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Estradiol dienantate

From Wikipedia, the free encyclopedia
Chemical compound
Not to be confused withEstradiol enanthate.
Pharmaceutical compound
Estradiol dienantate
Clinical data
Trade namesClimacteron, Amenose, Lactimex, Lactostat (all combinations)
Other namesEstradiol dienantate; EDE; EDEn; E2-EDN; Estradiol diheptanoate; Estra-1,3,5(10)-triene-3,17β-diol 3,17β-diheptanoate
Routes of
administration
Intramuscular injection
Drug classEstrogen;Estrogen ester
Identifiers
  • [(8R,9S,13S,14S,17S)-3-heptanoyloxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] heptanoate
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.028.903Edit this at Wikidata
Chemical and physical data
FormulaC32H48O4
Molar mass496.732 g·mol−1
3D model (JSmol)
  • CCCCCCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C3C=CC(=C4)OC(=O)CCCCCC)C
  • InChI=1S/C32H48O4/c1-4-6-8-10-12-30(33)35-24-15-17-25-23(22-24)14-16-27-26(25)20-21-32(3)28(27)18-19-29(32)36-31(34)13-11-9-7-5-2/h15,17,22,26-29H,4-14,16,18-21H2,1-3H3/t26-,27-,28+,29+,32+/m1/s1
  • Key:OVAHZPTYWMWNKO-CAHAWPIUSA-N

Estradiol dienanthate (EDE), sold under the brand namesClimacteron among others, is a long-actingestrogen medication which was previously used inmenopausal hormone therapy for women and to suppresslactation in women.[1][2][3][4] It was formulated incombination withestradiol benzoate (EB), a short-acting estrogen, andtestosterone enanthate benzilic acid hydrazone (TEBH), a long-actingandrogen/anabolic steroid.[2][3][4] EDE has not been made available for medical use alone.[5] The medication, in combination with EB and TEBH, was given byinjection into muscle once or at regular intervals, for instance once every 6 weeks.[6][7][8]

Side effects of EDE includebreast tenderness,breast enlargement,nausea,headache, andfluid retention.[9] EDE is anestrogen and hence is anagonist of theestrogen receptor, thebiological target ofestrogens likeestradiol.[10][11] It is anestrogen ester and aprodrug ofestradiol in the body.[11][10] Because of this, it is considered to be anatural andbioidentical form of estrogen.[11]

EDE was first described by 1959.[12][13] It was previously available inCanada andGermany but was discontinued by 2005.[14][15][16] The medication is no longer available in any form.[5]

Medical uses

[edit]

EDE, a long-acting estrogen, was used in combination with EB, a short-acting estrogen, and TEBH, a long-acting androgen/anabolic steroid, inmenopausal hormone therapy inperimenopausal,postmenopausal,hypogonadal, andoophorectomized women, as well as for suppression oflactation inpostpartum women.[6][8][7]

Available forms

[edit]
See also:Estradiol benzoate/estradiol dienanthate/testosterone enanthate benzilic acid hydrazone

EDE was available only in combination EB and TEBH.[17] The combination was available in two different dose forms, one for menopausal hormone therapy (brand names Climacteron, Amenose) and the other for lactation suppression (brand names Lactimex, Lactostat). Climacteron and Amenose contained 1.0 mg EB, 7.5 mg EDE, and 150 mg TEBH (69 mg freetestosterone) and was given by repeated intramuscular injection at regular intervals.[6][18][8] Lactimex and Lactostat contained 6 mg EB, 15 mg EDE, and 300 mg TEBH in 2 mL ofcorn oil and was administered as a single intramuscular injection afterchildbirth or duringbreastfeeding.[7][19][20][21]

Pharmacology

[edit]
Estradiol, theactive form of EDE.

