Vullo Daniela, Innocenti Alessio, Nishimori Isao, Scozzafava Andrea, Kaila Kai, Supuran Claudiu T
Università degli Studi di Firenze, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, I-50019 Sesto Fiorentino (Firenze), Italy.
Bioorg Med Chem Lett. 2007 Aug 1;17(15):4107-12. doi: 10.1016/j.bmcl.2007.05.052. Epub 2007 May 21.
An activation study of the human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes VII and XIV using a small library of natural/non-natural amino acids and aromatic/heterocyclic amines is reported. hCA VII was efficiently activated by L-/D-His, dopamine and serotonin (K(A)s of 0.71-0.93 microM). The best hCA XIV activators were histamine (K(A) of 10 nM), L-Phe, L-/D-His and 4-amino-L-Phe (K(A)s of 0.24-2.90 microM). In view of the significant expression levels of CA VII and CA XIV in the brain, selective activation of these isoforms may be useful when developing pharmacologic agents for the management of major disorders such as epilepsy and Alzheimer's disease.
报道了一项使用天然/非天然氨基酸和芳香/杂环胺的小型文库对人类碳酸酐酶(hCA,EC 4.2.1.1)同工酶VII和XIV进行的激活研究。hCA VII被L-/D-组氨酸、多巴胺和血清素有效激活(K(A)为0.71 - 0.93 microM)。最佳的hCA XIV激活剂是组胺(K(A)为10 nM)、L-苯丙氨酸、L-/D-组氨酸和4-氨基-L-苯丙氨酸(K(A)为0.24 - 2.90 microM)。鉴于CA VII和CA XIV在大脑中的显著表达水平,在开发用于治疗癫痫和阿尔茨海默病等主要疾病的药物时,选择性激活这些同工型可能是有用的。