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Dihydrorotenone

Catalog No. TN1586Cas No. 6659-45-6

Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.

Dihydrorotenone

Dihydrorotenone

Purity: 99.58%
Catalog No. TN1586Cas No. 6659-45-6
Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.
Pack SizePriceAvailabilityQuantity
1 mg$115In Stock
5 mg$279In Stock
10 mg$443In Stock
25 mg$733In Stock
50 mg$987In Stock
1 mL x 10 mM (in DMSO)$335In Stock
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Purity:99.58%
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Product Introduction

Bioactivity
Description
Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.
In vitro
Dihydrorotenone arrested human plasma cancer cells at the G0/G1 phase of the cell cycle. Dihydrorotenone inhibited cyclin D2 transactivation, thus inhibiting its mRNA expression. In addition, Dihydrorotenone upregulated the cell cycle repressors p21 and p53. Dihydrorotenone also increased the phosphorylation level of p53, suggesting the upregulated transactivation function of p53, which was confirmed by the induction of p21, a substrate of activated p53. Moreover, Dihydrorotenone downregulated AKT and ERK phosphorylation, an incentive of cell cycle progression.
Chemical Properties
Molecular Weight396.43
FormulaC23H24O6
Cas No.6659-45-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 27.5 mg/mL (69.37 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5225 mL12.6126 mL25.2251 mL126.1257 mL
5 mM0.5045 mL2.5225 mL5.0450 mL25.2251 mL
10 mM0.2523 mL1.2613 mL2.5225 mL12.6126 mL
20 mM0.1261 mL0.6306 mL1.2613 mL6.3063 mL
50 mM0.0505 mL0.2523 mL0.5045 mL2.5225 mL

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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