Pharmacodynamics

[edit]
See also:Pharmacodynamics of estradiol

EDE is anestradiol ester, or aprodrug ofestradiol.[11][10] As such, it is anestrogen, or anagonist of theestrogen receptors.[11][10] EDE is of about 82% highermolecular weight than estradiol due to the presence of its C3 and C17βheptanoate (enanthate) esters. Because EDE is a prodrug of estradiol, it is considered to be anatural andbioidentical form of estrogen.[11]

Potencies and durations of natural estrogens by intramuscular injection
EstrogenFormDose (mg)Duration by dose (mg)
EPDCICD
EstradiolAq. soln.?<1 d
Oil soln.40–601–2 ≈ 1–2 d
Aq. susp.?3.50.5–2 ≈ 2–7 d; 3.5 ≈ >5 d
Microsph.?1 ≈ 30 d
Estradiol benzoateOil soln.25–351.66 ≈ 2–3 d; 5 ≈ 3–6 d
Aq. susp.2010 ≈ 16–21 d
Emulsion?10 ≈ 14–21 d
Estradiol dipropionateOil soln.25–305 ≈ 5–8 d
Estradiol valerateOil soln.20–3055 ≈ 7–8 d; 10 ≈ 10–14 d;
40 ≈ 14–21 d; 100 ≈ 21–28 d
Estradiol benz. butyrateOil soln.?1010 ≈ 21 d
Estradiol cypionateOil soln.20–305 ≈ 11–14 d
Aq. susp.?55 ≈ 14–24 d
Estradiol enanthateOil soln.?5–1010 ≈ 20–30 d
Estradiol dienanthateOil soln.?7.5 ≈ >40 d
Estradiol undecylateOil soln.?10–20 ≈ 40–60 d;
25–50 ≈ 60–120 d
Polyestradiol phosphateAq. soln.40–6040 ≈ 30 d; 80 ≈ 60 d;
160 ≈ 120 d
EstroneOil soln.?1–2 ≈ 2–3 d
Aq. susp.?0.1–2 ≈ 2–7 d
EstriolOil soln.?1–2 ≈ 1–4 d
Polyestriol phosphateAq. soln.?50 ≈ 30 d; 80 ≈ 60 d
Notes and sources
Notes: Allaqueous suspensions are ofmicrocrystallineparticle size.Estradiol production during themenstrual cycle is 30–640 µg/d (6.4–8.6 mg total per month or cycle). Thevaginalepithelium maturation dosage ofestradiol benzoate orestradiol valerate has been reported as 5 to 7 mg/week. An effectiveovulation-inhibiting dose ofestradiol undecylate is 20–30 mg/month.Sources: See template.
Hormone levels with estradiol benzoate/estradiol dienanthate/testosterone enanthate benzilic acid hydrazone by intramuscular injection

Pharmacokinetics

[edit]
See also:Pharmacokinetics of estradiol andEstradiol benzoate/estradiol dienanthate/testosterone enanthate benzilic acid hydrazone

Estradiol andtestosterone levels following a singleintramuscular injection of Climacteron (including 1 mg EB, 7.5 mg EDE, and 150 mg TEBH equivalent to 69 mg freetestosterone) versus 10 mgestradiol valerate have been studied over 28 days.[23][24]

Potencies and durations of natural estrogens by intramuscular injection
EstrogenFormDose (mg)Duration by dose (mg)
EPDCICD
EstradiolAq. soln.?<1 d
Oil soln.40–601–2 ≈ 1–2 d
Aq. susp.?3.50.5–2 ≈ 2–7 d; 3.5 ≈ >5 d
Microsph.?1 ≈ 30 d
Estradiol benzoateOil soln.25–351.66 ≈ 2–3 d; 5 ≈ 3–6 d
Aq. susp.2010 ≈ 16–21 d
Emulsion?10 ≈ 14–21 d
Estradiol dipropionateOil soln.25–305 ≈ 5–8 d
Estradiol valerateOil soln.20–3055 ≈ 7–8 d; 10 ≈ 10–14 d;
40 ≈ 14–21 d; 100 ≈ 21–28 d
Estradiol benz. butyrateOil soln.?1010 ≈ 21 d
Estradiol cypionateOil soln.20–305 ≈ 11–14 d
Aq. susp.?55 ≈ 14–24 d
Estradiol enanthateOil soln.?5–1010 ≈ 20–30 d
Estradiol dienanthateOil soln.?7.5 ≈ >40 d
Estradiol undecylateOil soln.?10–20 ≈ 40–60 d;
25–50 ≈ 60–120 d
Polyestradiol phosphateAq. soln.40–6040 ≈ 30 d; 80 ≈ 60 d;
160 ≈ 120 d
EstroneOil soln.?1–2 ≈ 2–3 d
Aq. susp.?0.1–2 ≈ 2–7 d
EstriolOil soln.?1–2 ≈ 1–4 d
Polyestriol phosphateAq. soln.?50 ≈ 30 d; 80 ≈ 60 d
Notes and sources
Notes: Allaqueous suspensions are ofmicrocrystallineparticle size.Estradiol production during themenstrual cycle is 30–640 µg/d (6.4–8.6 mg total per month or cycle). Thevaginalepithelium maturation dosage ofestradiol benzoate orestradiol valerate has been reported as 5 to 7 mg/week. An effectiveovulation-inhibiting dose ofestradiol undecylate is 20–30 mg/month.Sources: See template.

