https://www.selleckchem.com/pr....oducts/filanesib.htm
4LZI3 protein in complex with curcumin and catechin respectively. These systems exhibited the highest binding energies, while the major interacting residues conserved in all the complexes provides a route map for structure-based drug design of novel compounds with enhanced inhibitory potency against the G4LZI3 protein. This study suggests an alternative approach for the development of anti-schistosomal drugs using natural compounds. Conjugation to clinical-grade tumor penetrating iRGD peptide is a widely used strategy to improve tumor
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