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N‑SUBSTITUTED CHIRAL AROMATIC OXAZOLIDINES, SYNTHESIS PROCESS, PHARMACEUTICAL COMPOSITION AND USE

机译:N-取代的手性芳族乙二醛,合成过程,药物成分和用途

摘要

The present invention relates to the production of synthetic molecules of N‑substituted chiral aromatic oxazolidines, the process for the synthesis thereof, pharmaceutical compositions containing said molecules and to the use of these compositions, especially as anti‑tumour agents. The low‑molecular‑weight compounds obtained from the synthesis process promote the pharmacokinetic properties of the compositions and the efficacy of the therapy. These compounds further exhibit anti‑tumour activity, as observed in in‑vitro tests, against human tumour cell lines.
机译:本发明涉及N-取代的手性芳族恶唑烷的合成分子的生产,其合成方法,包含所述分子的药物组合物以及这些组合物特别是作为抗肿瘤剂的用途。从合成过程中获得的低分子量化合物促进了组合物的药代动力学特性和治疗效果。如体外试验中所观察到的,这些化合物还具有针对人类肿瘤细胞系的抗肿瘤活性。

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