AZD1152

722543-31-9

C26H31FN7O6P

DMSO : >= 33 mg/mL (56.17 mM)

Cell Cycle/DNA Damage; Epigenetics

AZD1152 is a pro-drug of Barasertib-hQPA, which is a highly selective Aurora B inhibitor with IC₅₀ of 0.37 nM in a cell-free assay. IC50 & Target: IC50: 0.37 nM (Aurora B) In Vitro: AZD1152 displays >3000-fold selectivity for Aurora B as compared with Aurora A which has an IC₅₀ of 1.368 uM. AZD1152 has even less activity against 50 other serine-threonine and tyrosine kinases including FLT3, JAK2, and Abl. AZD1152 inhibits the proliferation of hematopoietic malignant cells such as HL-60, NB4, MOLM13, PALL-1, PALL-2, MV4-11, EOL-1, THP-1, and K562 cells with IC₅₀ of 3-40 nM, displaying appr 100-fold potency than another Aurora kinase inhibitor ZM334739 which has IC₅₀ of 3-30 uM. AZD1152 inhibits the clonogenic growth of MOLM13 and MV4-11 cells with IC₅₀ of 1 nM and 2.8 nM, respectively, as well as the freshly isolated imatinib-resistant leukemia cells with IC₅₀ values of 1-3 nM, more significantly compared with bone marrow mononuclear cells with IC₅₀ values of >10 nM. AZD1152 induces accumulation of cells with 4N/8N DNA content, followed by apoptosis in a dose- and time-dependent manner^[1]. AZD1152 causes significant accumulation of cells with 4N/8N DNA content in KMS12 and U266 and induces apoptosis in KMS18 and U266. AZD1152 in combination with DEX, has negative effects on cell viability in comparison with single agent in PMI8226, KMS11 and U266^[3]. In Vivo: Administration of AZD1152 (25 mg/kg) alone markedly suppresses the growth of MOLM13 xenografts, confirmed by the observation of necrotic tissue with infiltration of phagocytic cells^[1]. In addition, AZD1152 (10-150 mg/kg/day) significantly inhibits the growth of a variety of human solid tumor xenografts, including colon, breast, and lung cancers, in a dose-dependent manner^[2]. AZD1152 (25 mg/kg/day) treatment reduces xenograft levels such that they are slightly lower levels than after the first round of treatment, but this is not statistically significant indicating that residual cells might be more resistant to a second cycle of AZD1152^[4].