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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >2,3-Disubstituted-1,4-naphthoquinones, 12H-benzo(b)phenothiazine-6,11-diones and related compounds: synthesis and biological evaluation as potential antiproliferative and antifungal agents.
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2,3-Disubstituted-1,4-naphthoquinones, 12H-benzo(b)phenothiazine-6,11-diones and related compounds: synthesis and biological evaluation as potential antiproliferative and antifungal agents.

机译:2,3-二取代-1,4-萘醌,12H-苯并(b)吩噻嗪-6,11-二酮及相关化合物:合成和生物学评估为潜在的抗增殖和抗真菌剂。

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摘要

A series of 2-chloro-3-arylsulfanyl-[1,4]naphthoquinones (2), 2,3-bis-arylsulfanyl-[1,4]naphthoquinones (3) and 12H-benzo[b]phenothiazine-6,11-diones and their analogs 6-8 were synthesized and evaluated for their antiproliferative activity against human cervical cancer (HeLa) cells. Compounds 3a and 3b were found to possess most potent antiproliferative and cell killing ability. Compounds 1-8 were also evaluated for antifungal activities. The structure-activity relationship of these compounds was studied and the results show that compound 2a (MIC(50)=1.56 microg/mL) exhibited in vitro potent antifungal activity compared to the clinically useful antifungal drug Fluconazole (MIC(50)=2.0 microg/mL) against Sporothrix. schenckii. Compound 2a (MIC(50)=1.56 microg/mL) also exhibited same antifungal activity compared to clinically useful drug Amphotericin-B (MIC(50)=1.56 microg/mL) against Trichophyton. mentagraphytes.
机译:一系列2-氯-3-芳基硫烷基-[1,4]萘醌(2),2,3-双-芳基硫烷基-[1,4]萘醌(3)和12H-苯并[b]吩噻嗪-6,11合成了二酮及其类似物6-8,并评估了其对人宫颈癌(HeLa)细胞的抗增殖活性。发现化合物3a和3b具有最有效的抗增殖和细胞杀伤能力。还评估了化合物1-8的抗真菌活性。研究了这些化合物的结构活性关系,结果表明与临床上有用的抗真菌药物氟康唑(MIC(50)= 2.0 microg)相比,化合物2a(MIC(50)= 1.56 microg / mL)表现出体外有效的抗真菌活性。 / mL)。申克化合物2a(MIC(50)= 1.56 microg / mL)与针对Trichophyton的临床有用药物两性霉素B(MIC(50)= 1.56 microg / mL)相比也显示出相同的抗真菌活性。薄荷油。

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