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. 2016 Oct 19;7(47):76995–77009. doi: 10.18632/oncotarget.12765

Table 1. Selected examples for the structure-activity-relationship of 1,2,3-triazole compounds.

graphic file with name oncotarget-07-76995-ig001.jpg
n R PC-3 (IC50, μM) DU-145 (IC50, μM)
SPS-1 1 C6H13 >10 >10
SPS-2 1 C8H17 >10 >10
SPS-3 1 C10H21 >10 9.7
SPS-4 1 C12H25 >10 >10
SPS-5 1 C14H29 4.9 4.7
SPS-6 1 C16H33 3.3 5.3
SPS-7 1 C18H37 3.0 4.6
SPS-8 1 C20H41 3.8 6.2
SPS-9 2 C16H33 6.2 nd
SPS-10 2 C14H29 >10 nd
SPS-11 3 C14H29 4.2 5.4
SPS-12 4 C13H27 9.0 6.6
SPS-13 graphic file with name oncotarget-07-76995-ig002.jpg >10 >10
SPS-14 graphic file with name oncotarget-07-76995-ig003.jpg 7.9 > 10
SPS-15 graphic file with name oncotarget-07-76995-ig004.jpg > 10 > 10
SPS-16 graphic file with name oncotarget-07-76995-ig005.jpg > 10 > 10
SPS-17 graphic file with name oncotarget-07-76995-ig006.jpg > 10 > 10

Cells were incubated in the absence or presence of the compound 48 hours. The cell proliferation was determined using sulforhodamine B assay.