Chemistry

[edit]
See also:Estrogen ester andList of estrogen esters § Estradiol esters

EDE is asyntheticestranesteroid and the C3 and C17βheptanoate (enanthate)diester ofestradiol.[1] It is also known as estradiol 3,17β-heptanoate or as estra-1,3,5(10)-triene-3,17β-diol 3,17β-diheptanoate.[1] EDE is structurally related toestradiol enanthate (estradiol 17β-heptanoate), which has a single heptanoate ester rather than two.[1]

Structural properties of selected estradiol esters
EstrogenStructureEster(s)Relative
mol. weight
Relative
E2 contentb
log Pc
Position(s)Moiet(ies)TypeLengtha
Estradiol
1.001.004.0
Estradiol acetate
C3Ethanoic acidStraight-chain fatty acid21.150.874.2
Estradiol benzoate
C3Benzoic acidAromatic fatty acid– (~4–5)1.380.724.7
Estradiol dipropionate
C3, C17βPropanoic acid (×2)Straight-chain fatty acid3 (×2)1.410.714.9
Estradiol valerate
C17βPentanoic acidStraight-chain fatty acid51.310.765.6–6.3
Estradiol benzoate butyrate
C3, C17βBenzoic acid,butyric acidMixed fatty acid– (~6, 2)1.640.616.3
Estradiol cypionate
C17βCyclopentylpropanoic acidCyclic fatty acid– (~6)1.460.696.9
Estradiol enanthate
C17βHeptanoic acidStraight-chain fatty acid71.410.716.7–7.3
Estradiol dienanthate
C3, C17βHeptanoic acid (×2)Straight-chain fatty acid7 (×2)1.820.558.1–10.4
Estradiol undecylate
C17βUndecanoic acidStraight-chain fatty acid111.620.629.2–9.8
Estradiol stearate
C17βOctadecanoic acidStraight-chain fatty acid181.980.5112.2–12.4
Estradiol distearate
C3, C17βOctadecanoic acid (×2)Straight-chain fatty acid18 (×2)2.960.3420.2
Estradiol sulfate
C3Sulfuric acidWater-soluble conjugate1.290.770.3–3.8
Estradiol glucuronide
C17βGlucuronic acidWater-soluble conjugate1.650.612.1–2.7
Estramustine phosphated
C3, C17βNormustine,phosphoric acidWater-soluble conjugate1.910.522.9–5.0
Polyestradiol phosphatee
C3–C17βPhosphoric acidWater-soluble conjugate1.23f0.81f2.9g
Footnotes:a = Length ofester incarbonatoms forstraight-chain fatty acids or approximate length of ester in carbon atoms foraromatic orcyclic fatty acids.b = Relative estradiol content by weight (i.e., relativeestrogenic exposure).c = Experimental or predictedoctanol/water partition coefficient (i.e.,lipophilicity/hydrophobicity). Retrieved fromPubChem,ChemSpider, andDrugBank.d = Also known asestradiol normustine phosphate.e =Polymer ofestradiol phosphate (~13repeat units).f = Relative molecular weight or estradiol content per repeat unit.g = log P of repeat unit (i.e., estradiol phosphate).Sources: See individual articles.

