Ethisterone

"Pregneninolone" redirects here. For the similarly named steroid, see Pregnenolone.

Ethisterone, also known as ethinyltestosterone, pregneninolone, and anhydrohydroxyprogesterone and formerly sold under the brand names Proluton C and Pranone among others, is a progestin medication which was used in the treatment of gynecological disorders but is now no longer available.^[3][4][5] It was used alone and was not formulated in combination with an estrogen.^[1][6] The medication is taken by mouth.^[4]

Ethisterone

Clinical data
Trade names	Proluton C, Pranone, others
Other names	Ethinyltestosterone; Ethynyltestosterone; Pregneninolone; Anhydrohydroxyprogesterone; Etisteron; Pregnin; Ethindrone
Routes of administration	By mouth, sublingual^[1]
Drug class	Progestogen; Progestin; Androgen; Anabolic steroid
ATC code	G03DC04 (WHO)
Pharmacokinetic data
Metabolites	• 5α-Dihydroethisterone^[2]
Identifiers
IUPAC name (8R,9S,10R,13R,14S,17R)-17-Ethynyl-17-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
CAS Number	434-03-7^Y
PubChem CID	5284557
ChemSpider	4447612^Y
UNII	P201BVY1MJ
ChEBI	CHEBI:34749^Y
ChEMBL	ChEMBL241694^Y
CompTox Dashboard (EPA)	DTXSID2023016
ECHA InfoCard	100.006.452
Chemical and physical data
Formula	C21H28O2
Molar mass	312.453 g·mol^−1
3D model (JSmol)	Interactive image
SMILES C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@]4(C#C)O)C
InChI InChI=1S/C21H28O2/c1-4-21(23)12-9-18-16-6-5-14-13-15(22)7-10-19(14,2)17(16)8-11-20(18,21)3/h1,13,16-18,23H,5-12H2,2-3H3/t16-,17+,18+,19+,20+,21+/m1/s1^Y Key:CHNXZKVNWQUJIB-CEGNMAFCSA-N^Y
(verify)

Side effects of ethisterone include masculinization among others.^[4][7][8] Ethisterone is a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progesterone.^[9] It has some androgenic and anabolic activity and no other important hormonal activity.^{[9][10][11][12][13]}

Ethisterone was discovered in 1938 and was introduced for medical use in Germany in 1939 and in the United States in 1945.^[14][15][16] It was the second progestogen to be marketed, following injected progesterone in 1934, and was both the first orally active progestogen and the first progestin to be introduced.^[17][18][15] Ethisterone was followed by the improved and much more widely used and known progestin norethisterone in 1957.^[19][20]

Medical uses

Ethisterone was used in the treatment of gynecological disorders such as irregular menstruation, amenorrhea, and premenstrual syndrome.^[3][21]

Available forms

Ethisterone was available in the form of 5, 10, and 25 mg oral and sublingual tablets, as well as 50 , 100 , and 250 mg oral capsules.^[1][6][22] The usual dosage was 25 mg, up to four times per day.^[6]

Side effects

See also: Progestin § Side effects, and Anabolic steroid § Adverse effects

Side effects of ethisterone reportedly include symptoms of masculinization such as acne and hirsutism among others.^[4][7][8] Findings are mixed on the anabolic effects of high doses of ethisterone.^[23]

Pharmacology

Pharmacodynamics

Ethisterone has weak progestogenic activity and weak androgenic activity, but does not seem to have estrogenic activity.^[9][12][24]

Ethisterone is a major active metabolite of danazol (2,3-isoxazolethisterone), and is thought to contribute importantly to its effects.^[24]

Progestogenic activity

Ethisterone is a progestogen, or an agonist of the progesterone receptors.^[9] It has about 44% of the affinity of progesterone for the progesterone receptor.^[25] The medication is described as a relatively weak progestogen, similarly to its analogue dimethisterone.^[26] Its total endometrial transformation dosage per 10 to 14 days in women is 200 to 700 mg.^{[27][additional citation(s) needed]} Ethisterone has about 20-fold lower potency as a progestogen relative to norethisterone.^[28] It is said to have minimal antigonadotropic effect and to not suppress ovulation, which has precluded its use in hormonal contraception.^[24]

