Testosterone sulfate

Testosterone sulfate
Names
	Preferred 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
	Other names Testosterone 17β-sulfate; Testosterone 17β-sulfuric acid; 17β-(Sulfooxy)androst-4-en-3-one
Identifiers
CAS Number	651-45-6;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:84094;
ChemSpider	106493;
PubChem CID	119207;
	InChI 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;
	SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2OS(=O)(=O)O)CCC4=CC(=O)CC[C@]34C;
Properties
Chemical formula	C19H28O5S
Molar mass	368.488 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Testosterone sulfate is an endogenous, naturally occurring steroid and minor urinary metabolite of testosterone.[1]

References

Wishart, David S.; Djombou Feunang, Yannick; Marcu, Ana; Guo, An Chi; Liang, Kevin; Vázquez Fresno, Rosa; Sajed, Tanvir; Johnson, Daniel; Li, Carin; Karu, Naama; Sayeeda, Zinat; Lo, Elvis; Assempour, Nazanin; Berjanskii, Mark; Singhal, Sandeep; Arndt, David; Liang, Yonjie; Badran, Hasan; Grant, Jason; Serra Cayuela, Arnau; Liu, Yifeng; Mandal, Rupa; Neveu, Vanessa; Pon, Allison; Knox, Craig; Wilson, Michael; Manach, Claudine; Scalbert, Augustin. "Showing metabocard for Testosterone sulfate (HMDB02833)". Human Metabolome Database, HMDB. 4.0.

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