TY - JOUR
T1 - Thiazole-pyrazoline hybrids as potential antimicrobial agent
T2 - Synthesis, biological evaluation, molecular docking, DFT studies and POM analysis
AU - Salih, Rezan Huseen Hama
AU - Hasan, Aso Hameed
AU - Hussen, Narmin Hamaamin
AU - Hawaiz, Farouq Emam
AU - Hadda, Taibi Ben
AU - Jamalis, Joazaizulfazli
AU - Almalki, Faisal A.
AU - Adeyinka, Adedapo S.
AU - Coetzee, Louis Charl C.
AU - Oyebamiji, Abel Kolawole
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/6/15
Y1 - 2023/6/15
N2 - In this study, an efficient synthesis of new thiazole-pyrazoline hybrids was investigated and hybrids were screened for their antimicrobial activities against four species of pathogenic bacteria and one fungal strain utilizing the well-diffusion and MIC assays using ciprofloxacin and fluconazole as the positive controls. The obtained results revealed excellent to moderate antibacterial and antifungal activity. Among them, compound 11b showed potent antibacterial activity against A. baumannii with MIC of 16 µg/mL, while ciprofloxacin was ineffective. Molecular docking studies showed that compound 11b had a stronger binding affinity of about 1 kcal/mol to gram-positive and gram-negative bacteria than compared with compound 11a. Furthermore, the results of the POM (Petra, Osiris, Molinspiration) bioinformatics investigations show that the two studied heterocycles present a very good non toxicity profile, a bad bioavailability, and pharmacokinetics. Finally, an antibacterial pharmacophore (Nδ−, HNδ−) and two antifungal pharmacophores (Nδ−, Sδ−) and (Nδ−, Nδ−) were evaluated in the POM investigations and deserves all our attention to be tested against other pathogenic microorganisms. The more potent compound 11b compared to that of 11a can also be attributed to its lower HOMO-LUMO gap which is an indicator of greater reactivity.
AB - In this study, an efficient synthesis of new thiazole-pyrazoline hybrids was investigated and hybrids were screened for their antimicrobial activities against four species of pathogenic bacteria and one fungal strain utilizing the well-diffusion and MIC assays using ciprofloxacin and fluconazole as the positive controls. The obtained results revealed excellent to moderate antibacterial and antifungal activity. Among them, compound 11b showed potent antibacterial activity against A. baumannii with MIC of 16 µg/mL, while ciprofloxacin was ineffective. Molecular docking studies showed that compound 11b had a stronger binding affinity of about 1 kcal/mol to gram-positive and gram-negative bacteria than compared with compound 11a. Furthermore, the results of the POM (Petra, Osiris, Molinspiration) bioinformatics investigations show that the two studied heterocycles present a very good non toxicity profile, a bad bioavailability, and pharmacokinetics. Finally, an antibacterial pharmacophore (Nδ−, HNδ−) and two antifungal pharmacophores (Nδ−, Sδ−) and (Nδ−, Nδ−) were evaluated in the POM investigations and deserves all our attention to be tested against other pathogenic microorganisms. The more potent compound 11b compared to that of 11a can also be attributed to its lower HOMO-LUMO gap which is an indicator of greater reactivity.
KW - Antimicrobial
KW - DFT
KW - HOMO-LUMO
KW - Pharmacophore sites identification
KW - Pom theory
KW - Pyrazoline
KW - Thiazole
UR - http://www.scopus.com/inward/record.url?scp=85149057947&partnerID=8YFLogxK
U2 - 10.1016/j.molstruc.2023.135191
DO - 10.1016/j.molstruc.2023.135191
M3 - Article
AN - SCOPUS:85149057947
SN - 0022-2860
VL - 1282
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
M1 - 135191
ER -