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Synthesis and biological evaluation of some new N4-aryl substituted 5-chloroisatin-3-thiosemicarbazones
- Source :
- Medicinal chemistry (Shariqah (United Arab Emirates)). 8(3)
- Publication Year :
- 2011
-
Abstract
- A new series of sixteen N4-aryl substituted 5-chloroisatin-3-thiosemicarbazones 2a-2p has been synthesized, characterized and tested for selected biological activities i.e. cytotoxicity, phytotoxicity and urease inhibition. In the brine shrimp bioassay, all the synthesized compounds gave LD50 values >2.30 X 10-4 M - 2.79 X 10-4 M and were, therefore, found to be almost inactive, whereas in phytotoxicity assay, regardless of the nature of aryl substituents, they displayed weak to moderate (5-40%) phytotoxic activity at the highest tested concentrations (500 or 1000 μg/mL). In urease inhibition bioassay, compounds 2a, 2c, 2e, 2f, 2k and 2m exhibited relatively a higher degree of urease inhibition with IC50 values ranging from 38.91 μM to 76.65 μM and thus proved to be potent inhibitors of the enzyme. Of these, 2f and 2m displayed pronounced inhibition with IC50 values 38.91 μM and 39.50 μM, respectively, and may act as lead compounds for further studies. Structure-activity relationship (SAR) studies revealed that electronic effects of the substituents about the phenyl ring at N4 of the thiosemicarbazone moiety played an important role in enhancing the urease inhibitory potential of some of the synthesized compounds.
- Subjects :
- Isatin
Thiosemicarbazones
Urease
Stereochemistry
Medicinal chemistry
chemistry.chemical_compound
Structure-Activity Relationship
Drug Discovery
Bioassay
Moiety
Animals
Araceae
Enzyme Inhibitors
Cytotoxicity
Semicarbazone
chemistry.chemical_classification
biology
Dose-Response Relationship, Drug
Molecular Structure
Aryl
Stereoisomerism
Enzyme
chemistry
biology.protein
Phytotoxicity
Artemia
Subjects
Details
- ISSN :
- 18756638
- Volume :
- 8
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Medicinal chemistry (Shariqah (United Arab Emirates))
- Accession number :
- edsair.doi.dedup.....3b583c89c6da3e320da59ce01612158f