Estradiol stearate

Estradiol stearate
Clinical data
Trade names	Depofollan
Other names	E2-17-St; Estradiol octadecanoate; Estradiol 17β-stearate; Estradiol 17β-octadecanoate
Routes of; administration	Intramuscular injection
Drug class	Estrogen; Estrogen ester
Identifiers
	show IUPAC name
CAS Number	82205-00-3;
PubChem CID	67100;
ChemSpider	60448;
CompTox Dashboard (EPA)	DTXSID401002548 ;
Chemical and physical data
Formula	C36H58O3
Molar mass	538.857 g·mol−1
3D model (JSmol)	Interactive image;
	show SMILES
	show InChI

Estradiol stearate (E2-17-St), also known as estradiol octadecanoate and sold under the brand name Depofollan, is a naturally occurring estrogen and an estrogen ester – specifically, the C17β stearate ester of estradiol.^[1]^[2]^[3]^[4]^[5] It occurs in the body as a very long-lasting metabolite and prohormone of estradiol.^[5] The compound is one of the components that collectively constitute lipoidal estradiol, another of which is estradiol palmitate.^[6]^[5] It is extremely lipophilic and hydrophobic.^[5] Estradiol stearate has no affinity for the estrogen receptor, requiring transformation into estradiol via esterases for its estrogenic activity.^[7]^[8]^[9]^[5] The compound does not bind to sex hormone-binding globulin or α-fetoprotein, instead being transported by lipoproteins such as high-density lipoprotein and low-density lipoprotein.^[5]

Estradiol stearate has a prolonged duration of action relative to estradiol regardless of whether it is given by intravenous injection or subcutaneous injection.^[7] This is in contrast to short-chain fatty acid esters of estradiol, such as estradiol benzoate, which do not show a prolonged duration with intravenous injection.^[10] When administered by intravenous injection in rodents, estradiol stearate has a greatly increased terminal half-life relative to estradiol (6 hours vs. 2 minutes).^[7] Estradiol stearate also had a half-life that was 60% longer than that of estradiol arachidonate, despite similar ester chain lengths.^[7] In contrast to the long-chain esters, the half-lives of short-chain estradiol esters such as estradiol acetate and estradiol hexanoate were the same as that of estradiol.^[7] As such, whereas short-chain estradiol esters are rapidly hydrolyzed, long-chain estradiol esters like estradiol stearate are resistant to metabolism.^[7] Thus, the prolongation of effect of short-chain estradiol esters is purely due to their increased lipophilicity and slow release from the injected depot, whereas the prolonged duration of long-chain estradiol esters is due both to this property and to their resistance to metabolism.^[7] Estradiol stearate is susceptible to first-pass metabolism in the liver, and hence has much greater potency by subcutaneous injection than by oral administration.^[7]

In addition to its endogenous role, estradiol stearate was previously available as a pharmaceutical drug for use via depot intramuscular injection.^[1]^[2] The medication was introduced between 1938 and 1941 under the brand name Depofollan.^[11]^[12] It has been used to treat prostate cancer.^[13]^[14] Estradiol stearate is a long-acting estrogen^[15]^[12] and is said to have been the first long-acting estrogen used in medicine, although it was never widely employed.^[12] It was reported to have a duration of more than one month.^[12] The medication was provided as an oil solution in ampoules containing 15 mg estradiol stearate.^[15]^[14] It was manufactured by Chinoin, a Hungarian pharmaceutical company.^[15]^[14]^[11]^[16] The compound was studied by Karl Miescher in 1938^[17] and was patented by Miescher and Chinoin in 1939 and 1941, respectively.^[18]^[19] A similar long-acting estradiol ester is estradiol undecylate, which has 11 carbon atoms instead of the 18 carbon atoms in estradiol stearate.^[1]^[2]

