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Estrone sulfate
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{{cs1 config|name-list-style=vanc}} {{About|estrone sulfate as a hormone|its use as a medication|Estrone sulfate (medication)}} {{Use dmy dates|date=August 2018}} {{Chembox <!-- Images --> | ImageFile = Estrone sulfate.svg | ImageClass = skin-invert | ImageSize = 250px | ImageAlt = Skeletal formula of estrone sulfate | ImageFile2 = Estrone sulfate 3D ball.png | ImageSize2 = 250px | ImageAlt2 = Space-filling model of the estrone sulfate molecule <!-- Names --> | IUPACName = 17-Oxoestra-1,3,5(10)-trien-3-yl hydrogen sulfate | SystematicName = (3a''S'',3b''R'',9b''S'',11a''S'')-11a-Methyl-1-oxo-2,3,3a,3b,4,5,9b,10,11,11a-decahydro-1''H''-cyclopenta[''a'']phenanthren-7-yl hydrogen sulfate | OtherNames = E1S; Oestrone sulfate; Estrone 3-sulfate; Estra-1,3,5(10)-trien-17-one 3-sulfate <!-- Sections --> | Section1 = {{Chembox Identifiers | CASNo = 481-97-0 | CASNoOther = 438-67-5 (sodium salt) | ChEBI = 17474 | ChEMBL = 494753 | ChemSpiderID = 2272513 | DrugBank = DB04574 | EC_number = 207-120-4 | InChI = 1S/C18H22O5S/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,20,21,22)/t14-,15-,16+,18+/m1/s1 | InChIKey = JKKFKPJIXZFSSB-CBZIJGRNSA-N | KEGG = C02538 | PubChem = 3001028 | SMILES = C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)CCC4=C3C=CC(=C4)OS(=O)(=O)O | UNII = QTL48N278K }} | Section2 = {{Chembox Properties | C=18 | H=22 | O=5 | S=1 | MolarMass = 350.429 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} '''Estrone sulfate''', also known as '''E1S''', '''E1SO4''' and '''estrone 3-sulfate''', is a [[natural product|natural]], [[endogenous]] [[steroid]] and an [[estrogen ester]] and [[estrogen conjugate|conjugate]].<ref name="pmid27960570">{{cite journal | vauthors = Rezvanpour A, Don-Wauchope AC | title = Clinical implications of estrone sulfate measurement in laboratory medicine | journal = Crit Rev Clin Lab Sci | volume = 54 | issue = 2 | pages = 73–86 | date = March 2017 | pmid = 27960570 | doi = 10.1080/10408363.2016.1252310 | s2cid = 1825531 }}</ref><ref name="Lobo2007">{{cite book| first = Rogerio A. | last = Lobo |title=Treatment of the Postmenopausal Woman: Basic and Clinical Aspects|url=https://books.google.com/books?id=gywV9hkcyOMC&pg=PA768|date=5 June 2007|publisher=Academic Press|isbn=978-0-08-055309-2|pages=768–}}</ref><ref name="pmid16112947">{{cite journal | vauthors = Kuhl H | title = Pharmacology of estrogens and progestogens: influence of different routes of administration | journal = Climacteric | volume = 8 | pages = 3–63 | year = 2005 | issue = Suppl 1 | pmid = 16112947 | doi = 10.1080/13697130500148875 | s2cid = 24616324 | url = http://hormonebalance.org/images/documents/Kuhl%2005%20%20Pharm%20Estro%20Progest%20Climacteric_1313155660.pdf}}</ref> In addition to its role as a natural hormone, estrone sulfate is used as a [[medication]], for instance in [[menopausal hormone therapy]]; for information on estrone sulfate as a medication, see the [[estrone sulfate (medication)]] article.
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