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PROT-IN-1

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Catalog No. T67938Cas No. 329935-45-7

PROT-IN-1 is a potent high-affinity inhibitor of L-proline transporter and a candidate compound for the treatment of neurological diseases.

PROT-IN-1

PROT-IN-1

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Purity: 98.55%
Catalog No. T67938Cas No. 329935-45-7
PROT-IN-1 is a potent high-affinity inhibitor of L-proline transporter and a candidate compound for the treatment of neurological diseases.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$33In StockIn Stock
10 mg$54In StockIn Stock
25 mg$92In StockIn Stock
50 mg$137In StockIn Stock
100 mg$203In StockIn Stock
500 mg$483-In Stock
1 mL x 10 mM (in DMSO)$39In 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:98.55%
Appearance:Solid
Color:White
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Product Introduction

PROT-IN-1 AI Summary
PROT-IN-1 displays multiple bioactivities. It is a potent modulator of miRNAs, particularly activating miR-21, and demonstrates significant inhibitory activity against Bacillus subtilis Sfp PPTase. Furthermore, it acts as an inhibitor targeting the Menin-MLL interaction in MLL-related leukemias and shows inhibitory effects on DNA Polymerase Beta. It also inhibits activity in the Nrf2 qHTS screen and re-activates p53 using a Luc reporter. In human embryonic kidney cells, it inhibits ELG1-dependent DNA repair. Additionally, it exhibits delayed death inhibition of the malarial parasite plastid, inhibits firefly luciferase, and induces DNA re-replication in SW480 colon adenocarcinoma cells. PROT-IN-1 also functions as a TDP-43 inhibitor, inhibits PTHR, and has been screened as a potential antiviral against the Foot and Mouth Disease Virus. Lastly, it inhibits the human high-affinity L-proline transporter expressed in COS1 cells, with an IC50 value of 1480.0 nM as determined through a [3H]proline uptake assay..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
PROT-IN-1 is a potent high-affinity inhibitor of L-proline transporter and a candidate compound for the treatment of neurological diseases.
Chemical Properties
Molecular Weight342.43
FormulaC23H22N2O
Cas No.329935-45-7
SmilesC(=O)(C1=CC=C(C=C1)C2=CC=CC=C2)N3CCN(CC3)C4=CC=CC=C4
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: 27.5 mg/mL (80.31 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9203 mL14.6015 mL29.2030 mL146.0152 mL
5 mM0.5841 mL2.9203 mL5.8406 mL29.2030 mL
10 mM0.2920 mL1.4602 mL2.9203 mL14.6015 mL
20 mM0.1460 mL0.7301 mL1.4602 mL7.3008 mL
50 mM0.0584 mL0.2920 mL0.5841 mL2.9203 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:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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