In silico design and ADMET evaluation of new inhibitors for …
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- DOI 10.1016/j.heliyon.2024.e38309
- PMID https://pubmed.ncbi.nlm.nih.gov/39397962
- PMCID https://www.ncbi.nlm.nih.gov/pmc/articles/11467636
- OpenAlex ID W4402813265
- Type Article
- Language EN
- Published 24 Sep 2024
- Volume 10 (19)
- Pages e38309
- Source Heliyon
- Publisher Elsevier BV
- FWCI 2.97
- Countries 1
- Institutions 1
- Added 25 Sep 2024
- Updated 29 Oct 2026
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In silico design and ADMET evaluation of new inhibitors for PIM1 kinase using QSAR studies, molecular docking, and molecular dynamic simulation
Article 2024 EN Gold
The proviral Integration site of Moloney (PIM) kinase is highly expressed in various diseases, including cancer, making the development of selective inhibitors for this protein important. A series of PIM1 inhibitors, triazolo [4, 3-b] pyridazin-3-yl-quinoline derivatives, have been studied to design new inhibitors. The activity and structural features of these derivatives were investigated to unde…
14
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39
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2
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2.97
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UN Sustainable Development Goals
1 SDGsAuthors & Affiliations
2 authors| # | Author | Institutions | ORCID |
|---|---|---|---|
| 1 | Fereshteh Golestanifar | Shahid Bahonar University of K… (IR) | — |
| 2 | Zahra Garkani‐Nejad Corresponding | Shahid Bahonar University of K… (IR) |
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