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BI-69A11

Chemical Structure : BI-69A11

CAS No.: 1233322-09-2

BI-69A11 (BI 69A11)

Catalog No.: PC-70086Not For Human Use, Lab Use Only.

BI-69A11 is a potent, selective, ATP competitive AKT inhibitor with IC50 of 2.3 uM for Akt1.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    BI-69A11 is a potent, selective, ATP competitive AKT inhibitor with IC50 of 2.3 uM for Akt1.
    BI-69A11 displays no activity for other protein kinases including Abl1, p38α, JNK, and PI3K (IC50>100 uM).
    BI-69A11 causes partial inhibition of AKT phosphorylation on S473 on melanoma cells at 3 uM.
    BI-69A11 reduces AKT protein expression and AKT association with HSP-90.|
    BI-69A11 caused effective regression of melanoma tumor xenografts.

    Physicochemical Properties

    M.Wt 425.872
    Formula C25H16ClN3O2
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20 °C 12 Months; 4°C 6 Months
    In Solvent
    -80 °C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    (E)-3-(3-(1H-benzo[d]imidazol-2-yl)acryloyl)-6-chloro-4-phenylquinolin-2(1H)-one(E)-3-(3-(1H-benzo[d]imidazol-2-yl)acryloyl)-6-chloro-4-phenylquinolin-2(1H)-one

    References

    1. Gaitonde S, et al. Pigment Cell Melanoma Res. 2009 Apr;22(2):187-95.

    2. Feng Y, et al. Pigment Cell Melanoma Res. 2013 Jan;26(1):136-42.

    3. Pal I, et al. Br J Cancer. 2014 Jul 8;111(1):101-11.

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