Topterone
Topterone
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| Names |
| IUPAC name
(8R,9S,10R,13S,14S,17S)-17-Hydroxy-10,13-dimethyl-17-propyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one |
| Identifiers |
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60607-35-4 |
| Jmol interactive 3D |
Image |
| PubChem |
9797605 |
InChI=1S/C22H34O2/c1-4-10-22(24)13-9-19-17-6-5-15-14-16(23)7-11-20(15,2)18(17)8-12-21(19,22)3/h14,17-19,24H,4-13H2,1-3H3/t17-,18+,19+,20+,21+,22+/m1/s1 Key: LZSOOHLAZHOTHJ-GUCLMQHLSA-N
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CCC[C@@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C)O
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| Properties |
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C22H34O2 |
| Molar mass |
330.51 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
| Infobox references |
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Topterone is an antiandrogen.[1]
See also
References
- ↑ Ferrari, RA; Chakrabarty, K; Creange, JE; Beyler, AL; Potts, OG; Schane, HP (1980). "Endocrine profile of topterone, a topical antiandrogen, in three species of laboratory animals". Methods and findings in experimental and clinical pharmacology 2 (2): 65–9. PMID 7339330.
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| Receptor (ligands) | |
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| | Enzyme | |
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| | Others | Precursors/prohormones | |
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| Indirect |
- Antigonadotropins (e.g., estrogens, progestogens, prolactin)
- GnRH agonists (e,g, GnRH, leuprorelin)
- GnRH antagonists (e.g., cetrorelix)
- Gonadotropins (e.g., FSH, hCG, LH)
- Kisspeptin
- Plasma proteins (ABP, albumin, SHBG)
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| See also: Estrogenics • Glucocorticoids • Mineralocorticoids • Progestogenics |
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