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Benzofuranyl Esters: Synthesis, Crystal Structure Determination, Antimicrobial and Antioxidant Activities.
Kumar, C S Chidan; Then, Li Yee; Chia, Tze Shyang; Chandraju, Siddegowda; Win, Yip-Foo; Sulaiman, Shaida Fariza; Hashim, Nurul Shafiqah; Ooi, Kheng Leong; Quah, Ching Kheng; Fun, Hoong-Kun.
Afiliação
  • Kumar CS; X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, Penang 11800, Malaysia. chidankumar@aiet.org.in.
  • Then LY; Department of Engineering Chemistry, Alva's Institute of Engineering & Technology, Visvesvaraya Technological University, Mijar, Moodbidri 574225, Karnataka, India. chidankumar@aiet.org.in.
  • Chia TS; X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, Penang 11800, Malaysia. lyeeth0923@hotmail.com.
  • Chandraju S; X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, Penang 11800, Malaysia. chiatzeshyang@hotmail.com.
  • Win YF; Department of Sugar Technology & Chemistry, University of Mysore, Sir M. V. PG Center, Tubinakere, Mandya 571402, Karnataka, India. chandraju1@yahoo.com.
  • Sulaiman SF; Department of Chemical Science, Faculty of Science, Universiti Tunku Abdul Rahman, Perak Campus, Jalan Universiti, Bandar Barat, Kampar 31900, Malaysia. yipfw@utar.edu.my.
  • Hashim NS; School of Biological Sciences, Universiti Sains Malaysia, Penang 11800, Malaysia. shaida@usm.my.
  • Ooi KL; School of Biological Sciences, Universiti Sains Malaysia, Penang 11800, Malaysia. nshafiqah25@gmail.com.
  • Quah CK; School of Biological Sciences, Universiti Sains Malaysia, Penang 11800, Malaysia. ooilng@yahoo.com.
  • Fun HK; X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, Penang 11800, Malaysia. ckquah@usm.my.
Molecules ; 20(9): 16566-81, 2015 Sep 11.
Article em En | MEDLINE | ID: mdl-26378514
ABSTRACT
A series of five new 2-(1-benzofuran-2-yl)-2-oxoethyl 4-(un/substituted)benzoates 4(a-e), with the general formula of C8H5O(C=O)CH2O(C=O)C6H4X, X = H, Cl, CH3, OCH3 or NO2, was synthesized in high purity and good yield under mild conditions. The synthesized products 4(a-e) were characterized by FTIR, ¹H-, (13)C- and ¹H-(13)C HMQC NMR spectroscopic analysis and their 3D structures were confirmed by single-crystal X-ray diffraction studies. These compounds were screened for their antimicrobial and antioxidant activities. The tested compounds showed antimicrobial ability in the order of 4b < 4a < 4c < 4d < 4e and the highest potency with minimum inhibition concentration (MIC) value of 125 µg/mL was observed for 4e. The results of antioxidant activities revealed the highest activity for compound 4e (32.62% ± 1.34%) in diphenyl-2-picrylhydrazyl (DPPH) radical scavenging, 4d (31.01% ± 4.35%) in ferric reducing antioxidant power (FRAP) assay and 4a (27.11% ± 1.06%) in metal chelating (MC) activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzofuranos / Ésteres / Antioxidantes Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzofuranos / Ésteres / Antioxidantes Idioma: En Ano de publicação: 2015 Tipo de documento: Article