Agarwal Ankita, Paliwal Sarvesh, Mishra Ruchi, Sharma Swapnil, Kumar Dwivedi Anil, Tripathi Renu, Gunjan Sarika
Department of Pharmacy, Banasthali University, Rajasthan, 304022, India.
Pharmaceutics Division, CSIR- Central Drug Research Institute (CSIR-CDRI), Sector 10, Jankipuram Extension, Sitapur Road, Lucknow, 226031, India.
Sci Rep. 2015 Sep 8;5:13838. doi: 10.1038/srep13838.
In recent years the DNA minor groove has attracted much attention for the development of anti-malarial agents. In view of this we have attempted to discover novel DNA minor groove binders through in-silico and in-vitro workflow. A rigorously validated pharmacophore model comprising of two positive ionizable (PI), one hydrophobic (HY) and one ring aromatic (RA) features was used to mine NCI chemical compound database. This led to retrieval of many hits which were screened on the basis of estimated activity, fit value and Lipinski's violation. Finally two compounds NSC639017 and NSC371488 were evaluated for their in-vitro anti-malarial activities against Plasmodium falciparum 3D7 (CQ sensitive) and K1 (CQ resistant) strains by SYBR green-I based fluorescence assay. The results revealed that out of two, NSC639017 posses excellent anti-malarial activity particularly against chloroquine resistant strain and moreover NSC639017 also appeared to be safe (CC50 126.04 μg/ml) and selective during cytotoxicity evaluation.
近年来,DNA小沟在抗疟药物的研发中备受关注。鉴于此,我们尝试通过计算机模拟和体外实验流程来发现新型DNA小沟结合剂。使用一个经过严格验证的药效团模型,该模型包含两个可电离的正电荷(PI)、一个疏水性(HY)和一个环状芳香性(RA)特征,用于挖掘美国国立癌症研究所(NCI)化合物数据库。这导致检索到许多命中化合物,这些化合物根据估计活性、拟合值和违反Lipinski规则的情况进行筛选。最后,通过基于SYBR Green-I的荧光测定法,评估了两种化合物NSC639017和NSC371488对恶性疟原虫3D7(氯喹敏感)和K1(氯喹耐药)菌株的体外抗疟活性。结果显示,在这两种化合物中,NSC639017具有出色的抗疟活性,尤其是对氯喹耐药菌株,此外,在细胞毒性评估中,NSC639017似乎也是安全的(CC50为126.04μg/ml)且具有选择性。