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3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone

Name: 3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone
Brand: TargetMol
SKU: T83366
Price: -1 USD
Availability: InStock
Rating: 4.5 (1 reviews)

Catalog No. T83366Cas No. 90850-99-0

3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone, a natural product isolated from the fruits of Vitex rotundifolia, exhibits potent cytotoxic activity against A549 and HepG-2 cell lines [1].

3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone

Catalog No. T83366Cas No. 90850-99-0

3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone, a natural product isolated from the fruits of Vitex rotundifolia, exhibits potent cytotoxic activity against A549 and HepG-2 cell lines [1].

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Product Introduction

Bioactivity

Description	3′,5-Dihydroxy-4′,6,7-trimethoxyflavanone, a natural product isolated from the fruits of Vitex rotundifolia, exhibits potent cytotoxic activity against A549 and HepG-2 cell lines [1].
In vitro	The compound 3,5-Dihydroxy-4',6,7-trimethoxyflavanone (referred to as compound 10; 36 h) exhibits cytotoxic activity, with IC50 values of 35 μM and >100 μM against HepG-2 and A549 cells, respectively [1].

Chemical Properties

Molecular Weight	346.33
Formula	C₁₈H₁₈O₇
Cas No.	90850-99-0

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For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments

A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent

DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。

Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO TargetMol | reagent

(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.

Preparation method for in vivo formula: Take 50 μL DMSO TargetMol | reagent

main solution, add 300 μLPEG300 TargetMol | reagent

mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O TargetMol | reagent

mix well and clarify

For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.

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