[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki19\/bolasterone-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki19\/bolasterone-wikipedia\/","headline":"Bolasterone – Wikipedia","name":"Bolasterone – Wikipedia","description":"From Wikipedia, the free encyclopedia Chemical compound Bolasterone Clinical data Trade names Myagen, Methosarb Other names U-19763; NSC-66233; 7\u03b1,17\u03b1-Dimethyltestosterone; 7\u03b1,17\u03b1-Dimethylandrost-4-en-17\u03b2-ol-3-one","datePublished":"2015-09-27","dateModified":"2015-09-27","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki19\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki19\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c7\/Bolasterone.png\/215px-Bolasterone.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c7\/Bolasterone.png\/215px-Bolasterone.png","height":"141","width":"215"},"url":"https:\/\/wiki.edu.vn\/en\/wiki19\/bolasterone-wikipedia\/","wordCount":3283,"articleBody":"From Wikipedia, the free encyclopediaChemical compoundBolasteroneClinical dataTrade namesMyagen, MethosarbOther namesU-19763; NSC-66233; 7\u03b1,17\u03b1-Dimethyltestosterone; 7\u03b1,17\u03b1-Dimethylandrost-4-en-17\u03b2-ol-3-oneRoutes ofadministrationBy mouthIdentifiers(7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,10,13,17-tetramethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-oneCAS NumberPubChem CIDChemSpiderUNIIChEMBLCompTox Dashboard (EPA)ECHA InfoCard100.015.018 Chemical and physical dataFormulaC21H32O2Molar mass316.485\u00a0g\u00b7mol\u221213D model (JSmol)O=C4C=C3\/[C@]([C@H]2CC[C@]1([C@@H](CC[C@@]1(O)C)[C@@H]2[C@H](C)C3)C)(C)CC4InChI=1S\/C21H32O2\/c1-13-11-14-12-15(22)5-8-19(14,2)16-6-9-20(3)17(18(13)16)7-10-21(20,4)23\/h12-13,16-18,23H,5-11H2,1-4H3\/t13-,16+,17+,18-,19+,20+,21+\/m1\/s1Key:IVFYLRMMHVYGJH-VLOLGRDOSA-NBolasterone (INN, USAN) (brand names Myagen, Methosarb; former developmental code name U-19763), also known as 7\u03b1,17\u03b1-dimethyltestosterone, is a 17\u03b1-alkylated androgen\/anabolic steroid (AAS) which is used in veterinary medicine.[1][2] It has close structural similarity to testosterone, and like methyltestosterone has a methyl group at C17\u03b1 in order to increase oral bioavailability.[1] In addition, it is also 7\u03b1-methylated, similar to its 7\u03b2-methylated isomer calusterone.[1] The medication has a low to moderate ratio of anabolic to androgenic activity, similar to that of fluoxymesterone.[3]Bolasterone is on the World Anti-Doping Agency’s list of prohibited substances,[4] and is therefore banned from use in most major sports.References[edit]^ a b c Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp.\u00a0646\u2013. ISBN\u00a0978-1-4757-2085-3.^ Morton IK, Hall JS (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp.\u00a052\u2013. ISBN\u00a0978-94-011-4439-1.^ Kochakian CD (6 December 2012). Anabolic-Androgenic Steroids. Springer Science & Business Media. pp.\u00a0377, 401. ISBN\u00a0978-3-642-66353-6.^ “The World Anti-Doping Code: The 2020 Prohibited List” (PDF). World Anti-Doping Agency. Retrieved 2019-12-28.li{counter-increment:listitem}.mw-parser-output .hlist ol>li::before{content:\" \"counter(listitem)\"a0 \"}.mw-parser-output .hlist dd ol>li:first-child::before,.mw-parser-output .hlist dt ol>li:first-child::before,.mw-parser-output .hlist li ol>li:first-child::before{content:\" (\"counter(listitem)\"a0 \"}]]>.navbox-abovebelow,.mw-parser-output tr+tr>.navbox-group,.mw-parser-output tr+tr>.navbox-image,.mw-parser-output tr+tr>.navbox-list{border-top:2px solid #fdfdfd}.mw-parser-output .navbox-title{background-color:#ccf}.mw-parser-output .navbox-abovebelow,.mw-parser-output .navbox-group,.mw-parser-output .navbox-subgroup .navbox-title{background-color:#ddf}.mw-parser-output .navbox-subgroup .navbox-group,.mw-parser-output .navbox-subgroup .navbox-abovebelow{background-color:#e6e6ff}.mw-parser-output .navbox-even{background-color:#f7f7f7}.mw-parser-output .navbox-odd{background-color:transparent}.mw-parser-output .navbox .hlist td dl,.mw-parser-output .navbox .hlist td ol,.mw-parser-output .navbox .hlist td ul,.mw-parser-output .navbox td.hlist dl,.mw-parser-output .navbox td.hlist ol,.mw-parser-output .navbox td.hlist ul{padding:0.125em 0}.mw-parser-output .navbox .navbar{display:block;font-size:100%}.mw-parser-output .navbox-title .navbar{float:left;text-align:left;margin-right:0.5em}]]>span,.mw-parser-output .navbar a>abbr{text-decoration:inherit}.mw-parser-output .navbar-mini abbr{font-variant:small-caps;border-bottom:none;text-decoration:none;cursor:inherit}.mw-parser-output .navbar-ct-full{font-size:114%;margin:0 7em}.mw-parser-output .navbar-ct-mini{font-size:114%;margin:0 4em}]]>Androgens(incl. AAS)AR agonistsProgonadotropinsAntiandrogensAR antagonistsSteroidogenesisinhibitorsAntigonadotropinsD2 receptor antagonists (prolactin releasers) (e.g., domperidone, metoclopramide, risperidone, haloperidol, chlorpromazine, sulpiride)Estrogens (e.g., bifluranol, diethylstilbestrol, estradiol, estradiol esters, ethinylestradiol, ethinylestradiol sulfonate, paroxypropione)GnRH agonists (e.g., leuprorelin)GnRH antagonists (e.g., cetrorelix)Progestogens (incl., chlormadinone acetate, cyproterone acetate, hydroxyprogesterone caproate, gestonorone caproate, medroxyprogesterone acetate, megestrol acetate)OthersWikimedia ErrorOur servers are currently under maintenance or experiencing a technical problem.Please try again in a few\u00a0minutes.See the error message at the bottom of this page for more\u00a0information. 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