Metilestrenolona

Metilestrenolona
Fórmula molecular	?
Identificadores
ChEMBL	269549
ChemSpider	4447645
PubChem	5284597
UNII	743F1Z557A
	SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@]2(C)O)CCC4=CC(=O)CC[C@H]34
	InChI InChI=1S/C19H28O2/c1-18-9-7-15-14-6-4-13(20)11-12(14)3-5-16(15)17(18)8-10-19(18,2)21/h11,14-17,21H,3-10H2,1-2H3/t14-,15+,16+,17-,18-,19-/m0/s1; Key: ZXSWTMLNIIZPET-ZOFHRBRSSA-N
	[editar datos en Wikidata]

La Metilestrenolona (nombres comerciales Metalutina, Orgasteron, Lutenina, Matronal), conocida también como normetandrona y normetisterona, como así también 17α-metil-19-nortestosterona, es una progestina y andrógeno capaz de actuar como esteroide anabólico.^[1]^[2]^[3]^[4]

Véase también[editar]

Trestolona

Referencias[editar]

↑ J. Elks (14 de noviembre de 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 888-. ISBN 978-1-4757-2085-3.
↑ Begni-Calvet, D. (1959). «Two properties of methylestrenolone (17-alpha-methyl-19-nortestosterone): Its effectiveness in the treatment of dysmenorrhea, its anabolic action». Gynecologie pratique 10: 261-272. PMID 13798272.
↑ Grunwell, J. F.; Benson, H. D.; Johnston, J. O.; Petrow, V (1976). «Antiprogestational agents. The synthesis of 7-alkyl steroidal ketones with anti-implantational and antidecidual activity». Steroids 27 (6): 759-71. PMID 941191.
↑ Djerassi, C.; Miramontes, L.; Rosenkranz, G.; Sondheimer, F. (1954). «Steroids. LIV.1Synthesis of 19-Nov-17α-ethynyltestosterone and 19-Nor-17α-methyltestosterone2». Journal of the American Chemical Society 76 (16): 4092. doi:10.1021/ja01645a010.

Datos: Q24960263

[Elks2014-1] J. Elks (14 de noviembre de 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 888-. ISBN 978-1-4757-2085-3.

[2] Begni-Calvet, D. (1959). «Two properties of methylestrenolone (17-alpha-methyl-19-nortestosterone): Its effectiveness in the treatment of dysmenorrhea, its anabolic action». Gynecologie pratique 10: 261-272. PMID 13798272.

[3] Grunwell, J. F.; Benson, H. D.; Johnston, J. O.; Petrow, V (1976). «Antiprogestational agents. The synthesis of 7-alkyl steroidal ketones with anti-implantational and antidecidual activity». Steroids 27 (6): 759-71. PMID 941191.

[4] Djerassi, C.; Miramontes, L.; Rosenkranz, G.; Sondheimer, F. (1954). «Steroids. LIV.1Synthesis of 19-Nov-17α-ethynyltestosterone and 19-Nor-17α-methyltestosterone2». Journal of the American Chemical Society 76 (16): 4092. doi:10.1021/ja01645a010.

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