[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/mesterolone-cipionate-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki41\/mesterolone-cipionate-wikipedia\/","headline":"Mesterolone cipionate – Wikipedia","name":"Mesterolone cipionate – Wikipedia","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 Steroid Mesterolone cipionate Clinical data Other names Mesterolone cypionate; Mesterolone cyclopentylpropionate; Mesterolone cyclopentanepropionate","datePublished":"2022-10-13","dateModified":"2022-10-13","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki41\/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\/d\/da\/Mesterolone_cipionate.svg\/250px-Mesterolone_cipionate.svg.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/d\/da\/Mesterolone_cipionate.svg\/250px-Mesterolone_cipionate.svg.png","height":"147","width":"250"},"url":"https:\/\/wiki.edu.vn\/en\/wiki41\/mesterolone-cipionate-wikipedia\/","wordCount":2432,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4SteroidMesterolone cipionateClinical dataOther namesMesterolone cypionate; Mesterolone cyclopentylpropionate; Mesterolone cyclopentanepropionateRoutes ofadministrationIntramuscular injectionDrug classAndrogen; Anabolic steroid; Androgen esterIdentifiers[(1S,5S,8R,9S,10S,13S,14S,17S)-1,10,13-trimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] 3-cyclopentylpropanoateChemical and physical dataFormulaC29H44O3Molar mass440.668\u00a0g\u00b7mol\u221213D model (JSmol)[H][C@@]12CC[C@H](OC(=O)CCC3CCCC3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2(C)CC(=O)C[C@H](C)[C@]12CInChI=1S\/C29H44O3\/c1-19-17-21(30)18-27(2)15-13-22-23-10-11-25(28(23,3)16-14-24(22)29(19,27)4)32-26(31)12-9-20-7-5-6-8-20\/h20,22-24H,5-18H2,1-4H3\/t22-,23-,24-,27-,28-,29+\/m0\/s1Key:TWDIZPBGCLXSNS-PAXVTGJLSA-NMesterolone cipionate is a synthetic anabolic\u2013androgenic steroid and an androgen ester \u2013 specifically, the C17\u03b2 cypionate ester of mesterolone \u2013 which was never marketed.[1][2][3] It is administered via intramuscular injection once every two weeks and acts as a long-acting prodrug of mesterolone.[3] The drug was studied in the treatment of depression in men along with mesterolone in the mid-1970s but was never introduced for medical use.[1][3]       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4See also[edit]References[edit]^ a b Herrmann, W. M., Horowski, R., Itil, T. M., Kehr, W., Palenschat, D., Paschelke, G., & Wachtel, H. (1975). U.S. Patent No. 3,908,007. Treatment of mental depression. Washington, DC: U.S. Patent and Trademark Office. https:\/\/www.google.com\/patents\/US3908007^ Spona J (1976). “Action of steroids on LH-RH provoked gonadotropin release”. Endocrinol. Exp. 10 (2): 91\u2013100. PMID\u00a0776594.^ a b c K\u00f6vary PM, Lenau H, Niermann H, Zierden E, Wagner H (1977). “Testosterone levels and gonadotrophins in Klinefelter’s patients treated with injections of mesterolone cipionate”. Arch Dermatol Res. 258 (3): 289\u201394. doi:10.1007\/bf00561132. PMID\u00a0883846. 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