Antimicrobial activity of amino acid, imidazole, and sulfonamide derivatives of pyrazolo[3,4-d]pyrimidine
β Scribed by M. M. Ghorab; Zeinab H. Ismail; Soad M. Abdel-Gawad; Anhar Abdel Aziem
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 100 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.10212
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β¦ Synopsis
Abstract
Derivatives of pyrazolo[3,4βd]pyrimidine with amino acid 3aβd, imidazole 4aβd, carbonyl 6β9, pyrazole 10, pyrazolone 11, and sulfonamide 12β17 moieties were synthesized. Structure of the new compounds were established by their elemental analyses and spectral data. Some of the synthesized compounds were tested in vitro for their antimicrobial activity. Compounds 4b, 12, and 16 were almost as potent as the standard antibiotic Chloramphenicol as positive control. Also, compounds 3b, 3c, 12, and 16 were nearly as active as Terbinafine as positive control. Β© 2003 Wiley Periodicals, Inc. 15:57β62, 2004; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/.hc10212
π SIMILAR VOLUMES
## Abstract 2βBenzylβ and 2βaryloxymethylβ3βaminoβ1βphenylβpyrazolo[3,4β__d__]pyrimidineβ4βones **__5aβf__** have been synthesized by reacting the corresponding arylacetylamino derivatives **__3aβf__** with hydrazine hydrate. Thionation of compounds **__5dβf__** by action of P~2~S~5~ in pyridine yi