v
t
Affinities and estrogenic potencies of estrogen esters and ethers at the estrogen receptors show
Estrogen	Other names	RBA (%)^a	REP (%)^b
Estrogen	Other names	ER	ERα	ERβ
Estradiol	E2	100	100	100
Estradiol 3-sulfate	E2S; E2-3S	?	0.02	0.04
Estradiol 3-glucuronide	E2-3G	?	0.02	0.09
Estradiol 17β-glucuronide	E2-17G	?	0.002	0.0002
Estradiol benzoate	EB; Estradiol 3-benzoate	10	1.1	0.52
Estradiol 17β-acetate	E2-17A	31–45	24	?
Estradiol diacetate	EDA; Estradiol 3,17β-diacetate	?	0.79	?
Estradiol propionate	EP; Estradiol 17β-propionate	19–26	2.6	?
Estradiol valerate	EV; Estradiol 17β-valerate	2–11	0.04–21	?
Estradiol cypionate	EC; Estradiol 17β-cypionate	?^c	4.0	?
Estradiol palmitate	Estradiol 17β-palmitate	0	?	?
Estradiol stearate	Estradiol 17β-stearate	0	?	?
Estrone	E1; 17-Ketoestradiol	11	5.3–38	14
Estrone sulfate	E1S; Estrone 3-sulfate	2	0.004	0.002
Estrone glucuronide	E1G; Estrone 3-glucuronide	?	<0.001	0.0006
Ethinylestradiol	EE; 17α-Ethynylestradiol	100	17–150	129
Mestranol	EE 3-methyl ether	1	1.3–8.2	0.16
Quinestrol	EE 3-cyclopentyl ether	?	0.37	?
Footnotes: ^a = Relative binding affinities (RBAs) were determined via in-vitro displacement of labeled estradiol from estrogen receptors (ERs) generally of rodent uterine cytosol. Estrogen esters are variably hydrolyzed into estrogens in these systems (shorter ester chain length -> greater rate of hydrolysis) and the ER RBAs of the esters decrease strongly when hydrolysis is prevented. ^b = Relative estrogenic potencies (REPs) were calculated from half-maximal effective concentrations (EC₅₀) that were determined via in-vitro β‐galactosidase (β-gal) and green fluorescent protein (GFP) production assays in yeast expressing human ERα and human ERβ. Both mammalian cells and yeast have the capacity to hydrolyze estrogen esters. ^c = The affinities of estradiol cypionate for the ERs are similar to those of estradiol valerate and estradiol benzoate (figure). Sources: See template page.

v
t
Structural properties of selected estradiol esters show
Estrogen	Structure	Ester(s)				Relative mol. weight	Relative E2 content^b	logP^c
Estrogen	Structure	Position(s)	Moiet(ies)	Type	Length^a	Relative mol. weight	Relative E2 content^b	logP^c
Estradiol		–	–	–	–	1.00	1.00	4.0
Estradiol acetate		C3	Ethanoic acid	Straight-chain fatty acid	2	1.15	0.87	4.2
Estradiol benzoate		C3	Benzenecarboxylic acid	Aromatic fatty acid	– (~4–5)	1.38	0.72	4.7
Estradiol dipropionate		C3, C17β	Propanoic acid (×2)	Straight-chain fatty acid	3 (×2)	1.41	0.71	4.9
Estradiol valerate		C17β	Pentanoic acid	Straight-chain fatty acid	5	1.31	0.76	5.6–6.3
Estradiol benzoate butyrate		C3, C17β	Benzoic acid, butyric acid	Mixed fatty acid	– (~6, 2)	1.64	0.61	6.3
Estradiol cypionate		C17β	Cyclopentylpropanoic acid	Aromatic fatty acid	– (~6)	1.46	0.69	6.9
Estradiol enanthate		C17β	Heptanoic acid	Straight-chain fatty acid	7	1.41	0.71	6.7–7.3
Estradiol dienanthate		C3, C17β	Heptanoic acid (×2)	Straight-chain fatty acid	7 (×2)	1.82	0.55	8.1–10.4
Estradiol undecylate		C17β	Undecanoic acid	Straight-chain fatty acid	11	1.62	0.62	9.2–9.8
Estradiol stearate		C17β	Octadecanoic acid	Straight-chain fatty acid	18	1.98	0.51	12.2–12.4
Estradiol distearate		C3, C17β	Octadecanoic acid (×2)	Straight-chain fatty acid	18 (×2)	2.96	0.34	20.2
Estradiol sulfate		C3	Sulfuric acid	Water-soluble conjugate	–	1.29	0.77	0.3–3.8
Estradiol glucuronide		C17β	Glucuronic acid	Water-soluble conjugate	–	1.65	0.61	2.1–2.7
Estramustine phosphate^d		C3, C17β	Normustine, phosphoric acid	Water-soluble conjugate	–	1.91	0.52	2.9–5.0
Polyestradiol phosphate^e		C3–C17β	Phosphoric acid	Water-soluble conjugate	–	1.23^f	0.81^f	2.9^g
Footnotes: ^a = Length of ester in carbon atoms for straight-chain fatty acids or approximate length of ester in carbon atoms for aromatic fatty acids. ^b = Relative estradiol content by weight (i.e., relative estrogenic exposure). ^c = Experimental or predicted octanol/water partition coefficient (i.e., lipophilicity/hydrophobicity). Retrieved from PubChem, ChemSpider, and DrugBank. ^d = Also known as estradiol normustine phosphate. ^e = Polymer of estradiol phosphate (~13 repeat units). ^f = Relative molecular weight or estradiol content per repeat unit. ^g = logP of repeat unit (i.e., estradiol phosphate). Sources: See individual articles.

