Triadimenol
CAS No. 55219-65-3
Triadimenol( —— )
Catalog No. M34724 CAS No. 55219-65-3
Triadimenol (UK 199) is a triazole fungicide that is cardiotoxic, promotes reactive oxygen species (ROS) production and apoptosis in zebrafish, and induces morphologic changes in zebrafish eyes and body length, as well as yolk sac and cardiac edema.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameTriadimenol
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NoteResearch use only, not for human use.
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Brief DescriptionTriadimenol (UK 199) is a triazole fungicide that is cardiotoxic, promotes reactive oxygen species (ROS) production and apoptosis in zebrafish, and induces morphologic changes in zebrafish eyes and body length, as well as yolk sac and cardiac edema.
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DescriptionTriadimenol is a triazole fungicide and has been widely used in agriculture. Triadimenol has certain toxicity to animals.
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In Vitro——
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In VivoAnimal Model:9.5 day-old Rat embryosDosage:6.25-125 μM Administration:Cultured for 48 h in rat serum Result:Showed specific cranial nerve and ganglia abnormalities.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetAntifungal
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RecptorAntifungal
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Research Area——
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Indication——
Chemical Information
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CAS Number55219-65-3
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Formula Weight295.77
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Molecular FormulaC14H18ClN3O2
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Purity>98% (HPLC)
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Solubility——
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SMILESClC1=CC=C(OC(N2N=CN=C2)C(O)C(C)(C)C)C=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Neticonazole
Neticonazole (SS717) is an imidazole derivative with antifungal activity that inhibits exosome secretion.
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SDH-IN-2
SDH-IN-2, a potent succinate dehydrogenase (SDH) inhibitor with an IC50 of 0.55 μg/mL, demonstrates antifungal activity against plant pathogenic fungi, with EC50 values ranging from 3.82 to 9.81 μg/mL.
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Pentamidine
Pentamidine is an antifungal and antiprotozoal agent, interacting directly with the pathogen genome by binding to AT-rich regions of duplex DNA and the minor groove of DNA, thereby interfering with DNA replication.Pentamidine is effective in therapy for the hemolymphatic stage of Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia.
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