Kemnitzer William, Sirisoma Nilantha, Nguyen Bao, Jiang Songchun, Kasibhatla Shailaja, Crogan-Grundy Candace, Tseng Ben, Drewe John, Cai Sui Xiong
Epicept Corporation, Inc, San Diego, CA 92121, USA.
Bioorg Med Chem Lett. 2009 Jun 1;19(11):3045-9. doi: 10.1016/j.bmcl.2009.04.009. Epub 2009 Apr 8.
N-(2-Methylphenyl)-9-oxo-9H-fluorene-1-carboxamide (2a) was identified as a novel apoptosis inducer through our caspase- and cell-based high-throughput screening assay. Compound 2a was found to be active with sub-micromolar potencies for both caspase induction and growth inhibition in T47D human breast cancer, HCT116 human colon cancer, and SNU398 hepatocellular carcinoma cancer cells. It arrested HCT116 cells in G(2)/M followed by apoptosis as assayed by the flow cytometry. Structure-activity relationship (SAR) studies of the carboxamide group identified the lead compound N-(2-(1H-pyrazol-1-yl)phenyl)-9-oxo-9H-fluorene-1-carboxamide (6s). Compound 6s, with increased aqueous solubility, was found to retain the broad activity in the caspase activation assay and in the cell growth inhibition assay with sub-micromolar EC(50) and GI(50) values in T47D, HCT116, and SNU398 cells, respectively.
通过我们基于半胱天冬酶和细胞的高通量筛选试验,N-(2-甲基苯基)-9-氧代-9H-芴-1-甲酰胺(2a)被鉴定为一种新型凋亡诱导剂。发现化合物2a在T47D人乳腺癌、HCT116人结肠癌和SNU398肝癌细胞中对半胱天冬酶诱导和生长抑制均具有亚微摩尔效力的活性。通过流式细胞术检测,它使HCT116细胞停滞在G(2)/M期,随后发生凋亡。对甲酰胺基团的构效关系(SAR)研究确定了先导化合物N-(2-(1H-吡唑-1-基)苯基)-9-氧代-9H-芴-1-甲酰胺(6s)。发现具有增加水溶性的化合物6s在半胱天冬酶激活试验和细胞生长抑制试验中分别在T47D、HCT116和SNU398细胞中具有亚微摩尔EC(50)和GI(50)值的广泛活性。