Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

CHEN Huan, LI Ke. Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives[J]. Journal of Pharmaceutical Practice and Service, 2013, 31(1): 5-10,71. doi: 10.3969/j.issn.1006-0111.2013.01.002
Citation: CHEN Huan, LI Ke. Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives[J]. Journal of Pharmaceutical Practice and Service, 2013, 31(1): 5-10,71. doi: 10.3969/j.issn.1006-0111.2013.01.002

Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives

doi: 10.3969/j.issn.1006-0111.2013.01.002
  • Received Date: 2011-03-14
  • Rev Recd Date: 2012-06-10
  • Benzofuran derivatives were a series of attracting heterocyclic compounds with a variety of biological activity. Based on the recently published literatures, these derivatives had shown antitumor, antioxidant, calcium influx blockade, angiotensin II receptor antagonistic, adenosine A1 receptor antagonistic, antifungal, antibacterial and platelet aggregation antagonistic activities. As Benzofuran derivatives had broad activity, which had attracted many research interests. In order to better study of these compounds both in synthesis and biological activity, the review focused on the biological activity and synthetic methods of 2-substituted Benzofuran derivatives in recent years, which would provide valuable information for the development of 2-substituted benzofuran compounds.
  • [1] Katritzky AR, Rees CW, Scriven EF, et al. Comprehensive Heterocyclic Chemistry II[M]. Oxford:Pergamon Press, 1996: 167.
    [2] Fikret K, Murat K, Haki K, et al. Synthesis and oxidant properties of novel (5-bromobenzofuran-2-yl)(3-methyl-3-mesitylcyclobutyl)ketonethiosemicarbazone[J]. Eur J Med Chem, 2006, 41(5): 664.
    [3] Cumhur K, Misir A, Murat K.Synthesis and antimicrobial activity of some novel derivatives of benzofuran: Part 2. The synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives[J]. Eur J Med Chem, 2008, 43(8): 300.
    [4] Bakr F,Abdel W, Hatem A,et al. Synthesis and antimicrobial evaluation of 1-(benzofuran-2-yl)-4-nitro-3-arylbutan-1-ones and 3-(benzofuran-2-yl)-4,5-dihydro-5-aryl-1-[4-(aryl)-1,3-thiazol-2-yl]-1H-pyrazoles[J]. Eur J Med Chem, 2009, 44(16): 2632.
    [5] Stephane P, Sook WY, Martyn J, et al. Synthesis and CYP26A1 inhibitory activity of 1-[benzofuran-2-yl-(4-alkyl/aryl-phenyl)-methyl]-1H-triazoles][J]. Bioorg Med Chem, 2006, 14(11): 3643.
    [6] Jerzy K, Kinga O, Irena W, et al. Synthesis and structural characterization of derivatives of 2-and 3-benzo[b]furan carboxylic acids with potential cytotoxic activity[J]. IL FARMACO, 2005, 60(6-7): 519.
    [7] Romeo R, Pier G, Taradas S,et al. Synthesis and biological evaluation of 2-(3',4',5'-trimethoxybenzoyl)-3-N,N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization[J]. Bioorg Med Chem, 2008, 16(18): 8419.
    [8] Pierre YM, Jennifer DA, Timothy AG, et al. Design, synthesis and structure-activity relationship of novel RXR-selective modulators[J]. Bioorg Med Chem Lett, 2004, 14(6): 1593.
    [9] Masahiro I, Shingo N, Shingo Y,et al. Discovery of a new chemical lead for a matrix metalloproteinase inhibitor[J]. Bioorg Med Chem, 2006, 14(12): 4241.
    [10] Siavosh M, Andrea U, Christophe C,et al. Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[b]furan-2-yl)methanones[J]. Bioorg Med Chem, 2007, 15(5): 187.
    [11] Manish D, Brajendra K, Akhilesh K,et al. Synthesis of benzofuran scaffold-based potential PTP-1B inhibitors[J]. Bioorg Med Chem, 2007, 15(2): 727.
