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Chemical compound
Bolenol![](https://upload.wikimedia.org/wikipedia/commons/thumb/8/84/Bolenol.png/200px-Bolenol.png) |
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Other names | Ethylnorandrostenol; 17α-Ethyl-19-norandrost-5-en-17β-ol |
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Routes of administration | By mouth |
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(8R,9S,10R,13S,14S,17S)-17-ethyl-13-methyl-2,3,4,7,8,9,10,11,12,14,15,
16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol
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CompTox Dashboard (EPA) | |
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ECHA InfoCard | 100.037.226 ![Edit this at Wikidata](https://upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png) |
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Formula | C20H32O |
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Molar mass | 288.475 g·mol−1 |
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3D model (JSmol) | |
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CC[C@@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@H]3CCCC4)C)O
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InChI=1S/C20H32O/c1-3-20(21)13-11-18-17-9-8-14-6-4-5-7-15(14)16(17)10-12-19(18,20)2/h8,15-18,21H,3-7,9-13H2,1-2H3/t15-,16+,17+,18-,19-,20-/m0/s1 NKey:VGXLQFPZGUQVQW-XGXHKTLJSA-N N
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Bolenol (INNTooltip International Nonproprietary Name, USANTooltip United States Adopted Name), also known as 17α-ethyl-19-norandrost-5-en-17β-ol (ethylnorandrostenol), is a synthetic, orally active anabolic-androgenic steroid (AAS) and a 17α-alkylated derivative of 19-nortestosterone (nandrolone) that was never marketed.[1] It was described in the literature in 1969.[1]
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ARTooltip Androgen receptor | Agonists | |
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SARMsTooltip Selective androgen receptor modulator | |
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GPRC6A | |
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