يعرض 141 - 160 نتائج من 8,976 نتيجة بحث عن '(( 5 ppm decrease ) OR ((( 50 nn decrease ) OR ((( 50 μ decrease ) OR ( 50 we decrease ))))))', وقت الاستعلام: 0.41s تنقيح النتائج
  1. 141

    Cytotoxicity assay. حسب Rodrigo Rollin-Pinheiro (239450)

    منشور في 2023
    الموضوعات:
  2. 142

    Cytotoxicity assay. حسب Rodrigo Rollin-Pinheiro (239450)

    منشور في 2023
    الموضوعات:
  3. 143
  4. 144
  5. 145

    Preformed biofilm. حسب Rodrigo Rollin-Pinheiro (239450)

    منشور في 2023
    الموضوعات:
  6. 146
  7. 147
  8. 148
  9. 149
  10. 150
  11. 151
  12. 152
  13. 153

    Biofilm formation. حسب Rodrigo Rollin-Pinheiro (239450)

    منشور في 2023
    الموضوعات:
  14. 154
  15. 155
  16. 156

    Antimicrobial activity of RP-1 peptide conjugate with ferrocene group حسب Natalia C. S. Costa (8626206)

    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. …"
  17. 157

    Synthesis and Biological Evaluation of New Chalcogen Semicarbazone (<i>S</i>, <i>Se</i>) and Their Azole Derivatives against Chagas Disease حسب Mercedes Rubio-Hernández (20036142)

    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. …"
  18. 158

    Synthesis and Biological Evaluation of New Chalcogen Semicarbazone (<i>S</i>, <i>Se</i>) and Their Azole Derivatives against Chagas Disease حسب Mercedes Rubio-Hernández (20036142)

    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. …"
  19. 159

    Potent 5‑Cyano-6-phenyl-pyrimidin-Based Derivatives Targeting DCN1–UBE2M Interaction حسب Wenjuan Zhou (115285)

    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). …"
  20. 160