Synthesis, in vitro urease inhibition and molecular docking studies of some novel quinazolin-4(3H)-one derivatives containing triazole, thiadiazole and thiosemicarbazide functionalities

Mentese E., Akyuz G., Emirik M., Baltas N.

BIOORGANIC CHEMISTRY, cilt.83, ss.289-296, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 83
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1016/j.bioorg.2018.10.031
  • Dergi Adı: BIOORGANIC CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.289-296
  • Anahtar Kelimeler: Quinazolin-4(3H)-one, Triazole, Thiadiazole, Molecular docking, Urease inhibition, QUINAZOLINONE DERIVATIVES, BIOLOGICAL EVALUATION, ANTI-UREASE, DESIGN, CHEMISTRY, LIBRARY, IDENTIFICATION, ANTIOXIDANT, SILICO
  • Recep Tayyip Erdoğan Üniversitesi Adresli: Evet

Özet

A new series of quinazolinone derivatives containing triazole, thiadiazole, thiosemicarbazide functionalities was synthesized and then screened for their in vitro urease inhibition properties. Most of the compounds showed excellent activity with IC50 values ranging between 1.88 +/- 0.17 and 6.42 +/- 0.23 mu g/mL, compared to that of thiourea (IC50 = 15.06 +/- 0.68) and acetohydroxamic acid (IC50 = 21.03 +/- 0.94), as reference inhibitors. Among the synthesized molecules, compounds 5c, 5e and 5a showed the best inhibitory effect against urease enzyme with IC50 values of 1.88 +/- 0.17 mu g/mL, 1.90 +/- 0.10 and 1.96 +/- 0.07 mu g/mL, respectively. Moreover in order to give better understanding of the inhibitory activity of synthesized compounds, molecular docking studies were applied at the target sites of jack bean urease enzyme (JBU). Their binding poses and energy calculations were analyzed using induced fit docking (IFD) and prime-MMGBSA tool. Binding poses of studied compounds were determined using induced fit docking (IFD) algorithms.