Novel 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-one derivatives as potential anti-cancer agents

Authors
Devegowda, Vani N.Kim, Jung HyunHan, Ki-CheolYang, Eun GyeongChoo, HyunahPae, Ae NimNam, GhilsooChoi, Kyung Il
Issue Date
2010-03-01
Publisher
Pergamon Press Ltd.
Citation
Bioorganic & Medicinal Chemistry Letters, v.20, no.5, pp.1630 - 1633
Abstract
A novel series of 3,5,6-trisubstituted pyrazolo[4,3-d] pyrimidin-7-one derivatives, especially 6-N-arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-ones were synthesized and evaluated for their in vitro anticancer activities against various human cancer cell lines. The inhibitory activities for several kinases have also been tested. The prepared compounds library exhibited significant anticancer activity towards HT-29 colon and DU-145 prostate cancer cell lines. The structure-activity relationships of the 6-N-arylcarboxamidopyrazolo[4,3-d] pyrimidin-7-one scaffold at R-1, R-2 and R-3 have been elucidated. Among the synthesized compounds, 12b was the most active compound with GI(50) value of 0.44 mu M and 1.07 mu M against HT-29 and DU-145 cell lines, respectively, and 13a was the most selective compound towards colon cancer cell line. (C) 2010 Published by Elsevier Ltd.
Keywords
CANCER-RESEARCH; INHIBITORS; PHOSPHODIESTERASE-5; CANCER-RESEARCH; INHIBITORS; PHOSPHODIESTERASE-5; 6-N-Arylcarboxamidopyrazolo[4,3-d]pyrimidin-7-one; Anticancer activity; Structure-activity relationship
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/131645
DOI
10.1016/j.bmcl.2010.01.029
Appears in Collections:
KIST Article > 2010
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