Androgenic activity

Based on in vitro research, ethisterone and norethisterone are about equipotent in their EC₅₀ values for activation of the androgen receptor (AR), whereas, conversely, norethisterone shows markedly increased potency relative to ethisterone in terms of its EC₅₀ for the progesterone receptor.^[9] As such, there is a considerable separation in the ratios of androgenic and progestogenic activity for ethisterone and norethisterone.^[9] Moreover, at the larger dosages in which it is used to achieve equivalent progestogenic effect, ethisterone has more androgenic effect relative to norethisterone and other 19-nortestosterone progestins.^[10][11] However, the androgenic activity of ethisterone has in any case been described as weak.^[24] Due to its androgenic activity, ethisterone has been associated with the masculinization of female fetuses in women who have taken it during pregnancy.^[8] The 5α-reduced metabolite of ethisterone, 5α-dihydroethisterone, has been found to show reduced androgenic activity relative to ethisterone.^[2] Interestingly, ethisterone showed antiandrogenic activity when co-administered with dihydrotestosterone (DHT) in animals, whereas 5α-dihydroethisterone did not.^[2]

Estrogenic activity

Testosterone is aromatized into estradiol, and norethisterone, the 19-nortestosterone analogue of ethisterone, has similarly been shown to be aromatized into ethinylestradiol.^[29] In accordance, high doses of norethisterone have been found to be associated with marked increases in urinary estrogen excretion (due to metabolism into ethinylestradiol), as well as with high rates of estrogenic side effects such as breast enlargement in women and gynecomastia in men and improvement of menopausal symptoms in postmenopausal women.^[12][30] In contrast, ethisterone and other progestogens such as progesterone and hydroxyprogesterone caproate do not increase estrogen excretion and are not associated with estrogenic effects, indicating that they have little or no estrogenic activity.^[12][13] Similarly, although ethisterone showed estrogenic effects in the uterus and vagina in rats, few or no such effects were observed in women treated with the medication, even at very high doses.^[31][32] As such, ethisterone does not appear to share the estrogenic activity of norethisterone, at least in humans.^[12][13][24] Aside from ethinylestradiol, 17α-ethynyl-3α-androstanediol and 17α-ethynyl-3β-androstanediol may be estrogenic metabolites of ethisterone.^[33]

Pharmacokinetics

Absorption

Ethisterone is active both orally and sublingually in humans.^[34] Good oral bioavailability of ethisterone has been observed in rats.^[34] The medication was the first orally active progestin to be discovered and introduced for clinical use.^[34]

Distribution

Ethisterone has relatively high affinity for sex hormone-binding globulin, about 14% of that of dihydrotestosterone and 49% of that of testosterone in one study.^[35]

Metabolism

In terms of metabolism, ethisterone is not converted into pregnanediol in humans.^[34] This indicates that it is not metabolized into progesterone.^[34] No aromatization of ethisterone has been detected in vivo, and no estrogenic metabolites were observed in vitro upon incubation of ethisterone in placental homogenates.^[34] This suggests that ethisterone may not be transformed into ethinylestradiol (17α-ethynylestradiol).^[34] 5α-Dihydroethisterone (5α-dihydro-17α-ethynyltestosterone), formed by 5α-reductase, is an active metabolite of ethisterone.^[2] 17α-Ethynyl-3α-androstanediol and 17α-ethynyl-3β-androstanediol, also formed via 5α-reductase, as well as other enzymes, are also potential metabolites of ethisterone.^[33]

Chemistry

See also: List of progestogens and List of androgens/anabolic steroids

Ethisterone is a synthetic androstane steroid which was derived from testosterone and is also known by the following synonyms:^[36][37]

• 17α-Ethynyltestosterone (or simply ethinyltestosterone or ethynyltestosterone)
• 17α-Ethynylandrost-4-en-17β-ol-3-one
• 17α-Pregn-4-en-20-yn-17β-ol-3-one (or simply pregneninolone or pregnenynolone)^[38][39]
• 20,21-Anhydro-17β-hydroxyprogesterone (or simply anhydrohydroxyprogesterone)^[40]

Closely related analogues of ethisterone include dimethisterone (6α,21-dimethylethisterone), norethisterone (19-norethisterone), and danazol (the 2,3-d-isoxazole ring-fused derivative of ethisterone), as well as vinyltestosterone, allyltestosterone, methyltestosterone, ethyltestosterone, and propyltestosterone. Other ethisterone analogues include ethinylandrostenediol (17α-ethynyl-5-androstenediol), ethandrostate (17α-ethynyl-5-androstenediol 3β-cyclohexylpropionate), 17α-ethynyl-3α-androstanediol, and 17α-ethynyl-3β-androstanediol.

