Ridaifen-B (C09-1027-251)

Ridaifen-B is a novel tamoxifen (TAM) analog which significantly augments apoptosis-inducing effect of TAM in estrogen receptor (ER)-negatives cells. It induces mitochondria-involved apoptosis in Jurkat cells, as evidenced by chromatin-condensed cells as well as downstream activation of caspases (caspase-3, -8 and -9) in a dose- and time-dependent manner. At 4 hours of incubation, IC|50|for RID-B is 4 μM (30 μM for TAM). And at prolonged treatment of 48 hours, IC|50|for RID-B is 0.1 μM. In a related report on the global anti-tumor activity, RID-B strongly inhibits 39 human cancer cells (JFCR 39), both ER-+ or ER-- at concentrations of equal or less than 1 μM (e.g., at 0.38 μM for SF-539 [central nervous system], at 0.58 μM for HT-29 [colon], at 0.20 μM for DMS114 [lung], at 0.21μM for LOX-IMVI [melanoma], and at 0.23 μM for MKN74 [stomach]. The binding protein of RID-B that exerts the apoptosis events is currently under investigation. Specification: ≥98% Molecular Formula: C34H42N2O2 Molecular Weight: 510.71 PubChem CID: 11548000 Isomeric SMILES: CCC(=C(C1=CC=C(C=C1)OCCN2CCCC2)C3=CC=C(C=C3)OCCN4CCCC4)C5=CC=CC=C5 Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/R333279-SCI_d814900a8b9600b38ecd7b4266b7f2c9.pdf