2. Academic Validation
  3. Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach

Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach

  • Eur J Med Chem. 2016 Jul 19:117:241-55. doi: 10.1016/j.ejmech.2016.04.024.
Bin Yu 1,  Ping-Ping Qi 1,  Xiao-Jing Shi 1,  Ruilei Huang 2,  Hao Guo 3,  Yi-Chao Zheng 1,  De-Quan Yu 4,  Hong-Min Liu 5
Affiliations

Affiliations

  • 1 School of Pharmaceutical Sciences & Collaborative Innovation Center of New Drug Research and Safety Evaluation, Zhengzhou University, Zhengzhou, 450001, China.
  • 2 School of Pharmaceutical Sciences, Central South University, Changsha, 410000, China.
  • 3 Chongqing Institute of Forensic Science, Chongqing, 400021, China.
  • 4 School of Pharmaceutical Sciences & Collaborative Innovation Center of New Drug Research and Safety Evaluation, Zhengzhou University, Zhengzhou, 450001, China. Electronic address: dqyu@imm.ac.cn.
  • 5 School of Pharmaceutical Sciences & Collaborative Innovation Center of New Drug Research and Safety Evaluation, Zhengzhou University, Zhengzhou, 450001, China. Electronic address: liuhm@zzu.edu.cn.
PMID: 27105028 DOI: 10.1016/j.ejmech.2016.04.024
Abstract

A series of steroidal hybrids with different terminal bioactive scaffolds were synthesized using the molecular hybridization approach and further evaluated for their antiproliferative activity against several Cancer cell lines of different origins using the MTT assay. The preliminary results indicated that compounds 12a-h with the terminal isatin motif were remarkably sensitive to SH-SY5Y cells, thereby exerting potent growth inhibition in vitro. This selectivity is possibly attributed to LSD1 inactivation (IC50 = 3.18 μM). Besides, we also found that the chloro atom at the 7-position on the isatin core was beneficial for the activity through the SARs studies. Among this series, compound 12g showed the best inhibitory activity (IC50 = 4.06 μM) against SH-SY5Y cells, which was comparable to that of 5-FU. Compound 12g arrested cell cycle at G2/M phase, induced Apoptosis accompanied with decrease of mitochondrial membrane potential, and inhibited LSD1 potently (IC50 = 3.18 μM). Docking studies showed that compound 12g formed interactions with surrounding amino acid residues and the steroid nucleus occupied the tubular hydrophobic cavity of the active site. Compounds 13-18 represented weak to moderate activity against the tested Cancer cell lines. The steroidal dimer 20 and the structurally simplified non-steroidal dimer 21 were found to be devoid of the inhibitory activity.

Keywords

Antiproliferative activity; Apoptosis; Cell cycle arrest; Docking simulations; LSD1 inactivation; Molecular hybridization; Steroids.

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