Dipartimento di Chimica "U. Schiff", Università di Firenze, Sesto Fiorentino, Italy.
Curr Med Chem. 2010;17(10):915-28. doi: 10.2174/092986710790820697.
2,3-dihydrobenzo[b][1,4]oxathiine represents a valuable pharmacophoric heterocyclic nucleus known since very long time. Initially, together with some patents reporting the use of these compounds as herbicides or lipogenesis inhibitors, several papers reported their ability as melatonin, histamine and serotonin receptor ligands, alpha-adrenoreceptor blockers as well as non-glycoside sweeteners. This wide range of biological activities has been recently further improved by studies stating their activity as antimycotics, multi-defense antioxidants and estrogen receptor ligands. The last insights regarding the preparation, the biological activity and the structure activity relationship (SAR) of derivatives containing the dihydrobenzoxathiine skeleton will be discussed in this review.
2,3-二氢苯并[b][1,4]硫氮杂卓代表了一种有价值的药效团杂环核,很早就为人所知。最初,除了一些专利报道这些化合物可用作除草剂或脂肪生成抑制剂外,还有一些论文报道了它们作为褪黑激素、组胺和血清素受体配体、α-肾上腺素受体阻滞剂以及非糖苷甜味剂的能力。最近的研究进一步表明,它们具有抗真菌、多防御抗氧化剂和雌激素受体配体的活性,从而进一步提高了它们的生物活性。本文综述了含二氢苯并硫氮杂卓骨架的衍生物的制备、生物活性和构效关系(SAR)的最新进展。