Cholinesterase Inhibition and Anticancer Properties of [4-(Benzyloxy) phenyl]{Methylidene}hydrazinylidene]-1,3-dihydro-2H-Indol-2-ones Using Swiss Target-guided Prediction

dc.contributor.authorMaliyakkal, Naseer
dc.contributor.authorTaslimi, Parham
dc.contributor.authorTuzun, Burak
dc.contributor.authorMenadi, Soumaya
dc.contributor.authorCacan, Ercan
dc.contributor.authorBeeran, Asmy Appadath
dc.contributor.authorBindra, Sandeep
dc.contributor.authorTaslimi, Parham
dc.contributor.otherFen Fakültesi, Biyoteknoloji Bölümü
dc.date.accessioned2026-10-09T08:21:52Z
dc.date.created2026
dc.date.issued2026
dc.departmentFakülteler, Fen Fakültesi, Biyoteknoloji Bölümü
dc.description.abstractIntroduction Our group previously reported isatin-based hydrazones (ISB1-ISB6) were further evaluated for their in vitro acetylcholine esterase, butylcholinestrase and cytotoxic effects on cancer cell lines. The compounds successfully suppressed AChE and BChE, with Ki values ranging from 1.06 +/- 0.07 to 23.57 +/- 1.64 nM for AChE and 15.31 +/- 1.28 to 84.41 +/- 8.04 nM for BChE. However, the IC50 values of these compounds for AChE and BChE were found to be in the ranges of 1.45-25.51 nM and 16.38-92.90 nM, respectively.Method Furthermore, to explore the anti-tumor potential of our newly synthesized compounds, we conducted a cytotoxic MTT assay to assess their impact on two different cancer cell lines: MCF7 and A2780.Results Our findings highlight diverse cytotoxic profiles among the compounds. Specifically, ISB2, ISB3, and ISB4 demonstrated potential cytotoxicity in the A2780 cell line, while ISB6 exhibited significant cytotoxicity in the MCF7 cell line. This suggests that these compounds have different effects on cancer cell types, indicating the need for further investigation into their potential applications in cancer therapy.Conclusion Finally, molecular docking and dynamic study revealed that lead molecule ISB3 provides stability in the AChE and BChE protein-ligand complex.
dc.identifier.citationMaliyakkal, N., Taslimi, P., Tüzün, B., Menadi, S., Cacan, E., Beeran, A. A., Bindra, S., Payyaula, N., Kumar, S., & Mathew, B. (2026). Cholinesterase inhibition and anticancer properties of [4-(benzyloxy) phenyl]{methylidene}hydrazinylidene]-1,3-dihydro-2H-indol-2-ones using Swiss target-guided prediction. Current Computer-Aided Drug Design, 22(4), 267–281. https://doi.org/10.2174/0115734099359621250320073543
dc.identifier.doi10.2174/0115734099359621250320073543
dc.identifier.endpage281
dc.identifier.issue4
dc.identifier.startpage267
dc.identifier.urihttps://doi.org/10.2174/0115734099359621250320073543
dc.identifier.urihttps://hdl.handle.net/11772/28100
dc.identifier.volume22
dc.identifier.wosWOS:001812434000001
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.relation.ispartofCURRENT COMPUTER-AIDED DRUG DESIGN
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgN/A
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectIsatin
dc.subjecthydrazone
dc.subjectacetylcholinesterase
dc.subjectbutylcholinestrase
dc.subjectMTT assay
dc.subjectmolecular dynamics
dc.subjectİsatin
dc.subjecthidrazon
dc.subjectasetilkolinesteraz
dc.subjectbütilkolinesteraz
dc.subjectMTT testi
dc.subjectmoleküler dinamik
dc.titleCholinesterase Inhibition and Anticancer Properties of [4-(Benzyloxy) phenyl]{Methylidene}hydrazinylidene]-1,3-dihydro-2H-Indol-2-ones Using Swiss Target-guided Prediction
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationdadfa319-65b8-4543-92b4-bea49e0139e9
relation.isAuthorOfPublication.latestForDiscoverydadfa319-65b8-4543-92b4-bea49e0139e9
relation.isOrgUnitOfPublication26d2cfa4-ade2-42cc-bd0e-b1e2292e2b42
relation.isOrgUnitOfPublication.latestForDiscovery26d2cfa4-ade2-42cc-bd0e-b1e2292e2b42

Dosyalar

Lisans paketi

Listeleniyor 1 - 1 / 1
Yükleniyor...
Küçük Resim
İsim:
license.txt
Boyut:
1.17 KB
Biçim:
Item-specific license agreed upon to submission
Açıklama: