Description
A mycotoxin first isolated from P. roqueforti that displays neurotoxic properties; activates a P-glycoprotein transport system involved in the efflux of xenobiotics and inhibits cytochrome P450 3A detoxification enzymes
Formal name: (3E,5aS,10bR)-10b-(1,1-dimethyl-2-propen-1-yl)-6,10b,11,11aS-tetrahydro-3-(1H-imidazol-5-ylmethylene)-2H-pyrazino[1′,2′:1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione
Synonyms: NSC 292134
Molecular weight: 389.5
CAS: 58735-64-1
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Small Molecule Inhibitors|Cytochrome P450||Product Type|Biochemicals|Small Molecule Inhibitors|MMPs||Product Type|Biochemicals|Toxins|Mycotoxins||Product Type|Biochemicals|Transporter & Exchanger Modulators||Research Area|Neuroscience||Research Area|Toxicology|Drug Metabolism|Cytochrome P450||Research Area|Toxicology|Drug Metabolism|Xenobiotic Sensing