References[]

^ Jump up to: ^a ^b ^c J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 898. ISBN 978-1-4757-2085-3.
^ Jump up to: ^a ^b ^c Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 405–. ISBN 978-3-88763-075-1.
^ Martin Negwer (1987). Organic-chemical Drugs and Their Synonyms: (an International Survey). VCH Publishers. ISBN 978-0-89573-552-2. Estra-1,3,5(10)-triene-3,173-diol 17-octadecanoate = 3,173-Estradiol 17-stearate = (173)-Estra-1,3,5- (10)-triene-3,17-diol 17-octadecanoate (e) S Depofollan, Estradiol stearate, Ostradiolstearat U Depot-estrogen 8103
^ Edith Josephy; F. Radt (1956). Elsevier's Encyclopædia of Organic Chemistry. pp. 1974–1976.
^ Jump up to: ^a ^b ^c ^d ^e ^f Hochberg RB, Pahuja SL, Larner JM, Zielinski JE (1990). "Estradiol-fatty acid esters. Endogenous long-lived estrogens". Ann. N. Y. Acad. Sci. 595 (1): 74–92. Bibcode:1990NYASA.595...74H. doi:10.1111/j.1749-6632.1990.tb34284.x. PMID 2197972. S2CID 19866729.
^ Michael Oettel; Ekkehard Schillinger (6 December 2012). Estrogens and Antiestrogens I: Physiology and Mechanisms of Action of Estrogens and Antiestrogens. Springer Science & Business Media. pp. 235–237. ISBN 978-3-642-58616-3.
^ Jump up to: ^a ^b ^c ^d ^e ^f ^g ^h Hochberg RB (June 1998). "Biological esterification of steroids". Endocr. Rev. 19 (3): 331–48. doi:10.1210/edrv.19.3.0330. PMID 9626557.
^ Janocko, Laura; Larner, Janice M.; Hochberg, Richard B. (1984). "The Interaction of C-17 Esters of Estradiol with the Estrogen Receptor*". Endocrinology. 114 (4): 1180–1186. doi:10.1210/endo-114-4-1180. ISSN 0013-7227. PMID 6705734.
^ Vazquez-Alcantara, Marco Aurelio; Menjivar, Marta; Garcia, Gustavo A.; Díaz-Zagoya, Juan C.; Garza-Flores, Josue (1989). "Long-acting estrogenic responses of estradiol fatty acid esters". Journal of Steroid Biochemistry. 33 (6): 1111–1118. doi:10.1016/0022-4731(89)90417-2. ISSN 0022-4731. PMID 2515394.
^ Parkes AS (February 1938). "Effective Absorption of Hormones". Br Med J. 1 (4024): 371–3. doi:10.1136/bmj.1.4024.371. PMC 2085798. PMID 20781252.
^ Jump up to: ^a ^b Antalné, S., Géza, B., István, B., & Dezső, K. (1996). A Chinoin története (1910–1995). http://www.gyogyszeresztortenet.hu/wp-content/uploads/2013/08/Egy-mindig-meg%C3%BAjul%C3%B3-v%C3%A1llalat-a-Chinoin-t%C3%B6rt%C3%A9nete.pdf From the middle of the vitamin D and hannincas years, the research and production of steroid sex hormones was directed by Rezső Weisz. (n) In the latter, the collection of animal raw materials, in addition to chemical operations, required considerable organizational work similar to that of insulin. The intensification of attempts to produce steroid hormones and synthetic steroids, estrogens, over four years may have surpassed even 36 studies of sulfone JDid. Weisz et al., Primarily Kálmán Lányi, developed the most important estrone derivatives of industrial and therapeutic interest, Hogival (estrone acetate), Acrafalin (estradiol propionate) and Depofollan (estradiol stearate), which were marketed in 1938-1940.
^ Jump up to: ^a ^b ^c ^d Orvostudomány. Magyar Tudomanyos Akadémia V. Orvosi Tudományok Osztálya. 1960. p. 11.
^ Medgyaszay, A. (1963). "Intraokularer Druck und Hormonbehandlung". Ophthalmologica. 145 (3): 243–248. doi:10.1159/000304442. ISSN 1423-0267. PMID 13934365.
^ Jump up to: ^a ^b ^c Camillo Sellei (1970). Chemotherapy of Neoplastic Diseases. Acad. Press. p. 251.
^ Jump up to: ^a ^b ^c Endokrinologie. Johann Ambrosius Barth Verlag. 1951.
^ Alkaloida Vegyészeti Gyár Rt, Tiszavasvári T. Novák K., Hermecz I. szerk. (2005): Esti beszélgetés – Magyar Gyógyszerkutatók portréi. MTA Gyógyszerkémiai és Gyógyszertechnológiai Munkabizottsága, Budapest http://www.gyogyszeresztortenet.hu/wp-content/uploads/2013/08/Esti-besz%C3%A9lget%C3%A9s.pdf Archived 2016-08-05 at the Wayback Machine "Chinoin has achieved good results in the steroid hormones, synthetic steroids, and estrogens since the twenties, protected by 36 patents. The company was one of the first in the world to produce vitamin D, but was also a successful product for Hogival (estrone acetate), Acrofollin (estradiol propionate), Depofollan (estradiol stearate), Acrolutin (progesterone)."
^ Miescher K, Scholz C, Tschopp E (August 1938). "The activation of female sex hormones: Mono-esters of alpha-oestradiol". Biochem. J. 32 (8): 1273–80. doi:10.1042/bj0321273b. PMC 1264184. PMID 16746750.
^ "Estradiol esters esterified in 3-position and process of making same".
^ "Estradiol higher fatty acid ester".

