Bioorganic & Medicinal Chemistry Letters 2010-04-01

Synthesis and evaluation of tricyclic derivatives containing a non-aromatic amide as inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1).

Chun-Ho Park, Kwangwoo Chun, Bo-Young Joe, Ji-Seon Park, Young-Chul Kim, Ji-Soo Choi, Dong-Kyu Ryu, Seong-Ho Koh, Goang Won Cho, Seung Hyun Kim, Myung-Hwa Kim

文献索引：Bioorg. Med. Chem. Lett. 20(7) , 2250-3, (2010)

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摘要

Highly potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors, including 9-hydroxy-1,2-dihydro-4H-thiopyrano[3,4-c]quinolin-5(6H)-one derivatives with a non-aromatic A-ring, were synthesized. Among the derivatives, 12a showed low nanomolar enzyme and cellular activity (IC(50) = 42 nM, ED(50) = 220 nM) with good water solubility. Further, 12a exhibited microsomal stability in vitro and brain permeability in vivo.2010 Elsevier Ltd. All rights reserved.