The Importance of Being Casiopeina as Polypharmacologycal Profile (Mixed Chelate-Copper (II) Complexes and Their In Vitro and In Vivo Activities)

被引:18
作者
Aguilar-Jimenez, Zenayda [1 ]
Espinoza-Guillen, Adrian [1 ]
Resendiz-Acevedo, Karen [1 ]
Fuentes-Noriega, Ines [2 ]
Mejia, Carmen [3 ]
Ruiz-Azuara, Lena [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Chem, Inorgan Chem Dept, Av Univ 3000,Circuito Exterior S-N,CU, Mexico City 04510, Mexico
[2] Univ Nacl Autonoma Mexico, Pharm Dept, Av Univ 3000,Circuito Exterior S-N,CU, Mexico City 04510, Mexico
[3] Univ Queretaro, Fac Nat Sciencies, Interdisciplinary Biomed Lab, Juriquilla 76230, Queretaro, Mexico
关键词
cancer; copper; antiparasitic; antiviral; drug delivery; Casiopeinas (R); MITOCHONDRIAL PERMEABILITY TRANSITION; CANCER-THERAPY; DNA-BINDING; COORDINATION-COMPLEXES; MOLECULAR-MECHANISMS; ANTICANCER AGENT; ARSENIC TRIOXIDE; CISPLATIN; CELLS; APOPTOSIS;
D O I
10.3390/inorganics11100394
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this review, we present a timeline that shows the origin of mixed chelate copper (II) complexes, registered as Mark Title Casiopeinas (R), as the first copper (II) compounds proposed as anticancer drugs in 1988 and 1992. In the late twentieth century, the use of essential metals as anticancer agents was not even considered, except for their antifungal or antibacterial effects; also, copper, as gold salts, was used for arthritis problems. The use of essential metals as anticancer drugs to diminish the secondary toxic effects of Cisplatin was our driving force: to find less toxic and even more economical compounds under the rational design of metal chelate complexes. Due to their chemical properties, copper compounds were the choice to continue anticancer drug development. In this order of ideas, the rational designs of mixed chelate-copper (II) complexes (Casiopeinas, (Cas) homoleptic or heteroleptic, depending on the nature of the secondary ligand) were synthesized and fully characterized. In the search for new, more effective, and less toxic drugs, Casiopeina (R) (Cas) emerged as a family of approximately 100 compounds synthesized from coordinated Cu(II) complexes with proven antineoplastic potential through cytotoxic action. The Cas have the general formula [Cu(N-N)(N-O)]NO3 and [Cu(N-N)(O-O)]NO3, where N-N is an aromatic substituted diimine (1,10-phenanthroline or 2,2 '-bipyridine), and the oxygen donor (O-O) is acetylacetonate or salicylaldehyde. Lately, some similar compounds have been developed by other research groups considering a similar hypothesis after Casiopeina's discoveries had been published, as described herein. As an example of translational medicine criteria, we have covered each step of the established normative process for drug development, and consequently, one of the molecules (Casiopeina III ia (CasIIIia)) has reached the clinical phase I. For these copper compounds, other activities, such as antibacterial, antiparasitic and antiviral, have been discovered.
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页数:23
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