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74(13):3546-55
InChiKey: GEPYBHCJBORHCE-SFHVURJKSA-N
It can inhibit the enzymatic activity of IDH1 R132H in vitro with an IC50 < 0
1 nM in a BT20 cell assay
The RAD51-stimulatory compound RS-1 can exploit the RAD51 overexpression that exists in cancer cells and tumors
PF-04979064 - PI3K/mTOR Dual Inhibitor. CAS# 1220699-06-8 hylase 74(13):3546-55PF 04979064, CAS No. 1220699 06 8, is a highly potent and orally bioavailable PI3K mTOR dual inhibitor developed through structure based drug design. It inhibited mTOR, PI3K, , and isoforms and AKT phosphorylation with IC50 as 2. 64 nM, 0. 395 nM, 0. 111 nM, 0. 122 nM and 28. 3 nM, respectively. PF 04979064 exhibited cellular potency with an IC50 of 9. 1 nM in a BT20 cell assay. PF 04979064 exhibited excellent in vitro potency, very good solubility,
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