Search Results - "Pattnaik, Banita"

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  1. 1

    Conformation of flexibly linked triterpene dimers by using RDC-enhanced NMR spectroscopy by Lakshmi, Jerripothula K., Pattnaik, Banita, Kavitha, Rachineni, Mallavadhani, Uppuluri V., Jagadeesh, Bharatam

    Published in Journal of molecular structure (15-06-2018)
    “…Dimers of flexibly linked pentacyclic triterpene ursolic acid (UA) and its related frameworks such as asiatic acid (AA) and oleanolic acid (OA) have recently…”
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  2. 2

    Synthesis of ring-C modified oleanolic acid derivatives and their cytotoxic evaluation by Pattnaik, Banita, Lakshma Nayak, Vadithe, Ramakrishna, Sistla, Venkata Mallavadhani, Uppuluri

    Published in Bioorganic chemistry (01-10-2016)
    “…[Display omitted] •Oleanolic acid ring-C was chemically modified.•Dienes, α,β-unsaturated ketone, saturated and unsaturated lactones were synthesized.•The…”
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  3. 3
  4. 4

    A rapid and highly sensitive UPLC-QTOF MS method for quantitative evaluation of Nardostachys jatamansi using Nardin as the marker by Mallavadhani, Uppuluri Venkata, Panigrahi, Reba, Pattnaik, Banita

    Published in Biomedical chromatography (01-08-2011)
    “…Nardostachys jatamansi DC. is a highly reputed Medhya and Nootropic (Learning and Memory) Ayurvedic medicinal plant. Its use as herbal medicine singly and as…”
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  5. 5

    Synthesis and anti-cancer activity of some novel C-17 analogs of ursolic and oleanolic acids by Mallavadhani, Uppuluri V., Mahapatra, Anita, Pattnaik, Banita, Vanga, Nagireddy, Suri, Nitasha, Saxena, Ajit K.

    Published in Medicinal chemistry research (01-03-2013)
    “…A series of seventeen novel analogs of ursolic and oleanolic acid were synthesized (60–98 %), and evaluated for their anti-cancer potential against a panel of…”
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    Journal Article
  6. 6

    Novel C-ring analogs of ursolic acid: synthesis and cytotoxic evaluation by Mallavadhania, Uppuluri V, Pattnaik, Banita, Suri, Nitasha, Saxena, Ajit K

    Published in Natural product communications (01-12-2014)
    “…Ursolic acid (1), a natural pentacyclic triterpenic acid, afforded a variety of ring-C transformed products (5-11) when treated with N-bromosuccinimide under…”
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    Journal Article