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G0507

(Synonyms: G 0507, 5-(4-methoxyphenyl)-6-(5-methyl-2-thienyl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione) Copy Product Info
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Synonyms: G 0507, 5-(4-methoxyphenyl)-6-(5-methyl-2-thienyl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione

Catalog No. T11343 Copy Product Info
Purity: 98.98%
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G0507 (5-(4-methoxyphenyl)-6-(5-methyl-2-thienyl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione) is a pyrrolopyrimidinedione compound that effectively inhibits the LolCDE ABC transporter. It suppresses the growth of Escherichia coli and induces the extracytoplasmic σE stress response. G0507 is commonly used as a chemical probe to study lipoprotein transport in Gram-negative bacteria.
G0507
Cas No. 1223998-29-5
Pack SizePriceUSA StockGlobal StockQuantity
5 mg$4976-8 weeks6-8 weeks
25 mg$1,2706-8 weeks6-8 weeks
50 mg$1,6506-8 weeks6-8 weeks
100 mg$2,5006-8 weeks6-8 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:98.98%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
G0507 (5-(4-methoxyphenyl)-6-(5-methyl-2-thienyl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione) is a pyrrolopyrimidinedione compound that effectively inhibits the LolCDE ABC transporter. It suppresses the growth of Escherichia coli and induces the extracytoplasmic σE stress response. G0507 is commonly used as a chemical probe to study lipoprotein transport in Gram-negative bacteria.
In vitro
Method: E. coli imp4213 strain was treated with G0507 (4× MIC, i.e., 4 μg/ml) for 2 hours. Morphological changes were observed by fluorescence microscopy. Localization of Lpp was analyzed by sucrose density gradient centrifugation combined with Western blot. Processing status of Lpp was assessed by SDS-PAGE and LC-MS.
Result: G0507 caused swelling of the periplasmic space at the bacterial poles. Lpp abnormally accumulated in the inner membrane. The accumulated Lpp was fully processed. The MIC values of G0507 against imp4213 and ΔtolC strains were 1 μg/ml and 0.5 μg/ml, respectively, while it showed no activity against wild-type MG1655 (>64 μg/ml)[1].
SynonymsG 0507, 5-(4-methoxyphenyl)-6-(5-methyl-2-thienyl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione
Chemical Properties
Molecular Weight353.40
FormulaC18H15N3O3S
Cas No.1223998-29-5
SmilesO=C1NC(=O)C2=C(N1)NC(C=3SC(=CC3)C)=C2C=4C=CC(OC)=CC4
Relative Density.1.359 g/cm3 (Predicted)
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: 5.00 mg/mL (14.15 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8297 mL14.1483 mL28.2965 mL141.4827 mL
5 mM0.5659 mL2.8297 mL5.6593 mL28.2965 mL
10 mM0.2830 mL1.4148 mL2.8297 mL14.1483 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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g
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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Keywords

Related Tags: G0507 chemical structure | G0507 in vitro | G0507 formula | G0507 molecular weight