History

[edit]

EDE was first described and introduced for medical use by 1959.[12][13]

Society and culture

[edit]

Brand names

[edit]

EDE was marketed in combination with EB and TEBH under the brand names Climacteron, Amenose, Lactimex, and Lactostat.[17][8]

Availability

[edit]

EDE is no longer available but was previously used inCanada,Germany and other countries.[5][17][7][21]

See also

[edit]

References

[edit]
  1. ^abcdElks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 898.ISBN 978-1-4757-2085-3.
  2. ^abGinsburg ES (1999). "Androgen Replacement in Postmenopausal Women". In Seifer DB, Kennard EA (eds.).Menopause. Vol. 18. pp. 209–219.doi:10.1007/978-1-59259-246-3_13.ISBN 978-1-61737-129-5.
  3. ^abGreenblatt RB, Barfield WE, Jungck EC (January 1962)."The treatment of the menopause".Canadian Medical Association Journal.86 (3):113–114.PMC 1848811.PMID 13901504.
  4. ^abLeondires MP, Segars JH, Walsh BW (27 July 1999)."The Use of Antiestrogens in the Postmenopausal Woman". In Seifer DB, Kennard EA (eds.).Menopause: Endocrinology and Management. Springer Science & Business Media. pp. 183–.doi:10.1007/978-1-59259-246-3_12.ISBN 978-1-59259-246-3.
  5. ^abc"Estradiol: Uses, Dosage & Side Effects".Drugs.com.
  6. ^abc"Climacteron Drug Information, Professional".Drugs.com. Archived fromthe original on 2 June 2019. Retrieved2 June 2019.
  7. ^abcdGeburtshilfe und Frauenheilkunde: Ergebnisse der Forschung für die Praxis. Georg Thieme Verlag. 1969. p. 387,390.[Kelly and Primose and Dodek found the following androgen-estrogen combination to be particularly effective and well-tolerated: 300 mg 3-benzilic acid hydrazone-testosterone-17-enanthate, 15 mg estradiol di-enanthate, 6 mg estradiol benzoate in 2 ml corn oil. This product is sold in Germany under the name Lactimex and has been clinically examined by us.] [...] Of 1200 postpartum patients one quarter stopped breast feeding for a variety of reasons and received an injection of Lactimex (Protina: Benzil acid hydrazon-testosteron-oenanthat 300 mg, Oestradiol-di-oenanthat 15 mg and Oestradiol-benzoate 6 mg in 1.0 ml of oil). In 76% of cases one injection was sufficient and the remaining 24% required a second injection. A second injection was required rarer if the first injection had been longer after delivery. A higher dosage of Lactimex was not necessary in cases with a preceding medical induction with intraveinous Oxytocin (Orasthin). Mothers who had been treated postpartum with methylergobasin did not as often require a second injection. No localized or generalized adverse reaction to the drug was noticed.
  8. ^abcdBundesverband der Pharmazeutischen Industrie (Germany) (1974).Rote Liste: Verzeichnis pharmazeutischer Spezialpräparate. Editio Cantor.ISBN 9783871930133.49035 В Amenose® Rp Ampullen Zus.: 1 Amp. 1 ml enth.: Benzilsäurehydrazid-N-testosteron-hydrazon-17-oenanthat 150 mg, Oestradiol-di-oenanthat 7.5 mg. Oestradiolbenzoat 1 mg in öl-Lösg. Ind.: Androgen-Oestrogen-Gemisch. Gegen Ausfallserscheinungen im Klimakterium und nach Ovarektomie. Osteoporose. Kontraind.: A 90, О 5 Dos.: Durchschnittl. alle 6 Wochen 1 Amp. im. 1 Amp. I ml 6.75 3 Amp 17.40 AP.: 10 Amp.
  9. ^Ghosh AK (23 September 2010).Mayo Clinic Internal Medicine Board Review. OUP USA. pp. 222–.ISBN 978-0-19-975569-1.
  10. ^abcdKuhl H (August 2005). "Pharmacology of estrogens and progestogens: influence of different routes of administration".Climacteric.8 (Suppl 1):3–63.doi:10.1080/13697130500148875.PMID 16112947.S2CID 24616324.
