بدائل البحث:
ppm decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), pa decreased (توسيع البحث)
nn decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), mean decrease (توسيع البحث)
μ decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), _ decreased (توسيع البحث)
we decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), mean decrease (توسيع البحث)
50 nn » 50 ns (توسيع البحث), 50 ng (توسيع البحث), 50 n (توسيع البحث)
50 μ » 10 μ (توسيع البحث), 5 μ (توسيع البحث)
ppm decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), pa decreased (توسيع البحث)
nn decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), mean decrease (توسيع البحث)
μ decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), _ decreased (توسيع البحث)
we decrease » _ decrease (توسيع البحث), a decrease (توسيع البحث), mean decrease (توسيع البحث)
50 nn » 50 ns (توسيع البحث), 50 ng (توسيع البحث), 50 n (توسيع البحث)
50 μ » 10 μ (توسيع البحث), 5 μ (توسيع البحث)
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Morphological alterations on <i>S</i>. <i>aurantiacum</i> biofilm by scanning electron microscopy.
منشور في 2023الموضوعات: -
152
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In Vitro Screening for ToxCast Chemicals Binding to Thyroxine-Binding Globulin
منشور في 2024الموضوعات: -
156
Antimicrobial activity of RP-1 peptide conjugate with ferrocene group
منشور في 2020"…The Fc-RP1 presented anti-amastigote activity against <i>Leishmania amazonensis</i> (IC<sub>50</sub> = 0.25 μmol L<sup>–1</sup>). In comparison with amphotericin B, a second-line drug approved for leishmaniasis treatment, (IC<sub>50</sub> = 0.63 μmol L<sup>-1</sup>), Fc-RP1 was more active and showed a 2.5-fold higher selectivity index. …"
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157
Synthesis and Biological Evaluation of New Chalcogen Semicarbazone (<i>S</i>, <i>Se</i>) and Their Azole Derivatives against Chagas Disease
منشور في 2024"…Three compounds were selected, based on their activity against the intracellular amastigotes (EC<sub>50</sub> < 1 μM, SI > 10) and cruzain (IC<sub>50</sub> < 100 nM, SI > 5.55) which compared favorably with the approved drug, Benznidazole, and the well-established cruzain inhibitor K777. …"
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158
Synthesis and Biological Evaluation of New Chalcogen Semicarbazone (<i>S</i>, <i>Se</i>) and Their Azole Derivatives against Chagas Disease
منشور في 2024"…Three compounds were selected, based on their activity against the intracellular amastigotes (EC<sub>50</sub> < 1 μM, SI > 10) and cruzain (IC<sub>50</sub> < 100 nM, SI > 5.55) which compared favorably with the approved drug, Benznidazole, and the well-established cruzain inhibitor K777. …"
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159
Potent 5‑Cyano-6-phenyl-pyrimidin-Based Derivatives Targeting DCN1–UBE2M Interaction
منشور في 2019"…After finding a novel inhibitor <b>DC-1</b> with IC<sub>50</sub> = 1.2 μM, we performed a series of chemical optimizations, which finally led to the discovery of a potent thiazole containing 5-cyano-6-phenylpyrimidin-based inhibitor <b>DC-2</b> (IC<sub>50</sub> = 15 nM). …"
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160