Synthesis, biological evaluation and in silico studies of tetrazole-heterocycle hybrids

被引:27
|
作者
Sribalan, Rajendran [1 ]
Banuppriya, Govindharasu [1 ]
Kirubavathi, Maruthan [1 ]
Padmini, Vediappen [1 ]
机构
[1] Madurai Kamaraj Univ, Sch Chem, Dept Organ Chem, Madurai 625021, Tamil Nadu, India
关键词
Hybrid tetrazole; Antimicrobial; Anti-inflammatory; Molecular docking; Molecular orbitals; ANTIBACTERIAL ACTIVITY; MOLECULAR DOCKING; DERIVATIVES;
D O I
10.1016/j.molstruc.2018.07.114
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The series of three different chemical entities of tetrazole-heterocycle hybrids such as thiophene, pyridine and quinoline tetrazoles were synthesized and characterized for the purpose to develop new lead molecules. Biological evaluations such as in vitro antimicrobial and anti-inflammatory activities were studied. Further, the in silico studies such as Molecular docking (with COX-1, COX-2 and 3TTZ), OFT calculations, the Molecular electrostatic potential (MEP) and ACME were investigated. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:577 / 586
页数:10
相关论文
共 50 条
  • [41] Synthesis, characterization, in silico studies and in vitro biological evaluation of isoniazid-hydrazone complexes
    Rajan, M. P. Ramya
    Rathikha, Ramaswamy
    Nithyabalaji, Rajendran
    Sribalan, Rajendran
    JOURNAL OF MOLECULAR STRUCTURE, 2020, 1216
  • [42] Synthesis, biological evaluation, molecular docking studies and In-silico ADMET evaluation of pyrazines of pentacyclic triterpenes
    Lopez-Huerta, Fabiola A.
    Teresa Ramirez-Apan, Maria
    Mendez-Cuesta, Carlos A.
    Nieto-Camacho, Antonio
    Hernandez-Ortega, Simon
    Almeida-Aguirre, Ericka K. P.
    Cerbon, Marco A.
    Delgado, Guillermo
    BIOORGANIC CHEMISTRY, 2022, 125
  • [43] Synthesis, single crystal analysis, biological and docking evaluation of tetrazole derivatives
    Aziz, Hamid
    Saeed, Aamer
    Jabeen, Farukh
    Din, Noor Ud
    Floerke, Ulrich
    HELIYON, 2018, 4 (09):
  • [44] Design, Synthesis and Biological Evaluation of Triptorelin Analogs Containing Tetrazole Moiety
    Sohbati, Hamidreza
    Alipour, Mohsen
    Hosseinkhani, Saman
    Balalaie, Saeed
    Hamdan, Fatima
    CHEMISTRYSELECT, 2020, 5 (04): : 1443 - 1449
  • [45] Synthesis and biological evaluation of tetrazole containing compounds as possible anticancer agents
    Kumar, Chebolu Naga Sesha Sai Pavan
    Parida, Dusmant Kumar
    Santhoshi, Amlipur
    Kota, Anil Kumar
    Sridhar, Balasubramanian
    Rao, Vaidya Jayathirtha
    MEDCHEMCOMM, 2011, 2 (06) : 486 - 492
  • [46] Synthesis and biological evaluation of tetrazole fused imidazopyridine derivatives as anticancer agents
    Vanam, Narendhar Reddy
    Anireddy, Jaya Shree
    CHEMICAL DATA COLLECTIONS, 2023, 48
  • [47] Synthesis of Oxindole Analogues, Biological Activity, and In Silico Studies
    Lotfy, Gehad
    Aziz, Yasmine M. Abdel
    Said, Mohamed M.
    El Ashry, El Sayed H.
    El Tamany, El Sayed H.
    Barakat, Assem
    Ghabbour, Hazem A.
    Yousuf, Sammer
    Ul-Haq, Zaheer
    Choudhary, M. Iqbal
    CHEMISTRYSELECT, 2019, 4 (35): : 10510 - 10516
  • [48] Furanchalcone–biphenyl hybrids: synthesis, in silico studies, antitrypanosomal and cytotoxic activities
    Elisa García
    Rodrigo Ochoa
    Isabel Vásquez
    Laura Conesa-Milián
    Miguel Carda
    Andrés Yepes
    Iván D. Vélez
    Sara M. Robledo
    Wilson Cardona-G
    Medicinal Chemistry Research, 2019, 28 : 608 - 622
  • [49] Stereoisomers of oseltamivir - synthesis, in silico prediction and biological evaluation
    Hajzer, Viktoria
    Fisera, Roman
    Latika, Attila
    Durmis, Julius
    Kollar, Jakub
    Frecer, Vladimir
    Tucekova, Zuzana
    Miertus, Stanislav
    Kostolansky, Frantisek
    Vareckova, Eva
    Sebesta, Radovan
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2017, 15 (08) : 1828 - 1841
  • [50] Synthesis and biological evaluation of paclitaxel-thiocoichicine hybrids
    Danieli, B
    Giardini, A
    Lesma, G
    Passarella, D
    Silvani, A
    Appendino, G
    Noncovich, A
    Fontana, G
    Bombardelli, E
    Sterner, O
    CHEMISTRY & BIODIVERSITY, 2004, 1 (02) : 327 - 345