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新型铱噻唑配合物的合成、细胞抑制和抗肿瘤活性。

Synthesis, cytostatic, and antitumor properties of new rh(i) thiazole complexes.

机构信息

Department of Inorganic and Analytical Chemistry, Faculty ofPharmacy, Madrid-3, Spain.

出版信息

Biol Trace Elem Res. 1985 Dec;8(4):251-61. doi: 10.1007/BF02989580.

Abstract

Six new organometallic derivatives of Rh(I), belonging to the general structure [Rh(CO)2(L)(Cl)], were synthesized and characterized by chemical analysis and IR determinations. The following ligands (L) were employed: 2-aminothiazole, thiazole, 2-amino-6-bromobenzothiazole, 5-chloro-2-methylthiobenzothiazole, 2-bromo-thiazole, and 2-isopropylthiazole. These new complexes were assayed in vitro with KB cells and in vivo with mice bearing established P388 and L1210 leukemias. Assays against S180 and Ehrlich ascitic tumors were also performed. Two complexes displayed antitumor activity against ascitic tumors.

摘要

六种新型的铑(I)有机金属衍生物,属于一般结构[Rh(CO)2(L)(Cl)],通过化学分析和红外测定进行了合成和表征。使用了以下配体(L):2-氨基噻唑、噻唑、2-氨基-6-溴苯并噻唑、5-氯-2-甲基噻唑、2-溴噻唑和 2-异丙基噻唑。这些新的配合物在体外与 KB 细胞进行了检测,并在体内与患有已建立的 P388 和 L1210 白血病的小鼠进行了检测。还对 S180 和艾氏腹水瘤进行了检测。有两个复合物对腹水瘤显示出抗肿瘤活性。

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