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首页> 外文期刊>Turkish journal of chemistry >Synthesis, and prediction of molecular properties and antimicrobial activity of some acylhydrazones derived from $N$-(arylsulfonyl)methionine
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Synthesis, and prediction of molecular properties and antimicrobial activity of some acylhydrazones derived from $N$-(arylsulfonyl)methionine

机译:$ N $-(芳基磺酰基)蛋氨酸衍生的某些酰基hydr的合成,分子性质和抗菌活性的预测

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摘要

A series of 38 new acylhydrazones [ 3 - 40 ], derived from (2$S)$-4-(methylsulfanyl)-2-[[(4-methylphenyl)sulfonyl] amino]butanoic acid hydrazide [ 2 ], were synthesized and evaluated for their anti-HIV and antimicrobial activity with the further aim to develop acylhydrazones carrying an amino acid side chain. All tested compounds possess stronger activity against gram (+) bacteria. Compound 23 was found active against methicillin-resistant Staphylococcus aureus (MRSA) with a MIC value of 3.9 $mu $g/mL. The MIC value of compound 30 against Enterococcus faecalis , Listeria monocytogenes , and Bacillus cereus was 8 $mu $g/mL. A computational study for prediction of ADME and drug-like properties (solubility, drug-likeness, and drug score) as well as potential toxicity profiles of compounds 2 - 40 was performed using the Molinspiration online property calculation toolkit and Osiris Property Explorer. As most of our compounds meet Lipinski's rule of five, they promise good solubility and permeability. According to Osiris calculations, the majority of our compounds are supposed to be nonmutagenic and nonirritating.
机译:合成了一系列由(2 $ S)$-4-(methylsulfanyl)-2-[[[(4-methylphenyl)磺酰基]氨基]丁酸酰肼[2]衍生的新酰基hydr [3-40],并评估其抗HIV和抗菌活性,其进一步目的是开发带有氨基酸侧链的酰基hydr。所有测试的化合物对革兰氏阳性菌都有更强的活性。发现化合物23对耐甲氧西林的金黄色葡萄球菌(MRSA)具有活性,其MIC值为3.9μg/ g / mL。化合物30对粪肠球菌,单核细胞增生性李斯特菌和蜡状芽孢杆菌的MIC值为8μg/μg/ mL。使用Molinspiration在线属性计算工具包和Osiris Property Explorer,对ADME和类药物特性(溶解度,类药物和药物评分)以及化合物2-40的潜在毒性特征进行了预测研究。由于我们的大多数化合物都符合Lipinski的五个规则,因此它们具有良好的溶解性和渗透性。根据奥西里斯(Osiris)的计算,我们大多数化合物被认为是非诱变和无刺激性的。

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