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LGD-2941

(Synonyms: LGD2941, LGD 2941) Copy Product Info
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Synonyms: LGD2941, LGD 2941

Catalog No. T27826 Copy Product Info
Purity: 99.90%
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LGD-2941 is a non-steroidal selective androgen receptor modulator (SARM) that selectively agonizes the androgen receptor to exert anabolic effects and is used in endocrine-related research on hypogonadism and osteoporosis.
LGD-2941
Cas No. 847235-85-2
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$413-In Stock
5 mg$982-In Stock
10 mg$1,320-In Stock
25 mg$1,970-In Stock
50 mg$2,580-In Stock
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:99.90%
Appearance:Solid
Color:Yellow
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Product Information

Bioactivity
Description
LGD-2941 is a non-steroidal selective androgen receptor modulator (SARM) that selectively agonizes the androgen receptor to exert anabolic effects and is used in endocrine-related research on hypogonadism and osteoporosis.
In vivo
Method: Twenty-four male cynomolgus monkeys were divided into four groups of six and treated for 90 days; the LGD-2941 group received 1 mg/kg daily. Whole-blood samples collected before treatment and on days 16 and 90 were analyzed for 37 candidate genes by qRT-PCR.
Result: LGD-2941 significantly altered six of the 37 genes, including CD30L, Fas, TNFR1, TNFR2, IL-12B and IL-15, indicating a measurable androgen-receptor-ligand gene-expression signature in whole blood.[1]
SynonymsLGD2941, LGD 2941
Chemical Properties
Molecular Weight394.31
FormulaC17H16F6N2O2
Cas No.847235-85-2
Smiles[C@@H](C(F)(F)F)(O)[C@@]1(N([C@H](C)CC1)C=2C=C3C(=CC2)NC(=O)C=C3C(F)(F)F)[H]
Relative Density.1.422 g/cm3 (Predicted)
Storage & Solubility Information
StorageKeep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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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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2 Enter the in vivo formulation:
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%
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Keywords

Related Tags: LGD-2941 chemical structure | LGD-2941 in vivo | LGD-2941 formula | LGD-2941 molecular weight