Benzimidazole derivatives as potential dual inhibitors for PARP-1 and DHODH

被引:34
作者
Abdullah, Iskandar [1 ]
Chee, Chin Fei [1 ,2 ,5 ]
Lee, Yean-Kee [1 ]
Thunuguntla, Siva Sanjeeva Rao [3 ]
Reddy, K. Satish [3 ]
Nellore, Kavitha [3 ]
Antony, Thomas [3 ]
Verma, Jitender [3 ]
Mun, Kong Wai [2 ]
Othman, Shatrah [1 ,4 ]
Subramanya, Hosahalli [3 ]
Rahman, Noorsaadah Abd. [1 ]
机构
[1] Univ Malaya, Fac Sci, Dept Chem, Drug Design & Dev Res Grp, Kuala Lumpur, Malaysia
[2] Aurigene Discovery Technol Malaysia, Sdn Bhd, Malaysia
[3] Aurigene Discovery Technol India Ltd, Bangalore, Karnataka, India
[4] Univ Malaya, Fac Med, Dept Mol Med, Kuala Lumpur, Malaysia
[5] Int Med Univ, Sch Pharm, Kuala Lumpur 57000, Malaysia
关键词
Poly (ADP-ribose) polymerase; PARP; PARP-1; Dihydroorotate dehydrogenase; DHODH; Benzimidazole; POLY(ADP-RIBOSE) POLYMERASE PARP; RESISTANCE-MODIFYING AGENTS; ACID SODIUM-SALT; DNA-REPAIR; BIOLOGICAL-PROPERTIES; DISCOVERY; PARTHANATOS; BREQUINAR; DRUG; SAR;
D O I
10.1016/j.bmc.2015.05.051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly (ADP-ribose) polymerases (PARPs) play diverse roles in various cellular processes that involve DNA repair and programmed cell death. Amongst these polymerases is PARP-1 which is the key DNA damage-sensing enzyme that acts as an initiator for the DNA repair mechanism. Dihydroorotate dehydrogenase (DHODH) is an enzyme in the pyrimidine biosynthetic pathway which is an important target for anti-hyperproliferative and anti-inflammatory drug design. Since these enzymes share a common role in the DNA replication and repair mechanisms, it may be beneficial to target both PARP-1 and DHODH in attempts to design new anti-cancer agents. Benzimidazole derivatives have shown a wide variety of pharmacological activities including PARP and DHODH inhibition. We hereby report the design, synthesis and bioactivities of a series of benzimidazole derivatives as inhibitors of both the PARP-1 and DHODH enzymes. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4669 / 4680
页数:12
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