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Synthesis and structure-activity relationship study of chemical probes as hypoxia induced factor-1α/malate dehydrogenase 2 inhibitors.

Abstract
A structure-activity relationship study of hypoxia inducible factor-1α inhibitor 3-aminobenzoic acid-based chemical probes, which were previously identified to bind to mitochondrial malate dehydrogenase 2, was performed to provide a better understanding of the pharmacological effects of LW6 and its relation to hypoxia inducible factor-1α (HIF-1α) and malate dehydrogenase 2 (MDH2). A variety of multifunctional probes including the benzophenone or the trifluoromethyl diazirine for photoaffinity labeling and click reaction were prepared and evaluated for their biological activity using a cell-based HRE-luciferase assay as well as a MDH2 assay in human colorectal cancer HCT116 cells. Among them, the diazirine probe 4a showed strong inhibitory activity against both HIF-1α and MDH2. Significantly, the inhibitory effect of the probes on HIF-1α activity was consistent with that of the MDH2 enzyme assay, which was further confirmed by the effect on in vitro binding activity to recombinant human MDH2, oxygen consumption, ATP production, and AMP activated protein kinase (AMPK) activation. Competitive binding modes of LW6 and probe 4a to MDH2 were also demonstrated.
AuthorsRavi Naik, Misun Won, Hyun Seung Ban, Deepak Bhattarai, Xuezhen Xu, Yumi Eo, Ye Seul Hong, Sarbjit Singh, Yongseok Choi, Hee-Chul Ahn, Kyeong Lee
JournalJournal of medicinal chemistry (J Med Chem) Vol. 57 Issue 22 Pg. 9522-38 (Nov 26 2014) ISSN: 1520-4804 [Electronic] United States
PMID25356789 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Benzophenones
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Recombinant Proteins
  • meta-Aminobenzoates
  • benzophenone
  • Adenosine Triphosphate
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2
  • 3-aminobenzoic acid
Topics
  • Adenosine Triphosphate (chemistry)
  • Benzophenones (chemistry)
  • Binding, Competitive
  • Cell Line, Tumor
  • Chemistry, Pharmaceutical (methods)
  • Chromatography, Affinity (methods)
  • Drug Design
  • Drug Discovery
  • HCT116 Cells
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit (antagonists & inhibitors)
  • Inhibitory Concentration 50
  • Kinetics
  • Oxygen Consumption
  • Proto-Oncogene Proteins c-mdm2 (antagonists & inhibitors)
  • Recombinant Proteins (chemistry)
  • Structure-Activity Relationship
  • meta-Aminobenzoates (chemistry)

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