Page last updated: 2024-09-03

estrone-3-o-sulfamate and sulpiride

estrone-3-o-sulfamate has been researched along with sulpiride in 2 studies

Compound Research Comparison

Studies
(estrone-3-o-sulfamate)
Trials
(estrone-3-o-sulfamate)
Recent Studies (post-2010)
(estrone-3-o-sulfamate)
Studies
(sulpiride)
Trials
(sulpiride)
Recent Studies (post-2010) (sulpiride)
890154,152427635

Protein Interaction Comparison

ProteinTaxonomyestrone-3-o-sulfamate (IC50)sulpiride (IC50)
Carbonic anhydrase 1Homo sapiens (human)1.2
Carbonic anhydrase 2Homo sapiens (human)0.04
Alpha-2A adrenergic receptorHomo sapiens (human)2.019
D(2) dopamine receptorHomo sapiens (human)0.0858
D(3) dopamine receptorHomo sapiens (human)0.2651
D(2) dopamine receptorRattus norvegicus (Norway rat)0.2215
Carbonic anhydrase 4Bos taurus (cattle)0.62
D(2) dopamine receptorCanis lupus familiaris (dog)0.2

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abbate, F; Casini, A; Ciattini, S; Coetzee, A; Scozzafava, A; Supuran, CT1
Alterio, V; De Simone, G; Di Fiore, A; Menchise, V; Pedone, C; Scozzafava, A; Supuran, CT1

Other Studies

2 other study(ies) available for estrone-3-o-sulfamate and sulpiride

ArticleYear
Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with the antipsychotic drug sulpiride.
    Bioorganic & medicinal chemistry letters, 2004, Jan-19, Volume: 14, Issue:2

    Topics: Antipsychotic Agents; Binding Sites; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Crystallography, X-Ray; Humans; Isoenzymes; Sulpiride

2004
Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme II.
    Journal of medicinal chemistry, 2005, Sep-08, Volume: 48, Issue:18

    Topics: Antigens, Neoplasm; Antineoplastic Agents; Binding Sites; Biomarkers, Tumor; Carbonic Anhydrase II; Carbonic Anhydrase IX; Carbonic Anhydrases; Cell Membrane Permeability; Crystallography, X-Ray; Humans; Isoenzymes; Models, Molecular; Molecular Structure; Protein Binding; Pyridinium Compounds; Quantitative Structure-Activity Relationship; Recombinant Proteins; Sulfonamides

2005