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Ostarine

Catalog No. T2408   CAS 841205-47-8
Synonyms: MK-2866, GTX-024, Enobosarm

Ostarine (MK-2866) is a non-steroidal agent with anabolic activity. Selective androgen receptor modulator (SARM) GTx-024 is designed to work like testosterone, thus promoting and/or maintaining libido, fertility, prostate growth, and muscle growth and strength. Mimicking testosterone's action, this agent may increase lean body mass, thereby ameliorating muscle wasting in the hypermetabolic state of cancer cachexia.

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Ostarine Chemical Structure
Ostarine, CAS 841205-47-8
Pack Size Availability Price/USD Quantity
25 mg In stock $ 36.00
50 mg In stock $ 72.00
100 mg In stock $ 122.00
500 mg In stock $ 295.00
1 mL * 10 mM (in DMSO) In stock $ 30.00
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Purity: 99.9%
Purity: 99.35%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Ostarine (MK-2866) is a non-steroidal agent with anabolic activity. Selective androgen receptor modulator (SARM) GTx-024 is designed to work like testosterone, thus promoting and/or maintaining libido, fertility, prostate growth, and muscle growth and strength. Mimicking testosterone's action, this agent may increase lean body mass, thereby ameliorating muscle wasting in the hypermetabolic state of cancer cachexia.
Targets&IC50 Androgen receptor:3.8 nM(Ki)
In vitro Compared to any non-steroidal androgen receptor (AR) agonists, Ostarine exhibits the highest androgenic and anabolic activity in the body, particularly affecting the prostate, seminal vesicles, and levator ani muscle, with ED50 values of 0.12, 0.39, and 0.03 mg/day, respectively. This makes it four times more effective on the levator ani muscle than testosterone propionate. At a low dose of 0.03 mg/day, Ostarine demonstrates effective and selective activity in anabolic tissues. Following a single intravenous injection of 10 mg/kg, Ostarine presents a slow decline in plasma concentration with a longer half-life of 6 hours, compared to the 2.6-4.0 hours half-life when targeting other cyan/nitro substituted Selective Androgen Receptor Modulators (SARMs). In castrated male rats, Ostarine shows significant androgenic and anabolic activity, more effectively stimulating growth in the prostate, seminal vesicles, and levator ani muscle than other cyan/nitro substituted SARMs. Ostarine facilitated recovery of prostate weight by 39.2%, seminal vesicle weight by 78.8%, and notably stimulated levator ani muscle growth beyond other male organs to 141.9%.
In vivo Ostarine (10 nM) modulates the transcriptional activity of the androgen receptor (AR) in CV-1 cells co-transfected with human androgen receptor expression vectors, luciferase reporter vectors, and β-galactosidase control vectors. Ostarine binds to the androgen receptor with the highest affinity among selective androgen receptor modulators (SARMs), exhibiting a Ki value of 3.8 nM.
Synonyms MK-2866, GTX-024, Enobosarm
Molecular Weight 389.33
Formula C19H14F3N3O3
CAS No. 841205-47-8

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: 72 mg/mL (184.9 mM)

DMSO: 72 mg/mL (184.9 mM)

TargetMolReferences and Literature

1. Kim J, et al. J Pharmacol Exp Ther, 2005, 315(1), 230-239. 2. Duke CB, et al. J Med Chem, 2011, 54(11), 3973-3976.

Related compound libraries

This product is contained In the following compound libraries:
Fluorochemical Library

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Keywords

Ostarine 841205-47-8 Endocrinology/Hormones Androgen Receptor MK2866 MK-2866 GTX-024 GTX 024 Enobosarm GTX024 MK 2866 inhibitor inhibit

 

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