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Hu7691 free base
Cat. No.:
OB0225WX-1637
Appearance:
Solid
Purity:
≥98%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
Hu7691 free base is a potent, orally active Akt inhibitor that targets all three isoforms (Akt1, 2, and 3) to induce cellular differentiation and arrest proliferation.
Synonym:
Hu7691 (free base); 2241232-43-7; GTPL12722; Hu-7691; N-((3s,4s)-4-(3,4-difluorophenyl) piperidin-3-yl)-2-fluoro-4-(1-methyl-1h-pyrazol-5-yl)benzamide; N-[(3S,4S)-4-(3,4-difluorophenyl)piperidin-3-yl]-2-fluoro-4-(2-methylpyrazol-3-yl)benzamide
CAS No.:
2241232-43-7
Compound CID:
135274950
Formula:
C22H21F3N4
Formula Weight:
414.423
Specification
Targets&IC50:
Akt2: 97.5 nM (IC50); PKA: 11 nM; AKT1: 4.0 nM; mTOR (p70S6K): 229 nM; AKT3: 28 nM; RSK1: 756 nM (IC50); RSK1: 756 nM; AKT2: 97.5 nM; Akt1: 4.0 nM (IC50); Akt3: 28 nM (IC50); PKCη: 629 nM (IC50); PKCη: 629 nM; PKA: 11 nM (IC50); ROCK1: 354 nM; p70 S6K: 229 nM (IC50); ROCK1: 354 nM (IC50)
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Hu7691 free base is employed in medicinal chemistry research as a potent kinase inhibitor to study its pharmacodynamic profile and efficacy within the Akt signaling axis.
Library Information
Target:
Akt
Receptor:
Akt
Pathways:
Cytoskeletal signaling; PI3K/Akt/mTOR signaling
Plate Number:
AOCL-22
Plate Location:
a2
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO





