Compounds > sinensetin
Page last updated: 2024-09-04

sinensetin and fisetin

sinensetin has been researched along with fisetin in 5 studies

Compound Research Comparison

Studies
(sinensetin)		Trials
(sinensetin)		Recent Studies (post-2010)
(sinensetin)		Studies
(fisetin)		Trials
(fisetin)		Recent Studies (post-2010) (fisetin)
560426674507

Protein Interaction Comparison

ProteinTaxonomysinensetin (IC50)fisetin (IC50)
Chain B, Cell division protein kinase 6Homo sapiens (human)0.85
G2/mitotic-specific cyclin-B2Homo sapiens (human)0.79
Cyclin-dependent kinase 1Homo sapiens (human)0.79
Serine/threonine-protein kinase pim-1Homo sapiens (human)0.85
Pyruvate kinase PKMHomo sapiens (human)0.9
G2/mitotic-specific cyclin-B1Homo sapiens (human)0.79
G2/mitotic-specific cyclin-BMarthasterias glacialis (spiny starfish)0.6575
Polyunsaturated fatty acid lipoxygenase ALOX15Homo sapiens (human)1.4
Polyunsaturated fatty acid lipoxygenase ALOX12Homo sapiens (human)0.95
Glycogen synthase kinase-3 betaRattus norvegicus (Norway rat)0.6575
Casein kinase II subunit alpha'Homo sapiens (human)0.5667
Cyclin-dependent kinase 2Homo sapiens (human)5
1-deoxy-D-xylulose 5-phosphate reductoisomeraseEscherichia coli K-123.5
Xanthine dehydrogenase/oxidaseHomo sapiens (human)4.33
Glycogen synthase kinase-3 alphaHomo sapiens (human)0.42
Glycogen synthase kinase-3 betaHomo sapiens (human)0.42
Mitogen-activated protein kinase 10Homo sapiens (human)2.65
Casein kinase II subunit betaHomo sapiens (human)0.5667
Casein kinase II subunit alphaHomo sapiens (human)0.5667
Cyclin-dependent kinase 6Homo sapiens (human)0.696
Cyclin-dependent-like kinase 5 Homo sapiens (human)0.64
Cyclin homologHerpesvirus saimiri (strain 11)0.6575
Cyclin-dependent kinase 5 activator 1Homo sapiens (human)0.64
Mitogen-activated protein kinase 14Homo sapiens (human)2.65
Integrase Human immunodeficiency virus 18.5
Casein kinase II subunit alpha 3Homo sapiens (human)0.35
G2/mitotic-specific cyclin-B3Homo sapiens (human)0.79
Enoyl-acyl-carrier protein reductase Plasmodium falciparum (malaria parasite P. falciparum)1
3-oxoacyl-acyl-carrier protein reductase Plasmodium falciparum (malaria parasite P. falciparum)4.1
Beta-hydroxyacyl-ACP dehydratase precursor (Fatty acid synthesis protein)Plasmodium falciparum (malaria parasite P. falciparum)2
Aurora kinase BHomo sapiens (human)2.63
Cyclin-dependent kinase 1Oryzias latipes (Japanese medaka)0.6575

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Augereau, JM; Billon, M; Gleye, J; Herbert, JM; Lale, A; Leconte, M1
Ash, K; Grohmann, K; Manthey, CL; Manthey, JA; Montanari, A1
Debyser, Z; Glisic, S; Mouscadet, JF; Veljkovic, N; Veljkovic, V1
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P1
Ahn, S; Jung, H; Jung, Y; Lee, YH; Lim, Y; Shin, SY; Yong, Y1

Other Studies

5 other study(ies) available for sinensetin and fisetin

ArticleYear
Ability of different flavonoids to inhibit the procoagulant activity of adherent human monocytes.
    Journal of natural products, 1996, Volume: 59, Issue:3

    Topics: Amino Acid Sequence; Blood Coagulation; Cell Adhesion; Endotoxins; Flavonoids; Humans; In Vitro Techniques; Interleukin-1; Molecular Sequence Data; Monocytes

1996
Polymethoxylated flavones derived from citrus suppress tumor necrosis factor-alpha expression by human monocytes.
    Journal of natural products, 1999, Volume: 62, Issue:3

    Topics: Citrus; Cyclic AMP; Flavonoids; Humans; In Vitro Techniques; Lipopolysaccharides; Monocytes; Phosphodiesterase Inhibitors; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tumor Necrosis Factor-alpha

1999
Simple criterion for selection of flavonoid compounds with anti-HIV activity.
    Bioorganic & medicinal chemistry letters, 2007, Mar-01, Volume: 17, Issue:5

    Topics: Anti-HIV Agents; Computational Biology; Flavonoids; Humans; Models, Molecular; Quantitative Structure-Activity Relationship

2007
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
    Bioorganic & medicinal chemistry, 2012, Nov-15, Volume: 20, Issue:22

    Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship

2012
Plant-derived flavones as inhibitors of aurora B kinase and their quantitative structure-activity relationships.
    Chemical biology & drug design, 2015, Volume: 85, Issue:5

    Topics: Apoptosis; Aurora Kinase A; Aurora Kinase B; Aurora Kinase C; Binding Sites; Chromones; Eriocaulaceae; Flavones; G2 Phase Cell Cycle Checkpoints; HCT116 Cells; Humans; M Phase Cell Cycle Checkpoints; Microscopy, Fluorescence; Molecular Docking Simulation; Phosphorylation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Quantitative Structure-Activity Relationship

2015