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β-Anhydroicaritin

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Catalog No. T6S2140Cas No. 38226-86-7
Alias Beta-Anhydroicaritin, Anhydroicaritin

1. β-Anhydroicaritin exhibits immunosuppressive effect on the mouse macrophages stimulated by LPS. 2. β-Anhydroicaritin phytosomes can inhibit enhanced bone turnover induced by ovariectomy, improve BMD the biomechanical properties of vertebrae, without any stimulation on uterus. 3. β-Anhydroicaritin possesses significant protective effects on the zymosan-induced peritonitis mice, which might be associated with the regulation of Ca(2+); influx in macrophages and iNOS expression.

β-Anhydroicaritin

β-Anhydroicaritin

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🥰Excellent
Purity: 99.09%
Catalog No. T6S2140Alias Beta-Anhydroicaritin, AnhydroicaritinCas No. 38226-86-7
1. β-Anhydroicaritin exhibits immunosuppressive effect on the mouse macrophages stimulated by LPS. 2. β-Anhydroicaritin phytosomes can inhibit enhanced bone turnover induced by ovariectomy, improve BMD the biomechanical properties of vertebrae, without any stimulation on uterus. 3. β-Anhydroicaritin possesses significant protective effects on the zymosan-induced peritonitis mice, which might be associated with the regulation of Ca(2+); influx in macrophages and iNOS expression.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$40In StockIn Stock
10 mg$68In StockIn Stock
25 mg$123In StockIn Stock
50 mg$183In StockIn Stock
100 mg$272In StockIn Stock
1 mL x 10 mM (in DMSO)$44In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.09%
Appearance:Solid
Color:Yellow
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Product Introduction

β-Anhydroicaritin AI Summary
β-Anhydroicaritin is an inhibitor of human recombinant PDE5A1 expressed in COS7 cells, with an IC50 value of 45,500 nM, indicating its bioactivity against this enzyme. The compound also counters P-glycoprotein (P-gp)-mediated multidrug resistance in human MCF7/ADR cells, enhancing the cytotoxicity of adriamycin with a fold change of 10.0. It modulates the concentration of adriamycin needed for cytotoxic effect at various dosages, showing modulation factors of 2.33, 4.35, and 10.07 at 1 μM, 10 μM, and 25 μM, respectively. Moreover, β-Anhydroicaritin demonstrates cytotoxicity against MCF7/ADR cells with an IC50 greater than 100,000 nM and exhibits P-gp inhibitory effects in human Caco-2 cells by increasing influx permeability by 39.6% and decreasing efflux permeability by the same percentage at 50 μM after 120 minutes..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. β-Anhydroicaritin exhibits immunosuppressive effect on the mouse macrophages stimulated by LPS. 2. β-Anhydroicaritin phytosomes can inhibit enhanced bone turnover induced by ovariectomy, improve BMD the biomechanical properties of vertebrae, without any stimulation on uterus. 3. β-Anhydroicaritin possesses significant protective effects on the zymosan-induced peritonitis mice, which might be associated with the regulation of Ca(2+); influx in macrophages and iNOS expression.
SynonymsBeta-Anhydroicaritin, Anhydroicaritin
Chemical Properties
Molecular Weight368.38
FormulaC21H20O6
Cas No.38226-86-7
SmilesCOc1ccc(cc1)-c1oc2c3CCC(C)(C)Oc3cc(O)c2c(=O)c1O
Relative Density.1.349 g/cm3
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 3.69 mg/mL (10.02 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7146 mL13.5729 mL27.1459 mL135.7294 mL
5 mM0.5429 mL2.7146 mL5.4292 mL27.1459 mL
10 mM0.2715 mL1.3573 mL2.7146 mL13.5729 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
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.
1 Enter information below:
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2 Enter the in vivo formulation:
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