Del Carpio Edgar, Hernández Lino, Ciangherotti Carlos, Villalobos Coa Valentina, Jiménez Lissette, Lubes Vito, Lubes Giuseppe
Laboratorio de Equilibrios en Solución, Universidad Simón Bolívar (USB), Apartado 89000, Caracas 1080 A, Venezuela.
Unidad de Química Medicinal, Facultad de Farmacia, Escuela "Dr. Jesús María Bianco", Universidad Central de Venezuela, Venezuela.
Coord Chem Rev. 2018 Oct 1;372:117-140. doi: 10.1016/j.ccr.2018.06.002. Epub 2018 Jun 21.
In the last 30 years, since the discovery that vanadium is a cofactor found in certain enzymes of tunicates and possibly in mammals, different vanadium-based drugs have been developed targeting to treat different pathologies. So far, the studies of the insulin mimetic, antitumor and antiparasitic activity of certain compounds of vanadium have resulted in a great boom of its inorganic and bioinorganic chemistry. Chemical speciation studies of vanadium with amino acids under controlled conditions or, even in blood plasma, are essential for the understanding of the biotransformation of e.g. vanadium antidiabetic complexes at the physiological level, providing clues of their mechanism of action. The present article carries out a bibliographical research emphaticizing the chemical speciation of the vanadium with different amino acids and reviewing also some other important aspects such as its chemistry and therapeutical applications of several vanadium complexes.
在过去30年里,自从发现钒是被囊动物某些酶中以及可能在哺乳动物体内发现的一种辅因子以来,已经开发出了不同的钒基药物用于治疗不同的病症。到目前为止,对某些钒化合物的胰岛素模拟、抗肿瘤和抗寄生虫活性的研究导致了其无机和生物无机化学的极大繁荣。在受控条件下甚至在血浆中对钒与氨基酸的化学形态研究,对于理解例如钒抗糖尿病复合物在生理水平上的生物转化至关重要,为其作用机制提供线索。本文进行了一项文献研究,着重强调了钒与不同氨基酸的化学形态,并回顾了其他一些重要方面,如几种钒配合物的化学及其治疗应用。