1. Apoptosis TGF-beta/Smad Stem Cell/Wnt NF-κB Anti-infection
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  3. Gliotoxin

Gliotoxin is a secondary metabolite, the most abundant mycotoxin secreted by A. fumigatus, inhibits the phagocytosis of macrophages and the immune functions of other immune cells . Gliotoxin inhibits inducible NF-κB activity by preventing IκB degradation, which consequently induces host-cell apoptosis. Gliotoxin activates PKA and increases intracellular cAMP concentration; modulates actin cytoskeleton rearrangement to facilitate A. fumigatus internalization into lung epithelial cells. Gliotoxin is a potent NOTCH2 transactivation inhibitor, can effectively induce apoptosis of chronic lymphocytic leukemia (CLL) cells.

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Gliotoxin

Gliotoxin Chemical Structure

CAS No. : 67-99-2

Size Prix Stock Quantité
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
En stock
Solution
10 mM * 1 mL in DMSO En stock
Solid
1 mg En stock
5 mg En stock
10 mg En stock
25 mg En stock
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100 mg   Obtenir un devis  

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Description

Gliotoxin is a secondary metabolite, the most abundant mycotoxin secreted by A. fumigatus, inhibits the phagocytosis of macrophages and the immune functions of other immune cells [1]. Gliotoxin inhibits inducible NF-κB activity by preventing IκB degradation, which consequently induces host-cell apoptosis[2]. Gliotoxin activates PKA and increases intracellular cAMP concentration; modulates actin cytoskeleton rearrangement to facilitate A. fumigatus internalization into lung epithelial cells[3]. Gliotoxin is a potent NOTCH2 transactivation inhibitor, can effectively induce apoptosis of chronic lymphocytic leukemia (CLL) cells[4].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
0.003 3
Compound: 10
Cytotoxicity against human A549 cells
Cytotoxicity against human A549 cells
[PMID: 20303767]
A549 IC50
0.003 3
Compound: 10
Cytotoxicity against human A549 cells
Cytotoxicity against human A549 cells
[PMID: 20303767]
CCRF-CEM IC50
0.15 3
Compound: gliotoxin
Cytotoxicity against human CEM cells after 96 hrs
Cytotoxicity against human CEM cells after 96 hrs
[PMID: 16124785]
CCRF-CEM IC50
0.15 3
Compound: gliotoxin
Cytotoxicity against human CEM cells after 96 hrs
Cytotoxicity against human CEM cells after 96 hrs
[PMID: 16124785]
CCRF-CEM IC50
0.15 3
Compound: gliotoxin
Cytotoxicity against human CEM cells after 96 hrs
Cytotoxicity against human CEM cells after 96 hrs
[PMID: 16124785]
Jurkat IC50
< 1 3
Compound: 10
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
[PMID: 20303767]
HCT-116 IC50
0.41 3
Compound: 311
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
[PMID: 38181652]
P388 IC50
0.024 3
Compound: 6
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
[PMID: 22148349]
HeLa IC50
2.45 3
Compound: 10
Cytotoxicity against human HeLa cells
Cytotoxicity against human HeLa cells
[PMID: 20303767]
HCT-116 IC50
1.24 3
Compound: 311
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
Cytotoxicity against human HCT-116 cells assessed as reduction in cell viability incubated for 24 hrs by MTT assay
[PMID: 38181652]
HUVEC IC50
0.123 3
Compound: 10
Cytotoxicity against HUVEC
Cytotoxicity against HUVEC
[PMID: 20303767]
HEK293 IC50
1.58 3
Compound: 311
Cytotoxicity against HEK293 cells assessed as cell growth inhibition
Cytotoxicity against HEK293 cells assessed as cell growth inhibition
[PMID: 38181652]
Jurkat IC50
<1 3
Compound: 10
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
[PMID: 20303767]
HUVEC IC50
0.123 3
Compound: 10
Cytotoxicity against HUVEC
Cytotoxicity against HUVEC
[PMID: 20303767]
Macrophage ED50
0.104 3
Compound: 10
Immunomodulatory activity in macrophage assessed as inhibition of phagocytosis
Immunomodulatory activity in macrophage assessed as inhibition of phagocytosis
[PMID: 20303767]
HeLa IC50
2.45 3
Compound: 10
Cytotoxicity against human HeLa cells
Cytotoxicity against human HeLa cells
[PMID: 20303767]
P388 IC50
0.024 3
Compound: 6
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
[PMID: 22148349]
HepG2 IC50
0.21 3
Compound: 311
Cytotoxicity against human HepG2 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
[PMID: 38181652]
P815 ED50
2 3
Compound: Gliotoxin
Compound was evaluated for Thymidine incorporation in P815 cell lines
Compound was evaluated for Thymidine incorporation in P815 cell lines
10.1016/S0960-894X(97)10052-X
HepG2 IC50
0.24 3
Compound: 311
Cytotoxicity against human HepG2 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
[PMID: 38181652]
Jurkat IC50
< 1 3
Compound: 10
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
Cytotoxicity against human Jurkat cells after 40 hrs bioluminescence assay
[PMID: 20303767]
MCF7 IC50
0.08 3
Compound: 311
Cytotoxicity against human MCF7 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
[PMID: 38181652]
MCF7 IC50
0.08 3
Compound: 311
Cytotoxicity against human MCF7 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
Cytotoxicity against human MCF7 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
[PMID: 38181652]
Macrophage ED50
0.104 3
Compound: 10
Immunomodulatory activity in macrophage assessed as inhibition of phagocytosis
Immunomodulatory activity in macrophage assessed as inhibition of phagocytosis
[PMID: 20303767]
NCI-H460 IC50
0.21 3
Compound: 311
Cytotoxicity against human NCI-H460 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
Cytotoxicity against human NCI-H460 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
[PMID: 38181652]
NCI-H460 IC50
0.24 3
Compound: 311
Cytotoxicity against human NCI-H460 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
Cytotoxicity against human NCI-H460 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
[PMID: 38181652]
P388 IC50
0.024 3
Compound: 6
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
Cytotoxicity against mouse P388 cells after 96 hrs by MTT assay
[PMID: 22148349]
P815 ED50
2 3
Compound: Gliotoxin
Compound was evaluated for Thymidine incorporation in P815 cell lines
Compound was evaluated for Thymidine incorporation in P815 cell lines
10.1016/S0960-894X(97)10052-X
PC-3 IC50
0.39 3
Compound: 311
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability
[PMID: 38181652]
PC-3 IC50
15.87 3
Compound: 311
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability measured after 72 hrs by MTT assay
[PMID: 38181652]
RKO IC50
0.8 3
Compound: 311
Cytotoxicity against human RKO cells assessed as inhibition of cell growth measured after 48 hrs by MTT assay
Cytotoxicity against human RKO cells assessed as inhibition of cell growth measured after 48 hrs by MTT assay
[PMID: 38181652]
SF-268 IC50
0.24 3
Compound: 311
Cytotoxicity against human SF-268 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
Cytotoxicity against human SF-268 cells assessed as reduction in cell growth incubated for 48 hrs by SRB assay
[PMID: 38181652]
SF-268 IC50
0.24 3
Compound: 311
Cytotoxicity against human SF-268 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
Cytotoxicity against human SF-268 cells assessed as reduction in cell growth incubated for 72 hrs by SRB assay
[PMID: 38181652]
U-937 IC50
0.2 3
Compound: 311
Cytotoxicity against human U-937 cells assessed as reduction in cell viability
Cytotoxicity against human U-937 cells assessed as reduction in cell viability
[PMID: 38181652]
U-937 IC50
0.52 3
Compound: 311
Cytotoxicity against human U-937 cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
Cytotoxicity against human U-937 cells assessed as reduction in cell viability incubated for 72 hrs by MTT assay
[PMID: 38181652]
In Vitro

