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DESIGN OF ALLOSTERIC INHIBITORS OF GALECTIN-1 CARBOHYDRATE BINDING.

机译:半凝集素-1碳水化合物结合的变构抑制剂设计。

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Galectins are a family of lectins with a conserved carbohydrate-recognition domain, that were identified for their propensity to bind galactosides. Depending on cell type and state of cell differentiation, galectins can be found in the nucleus, cytoplasm, on the cell surface, or within the extracellular matrix. By binding to glycoconjugates on cells, galectins mediate cell adhesion and migration. Consequently, they are important regulators of these processes, and are involved in a number of pathological disorders (e.g., 1). Galectin-1 (Gal-1) in particular is an important regulator of angiogenesis and tumorogenesis, and the inhibition of angiogenesis has become a promising avenue for cancer treatment, and as such, galectins in general have become attractive targets for the development of anti-angiogenesis and anti-cancer agents.
机译:半乳酸汀是一种凝集素,具有保守的碳水化合物 - 识别结构域,其被鉴定为其结合半乳糖糖苷的倾向。取决于细胞类型和细胞分化状态,可以在细胞核,细胞质,细胞表面或细胞外基质内发现半乳糖蛋白。通过对细胞的糖缀合物结合,半乳糖蛋白介导细胞粘附和迁移。因此,它们是这些过程的重要调节因素,并且参与了许多病理疾病(例如,1)。 Galectin-1(Gal-1)特别是血管生成和肿瘤发生的重要调节剂,血管生成的抑制已成为癌症治疗的有希望的大道,因此,Galectins通常已成为抗 - 抗议性的有吸引力的目标。血管生成和抗癌剂。

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