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Both materials showed good affinity for cell attachment.
Excellent extraction efficiency of this fiber was demonstrated, indicating its good affinity for both non-/less polar and polar compounds.
Compounds Ve and Vf have shown good affinity for receptor GST, as well as in vitro anti-filarial potency.
The flexibility of our structure offered the potential to preserve good affinity for mutant FGFR, which is important for developing TKIs with long-term efficacy.
CNTs with good affinity for drug molecules, improved solubility, and lower tendency to aggregate have potential as DDS for enhancing the efficacy of medicines.
In silico ADMET predictions revealed that the compound 19 had good oral absorption, aqueous solubility, non-hepatotoxic and good affinity for plasma protein binding.
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Compound 8 present good selectivity for MT2 over MT1 (MT1/MT2 = 19) and compound 13 have good affinities for both MT1 (Ki :28 nM) and MT2 (Ki : 8 nM).
Anion binding studies carried out using fluorescence spectroscopy and 1H NMR revealed that this compound displays good affinities for bromide ion.
Anion binding studies carried out using 1H NMR and UV vis revealed that this compound displays good affinities for Y-shaped anions such as acetate and benzoate, while binding spherical-shaped anions and tetrahedral-shaped anions only weakly.
Compounds 2a and 2b, on the other hand, show greater affinity for Alk and Met, and good affinities for both EGFR variants.
Another level of local homoeostatic control appears to be intrinsic to the structures of the enzymes themselves, as in addition to their catalytic domain, some of these possess additional PI-binding domains with good affinities for their substrate.
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