| Iupac name | [(8R,9S,13S,14S,17S)-13-Methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] pyridine-3-carboxylate |
|---|---|
| Width | 250px |
| Routes of administration | Intramuscular injection |
| Class | Estrogen; Estrogen ester |
| Cas number | 4140-20-9 |
| Unii | BC621AC03L |
| Pubchem | 66433 |
| Chemspiderid | 59806 |
| Synonyms | Estradiol propionicotinate; Estradiol propionate nicotinate; Estradiol nicotinate propionate; Estradiol 17β-nicotinate 3-propionate |
| C | 27 |
| H | 31 |
| N | 1 |
| O | 4 |
| Smiles | CCC(=O)OC1=CC2=C(C=C1)C3CCC4(C(C3CC2)CCC4OC(=O)C5=CN=CC=C5)C |
| Stdinchi | 1S/C27H31NO4/c1-3-25(29)31-19-7-9-20-17(15-19)6-8-22-21(20)12-13-27(2)23(22)10-11-24(27)32-26(30)18-5-4-14-28-16-18/h4-5,7,9,14-16,21-24H,3,6,8,10-13H2,1-2H3/t21-,22-,23+,24+,27+/m1/s1 |
| Stdinchikey | FXMSQUVSUXBBAB-TXDQRGGKSA-N |
Estrapronicate (INN), also known as estradiol nicotinate propionate is an estrogen medication and estrogen ester which was never marketed.[1] It was studied as a component of the experimental tristeroid combination drug Trophobolene, which contained nandrolone decanoate, estrapronicate, and hydroxyprogesterone heptanoate.[2][3]
See also
- List of estrogen esters § Estradiol esters
- Estrapronicate/hydroxyprogesterone heptanoate/nandrolone undecanoate
References
- ^ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 898–. ISBN 978-1-4757-2085-3.
- ^ Excerpta medica. Section 8, Neurology and neurosurgery. 1981. p. 10.
- ^ Testosterone Congeners—Advances in Research and Application: 2013 Edition: ScholarlyBrief. ScholarlyEditions. 21 June 2013. pp. 137–. ISBN 978-1-4816-9288-5.