New 4-aminopyrazolo[3,4-d]pyrimidines bearing various substituents at the position 1 and 6, were synthesized. The new compounds showed antiproliferative activity toward A431 cells, were found to be inhibitors of Src phosphorylation, and induced apoptotic cell death. In particular, 2h was a better inhibitor of Src phosphorylation than the reference compound PP2
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
Pyrazolopyrimidines are fused heterocyclic ring systems which structurally can consider as bioisoste...
New 4-aminopyrazolo[3,4-d]pyrimidines bearing various substituents at the position 1 and 6, were syn...
We report here the synthesis of new pyrazolo[3,4-d]pyrimidine derivatives along with their biologica...
We report here the synthesis of new pyrazolo[3,4-d]pyrimidine derivatives along with their biologica...
Novel 1,4,6-trisubstituted pyrazolo[3,4-d]pyrimidines are reported with preliminary in vitro activit...
Novel 1,4,6-trisubstituted pyrazolo[3,4-d]pyrimidines are reported with preliminary in vitro activit...
The synthesis of new 4-amino substituted pyrazolo[3,4-d]pyrimidines along with their activity in cel...
The synthesis of new 4-amino substituted pyrazolo[3,4-d]pyrimidines along with their activity in cel...
In a cell-based screen of novel anticancer agents, the hit compound 1a which bears a pyrazolo[3,4-d]...
Synthesis and biological evaluation of a new class of 1-aryl-4-amino-1H- pyrazolo[3,4-d]pyrimidine d...
The current study was designed to identify new compounds as potential antiproliferative drug candida...
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
Pyrazolopyrimidines are fused heterocyclic ring systems which structurally can consider as bioisoste...
New 4-aminopyrazolo[3,4-d]pyrimidines bearing various substituents at the position 1 and 6, were syn...
We report here the synthesis of new pyrazolo[3,4-d]pyrimidine derivatives along with their biologica...
We report here the synthesis of new pyrazolo[3,4-d]pyrimidine derivatives along with their biologica...
Novel 1,4,6-trisubstituted pyrazolo[3,4-d]pyrimidines are reported with preliminary in vitro activit...
Novel 1,4,6-trisubstituted pyrazolo[3,4-d]pyrimidines are reported with preliminary in vitro activit...
The synthesis of new 4-amino substituted pyrazolo[3,4-d]pyrimidines along with their activity in cel...
The synthesis of new 4-amino substituted pyrazolo[3,4-d]pyrimidines along with their activity in cel...
In a cell-based screen of novel anticancer agents, the hit compound 1a which bears a pyrazolo[3,4-d]...
Synthesis and biological evaluation of a new class of 1-aryl-4-amino-1H- pyrazolo[3,4-d]pyrimidine d...
The current study was designed to identify new compounds as potential antiproliferative drug candida...
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
New pyrazolo[3,4-d]pyrimidines were synthesized and found to inhibit Src phosphorylation in a cell-f...
Pyrazolopyrimidines are fused heterocyclic ring systems which structurally can consider as bioisoste...