An immunosuppressive mycotoxin with diverse biological effects
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Labeled Version(s)
9003827Gliotoxin-13C13
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Gliotoxin

Item No. 11433

Technical Information
Formal Name
2,3R,5aS,6S-tetrahydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3,10aR-epidithiopyrazino[1,2-a]indole-1,4-dione
CAS Number
67-99-2
Synonyms
  • Aspergillin
Molecular Formula
C13H14N2O4S2
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 5 mg/mlDMSO: 5 mg/mlDMSO:PBS (pH 7.2)(1:5): 0.5 mg/ml
λmax
202, 269 nm
SMILES
O[C@H]1C=CC=C2[C@@H]1N(C([C@]3(CO)N(C)C4=O)=O)[C@@]4(SS3)C2
InChi Code
InChI=1S/C13H14N2O4S2/c1-14-10(18)12-5-7-3-2-4-8(17)9(7)15(12)11(19)13(14,6-16)21-20-12/h2-4,8-9,16-17H,5-6H2,1H3/t8-,9-,12+,13?/m0/s1
InChi Key
FIVPIPIDMRVLAY-ZKVOIBSNSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Gliotoxin is an immunosuppressive mycotoxin produced by pathogenic strains of Aspergillus and other fungi with diverse biological activities.1,2,3,4,5,6,7,8 It inhibits 20S proteasomal chymotrypsin activity (IC50 = 10 μM), blocking the degradation of IκBα and preventing the activation of NF-κB.2,3 Gliotoxin induces apoptosis in monocytes and dendritic cells and reduces phagocytosis by neutrophils.4,5 It suppresses viral infection by Nipah and Hendra virus in HEK293T cells (IC50s = 149 and 579 nM, respectively).6 Under reducing conditions, gliotoxin inhibits leukotriene A4 hydrolase (LTA4H; Item No. 10007817) epoxide hydrolase activity, but not aminopeptidase activity, and leukotriene B4 (LTB4; Item No. 20110) synthesis in neutrophils and monocytes.7 In vivo, gliotoxin (5 mg/kg) reduces LTB4 plasma levels and blocks peritoneal neutrophil infiltration in a mouse model of peritonitis induced by zymosan A (Item No. 21175). It also inhibits geranylgeranyltransferase I and farnesyltransferase (IC50s = 17 and 80 μM, respectively).8

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kwon-Chung, K.J., and Sugui, J.A. What do we know about the role of gliotoxin in the pathobiology of Aspergillus fumigatus? Med. Mycol. 47(Suppl 1), S97-S103 (2009).

    2. Kroll, M., Arenzana-Seisdedos, F., Bachelerie, F., et alThe secondary fungal metabolite gliotoxin targets proteolytic activities of the proteasome. Chem. Biol. 6(10), 689-698 (1999).

    3. Pahl, H.L., Krauss, B., Schulze-Osthoff, K., et alThe immunosuppressive fungal metabolite gliotoxin specifically inhibits transcription factor NF-κB. J. Exp. Med. 183(4), 1829-1840 (1996).

    4. Anselmi, K., Stolz, D.B., Nalesnik, M., et alGliotoxin causes apoptosis and necrosis of rat Kupffer cells in vitro and in vivo in the absence of oxidative stress: Exacerbation by caspase and serine protease inhibition. J. Hepatol. 47(1), 103-113 (2007).

    5. Orciuolo, E., Stanzani, M., Canestraro, M., et alEffects of Aspergillus fumigatus gliotoxin and methylprednisolone on human neutrophils: Implications for the pathogenesis of invasive aspergillosis. J. Leukoc. Biol. 82(4), 839-848 (2007).

    6. Aljofan, M., Sganga, M.L., Lo, M.K., et alAntiviral activity of gliotoxin, gentian violet and brilliant green against Nipah and Hendra virus in vitro. Virol. J. 6, 187 (2009).

    7. König, Pace, S., Pein, H., et alGliotoxin from Aspergillus fumigatus abrogates leukotriene B4 formation through inhibition of leukotriene A4 hydrolase. Cell. Chem. Biol. 26(4), 524-534 (2019).

    8. Vigushin, D.M., Mirsaidi, N., Brooke, G., et alGliotoxin is a dual inhibitor of farnesyltransferase and geranylgeranyltransferase I with antitumor activity against breast cancer in vivo. Med. Oncol. 21(1), 21-30 (2004).