897932-88-6Relevant articles and documents
Dithiocarbamate/piperazine bridged pyrrolobenzodiazepines as DNA-minor groove binders: Synthesis, DNA-binding affinity and cytotoxic activity
Kamal, Ahmed,Sreekanth, Kokkonda,Shankaraiah, Nagula,Sathish, Manda,Nekkanti, Shalini,Srinivasulu, Vunnam
, p. 23 - 30 (2015/02/19)
A new series of C8-linked dithiocarbamate/piperazine bridged pyrrolo[2,1-c][1,4]benzodiazepine conjugates (5a-c, 6a,b) have been synthesized and evaluated for their cytotoxic potential and DNA-binding ability. The representative conjugates 5a and 5b have
Dithiocarbamic acid esters as anticancer agent. Part 1: 4-Substituted-piperazine-1-carbodithioic acid 3-cyano-3,3-diphenyl-propyl esters
Hou, Xueling,Ge, Zemei,Wang, Tingmin,Guo, Wei,Cui, Jingrong,Cheng, Tieming,Lai, Chingshan,Li, Runtao
, p. 4214 - 4219 (2007/10/03)
A variety of 4-N atom substituted derivatives were synthesized and evaluated for their in vitro anticancer activities using 4-methylpiperazine-1-carbodithioic acid 3-cyano-3,3-diphenyl-propyl ester 4 as lead compound. Among them, compound 6a without any substituent on 4-N atom (R1 = H) was found to be the most active anticancer agent with IC50 = 5.3 μM against HL-60 and IC50 = 11.5 μM against Bel-7402, respectively. Increase in the polarity and/or introduction of suitable acyl groups at the 4-N atom of the lead compound 4 are favorable for the improvement of activity.