Evidence map›Paper›PMID 36101854›Full record

ArticleJournal of molecular liquids2022

SARS-CoV-2 main protease (3CL

Sonaimuthu Mohandoss, Ramaraj Sukanya, Sivarasan Ganesan, Fatemah H Alkallas, Amira Ben Gouider Trabelsi, Fedor V Kusmartsev, Kuppu Sakthi Velu, Thambusamy Stalin, Huang-Mu Lo, Yong Rok Lee

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular liquids, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Prediction of Drug-Target Affinity Using Attention Neural Network.International journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 5 countries.

Sonaimuthu MohandossSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Ramaraj SukanyaSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Sivarasan GanesanDepartment of Environmental Engineering and Management, Chaoyang University of Technology, Taichung 41349, Taiwan.
Fatemah H AlkallasDepartment of Physics, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Amira Ben Gouider TrabelsiDepartment of Physics, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Fedor V KusmartsevDepartment of Physics, Khalifa University of Science and Technology, Abu Dhabi 127788, United Arab Emirates.
Kuppu Sakthi VeluDepartment of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630003, Tamilnadu, India.
Thambusamy StalinDepartment of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630003, Tamilnadu, India.
Huang-Mu LoDepartment of Environmental Engineering and Management, Chaoyang University of Technology, Taichung 41349, Taiwan.
Yong Rok LeeSchool of Chemical Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Yeungnam University · KRAlagappa University · INChaoyang University of Technology · TWPrincess Nourah bint Abdulrahman University · SAKhalifa University of Science and Technology · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the current outbreak of the novel coronavirus disease 2019 (COVID-19), researchers have examined several antiviral drugs with the potential to inhibit the proliferation of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The antiviral drug acyclovir (AVR), which is used to treat COVID-19, in complex with methyl-β-cyclodextrin (Mβ-CD) was examined in the solution and solid phases. UV-visible and fluorescence spectroscopic analyses confirmed that the guest (AVR) was included inside the host (Mβ-CD) cavity. A solid inclusion complex of AVR was prepared by co-precipitation, physical mixing, kneading, and bath sonication methods at a 1:1 ratio of Mβ-CD:AVR. The prepared Mβ-CD:AVR inclusion complex was characterized using Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) analysis. Phase solubility studies indicated the Mβ-CD:AVR inclusion complex exhibited a higher stability constant and linear enhancement in AVR solubility with increasing Mβ-CD concentrations.

Indexed as

Antiviral drugCOVID-19Inclusion complexIn silicoMβ-CDSARS-CoV-2 (3CLPro) inhibitor

Identifiers

PMID36101854
PMCPMC9458544
OpenAlexW4295196970

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.