1233322-09-2

1233322-09-2 structure

Name: BI-69A11
Chemical Name: 3-[(2E)-3-(1H-Benzimidazol-2-yl)-2-propenoyl]-6-chloro-4-phenyl-2(1H)-quinolinone
CAS Number: 1233322-09-2
Molecular Formula: C₂₅H₁₆ClN₃O₂
Molecular Weight: 425.866
Create Date: 2020-01-11 20:29:49
Modify Date: 2025-08-25 11:37:15
A potent, selective, ATP competitive AKT inhibitor with IC50 of 2.3 uM for Akt1; displays no activity for other protein kinases including Abl1, p38α, JNK, and PI3K (IC50>100 uM); causes partial inhibition of AKT phosphorylation on S473 on melanoma cells at 3 uM; reduces AKT protein expression and AKT association with HSP-90; caused effective regression of melanoma tumor xenografts.

Name	3-[(2E)-3-(1H-Benzimidazol-2-yl)-2-propenoyl]-6-chloro-4-phenyl-2(1H)-quinolinone
Synonyms	3-[(2E)-3-(1H-Benzimidazol-2-yl)-2-propenoyl]-6-chloro-4-phenyl-2(1H)-quinolinone 2(1H)-Quinolinone, 3-[(2E)-3-(1H-benzimidazol-2-yl)-1-oxo-2-propen-1-yl]-6-chloro-4-phenyl- MFCD00186600 (2E)-3-(1H-benzimidazol-2-yl)-1-(6-chloro-2-hydroxy-4-phenylquinolin-3-yl)prop-2-en-1-one

Description	A potent, selective, ATP competitive AKT inhibitor with IC50 of 2.3 uM for Akt1; displays no activity for other protein kinases including Abl1, p38α, JNK, and PI3K (IC50>100 uM); causes partial inhibition of AKT phosphorylation on S473 on melanoma cells at 3 uM; reduces AKT protein expression and AKT association with HSP-90; caused effective regression of melanoma tumor xenografts.
References	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. View Related Products by Target Akt