1. Metabolic Enzyme/Protease
  2. Cytochrome P450
  3. Dapaconazole

Dapaconazole 

Cat. No.: HY-16719 Purity: 98.95%
Handling Instructions

Dapaconazole, as an antifungal agent, inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 μM.

For research use only. We do not sell to patients.

Dapaconazole Chemical Structure

Dapaconazole Chemical Structure

CAS No. : 1269726-67-1

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5 mg USD 300 In-stock
Estimated Time of Arrival: December 31
10 mg USD 480 In-stock
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25 mg USD 950 In-stock
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50 mg USD 1450 In-stock
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100 mg USD 2250 In-stock
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Based on 1 publication(s) in Google Scholar

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Description

Dapaconazole, as an antifungal agent, inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 μM[1].

IC50 & Target[1]

Cytochrome P450 (CYP26)

1.4 μM (IC50)

In Vitro

Dapaconazole inhibits sterol 14α-demethylase cytochrome P450 activity with an IC50 of 1.4 ± 0.3 μM[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Dapaconazole (20 mg/kg; p.o.) shows that the bioavailability is 97.3 %[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male beagle dogs[1]
Dosage: 20 mg/kg (Pharmacokinetic Analysis)
Administration: P.o.
Result: Showed that the bioavailability was 97.3 %.
Molecular Weight

415.24

Formula

C₁₉H₁₅Cl₂F₃N₂O

CAS No.
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
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Product Name:
Dapaconazole
Cat. No.:
HY-16719
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