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Synthesis, identification and in vitro biological evaluation of some novel quinoline incorporated 1,3-thiazinan-4-one derivatives
被引:16
|作者:
Umamatheswari, S.
[1
]
Sankar, C.
[2
]
机构:
[1] Govt Arts Coll, Dept Chem, Tiruchirappalli 620022, Tamil Nadu, India
[2] TRP Engn Coll, Dept Chem, Tiruchirappalli 621105, Tamil Nadu, India
关键词:
Tuberculosis;
Quinoline;
Thiazinan-4-one;
Antimalarial;
MEFLOQUINE-BASED LIGANDS;
DESIGN;
POTENT;
QUINOLINE-3-CARBOHYDRAZIDE;
TUBERCULOSIS;
MOXIFLOXACIN;
HYDRAZONES;
INHIBITORS;
HYBRIDS;
AGENTS;
D O I:
10.1016/j.bmcl.2016.06.038
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
The present study describes the synthesis of two new series of 3-hydroxy-N-(4-oxo-2-phenyl-1,3-thiazinan-3-y1)-8-(trifluoromethyl)quinoline-2-carboxamide derivatives (4a-j) and 3((7-chloroquinolin-4-ylamino)methyl)-2-phenyl-1,3-thiazinan-4-one derivatives (5a-7j). All the compounds were synthesized in moderate to good yield by one-pot three component cyclo-condensation reaction. The newly synthesized compounds were characterized by FT-IR,H-1,C-13 NMR and elemental analysis. The compounds were screened for their in vitro antibacterial activity against a panel of pathogenic bacterial strains, antitubercular activity against Mycobacterium tuberculosis H(37)Rv and also for their in vitro antimalarial activity against Plasmodium falciparum. Among the synthesized compounds two of them (4f and 5f) showed excellent antibacterial activity against C tetani at 15.6 mu g/mL. Some of them exhibited excellent antitubercular (4f & 5f) and good antimalarial (4f, 5f & 6f) activity compared with the first line drugs. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:695 / 699
页数:5
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