  11. ^abcdefOettel M, Schillinger E (6 December 2012).Estrogens and Antiestrogens II: Pharmacology and Clinical Application of Estrogens and Antiestrogen. Springer Science & Business Media. p. 261.ISBN 978-3-642-60107-1.Natural estrogens considered here include: [...] Esters of 17β-estradiol, such as estradiol valerate, estradiol benzoate and estradiol cypionate. Esterification aims at either better absorption after oral administration or a sustained release from the depot after intramuscular administration. During absorption, the esters are cleaved by endogenous esterases and the pharmacologically active 17β-estradiol is released; therefore, the esters are considered as natural estrogens.
  12. ^abVademecum International. J. Morgan Jones Publications. 1959. pp. 121–122.
  13. ^abKelly MJ, Primrose T (December 1960)."Evaluation of a new preparation for the suppression of lactation".Canadian Medical Association Journal.83 (24):1240–1242.PMC 1938994.PMID 13752392.
  14. ^Al-Imari L, Wolfman WL (September 2012). "The safety of testosterone therapy in women".Journal of Obstetrics and Gynaecology Canada.34 (9):859–865.doi:10.1016/S1701-2163(16)35385-3.PMID 22971455.
  15. ^Lexchin, Joel (2010)."Drug safety and Health Canada".International Journal of Risk & Safety in Medicine.22 (1):41–53.doi:10.3233/JRS-2010-0490.
  16. ^"Discontinuation of CLIMACTERON® Injection (estradiol dienanthate ⁄ estradiol benzoate and testosterone enanthate benzilic acid hydrazone injection in corn oil)"(PDF).Sandoz. Health Canada. 23 November 2005. Archived fromthe original(PDF) on 2013-01-11. Retrieved2 June 2019.
  17. ^abc"MDX Pharmaceutical Knowledge". Merative US L.P.
  18. ^Sherwin BB (1988). "Estrogen and/or androgen replacement therapy and cognitive functioning in surgically menopausal women".Psychoneuroendocrinology.13 (4):345–357.doi:10.1016/0306-4530(88)90060-1.PMID 3067252.S2CID 24695692.
  19. ^Zentralblatt für Gynäkologie. J. A. Barth. 1971.The preparation Lactimex (300 mg 3-benzyl hydrazone-testosterone-17-enanthate + 15 mg estradiol-dienanthate + 6 mg estradiol benzoate in 2 ml corn oil) was injected. [...]
  20. ^Vorherr H (2 December 2012).The Breast: Morphology, Physiology, and Lactation. Elsevier Science. pp. 201–.ISBN 978-0-323-15726-1.
  21. ^abCompendium of Pharmaceuticals and Specialties. Canadian Pharmaceutical Association. 1983.ISBN 978-0-919115-04-0.LACTOSTAT [...] Each 2 mL of injectable solution contains testosteorne enanthate benzilic acid hydrazone 300 mg, estradiol dienanthate 15 mg, estradiol benzoate 6 mg, benzyl alcohol 7.5% as preservative, benzyl benzoate 0.75 mg, corn oil q.s. Available in 2 mL ampuls, boxes of 25.
  22. ^abcSherwin, Barbara B.; Gelfand, Morrie M. (1987). "Individual differences in mood with menopausal replacement therapy: possible role of sex hormone-binding globulin".Journal of Psychosomatic Obstetrics & Gynecology.6 (2):121–131.doi:10.3109/01674828709016773.ISSN 0167-482X.
  23. ^abcdSherwin BB, Gelfand MM, Schucher R, Gabor J (February 1987). "Postmenopausal estrogen and androgen replacement and lipoprotein lipid concentrations".Am. J. Obstet. Gynecol.156 (2):414–9.doi:10.1016/0002-9378(87)90295-X.PMID 3826177.
  24. ^abcdSherwin BB (1988). "Affective changes with estrogen and androgen replacement therapy in surgically menopausal women".J Affect Disord.14 (2):177–87.doi:10.1016/0165-0327(88)90061-4.PMID 2966832.
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