Page last updated: 2024-08-16

saccharin and suramin

saccharin has been researched along with suramin in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bauer, I; Bonaccini, C; Brosch, G; Caroli, A; Castellano, S; Mai, A; Ragno, R; Sbardella, G; Simeoni, S; Tramontano, A; Trojer, P; Vicidomini, C	1
Auld, DS; Blackburn, EA; Boxer, MB; Fothergill-Gilmore, LA; McNae, IW; Michels, PA; Morgan, HP; Nowicki, MW; Shen, M; Veith, H; Walkinshaw, MD; Walsh, MJ; Wear, MA	1

Other Studies

2 other study(ies) available for saccharin and suramin

Article	Year
Small molecule inhibitors of histone arginine methyltransferases: homology modeling, molecular docking, binding mode analysis, and biological evaluations. Journal of medicinal chemistry, 2007, Mar-22, Volume: 50, Issue:6 Topics: Amino Acid Sequence; Animals; Aspergillus nidulans; Benzoates; Binding Sites; Catalytic Domain; Databases, Protein; Humans; Ligands; Models, Molecular; Molecular Sequence Data; Naphthalenes; Protein Conformation; Protein-Arginine N-Methyltransferases; Quantitative Structure-Activity Relationship; Rats; Repressor Proteins; Sequence Homology, Amino Acid; Sulfonic Acids; Triazines; Xanthenes	2007
A new family of covalent inhibitors block nucleotide binding to the active site of pyruvate kinase. The Biochemical journal, 2012, Nov-15, Volume: 448, Issue:1 Topics: Adenosine Diphosphate; Adenosine Triphosphate; Animals; Arginine; Benzoates; Catalytic Domain; Conserved Sequence; Crystallography, X-Ray; Enzyme Inhibitors; High-Throughput Screening Assays; Humans; Isoenzymes; Leishmania mexicana; Lysine; Models, Molecular; Protein Binding; Protein Conformation; Pyruvate Kinase; Recombinant Proteins; Saccharin; Species Specificity; Structure-Activity Relationship; Suramin	2012

Article

Year

Small molecule inhibitors of histone arginine methyltransferases: homology modeling, molecular docking, binding mode analysis, and biological evaluations.

Journal of medicinal chemistry, 2007, Mar-22, Volume: 50, Issue:6

Topics: Amino Acid Sequence; Animals; Aspergillus nidulans; Benzoates; Binding Sites; Catalytic Domain; Databases, Protein; Humans; Ligands; Models, Molecular; Molecular Sequence Data; Naphthalenes; Protein Conformation; Protein-Arginine N-Methyltransferases; Quantitative Structure-Activity Relationship; Rats; Repressor Proteins; Sequence Homology, Amino Acid; Sulfonic Acids; Triazines; Xanthenes

2007

A new family of covalent inhibitors block nucleotide binding to the active site of pyruvate kinase.

The Biochemical journal, 2012, Nov-15, Volume: 448, Issue:1

Topics: Adenosine Diphosphate; Adenosine Triphosphate; Animals; Arginine; Benzoates; Catalytic Domain; Conserved Sequence; Crystallography, X-Ray; Enzyme Inhibitors; High-Throughput Screening Assays; Humans; Isoenzymes; Leishmania mexicana; Lysine; Models, Molecular; Protein Binding; Protein Conformation; Pyruvate Kinase; Recombinant Proteins; Saccharin; Species Specificity; Structure-Activity Relationship; Suramin

2012