Synthesis and SAR of novel, potent and orally bioavailable benzimidazole inhibitors of poly(ADP-ribose) polymerase (PARP) with a quaternary methylene-amino substituent
2008; Elsevier BV; Volume: 18; Issue: 14 Linguagem: Inglês
10.1016/j.bmcl.2008.06.023
ISSN1464-3405
AutoresGui‐Dong Zhu, Viraj B. Gandhi, Jianchun Gong, Sheela A. Thomas, Yan Luo, Xuesong Liu, Yan Shi, Vered Klinghofer, Eric F. Johnson, David J. Frost, Cherrie K. Donawho, Ken Jarvis, Jennifer J. Bouska, Kennan C. Marsh, Saul H. Rosenberg, Vincent L. Giranda, Thomas D. Penning,
Tópico(s)DNA Repair Mechanisms
ResumoPoly(ADP-ribose) polymerases (PARPs) play significant roles in various cellular functions including DNA repair and control of RNA transcription. PARP inhibitors have been demonstrated to potentiate the effect of cytotoxic agents or radiation in a number of animal tumor models. Utilizing a benzimidazole carboxamide scaffold in which the amide forms a key intramolecular hydrogen bond for optimal interaction with the enzyme, we have identified a novel series of PARP inhibitors containing a quaternary methylene-amino substituent at the C-2 position of the benzimidazole. Geminal dimethyl analogs at the methylene-amino substituent were typically more potent than mono-methyl derivatives in both intrinsic and cellular assays. Smaller cycloalkanes such as cyclopropyl or cyclobutyl were tolerated at the quaternary carbon while larger rings were detrimental to potency. In vivo efficacy data in a B16F10 murine flank melanoma model in combination with temozolomide (TMZ) are described for two optimized analogs.
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