Literature DB >> 19921590

Synthesis, phytotoxic, cytotoxic, acetylcholinesterase and butrylcholinesterase activities of N,N'-diaryl unsymmetrically substituted thioureas.

Saeedan Begum1, M Iqbal Choudhary, Khalid M Khan.   

Abstract

Fourteen N,N'-diaryl unsymmetrically substituted thioureas were synthesised and their cytotoxic (in vitro), phytotoxic (in vitro), acetylcholinesterase and butrylcholinesterase activities were determined. Thiourea 16 exhibited high, and 1 and 3 showed significant phytotoxic activity. Thioureas 1, 3, 4, 6 and 10 showed significant activity and 2, 6 and 7 indicated moderate cytotoxic activities. Compound 12 exhibited butrylcholinesterase activity higher than a standard reference.

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Year:  2009        PMID: 19921590     DOI: 10.1080/14786410802223778

Source DB:  PubMed          Journal:  Nat Prod Res        ISSN: 1478-6419            Impact factor:   2.861


  2 in total

1.  Convenient diastereoselective synthesis of annulated 3-substituted-(5S*,6S*,Z)-2-(2-(2,4-dinitrophenyl)hydrazono)-5,6-diphenyl-1,3-thiazinan-4-ones.

Authors:  Alaa A Hassan; Nasr K Mohamed; Ashraf A Aly; Hendawy N Tawfeek; Henning Hopf; Stefan Bräse; Martin Nieger
Journal:  Mol Divers       Date:  2019-01-03       Impact factor: 2.943

2.  One-step construction of unsymmetrical thioureas and oxazolidinethiones from amines and carbon disulfide via a cascade reaction sequence.

Authors:  Chaochao Ding; Shaoli Wang; Yaoguang Sheng; Qian Dai; Yunjie Zhao; Guang Liang; Zengqiang Song
Journal:  RSC Adv       Date:  2019-08-27       Impact factor: 4.036

  2 in total

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