1. Academic Validation
  2. Design, Synthesis, and Biological Application of Novel Photoaffinity Probes of Dihydropyridine Derivatives, BAY R3401

Design, Synthesis, and Biological Application of Novel Photoaffinity Probes of Dihydropyridine Derivatives, BAY R3401

  • Molecules. 2019 Jun 28;24(13):2394. doi: 10.3390/molecules24132394.
Liying Zhang 1 Zhiwei Yan 2 Youde Wang 2 Chengjun Song 3 Guangxin Miao 2
Affiliations

Affiliations

  • 1 Key Laboratory of Traditional Chinese Medicine Research and Development of Hebei Province, Institute of Traditional Chinese Medicine, Chengde Medical University, Chengde 067000, China. zzzhangliying@126.com.
  • 2 Key Laboratory of Traditional Chinese Medicine Research and Development of Hebei Province, Institute of Traditional Chinese Medicine, Chengde Medical University, Chengde 067000, China.
  • 3 Department of Human Anatomy, Chengde Medical University, Chengde 067000, China.
Abstract

To explore the molecular mechanisms of BAY R3401, four types of novel photoaffinity probes bearing different secondary tags were synthesized. Their potency for glycogenolysis was evaluated in primary human liver HL-7702 cells and HepG2 cells. Probe 2d showed the best activity in primary human liver HL-7702 cells and HepG2 cells, with IC50 values of 4.45 μM and 28.49 μM, respectively. Likewise, probe 5d showed IC50 values of 6.46 μM in primary human liver HL-7702 cells and 15.29 μM in HepG2 cells, respectively. Photoaffinity labeling experiments were also performed and protein bands larger than 170 kDa were specifically tagged by probe 2d. The results suggest that the synthesized probe 2d might be a very promising tool for the isolation of the target proteins of BAY R3401.

Keywords

BAY R3401; glycogenolysis; molecular mechanism; photoaffinity labeling; photoaffinity probe; target proteins; type 2 diabetes.

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