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Tebuconazole

Cat. No. M11176
Tebuconazole Structure
Size Price Availability Quantity
250mg USD 60  USD60 In stock
1g USD 105  USD105 In stock
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Quality Control & Documentation
Biological Activity

Tebuconazole is an agricultural azole fungicide that also inhibits CYP51 for Candida albicans CYP51 (CaCYP51) and truncated human CYP51 (Δ60HsCYP51). IC50 The values are 0.9 and 1.3 μM, respectively.

Chemical Information
Molecular Weight 307.82
Formula C16H22ClN3O
CAS Number 107534-96-3
Solubility (25°C) DMSO ≥ 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Lingxi Han, et al. Environ Pollut. Repeated exposure to fungicide tebuconazole alters the degradation characteristics, soil microbial community and functional profiles

[2] Tingting Ku, et al. Ecotoxicol Environ Saf. Tebuconazole induces liver injury coupled with ROS-mediated hepatic metabolism disorder

[3] Nagapooja Yogendraiah Matadha, et al. Food Chem. Distribution of fluopyram and tebuconazole in pomegranate tissues and their risk assessment

[4] Feifei Ma, et al. Chemosphere. Gestational exposure to tebuconazole affects the development of rat fetal Leydig cells

[5] Yosra Ben Othmne, et al. Food Chem Toxicol. Tebuconazole induced cardiotoxicity in male adult rat

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Keywords: Tebuconazole supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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