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Dihydroisotanshinone I

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Catalog No. TN1588Cas No. 20958-18-3

Dihydroisotanshinone I is a natural product isolated from the dried roots of Salvia miltiorrhiza, a traditional Chinese medicine, and exhibits various biological activities. Dihydroisotanshinone I alleviates menadione-induced liver injury through antioxidant effects such as scavenging free radicals and inhibiting lipid peroxidation; it also inhibits the migration of prostate cancer cells and induces cancer cell apoptosis.

Dihydroisotanshinone I

Dihydroisotanshinone I

😃Good
Purity: 99.75%
Catalog No. TN1588Cas No. 20958-18-3
Dihydroisotanshinone I is a natural product isolated from the dried roots of Salvia miltiorrhiza, a traditional Chinese medicine, and exhibits various biological activities. Dihydroisotanshinone I alleviates menadione-induced liver injury through antioxidant effects such as scavenging free radicals and inhibiting lipid peroxidation; it also inhibits the migration of prostate cancer cells and induces cancer cell apoptosis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$818-In Stock
5 mg$1,800-In Stock
10 mg$2,700-In Stock
25 mg$4,590-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.75%
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Product Introduction

Bioactivity
Description
Dihydroisotanshinone I is a natural product isolated from the dried roots of Salvia miltiorrhiza, a traditional Chinese medicine, and exhibits various biological activities. Dihydroisotanshinone I alleviates menadione-induced liver injury through antioxidant effects such as scavenging free radicals and inhibiting lipid peroxidation; it also inhibits the migration of prostate cancer cells and induces cancer cell apoptosis.
In vitro
Dihydroisotanshinone I induces cell cycle G1 arrest by inhibiting the expression of cyclin D1, cyclin E1, CDK2, CDK4, CDK6, p-Rb, E2F1 and SKP2, and suppresses the proliferation of human osteosarcoma 143B cells in a dose- and time-dependent manner.
Dihydroisotanshinone I induces apoptosis via activating caspase-3, caspase-8, caspase-9 and cleaving PARP, and inhibits cell migration by down-regulating VCAM-1 and ICAM-1.
In vivo
In xenograft tumor models, Dihydroisotanshinone I inhibits the proliferation of Hela human cervical cancer cells. It enhances radiation-induced apoptosis and significantly inhibits proliferation in Hela cells mainly by prolonging radiation-induced G2/M arrest and reducing the expression levels of Bcl-XL, Bcl-2 and HPV E6 protein.
Chemical Properties
Molecular Weight278.31
FormulaC18H14O3
Cas No.20958-18-3
SmilesO=C1C=2OCC(C2C(=O)C3=CC=C4C(C=CC=C4C)=C13)C
Relative Density.1.32g/cm3
Storage & Solubility Information
Storagestore at low temperature | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 5.00 mg/mL (17.97 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.5931 mL17.9656 mL35.9312 mL179.6558 mL
5 mM0.7186 mL3.5931 mL7.1862 mL35.9312 mL
10 mM0.3593 mL1.7966 mL3.5931 mL17.9656 mL

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TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
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