Synthesis, pharmacological evaluation and docking studies of coumarin derivatives

被引:41
|
作者
Sandhya, B. [1 ]
Giles, D. [1 ]
Mathew, Vinod [1 ]
Basavarajaswamy, Guru [1 ]
Abraham, Rekha [1 ]
机构
[1] Acharya & BM Reddy Coll Pharm, Dept Pharmaceut Chem, Bangalore 560090, Karnataka, India
关键词
Docking; Analgesic; Coumarin; Antimicrobial; Anti-inflammatory; Cyclooxygenase;
D O I
10.1016/j.ejmech.2011.07.013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We synthesized coumarin derivatives using various aromatic and heterocyclic amines, and tested the target compound for its analgesic, anti-inflammatory, antimicrobial activities. Compounds 31, 3m and 3n showed significant anti-inflammatory, analgesic and antimicrobial activities. The synthesized compounds, then docked on COX-2 to predict the binding affinity and orientation at the active site of the receptor. It was found that the active compounds 31, 3m and 3n intact mainly with Arg 44 amino acid, which may be involved in COX-2 inhibition. The compounds which bind with Arg 44 have significant anti-inflammatory activity. This could be due to the formation of more effective hydrogen bond with the receptor. Comparing pharmacological activity and docking results, we conclude that heterocyclic derivatives linked with nitrogen at 7-position of coumarin seem to be potentially active drug. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
下载
收藏
页码:4696 / 4701
页数:6
相关论文
共 50 条
  • [31] Synthesis, Pharmacological Evaluation, and In-Silico Studies of Thiophene Derivatives
    Mishra, Raghav
    Kumar, Nitin
    Sachan, Neetu
    ONCOLOGIE, 2021, 23 (04) : 493 - 514
  • [32] Design, Synthesis, Pharmacological Evaluation and Molecular Docking Studies of Substituted Oxadiazolyl-2-Oxoindolinylidene Propane Hydrazide Derivatives
    Kerzare, Deweshri
    Chikhale, Rupesh
    Bansode, Ratnadeep
    Amnerkar, Nikhil
    Karodia, Nazira
    Paradkar, Anant
    Khedekar, Pramod
    JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2016, 27 (11) : 1998 - 2010
  • [33] Heteroaromatization of Coumarin Part III: One-Pot Synthesis, Antitumor Activity, DFT Studies, and Molecular Docking of Coumarin Derivatives
    Alamri, Abdullah A.
    Borik, Rita M. A.
    Abd El-Wahab, Ashraf H. F.
    Al-Dies, Al-Anood M.
    Mohamed, Hany M.
    Ibrahim, Diaa A.
    CURRENT ORGANIC CHEMISTRY, 2024,
  • [34] Synthesis, spectral studies, biological evaluation and molecular docking studies of metal complexes from coumarin derivative
    Sunitha, N.
    Raj, C. Isac Sobana
    Kumari, B. Sindhu
    JOURNAL OF MOLECULAR STRUCTURE, 2023, 1285
  • [35] Synthesis via carbon suboxide and pharmacological activity of coumarin derivatives
    Bonsignore, L
    Cottiglia, F
    Lavagna, SM
    Loy, G
    Secci, D
    FARMACO, 1998, 53 (10-11): : 693 - 697
  • [36] Design, Synthesis and Cytotoxicity of New Coumarin-1,2,3-triazole Derivatives: Evaluation of Anticancer Activity and Molecular Docking Studies
    Miriyala, Victor Premsagar
    Thommandru, Prakash Raj
    Kashanna, Jajula
    Govinda, Varadhi
    Ravi, Guguloth
    Kishore, Ravada
    CHEMISTRY & BIODIVERSITY, 2023, 20 (07)
  • [37] Synthesis, biological evaluation and molecular docking studies of some pyrimidine derivatives
    Fargualy, Ahmed M.
    Habib, Nargues S.
    Ismail, Khadiga A.
    Hassan, Ahmed M. M.
    Sarg, Marwa T. M.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 66 : 276 - 295
  • [38] Synthesis, antimalarial evaluation and molecular docking studies of some thiolactone derivatives
    Sainy, Jitendra
    Sharma, Rajesh
    JOURNAL OF MOLECULAR STRUCTURE, 2017, 1134 : 350 - 359
  • [39] Synthesis, antimicrobial evaluation, and molecular docking studies of new tetrahydrocarbazole derivatives
    Neama A. Mohamed
    Walaa S. El-Serwy
    Somaia S. Abd El-Karim
    Ghada E. A. Awad
    Samia A. Elseginy
    Research on Chemical Intermediates, 2016, 42 : 1363 - 1386
  • [40] Design, synthesis, biological evaluation and molecular docking studies of thiophene derivatives
    Shah, Rashmi
    Verma, Prabhakar Kumar
    Shah, Manisha
    Kumar, Satendra
    JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2024, 21 (09) : 2501 - 2515