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.
引用
收藏
页数:19
相关论文
共 56 条
  • [1] Coronavirus Disease (COVID-19) Control between Drug Repurposing and Vaccination: A Comprehensive Overview
    Al-Karmalawy, Ahmed A.
    Soltane, Raya
    Abo Elmaaty, Ayman
    Tantawy, Mohamed A.
    Antar, Samar A.
    Yahya, Galal
    Chrouda, Amani
    Pashameah, Rami Adel
    Mustafa, Muhamad
    Abu Mraheil, Mobarak
    Mostafa, Ahmed
    [J]. VACCINES, 2021, 9 (11)
  • [2] Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphone Function
    Al-Majid, Abdullah Mohammed
    Soliman, Saied M.
    Haukka, Matti
    Ali, M.
    Islam, Mohammad Shahidul
    Shaik, Mohammed Rafi
    Barakat, Assem
    [J]. SYMMETRY-BASEL, 2020, 12 (08): : 1 - 15
  • [3] Synthesis and characterization of a spiroindolone pyrothiazole analog via X-ray, biological, and computational studies
    Altowyan, Mezna Saleh
    Atef, Saleh
    Al-Agamy, Mohamed H.
    Soliman, Saied M.
    Ali, M.
    Shaik, Mohammed Rafi
    Choudhary, M. Iqbal
    Ghabbour, Hazem A.
    Barakat, Assem
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2019, 1186 : 384 - 392
  • [4] Vaccine hesitancy: a generation at risk
    不详
    [J]. LANCET CHILD & ADOLESCENT HEALTH, 2019, 3 (05) : 281 - 281
  • [5] Design, Synthesis, Chemical and Biochemical Insights Into Novel Hybrid Spirooxindole-Based p53-MDM2 Inhibitors With Potential Bcl2 Signaling Attenuation
    Aziz, Yasmine M. Abdel
    Lotfy, Gehad
    Said, Mohamed M.
    El Ashry, El Sayed H.
    El Tamany, El Sayed H.
    Soliman, Saied M.
    Abu-Serie, Marwa M.
    Teleb, Mohamed
    Yousuf, Sammer
    Doemling, Alexander
    Domingo, Luis R.
    Barakat, Assem
    [J]. FRONTIERS IN CHEMISTRY, 2021, 9
  • [6] Determination of potential inhibitors based on isatin derivatives against SARS-CoV-2 main protease (mpro): a molecular docking, molecular dynamics and structure-activity relationship studies
    Badavath, Vishnu Nayak
    Kumar, Akhil
    Samanta, Pralok K.
    Maji, Siddhartha
    Das, Anik
    Blum, Galia
    Jha, Anjali
    Sen, Anik
    [J]. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2022, 40 (07) : 3110 - 3128
  • [7] Barakat A., 2021, Med. J, V3, P104, DOI [10.2991/dsahmj.k.210810.001, DOI 10.2991/DSAHMJ.K.210810.001]
  • [8] Design and synthesis of new substituted spirooxindoles as potential inhibitors of the MDM2-p53 interaction
    Barakat, Assem
    Islam, Mohammad Shahidul
    Ghawas, Hussien Mansur
    Al-Majid, Abdullah Mohammed
    El-Senduny, Fardous F.
    Badria, Farid A.
    Elshaier, Yaseen A. M. M.
    Ghabbour, Hazem A.
    [J]. BIOORGANIC CHEMISTRY, 2019, 86 : 598 - 608
  • [9] Substituted spirooxindole derivatives as potent anticancer agents through inhibition of phosphodiesterase 1
    Barakat, Assem
    Islam, Mohammad Shahidul
    Ghawas, Hussien Mansur
    Al-Majid, Abdullah Mohammed
    El-Senduny, Fardous F.
    Badria, Farid A.
    Elshaier, Yaseen A. M. M.
    Ghabbour, Hazem A.
    [J]. RSC ADVANCES, 2018, 8 (26) : 14335 - 14346
  • [10] Arbidol:: A broad-spectrum antiviral compound that blocks viral fusion
    Boriskin, Y. S.
    Leneva, I. A.
    Pecheur, E. -I.
    Polyak, S. J.
    [J]. CURRENT MEDICINAL CHEMISTRY, 2008, 15 (10) : 997 - 1005