2017
DOI: 10.1007/s11094-017-1688-y
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Synthesis and Antitumor Activity of 2-N-,3-S-Substituted 5-(4-Benzyloxyphenyl)-1,2,4-Triazoles

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Cited by 2 publications
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“…[144] Three Mannich bases 148 (Figure 18) having a fluoroquinolone antibiotic as amine moiety introduced through aminomethylation of the triazolthione substrate (X = S) were shown to inhibit the growth of PC-3 prostate cancer cell line by 46 % to 56 % at 10 μM. [145] In a series of papers, the antitumor activity of Mannich bases 149, 150 and 151 (Figure 18) against two models of grafted murine tumors (Ehrlich ascites carcinoma and S-37) has been investigated, [146][147][148] and their ability to inhibit methylation of DNA in tumors was determined to be relatively poor to modest. [146,147] Out of these Mannich bases, compound 150 (R = C 6 H 5 , n = 1) exhibited 54 % tumor growth inhibition of S-37 at 155 mg/kg, and increased the lifespan of mice with Ehrlich ascites carcinoma by 35 %.…”
Section: Anticancer and Cytotoxic Activity Of Mannich Bases Obtained ...mentioning
confidence: 99%
“…[144] Three Mannich bases 148 (Figure 18) having a fluoroquinolone antibiotic as amine moiety introduced through aminomethylation of the triazolthione substrate (X = S) were shown to inhibit the growth of PC-3 prostate cancer cell line by 46 % to 56 % at 10 μM. [145] In a series of papers, the antitumor activity of Mannich bases 149, 150 and 151 (Figure 18) against two models of grafted murine tumors (Ehrlich ascites carcinoma and S-37) has been investigated, [146][147][148] and their ability to inhibit methylation of DNA in tumors was determined to be relatively poor to modest. [146,147] Out of these Mannich bases, compound 150 (R = C 6 H 5 , n = 1) exhibited 54 % tumor growth inhibition of S-37 at 155 mg/kg, and increased the lifespan of mice with Ehrlich ascites carcinoma by 35 %.…”
Section: Anticancer and Cytotoxic Activity Of Mannich Bases Obtained ...mentioning
confidence: 99%