Process to obtain new mixed copper aminoacidate complexes from phenanthrolines and their alkyl derivatives to be used as anticancerigenic agents
申请人:UNIVERSIDAD NACIONAL AUTONOMA DE MEXICO
公开号:EP0434445A2
公开(公告)日:1991-06-26
This invention refers to a process to obtain new mixed copper aminoacidates from phenanthrolines and their alkyl derivates of an aromatic type to be used as anticancerigenic, agents preferably with a therapeutic use for the treatment of liquid and solid cancerigenic tumours such as leukemia. The complexes obtained are of the [Cu (N-N) (N-O)]⁺⁻ NO₃ type in which the N-N ligand corresponds to 4, 7-dimethyl-1, 10 phenanthroline and the N-O ligand preferably correponds to one of the aminoacidates such as tyrosine-alaninate, treoninate, triptophanate, valinate, isoleucinate, cisteinate, diglycinate, phenylalaninate, glycinate, hystidinate, serinate, tyrosinate, aspartate, alaninate and phenylalaninate. The process is characterized because it includes the following steps: making an aqueous solution based on an aliphatic alcohol and 4, 7-dimethyl-1, 10 phenanthroline react with a copper complex preferably CuNO₃5H₂O at room temperature, and immediately after making the obtained product react in an aqueous aminoacidate solution adjusting a slightly alkaline pH.
本发明涉及一种从
菲罗啉及其芳香族烷基衍
生物中获得新的混合
氨基酸铜的工艺,该工艺可用作抗癌剂,优选用于治疗液态和固态致癌肿瘤,如白血病。所获得的配合物为[Cu (N-N) (N-O)]⁺- NO₃型,其中 N-N
配体对应于 4,7-二甲基-1,10-
菲罗啉,N-O
配体最好对应于
氨基酸盐之一,如
酪氨酸丙
氨酸盐、曲安酸盐、三色
氨酸盐、
氨酸、三色
氨酸、缬
氨酸、
异亮氨酸、
肌氨酸、二甘
氨酸、苯丙
氨酸、甘
氨酸、胱
氨酸、
丝氨酸、
酪氨酸、天门冬
氨酸、丙
氨酸和苯丙
氨酸。该工艺的特点是包括以下步骤:在室温下,使基于
脂肪醇和 4,7-二甲基-1,10-
菲罗啉的
水溶液与
铜络合物(最好是 CuNO₃5H₂O)反应,然后立即使得到的产物在调节 pH 值为微碱性的
氨基酸水溶液中反应。