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Deepak Bhattarai

Researcher at University of Kentucky

Publications -  30
Citations -  417

Deepak Bhattarai is an academic researcher from University of Kentucky. The author has contributed to research in topics: Cancer & Antibacterial activity. The author has an hindex of 9, co-authored 29 publications receiving 282 citations. Previous affiliations of Deepak Bhattarai include Korea University of Science and Technology & Dongguk University.

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Hypoxia-inducible factor-1 (HIF-1) inhibitors from the last decade (2007 to 2016): A "structure-activity relationship" perspective.

TL;DR: This review will summarize the structure–activity relationship of ten different chemotypes reported to be HIF‐1 inhibitors in the last decade, their mechanisms of action for Hif‐1 inhibition, progress in the way of target‐specific inhibitors, and problems associated with current inhibitors.
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Recent Advances in the Development of Pharmacologically Active Compounds that Contain a Benzoxazole Scaffold

TL;DR: This focus review, which highlights recent advancements in the development of benzoxazole-based pharmacologically active compounds since the year 2000, highlights the importance of knowing the carrier and removal status of this substance.
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Synthesis and structure-activity relationship study of chemical probes as hypoxia induced factor-1α/malate dehydrogenase 2 inhibitors.

TL;DR: The inhibitory effect of the probes on HIF-1α activity was consistent with that of theMDH2 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.
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Cytoplasmic synthesis of endogenous Alu complementary DNA via reverse transcription and implications in age-related macular degeneration

Shinichi Fukuda, +70 more
TL;DR: In this article, the authors reported that Alu RNA-induced RPE degeneration is mediated via cytoplasmic L1-reverse-transcribed Alu cDNA independently of retrotransposition.
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Targeting the interaction of AIMP2-DX2 with HSP70 suppresses cancer development.

TL;DR: The cellular stability of an oncogenic factor, AIMP2-DX2, is increased via association with HSP70, and interference with this interaction by a small-molecule compound promotes ubiquitin-mediated degradation and reduces cancer cell growth.