Please use this identifier to cite or link to this item: http://dspace2020.uniten.edu.my:8080/handle/123456789/9736
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dc.contributor.authorAbdullah, I.
dc.contributor.authorChee, C.F.
dc.contributor.authorLee, Y.-K.
dc.contributor.authorThunuguntla, S.S.R.
dc.contributor.authorSatish Reddy, K.
dc.contributor.authorNellore, K.
dc.contributor.authorAntony, T.
dc.contributor.authorVerma, J.
dc.contributor.authorMun, K.W.
dc.contributor.authorOthman, S.
dc.contributor.authorSubramanya, H.
dc.contributor.authorRahman, N.A.
dc.date.accessioned2018-03-06T03:49:14Z-
dc.date.available2018-03-06T03:49:14Z-
dc.date.issued2015
dc.identifier.urihttp://dspace.uniten.edu.my/jspui/handle/123456789/9736-
dc.description.abstractPoly (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. © 2015 Elsevier Ltd. All rights reserved.
dc.titleBenzimidazole derivatives as potential dual inhibitors for PARP-1 and DHODH
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptUniversiti Tenaga Nasional-
Appears in Collections:COE Scholarly Publication
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