Design, Synthesis and In Vitro Evaluation of Spirooxindole-Based Phenylsulfonyl Moiety as a Candidate Anti-SAR-CoV-2 and MERS-CoV-2 with the Implementation of Combination Studies

被引:13
作者
Barakat, Assem [1 ]
Mostafa, Ahmed [2 ]
Ali, M. [1 ]
Al-Majid, Abdullah Mohammed [1 ]
Domingo, Luis R. [3 ]
Kutkat, Omnia [2 ]
Moatasim, Yassmin [2 ]
Zia, Komal [4 ]
Ul-Haq, Zaheer [4 ,5 ]
Elshaier, Yaseen A. M. M. [6 ]
机构
[1] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia
[2] Natl Res Ctr, Ctr Sci Excellence Influenza Viruses, Giza 12622, Egypt
[3] Univ Valencia, Dept Organ Chem, Dr Moliner 50, Valencia 46100, Spain
[4] Univ Karachi, Dr Panjwani Ctr Mol Med & Drug Res, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[5] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan
[6] Univ Sadat City, Fac Pharm, Dept Organ & Med Chem, Menoufia 32958, Egypt
关键词
spirooxindole; SARS-CoV-2; drug combination protocol; molecular dynamic simulation (MDS); ADMET; REVERSE-TRANSCRIPTASE; WILD-TYPE; DERIVATIVES; POTENT; PROTEASE; INHIBITORS; COVID-19; INDOLYLARYLSULFONES; DISCOVERY; DOCKING;
D O I
10.3390/ijms231911861
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 search for an effective anti-viral to inhibit COVID-19 is a challenge for the specialized scientific research community. This work investigated the anti-coronavirus activity for spirooxindole-based phenylsulfone cycloadducts in a single and combination protocols. The newly designed anti-SARS-CoV-2 therapeutics spirooxindoles synthesized by [3 + 2] cycloaddition reactions represent an efficient approach. One-pot multicomponent reactions between phenyl vinyl sulfone, substituted isatins, and amines afforded highly stereoselective anti-SARS-CoV-2 therapeutics spirooxindoles with three stereogenic centers. Herein, the newly synthesized spirooxindoles were assessed individually against the highly pathogenic human coronaviruses and proved to be highly potent and safer. Interestingly, the synergistic effect by combining the potent, tested spirooxindoles resulted in an improved antiviral activity as well as better host-cell safety. Compounds 4i and 4d represented the most potent activity against MERS-CoV with IC50 values of 11 and 23 mu M, respectively. Both compounds 4c and 4e showed equipotent activity with the best IC50 against SARS-CoV-2 with values of 17 and 18 mu M, respectively, then compounds 4d and 4k with IC50 values of 24 and 27 mu M, respectively. Then, our attention oriented to perform a combination protocol as anti-SARS-CoV-2 for the best compounds with a different binding mode and accompanied with different pharmacophores. Combination of compound 4k with 4c and combination of compounds 4k with 4i proved to be more active and safer. Compounds 4k with 4i displayed IC50 = 3.275 mu M and half maximal cytotoxic-concentration CC50 = 11832 mu M. MD simulation of the most potential compounds as well as in silico ADMET properties were investigated. This study highlights the potential drug-like properties of spirooxindoles as a cocktail anti-coronavirus protocol.
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页数:19
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