
Chemical Name : CAL101
CAS : 870281-82-6
Synonyms: (S)-2-(1-(1H-purin-6-ylamino)propyl)-5-fluoro-3-phenylquinazolin-4(3H)-one
Storage:-20C 2 years
Biologieal
CAL-101 is a potent PI3K p110 inhibitor with an IC50 of 65 nM. CAL-101 blocked constitutive phosphatidylinositol-3-kinase signaling, resulting in decreased phosphorylation of Akt and other downstream effectors, an increase in poly(ADP-ribose) polymerase and caspase cleavage and an induction of apoptosis. CAL-101 has 40 to 300-fold selectivity compared to other PI3K isoforms. In vitro studies of 0.1 to 10 µM CAL-101 showed inhibition of pAKT expression and/or apoptotic effects against primary chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML) cells and against a range of leukemia and lymphoma cell lines.
Reference
[1] http://www.asco.org/ASCOv2/Meetings/Abstracts?&vmview=abst_detail_view&confID=65&abstractID=34213 [2] Lannutti BJ et al. Blood. 2011 Jan 13;117(2):591-4.
GDC-0941/GDC0941
957054-30-7
ZSTK474/ZSTK-474/
475110-96-4
YM201636
371942-69-7
BEZ235/NVP-BEZ235/BE-Z235/
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