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Literature summary extracted from

  • Ferreira, C.V.; Justo, G.Z.; Souza, A.C.; Queiroz, K.C.; Zambuzzi, W.F.; Aoyama, H.; Peppelenbosch, M.P.
    Natural compounds as a source of protein tyrosine phosphatase inhibitors: application to the rational design of small-molecule derivatives (2006), Biochimie, 88, 1859-1873.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.1.3.48 (7bS,9R,13bR,15R)-7-amino-9-(hydroxymethyl)-10,13-dioxo-2,3,3a,3b,4,5,6,7,7a,7b,9,10,13,13b-tetradecahydro-1H-6,8-methanobenzo[h]imidazo[1,2-a]pyrido[3,2-c][1,5]naphthyridine-15-carbonitrile inhibits Cdc25B modestly Homo sapiens
3.1.3.48 (7bS,9R,13bR,15S)-7-amino-15-hydroxy-9-(hydroxymethyl)-2,3,3a,3b,4,5,6,7,7a,7b,9,13b-dodecahydro-1H-6,8-methanobenzo[h]imidazo[1,2-a]pyrido[3,2-c][1,5]naphthyridine-10,13-dione
-
 Homo sapiens
3.1.3.48 ([2-bromo-4-(3-oxo-2,3-diphenylpropyl)phenyl](difluoro)methyl)phosphonic acid
-
 Homo sapiens
3.1.3.48 4-isoavenaciolide potent irreversible inhibitor of VHR; potent irreversible inhibitor of VHR; potent irreversible inhibitor of VHR Homo sapiens
3.1.3.48 4-methoxy-3-(5-methoxy-1-benzofuran-6-yl)-5-(4-methoxyphenyl)isoxazole
-
 Homo sapiens
3.1.3.48 4-methoxy-3-(5-methoxy-1-benzofuran-6-yl)-5-phenylisoxazole
-
 Homo sapiens
3.1.3.48 5-(2-fluoro-5-((1E)-3-[3-hydroxy-2-(methoxycarbonyl)phenoxy]prop-1-en-1-yl)phenyl)isoxazole-3-carboxylic acid
-
 Homo sapiens
3.1.3.48 dysidiolide inhibits Cdc25A Homo sapiens
3.1.3.48 ethyl-3,4-dephostatin
-
 Homo sapiens
3.1.3.48 hexadecanoyl-5-hydroxymethyl tetronic acid potent irreversible inhibitor of VHR; potent irreversible inhibitor of VHR; potent irreversible inhibitor of VHR Homo sapiens
3.1.3.48 kanjone
-
 Homo sapiens
3.1.3.48 karanjin
-
 Homo sapiens
3.1.3.48 menadione inhibits Cdc25B irreversibly Homo sapiens
3.1.3.48 methyl 2-[4-[(4-[[ethoxy(oxo)acetyl][2-(methoxycarbonyl)phenyl]amino]-3-ethylphenylalanyl)amino]butoxy]-6-hydroxybenzoate
-
 Homo sapiens
3.1.3.48 nocardione A inhibits Cdc25B Homo sapiens
3.1.3.48 nocardione B inhibits Cdc25B Homo sapiens
3.1.3.48 Sodium vanadate
-
 Homo sapiens
3.1.3.48 stevastelin inhibits VHR; inhibits VHR; inhibits VHR Homo sapiens
3.1.3.48 sulfircin inhibits Cdc25A Homo sapiens
3.1.3.48 vanadate
-
 Homo sapiens
3.1.3.48 [(4-[(4E)-2-(1H-benzotriazol-1-yl)-2-[4-(methoxycarbonyl)phenyl]-5-phenylpent-4-en-1-yl]phenyl)(difluoro)methyl]phosphonic acid
-
 Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
3.1.3.48 Homo sapiens
-
-
-
3.1.3.48 Homo sapiens P30304
-
-
3.1.3.48 Homo sapiens P30305 Cdc25B
-
3.1.3.48 Homo sapiens P30307 Cdc25C
-

Synonyms

EC Number Synonyms Comment Organism
3.1.3.48 Cdc25A
-
 Homo sapiens
3.1.3.48 Cdc25B
-
 Homo sapiens
3.1.3.48 Cdc25C
-
 Homo sapiens
3.1.3.48 protein tyrosine phosphatase
-
 Homo sapiens
3.1.3.48 PTP
-
 Homo sapiens
3.1.3.48 PTP1B
-
 Homo sapiens
3.1.3.48 VHR
-
 Homo sapiens

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.1.3.48 0.0562
-
-
 Homo sapiens Sodium vanadate
3.1.3.48 0.0796
-
-
 Homo sapiens 4-methoxy-3-(5-methoxy-1-benzofuran-6-yl)-5-(4-methoxyphenyl)isoxazole
3.1.3.48 0.0804
-
-
 Homo sapiens 4-methoxy-3-(5-methoxy-1-benzofuran-6-yl)-5-phenylisoxazole