Description
Aflatoxin Q1 is a hydroxy metabolite of the mycotoxin aflatoxin B1. Human CYP3A4 study suggests aflatoxin Q1 is a detoxification product that is no longer mutagenic.
Product Unit Size | Cost | Quantity | Stock |
---|
Aflatoxin Q1 is a hydroxy metabolite of the mycotoxin aflatoxin B1. Human CYP3A4 study suggests aflatoxin Q1 is a detoxification product that is no longer mutagenic.
Cas No. | 52819-96-2 |
---|---|
Purity | ≥98% |
Formula | C17H12O7 |
Formula Wt. | 328.27 |
Chemical Name | (3S,6aR,9aS)-3-hydroxy-4-methoxy-2,3-dihydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene-1,11(6aH,9aH)-dione |
IUPAC Name | (3S,6aR,9aS)-3-Hydroxy-4-methoxy-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene-1,11-dione |
Synonym | AFQ1 |
Appearance | Off white powder |
Store Temp | 4°C |
---|---|
Ship Temp | Ambient |
Info Sheet |
---|
Yourtee DM, Bean TA, Kirk-Yourtee CL. Human aflatoxin B1 metabolism: an investigation of the importance of aflatoxin Q1 as a metabolite of hepatic post-mitochondrial fraction. Toxicol Lett. 198738(3):213-24. doi: 10.1016/0378-4274(87)90002-6, PMID: 3116726
M. Yamada , K. Hatsuta , M Niikawa, et al. Detoxification of Aflatoxin B1 Contaminated Maize Using Human CYP3A4 J. Microbiol Biotechnol 2020, 28;30(8):1207-1213. doi: 10.4014/jmb.2003.03032 PMID: 32423188
Macrolide antibiotic; peptidyl transferase inhi...
NO donor.
Benzimidazole; microtubule polymerization inhib...
MEK1/2 inhibitor.
NDRI inhibitor
Endogenous precursor to all steroid hormones; T...
Everolimus impurity
Piperazine; FIASMA, D2 antagonist, hERG K+ chan...
Antioxidant, vitamin E derivative found in vege...
Peptide, derivative of AT I, cleavage product o...
Peptide, involved in neutrophil activation; FPR...
inhibits inflammatory signaling
Sulfonamide; carbonic anhydrase inhibitor, volt...
Potent and selective inhibitor
α-glucosidase inhibitor.