An internal standard for the quantification of gliotoxin
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Unlabeled Version(s)
11433Gliotoxin
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Gliotoxin-13C13

Item No. 9003827

Technical Information
Formal Name
(3R,5aS,6S,10aR)-6-hydroxy-3-(hydroxymethyl-13C)-2-(methyl-13C)-2,3,5a,6-tetrahydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione-1,3,4,5a,6,7,8,9,9a,10,10a-13C11
Synonyms
  • Aspergillin-13C13
Molecular Formula
[13C]13H14N2O4S2
Formula Weight
Purity
≥95%
A solution in acetonitrile
Acetonitrile: 3 mg/ml
λmax
265 nm
SMILES
O=[13C]([13C@]1(SS2)[13CH2][13C]3=[13CH][13CH]=[13CH][13C@H](O)[13C@H]3N14)N([13CH3])[13C@@]2([13CH2]O)[13C]4=O
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/i1+1,2+1,3+1,4+1,5+1,6+1,7+1,8+1,9+1,10+1,11+1,12+1,13+1
InChi Key
FIVPIPIDMRVLAY-DKOZNSHBSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Gliotoxin-13C13 is intended for use as an internal standard for the quantification of gliotoxin (Item No. 11433) by GC- or LC-MS. 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).