Ligand boldenone
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Basic Ligand Information
Molecular Structure

C19H26O2
boldenone
RSIHSRDYCUFFLA-DYKIIFRCSA-N
1,4-androstadien-17beta-ol-3-one, 1,4-androstadiene-17beta-ol-3-one, 1-dehydrotestosterone, 17beta-Hydroxy-1,4-androstadien-3-one, 17beta-Hydroxyandrost-1,4-diene-3-one, 17beta-hydroxyandrosta-1,4-dien-3-one, 17beta-hydroxyandrosta-1,4-diene-3-one, dehydrotestosterone
Roles as Enzyme Ligand
In Vivo Substrate in Enzyme-catalyzed Reactions (1 result)
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UDP-D-glucuronate + dehydrotestosterone = UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
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Substrate in Enzyme-catalyzed Reactions (3 results)
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1-dehydrotestosterone + H2O + 2,6-dichlorophenolindophenol = ? + reduced 2,6-dichlorophenolindophenol
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1,4-androstadien-17beta-ol-3-one + NADPH + H+ = ?
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UDP-D-glucuronate + dehydrotestosterone = UDP + dehydrotestosterone 17-O-beta-D-glucuronoside
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Product in Enzyme-catalyzed Reactions (5 results)
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4-androstene-17beta-ol-3-one + 2,6-dichlorophenol-indophenol = 1,4-androstadiene-17beta-ol-3-one + reduced 2,6-dichlorophenol-indophenol
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testosterone + 2,6-dichlorophenol-indophenol = 17beta-hydroxyandrost-1,4-diene-3-one + reduced 2,6-dichlorophenol-indophenol
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testosterone + acceptor = 17beta-hydroxyandrost-1,4-diene-3-one + reduced acceptor
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boldenone 17-sulfate + H2O = boldenone + sulfate
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boldenone 17-sulfate + H2O = boldenone + sulfate
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Inhibitor in Enzyme-catalyzed Reactions (3 results)
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Enzyme Kinetic Parameters
kcat Value (Turnover Number) (1 result)
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KM Value (1 result)
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Ki Value (1 result)
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IC50 Value (5 results)
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0.0494
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pH 8.0, temperature not specified in the publication
0.0915
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presence of 0.1 M ADP, pH 8.0, temperature not specified in the publication
0.494
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pH 8.0, temperature not specified in the publication
0.814
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presence of 0.1 M ADP, pH 8.0, temperature not specified in the publication
References & Links
Literature References (6)
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Some characteristics of the microsomal steroid reductase (5alpha) of rat liver
1960
McGuire, J.S.; Hollis, V.W.; Tomkins, G.M.
J. Biol. Chem.
235
3112-3117
Butyrylcholinesterase inhibitory activity of testosterone and some of its metabolites
2008
Al-Aboudi, A.; Odeh, H.; Khalid, A.; Naz, Q.; Choudhary, M.I.
J. Enzyme Inhib. Med. Chem.
24
553-558
Inactivation by UDP-glucuronosyltransferase enzymes: the end of androgen signaling
2008
Chouinard, S.; Yueh, M.F.; Tukey, R.H.; Giton, F.; Fiet, J.; Pelletier, G.; Barbier, O.; Belanger, A.
J. Steroid Biochem. Mol. Biol.
109
247-253
Substrate specificity and inhibitor analyses of human steroid 5beta-reductase (AKR1D1)
2011
Chen, M.; Drury, J.E.; Penning, T.M.
Steroids
76
484-490
Widening spectrum of cellular and subcellular expression of human GLUD1 and GLUD2 glutamate dehydrogenases suggests novel functions
2017
Spanaki, C.; Kotzamani, D.; Plaitakis, A.
Neurochem. Res.
42
92-107
Integrated multi-omics analyses reveal the biochemical mechanisms and phylogenetic relevance of anaerobic androgen biodegradation in the environment
2016
Yang, F.; Chen, Y.; Tang, S.; Yu, C.; Wang, P.; Ismail, W.; Wang, C.; Ding, J.; Yang, C.; Yang, C.; Chiang, Y.
ISME J.
10
1967-1983
Links to other databases for boldenone