    [12] Kuntal M, Yadvendra K, Agrawa D,et al. Synthesis, and antitubercular evaluation of novel series benzofuran-5-aryl-1-pyrazolyl-pyridylmethanone and 3-benzofuran-5-aryl-1-pyrazolylcarbonyl-4-oxo-naphthyridin analogs[J]. Eur J Med Chem, 2010, 10(9): 1016.
    [13] Kham MW, Alam MJ, Rashid MA,et al. A new structural alternative in benzo[b]furans for antimicrobial activity[J]. Bioorg Med Che, 2005, 13(16): 4796.
    [14] Bernd P, Sonja B, Rolf H,et al. Benzo[b]thiophene-2-carboxamides and benzo[b]furan-2-carboxamides are potent antagonists of the human H3-receptor[J]. Bioorg Med Chem Lett, 2006, 16(12): 3162.
    [15] Jung WH, Da HC, Jae H,et al. Facile Preparation of 2-Arylbenzo[b]furan Molecules and Their Antiinflammatory Effects[J]. Bull Korean Chem Soc, 2010, 31(4): 4965.
    [16] Michael CW, Dawn T, Adam TG,et al. Palladium-catalysed intramolecular enolate O-arylation and thio-enolate S-arylation: synthesis of benzo[b]furans and benzo[b]thiophenes[J]. Tetrahedron,2006, 62(49): 11513.
    [17] Sanjay SP, Vijaykumar S, More KV,et al. Ultrasound promoted copper-, ligand-and amine-free synthesis of benzo [b]furans/nitro benzo[b]furans via Sonogashira coupling-5-endo-dig-cyclization[J]. Ultrason Sonochem, 2008, 15(5): 853.
    [18] Antonella B, Lucia C, Maria F,et al. Effcient synthesis of 5-nitro-benzo[b]furans via 2-bromo-4-nitro-phenyl acetates[J]. Tetrahedron Lett, 2010, 51(21): 2824.
    [19] Hu J, Wang XC, Guo LN,et al. Pd/C-catalyzed cyclization/isomerization: A new route to 2-aroyl-3-vinyl benzo[b]furans via carbon-carbon bond formation[J]. Catal Commun, 2010, 11(5): 346.
    [20] Pei LX,Li YM,Bu XI,et al. One-pot synthesis of 5.6-dihydroxylated benzo[b]furan derivatives[J]. Tetrahedron Lett, 2006, 47(15): 2615.
    [21] Li HF,Liu J,Yan B,et al. Newdomino approach for the synthesis of 2,3-disubstituted benzo[b]furans via copper-catalyzed multi-component coupling reactions followed by cyclization[J]. Tetrahedron Lett, 2009, 50(20): 2353.
  • 加载中
通讯作者: 陈斌, [email protected]
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(4630) PDF downloads(232) Cited by()

Related
Proportional views

Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives

doi: 10.3969/j.issn.1006-0111.2013.01.002

Abstract: Benzofuran derivatives were a series of attracting heterocyclic compounds with a variety of biological activity. Based on the recently published literatures, these derivatives had shown antitumor, antioxidant, calcium influx blockade, angiotensin II receptor antagonistic, adenosine A1 receptor antagonistic, antifungal, antibacterial and platelet aggregation antagonistic activities. As Benzofuran derivatives had broad activity, which had attracted many research interests. In order to better study of these compounds both in synthesis and biological activity, the review focused on the biological activity and synthetic methods of 2-substituted Benzofuran derivatives in recent years, which would provide valuable information for the development of 2-substituted benzofuran compounds.

CHEN Huan, LI Ke. Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives[J]. Journal of Pharmaceutical Practice and Service, 2013, 31(1): 5-10,71. doi: 10.3969/j.issn.1006-0111.2013.01.002
Citation: CHEN Huan, LI Ke. Recent progress on biological activity and synthesis of 2-substituted Benzofuran derivatives[J]. Journal of Pharmaceutical Practice and Service, 2013, 31(1): 5-10,71. doi: 10.3969/j.issn.1006-0111.2013.01.002
Reference (21)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return