TY - JOUR
T1 - Synthesis, characterization and antimicrobial, antioxidant properties of some benzopyrone derivatives
AU - Jayashree, B.S.
AU - Kuppast, B.K.
AU - Venugopala, K.N.
N1 - Cited By :4
Export Date: 10 November 2017
CODEN: AJCHE
Correspondence Address: Jayashree, B.S.; Department of Pharmaceutical Chemistry, Manipal College of Pharmaceutical Sciences, Manipal-576104, India; email: [email protected]
References: Karale, B.K., Hangargo, R.V., Mane, A.S., Gill, C.H., Shingare, M.S., (2001) Indian J. Heterocycl. Chem, 11, p. 81; Emim, J.A.D.S., Oliveira, A.B., Lapa, A.J., (1992) J. Pharm. Pharmacol, 46, p. 118; Malterud, K.E., Diep, O.H., Sund, R.B., (1996) Pharmacol. Toxic, 78, p. 111; Nakane, H., Ono, K., (1990) Biochemistry, 29, p. 2841; Cassady, J.M., (1990) J. Nat. Prod, 35, p. 23; Imai, K., Nakachi, K., (1995) British Med. J, 310, p. 693; Fritz, B., Tobias, S., Albrecht, K., Charlotte, B., Kent, C., Anni, A., Franz, J., Joseph, K., (1996) Am. Soc. Biochem. Mol. Bio, 271, p. 2262; I. L. Finar, Organic Chemistry, Pearson Education, (Singapore) Pvt. Ltd., edn. 6, 1, p. 704 (2003); Lynda, L.S., Jerome, K.W., Sang, K., Lee, C.G., Daiel, L., Richard, C.M., Robert, M.M., John, M.P., (1991) Cancer Res, 59, p. 578; Garg, C.P., Sharma, V.P., Kapoor, R.P., (1985) Indian J. Chem, 24 B, p. 1197; http://www.niaid.nih.gov; Vani, T., Rajani, M., Sarkar, S., Shishhoo, C.J., (1997) Int. J. Pharmacog, 35, p. 313; Kavanagh, F., (1963) Analytical Microbiology, p. 125. , Academic Press, New York, p; Lowdi, E., Odenholt, I., Bengtsson, S., Cars, O., (1993) Antimicrob. Agents Chemother, 37, p. 2200
PY - 2007
Y1 - 2007
N2 - The purpose of present study is to develop potential antimicrobial and antioxidant agents. In this attempt three series of the substituted flavones such as 3-hydroxy flavones (4a-j), 3-methoxy flavones (5a-e) and 3-acetyloxy flavones (6a-g) were synthesized and characterized by IR, 1H NMR and mass spectral analysis. Test compounds were subjected for the determination of lipophillic parameter and pharmacological activities such as quantitative antibacterial activity and antioxidant activity by MIC (ELISA) and DPPH* method, respectively.
AB - The purpose of present study is to develop potential antimicrobial and antioxidant agents. In this attempt three series of the substituted flavones such as 3-hydroxy flavones (4a-j), 3-methoxy flavones (5a-e) and 3-acetyloxy flavones (6a-g) were synthesized and characterized by IR, 1H NMR and mass spectral analysis. Test compounds were subjected for the determination of lipophillic parameter and pharmacological activities such as quantitative antibacterial activity and antioxidant activity by MIC (ELISA) and DPPH* method, respectively.
M3 - Article
SN - 0970-7077
VL - 19
SP - 1415
EP - 1422
JO - Asian Journal of Chemistry
JF - Asian Journal of Chemistry
IS - 2
ER -