Synthesis

Chemical syntheses of ethisterone have been published.^[34]

History

Ethisterone was synthesized in 1938 by Hans Herloff Inhoffen, Willy Logemann, Walter Hohlweg, and Arthur Serini at Schering AG in Berlin.^[14] It was derived from testosterone via ethynylation at the C17α position, and it was hoped, that, analogously to estradiol and ethinylestradiol, ethisterone would be an orally active form of testosterone.^[41] However, the androgenic activity of ethisterone was attenuated and it showed considerable progestogenic activity.^[41] As such, it was developed as a progestogen instead and was introduced for medical use in Germany in 1939 as Proluton C and by Schering in the United States in 1945 as Pranone.^[15][16] Ethisterone remained in use as late as 2000.^[37]

Society and culture

Generic names

Ethisterone is the generic name of the drug and its INN, USAN, and BAN, while ethistérone is its DCF.^[36][37][4] It has also been referred to as ethinyltestosterone, pregneninolone, and anhydrohydroxyprogesterone.^[36][37][4]

Brand names

Ethisterone has been marketed under a variety of brand names including Amenoren, Cycloestrol-AH Progestérone, Duosterone, Estormon, Etherone, Ethisteron, Luteosterone, Lutocyclin, Lutocylol, Lutogynestryl, Menstrogen, Nugestoral, Oophormin Luteum, Ora-Lutin, Orasecron, Pranone, Pre Ciclo, Prodroxan, Produxan, Progestab, Progesteron lingvalete, Progestoral, Proluton C, Syngestrotabs, and Trosinone among others.^{[36][37][22][42]}

Availability

Ethisterone was previously available in France, Germany, Italy, Japan, the United Kingdom, and the United States, among other countries.^[22] It is no longer marketed and hence is no longer available in any country.^[43]

References

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15. Lauritzen C, Studd JW (22 June 2005). Current Management of the Menopause. CRC Press. p. 45. ISBN 978-0-203-48612-2. Ethisterone, the first orally effective progestagen, was synthesized by Inhoffen and Hohlweg in 1938. Norethisterone, a progestogen still used worldwide, was synthesized by Djerassi in 1951. But this progestogen was not used immediately and in 1953 Colton discovered norethynodrel, used by Pincus in the first oral contraceptive. Numerous other progestogens were subsequently synthesized, e.g., lynestrenol and ethynodiol diacetate, which were, in fact, prhormones converted in vivo to norethisterone. All these progestogens were also able to induce androgenic effects when high doses were used. More potent progestogens were synthesized in the 1960s, e.g. norgestrel, norgestrienone. These progestogens were also more androgenic.
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Further reading

• Djerassi C (January 2006). "Chemical birth of the pill. 1992". American Journal of Obstetrics and Gynecology. 194 (1): 290–298. doi:10.1016/j.ajog.2005.06.010. PMID 16389046.
• Inhoffen HH, Logemann W, Hohlweg W, Serini A (May 4, 1938). "Untersuchungen in der Sexualhormon-Reihe (Investigations in the sex hormone series)". Ber Dtsch Chem Ges. 71 (5): 1024–32. doi:10.1002/cber.19380710520.
• Kugener A (2004). . Archived from the original on 2004-10-19.
• Petrow V (December 1970). "The contraceptive progestagens". Chemical Reviews. 70 (6): 713–726. doi:10.1021/cr60268a004. PMID 4098492.
• Quinkert G (2004). "Hans Herloff Inhoffen in His Times (1906-1992)". European Journal of Organic Chemistry. 2004 (17): 3727–48. doi:10.1002/ejoc.200300813.
• Sneader W (2005). "Hormone analogues". Drug discovery : a history. Hoboken NJ: John Wiley & Sons. pp. 188–225. ISBN 0-471-89980-1.