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Gut restricted-7

(Synonyms: GR-7) Copy Product Info
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Synonyms: GR-7

Catalog No. T11515 Copy Product Info
Purity: 99.27%
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Gut restricted-7 (GR-7) is a potent, covalent, orally administered, gut-selective bile salt hydrolase (BSH) inhibitor with tissue specificity that localizes to the gut. Gut restricted-7 reduces BSH activity in gut bacteria and decreases levels of unconjugated bile acids in mouse feces, making it suitable for research into metabolism, inflammation, and intestinal diseases.
Gut restricted-7
Cas No. 2553218-46-3
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$139In StockIn Stock
5 mg$332In StockIn Stock
10 mg$532In StockIn Stock
25 mg$863In StockIn Stock
50 mg$1,190-In Stock
1 mL x 10 mM (in DMSO)$373In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.27%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Gut restricted-7 (GR-7) is a potent, covalent, orally administered, gut-selective bile salt hydrolase (BSH) inhibitor with tissue specificity that localizes to the gut. Gut restricted-7 reduces BSH activity in gut bacteria and decreases levels of unconjugated bile acids in mouse feces, making it suitable for research into metabolism, inflammation, and intestinal diseases.
In vitro
Methods: Six human gut symbionts (3 Gram-negative: B. theta, B. fragilis, B. vulgatus; 3 Gram-positive: L. plantarum, C. perfringens, B. adolescentis). Pre-log phase bacteria were co-incubated with Gut restricted-7 (100 μM) and mixed bile acid substrate (100 μM), monitoring deglycolysis activity over 21 hours.
Results: Gut restricted-7 nearly completely inhibited bile acid deconjugation activity in all 6 strains. [1]
In vivo
Methods: Conventional mice were administered a single oral dose of Gut restricted-7 (10 mg/kg) or a solvent control. Feces were collected 30 hours after dosing, and BSH activity and bile acid composition were measured.
Results: Levels of unconjugated bile acids in feces decreased, while the proportion of conjugated bile acids increased, confirming in vivo target inhibition and alterations in the bile acid profile. [1]
SynonymsGR-7
Chemical Properties
Molecular Weight510.64
FormulaC25H40FNaO6S
Cas No.2553218-46-3
SmilesO[C@H]1[C@]2([H])[C@@](CC[C@]3([C@@]2([H])CC[C@]3([H])[C@H](C)CCC(CF)=O)C)([H])[C@@]4([C@](C[C@@H](CC4)OS(=O)([O-])=O)([H])C1)C.[Na+]
Relative Density.no data available
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: 250 mg/mL (489.58 mM), Sonication is recommended.
H2O: 100 mg/mL (195.83 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (9.79 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
H2O/DMSO
1mg5mg10mg50mg
1 mM1.9583 mL9.7916 mL19.5833 mL97.9163 mL
5 mM0.3917 mL1.9583 mL3.9167 mL19.5833 mL
10 mM0.1958 mL0.9792 mL1.9583 mL9.7916 mL
20 mM0.0979 mL0.4896 mL0.9792 mL4.8958 mL
50 mM0.0392 mL0.1958 mL0.3917 mL1.9583 mL
100 mM0.0196 mL0.0979 mL0.1958 mL0.9792 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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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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Keywords

Related Tags: Gut restricted-7 chemical structure | Gut restricted-7 in vivo | Gut restricted-7 in vitro | Gut restricted-7 formula | Gut restricted-7 molecular weight