Gliotoxin (50 ng/ml, 48 hours) promotes the internalization of Aspergillus fumigatus by A549 type II human pneumocytes through inducing cofilin phosphorylation and actin cytoskeleton rearrangement[3].
Gliotoxin (2.5%, 5%, 10%, 20% culture filtrates of Aspergillus fumigatus containing Gliotoxin, 16 hours) induces apoptosis in EL4 thymoma cells through Bak-dependent mechanisms and activation of caspase 3, leading to phosphatidylserine translocation and cell death[5].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[3]

Cell Line: A549 type II human pneumocytes
Concentration: 50 ng/ml
Incubation Time: 48 hours
Result: Induced cofilin phosphorylation, promoting actin cytoskeleton rearrangement and facilitating internalization of Aspergillus fumigatus.
In Vivo

Gliotoxin (50 ng/ml, Intranasal administration, single dose) enhances the invasiveness of Aspergillus fumigatus in Hydrocortisone (HY-N0583)-induced immunosuppressed C57BL/6 mouse models by promoting lung tissue invasion and increasing fungal burden[3].
Gliotoxin (Intranasal administration, single dose) significantly increases fungal burden in the lungs and mortality in Hydrocortisone (HY-N0583)-induced immunosuppressed BALB/c and 129/Sv mouse models, contributing to the virulence of Aspergillus fumigatus[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Hydrocortisone (HY-N0583)-induced immunosuppressed C57BL/6 mice[3]
Dosage: 50 ng/ml
Administration: Intranasal administration, single dose
Result: Helped the gliP mutant strain (which cannot produce Gliotoxin) invade lung tissues, leading to increased fungal burden in the lungs of immunosuppressed mice.
Animal Model: Hydrocortisone (HY-N0583)-induced immunosuppressed BALB/c and 129/Sv mouse models[4]
Dosage: Gliotoxin concentration not explicitly mentioned, present in Aspergillus fumigatus culture filtrates
Administration: Intranasal administration of culture filtrates containing gliotoxin, single dose
Result: Increased lung tissue fungal burden and mortality in immunosuppressed mice. The gliP deletion strain, which cannot produce gliotoxin, showed reduced virulence.
Masse moléculaire

326.39

Formule

C13H14N2O4S2

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C1N([C@]2(C(N3[C@]1(CC4=CC=C[C@@H]([C@@]34[H])O)SS2)=O)CO)C

Structure Classification
Initial Source

Aspergillus fumigatus

Livraison

Room temperature in continental US; may vary elsewhere.

Stockage
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
Solvant et solubilité
In Vitro: 

DMSO : 5 mg/mL (15.32 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

DMF : 5 mg/mL (15.32 mM; Need ultrasonic and warming)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.0638 mL 15.3191 mL 30.6382 mL
5 mM 0.6128 mL 3.0638 mL 6.1276 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Pureté et documentation

Purity: 99.51%

Références

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO / DMF 1 mM 3.0638 mL 15.3191 mL 30.6382 mL 76.5955 mL
5 mM 0.6128 mL 3.0638 mL 6.1276 mL 15.3191 mL
10 mM 0.3064 mL 1.5319 mL 3.0638 mL 7.6595 mL
15 mM 0.2043 mL 1.0213 mL 2.0425 mL 5.1064 mL
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Nom du produit:
Gliotoxin
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