Description
Triadimefon is a mutagenic antifungal compound used to manage fungal infections in agricultural crops. Triadimefon may be neurotoxic, as it regulates retinoic acid levels and alters learning and memory function in vivo.
Product Unit Size | Cost | Quantity | Stock |
---|
Triadimefon is a mutagenic antifungal compound used to manage fungal infections in agricultural crops. Triadimefon may be neurotoxic, as it regulates retinoic acid levels and alters learning and memory function in vivo.
Cas No. | 43121-43-3 |
---|---|
Purity | ≥98% |
Formula | C14H16ClN3O2 |
Formula Wt. | 293.75 |
Chemical Name | 1-(4-Chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-trazol-1-yl)-2-butanone |
IUPAC Name | 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one |
Synonym | BAY MEB 6447, Bayleton |
Melting Point | 82°C |
Solubility | Soluble in water. Moderately soluble in most organic solvents |
Appearance | White to yellowish crystalline powder |
Store Temp | Ambient |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Xi J, Yang Z, Zeng C, et al. Suppressive effect of triadimefon, a triazole fungicide, on spatial learning and reference memory in rats. Behav Pharmacol. 2012 Dec;23(8):727-34. PMID: 23080312.
Di Renzo F, Broccia ML, Giavini E, et al. Stage-dependent abnormalities induced by the fungicide triadimefon in the mouse. Reprod Toxicol. 2011 Feb;31(2):194-9. PMID: 21055463.
Berg D, Draber W, von Hugo H, et al. The effect of clotrimazole and triadimefon on 3-hydroxy-3-methyl-glutaryl-CoA-reductase-[EC 1.1.1.34]-activity in Saccharomyces cerevisiae. Z Naturforsch C. 1981 Sep-Oct;36(9-10):798-803. PMID: 7029940.
PKA inhibitor, potential ROCK, S6K1, MSK1, PKB ...
Rapamycin analog
GSK-3 and CDK inhibitor.
Glutathione-ITC conjugate, antioxidant.
PORCN inhibitor.
Endogenous peptide hormone, involved in cell gr...
Nucleoside (adenosine) analog; DNA chain termin...
Voltage-gated Na+ channel blocker, mAChR antago...
Synthetic analog of 1,4-naphthoquinone, precurs...
Peptide, IgG derivative, tuftsin analog.
MAO-A/B inhibitor.
p110α PI3K inhibitor.
Peptide, vasopressin analog; V1/2 agonist.
Endogenous catecholamine precursor, also found ...
Selective HDAC4 and HDAC5 inhibitor.
Centrally acting muscle relaxant.
Quinazoline; α1-adrenergic antagonist.
Thioamide; thyroid peroxidase inhibitor.
PDEδ inhibitor.
Potential PKD binding agent.