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DC Field | Value | Language |
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dc.contributor.author | Abdullah, I. | |
dc.contributor.author | Chee, C.F. | |
dc.contributor.author | Lee, Y.-K. | |
dc.contributor.author | Thunuguntla, S.S.R. | |
dc.contributor.author | Satish Reddy, K. | |
dc.contributor.author | Nellore, K. | |
dc.contributor.author | Antony, T. | |
dc.contributor.author | Verma, J. | |
dc.contributor.author | Mun, K.W. | |
dc.contributor.author | Othman, S. | |
dc.contributor.author | Subramanya, H. | |
dc.contributor.author | Rahman, N.A. | |
dc.date.accessioned | 2018-03-06T03:49:14Z | - |
dc.date.available | 2018-03-06T03:49:14Z | - |
dc.date.issued | 2015 | |
dc.identifier.uri | http://dspace.uniten.edu.my/jspui/handle/123456789/9736 | - |
dc.description.abstract | 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. © 2015 Elsevier Ltd. All rights reserved. | |
dc.title | Benzimidazole derivatives as potential dual inhibitors for PARP-1 and DHODH | |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
crisitem.author.dept | Universiti Tenaga Nasional | - |
Appears in Collections: | COE Scholarly Publication |
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