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Using fungal naphthopyran-8,9-diones as inhibitors of aspartyl protease, useful for treatment of infection by Candida or human immune deficiency virus

机译:使用真菌萘并吡喃-8,9-二酮作为天冬氨酰蛋白酶的抑制剂,可用于治疗念珠菌或人类免疫缺陷病毒的感染

摘要

Use of laccaridiones (I) as inhibitors of SAP and HIV proteases. Use of laccaridiones of formula (I) as inhibitors of SAP and HIV proteases. [Image] R1 -R3hydroxy, 1-8C alkoxy or 2-8C alkanoyloxy. ACTIVITY : Fungicide; Anti-HIV. MECHANISM OF ACTION : Inhibition of (a) aspartyl proteases and (b) adhesion of Candida to epithelial and/or endothelial cells. Laccaridione B ((I) with R1 = methoxy; R2 = hydroxy and R3 = ethoxy) was tested for inhibition of release of the SAP protease from Candida CBS 5982. It was added every 42 hours and extinction measured at 450 nm. At a concentration of 50 Microg/ml, extinction was about 7% of that in a control. A further test showed that at 50 Microg/ml the same compound had 100% inhibition of adhesion of CBS 5982 to HeLa S3 cells.
机译:laccaridiones(I)作为SAP和HIV蛋白酶抑制剂的用途。式(I)的laccaridiones作为SAP和HIV蛋白酶的抑制剂的用途。 [图像] R1-R3羟基,1-8C烷氧基或2-8C烷酰氧基。活动:杀菌剂;抗艾滋病毒。作用机理:(a)天冬氨酰蛋白酶的抑制和(b)念珠菌对上皮和/或内皮细胞的粘附。测试了Laccaridione B((I),R1 =甲氧基; R2 =羟基,R3 =乙氧基)对SAP蛋白酶从假丝酵母CBS 5982释放的抑制作用。每42小时添加一次,在450 nm处消光。在50微克/毫升的浓度下,消光约为对照组的7%。进一步的测试表明,在50微克/毫升下,相同的化合物对CBS 5982对HeLa S3细胞的粘附具有100%的抑制作用。

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