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Afuresertib
Cat. No.:
0225LY-1091
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and LC-MS.
Size:
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Product Overview
Description:
Afuresertib is an orally active inhibitor of Akt (protein kinase B) currently being studied for its antineoplastic potential.
Synonym:
GSK2110183C; GSK2110183; 1047644-62-1; GSK-2110183; GSK2110183C; N-[(2S)-1-amino-3-(3-fluorophenyl)propan-2-yl]-5-chloro-4-(4-chloro-2-methylpyrazol-3-yl)thiophene-2-carboxamide; 2-Thiophenecarboxamide, N-((1S)-2-amino-1-((3-fluorophenyl)methyl)ethyl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)-; N-((1S)-1-(aminomethyl)-2-(3-fluorophenyl)ethyl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxamide; N-((S)-1-amino-3-(3-fluorophenyl)propan-2-yl)-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxamide; N-[(2S)-1-amino-3-(3-fluorophenyl)propan-2-yl]-5-chloro-4-(4-chloro-1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxamide; afuresertibum
CAS No.:
1047644-62-1
Compound CID:
46843057
Formula:
C18H17Cl2FN4OS
Formula Weight:
427.32
Specification
Targets&IC50:
Akt3: 2.6 nM(Ki); Akt1: 0.08 nM(Ki); Akt2: 2 nM(Ki)
Relative Density:
1.49 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Afuresertib can be used in drug screening assays to evaluate the therapeutic potential of targeting the AKT pathway in resistant cancers.
Library Information
Target:
ROCK; Akt; PKC
Receptor:
Akt1; Akt2; Akt3; PKC; ROCK
Pathways:
Stem cell regulation; Cytoskeletal signaling; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Cell cycle/Checkpoint
Plate Number:
AOCL-15
Plate Location:
a7
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
250 mg/mL; 585.04 mM
Ethanol Max Solubility:
79 mg/mL; 184.87 mM
ALogP:
3.884
HBA_Count:
2
HBD_Count:
2
Rotatable Bond:
6





