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O-Propargyl-Puromycin

(Synonyms: O-Propargylpuromycin, OP-puro) Copy Product Info
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Synonyms: O-Propargylpuromycin, OP-puro

Catalog No. T12284 Copy Product Info
Purity: 99.45%
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O-Propargyl-Puromycin ( OP-puro) is a natural product derivative and a protein synthesis inhibitor with cell permeability. It terminates translational elongation by incorporation into nascent peptide chains, and is widely used for nascent protein labeling and detection, enabling fluorescence imaging or affinity enrichment when combined with click chemistry.
O-Propargyl-Puromycin
Cas No. 1416561-90-4
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Pack SizePriceUSA StockGlobal StockQuantity
500 μg$46In StockIn Stock
1 mg$66In StockIn Stock
5 mg$158In StockIn Stock
10 mg$248In StockIn Stock
25 mg$397In StockIn Stock
50 mg$569In StockIn Stock
1 mL x 10 mM (in DMSO)$175In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.45%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
O-Propargyl-Puromycin ( OP-puro) is a natural product derivative and a protein synthesis inhibitor with cell permeability. It terminates translational elongation by incorporation into nascent peptide chains, and is widely used for nascent protein labeling and detection, enabling fluorescence imaging or affinity enrichment when combined with click chemistry.
In vitro
Methods: Reticulocyte lysates and 293T cells were treated with O-Propargyl-Puromycin (25 μM) for 1 hour, and protein synthesis inhibition was detected by SDS-PAGE and autoradiography. Nascent polypeptide labeling was assessed through copper-catalyzed click chemistry combined with affinity purification.
Results: O-Propargyl-Puromycin inhibited protein synthesis with an efficacy of 1/2 to 1/3 that of puromycin, covalently bound to nascent peptide chains, and was rapidly degraded by the proteasome, making it applicable for imaging of nascent proteins in cells and tissues. [1]
In vivo
Methods: Intraperitoneal injection of O-Propargyl-Puromycin (20 mM, 100 μL, dissolved in PBS) was administered to 3-week-old mice. Tissues were harvested and fixed 1 hour post-injection, followed by CuAAC staining with TMR-azide. PBS-injected mice served as controls.
Results: Strong staining was observed in the small intestinal crypts and Paneth cells of injected mice, with distinct labeling of secretory granules, confirming that O-Propargyl-Puromycin can specifically label nascent proteins in vivo. [1]
SynonymsO-Propargylpuromycin, OP-puro
Chemical Properties
Molecular Weight495.53
FormulaC24H29N7O5
Cas No.1416561-90-4
SmilesCN(C)c1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](NC(=O)[C@@H](N)Cc2ccc(OCC#C)cc2)[C@H]1O
Relative Density.1.44 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: 257.5 mg/mL (519.65 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (10.09 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
1mg5mg10mg50mg
1 mM2.0180 mL10.0902 mL20.1804 mL100.9021 mL
5 mM0.4036 mL2.0180 mL4.0361 mL20.1804 mL
10 mM0.2018 mL1.0090 mL2.0180 mL10.0902 mL
20 mM0.1009 mL0.5045 mL1.0090 mL5.0451 mL
50 mM0.0404 mL0.2018 mL0.4036 mL2.0180 mL
100 mM0.0202 mL0.1009 mL0.2018 mL1.0090 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: O-Propargyl-Puromycin chemical structure | O-Propargyl-Puromycin in vivo | O-Propargyl-Puromycin in vitro | O-Propargyl-Puromycin formula | O-Propargyl-Puromycin molecular weight