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Virinder S. Parmar

Researcher at City University of New York

Publications -  417
Citations -  9115

Virinder S. Parmar is an academic researcher from City University of New York. The author has contributed to research in topics: Lipase & Catalysis. The author has an hindex of 42, co-authored 412 publications receiving 8300 citations. Previous affiliations of Virinder S. Parmar include University of Massachusetts Lowell & Dartmouth College.

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Phytochemistry of the genus Piper

TL;DR: The secondary metabolites isolated from Piper species for the period 1907 to June 1996 have been reviewed in this paper, where nearly six hundred chemical constituents belonging to different classes of bioactive compounds are listed together with their source(s) and references.
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N,N,N′,N′‐Tetraoctyl Diglycolamide (TODGA): A Promising Extractant for Actinide‐Partitioning from High‐Level Waste (HLW)

TL;DR: In this article, the authors evaluated TODGA as an extractant for the partitioning of minor actinides from simulated high level nuclear waste solutions and found that TODGA molecules display a tendency toward aggregation in n−dodecane at lower acidities.
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Naturally occurring aristolactams, aristolochic acids and dioxoaporphines and their biological activities

TL;DR: Aristolactams, having a phenanthrene chromophore are a small group of compounds mainly found in the Aristolochiaceae together with the aristolochic acids and 4,5-dioxoaporphines, which are reviewed and classified on the basis of their oxygenation pattern.
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Synthetic and biological activity evaluation studies on novel 1,3-diarylpropenones.

TL;DR: Out of the twelve chalcones tested, three were found to exhibit potent anti-invasive activity and a prenylated acetophenone carrying two methoxy groups and two free phenolic hydroxy functions was found to be a potential antioxidant.
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Novel chalcone derivatives as potent Nrf2 activators in mice and human lung epithelial cells.

TL;DR: The studies showed 2-trifluoromethyl-2'-methoxychalone (2b) to be a potent activator of Nrf2, both in vitro and in mice, and showed that the activation of NRF2 by this compound is independent of reactive oxygen species or redox changes.