بدائل البحث:
significant decrease » significant increase (توسيع البحث), significantly increased (توسيع البحث)
significant binding » significant burden (توسيع البحث), significant benefits (توسيع البحث)
binding decrease » binding database (توسيع البحث)
significant decrease » significant increase (توسيع البحث), significantly increased (توسيع البحث)
significant binding » significant burden (توسيع البحث), significant benefits (توسيع البحث)
binding decrease » binding database (توسيع البحث)
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401
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402
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403
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404
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405
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406
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407
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415
Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer
منشور في 2024"…Among them, <b>E35</b> demonstrated excellent inhibitory activities against the binding of Skp2–Cks1. In addition, compound <b>E35</b> significantly inhibited colony formation and migration, as well as arrested the cell cycle at the S-phase. …"
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416
Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer
منشور في 2024"…Among them, <b>E35</b> demonstrated excellent inhibitory activities against the binding of Skp2–Cks1. In addition, compound <b>E35</b> significantly inhibited colony formation and migration, as well as arrested the cell cycle at the S-phase. …"
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417
Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer
منشور في 2024"…Among them, <b>E35</b> demonstrated excellent inhibitory activities against the binding of Skp2–Cks1. In addition, compound <b>E35</b> significantly inhibited colony formation and migration, as well as arrested the cell cycle at the S-phase. …"
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418
Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer
منشور في 2024"…Among them, <b>E35</b> demonstrated excellent inhibitory activities against the binding of Skp2–Cks1. In addition, compound <b>E35</b> significantly inhibited colony formation and migration, as well as arrested the cell cycle at the S-phase. …"
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419
Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer
منشور في 2024"…Among them, <b>E35</b> demonstrated excellent inhibitory activities against the binding of Skp2–Cks1. In addition, compound <b>E35</b> significantly inhibited colony formation and migration, as well as arrested the cell cycle at the S-phase. …"
-
420