[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki40\/trendione-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki40\/trendione-wikipedia\/","headline":"Trendione – Wikipedia","name":"Trendione – Wikipedia","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 Chemical compound Trendione Other names RU-2065; Trenavar; Triendione; Estra-4,9,11-triene-3,17-dione Drug class Androgen; Anabolic","datePublished":"2016-05-06","dateModified":"2016-05-06","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki40\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki40\/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\/0\/0b\/Trendione.svg\/200px-Trendione.svg.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/0\/0b\/Trendione.svg\/200px-Trendione.svg.png","height":"140","width":"200"},"url":"https:\/\/wiki.edu.vn\/en\/wiki40\/trendione-wikipedia\/","wordCount":3169,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Chemical compoundTrendioneOther namesRU-2065; Trenavar; Triendione; Estra-4,9,11-triene-3,17-dioneDrug classAndrogen; Anabolic steroid; Progestogen(8S,13S,14S)-13-Methyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthrene-3,17-dioneCAS NumberPubChem CIDChemSpiderUNIICompTox Dashboard (EPA)FormulaC18H20O2Molar mass268.356\u00a0g\u00b7mol\u221213D model (JSmol)C[C@]12C=CC3=C4CCC(=O)C=C4CC[C@H]3[C@@H]1CCC2=O       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4InChI=1S\/C18H20O2\/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20\/h8-10,15-16H,2-7H2,1H3\/t15-,16+,18+\/m1\/s1Key:KBSXJBBFQODDTQ-RYRKJORJSA-NTrendione (developmental code name RU-2065; nickname Trenavar), also known as estra-4,9,11-triene-3,17-dione, is an androgen prohormone as well as metabolite of the anabolic steroid trenbolone.[1][2][3][4][5] Trendione is to trenbolone as androstenedione is to testosterone.[6] The compound is inactive itself, showing more than 100-fold lower affinity for the androgen and progesterone receptors than trenbolone.[7][8] It is a designer steroid and has been sold on the internet as a “nutritional supplement”.[1] Trendione is listed in the United States Designer Anabolic Steroid Control Act of 2014.[1]See also[edit]References[edit]^ a b c Liane BJ, Magee C (October 2016). “Guerilla Warfare on the Pancreas? A Case of Acute Pancreatitis From a Supplement Known to Contain Anabolic-Androgenic Steroids”. Mil Med. 181 (10): e1395\u2013e1397. doi:10.7205\/MILMED-D-15-00575. PMID\u00a027753588.^ Yarrow JF, McCoy SC, Borst SE (June 2010). “Tissue selectivity and potential clinical applications of trenbolone (17beta-hydroxyestra-4,9,11-trien-3-one): A potent anabolic steroid with reduced androgenic and estrogenic activity”. Steroids. 75 (6): 377\u201389. doi:10.1016\/j.steroids.2010.01.019. PMID\u00a020138077. S2CID\u00a0205253265.^ Metzler M (April 1989). “Metabolism of some anabolic agents: toxicological and analytical aspects”. J. Chromatogr. 489 (1): 11\u201321. doi:10.1016\/s0378-4347(00)82880-7. PMID\u00a02745641.^ Yarrow JF, Conover CF, McCoy SC, Lipinska JA, Santillana CA, Hance JM, Cannady DF, VanPelt TD, Sanchez J, Conrad BP, Pingel JE, Wronski TJ, Borst SE (April 2011). “17\u03b2-Hydroxyestra-4,9,11-trien-3-one (trenbolone) exhibits tissue selective anabolic activity: effects on muscle, bone, adiposity, hemoglobin, and prostate”. Am. J. Physiol. Endocrinol. Metab. 300 (4): E650\u201360. doi:10.1152\/ajpendo.00440.2010. PMC\u00a06189634. PMID\u00a021266670.^ Spranger B, Metzler M (April 1991). “Disposition of 17 beta-trenbolone in humans”. J. Chromatogr. 564 (2): 485\u201392. doi:10.1016\/0378-4347(91)80517-g. PMID\u00a01874853.^ Advances in Agronomy. Elsevier. 13 April 2007. pp.\u00a016\u2013. ISBN\u00a0978-0-08-048819-6.^ Bauer ER, Daxenberger A, Petri T, Sauerwein H, Meyer HH (December 2000). “Characterisation of the affinity of different anabolics and synthetic hormones to the human androgen receptor, human sex hormone binding globulin and to the bovine progestin receptor”. APMIS. 108 (12): 838\u201346. doi:10.1111\/j.1600-0463.2000.tb00007.x. PMID\u00a011252818. S2CID\u00a022776408.^ Delettr\u00e9 J, Mornon JP, Lepicard G, Ojasoo T, Raynaud JP (January 1980). “Steroid flexibility and receptor specificity”. J. Steroid Biochem. 13 (1): 45\u201359. doi:10.1016\/0022-4731(80)90112-0. PMID\u00a07382482.PRAgonistsTestosterone derivatives: Progestins: 6,6-Difluoronorethisterone6,6-Difluoronorethisterone acetate17\u03b1-Allyl-19-nortestosteroneAllylestrenolAltrenogestChloroethynylnorgestrelCingestolDanazolDesogestrelDienogestEthinylandrostenediolEthisteroneEthyneroneEtonogestrelEtynodiolEtynodiol diacetateGestodeneGestrinoneLevonorgestrelLevonorgestrel esters (e.g., levonorgestrel butanoate)LynestrenolLynestrenol phenylpropionateMetynodiolMetynodiol diacetateNorelgestrominNorethisterone (norethindrone)Norethisterone esters (e.g., norethisterone acetate, norethisterone enanthate)NoretynodrelNorgesteroneNorgestimateNorgestrelNorgestrienoneNorvinisteroneOxendoloneQuingestanolQuingestanol acetateTiboloneTigestolTosagestin; Anabolic\u2013androgenic steroids: 11\u03b2-Methyl-19-nortestosterone11\u03b2-Methyl-19-nortestosterone dodecylcarbonate19-Nor-5-androstenediol19-Nor-5-androstenedione19-NordehydroepiandrosteroneBolandiolBolandiol dipropionateBolandioneDimethisteroneDienedioneDienoloneDimethandroloneDimethandrolone buciclateDimethandrolone dodecylcarbonateDimethandrolone undecanoateDimethyldienoloneDimethyltrienoloneEthyldienoloneEthylestrenol (ethylnandrol)MethyldienoloneMetribolone (R-1881)Methoxydienone (methoxygonadiene)MiboleroneNandroloneNandrolone esters (e.g., nandrolone decanoate, nandrolone phenylpropionate)NorethandroloneNormethandrone (methylestrenolone, normethandrolone, normethisterone)RU-2309TetrahydrogestrinoneTrenbolone (trienolone)Trenbolone esters (e.g., trenbolone acetate, trenbolone enanthate)TrendioneTrestoloneTrestolone acetateMixed(SPRMs)AntagonistsmPR(PAQR)       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4     (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki40\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki40\/trendione-wikipedia\/#breadcrumbitem","name":"Trendione – Wikipedia"}}]}]