms in aconitine intoxication.  |  Jeon, SY., et al. 2021. Am J Emerg Med. 40: 184-187. PMID: 33243534
  12. An Effective Phytoconstituent Aconitine: A Realistic Approach for the Treatment of Trigeminal Neuralgia.  |  Çankal, D., et al. 2021. Mediators Inflamm. 2021: 6676063. PMID: 33935591
  13. Inhibition of SLC7A11-GPX4 signal pathway is involved in aconitine-induced ferroptosis in vivo and in vitro.  |  Li, Q., et al. 2023. J Ethnopharmacol. 303: 116029. PMID: 36503029

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Aconitine, 25 mg

sc-202441
25 mg
$300.00

Aconitine, 50 mg

sc-202441A
50 mg
$450.00

Aconitine, 100 mg

sc-202441B
100 mg
$650.00

Aconitine, 250 mg

sc-202441C
250 mg
$1252.00

Aconitine, 500 mg

sc-202441D
500 mg
$2050.00