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Literature summary extracted from

  • Bulbul, M.; Erat, M.
    Investigation of the effects of some sulfonamide derivatives on the activities of glucose-6-phosphate dehydrogenase, 6-phospho gluconate dehydrogenase and glutathione reductase from human erythrocytes (2008), J. Enzyme Inhib. Med. Chem., 23, 418-423.
    View publication on PubMed

Activating Compound

EC Number Activating Compound Comment Organism Structure
1.1.1.44 5-(3alpha-acetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide activates Homo sapiens
1.1.1.44 5-(3alpha-hydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide activates Homo sapiens
1.1.1.49 5-(3alpha,12alpha-dihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide weak activation Homo sapiens
1.1.1.49 5-(3alpha,acetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide activates Homo sapiens
1.1.1.49 acetazolamide activates Homo sapiens

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.1.1.43 5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.43 5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.43 dorzolamide
-
Homo sapiens
1.1.1.43 additional information not inhibited by 5-(3alpha-hydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide, 5-(3alpha,12alpha-dihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide, 5-(3alpha,acetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide, 5-(3,7,12-trioxo-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide, and acetazolamide Homo sapiens
1.1.1.44 (4S)-trans-4-ethylammonio-6-methyl-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide i.e. dorzolamide, competitive Homo sapiens
1.1.1.44 5-(3,7,12-trioxo-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide weak inhibition Homo sapiens
1.1.1.44 5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide competitive Homo sapiens
1.1.1.44 5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide competitive Homo sapiens
1.1.1.49 5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide weak inhibition Homo sapiens
1.1.1.49 5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide weak inhibition Homo sapiens
1.8.1.7 5-(3alpha,12alpha-dihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.8.1.7 5-(3alpha-hydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
1.1.1.43 Homo sapiens
-
-
-
1.1.1.44 Homo sapiens
-
-
-
1.1.1.49 Homo sapiens
-
-
-
1.8.1.7 Homo sapiens
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
1.1.1.43 ammonium sulfate precipitation, 2',5'-ADP Sepharose 4B affinity chromatography, and Sephadex G-200 gel filtration Homo sapiens
1.1.1.44
-
Homo sapiens
1.1.1.49
-
Homo sapiens

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.1.1.43 erythrocyte
-
Homo sapiens
-
1.1.1.49 erythrocyte
-
Homo sapiens
-
1.8.1.7 erythrocyte
-
Homo sapiens
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.1.1.44 6-phospho-D-gluconate + NADP+
-
Homo sapiens D-ribulose 5-phosphate + CO2 + NADPH + H+
-
?

Synonyms

EC Number Synonyms Comment Organism
1.1.1.43 6-phosphogluconate dehydrogenase
-
Homo sapiens
1.1.1.44 6PGD
-
Homo sapiens
1.1.1.49 G6PD
-
Homo sapiens

Ki Value [mM]

EC Number Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
1.1.1.43 0.0042
-
5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.43 0.0878
-
5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.43 3.145
-
dorzolamide
-
Homo sapiens
1.1.1.44 0.0042
-
5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.44 0.0878
-
5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.1.1.44 3.14
-
(4S)-trans-4-ethylammonio-6-methyl-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide
-
Homo sapiens
1.8.1.7 0.0061
-
5-(3alpha,12alpha-dihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens
1.8.1.7 0.0723
-
5-(3alpha-hydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
-
Homo sapiens

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
1.1.1.43 0.00253
-
-
Homo sapiens 5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
1.1.1.43 0.0601
-
-
Homo sapiens 5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
1.1.1.43 1.41
-
-
Homo sapiens dorzolamide
1.1.1.44 0.00253
-
-
Homo sapiens 5-(3alpha,7alpha,12alpha-triacetoxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
1.1.1.44 0.0601
-
-
Homo sapiens 5-(3alpha,7alpha,12alpha-trihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
1.1.1.44 1.41
-
-
Homo sapiens (4S)-trans-4-ethylammonio-6-methyl-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide
1.8.1.7 0.0045
-
-
Homo sapiens 5-(3alpha,12alpha-dihydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide
1.8.1.7 0.0471
-
-
Homo sapiens 5-(3alpha-hydroxy-5-beta-cholanamido)-1,3,4-thiadiazole-2-sulfonamide