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MM41

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Catalog No. T60028Cas No. 1429028-96-5

MM41 is a human telomeric and gene promoter DNA quadruplex stabilizer with an IC50 of <10 nM against the MIA PaCa-2 pancreatic cancer cell line.

MM41

MM41

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Purity: 99.25%
Catalog No. T60028Cas No. 1429028-96-5
MM41 is a human telomeric and gene promoter DNA quadruplex stabilizer with an IC50 of <10 nM against the MIA PaCa-2 pancreatic cancer cell line.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$48-In Stock
5 mg$118-In Stock
10 mg$188-In Stock
25 mg$308-In Stock
50 mg$413-In Stock
100 mg$548-In Stock
200 mg$749-In Stock
1 mL x 10 mM (in DMSO)$163-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.25%
Appearance:Solid
Color:Blue
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Product Introduction

MM41 AI Summary
MM41 induces senescence in human MIAPaCa2 cells and modulates gene expression by downregulating SLX4, RASSF1, and PTEGES3, while upregulating PRKCB, PPARG, NHP2, and MYC genes. It exhibits cytotoxicity against various human cell lines such as PANC1, MIAPaCa2, MCF7, and A549, with varying IC50 values from 3.0 nM to 230.0 nM. Specifically, it has an IC50 value of 3.0 nM after 96 hours in human PANC1 cells, as determined by the SRB assay. In vivo studies show that the compound demonstrates antitumor activity against MIAPaCa2 xenografts in CD-1 nude mice, achieving significant reductions in tumor volume when administered at 15 mg/kg intravenously twice weekly for 4 weeks, though toxicity emerges at a maximum tolerated dose of 25.0 mg/kg. Additionally, MM41 selectively binds to various G-quadruplex RNA and DNA structures, including the human telomeric G-quadruplex and TERT hairpin duplex DNA, exhibiting binding affinities with dissociation equilibrium constants ranging from 2.0 nM to 10.0 nM. It stabilizes the promoter sequences of HSP90a and HSP90b, as well as the human telomeric G-quadruplex, indicated by significant changes in melting temperatures. These stabilizing effects vary, causing melting temperature increases from 4.9°C to 33.1°C for different DNA structures, and a reduced melting temperature change of less than 2.0°C for TERT hairpin duplex DNA. Such properties suggest its broad potential in cancer therapy, providing differential cytotoxic and binding activities that could be leveraged against diverse cell lines and DNA structures..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
MM41 is a human telomeric and gene promoter DNA quadruplex stabilizer with an IC50 of <10 nM against the MIA PaCa-2 pancreatic cancer cell line.
Chemical Properties
Molecular Weight831.06
FormulaC44H66N10O6
Cas No.1429028-96-5
SmilesCN1CCN(CCCNc2cc3c4c(c(NCCCN5CCN(C)CC5)cc5c4c2c(=O)n(CCCN2CCOCC2)c5=O)c(=O)n(CCCN2CCOCC2)c3=O)CC1
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: 30 mg/mL (36.1 mM), when pH is adjusted to 8 with HCl. Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.2033 mL6.0164 mL12.0328 mL60.1641 mL
5 mM0.2407 mL1.2033 mL2.4066 mL12.0328 mL
10 mM0.1203 mL0.6016 mL1.2033 mL6.0164 mL
20 mM0.0602 mL0.3008 mL0.6016 mL3.0082 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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2 Enter the in vivo formulation:
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