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词条 Estradiol 3-propionate
释义

  1. See also

  2. References

{{Drugbox
| Verifiedfields =
| Watchedfields =
| verifiedrevid =
| IUPAC_name = [(8R,9S,13S,14S,17S)-17-Hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] propanoate
| image = Estradiol 3-propionate.svg
| width = 250px
| tradename =
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration = Intramuscular, vaginal[1]
| class = Estrogen; Estrogen ester
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =
| CAS_number_Ref =
| CAS_number = 6045-51-8
| CAS_supplemental =
| ATC_prefix = None
| ATC_suffix =
| ATC_supplemental =
| PubChem =
| IUPHAR_ligand =
| DrugBank_Ref =
| DrugBank =
| ChemSpiderID_Ref =
| ChemSpiderID = 2298529
| UNII = DS9WS297BV
| KEGG =
| ChEBI =
| ChEMBL =
| synonyms = Estradiol 3-propanoate; 3-Propanoylestradiol; 3,17β-Hydroxyestra-1,3,5(10)-trien-3-yl propionate
| C=21 | H=28 | O=3
| molecular_weight = 328.445 g/mol
| SMILES = CCC(=O)Oc1ccc2c(c1)CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4O)C
| StdInChI_Ref =
| StdInChI = InChI=1S/C21H28O3/c1-3-20(23)24-14-5-7-15-13(12-14)4-6-17-16(15)10-11-21(2)18(17)8-9-19(21)22/h5,7,12,16-19,22H,3-4,6,8-11H2,1-2H3/t16-,17-,18+,19?,21?/m1/s1
| StdInChIKey_Ref =
| StdInChIKey = InChIKey=FONFXFZWMZJFCD-NYKHLBABSA-N
}}Estradiol 3-propionate, or 3-propanoylestradiol, also known as estra-1,3,5(10)-triene-3,17β-diol 3-propionate, is a semisynthetic, steroidal estrogen that was never marketed.[1][2] It is an estrogen ester, specifically, a propionic acid ester of estradiol, and acts as a prodrug to it in vivo.[1][2] The chemical structure of estradiol 3-propionate is contained within estradiol dipropionate, estrapronicate, and orestrate, all of which are also estradiol esters.[2]

See also

  • List of estrogen esters § Estradiol esters

References

1. ^{{cite journal | vauthors = Woolfson AD, Elliott GR, Gilligan CA, Passmore CM | title = Design of an intravaginal ring for the controlled delivery of 17 beta-estradiol as its 3-acetate ester | journal = J Control Release | volume = 61 | issue = 3 | pages = 319–28 | year = 1999 | pmid = 10477804 | doi = | url = }}
2. ^{{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=RA1-PA129|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|page=898}}
{{Estrogen receptor modulators}}{{Steroid-stub}}{{Genito-urinary-drug-stub}}

5 : Abandoned drugs|Estradiol esters|Estranes|Propionate esters|Synthetic estrogens

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