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Vanadium: History, chemistry, interactions with α-amino acids and potential therapeutic applications.
Del Carpio, Edgar; Hernández, Lino; Ciangherotti, Carlos; Villalobos Coa, Valentina; Jiménez, Lissette; Lubes, Vito; Lubes, Giuseppe.
Afiliación
  • Del Carpio E; Laboratorio de Equilibrios en Solución, Universidad Simón Bolívar (USB), Apartado 89000, Caracas 1080 A, Venezuela.
  • Hernández L; Unidad de Química Medicinal, Facultad de Farmacia, Escuela "Dr. Jesús María Bianco", Universidad Central de Venezuela, Venezuela.
  • Ciangherotti C; Laboratorio de Equilibrios en Solución, Universidad Simón Bolívar (USB), Apartado 89000, Caracas 1080 A, Venezuela.
  • Villalobos Coa V; Escuela de Quimica, Facultad de Ciencias, Universidad Central de Venezuela, Venezuela.
  • Jiménez L; Laboratorio de Neuropéptidos, Facultad de Farmacia, Escuela "Dr. Jesús María Bianco", Universidad Central de Venezuela, Venezuela.
  • Lubes V; Laboratorio de Bioquímica, Facultad de Farmacia, Escuela "Dr. Jesús María Bianco", Universidad Central de Venezuela, Venezuela.
  • Lubes G; Laboratorio de Equilibrios en Solución, Universidad Simón Bolívar (USB), Apartado 89000, Caracas 1080 A, Venezuela.
Coord Chem Rev ; 372: 117-140, 2018 Oct 01.
Article en En | MEDLINE | ID: mdl-32226092
ABSTRACT
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 in vitro 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.
Palabras clave
2,2'-bipy, 2,2-bipyridine; 6-mepic, 6-methylpicolinic acid; Ad, adenosine; Ala, alanine; Ala-Gly, alanylglycine; Ala-His, alanylhistidine; Ala-Ser, alanylserine; Amino acids; Antidiabetics; Antitumors; Asp, aspartic acid; BEOV, bis(ethylmaltolate)oxovanadium(IV); Chemical speciation; Cys, cysteine; Cyt, citrate; DMF, N,N-dimethylformamide; DNA, deoxyribonucleic acid; EPR, Electron Paramagnetic Resonance; G, Gauss; Glu, glutamic acid; Gly, glycine; GlyAla, glycylalanine; GlyGly, glycylglycine; GlyGlyCys, glycylglycylcysteine; GlyGlyGly, glycylglycylglycine; GlyGlyHis, glycylglycylhistidine; GlyPhe, glycylphenylalanine; GlyTyr, glycyltyrosine; GlyVal, glycylvaline; HIV, human immunodeficiency virus; HSA, albumin; Hb, hemoglobin; His, histidine; HisGlyGly, histidylglycylglycine; Ig, immunoglobulins; Im, imidazole; L-Glu(γ)HXM, l-glutamic acid γ-monohydroxamate; LD50, the amount of a toxic agent (such as a poison, virus, or radiation) that is sufficient to kill 50 percent of population of animals; Lac, lactate; MeCN, acetonitrile; NADH and NAD+, nicotinamide adenine dinucleotide; NEP, neutral endopeptidas; NMR, Nuclear Magnetic Resonance; Ox, oxalate; PI3K, phosphoinositide 3-kinase; PTP1B, protein tyrosine phosphatase 1B; Pic, picolinic acid; Pro, proline; Pro-Ala, prolylalanine; RNA, ribonucleic acid; SARS, severe acute respiratory syndrome; Sal-Ala, N-salicylidene-l-alaninate; SalGly, salicylglycine; SalGlyAla, salicylglycylalanine; Ser, serine; T, Tesla; THF, tetrahydrofuran; Thr, threonine; VBPO, vanadium bromoperoxidases; VanSer, Schiff base formed from o-vanillin and l-serine; Vanadium complexes; acac, acetylacetone; dhp, 1,2-dimethyl-3-hydroxy-4(1H)-pyridinone; dipic, dipicolinic acid; dmpp, 1,2-dimethyl-3-hydroxy-4-pyridinonate; hTf, transferring; hpno, 2-hydroxypyridine-N-oxide; l.m.m., low molecular mass; mal, maltol; py, pyridine; sal-l-Phe, N-salicylidene-l-tryptophanate; salGlyGly, N-salicylideneglycylglycinate; salSer, N-salicylideneserinate; salTrp, N-salicylidene-L tryptophanate; salVal, N-salicylidene-l-valinate; salophen, N,N'-bis(salicylidene)-o-phenylenediamine; saltrp, N-salicylidene-l-tryptophanate; γ-PGA, poly-γ-glutamic acid

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Coord Chem Rev Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Coord Chem Rev Año: 2018 Tipo del documento: Article