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Ibutamoren (Synonyms: MK-677, MK677, MK 677, L-163191, L163191, L 163191)

Catalog No. T20095 Copy Product Info
Purity: 97.59%
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Ibutamoren (MK-677) is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It also alters the metabolism of body fat and so may have an application in the treatment of obesity.

Ibutamoren

Copy Product Info
😃Good
Catalog No. T20095
Synonyms MK-677, MK677, MK 677, L-163191, L163191, L 163191

Ibutamoren (MK-677) is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It also alters the metabolism of body fat and so may have an application in the treatment of obesity.

Ibutamoren
Cas No. 159634-47-6
Pack SizePriceUSA StockGlobal StockQuantity
1 mL x 10 mM (in DMSO)$50In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:97.59%
Appearance:Solid
Color:White
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Product Introduction

Ibutamoren AI Summary
Ibutamoren exhibits potent bioactivity related to growth hormone secretion and strong binding affinity to growth hormone secretagogue receptors. In vitro assays demonstrate an EC50 value of 1.3 nM for stimulating growth hormone release from rat pituitary cells, and the compound shows high binding affinity to the human Growth Hormone Secretagogue Receptor type 1, with IC50 values ranging from 0.4 to 0.63 nM. Additionally, the compound displays competitive antagonistic activity against ghrelin and significant agonist activity, achieving up to 90% of the response of the reference compound, GHRP-6. In vivo studies confirm its bioactivity, with a low ED50 value of 0.084 µmol/kg for stimulating growth hormone release in pigs. Furthermore, Ibutamoren exhibits multi-faceted bioactivity, including a moderate binding affinity in different assays and moderate plasma protein binding across species. It has also shown some level of antiviral activity against SARS-CoV-2 and inhibitory activity against the human HDAC6 enzyme. Overall, Ibutamoren demonstrates significant potential in modulating growth hormone pathways and other biological activities..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Ibutamoren (MK-677) is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It also alters the metabolism of body fat and so may have an application in the treatment of obesity.
SynonymsMK-677, MK677, MK 677, L-163191, L163191, L 163191
Chemical Properties
Molecular Weight528.66
FormulaC27H36N4O5S
Cas No.159634-47-6
SmilesS(C)(=O)(=O)N1CC2(C=3C1=CC=CC3)CCN(C([C@@H](COCC4=CC=CC=C4)NC(C(C)(C)N)=O)=O)CC2
Relative Density.1.32g/cm3
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 (52.02 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8916 mL9.4579 mL18.9157 mL94.5787 mL
5 mM0.3783 mL1.8916 mL3.7831 mL18.9157 mL
10 mM0.1892 mL0.9458 mL1.8916 mL9.4579 mL
20 mM0.0946 mL0.4729 mL0.9458 mL4.7289 mL
50 mM0.0378 mL0.1892 mL0.3783 mL1.8916 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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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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