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Daphnoretin

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Catalog No. T4S1335Cas No. 2034-69-7
Alias Thymelol, Dephnoretin

1. Daphnoretin (Thymelol) has strong antiviral activity, mainly on the later phase of the replication cycle. 2. Daphnoretin has anticancer effects on leukemia, osteosarcoma and uterine cervix cancer cells, might through promoting apoptosis in a mitochondria-mediated way. 3. Daphnoretin causes death of HOS cells by blocking cells successively in G2/M phases and activating the caspase-3 pathway.

Daphnoretin

Daphnoretin

Copy Product Info
🥰Excellent
Purity: 99.85%
Catalog No. T4S1335Alias Thymelol, DephnoretinCas No. 2034-69-7
1. Daphnoretin (Thymelol) has strong antiviral activity, mainly on the later phase of the replication cycle. 2. Daphnoretin has anticancer effects on leukemia, osteosarcoma and uterine cervix cancer cells, might through promoting apoptosis in a mitochondria-mediated way. 3. Daphnoretin causes death of HOS cells by blocking cells successively in G2/M phases and activating the caspase-3 pathway.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$50In StockIn Stock
10 mg$70In StockIn Stock
25 mg$113In StockIn Stock
50 mg$163In StockIn Stock
100 mg$239In StockIn Stock
1 mL x 10 mM (in DMSO)$48In 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:99.85%
Color:White
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Product Introduction

Daphnoretin AI Summary
Daphnoretin demonstrates significant bioactivity across various biological targets and assays. It inhibits the growth of mouse EAC cells xenografted in CF1 mice at a dose of 3 mg/kg/day intraperitoneally, achieving an impressive inhibition rate of 97.0%. The compound also shows cytotoxicity against mouse P388 cells with effective doses (ED50) of 2.2 µg/mL and 3.4 µg/mL. Additionally, it inhibits rat DNA polymerase beta lyase activity with an IC50 value of 122300 nM after 30 minutes. Daphnoretin targets multiple enzymes and proteins, including hydroxysteroid dehydrogenase 4 (HSD17B4) with a potency of 31622.8 nM, and human Jumonji Domain Containing 2E (JMJD2E) with potencies of 35481.3 nM and 25118.9 nM. It inhibits Tyrosyl-DNA Phosphodiesterase (TDP1) at 35481.3 nM, Aldehyde Dehydrogenase 1 (ALDH1A1) at 25118.9 nM and 17782.8 nM, and Tau fibril formation at 44668.4 nM. The compound also shows inhibitory activity against Anthrax Lethal Toxin Internalization (12589.3 nM), 15-Hydroxyprostaglandin Dehydrogenase (HPGD) at 35481.3 nM, and DNA Polymerase Beta at 44668.4 nM. Furthermore, Daphnoretin acts as an activator and substrate of Cytochrome P450 3A4 with a potency of 501.2 nM, and modulates lipid storage at 35481.3 nM. It inhibits the Rango-Importin beta complex (35481.3 nM), polymerases Iota (63095.7 nM) and Kappa (354.8 nM), and the malarial parasite plastid (9285.0 nM). It induces DNA re-replication in MCF 10a normal breast cells at 20596.2 nM and inhibits Pin1 (79432.8 nM). Additionally, it acts as an agonist (79432.8 nM) and antagonist (50118.7 nM) of EPAC1, inhibits MBNL1-poly(CUG) RNA binding (6309.6 nM), and Human Apurinic/apyrimidinic Endonuclease 1 (APE1) at 44668.4 nM. In cellular models, Daphnoretin inhibits human Dipeptidyl Peptidase-4 (DPP4) with an IC50 of 87100.0 nM and induces cell cycle arrest in human MCF7 and MDA-MB-231 cells, with IC50 values of 2000.0 nM and 1000.0 nM, respectively, leading to accumulation of cells in G0-G1, S, and G2/M phases. It also exhibits inhibitory activity against porcine pancreas alpha-amylase and Saccharomyces cerevisiae alpha-glucosidase with IC50 values of 90.0 µg/mL and 86.0 µg/mL, respectively..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. Daphnoretin (Thymelol) has strong antiviral activity, mainly on the later phase of the replication cycle. 2. Daphnoretin has anticancer effects on leukemia, osteosarcoma and uterine cervix cancer cells, might through promoting apoptosis in a mitochondria-mediated way. 3. Daphnoretin causes death of HOS cells by blocking cells successively in G2/M phases and activating the caspase-3 pathway.
SynonymsThymelol, Dephnoretin
Chemical Properties
Molecular Weight352.29
FormulaC19H12O7
Cas No.2034-69-7
SmilesCOc1cc2cc(Oc3ccc4ccc(=O)oc4c3)c(=O)oc2cc1O
Relative Density.1.501g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 62.5 mg/mL (177.41 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8386 mL14.1929 mL28.3857 mL141.9285 mL
5 mM0.5677 mL2.8386 mL5.6771 mL28.3857 mL
10 mM0.2839 mL1.4193 mL2.8386 mL14.1929 mL
20 mM0.1419 mL0.7096 mL1.4193 mL7.0964 mL
50 mM0.0568 mL0.2839 mL0.5677 mL2.8386 mL
100 mM0.0284 mL0.1419 mL0.2839 mL1.4193 mL

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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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