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ALPHA-AMANITIN

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Products Intro: Product Name:α-Amanitin
CAS:23109-05-9
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CAS:23109-05-9
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CAS: 23109-05-9
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CAS:23109-05-9
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ALPHA-AMANITIN manufacturers

  • ALPHA-AMANITIN
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  • 2025-12-09
  • CAS:23109-05-9
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  • Purity: 0.99
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  • alpha-Amanitin
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  • $9.00 / 10g
  • 2024-05-11
  • CAS:23109-05-9
  • Min. Order: 10g
  • Purity: 99%
  • Supply Ability: 10 tons
  • α-Amanitin
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  • $60.00 / 50mg
  • 2024-01-08
  • CAS:23109-05-9
  • Min. Order: 1mg
  • Purity: 99.96%
  • Supply Ability: 1kg
ALPHA-AMANITIN Basic information
Product Name:ALPHA-AMANITIN
Synonyms:Aids004473;Aids-004473;AMANITIN, a-(RG);AMANITIN, a-(RG)(CALL);cyclo[L-Asparaginyl-4-hydroxy-L-proly-(R-4,5-dihydroxy-L-isoleucyl-6-hydroxy-2-mercapto-L-tryptophylglycyl-L-isoleucylglycyl-L-cysteinyl]cyclic(4-8)-sulfide(R)-S-oxide;alpha-AMantine, froM AManita Phalloides;AMANITIN, A-;ALPHA-AMANITIN
CAS:23109-05-9
MF:C39H54N10O14S
MW:918.98
EINECS:245-432-2
Product Categories:Alkaloids;DNA-RNA Transcription RegulatorsCell Signaling and Neuroscience;Gene Regulation and Expression;Cell Signaling and Neuroscience;Mushroom;Toxins and Venoms;Enzyme Inhibitors;Enzyme Inhibitors by Type;Other;Miscellaneous Enzyme;inhibitor
Mol File:23109-05-9.mol
ALPHA-AMANITIN Structure
ALPHA-AMANITIN Chemical Properties
Melting point 254-255 °C(lit.)
alpha D20 +191°
Boiling point 1622.2±65.0 °C(Predicted)
density 1.1626 (rough estimate)
refractive index 1.7400 (estimate)
storage temp. −20°C
solubility H2O: 1.0 mg/mL
form powder
pka9.63±0.70(Predicted)
color white to light yellow
biological sourceAmanita phalloides
Optical Rotation+19120 (H2O)
Water Solubility Soluble to 5 mM in ethanol and to 5 mM in water
ε(extinction coefficient)13,500 at 310nm in H2O at 1M
Merck 13,370
BRN 1071138
InChIKeyCIORWBWIBBPXCG-PWKRRBCNNA-N
Safety Information
Hazard Codes T+
Risk Statements 26/27/28-33-26/28
Safety Statements 36/37/39-45-36/37-28
RIDADR UN 3462 6.1/PG 2
WGK Germany 3
RTECS BD6195000
8-10-18-21
HazardClass 6.1(a)
PackingGroup I
HS Code 2934999090
Hazardous Substances Data23109-05-9(Hazardous Substances Data)
ToxicityLD50 i.p. in albino mice: 0.1 mg/kg (Wieland, Wieland)
MSDS Information
ProviderLanguage
SigmaAldrich English
ALPHA-AMANITIN Usage And Synthesis
Usesα-Amanitin has been used:
  • for inducing transcriptional arrest in NT2 cells prior to immunofluorescence assay
  • to induce nephrotoxicity in mice renal tissues
  • to induce and analyse genotoxicity in mice bone marrow cells by cell viability assay, comet assay and chromosomal aberration assay

Biological Activityα-amanitin, the most deleterious toxin of a. phalloides to humans, inhibits rna polymerase ii (rnapii), causing hepatic and renal failure.
Biochem/physiol ActionsThe major toxic constituent of the mushroom, Amanita phalloides, inhibits eukaryotic RNA polymerase II and III, but does not inhibit RNA polymerase I or bacterial RNA polymerase. Inhibits mammalian protein synthesis.
in vivo

The intravenous LD50 dose of alpha-Amanitin is 0.327 mg/kg body weight after intravenous injection into BALB/c mice. After 12 h of alpha-Amanitin injection in caudal vein, the levels of WBC, RBC and HGB decrease significantly, while those of BUN and Crea increase significantly in serum. alpha-Amanitin inhibits some genes (Hsp90b1, Irx4, etc.), whose encoded proteins regulate the RNA polymerase II activity. alpha-Amanitin down-regulates some proteins (Nmi, Trpc5, etc.) taking part in the transcription progress[1]. alpha-Amanitin has potent activity in DTC suppression. Mice injected with alpha-Amanitin (0.4 mg/kg, i.p.)-treated cells maintain their body weight, while those receiving a peritoneal injection of MKN45 cells show a constant decrease in body weight[2].

IC 50Traditional Cytotoxic Agents
storageStore at -20°C
ALPHA-AMANITIN Preparation Products And Raw materials
Tag:ALPHA-AMANITIN(23109-05-9) Related Product Information
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