2,4-Dihydroxycinnamic acid as spike ACE2 inhibitor and apigenin as RdRp inhibitor in Nimbamritadi Panchatiktam Kashayam against COVID-19: an in silico and in vitro approach

被引:4
|
作者
Murali, Maneesha [1 ,2 ]
Nair, Bhagyalakshmi [1 ,2 ]
Vishnu, V. R. [3 ]
Aneesh, T. P. [3 ]
Nath, Lekshmi R. [1 ]
机构
[1] Amrita Vishwa Vidyapeetham, Dept Pharmacognosy, Amrita Sch Pharm, AIMS Hlth Sci Campus, Kochi 682041, Kerala, India
[2] Amrita Vishwa Vidyapeetham, Dept Pharmacol, Amrita Sch Pharm, AIMS Hlth Sci Campus, Kochi 682041, Kerala, India
[3] Amrita Vishwa Vidyapeetham, Dept Pharmaceut Chem, Amrita Sch Pharm, AIMS Hlth Sci Campus, Kochi 682041, Kerala, India
关键词
Nimbamritadi Panchatiktam Kashayam; Spike ACE2; Viral replication; Pseudovirus inhibition assay; MOLECULAR DOCKING;
D O I
10.1007/s11030-022-10552-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nimbamritadi Panchatiktam Kashayam (NPK) is an ayurvedic formulation composed of ingredients with potent anti-viral activities. We studied the interaction energy of 144 phytoconstituents present in NPK against spike receptor-binding domain (RBD) complexed with ACE2 protein (PDB ID: 6LZG) and RNA-dependent RNA polymerase protein (PDB ID: 7BTF) using Biovia Drug Discovery studio. The result indicated that 2,4-hydroxycinnamic acid exerts more significant binding affinities (28.43 kcal/mol) than Umifenovir (21.24 kcal/mol) against spike ACE2. Apigenin exhibited the highest binding affinities (54.63 kcal/mol) compared with Remdesivir (24.52 kcal/mol) against RdRp. An in vitro analysis showed a reduction in the number of lentiviral particles on transfected HEK293T-hACE2 cells as assessed by pseudovirus inhibition assay. At the same time, the tested compounds showed non-toxic up to 100 mu g/ml in normal cells by MTT assay. The study highlights the plausible clinical utility of this traditional medicine against SARS CoV2. [GRAPHICS] .
引用
收藏
页码:2353 / 2363
页数:11
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