Evidence map›Paper›PMID 31083628›Full record

ArticleMolecules (Basel, Switzerland)2019

Targeting Caspase 8: Using Structural and Ligand-Based Approaches to Identify Potential Leads for the Treatment of Multi-Neurodegenerative Diseases.

Khurshid Ahmad, Vishal M Balaramnavar, Navaneet Chaturvedi, Saif Khan, Shafiul Haque, Yong-Ho Lee, Inho Choi

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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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

7 authors at 4 institutions in 4 countries.

Khurshid AhmadDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea. ahmadkhursheed2008@gmail.com.ORCID 0000-0002-1095-8445
Vishal M BalaramnavarDepartment of Pharmaceutical Chemistry, GIPER, Kashipur, Uttarakhand 44713, India. v.balaramnavar@gmail.com.
Navaneet ChaturvediUniversity of Information Science and Technology, St. Paul The Apostle, Ohrid 6000, Macedonia. 14.navneet@gmail.com.ORCID 0000-0002-4265-9255
Saif KhanCollege of Dentistry, Hail University, Hail 2440, Saudi Arabia. Saifkhan.bio@gmail.com.
Shafiul HaqueResearch and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan 45142, Saudi Arabia. shafiul.haque@hotmail.com.ORCID 0000-0002-2989-121X
Yong-Ho LeeDepartment of Biomedical Sciences, Daegu Catholic University, Gyeongsan 38430, Korea. ylee325@cu.ac.kr.
Inho ChoiDepartment of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Korea. inhochoi@ynu.ac.kr.
Yeungnam University · KRDaegu Catholic University · KRIndian Institute of Management Kashipur · INUniversity of Ha'il · SA

Funding

Creative Economy Leading Technology Development Program through the Gyeongsanbuk-Do and Gyeongbuk Science & Technology Promotion Center of Korea SF316001ANational Research Foundation of Korea NRF-2018R1A2B6001020
6 · The paper itself

Abstract

Caspase 8 is a central player in the apoptotic cell death pathway and is also essential for cytokine processing. The critical role of this protease in cell death pathways has generated research interest because its activation has also been linked with neural cell death. Thus, blocking the activity of caspase 8 is considered a potential therapy for neurodegenerative diseases. To extend the repertoire of caspase 8 inhibitors, we employed several computational approaches to identify potential caspase 8 inhibitors. Based on the structural information of reported inhibitors, we designed several individual and consensus pharmacophore models and then screened the ZINC database, which contains 105,480 compounds. Screening generated 5332 candidates, but after applying stringent criteria only two candidate compounds, ZINC19370490 and ZINC04534268, were evaluated by molecular dynamics simulations and subjected to Molecular Mechanics/Poisson Boltzmann Surface Area (MM-PBSA) analysis. These compounds were stable throughout simulations and interacted with targeted protein by forming hydrogen and van der Waal bonds. MM-PBSA analysis showed that these compounds were comparable or better than reported caspase 8 inhibitors. Furthermore, their physical properties were found to be acceptable, and they are non-toxic according to the ADMET online server. We suggest that the inhibitory efficacies of ZINC19370490 and ZINC04534268 be subjected to experimental validation.

Indexed as

Molecular Dynamics SimulationCaspase 8Hydrogen BondingMolecular Docking SimulationMolecular StructureNeurodegenerative DiseasesCaspase 8caspase 8ligandneurodegenerationpharmacophorevirtual screening

Identifiers

PMID31083628
PMCPMC6539313
OpenAlexW2944501102

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.