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[Elks2014-1] Jump up to: ^a ^b ^c J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 898. ISBN 978-1-4757-2085-3.

[IndexNominum2000-2] Jump up to: ^a ^b ^c Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 405–. ISBN 978-3-88763-075-1.

[Negwer1987-3] Martin Negwer (1987). Organic-chemical Drugs and Their Synonyms: (an International Survey). VCH Publishers. ISBN 978-0-89573-552-2. Estra-1,3,5(10)-triene-3,173-diol 17-octadecanoate = 3,173-Estradiol 17-stearate = (173)-Estra-1,3,5- (10)-triene-3,17-diol 17-octadecanoate (e) S Depofollan, Estradiol stearate, Ostradiolstearat U Depot-estrogen 8103

[JosephyRadt1956-4] Edith Josephy; F. Radt (1956). Elsevier's Encyclopædia of Organic Chemistry. pp. 1974–1976.

[pmid2197972-5] Jump up to: ^a ^b ^c ^d ^e ^f Hochberg RB, Pahuja SL, Larner JM, Zielinski JE (1990). "Estradiol-fatty acid esters. Endogenous long-lived estrogens". Ann. N. Y. Acad. Sci. 595 (1): 74–92. Bibcode:1990NYASA.595...74H. doi:10.1111/j.1749-6632.1990.tb34284.x. PMID 2197972. S2CID 19866729.

[OettelSchillinger2012-6] Michael Oettel; Ekkehard Schillinger (6 December 2012). Estrogens and Antiestrogens I: Physiology and Mechanisms of Action of Estrogens and Antiestrogens. Springer Science & Business Media. pp. 235–237. ISBN 978-3-642-58616-3.

[pmid9626557-7] Jump up to: ^a ^b ^c ^d ^e ^f ^g ^h Hochberg RB (June 1998). "Biological esterification of steroids". Endocr. Rev. 19 (3): 331–48. doi:10.1210/edrv.19.3.0330. PMID 9626557.

