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Malotilate

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Catalog No. T6576Cas No. 59937-28-9
Alias NKK 105, Malotilatum, Kantec

Malotilate (Kantec) is a medicine used for the therapy of liver cirrhosis.

Malotilate

Malotilate

Copy Product Info
🥰Excellent
Purity: 99.80%
Catalog No. T6576Alias NKK 105, Malotilatum, KantecCas No. 59937-28-9
Malotilate (Kantec) is a medicine used for the therapy of liver cirrhosis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$31In StockIn Stock
25 mg$48In StockIn Stock
50 mg$68In StockIn Stock
100 mg$98In StockIn Stock
500 mg$238In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn 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:99.80%
Appearance:Solid
Color:White
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Product Introduction

Malotilate AI Summary
Malotilate exhibits a diverse range of bioactivities across multiple assays and biological targets. It acts as a potent inhibitor of human tyrosyl-DNA phosphodiesterase 1, with inhibition potencies ranging from 18.37 to 56.234 nM. Furthermore, it shows significant efficacy against Plasmodium falciparum strains (3D7 and DD2), with potencies as low as 0.7 nM. In anti-Ebola virus screens, it demonstrates moderate to strong inhibitory effects, with AC50 values between 14.13 µM and 44.67 µM. Regarding SARS-CoV-2, Malotilate inhibits cell viability in Vero E6 cells infected with the virus (strain BavPat1) at a low MOI (0.002) with an inhibition index of 0.2262 after 72 hours. It also inhibits SARS-CoV-2 3CL-Pro protease activity by 23.6% at a 20 µM concentration and reduces SARS-CoV-2-induced cytotoxicity in Vero E6 cells by 0.28% at 10 µM after 48 hours. Additionally, Malotilate shows moderate binding affinity and bioactivity in various in vitro assays, notably displaying moderate inhibition with an AC50 value of 15000.0 nM in the assay targeting rat Gabra1. However, it generally exhibits binding affinities with AC50 values greater than 30000.0 nM across multiple assays for different biological targets..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Malotilate (Kantec) is a medicine used for the therapy of liver cirrhosis.
Targets&IC50
5-LOX:4.7 μM (IC50)
In vitro
Malotilate caused a significant decrease in the invasion of C-SST-2 cells in RLE monolayers.Malotilate inhibited the increased permeability of RLE monolayers by serum starvation. By enhancing the intercellular contact of endothelial cells, Malotilate prevented the invasion of tumor cells into the vascular endothelium and inhibited tumor metastasis. In multilayer cultures, Malotilate (0.1-100 μM) concentration-dependently increased collagenase activity but did not affect monolayer cells. In damaged multilayer cultures, Malotilate increased MMP-1 and MMP-3 secretion, also without affecting monolayer cells.
In vivo
Malotilate caused a significant decrease in the invasion of C-SST-2 cells in RLE monolayers.Malotilate inhibited the increased permeability of RLE monolayers by serum starvation. By enhancing the intercellular contact of endothelial cells, Malotilate prevented the invasion of tumor cells into the vascular endothelium and inhibited tumor metastasis. In multilayer cultures, Malotilate (0.1-100 μM) concentration-dependently increased collagenase activity but did not affect monolayer cells. In damaged multilayer cultures, Malotilate increased MMP-1 and MMP-3 secretion, also without affecting monolayer cells.
SynonymsNKK 105, Malotilatum, Kantec
Chemical Properties
Molecular Weight288.38
FormulaC12H16O4S2
Cas No.59937-28-9
SmilesC(C(OC(C)C)=O)(C(OC(C)C)=O)=C1SC=CS1
Relative Density.1.3727 g/cm3 (Estimated)
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
Ethanol: 58 mg/mL (201.12 mM), Sonication is recommended.
DMSO: 55 mg/mL (190.72 mM), Sonication is recommended.
H2O: < 1 mg/mL (insoluble or slightly soluble)
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.94 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO/Ethanol
1mg5mg10mg50mg
1 mM3.4676 mL17.3382 mL34.6765 mL173.3823 mL
5 mM0.6935 mL3.4676 mL6.9353 mL34.6765 mL
10 mM0.3468 mL1.7338 mL3.4676 mL17.3382 mL
20 mM0.1734 mL0.8669 mL1.7338 mL8.6691 mL
50 mM0.0694 mL0.3468 mL0.6935 mL3.4676 mL
100 mM0.0347 mL0.1734 mL0.3468 mL1.7338 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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