Date published: 2026-4-24

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β-Amanitin (CAS 21150-22-1)

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Application:
β-Amanitin is a specific and potent inhibitor of eukaryotic RNA polymerase II and a mild inhibitor of RNA polymerase III
CAS Number:
21150-22-1
Purity:
≥90%
Molecular Weight:
920.0
Molecular Formula:
C39H53N9O15S
Supplemental Information:
This is 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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β-Amanitin is an extremely toxic constituent of the mushroom, Amanita phalloides, that inhibits Rpb (eukaryotic RNA polymerase II) and eukaryotic RNA polymerase III. This toxin is synthesized as a proprotein, on ribosomes, 34 to 35 amino acids in length and then cleaved at specific proline residues by an enzyme belonging to the prolyl oligopeptidase (POP) subfamily. beta-Amanitin shows remarkable binding affinity for eukaryotic RNA polymerase II, slightly binds to RNA polymerase III, and shows no activity on RNA polymerase I it has been used to determine which types of RNA polymerase are present in a given sample. The toxin works by binding to the bridging helix of RNA polymerase II inhibiting the translocation of RNA and DNA needed to empty the site for the next round of synthesis thereby slowing the rate of transcription by over 1000 fold. Beta-Amanitin, a naturally occurring chemical compound found in certain fungi species like the Amanita genus, is a potent toxin that can result in severe liver damage and fatality upon ingestion. Although its mechanism of action is not entirely understood, it is known to interfere with the transcription of genetic material within cells.


β-Amanitin (CAS 21150-22-1) References

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  2. Cytotoxic constituents of Amanita subjunquillea.  |  Kim, KH., et al. 2008. Arch Pharm Res. 31: 579-86. PMID: 18481012
  3. Ribosomal biosynthesis of the cyclic peptide toxins of Amanita mushrooms.  |  Walton, JD., et al. 2010. Biopolymers. 94: 659-64. PMID: 20564017
  4. Cytotoxicity on L1210 leukemic cells of beta-amanitin-concanavalin A and phallacidin-concanavalin A conjugates.  |  Zhelev, Z., et al. 1990. Toxicon. 28: 1360-3. PMID: 2087697
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  6. Evaluation and comparison of alpha- and beta-amanitin toxicity on MCF-7 cell line.  |  Kaya, E., et al. 2014. Turk J Med Sci. 44: 728-32. PMID: 25539537
  7. Preparation of a beta-amanitin-concanavalin A conjugate of low toxicity.  |  Zhelev, Z., et al. 1987. Toxicon. 25: 981-7. PMID: 3124301
  8. Total Synthesis of α- and β-Amanitin.  |  Lutz, C., et al. 2020. Angew Chem Int Ed Engl. 59: 11390-11393. PMID: 32091645
  9. A therapeutic oxygen carrier isolated from Arenicola marina decreases amanitin-induced hepatotoxicity.  |  Le Daré, B., et al. 2021. Toxicon. 200: 87-91. PMID: 34274377
  10. Erdosteine reduces cytotoxicity induced by alpha- and beta-amanitin, but not gamma-amanitin, in CA3 hepatocyte cultures.  |  Bayram, R., et al. 2022. Toxicon. 213: 52-58. PMID: 35443191
  11. Toxicokinetics of β-Amanitin in Mice and In Vitro Drug-Drug Interaction Potential.  |  Bang, YY., et al. 2022. Pharmaceutics. 14: PMID: 35456608
  12. Rapid detection of α-amanitin and β-amanitin in rat plasma by ultra-performance liquid chromatography-tandem mass spectrometry and its application to the toxicokinetic study of Lepiota brunneoincarnata.  |  Mao, Z., et al. 2022. Forensic Toxicol. 40: 111-118. PMID: 36454499
  13. Analytical methods for amatoxins: A comprehensive review.  |  Barbosa, I., et al. 2023. J Pharm Biomed Anal. 232: 115421. PMID: 37146495
  14. The effects of amanitin poisoning on mouse kidney.  |  Fiume, L., et al. 1969. Br J Exp Pathol. 50: 270-6. PMID: 5792902
  15. Conformation of the mushroom toxin beta-amanitin in the crystalline state.  |  Kostansek, EC., et al. 1978. Biochemistry. 17: 3790-5. PMID: 698197

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

β-Amanitin, 1 mg

sc-202860
1 mg
$235.00

β-Amanitin, 10 mg

sc-202860A
10 mg
$2150.00