[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/chlormethenmadinone-acetate-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki41\/chlormethenmadinone-acetate-wikipedia\/","headline":"Chlormethenmadinone acetate – Wikipedia","name":"Chlormethenmadinone acetate – Wikipedia","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 Chemical compound Chlormethenmadinone acetate Trade names Biogest, Sterolibrin, Antigest B, Agelin Other names","datePublished":"2019-10-28","dateModified":"2019-10-28","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\/f\/f7\/Chlormethenmadinone_acetate.svg\/235px-Chlormethenmadinone_acetate.svg.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/f\/f7\/Chlormethenmadinone_acetate.svg\/235px-Chlormethenmadinone_acetate.svg.png","height":"188","width":"235"},"url":"https:\/\/wiki.edu.vn\/en\/wiki41\/chlormethenmadinone-acetate-wikipedia\/","about":["Wiki"],"wordCount":2721,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Chemical compoundChlormethenmadinone acetateTrade namesBiogest, Sterolibrin, Antigest B, AgelinOther namesSCH-12600; 6-Chloromethylene\u00addehydroacetoxy\u00adprogesterone; 17\u03b1-Acetoxy-6-chloro-16-methylene-6-dehydroprogesterone; 16-Methylene\u00adchlormadinone acetate; 17\u03b1-Acetoxy-6-chloro-16-methylenepregna-4,6-diene-3,20-dioneDrug classProgestogen; Progestin; Progestogen ester[(8R,9S,10R,13S,14S,17R)-17-Acetyl-6-chloro-10,13-dimethyl-16-methylidene-3-oxo-1,2,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-17-yl] acetateCAS NumberPubChem CIDChemSpiderChEMBLCompTox Dashboard (EPA)FormulaC24H29ClO4Molar mass416.94\u00a0g\u00b7mol\u221213D model (JSmol)CC(=O)[C@]1(C(=C)C[C@@H]2[C@@]1(CC[C@H]3[C@H]2C=C(C4=CC(=O)CC[C@]34C)Cl)C)OC(=O)C       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4InChI=1S\/C24H29ClO4\/c1-13-10-19-17-12-21(25)20-11-16(28)6-8-22(20,4)18(17)7-9-23(19,5)24(13,14(2)26)29-15(3)27\/h11-12,17-19H,1,6-10H2,2-5H3\/t17-,18+,19+,22-,23+,24+\/m1\/s1Key:MDTBKPVVPCIBIT-USYNNDFZSA-NChlormethenmadinone acetate (CMMA), also known as chlorsuperlutin, is a progestin medication which was developed in Czechoslovakia in the 1960s.[1] It has been used in combination with mestranol in birth control pills under the brand names Biogest, Sterolibrin, and Antigest B,[2][3] and in veterinary medicine under the brand name Agelin.[4]Analogues of CMMA include bromethenmadinone acetate (bromsuperlutin), which was assessed but was never marketed,[3][5] and melengestrol acetate (methylsuperlutin), which is used in veterinary medicine.[6]See also[edit]References[edit]^ Sterba, R. (1968). New biological application of contraceptive steroids. Endocrinologia Experimentalis, 2(2), 101-110. https:\/\/www.popline.org\/node\/469522 Archived 2018-09-16 at the Wayback Machine^ Melich H (July 1972). “[Biogest]”. Cas. Lek. Cesk. (in Czech). 111 (30): 694\u20135. PMID\u00a05079918. Archived from the original on 2018-09-16. Retrieved 2018-09-16.^ a b St\u0115rba R (March 1970). “[Towards a more physiological hormonal contraception]”. Zentralbl Gynakol (in German). 92 (10): 303\u201312. PMID\u00a04096927. Archived from the original on 2018-09-16. Retrieved 2018-09-16.^ Bekeov\u00e1 E, Krajnic\u00e1kov\u00e1 M, Hendrichovsk\u00fd V, Maracek I (November 1995). “[Thyroid and ovarian hormones in ewes treated with gestagens and PMSG in the spring season]”. Vet Med (Praha) (in Slovak). 40 (11): 345\u201352. PMID\u00a08659087.^ \u0160t\u011brba, R. (1971). “On the Way to a More Physiological Hormonal Contraception”. Current Problems in Fertility. pp.\u00a0154\u2013158. doi:10.1007\/978-1-4615-8651-7_28. ISBN\u00a0978-1-4615-8653-1. Archived from the original on 2018-09-16. Retrieved 2018-09-16.^ R. G. Denkewalter; M. Tishler; G. Ehrhart; J. H. Biel, B. K. B. Lum, J. B\u00fcchi, C. A. Winter, K. M\u00fcnzel, W. Kunz, E. J. Ari\u00ebns, F. Labhardt (8 March 2013). Fortschritte der Arzneimittelforschung \/ Progress in Drug Research \/ Progr\u00e8s des recherches pharmaceutiques. Birkh\u00e4user. pp.\u00a0407\u2013. ISBN\u00a0978-3-0348-7059-7.{{cite book}}:  CS1 maint: multiple names: authors list (link)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\/wiki41\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/chlormethenmadinone-acetate-wikipedia\/#breadcrumbitem","name":"Chlormethenmadinone acetate – Wikipedia"}}]}]