Page last updated: 2024-09-03

estrone-3-o-sulfamate and n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide

estrone-3-o-sulfamate has been researched along with n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide 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 (n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide)	Trials (n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide)	Recent Studies (post-2010) (n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide)
89	0	15	149	13	63

Protein Interaction Comparison

Protein	Taxonomy	n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide (IC50)
Tyrosine-protein kinase ABL1	Homo sapiens (human)	0.007
Carbonic anhydrase 1	Homo sapiens (human)	0.031
Carbonic anhydrase 2	Homo sapiens (human)	0.011
Dihydrofolate reductase	Escherichia coli K-12	0.007
Cyclin-dependent kinase 2	Homo sapiens (human)	0.007
Carbonic anhydrase 4	Bos taurus (cattle)	0.065

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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abbate, F; Casini, A; Ciattini, S; Coetzee, A; Scozzafava, A; Supuran, CT	1
Alterio, V; De Simone, G; Di Fiore, A; Menchise, V; Pedone, C; Scozzafava, A; Supuran, CT	1

Other Studies

2 other study(ies) available for estrone-3-o-sulfamate and n-(3-chloro-7-indolyl)-1,4-benzenedisulphonamide

Article	Year
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

Article

Year

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