Search Results - "Ambre, Premlata K"

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    New horizons in antimalarial drug discovery in the last decade by chemoinformatic approaches by Ambre, Premlata K, Wavhale, Ravindra D, Coutinho, Evans C

    “…Antimalarial drug discovery process is progressively carried out by a combination of innovation and knowledge based methods that include computational and…”
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    Journal Article
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    Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity by Wavhale, Ravindra D., Martis, Elvis A.F., Ambre, Premlata K., Wan, Baojie, Franzblau, Scott G., Iyer, Krishna R., Raikuvar, Kavita, Macegoniuk, Katarzyna, Berlicki, Łukasz, Nandan, Santosh R., Coutinho, Evans C.

    Published in Bioorganic & medicinal chemistry (01-09-2017)
    “…[Display omitted] BM212 [1,5-diaryl-2-methyl-3-(4-methylpiperazin-1-yl)-methyl-pyrrole] is a pyrrole derivative with strong inhibitory activity against drug…”
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    Journal Article
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    Extracting structural requirements for activity of GPR119 agonists: a hologram quantitative structure activity relationship (HQSAR) study by Ugarkar, Apoorva G, Ambre, Premlata K, Coutinho, Evans C, Nandan, Santosh, Pissurlenkar, Raghuvir R.S

    Published in Canadian journal of chemistry (01-07-2014)
    “…GPR119 is a potential target for the treatment of diabetes mellitus. GPR119 agonists minimize the side-effects observed with sulphonyl ureas and glucagon-like…”
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    Identification of new checkpoint kinase-1 (Chk1) inhibitors by docking, 3D-QSAR, and pharmacophore-modeling methods by Ambre, Premlata K, Pissurlenkar, Raghuvir R.S, Coutinho, Evans C, Iyer, Radhakrishnan P

    Published in Canadian journal of chemistry (01-08-2012)
    “…Inhibition of checkpoint kinase-1 (Chk1) by small molecules is of great therapeutic interest in the field of oncology and for understanding cell-cycle…”
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    Molecular docking and 3D-QSAR studies of HIV-1 protease inhibitors by Khedkar, Vijay M., Ambre, Premlata K., Verma, Jitender, Shaikh, Mushtaque S., Pissurlenkar, Raghuvir R. S., Coutinho, Evans C.

    Published in Journal of molecular modeling (01-07-2010)
    “…HIV-1 protease is an obligatory enzyme in the replication process of the HIV virus. The abundance of structural information on HIV-1PR has made the enzyme an…”
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    Journal Article
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    Antifolate agents against wild and mutant strains of plasmodium falciparum by Shaikh, M, Rana, J, Gaikwad, D, Leartsakulpanich, U, Ambre, Premlata, Pissurlenkar, R. R. S, Coutinho, E

    Published in Indian journal of pharmaceutical sciences (01-03-2014)
    “…Plasmodium falciparum dihydrofolate reductase is an important target for antimalarial chemotherapy. The emergence of resistance has significantly reduced the…”
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