Showing 141 - 160 results of 10,256 for search '(( 50 ng decrease ) OR ((((( 50 n decrease ) OR ( 50 μ decrease ))) OR ( 5 μ decrease ))))', query time: 0.99s Refine Results
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    Synthesis, Biological Evaluation, Structure–Activity Relationship, and Mechanism of Action Studies of Quinoline–Metronidazole Derivatives Against Experimental Visceral Leishmaniasi... by Akanksha Upadhyay (6732857)

    Published 2019
    “…Among all synthesized derivatives, <b>15b</b> and <b>15i</b> showed significant antileishmanial efficacy against both extracellular promastigote (IC<sub>50</sub> 9.54 and 5.42 μM, respectively) and intracellular amastigote (IC<sub>50</sub> 9.81 and 3.75 μM, respectively) forms of Leishmania donovani with negligible cytotoxicity toward the host (J774 macrophages, Vero cells). …”
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    <i>In vitro</i> activity of aryl-thiazole derivatives against <i>Schistosoma mansoni</i> schistosomula and adult worms by Adriana S. A. Pereira (5900249)

    Published 2019
    “…Adult worms’ treatment with 50 μM NJ05, NJ07 or NJ05 + NJ07 showed decreased motility to 30–50% compared with controls. …”
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    Cost-effectiveness and budget impact of immediate antiretroviral therapy initiation for treatment of HIV infection in Côte d’Ivoire: A model-based analysis by Eric N. Ouattara (6890174)

    Published 2019
    “…<i>Immediate ART</i> increased the 5-year HIV care budget from $801.9M to $812.6M compared to <i>ART<350/μL</i>.…”
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    Synthesis and Biological Evaluation of Heterocyclic Ring-Fused 20(<i>S</i>)‑Protopanaxadiol Derivatives as Potent Antiosteoporosis Agents by Shuan-Jing Wang (16854232)

    Published 2023
    “…Among these compounds, <b>33</b> (SH491, IC<sub>50</sub> = 11.8 nM) showed the highest potency with 100% inhibition at 0.1 μM and 44.4% inhibition at an even lower concentration of 0.01 μM, which was much more potent than the lead compound PPD (IC<sub>50</sub> = 10.3 μM). …”