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S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺

Andarine

CAS:

Molecular Formula: C19H18F3N3O6

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S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺 - Names and Identifiers

Name Andarine
Synonyms GTX007
CS-418
GTX 007
Andarine
(1132656-73-5) ostarine
Andarine(S4),whnohe_lucy(at)163.com
Andarine(S4) whnohe_caroline(at)163.com
S-3-(4-acetylamino-phenoxy)-2-hydroxy-2-methyl-N-(4-nitro-3-trifluoromethyl-phenyl)-propionamide
N-[4-Nitro-3-(trifluoromethyl)phenyl]-(2S)-3-[4-(acetylamino)phenoxy]-2-hydroxy-2-methylpropanamide
EINECS 803-892-7
InChIKey YVXVTLGIDOACBJ-SFHVURJKSA-N

S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺 - Physico-chemical Properties

Molecular FormulaC19H18F3N3O6
Molar Mass441.36
Density1.47
Melting Point70-74℃
Boling Point698.7±55.0 °C(Predicted)
Water Solubility1.2 mg/mL in water
Solubility DMSO (Slightly), Methanol (Slightly)
Appearanceneat
ColorLight Yellow
BRN9666695
pKa12.13±0.29(Predicted)
Storage ConditionRefrigerator
In vitro studyIn Vitro, Andarine binds with high affinity to the androgen receptor with a K I of 4 nM. Moreover, 10 nM Andarine stimulated androgen receptor-regulated transcription by 93%.
In vivo studyIn Vivo, Andarine has potent anabolic activity and stimulates the growth of prostate, seminal vesicle, and levator ani muscle with ED50 of 0.43 mg/day and 0.55 mg/day, respectively, and 0.14 mg/day, the effect was dose-dependent. In addition, Andarine acted on FSH, did not affect some physiological changes caused by castration, and treated with 0.5 mg or more per day, partially inhibited LH production. Intravenous administration of 0.1, 1, 3, and 10 mg/kg Andarine to dogs, total body clearance (CL) from 7.4 mL/min/kg to 3.1 mL/min/kg, the steady state volume of distribution (Vss) is 1.39 L/kg, and the Half-Life is 229 minutes. In addition, the oral bioavailability of Andarine at doses of 10 mg/kg, 1 mg/kg, and 0.1 mg/kg was 38%, 62%, and 91%, respectively. Andarine has tissue-selective pharmacological activity and treatment of intact rats at a concentration of 0.5 mg/day significantly reduced prostate weight to 79.4%.

S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36 - Irritating to the eyes
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3

S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺 - Reference Information

biological activity Andarine is a selective non-steroidal androgen receptor (AR)(androgen receptor) agonist with Ki of 4 nM and tissue selectivity for anabolic organs. Phase 3.
Andarine (GTx-007, S-4) is a selective non-steroidal androgen receptor (AR)(androgen receptor) agonist with Ki of 4 nM and tissue selectivity for anabolic organs. Phase 3.
features Andarine are non-steroid androgen receptor (AR) selective stimulants.
TargetValue
Androgen Receptor 4 nM(Ki)
Last Update:2024-04-09 19:05:07
S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺
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S-3-(4-乙酰氨基苯氧基)-2-羟基-2-甲基-N-(4-硝基-3-三氟甲基苯基)丙酰胺
2-氨基-4-碘苯酚
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C.I.15530
(2-(4-((4-氟苄基)氨基甲酰基)-5-羟基-6-氧代-1,6-二氢嘧啶-2-基)丙-2-基)氨基甲酸叔丁酯
2-(4-甲基-1-哌嗪基)-5-硝基吡啶
全氟(4-甲基-2-戊烯酸)
2-乙氧基-6-{[((丙-2-基)氨基]甲基}苯酚
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