3β-Hydroxytibolone
3β-Hydroxytibolone (developmental code name ORG-30126) is a synthetic steroidal estrogen which was never marketed.[1][2] Along with 3α-hydroxytibolone and δ4-tibolone, it is a major active metabolite of tibolone, and 3α-hydroxytibolone and 3β-hydroxytibolone are thought to be responsible for the estrogenic activity of tibolone.[1][2]
Compound | Code name | PR | AR | ER | GR | MR | SHBG | CBG |
---|---|---|---|---|---|---|---|---|
Noretynodrel | – | 6 | 0 | 2 | 0 | 0 | 0 | 0 |
Norethisterone (δ4-NYD) | – | 67–75 | 15 | 0 | 0–1 | 0–3 | 16 | 0 |
3α-Hydroxynoretynodrel | – | ? | ? | ? | ? | ? | ? | ? |
3β-Hydroxynoretynodrel | – | ? | ? | ? | ? | ? | ? | ? |
Ethinylestradiol | – | 15–25 | 1–3 | 112 | 1–3 | <1 | 0.18 | <0.1 |
Tibolone (7α-Me-NYD) | ORG-OD-14 | 6 | 6 | 1 | ? | ? | ? | ? |
Δ4-Tibolone | ORG-OM-38 | 90 | 35 | 1 | 0 | 2 | 1 | 0 |
3α-Hydroxytibolone | ORG-4094 | 0 | 3 | 4–6 | 0 | ? | ? | ? |
3β-Hydroxytibolone | ORG-301260 | 0 | 4 | 3–29 | 0 | ? | ? | ? |
7α-Methylethinylestradiol | – | ? | ? | ? | ? | ? | ? | ? |
Notes: Values are percentages (%). Reference ligands (100%) were promegestone for the PR, metribolone for the AR, E2 for the ER, DEXA for the GR, aldosterone for the MR, DHT for SHBG, and cortisol for CBG. Sources: See template. |
Compound | Code name | PR | AR | ERα | ERβ | GR | MR |
---|---|---|---|---|---|---|---|
Tibolone | ORG-OD-14 | 123 | 1.05 | 4 | 105 | 2410* | 170* |
Δ4-Tibolone | ORG-OM-38 | 46 | 0.2 | 26 | 300 | 1760* | 30* |
3α-Hydroxytibolone | ORG-4094 | 2400* | 135* | 1.7 | 100 | ND* | 1160* |
3β-Hydroxytibolone | ORG-30126 | 20000* | ND* | 2.4 | 115 | ND* | 3310* |
Notes: Values are affinities (nM). Non-italicized values are EC50. Italicized values with an asterisk (*) are IC50. Reference ligands (EC50) were promegestone (5 nM for PR), metribolone (0.1 nM for AR), estradiol (0.018 nM for ERα, 0.08 nM for ERβ), dexamethasone (6 nM for GR), and aldosterone (0.36 nM for MR). Sources: See template. |
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Other names | ORG-30126; 7α-Methyl-17α-ethynylestr-5(10)-ene-3β,17β-diol |
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Formula | C21H30O2 |
Molar mass | 314.469 g·mol−1 |
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References
- Kuhl, H (2005). "Pharmacology of estrogens and progestogens: influence of different routes of administration". Climacteric. 8 (sup1): 3–63. doi:10.1080/13697130500148875. ISSN 1369-7137. PMID 16112947.
- Escande A, Servant N, Rabenoelina F, Auzou G, Kloosterboer H, Cavaillès V, Balaguer P, Maudelonde T (2009). "Regulation of activities of steroid hormone receptors by tibolone and its primary metabolites". J. Steroid Biochem. Mol. Biol. 116 (1–2): 8–14. doi:10.1016/j.jsbmb.2009.03.008. PMID 19464167.
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