Mostrando 121 - 140 Resultados de 326 Para Buscar '"Suramin"', tiempo de consulta: 0.18s Limitar resultados
  1. 121
    por Chakraborty, Sandeep
    Publicado 2016
    “…The conformational changes in the suramin molecule on binding highlights the challenges in docking flexible ligands into an already ’plastic’ binding site. …”
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  2. 122
  3. 123
    “…In present study, four-month-old APP/PS1 mice were administered resveratrol (RSV) or suramin once daily for two months, following which their spatial learning and memory were assessed using the Morris water maze test. …”
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  4. 124
    por Ullah, Anwar, Ullah, Kifayat
    Publicado 2021
    “…The global binding energy of Suramin, 2S albumin, and flocculating proteins were −41.96, −9.12, and −14.78 kJ/mol, respectively. …”
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  5. 125
    “…These changes of both cells at 3 dpi were mostly decayed at 7 dpi and were suppressed by any of IL-10, IL-4, suramin (P2 receptor inhibitor) and 4-AP (K(+) channel blocker). …”
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  6. 126
    “…In addition, treatment of C. elegans wild-type N2 and the oga-1 mutant with PUGNAc + suramin and suramin (an ubiquitination inhibitor), respectively has resulted in increased sensitivity to S. aureus infection. …”
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  7. 127
    “…This depressant effect was antagonized by CPZ and suramin, but not by the P(2)X antagonist, 2', 3'-O-(2,4,6-trinitrophenyl) adenosine 5'-triphosphate (TNP-ATP). …”
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  8. 128
    “…A 7-min OGD induced tissue anoxic depolarization and was invariably followed by irreversible loss of fEPSP. PPADS, suramin, MRS2179 or BBG (brilliant blue G) significantly prevented the irreversible failure of neurotransmission induced by 7-min OGD. …”
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  9. 129
    por Sharma, Bechan
    Publicado 2011
    “…The sensitivity of PFK from S. cervi towards antifilarials/anthelmintics was comparatively higher than that of mammalian PFK. With suramin, the Ki value for rat liver PFK was 40 times higher than PFK from S. cervi. …”
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  10. 130
    “…The extracellular H+ fluxes induced by ATP were mimicked by the P2Y1 agonist MRS 2365 and were significantly reduced by the P2 receptor blockers suramin and PPADS, suggesting activation of P2Y receptors. …”
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  11. 131
    “…The binding of s-adenosyl-L-methionine was examined along with the competitive binding of adenine, dATP, and suramin. Based on fluorescence spectroscopy experiments the dissociation constant for the four ligands and the target protein could be determined; SAM (1.4 ± 0.7 µM), adenine (17.8 ± 1.5 µM), dATP (15.8 ± 2.0 µM), and Suramin (6.3 ± 1.1 µM). …”
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  12. 132
    por Cruz, Ana Miguel, Beall, Craig
    Publicado 2020
    “…Acute and chronic treatment with ATPγS increased glycolytic rate in a manner that was differentially inhibited by PPADs and suramin, suggesting heterogeneous P2R activation in the control of cellular metabolism. …”
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  13. 133
    “…Results showed that, in general, hydrophobic drugs, such as remdesivir and sofosbuvir, bind better to both binding sites than relatively less hydrophobic drugs, such as alovudine, molnupiravir, zidovudine, favilavir, and ribavirin. However, suramin, which is a highly hydrophobic drug, unexpectedly showed overall weaker binding affinities in both binding sites when compared to other drugs. …”
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  14. 134
  15. 135
    “…At non-toxic concentrations, all significantly inhibited invasion (P< 0.05), although to varying degrees, suramin and Å5 almost completely and N-acetylcysteine the least. …”
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  16. 136
    “…On the other hand, ATPγS stimulated Jak2 and STAT3 activation which were inhibited by pretreatment with PPADS, suramin, Gö6983, Gö6976, Ro318220, GF109203X, Rottlerin, Edaravone, DPI, and apocynin in A549 cells. …”
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  17. 137
    “…Furthermore, our simulations predict that suramin may interfere ligand binding on P(2)Y(2) receptors or accelerate P(2)Y(2) receptor phosphorylation, which may partially be the reason for Ca(2+) wave attenuation by suramin. …”
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  18. 138
  19. 139
    “…The effects of the P2 receptor antagonists suramin and PPADS, the P2Y(14) receptor antagonist PPTN, and the P2Y(6) receptor antagonist MRS2578, were investigated. …”
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  20. 140
    “…The propagation distance was decreased when the purinergic receptor antagonists pyridoxalphosphate‐6‐azophenyl‐2′,4′‐disulfonic acid (PPADS; 50 μm) or suramin (150 μm) were added to the extracellular buffer. …”
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