Synthesis of some new 2,4-disubstituted thiazoles as possible antibacterial and driti-inflammatory agents

被引:294
作者
Holla, BS [1 ]
Malini, KV
Rao, BS
Sarojini, BK
Kumari, NS
机构
[1] Mangalore Univ, Dept Postgrad Studies & Res Chem, Mangalagangothri 574199, India
[2] KS Hegde Med Acad, Dept Biochem, Deralakatte, India
关键词
thiazoles; arylthiourea; arylaldehydethiosemicarbazone; arylfurfuraldehyde thiosemicarbazone; antibacterial activity; anti-inflammatory activity;
D O I
10.1016/S0223-5234(02)01447-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of arylthioureas (1), aromatic aldehyde thiosemicarbazones (2) and 5-aryl-2-furfuraldehyde thiosemicarbazones (3) were condensed with 2,4-dichloro-5-fluorophenacyl bromide to yield respective arylaminothiazoles, arylidene/5-aryl-2-furfurylidene hydrazinothiazoles (4). The newly synthesized compounds were characterized by IR, H-1-NMR and mass spectral studies. These compounds were also screened for their antibacterial and anti-inflammatory activities. Two of the newly synthesized compounds showed anti-inflammatory activity comparable with that of Ibuprofen. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:313 / 318
页数:6
相关论文
共 9 条
  • [1] BERLIN K D, 1991, Proceedings of the Oklahoma Academy of Science, V71, P29
  • [2] CRUICKSHANK R, 1975, MED MICROBIOLOGY, V2, P190
  • [3] Filler R., 1982, Biomedicinal Aspects of Fluorine Chemistry
  • [4] HANS N, Patent No. 1977592103
  • [5] Holla BS, 2002, EUR J MED CHEM, V37, P511
  • [6] Meir R, 1950, EXPERIENTIA, V6, P469
  • [7] Sharma P, 1998, INDIAN J CHEM A, V37, P371
  • [8] Synthesis of thiophene-2-carboxamidines containing 2-amino-thiazoles and their biological evaluation as urokinase inhibitors
    Wilson, KJ
    Illig, CR
    Subasinghe, N
    Hoffman, JB
    Rudolph, MJ
    Soll, R
    Molloy, CJ
    Bone, R
    Green, D
    Randall, T
    Zhang, M
    Lewandowski, FA
    Zhou, Z
    Sharp, C
    Maguire, D
    Grasberger, B
    DesJarlais, RL
    Spurlino, J
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (07) : 915 - 918
  • [9] WINTER CA, 1962, P SOC EXP BIOL MED, V111, P544