New Drug Design to Suppress Nonalcoholic Steatohepatitis

MakaleAçık ErişimScopus SJRQ3

Özet

A de novo designed biomolecule called INASHD was utilized through computer-aided drug design techniques to specifically target β2-spectrin, effectively suppressing and preventing NASH disease. Advanced computational software tools concerning the technologies of molecular docking and molecular dynamics (MD), were employed to showcase the drug's remarkable ability to efficiently suppress and control the α-helical topology of β2-spectrin. This protein is a vital component within the disease pathway. We successfully devised an effective design suppressing β2-spectrin, exhibiting an inhibition score surpassing any other molecule documented in scientific literature. With robust support from validated computational software, this bioorganic structure holds significant value and can be applied for a patent due to its innovative design. It shows promising potential for delivering positive outcomes in various stages, including in vitro, in vivo, ex vivo, and human phase studies.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/kostu/10429Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.18596/jotcsa.1395403Yayıncı resmi DOI adresi
İndeks kayıtları
Kaydın indeks veri tabanlarındaki sayfası (aktarımda alınan kayıt numarasıyla). Erişim, indeksin kendi koşullarına bağlıdır.
Atıflar
Scopus
2
OpenAlex
4
TR Dizin
3
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorAgar, Soykan
dc.contributor.authorAkkurt, Barbaros
dc.contributor.authorUlukaya, Engin
dc.date.accessioned2026-10-27T23:47:31.916534078Z
dc.date.available2026-10-27T23:47:31.916534078Z
dc.date.issued2024
dc.description.abstractA de novo designed biomolecule called INASHD was utilized through computer-aided drug design techniques to specifically target β2-spectrin, effectively suppressing and preventing NASH disease. Advanced computational software tools concerning the technologies of molecular docking and molecular dynamics (MD), were employed to showcase the drug's remarkable ability to efficiently suppress and control the α-helical topology of β2-spectrin. This protein is a vital component within the disease pathway. We successfully devised an effective design suppressing β2-spectrin, exhibiting an inhibition score surpassing any other molecule documented in scientific literature. With robust support from validated computational software, this bioorganic structure holds significant value and can be applied for a patent due to its innovative design. It shows promising potential for delivering positive outcomes in various stages, including in vitro, in vivo, ex vivo, and human phase studies.
dc.description.sponsorshipMolecular Cancer Research Association
dc.description.sponsorshipKalashnikov Izhevsk State Technical University, ISTU
dc.identifier.doi10.18596/jotcsa.1395403
dc.identifier.eissn2149-0120
dc.identifier.endpage590
dc.identifier.issn2149-0120
dc.identifier.issue2
dc.identifier.scopus2-s2.0-85188545376
dc.identifier.startpage585
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/kostu/10429
dc.identifier.volume11
dc.language.isoen
dc.publisherTurkish Chemical Society
dc.relation.ispartofJournal of the Turkish Chemical Society, Section A: Chemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectin silico drug design
dc.subjectmolecular docking
dc.subjectmolecular dynamics
dc.subjectNonalcoholic steatohepatitis
dc.subjectβ2-spectrin
dc.titleNew Drug Design to Suppress Nonalcoholic Steatohepatitis
dc.typeArticle
rdl.citation.openalex4
rdl.citation.scopus2
rdl.citation.trdizin3
rdl.oa.statusgold
rdl.oa.urlhttps://dergipark.org.tr/en/download/article-file/3557042
rdl.scopus.quartileQ3
rdl.source.indexSCOPUS
rdl.source.indexTRDIZIN