Design, Synthesis, and Biological Evaluation of Quinoxaline Bearing Tetrahydropyridine Derivatives as Anticancer, Antioxidant, and Anti-Tubercular Agents

被引:3
|
作者
Pavale, Ganesh [1 ]
Acharya, Poornima [1 ]
Korgavkar, Nilesh [2 ]
Ramana, M. M. V. [1 ]
机构
[1] Univ Mumbai, Dept Chem, Mumbai 400098, India
[2] Univ Mumbai, Mithibai Coll, Dept Chem, Mumbai, India
关键词
Quinoxaline; tetrahydropyridine; anticancer; antioxidant; anti-mycobacterial; molecular docking; ANTIPROLIFERATIVE ACTIVITY; MYCOBACTERIUM-TUBERCULOSIS; CHEMISTRY; ANTIBACTERIAL; ANTIFUNGAL; DIVERSITY; POTENT;
D O I
10.2174/1573409918666220804142753
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Quinoxaline and Tetrahydropyridine derivatives showed various biological properties. The combination of these two scaffolds may contribute to good biological activity and may give novel and efficacious bioactive candidates. Objective: The present study aimed to identify bioactive agents with quinoxaline bearing tetrahydropyridine derivatives possessing anticancer, antioxidant, and anti-tubercular agents. Methods: A series of novel quinoxaline bearing tetrahydropyridine derivatives have been designed and synthesized in good yields. The synthetic protocol involves three-component Povarov reactions of 6-amino quinoxaline, propenyl guaethol, and substituted aldehydes using BF3 center dot OEt2 as catalyst. The newly synthesized molecules were evaluated for their anticancer activity against four cell lines, i.e. A-549, MCF-7, PC-3, and HepG2. Results: The results from in vitro assay indicated that compound 4a proved to be as potent as the standard drug adriamycin against all cell lines with GI50 values <10 mu g/ml. Compounds 4b, 4f, and 4i exhibited good cytotoxicity against A-549 cell line. All synthesized molecules were evaluated for their antioxidant activity and the results revealed that the compounds 4a, 4b, and 4i showed promising antioxidant activities against DPPH and H2O2 scavenging. In addition, the anti-mycobacterial activity of the synthesized compounds against MTB H37Rv strain was determined using the MABA method. The results indicate that the compounds 4a, 4b, 4g, and 4i showed better anti-mycobacterial activity than the standard drugs pyrazinamide, ciprofloxacin and streptomycin with an MIC value of 1.6 mu g/ml. Furthermore, molecular docking studies and ADME properties showed good pharmacokinetic profile and drug-likeness properties. Conclusion: These studies showed that a series of novel quinoxaline bearing tetrahydropyridine derivatives exhibit anticancer, anti-mycobacterial, and antioxidant activities.
引用
收藏
页码:414 / 424
页数:11
相关论文
共 50 条
  • [31] Synthesis and Biological Evaluation of Benzodioxole Derivatives as Potential Anticancer and Antioxidant agents
    Hawash, Mohammed
    Eid, Ahmad M.
    Jaradat, Nidal
    Abualhasan, Murad
    Amer, Johnny
    Zaid, Abdel Naser
    Draghmeh, Saja
    Daraghmeh, Donia
    Daraghmeh, Haifa
    Shtayeh, Tahrir
    Sawaftah, Hadeel
    Mousa, Ahmed
    HETEROCYCLIC COMMUNICATIONS, 2020, 26 (01) : 157 - 167
  • [32] Synthesis of carbohydrazides and carboxamides as anti-tubercular agents
    Kumar, Gautam
    Krishna, Vagolu Siva
    Sriram, Dharmarajan
    Jachak, Sanjay M.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2018, 156 : 871 - 884
  • [33] Design, synthesis and biological evaluation of isoxazole bearing N-Arylpyrazole derivatives as anticancer agents
    Chandavaram, Pardha saradhi
    Maddirala, Shambabu Joseph
    Vidavalur, Siddaiah
    Somaiah, Nalla
    CHEMICAL DATA COLLECTIONS, 2022, 41
  • [34] Design, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents
    İrfan Çapan
    Mohammed Hawash
    Nidal Jaradat
    Yusuf Sert
    Refik Servi
    İrfan Koca
    BMC Chemistry, 17
  • [35] Design, synthesis and biological evaluation of rhein derivatives as anticancer agents
    Huang, Junkai
    Zhang, Zhuo
    Huang, Peng
    He, Liqin
    Ling, Yong
    MEDCHEMCOMM, 2016, 7 (09) : 1812 - 1818
  • [36] Design, Docking, Synthesis, and In vitro Evaluation of Potent Anti-tubercular Agents Targeting DNA Gyrase
    Bhosale, Manjiri D.
    Thomas, Asha B.
    Lokhande, Kiran B.
    Swamy, Kakumani V.
    Basu, Soumya
    Chitlange, Sohan S.
    LETTERS IN DRUG DESIGN & DISCOVERY, 2024, 21 (11) : 2072 - 2092
  • [37] Design, synthesis, molecular docking and biological evaluation of new carbazole derivatives as anticancer, and antioxidant agents
    Capan, Irfan
    Hawash, Mohammed
    Jaradat, Nidal
    Sert, Yusuf
    Servi, Refik
    Koca, Irfan
    BMC CHEMISTRY, 2023, 17 (01)
  • [38] Indole-fused spirochromenes as potential anti-tubercular agents: design, synthesis and in vitro evaluation
    Dogamanti, Ashok
    Chiranjeevi, Pamula
    Aamate, Vikas Kumar
    Vagolu, Siva Krishna
    Sriram, Dharmarajan
    Balasubramanian, Sridhar
    Sarasija, Madderla
    MOLECULAR DIVERSITY, 2021, 25 (04) : 2137 - 2148
  • [39] Indole-fused spirochromenes as potential anti-tubercular agents: design, synthesis and in vitro evaluation
    Ashok Dogamanti
    Pamula Chiranjeevi
    Vikas Kumar Aamate
    Siva Krishna Vagolu
    Dharmarajan Sriram
    Sridhar Balasubramanian
    Madderla Sarasija
    Molecular Diversity, 2021, 25 : 2137 - 2148
  • [40] Synthesis and biological evaluation of some novel isoxazoles and cyanopyridines, a new class of potential anti-tubercular agents
    Doshi, R
    Kagthara, P
    Parekh, H
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1999, 38 (03): : 348 - 352