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Academician profile · DOÇENT

PINAR SİYAH

BAHÇEŞEHİR ÜNİVERSİTESİ

  • Ana Dal Fen Bilimleri ve Matematik Temel Alanı
  • Yan Dal Biyoloji
  • ECZACILIK FAKÜLTESİ
  • TEMEL ECZACILIK BİLİMLERİ BÖLÜMÜ
Articles YÖKSİS 22
Projects 1
Books 0
Proceedings 26
Patents 1
Artistic 1
Scopus (SJR)
Q1 15 Q2 3 Q3 3 Q4 0
WoS (JCR)
Q1 7 Q2 9 Q3 5 Q4 0
TR Index 1 articles

Scopus (SJR)

Q1 15 Q2 3 Q3 3 Q4 0

WoS (JCR)

Q1 7 Q2 9 Q3 5 Q4 0

TR Index

1 articles

22 publications total

Articles

  1. 2026 Computational discovery and preclinical validation of a novel nanodrug eEF2 kinase inhibitor for suppression of tumor growth in triple-negative breast cancer by induction of ferroptosis and apoptosis International Journal of Biological Macromolecules DOI 10.1016/j.ijbiomac.2026.151860
  2. 2026 Evaluating the Blue Economic Potential of the Invasive Alien Macroalga Stypopodium schimperi Thalassas: An International Journal of Marine Sciences DOI 10.1007/s41208-026-01065-9
  3. 2026 Functional Characterization of a Novel OTU-like Deubiquitinase from Neospora caninum and Discovery of Small-Molecule Inhibitors International Journal of Molecular Sciences DOI 10.3390/ijms27125178
  4. 2026 Repurposing drugs for EGFR-targeted cancer therapy: An in silico and in vitro study with pharmacophore-based insights Journal of Molecular Graphics and Modelling DOI 10.1016/j.jmgm.2026.109288
  5. 2026 Synthesis and Development of Novel Small-Molecule MEIS2 Inhibitors That Induce Cell Death in Breast Cancer Cells by Targeting the Homeobox Domain Pharmaceuticals DOI 10.3390/ph19060881
  6. 2025 Advanced AI-Driven in Silico Approaches for the Rapid Discovery of Potent BCL-2 Inhibitors in Cancer Therapy CHEMISTRYSELECT DOI 10.1002/slct.202504166
  7. 2025 Synthesis, in silico and bio-evaluation studies of new isothiocyanate derivatives with respect to COX inhibition and H2S release profiles RSC Medicinal Chemistry DOI 10.1039/D4MD00495G
  8. 2025 Endoplasmic Reticulum Stress-Mediated Apoptosis Induced by Kaempferol in Colorectal Cancer Cells CHEMISTRY & BIODIVERSITY DOI 10.1002/cbdv.202403305
  9. 2025 Targeting IL‐23 with Small Molecule Inhibitors: A New Horizon In Psoriasis Therapy ChemistrySelect DOI 10.1002/slct.202406013
  10. 2025 Dual-Functioning Metal-Organic Frameworks: Methotrexate-Loaded Gadolinium MOFs as Drug Carriers and Radiosensitizers CHEMISTRY-A EUROPEAN JOURNAL DOI 10.1002/chem.202404106
  11. 2024 Enhancing chemotherapeutic efficacy: Niosome‐encapsulated Dox‐Cis with MUC‐1 aptamer Cancer Medicine DOI 10.1002/cam4.70079
  12. 2024 Innovative Fluorescent Polymers in Niosomal Carriers: A Novel Approach to Enhancing Cancer Therapy and Imaging Macromolecular Bioscience DOI 10.1002/mabi.202400343
  13. 2024 Comparison of Candida colonization in intensive care unit patients with and without COVID-19: First prospective cohort study from Turkey Med Mycol . DOI 10.1093/mmy/myae035
  14. 2024 Synthesis and In Silico Evaluation of Piperazine-Substituted 2,3-Dichloro-5,8-dihydroxy-1,4-naphthoquinone Derivatives as Potential PARP-1 Inhibitors ACS Omega DOI 10.1021/acsomega.4c04915
  15. 2024 Advanced Computational Pipeline for FAK Inhibitor Discovery: Combining Multiple Docking Methods with MD and QSAR for Cancer Therapy Computation DOI 10.3390/computation12110222
  16. 2024 In Silico Prediction of EGFR Inhibitors from Thiophene Derivatives Black Sea Journal of Engineering and Science DOI 10.34248/bsengineering.1537989
  17. 2022 Novel etodolac derivatives as eukaryotic elongation factor 2 kinase (eEF2K) inhibitors for targeted cancer therapy Royal Society of Chemistry (RSC) DOI 10.1039/D2MD00105E
  18. 2021 Identification of first-in-class plasmodium OTU inhibitors with potent anti-malarial activity BIOCHEMICAL JOURNAL DOI 10.1042/BCJ20210481
  19. 2021 New nimesulide derivatives with amide/sulfonamide moieties: Selective COX-2 inhibition and antitumor effects European Journal of Medicinal Chemistry DOI 10.1016/j.ejmech.2021.113566
  20. 2020 Development of Small Molecule MEIS Inhibitors that modulate HSC activity Scientific Reports DOI 10.1038/s41598-020-64888-3

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