Ontology highlight
ABSTRACT:
SUBMITTER: Cawrse BM
PROVIDER: S-EPMC6680647 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature
Cawrse Brian M BM Robinson Nia'mani M NM Lee Nina C NC Wilson Gerald M GM Seley-Radtke Katherine L KL
Molecules (Basel, Switzerland) 20190723 14
Pyrrolo[3,2-<i>d</i>]pyrimidines have been studied for many years as potential lead compounds for the development of antiproliferative agents. Much of the focus has been on modifications to the pyrimidine ring, with enzymatic recognition often modulated by C2 and C4 substituents. In contrast, this work focuses on the N5 of the pyrrole ring by means of a series of novel N5-substituted pyrrolo[3,2-<i>d</i>]pyrimidines. The compounds were screened against the NCI-60 Human Tumor Cell Line panel, and ...[more]