Mangiferin from Enicostemma littorale Blume with in silico and in vitro anti-inflammatory potential

被引:4
作者
Kumar, Niraj [1 ,2 ]
Tripathi, Nancy [3 ]
Kumar, Sanjeev [4 ]
Kushwaha, Manoj [5 ]
Banerjee, Chiranjib [6 ]
Dey, Swapan [1 ,7 ]
机构
[1] Indian Inst Technol ISM, Dept Chem & Chem Biol, Dhanbad, India
[2] Cadila Pharmaceut Ltd, Alunedabad 380050, India
[3] IIT BHU, Dept Pharmaceut Engn & Technol, Varanasi, India
[4] Banaras Hindu Univ, Inst Med Sci, Varanasi, India
[5] Indian Inst Integrat Med, Fermentat & Microbial Biotechnol Div, CSIR, Jammu, India
[6] Gurukula Kangri, Dept Bot & Microbiol, Haridwar, India
[7] Indian Inst Technol ISM, Dept Chem & Chem Biol, Dhanbad 826004, Jharkhand, India
关键词
Anti-inflammatory; COX; Enicostemma littorale; mangiferin; swertiamarin; EXTRACT;
D O I
10.1080/07391102.2023.2253914
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
The bioassay-guided fractionation of the extract of aerial parts of Enicostemma littorale resulted in two fractions 3 and 4 with moderate and potent antioxidant activity, respectively. The purification of fraction 3 gave swertiamarin (1), while the LCMS profile of fraction 4 unveiled the presence of another constituent along with swertiamarin. The extensive purification of fraction 4 led to the unusual isolation of mangiferin (2) from E. littorale. The uncommon isolation of mangiferin from E. littorale motivated us to conduct its in silico and in vitro screening as an anti-inflammatory agent. Both studies have proved mangiferin to be a promising anti-inflammatory molecule with a binding energy of 9.17kcal/mol against Cyclooxygenase-2 protein and IC50 of 146.07 nanomolar. This study is the first report of the isolation of mangiferin, a xanthone glycoside from E. littorale.
引用
收藏
页码:9939 / 9948
页数:10
相关论文
共 32 条
[1]  
Ahmed M. F., 2012, International Journal of Pharmaceutical Applications, V3, P271
[2]   Structural insights into conformational stability of both wild-type and mutant EZH2 receptor [J].
Aier, Imlimaong ;
Varadwaj, Pritish Kumar ;
Raj, Utkarsh .
SCIENTIFIC REPORTS, 2016, 6
[3]   LIPIDS COX-2's new role in inflammation [J].
Chen, Chu .
NATURE CHEMICAL BIOLOGY, 2010, 6 (06) :401-402
[4]   Analgesic and antioxidant activity of mangiferin and its derivatives: the structure activity relationship [J].
Dar, A ;
Faizi, S ;
Naqvi, S ;
Roome, T ;
Zikr-ur-Rehman, S ;
Ali, M ;
Firdous, S ;
Moin, ST .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (04) :596-600
[5]  
Dassault Systemes, 2021, BIOVIA DASS SYST DIS
[6]   Mangiferin: An effective therapeutic agent against several disorders [J].
Du, Suya ;
Liu, Huirong ;
Lei, Tiantian ;
Xie, Xiaofang ;
Wang, Hailian ;
He, Xia ;
Tong, Rongsheng ;
Wang, Yi .
MOLECULAR MEDICINE REPORTS, 2018, 18 (06) :4775-4786
[7]   Molecular dynamics simulations and drug discovery [J].
Durrant, Jacob D. ;
McCammon, J. Andrew .
BMC BIOLOGY, 2011, 9
[8]   Temperature and solvent dependent NMR studies on mangiferin and complete NMR spectral assignments of its acyl and methyl derivatives [J].
Faizi, Shaheen ;
Zikr-ur-Rehman, Sadia ;
Ali, Muhammad ;
Naz, Aneela .
MAGNETIC RESONANCE IN CHEMISTRY, 2006, 44 (09) :838-844
[9]   Design, synthesis and bioactivity study of N-salicyloyl tryptamine derivatives as multifunctional agents for the treatment of neuroinflammation [J].
Fan, Xiaohong ;
Li, Junfang ;
Deng, Xuemei ;
Lu, Yingmei ;
Feng, Yiyue ;
Ma, Shumeng ;
Wen, Huaixiu ;
Zhao, Quanyi ;
Tan, Wen ;
Shi, Tao ;
Wang, Zhen .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 193
[10]   New insights into the role of COX 2 in inflammation [J].
Gilroy, DW ;
Colville-Nash, PR .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2000, 78 (03) :121-129