Synthesis, In Silico Study and Antimalarial Activity of Triazolo[1,5-a]pyrimidine Derivatives

被引:2
|
作者
Prajapati, Arvind N. [1 ,2 ]
Saiyad, Shaffiqali Y. [1 ,2 ]
Bhatt, Bhaktiben R. [3 ]
Patel, Tarosh S. [3 ]
Kataria, Vipul B. [3 ]
Dixit, Bharat C. [3 ]
Dixit, Ritu B. [1 ,2 ]
机构
[1] Ashok & Rita Patel Inst Integrated Study & Res Bio, Anand 388120, Gujarat, India
[2] Charutar Vidya Mandal Univ CVMU, Constitute Coll, Vallabh Vidyanagar, Gujarat, India
[3] Sardar Patel Univ, V P&R P T P Sci Coll, Chem Dept, Vallabh Vidyanagar 388120, Gujarat, India
来源
CHEMISTRYSELECT | 2024年 / 9卷 / 26期
关键词
Synthesis; Molecular docking; 3D-QSAR; ADME; Enzyme inhibition assay; Antimalarial activity; ONE-POT SYNTHESIS; MICROWAVE-ASSISTED SYNTHESIS; THIAMINE HYDROCHLORIDE VB1; BIOLOGICAL EVALUATION; IONIC-LIQUID; EFFICIENT PROMOTER; PREDICTION;
D O I
10.1002/slct.202401335
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The present study mainly focused on synthesizing novel triazolo[1,5-a]pyrimidine-6-carboxamide derivatives using multicomponent reaction. Synthesized derivatives were duly characterized using spectroscopic methods of analysis FT-IR and mass spectroscopy, and H-1 NMR and( 13)C NMR confirmed the structure of compounds. Further, the potential of the synthesized compounds against Plasmodium falciparum dihydrofolate reductase (Pf-DHFR) inhibitors was evaluated by in vitro antimalarial activity, and the results of the study showed moderate to good antimalarial profile of synthesized entities. In silico study of all the synthesized compounds was carried out using Schr & ouml;dinger LLC-2020-3 Software to explain the binding mode and interactions between molecules and pf DHFR enzyme. To study the drug likeliness of molecules, 3D QSAR and Pharmacokinetic studies have been carried out, and the results obtained showed a good pharmacokinetics profile of two compounds, namely AMP-24 and AMP-28, having good IC50 values concerning standard drugs. Further, the in vitro enzyme inhibition assay results suggested that the synthesized compound interacts nicely with the enzyme and might be used as a potent antimalarial agent.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Design, synthesis, and hypnotic activity of pyrazolo[1,5-a]pyrimidine derivatives
    Wang, SQ
    Fang, L
    Liu, XJ
    Zhao, K
    CHINESE CHEMICAL LETTERS, 2004, 15 (08) : 885 - 888
  • [2] Synthesis and Biological Activity of Diheterocyclic 5,7-Dimethyl-1,2,4-triazolo[1,5-a]pyrimidine Derivatives
    Ma, Zhong-Hua
    Liu, Zu-Ming
    Chen, Qiong
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2008, 28 (11) : 1965 - 1970
  • [3] Design, synthesis, biological assessment, and in-Silico studies of 1,2,4-triazolo[1,5-a]pyrimidine derivatives as tubulin polymerization inhibitors
    Mohamed, Heba S.
    Amin, Noha H.
    El-Saadi, Mohammed T.
    Abdel-Rahman, Hamdy M.
    BIOORGANIC CHEMISTRY, 2022, 121
  • [4] Design, synthesis, crystal structure and in vitro antimicrobial activity of novel 1,2,4-triazolo[1,5-a]pyrimidine-containing quinazolinone derivatives
    Du, Huan
    Ding, Muhan
    Luo, Na
    Shi, Jun
    Huang, Jian
    Bao, Xiaoping
    MOLECULAR DIVERSITY, 2021, 25 (02) : 711 - 722
  • [5] Synthesis of new sulfapyrimidine and pyrazolo[1,5-a]pyrimidine derivatives
    Ahmed, Ebtsam A. A.
    Elgemeie, Galal H. H.
    Azzam, Rasha A. A.
    SYNTHETIC COMMUNICATIONS, 2023, 53 (05) : 386 - 401
  • [6] Synthesis, in silico study and antimalarial activity of 2-thioxo-6-(trifluoromethyl)-1,2,3,4-tetrahydropyrimidine-5-carboxamide derivatives
    Arvind N Prajapati
    Shaffiqali Y Saiyad
    Tarosh S Patel
    Vipul B Kataria
    Bharat C Dixit
    Ritu B Dixit
    Journal of Chemical Sciences, 137 (2)
  • [7] Synthesis, anticancer activity, and molecular docking of new pyrazolo[1,5-a]pyrimidine derivatives
    Hossan, Aisha
    Alrefaei, Abdulmajeed F.
    Katouah, Hanadi A.
    Bayazeed, Abrar
    Asghar, Basim H.
    Shaaban, Fathy
    El-Metwaly, Nashwa M.
    JOURNAL OF SAUDI CHEMICAL SOCIETY, 2023, 27 (02)
  • [8] Pyrazole clubbed triazolo[1,5-a]pyrimidine hybrids as an anti-tubercular agents: Synthesis, in vitro screening and molecular docking study
    Bhatt, Jaimin D.
    Chudasama, Chaitanya J.
    Patel, Kanuprasad D.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2015, 23 (24) : 7711 - 7716
  • [9] Designing Potent Anti-Cancer Agents: Synthesis and Molecular Docking Studies of Thieno[2,3-d][1,2,4]triazolo[1,5-a]pyrimidine Derivatives
    Elsenbawy, Eman S. M.
    Alshehri, Zafer S.
    Babteen, Nouf A.
    Abdel-Rahman, Adel A. -H.
    El-Manawaty, Mai A.
    Nossier, Eman S.
    Arafa, Reem K.
    Hassan, Nasser A.
    MOLECULES, 2024, 29 (05):
  • [10] Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry
    Fischer, Gunther
    ADVANCES IN HETEROCYCLIC CHEMISTRY, VOL 128, 2019, 128 : 1 - 101