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Thiolutin

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Catalog No. T67708Cas No. 87-11-6
Alias Acetopyrrothin

Thiolutin (Acetopyrrothin) is an inhibitor of endothelial cell adhesion and produced by Streptomyces. Thiolutin shows antibiotic and anti-angiogenic properties. Thiolutin induces the phosphorylation of Hsp27 rapidly.

Thiolutin

Thiolutin

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Purity: 99.93%
Catalog No. T67708Alias AcetopyrrothinCas No. 87-11-6
Thiolutin (Acetopyrrothin) is an inhibitor of endothelial cell adhesion and produced by Streptomyces. Thiolutin shows antibiotic and anti-angiogenic properties. Thiolutin induces the phosphorylation of Hsp27 rapidly.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$122In StockIn Stock
5 mg$297In StockIn Stock
10 mg$488In StockIn Stock
25 mg$958In StockIn Stock
50 mg$1,330-In Stock
100 mg$1,790-In Stock
1 mL x 10 mM (in DMSO)$336In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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:99.93%
Appearance:Solid
Color:Yellow
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Product Introduction

Thiolutin AI Summary
Thiolutin exhibits broad-spectrum bioactivity, including significant antimicrobial and antifungal effects. It demonstrates antimicrobial activity against Staphylococcus epidermidis with a MIC of 6.25 µg/mL and an MBC of 12.5 µg/mL, indicating a moderate bactericidal effect with an MBC/MIC ratio of 2.0. Additionally, it shows RNA polymerase-mediated transcription inhibition in Staphylococcus epidermidis with an IC50 greater than 100.0 µg/mL. In antifungal assays, Thiolutin reveals specific efficacy against yeast strains expressing Candida albicans CaMdr1p with a 7.0 mm inhibition zone, while showing no inhibition against CaCdr1p. Beyond these, Thiolutin is effective across a variety of bioactivities such as inducing the erasure of genomic imprints, inhibiting tau fibril formation, inhibiting ROR gamma transcriptional activity, inhibiting the phosphopantetheinyl transferase Sfp in Bacillus subtilis, and disrupting the CBF-beta and RUNX1 interaction for treating Acute Myeloid Leukemia. Moreover, it demonstrates growth inhibition against diverse human tumor cell lines originating from renal, breast, lung, leukemia, prostate, melanoma, ovarian, and central nervous system tissues..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Thiolutin (Acetopyrrothin) is an inhibitor of endothelial cell adhesion and produced by Streptomyces. Thiolutin shows antibiotic and anti-angiogenic properties. Thiolutin induces the phosphorylation of Hsp27 rapidly.
SynonymsAcetopyrrothin
Chemical Properties
Molecular Weight228.29
FormulaC8H8N2O2S2
Cas No.87-11-6
SmilesCC(=O)Nc1c2sscc2n(C)c1=O
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: 4.5 mg/mL (19.71 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.3804 mL21.9020 mL43.8039 mL219.0197 mL
5 mM0.8761 mL4.3804 mL8.7608 mL43.8039 mL
10 mM0.4380 mL2.1902 mL4.3804 mL21.9020 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

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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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