Ibw-959z

Figure 1A (dose‑response curves) illustrates the steep inhibition profile for PI3K‑δ. IBW‑959z inhibited proliferation of PI3K‑δ‑dependent cell lines with GI₅₀ values in the low‑picomolar range (Table 2). In contrast, the PI3K‑α/β‑dependent A549 and MCF‑7 lines were ~100‑fold less sensitive (GI₅₀ ≈ 30–40 nM).

IBW‑959z: A Novel Small‑Molecule Inhibitor of the PI3K‑δ Pathway with Potent Antitumor Activity in Pre‑clinical Models IBW-959z

| Cell line | GI₅₀ (nM) | % Inhibition of p‑AKT (Ser473) at 1 nM | |-----------|----------|----------------------------------------| | OCI‑Ly3 | 0.12 ± 0.02 | 95 % | | MEC‑1 | 0.18 ± 0.03 | 92 % | | A549 | 31 ± 4 | 18 % | | MCF‑7 | 38 ± 5 | 22 % | University of Cambridge

¹ Department of Medicinal Chemistry, University of Cambridge, UK ² Institute of Molecular Pharmacology, Shanghai Jiao Tong University, China ³ Cancer Biology Program, Universidad Nacional Autónoma de México, Mexico ⁴ Department of Pharmacology, Seoul National University, South Korea ⁵ Department of Oncology, Johns Hopkins University School of Medicine, USA UK ² Institute of Molecular Pharmacology

4‑Fluorobenzaldehyde (10 mmol) was condensed with 2‑aminopyrimidine (10 mmol) in ethanol (30 mL) under reflux for 6 h to afford intermediate A (85 % yield).

Figure 2B shows dose‑dependent suppression of phospho‑AKT and phospho‑S6 in OCI‑Ly3 cells, confirming pathway blockade. Key PK parameters are summarized in Table 3 .