亲脂性
细胞毒性
化学
乙腈
色谱法
高效液相色谱法
甲醇
水溶液
立体化学
体外
有机化学
生物化学
作者
Judit Bartalis,Fathi T. Halaweish
标识
DOI:10.1016/j.jchromb.2004.12.020
摘要
Drug development of cucurbitacins requires derivatives that have lower cytotoxicity. Therefore, the effect of structural modification on in vitro cytotoxicity has been investigated. Lipophilicity or chromatographic hydrophobicity index (CHI) was chosen as molecular property. CHI was determined by RP-HPLC in both aqueous acetonitrile and aqueous methanol. Compounds CHI range was wide and better defined in acetonitrile (CHIACN = 46–88 and 38–102) than in methanol (CHIMeOH = 56–78). Higher resolution was achieved in acetonitrile, and higher precision on the shorter C18 column. Cucurbitacins cytotoxicity (IC50) was measured on the hepatocyte-derived HepG2 cells. Strong relationship between CHI and logarithmic IC50 was found. As a result, cytotoxicity increased linearly with increasing hydrophobicity (r ≥ 0.90). Other lipophilicity parameters, such as log P and C log P were also estimated. Cytotoxicity correlated well with log P (r = 0.95) and slightly with C log P (r = 0.74). The log P and C log P data showed good correlation with CHI (r > 0.92). Overall, alkylation of C1 hydroxyl, unsaturation of C1C2 bond, and acetylation of C25 hydroxyl increased both lipophilicity and cytotoxicity. This assay should prove useful for monitoring cucurbitacin homologues or other drug candidates for their cytotoxicity.
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