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Afuresertib hydrochloride
Cat. No.:
0225LY-1090
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and LC-MS.
Size:
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Product Overview
Description:
Afuresertib hydrochloride is a potent Akt kinase inhibitor with Kis of 0.08 nM, 2 nM, and 2.6 nM for Akt1, Akt2, and Akt3.
Synonym:
1047645-82-8; Afuresertib (hydrochloride); 2-Thiophenecarboxamide, N-((1S)-2-amino-1-((3-fluorophenyl)methyl)ethyl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-, hydrochloride (1:1); N-((S)-1-Amino-3-(3-fluorophenyl)propan-2-yl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxamide hydrochloride; N-[(2S)-1-amino-3-(3-fluorophenyl)propan-2-yl]-5-chloro-4-(4-chloro-2-methylpyrazol-3-yl)thiophene-2-carboxamide;hydrochloride
CAS No.:
1047645-82-8
Compound CID:
46843056
Formula:
C18H18Cl3FN4OS
Formula Weight:
463.8
Specification
Targets&IC50:
Akt3: 2.6 nM(Ki); Akt2: 2 nM(Ki); Akt1: 0.08 nM(Ki)
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Afuresertib hydrochloride can be used in clinical oncology research to investigate the potent inhibition of AKT isoforms in solid tumors.
Library Information
Target:
ROCK; Akt; PKC
Receptor:
ROCK; Akt; PKC
Pathways:
Stem cell regulation; Cell cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal signaling; PI3K/Akt/mTOR signaling
Plate Number:
AOCL-15
Plate Location:
a6
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
100 mg/mL; 215.61 mM





