Normethandrone is used in combination with an estrogen, either methylestradiol or estradiol valerate, in the treatment of amenorrhea and menopausal symptoms in women. It has also been used to treat dysmenorrhea in women. Normethandrone has been used successfully to inhibit libido in men with sexual deviance. Although normethandrone can be classified as an AAS and has strong such effects at sufficiently high doses, it is not typically used as such and is instead used medically only as a progestin. This is because it is so highly progestogenic in comparison.
Available forms
Normethandrone is marketed in combination with methylestradiol in the form of oral tablets containing 5 mg normethandrone and 0.3 mg methylestradiol.
Side effects
Normethandrone has been associated with symptoms of masculinization and hepatotoxicity.
Pharmacology
Pharmacodynamics
Normethandrone shows high progestogenic activity. With sublingual administration in women, it has at least 150 times the potency of sublingual progesterone and 50 times the potency of sublingual ethisterone. It also has 10 times the potency of injected progesterone via this route. The oral potency of normethandrone in terms of endometrial transformation is similar to that of norethisterone. It has been reported to inhibit ovulation in women. In addition to its progestogenic activity, normethandrone has anabolic and androgenic activity and can produce effects associated with this activity. It has a high ratio of anabolic to androgenic activity. The anabolic potency of normethandrone is similar to that of norethandrolone and is much greater than that of nandrolone or metandienone. It is also greater than that of ethylestrenol. Normethandrone has been found to increase nitrogen retention, a measure of anabolic effect, at a dosage of 30 mg/day. Analogously to nandrolone and norethandrolone, 5α-dihydronormethandrone, the 5α-reducedmetabolite of normethandrone, shows reduced affinity for the androgenreceptor relative to normethandrone. Its affinity for the androgen receptor is specifically about 33 to 60% of that of normethandrone. Normethandrone has estrogenic activity via aromatization into methylestradiol.
Pharmacokinetics
Normethandrone is metabolized by aromatase into methylestradiol in small quantities, similarly to methyltestosterone and metandienone. The metabolites of normethandrone have not been well-studied, but 5α-dihydronormethandrone is a likely metabolite formed by 5α-reductase. The pharmacokinetics of normethandrone have been reviewed.
Chemistry
Normethandrone, also known as 17α-methyl-19-nortestosterone or as 17α-methylestr-4-en-17β-ol-3-one, is a synthetic estrane steroid and a 17α-alkylatedderivative of nandrolone. It is specifically the 17α-methyl derivative of nandrolone as well as the 17α-methyl variant of norethandrolone and norethisterone.
Synthesis
of normethandrone have been published.
History
Normethandrone has been marketed for medical use since 1957. The combination of normethandrone and methylestradiol was introduced by at least 1966.
Society and culture
Generic names
Normethandrone has not been assigned an or other formal name designations. It is also known as methylestrenolone, methylnortestosterone, normethandrolone, and normethisterone.