Basic information Acute toxicity Safety Supplier Related

BETA-AMANITIN

Basic information Acute toxicity Safety Supplier Related

BETA-AMANITIN Basic information

Product Name:
BETA-AMANITIN
Synonyms:
  • BETA-AMANITIN
  • ,12,17,18,19,20,21,22,23,23a-octadecahydro-29-sec-butyl-2,14-dihydroxy-21-(2,3
  • 1-l-asparticacid-alpha-amaniti
  • 8,20,23,24,27,30,33-octaoxo--dihydroxy-1-methylpropyl)-11-oxide
  • beta-amatoxin
  • B-amanitin from amanita phalloides
  • alpha-Amanitin, 1-l-aspartic acid-
  • beta-Amanitine
CAS:
21150-22-1
MF:
C39H53N9O15S
MW:
919.95
EINECS:
244-244-8
Product Categories:
  • Cell Signaling and Neuroscience
  • DNA-RNA Transcription RegulatorsCell Signaling and Neuroscience
  • Gene Regulation and Expression
  • Mushroom
  • Toxins and Venoms
Mol File:
21150-22-1.mol
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BETA-AMANITIN Chemical Properties

Melting point:
300°
Boiling point:
1599.6±65.0 °C(Predicted)
Density 
1.1725 (rough estimate)
refractive index 
1.7400 (estimate)
storage temp. 
−20°C
solubility 
Water: 1 mg/ml
pka
4.02±0.10(Predicted)
form 
White to off-white powder.
color 
White to off-white
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Safety Information

Hazard Codes 
T+
Risk Statements 
26/27/28
Safety Statements 
7-28-36/37/39-45
RIDADR 
UN 3462 6.1/PG 1
WGK Germany 
3
RTECS 
NJ8324000
HazardClass 
6.1(a)
PackingGroup 
I
HS Code 
2934999090
Toxicity
LD50 i.p. in albino mice: 0.4 mg/kg (Wieland, Wieland)

MSDS

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BETA-AMANITIN Usage And Synthesis

Acute toxicity

peritoneal-mouse LD50: 0.4 mg/kg; unnamed-mouse LD50: 0.4 mg/kg

Mechanism of action

β-Amanitin is a cyclic peptide found in several species of the Amanita genus, as well as other poisonous fungi. It inhibits RNA polymerase II and III but not RNA polymerase I or bacterial RNA polymerase, thus preventing mammalian protein synthesis. The biological activity of this toxin is similar to that of α-amanitin but differs structurally by the presence of a carboxyl group, which is useful for coupling reactions.

Uses

β-Amanitin from Amanita phalloides has been used:

  • as a calibration standard for the quantification of β-Amanitin using liquid chromatography-high resolution-mass spectrometry/mass spectrometry (LC-HR-MS/MS) method.
  • to determine its concentration in urine samples by capillary zone electrophoresis (CZE).
  • in the analysis of β-amanitin in toxic mushrooms by liquid chromatography coupled to time-of-flight mass spectrometry.

Uses

As a tool in molecular biology.

General Description

β-Amanitin belongs to the family of amatoxins. Amanitins are made of bicyclic octapeptides. β-Amanitin is composed of a carboxyl group and is acidic in nature.

Biochem/physiol Actions

Toxic constituent of the mushroom, Amanita phalloides, inhibits eukaryotic RNA polymerase II and III, but not RNA polymerase I or bacterial RNA polymerase. Inhibits mammalian protein synthesis.

BETA-AMANITINSupplier

Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Email
isunpharm@qq.com
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Email
info@efebio.com
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Email
psaitong@jm-bio.com
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Email
sales@regentsciences.com
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