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Gliotoxin

Supplier:
Catalogue number:
g4434-10 mg
Size:
10 mg
Product is available in:
  • UK
  • Ireland
  • Europe
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  • Rest of World
£751.00 Estimated delivery Tue 28 Sep
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Toxin produced by Aspergillus.

Product Type:

Biochemicals

CAS Number:

67-99-2

Storage Temp:

4°C

Compound Purity:

≥98%

Molecular Weight:

326.39

Reference:

Nguyen VT, Lee JS, Qian ZJ, et al. Gliotoxin Isolated from Marine Fungus Aspergillus sp. Induces Apoptosis of Human Cervical Cancer and Chondrosarcoma Cells. Mar Drugs. 2013 Dec 24;12(1):69-87. PMID: 24368570. Hur JM, Yun HJ, Yang SH, et al. Gliotoxin enhances radiotherapy via inhibition of radiation-induced GADD45a, p38, and NFkappaB activation. J Cell Biochem. 2008 Aug 15;104(6):2174-84. PMID: 18425744. Orciuolo E, Stanzani M, Canestraro M, et al. Effects of Aspergillus fumigatus gliotoxin and methylprednisolone on human neutrophils: implications for the pathogenesis of invasive aspergillosis. J Leukoc Biol. 2007 Oct;82(4):839-48. PMID: 17626149. Hatabu T, Hagiwara M, Taguchi N, et al. Plasmodium falciparum: the fungal metabolite gliotoxin inhibits proteasome proteolytic activity and exerts a plasmodicidal effect on P. falciparum. Exp Parasitol. 2006 Mar;112(3):179-83. PMID: 16384554. Orr JG, Leel V, Cameron GA, et al. Mechanism of action of the antifibrogenic compound gliotoxin in rat liver cells. Hepatology. 2004 Jul;40(1):232-42. PMID: 15239107. Kweon YO, Paik YH, Schnabl B, et al. Gliotoxin-mediated apoptosis of activated human hepatic stellate cells. J Hepatol. 2003 Jul;39(1):38-46. PMID: 12821042.

Structure:

C13H14N2O4S2

Formula:

C13H14N2O4S2

UNSPSC Code:

51102800

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