Repository logo
Communities & Collections
All of DSpace
  • English
  • العربية
  • বাংলা
  • Català
  • Čeština
  • Deutsch
  • Ελληνικά
  • Español
  • Suomi
  • Français
  • Gàidhlig
  • हिंदी
  • Magyar
  • Italiano
  • Қазақ
  • Latviešu
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Srpski (lat)
  • Српски
  • Svenska
  • Türkçe
  • Yкраї́нська
  • Tiếng Việt
Log In
New user? Click here to register. Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "ABDELLAOUI Ouijdane"

Filter results by typing the first few letters
Now showing 1 - 1 of 1
  • Results Per Page
  • Sort Options
  • No Thumbnail Available
    Item
    In Silico Drug Design and Virtual Screening of Novel Tamoxifen and Mitomycin Derivatives : ADMET Profiling, Molecular Docking, and Molecular Dynamics Simulations
    (جامعة الوادي university of eloued, 2025) ABDELLAOUI Ouijdane; BENKHALIFA Djoumana; DJOUGHI Yamna; OUAKOUAK Roummaissa
    Breast cancer is one of the most significant global public health challenges, particularly in its subtypes characterized by hormone receptor positivity or HER2 protein overexpression, which require effective and targeted therapeutic strategies. Tamoxifen, a selective estrogen receptor modulator, is widely used; however, the development of cancer cell resistance often limits its efficacy. In contrast, Mitomycin, a DNA-interfering antitumor antibiotic, has shown promising activity, making it a molecule of interest for novel drug development. This study aims to design and evaluate 256 analogues for both Tamoxifen and Mitomycin using advanced computational approaches, including pharmacokinetic and toxicological profiling (ADMET), molecular docking, and molecular dynamics (MD) simulations. Results revealed that Tamoxifen analogues Tmx1, Tmx3, and Tmx4 demonstrated LD₅₀ values ranging from 1500 to 1530 mg/kg (toxicity class 4), were non-hepatotoxic (hepatotoxicity values between -0.50 and -0.53), and non-immunotoxic (up to -0.99), with low mutagenic and carcinogenic potential. During MD simulations, these compounds showed RMSD values below 2.5 Å, indicating high structural stability. On the other hand, the Mitomycin6 compound stood out with an LD₅₀ of 3000 mg/kg (toxicity class 5), very low hepatotoxicity (-0.51), negligible immunotoxicity (-0.99), strong biological activity, and excellent structural stability during simulations. Based on these findings, Tmx1, Tmx3, Tmx4, and Mitomycin6 are considered promising next-generation targeted therapy candidates for breast cancer, offering a balanced profile of efficacy and drug safety.

DSpace software copyright © 2002-2025 LYRASIS

  • Privacy policy
  • End User Agreement
  • Send Feedback