Bioorganic & Medicinal Chemistry 2002-09-01

Synthesis of new 2,5-disubstituted-1,3,4-thiadiazoles and preliminary evaluation of anticonvulsant and antimicrobial activities.

Hatice N Dogan, Arzu Duran, Sevim Rollas, Göksel Sener, Meral K Uysal, Dumrul Gülen

Index: Bioorg. Med. Chem. 10(9) , 2893-8, (2002)

Full Text: HTML

Abstract

Two new series of 2,5-disubstituted-1,3,4-thiadiazoles were synthesized for their possible anticonvulsant, antibacterial and antifungal activities. The degree of protection afforded by these compounds at a dose of 100mg/kg i.p. against pentylenetetrazole-induced convulsions in mice ranged from 0 to 90%. Among these compounds, 2a (90%) and 2g (70%) showed maximum protection. Antimicrobial tests showed that the MIC value of 3j against Pseudomanas aeruginosa was equal to that of penicillin.


Related Compounds

Related Articles:

Histochemical demonstration of protein-bound amino groups.

1954-01-01

[J. Histochem. Cytochem. 2(1) , 29-49, (1954)]

NADPH-dependent lipid peroxidation capacity in unfixed tissue sections: characterization of the pro-oxidizing conditions and optimization of the histochemical detection.

1994-03-01

[Histochem. J. 26(3) , 189-96, (1994)]

Imaging of oxidative stress at subcellular level by confocal laser scanning microscopy after fluorescent derivatization of cellular carbonyls.

1993-05-01

[Am. J. Pathol. 142(5) , 1353-7, (1993)]

The use of 3-hydroxy-2-naphthoic acid hydrazide and Fast Blue B for the histochemical detection of lipid peroxidation in animal tissues--a microphotometric study.

1991-01-01

[Histochemistry 95 , 255, (1991)]

Optimization of the histochemical demonstration of DNA using 3-hydroxy-2-naphthoic acid hydrazide and fast blue B.

1989-01-01

[Histochemistry 90 , 465, (1989)]

More Articles...