2005
DOI: 10.1016/j.ejmech.2005.02.002
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The synthesis and antimicrobial activity of some new methyl N-arylthiocarbamates, dimethyl N-aryldithiocarbonimidates and 2-arylamino-2-imidazolines

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Cited by 37 publications
(10 citation statements)
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“…Substituted thiadiazole derivatives have been found to show diverse pharmacological activities such as analgesic (Schenone et al, 2006), antidepressant and anxiolytic (Clerici and Pocar, 2001), anticonvulsant Chapleo et al, 1986), anti-inflammatory (Mullican et al, 1993), antimicrobial (Servi et al, 2005), antitubercular (Oruç et al, 2004), antitumor (Matysiak, 2006) and antiviral (Jones et al, 1965) activity. A series of 2-amino-5-sulfanyl-1,3,4-thiadiazoles originally been synthesized and evaluated for antidepressant and anxiolytic activity by Clerici and Pocar (2001).…”
Section: Introductionmentioning
confidence: 99%
“…Substituted thiadiazole derivatives have been found to show diverse pharmacological activities such as analgesic (Schenone et al, 2006), antidepressant and anxiolytic (Clerici and Pocar, 2001), anticonvulsant Chapleo et al, 1986), anti-inflammatory (Mullican et al, 1993), antimicrobial (Servi et al, 2005), antitubercular (Oruç et al, 2004), antitumor (Matysiak, 2006) and antiviral (Jones et al, 1965) activity. A series of 2-amino-5-sulfanyl-1,3,4-thiadiazoles originally been synthesized and evaluated for antidepressant and anxiolytic activity by Clerici and Pocar (2001).…”
Section: Introductionmentioning
confidence: 99%
“…These 1,3,4-thiadiazole compounds are associated with diverse pharmacological activities such as analgesic (Schenone et al, 2006), antidepressant and anxiolytic (Clerici and Pocar, 2001), anticonvulsant (Chapleo et al, 1986;Stillings et al, 1986), anti-inflamatory (Mullican et al, 1993), antimicrobial (Servi et al, 2005;Foroumadia et al, 2005), antitubercular (Oruç et al, 2004), antitumor (Matysiak, 2006), and antiviral (Jones et al, 1965) activity. A series of 2-amino-5-sulfanyl-1,3,4-thiadiazoles exemplified by the general structure in Fig.…”
Section: Introductionmentioning
confidence: 99%
“…THSG is one of the stilbene derivatives which are distributed abundantly in plants and have a number of interesting biological activities [7,8]. Although THSG is similar to other stilbene derivatives in their chemical structures, their effects on tyrosinase activity differ greatly.…”
Section: Discussionmentioning
confidence: 99%