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021217 T-2 Toxin CAS: 21259-20-1

Specifications
References
CAS Number
21259-20-1
Grade
Highly Purified
MDL Number
MFCD00871255
Molecular Formula
C₂₄H₃₄O₉
Molecular Weight
466.52
EU Commodity Code
38220090
Shipping Temp
Blue Ice
Storage Temp
-20°C
(3α,4β,8α)-12,13-Epoxytrichothec-9-ene-3,4,8,15-tetrol 4,15-Diacetate 8-(3-Methylbutanoate); 12,13-Epoxytrichothec-9-ene-3α,4β,8α,15-tetrol 4,15-Diacetate 8-Isovalerate; 4β,15-Diacetoxy-8α-(3-methylbutyryloxy)-|12,13-epoxytrichothec-9-en-3α-ol; 8α-(3-Methylbutyryloxy)-4β,15-|diacetoxyscirp-9-en-3α-ol; Fusariotoxin T 2; Insariotoxin; Mycotoxin T 2; NSC 138780; T 2; T 2 mycotoxin; T-2 Lienomycin; Toxin T 2

T-2 toxin is a common trichothecene mycotoxin produced by Fusarium species, which can infect grain crops causing alimentary toxic aleukia in humans and animals. It triggers a ribotoxic response through its high binding affinity to peptidyl transferase, which is an integral part of the 60S ribosomal subunit, resulting in activation of JNK/p38 MAPKs, interferes with the metabolism of membrane phospholipids, and increases liver lipid peroxides.1 T-2 toxin is highly cytotoxic to macrophages, inducing apoptosis in primary porcine alveolar macrophage cells with an IC50 value of 19.47 nM. At 3 nM it decreases the production of inflammatory mediators (IL-1β, TNFα, and nitric oxide), TLR4, and TLR2/6 agonists.2

Alternate Names
(3α,4β,8α)-12,13-Epoxytrichothec-9-ene-3,4,8,15-tetrol 4,15-Diacetate 8-(3-Methylbutanoate); 12,13-Epoxytrichothec-9-ene-3α,4β,8α,15-tetrol 4,15-Diacetate 8-Isovalerate; 4β,15-Diacetoxy-8α-(3-methylbutyryloxy)- 12,13-epoxytrichothec-9-en-3α-ol; 8α-(3-Methylbutyryloxy)-4β,15- diacetoxyscirp-9-en-3α-ol; Fusariotoxin T 2; Insariotoxin; Mycotoxin T 2; NSC 138780; T 2; T 2 mycotoxin; T-2 Lienomycin; Toxin T 2
CAS Number
21259-20-1
Appearance
White Solid
Purity
≥98%
Melting Point
140-143°C
Storage
-20˚C Freezer
Solubility
Cyclohexane (Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly)
Source
Synthetic
Purity
≥98%
Form
White Solid
Important Note
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
References
1. K. Doi and K. Uetsuka. Mechanisms of mycotoxin-induced neurotoxicity through oxidative stress-associated pathways. International Journal of Molecular Sciences 12, 5213-5237 (2011).|2. J. Seeboth, R. Solinhac, I. P. Oswald, et al. The fungal T-2 toxin alters the activation of primary macrophages induced by TLR-agonists resulting in a decrease of the inflammatory response in the pig. Veterinary Research 43, 1-18 (2012).|3. Kim, C., et al.: Cancer Res., 57, 3115 (1997)|4. Bottrel, R., et al.: Antimicrob. Agents Chemother., 1999, 43, 856 (1999)|5. Murray, P., et al.: J. Immunol., 178, 2623 (2007)|6. Choi, H., et al.: Toxicol. Appl. Pharmacol., 240, 46 (2009)|7. Amuzie, C., et al.: Toxicol. Sci., 113, 412 (2010)||
USBio References
No references available
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