Estriol acetate benzoate

Last updated
Estriol acetate benzoate
Estriol acetate benzoate.svg
Clinical data
Trade names Holin-Depot
Other namesOestriol diacetate benzoate; Estriol 3-benzoate 16,17-diacetate
Routes of
administration
Intramuscular injection
Drug class Estrogen; Estrogen ester
Identifiers
  • [(8R,9S,13S,14S,16R,17R)-16,17-diacetyloxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
Formula C29H32O6
Molar mass 476.569 g·mol−1
3D model (JSmol)
  • CC(=O)O[C@@H]1C[C@H]2[C@@H]3CCC4=C([C@H]3CC[C@@]2([C@H]1OC(=O)C)C)C=CC(=C4)OC(=O)C5=CC=CC=C5
  • InChI=1S/C29H32O6/c1-17(30)33-26-16-25-24-11-9-20-15-21(35-28(32)19-7-5-4-6-8-19)10-12-22(20)23(24)13-14-29(25,3)27(26)34-18(2)31/h4-8,10,12,15,23-27H,9,11,13-14,16H2,1-3H3/t23-,24-,25+,26-,27+,29+/m1/s1
  • Key:VQHGRIUWSVCJPX-HSZAMCLRSA-N

Estriol acetate benzoate (JAN Tooltip Japanese Accepted Name) (brand name Holin-Depot), or oestriol diacetate benzoate (BAN Tooltip British Approved Name), is an estrogen medication. [1] [2] It is an estrogen ester, specifically, an ester of estriol. [1]

See also

Related Research Articles

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Atrimustine, also known as bestrabucil or busramustine, is a cytostatic antineoplastic agent which was under development in Japan by Kureha Chemicals for the treatment of breast cancer and non-Hodgkin's lymphoma as well as for the prevention of graft-versus-host disease in bone marrow transplant recipients. It is the benzoate ester of an ester conjugate of estradiol and chlorambucil, which results in targeted/site-directed cytostatic activity toward estrogen receptor-positive tissues such as breast and bone. It reached preregistration for the treatment of cancer but was ultimately discontinued. Estrogenicic side effects of atrimustine in clinical trials included vaginal bleeding and gynecomastia. The drug was first patented in 1980.

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<span class="mw-page-title-main">Estradiol dienantate</span> Chemical compound

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<span class="mw-page-title-main">Estriol triacetate</span> Chemical compound

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<span class="mw-page-title-main">Estramustine</span> Chemical compound

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<span class="mw-page-title-main">Estriol (medication)</span> Chemical compound

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<span class="mw-page-title-main">Estrone benzoate</span> Chemical compound

Estrone benzoate, or estrone 3-benzoate, is a synthetic estrogen and estrogen ester – specifically, the C3 benzoate ester of estrone – which was first reported in 1932 and was never marketed. It led to the development in 1933 of the more active estradiol benzoate, the first estradiol ester to be introduced for medical use.

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Ethinylestradiol benzoate, or 17α-ethynylestradiol 3-benzoate, is a synthetic estrogen and estrogen ester – specifically, the C3 benzoate ester of ethinylestradiol – which was first described in the late 1930s and was never marketed.

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Estriol phosphate (E3P), or estriol 17β-phosphate, also known as estra-1,3,5(10)-triene-3,16α,17β-triol 17β-(dihydrogen phosphate), is an estrogen which was never marketed. It is an estrogen ester, specifically an ester of estriol with phosphoric acid, and acts as a prodrug of estriol by cleavage via phosphatase enzymes in the body. Estriol phosphate is contained within the chemical structure of polyestriol phosphate, and this medication has been marketed for medical use.

References

  1. 1 2 Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 899. ISBN   978-1-4757-2085-3.
  2. Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 114–. ISBN   978-94-011-4439-1.