CCT128930

CAS No. 885499-61-6

CCT128930 ( CCT 128930;CCT-128930 )

Catalog No. M16409 CAS No. 885499-61-6

CCT128930 is a potent, selective, ATP-competitive AKT inhibitor with IC50 of 6 nM (AKT2).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 59 In Stock
5MG 104 In Stock
10MG 188 In Stock
25MG 368 In Stock
50MG 536 In Stock
100MG 779 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CCT128930
  • Note
    Research use only, not for human use.
  • Brief Description
    CCT128930 is a potent, selective, ATP-competitive AKT inhibitor with IC50 of 6 nM (AKT2).
  • Description
    CCT128930 is a potent, selective, ATP-competitive AKT inhibitor with IC50 of 6 nM (AKT2), 28-fold selectivity over the closely related PKA; also exhibits 20-fold selectivity over p70S6K (IC50=120 nM); shows growth inhibition for U87MG human glioblastoma cells (IC50=6.3 uM), for LNCaP human prostate cancer cells (IC50=0.35 uM), and for PC3 human prostate cancer cells (IC50=1.9 uM) consistent with AKT pathway blockade; blocks the phosphorylation of several downstream AKT biomarkers in U87MG tumor xenografts, indicating AKT inhibition in vivo; demonstrates antitumor activity in U87MG and HER2-positive, PIK3CA-mutant BT474 human breast cancer xenografts.
  • Synonyms
    CCT 128930;CCT-128930
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Akt
  • Recptor
    Akt2 , p70 S6K , PKA
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    885499-61-6
  • Formula Weight
    341.80
  • Molecular Formula
    C18H20ClN5
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    NC1(CC2=CC=C(Cl)C=C2)CCN(C3=C4C(NC=C4)=NC=N3)CC1
  • Chemical Name
    4-Piperidinamine, 4-[(4-chlorophenyl)methyl]-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Caldwell JJ, et al. J Med Chem. 2008 Apr 10;51(7):2147-57.
2. Yap TA, et al. Mol Cancer Ther. 2011 Feb;10(2):360-71.
3. Yap TA, et al. Clin Cancer Res. 2012 Jul 15;18(14):3912-23.
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