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碳酸酐酶抑制剂:4-氨磺酰基苯基硫脲文库的首次树脂上筛选

Carbonic anhydrase inhibitors: the first on-resin screening of a 4-sulfamoylphenylthiourea library.

作者信息

Innocenti Alessio, Casini Angela, Alcaro Maria C, Papini Anna M, Scozzafava Andrea, Supuran Claudiu T

机构信息

Laboratory of Bioinorganic Chemistry, Department of Chemistry, University of Florence, Polo Scientifico, Rm. 188, Via della Lastruccia 3, I-50019 Sesto Fiorentino, Italy.

出版信息

J Med Chem. 2004 Oct 7;47(21):5224-9. doi: 10.1021/jm049692i.

Abstract

Sulfonamide carbonic anhydrase (CA) inhibitors are widely employed in the diagnosis and treatment of diverse diseases such as glaucoma and different neuromuscular disorders. Moreover, an emerging area is represented by their use in the prevention and treatment of tumors. In this paper we propose an optimized synthesis of on-resin CA inhibitor libraries to be used for a high-throughput biological screening. A library of 4-sulfamoylphenylthioureas, previously described to be attractive candidates as novel antiglaucoma drugs, has been synthesized by a solid-phase approach, avoiding the formation of thiohydantoin side products. The on-resin screening assay has been developed for the inhibition tests of different CA isozymes with the on-resin supported sulfonamides, allowing the direct identification of the biologically active lead compounds. These results allow the development of new designed libraries in the solid phase of sulfonamide CA inhibitors characterized by a set of prefixed parameters to be used as possible drug candidates.

摘要

磺酰胺碳酸酐酶(CA)抑制剂被广泛应用于青光眼和各种神经肌肉疾病等多种疾病的诊断和治疗。此外,它们在肿瘤预防和治疗方面的应用是一个新兴领域。在本文中,我们提出了一种用于高通量生物筛选的树脂上CA抑制剂文库的优化合成方法。通过固相方法合成了一个4-氨磺酰基苯基硫脲文库,该文库先前被描述为新型抗青光眼药物的有吸引力的候选物,避免了硫代乙内酰脲副产物的形成。已经开发了树脂上筛选测定法,用于用树脂负载的磺酰胺对不同CA同工酶进行抑制试验,从而直接鉴定具有生物活性的先导化合物。这些结果有助于开发以一组预先设定的参数为特征的磺酰胺CA抑制剂固相新设计文库,用作可能的候选药物。

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