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 47 条
  • [1] Abu-hashem A.A., 2015, AM J ORG CHEM, V5, P14, DOI [10.5923/j.ajoc.20150501.03, DOI 10.5923/J.AJOC.20150501.03]
  • [2] Adjiri A, 2016, ONCOL THER, V4, P17, DOI 10.1007/s40487-015-0015-6
  • [3] Synthesis and Antiproliferative Activity of Polysubstituted Tetrahydropyridine and Piperidin-4-one-3-carboxylate Derivatives
    Aeluri, Raghunath
    Alla, Manjula
    Bommena, Vittal Rao
    Murthy, Ramalinga
    Jain, Nishant
    [J]. ASIAN JOURNAL OF ORGANIC CHEMISTRY, 2012, 1 (01) : 71 - 79
  • [4] Chemistry and pharmacological diversity of quinoxaline motifs as anticancer agents
    Ajan, Olayinka O.
    Nlebemuo, Martins T.
    Adekoya, Joseph A.
    Ogunniran, Kehinde O.
    Siyanbola, Tolutope O.
    Ajanaku, Christiana O.
    [J]. ACTA PHARMACEUTICA, 2019, 69 (02) : 177 - 196
  • [5] Synthesis, Characterization and Biological Evaluation of Some Quinoxaline Derivatives: A Promising and Potent New Class of Antitumor and Antimicrobial Agents
    Al-Marhabi, Aisha R.
    Abbas, Hebat-Allah S.
    Ammar, Yousry A.
    [J]. MOLECULES, 2015, 20 (11): : 19805 - 19822
  • [6] A facile synthesis, antibacterial, and antitubercular studies of some piperidin-4-one and tetrahydropyridine derivatives
    Aridoss, Gopalakrishnan
    Amirthaganesan, Shanmugasundaram
    Kumar, Nanjundan Ashok
    Kim, Jong Tae
    Lim, Kwon Taek
    Kabilan, Senthamaraikannan
    Jeong, Yeon Tae
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (24) : 6542 - 6548
  • [7] An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles
    Baumann, Marcus
    Baxendale, Ian R.
    [J]. BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2013, 9 : 2265 - 2319
  • [8] Nucleophilic Dearomatization of Activated Pyridines
    Bertuzzi, Giulio
    Bernardi, Luca
    Fochi, Mariafrancesca
    [J]. CATALYSTS, 2018, 8 (12):
  • [9] Chemical Basis of Reactive Oxygen Species Reactivity and Involvement in Neurodegenerative Diseases
    Collin, Fabrice
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (10)
  • [10] Highly functionalized piperidines: Free radical scavenging, anticancer activity, DNA interaction and correlation with biological activity
    Das, Suvankar
    da Silva, Cristiane J.
    Silva, Marina de M.
    Dantas, Maria Dayanne de A.
    de Fatima, Angelo
    Gois Ruiz, Ana Lucia T.
    da Silva, Cleiton M.
    de Carvalho, Joao Ernesto
    Santos, Josue C. C.
    Figueiredo, Isis M.
    da Silva-Junior, Edeildo F.
    de Aquino, Thiago M.
    de Araujo-Junior, Joao X.
    Brahmachari, Goutam
    Modolo, Luzia Valentina
    [J]. JOURNAL OF ADVANCED RESEARCH, 2018, 9 : 51 - 61