[JanockoLarner1984-8] Janocko, Laura; Larner, Janice M.; Hochberg, Richard B. (1984). "The Interaction of C-17 Esters of Estradiol with the Estrogen Receptor*". Endocrinology. 114 (4): 1180–1186. doi:10.1210/endo-114-4-1180. ISSN 0013-7227. PMID 6705734.

[Vazquez-AlcantaraMenjivar1989-9] Vazquez-Alcantara, Marco Aurelio; Menjivar, Marta; Garcia, Gustavo A.; Díaz-Zagoya, Juan C.; Garza-Flores, Josue (1989). "Long-acting estrogenic responses of estradiol fatty acid esters". Journal of Steroid Biochemistry. 33 (6): 1111–1118. doi:10.1016/0022-4731(89)90417-2. ISSN 0022-4731. PMID 2515394.

[pmid20781252-10] Parkes AS (February 1938). "Effective Absorption of Hormones". Br Med J. 1 (4024): 371–3. doi:10.1136/bmj.1.4024.371. PMC 2085798. PMID 20781252.

[AntalnéGéza1996-11] Jump up to: ^a ^b Antalné, S., Géza, B., István, B., & Dezső, K. (1996). A Chinoin története (1910–1995). http://www.gyogyszeresztortenet.hu/wp-content/uploads/2013/08/Egy-mindig-meg%C3%BAjul%C3%B3-v%C3%A1llalat-a-Chinoin-t%C3%B6rt%C3%A9nete.pdf From the middle of the vitamin D and hannincas years, the research and production of steroid sex hormones was directed by Rezső Weisz. (n) In the latter, the collection of animal raw materials, in addition to chemical operations, required considerable organizational work similar to that of insulin. The intensification of attempts to produce steroid hormones and synthetic steroids, estrogens, over four years may have surpassed even 36 studies of sulfone JDid. Weisz et al., Primarily Kálmán Lányi, developed the most important estrone derivatives of industrial and therapeutic interest, Hogival (estrone acetate), Acrafalin (estradiol propionate) and Depofollan (estradiol stearate), which were marketed in 1938-1940.

[Orvostudomány1960-12] Jump up to: ^a ^b ^c ^d Orvostudomány. Magyar Tudomanyos Akadémia V. Orvosi Tudományok Osztálya. 1960. p. 11.

[Medgyaszay1963-13] Medgyaszay, A. (1963). "Intraokularer Druck und Hormonbehandlung". Ophthalmologica. 145 (3): 243–248. doi:10.1159/000304442. ISSN 1423-0267. PMID 13934365.

[Sellei1970-14] Jump up to: ^a ^b ^c Camillo Sellei (1970). Chemotherapy of Neoplastic Diseases. Acad. Press. p. 251.

[Barth1951-15] Jump up to: ^a ^b ^c Endokrinologie. Johann Ambrosius Barth Verlag. 1951.

[16] Alkaloida Vegyészeti Gyár Rt, Tiszavasvári T. Novák K., Hermecz I. szerk. (2005): Esti beszélgetés – Magyar Gyógyszerkutatók portréi. MTA Gyógyszerkémiai és Gyógyszertechnológiai Munkabizottsága, Budapest http://www.gyogyszeresztortenet.hu/wp-content/uploads/2013/08/Esti-besz%C3%A9lget%C3%A9s.pdf Archived 2016-08-05 at the Wayback Machine "Chinoin has achieved good results in the steroid hormones, synthetic steroids, and estrogens since the twenties, protected by 36 patents. The company was one of the first in the world to produce vitamin D, but was also a successful product for Hogival (estrone acetate), Acrofollin (estradiol propionate), Depofollan (estradiol stearate), Acrolutin (progesterone)."

[pmid16746750-17] Miescher K, Scholz C, Tschopp E (August 1938). "The activation of female sex hormones: Mono-esters of alpha-oestradiol". Biochem. J. 32 (8): 1273–80. doi:10.1042/bj0321273b. PMC 1264184. PMID 16746750.

[US2156599A-18] "Estradiol esters esterified in 3-position and process of making same".

[US2253669A-19] "Estradiol higher fatty acid ester".

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Estradiol stearate

See also[]

References[]