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Dihydroorotate Dehydrogenase Inhibitor
Known as:
Dihydroorotate Dehydrogenase Inhibitors
Any substance that inhibits dihydroorotate reductase, an enzyme required for de novo biosynthesis of pyrimidine. Inhibition of dihydroorotate…
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
In vitro selection predicts malaria parasite resistance to dihydroorotate dehydrogenase inhibitors in a mouse infection model
Rebecca E. K. Mandt
,
M. Lafuente-Monasterio
,
+10 authors
D. Wirth
Science Translational Medicine
2019
Corpus ID: 208641868
The malaria parasite Plasmodium falciparum readily develops resistance to dihydroorotate dehydrogenase inhibitors in vitro and in…
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2018
2018
Re-evaluation of Brequinar sodium, a dihydroorotate dehydrogenase inhibitor
G. Peters
Nucleosides, Nucleotides & Nucleic Acids
2018
Corpus ID: 58587302
Abstract DUP-785 (Brequinar sodium) is a potent inhibitor of the mitochondrial dihydroorotate dehydrogenase (DHO-DH), a rate…
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Highly Cited
2018
Highly Cited
2018
Antimalarial activity of single-dose DSM265, a novel plasmodium dihydroorotate dehydrogenase inhibitor, in patients with uncomplicated Plasmodium falciparum or Plasmodium vivax malaria infection: a…
A. Llanos-Cuentas
,
M. Casapia
,
+20 authors
S. Duparc
Lancet. Infectious Diseases (Print)
2018
Corpus ID: 49301774
2013
2013
The role of fluorine in stabilizing the bioactive conformation of dihydroorotate dehydrogenase inhibitors
S. Bonomo
,
P. Tosco
,
M. Giorgis
,
M. Lolli
,
R. Fruttero
Journal of Molecular Modeling
2013
Corpus ID: 207039023
Dihydroorotate dehydrogenase (DHODH) is an important drug target due to its prominent role in pyrimidine biosynthesis…
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2012
2012
Discovery of diverse human dihydroorotate dehydrogenase inhibitors as immunosuppressive agents by structure-based virtual screening.
Yanyan Diao
,
Weiqiang Lu
,
+10 authors
Honglin Li
Journal of Medicinal Chemistry
2012
Corpus ID: 19953391
This study applied an efficient virtual screening strategy integrating molecular docking with MM-GBSA rescoring to identify…
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2012
2012
3D-QSAR studies of triazolopyrimidine derivatives of Plasmodium falciparum dihydroorotate dehydrogenase inhibitors using a combination of molecular dynamics, docking, and genetic algorithm-based…
P. Shah
,
Sumit Kumar
,
S. Tiwari
,
M. Siddiqi
Journal of chemical biology
2012
Corpus ID: 44604381
A series of 35 triazolopyrimidine analogues reported as Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) inhibitors…
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Highly Cited
2010
Highly Cited
2010
Chemometric modeling, docking and in silico design of triazolopyrimidine-based dihydroorotate dehydrogenase inhibitors as antimalarials.
P. Ojha
,
K. Roy
European journal of medicinal chemistry
2010
Corpus ID: 24879544
Highly Cited
2009
Highly Cited
2009
Identification of a metabolically stable triazolopyrimidine-based dihydroorotate dehydrogenase inhibitor with antimalarial activity in mice.
R. Gujjar
,
A. Marwaha
,
+10 authors
M. Phillips
Journal of Medicinal Chemistry
2009
Corpus ID: 24940904
Plasmodium falciparum causes 1-2 million deaths annually. Yet current drug therapies are compromised by resistance. We previously…
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1998
1998
Dihydroorotate Dehydrogenase Inhibitors: Quantitative Structure-activity Relationship Analysis
S. Ren
,
Sharon K. Wu
,
E. Lien
Pharmaceutical Research
1998
Corpus ID: 23559680
AbstractPurpose. The main purpose of this study is to analyze the quantitative structure-activity relationship of two series of…
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Highly Cited
1996
Highly Cited
1996
Synthesis, structure-activity relationships, and pharmacokinetic properties of dihydroorotate dehydrogenase inhibitors: 2-cyano-3-cyclopropyl-3-hydroxy-N-[3'-methyl-4'-(trifluoromethyl)phenyl…
E. A. Kuo
,
P. Hambleton
,
+13 authors
Robert Westwood
Journal of Medicinal Chemistry
1996
Corpus ID: 37547285
The active metabolite (2) of the novel immunosuppressive agent leflunomide (1) has been shown to inhibit the enzyme…
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