Please use this identifier to cite or link to this item: http://ir.swu.ac.th/jspui/handle/123456789/15456
Title: Synthesis and novel bioactivities of substituted 6-propylthiouracils
Authors: Prachayasittikul S.
Sornsongkhram N.
Pingaew R.
Techatanachai S.
Ruchirawat S.
Prachayasittikul V.
Keywords: 6-propylthiouracils
Alkylation
Antibacterial
Antimalarial
Cytotoxic activities
Issue Date: 2009
Abstract: The synthetic design and novel bioactivities of substituted 6-n-propylthiouracils are reported. The target compounds were accomplished via base catalyzed alkylation (using RBr) of 6-n-propyl-2-thiouracil. The alkylation occurred primarily at a thione moiety to form S-substituted uracils 2a-d (R = n-C4H9, s-C4H9, CH2C6H11 and 1-adamantyl, respectively) together with N3-substitution product 4 (R = CH2C6H5). Bioactivities of the compounds were evaluated. Results show that the analogs 2a, 2c, 2d and 4 are novel antibacterial and cytotoxic agents. The compound 2d exhibits the most potent activity against Branhamella catarrhalis with MIC of 32 μg/mL, while 2c is the most potent cytotoxic against multidrug-resistant small cell lung cancer cell line (H69AR). The analogs 2c and 2d are identified to be novel antimalarials. These novel bioactive analogs are potential lead compounds to be developed as therapeutics. © EuroJournals Publishing, Inc. 2009.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-70349932179&partnerID=40&md5=c9c579c0eb77b9a39a66a024d1841970
http://ir.swu.ac.th/jspui/handle/123456789/15456
ISSN: 1450216X
Appears in Collections:SCOPUS 1983-2021

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