"目录号: HY-13671
LW6是新颖的HIF-1抑制剂，IC50值为4.4 μM。
相关产品
PT-2385-FG-4592-DMOG-PX-478-2-Methoxyestradiol-BAY 87-2243-Daprodustat-DASA-58-IOX2-Molidustat-FG-2216-JNJ-42041935-Paeoniflorin-Vadadustat-Oltipraz-
生物活性
Description
LW6 is a novelHIF-1inhibitor with anIC50of 4.4 μM.
IC50& Target
IC50: 4.4 μM (HIF-1)[1]
In Vitro
LW6 decreases HIF-1α protein expression without affecting HIF-1β expression. LW6 affects the stability of the HIF-1α protein. LW6 promotes the degradation of wild type HIF-1α, but not of a DM-HIF-1α with modifications of P402A and P564A, at hydroxylation sites in the oxygen-dependent degradation domain. LW6 induces the expression of von Hippel-Lindau (VHL), which interacts with prolyl-hydroxylated HIF-1α for proteasomal degradation. In the presence of LW6, knockdown of VHL does not abolish HIF-1α protein accumulation, indicating that LW6 degraded HIF-1α via regulation of VHL expression[2]. In MDCKII-BCRP cells overexpressing BCRP, LW6 enhances significantly the cellular accumulation of mitoxantrone, a BCRP substrate. LW6 also down-regulates BCRP expression at concentrations of 0.1-10 μM[3]. LW6 inhibits the expression of HIF 1α induced by hypoxia in A549 cells at 20 mM, independently of the von Hippel Lindau protein. LW6 induces hypoxia selective apoptosis together with a reduction in the mitochondrial membrane potential[4].
In Vivo
In mice carrying xenografts of human colon cancer HCT116 cells, LW6 demonstrates strong anti-tumor efficacyin vivoand causes a decrease in HIF-1α expression in frozen-tissue immunohistochemical staining[2].
References
[3].Song JG, et al. Discovery of LW6 as a new potent inhibitor of breast cancer resistance protein.
