Isolation and In Silico Anti-SARS-CoV-2 Papain-Like Protease Potentialities of Two Rare 2-Phenoxychromone Derivatives from Artemisia spp.

被引:27
作者
Suleimen, Yerlan M. [1 ,2 ]
Jose, Rani A. [3 ]
Suleimen, Raigul N. [4 ]
Arenz, Christoph [5 ]
Ishmuratova, Margarita [6 ]
Toppet, Suzanne [3 ]
Dehaen, Wim [3 ]
Alsfouk, Aisha A. [7 ]
Elkaeed, Eslam B. [8 ]
Eissa, Ibrahim H. [9 ]
Metwaly, Ahmed M. [10 ,11 ]
机构
[1] Int Ctr Interdisciplinary Solut Antibiot & Sec, Republ Collect Microorgan, Nur Sultan 010000, Kazakhstan
[2] Sh Ualikhanov Kokshetau Univ, Lab Engn Profile NMR Spect, Kokshetau 020000, Kazakhstan
[3] Katholieke Univ Leuven, Dept Chem, Mol Design & Synth, B-3001 Heverlee, Belgium
[4] LN Gumilyov Eurasian Natl Univ, Fac Syst Phys, Dept Nat Sci, Nur Sultan 010010, Kazakhstan
[5] Univ Berlin, Inst Chem Humboldt, D-12489 Berlin, Germany
[6] EA Buketov Karaganda Univ, Dept Bot, Karaganda 100024, Kazakhstan
[7] Princess Nourah Bint Abdulrahman Univ, Coll Pharm, Dept Pharmaceut Sci, POB 84428, Riyadh 11671, Saudi Arabia
[8] Al Maarefa Univ, Coll Pharm, Dept Pharmaceut Sci, Riyadh 13713, Saudi Arabia
[9] Al Azhar Univ, Fac Pharm Boys, Pharmaceut Med Chem & Drug Design Dept, Cairo 11884, Egypt
[10] Al Azhar Univ, Fac Pharm Boys, Pharmacognosy & Med Plants Dept, Cairo 11884, Egypt
[11] City Sci Res & Technol Applict SRTA, Genet Engn & Biotechnol Res Inst, Biopharmaceut Prod Res Dept, Alexandria 21934, Alexandria, Egypt
关键词
Artemisia commutate; 2-phenoxychromones; SARS-CoV-2; COVID-19 Papain-Like Protease; molecular docking; molecular fingerprints; ADMET; MD simulations; ALPHA-PYRONE DERIVATIVES; MOLECULAR-DYNAMICS; ANTIMICROBIAL ACTIVITY; ESSENTIAL OILS; COMPONENT COMPOSITION; BIOLOGICAL-ACTIVITY; DOCKING; CONSTITUENTS; SIMULATIONS; FLAVONOIDS;
D O I
10.3390/molecules27041216
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
Two rare 2-phenoxychromone derivatives, 6-demethoxy-4`-O-capillarsine (1) and tenuflorin C (2), were isolated from the areal parts of Artemisia commutata and A. glauca, respectively, for the first time. Being rare in nature, the inhibition potentialities of 1 and 2 against SARS-CoV-2 was investigated using multistage in silico techniques. At first, molecular similarity and fingerprint studies were conducted for 1 and 2 against co-crystallized ligands of eight different COVID-19 enzymes. The carried-out studies indicated the similarity of 1 and 2 with TTT, the co-crystallized ligand of COVID-19 Papain-Like Protease (PLP), (PDB ID: 3E9S). Therefore, molecular docking studies of 1 and 2 against the PLP were carried out and revealed correct binding inside the active site exhibiting binding energies of -18.86 and -18.37 Kcal/mol, respectively. Further, in silico ADMET in addition to toxicity evaluation of 1 and 2 against seven models indicated the general safety and the likeness of 1 and 2 to be drugs. Lastly, to authenticate the binding and to investigate the thermodynamic characters, molecular dynamics (MD) simulation studies were conducted on 1 and PLP.
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页数:18
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