From Wikipedia, the free encyclopedia
Testosterone sulfate
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Names
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IUPAC name
3-Oxoandrost-4-en-17β-yl hydrogen sulfate
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Systematic IUPAC name
(1S,3aS,3bR,9aR,9bS,11aS)-9a,11a-Dimethyl-7-oxo-2,3,3a,3b,4,5,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-1-yl hydrogen sulfate
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Other names
Testosterone 17β-sulfate; Testosterone 17β-sulfuric acid; 17β-(Sulfooxy)androst-4-en-3-one
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Identifiers
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ChEBI
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ChemSpider
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InChI=1S/C19H28O5S/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(24-25(21,22)23)19(15,2)10-8-16(14)18/h11,14-17H,3-10H2,1-2H3,(H,21,22,23)/t14-,15-,16-,17-,18-,19-/m0/s1 Key: WAQBISPOEAOCOG-DYKIIFRCSA-N
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C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OS(=O)(=O)O)CCC4=CC(=O)CC[C@]34C
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Properties
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C19H28O5S
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Molar mass
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368.488 g/mol
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Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound
Testosterone sulfate is an
endogenous,
naturally occurring
steroid and minor
urinary
metabolite of
testosterone.
[1]
See also
References
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^ Wishart, David S.; Guo, An Chi; Oler, Eponine; Wang, Fel; Anjum, Afia; Peters, Harrison; Dizon, Raynard; Sayeeda, Zinat; Tian, Siyang; Lee, Brian L.; Berjanskii, Mark; Mah, Robert; Yamamoto, Mai; Jovel Castillo, Juan; Torres Calzada, Claudia; Hiebert Giesbrecht, Mickel; Lui, Vicki W.; Varshavi, Dorna; Varshavi, Dorsa; Allen, Dana; Arndt, David; Khetarpal, Nitya; Sivakumaran, Aadhavya; Harford, Karxena; Sanford, Selena; Yee, Kristen; Cao, Xuan; Budinsky, Zachary; Liigand, Jaanus; Zhang, Lun; Zheng, Jiamin; Mandal, Rupasri; Karu, Naama; Dambrova, Maija; Schiöth, Helgi B.; Gautam, Vasuk.
"Showing metabocard for Testosterone sulfate (HMDB02833)".
Human Metabolome Database, HMDB. 5.0.