Trestolone enanthate
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Chemical compound
Clinical data | |
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Other names | Trestolone 17 |
Drug class | Androgen; Anabolic steroid; Androgen ester |
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CAS Number | |
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Chemical and physical data | |
Formula | C26H40O3 |
Molar mass | 400.603 g·mol−1 |
3D model (JSmol) | |
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Trestolone enanthate, also known as 7
See also
[edit]References
[edit]- ^ a b c Cunningham GR, Tindall DJ, Lobl TJ, Campbell JA, Means AR (September 1981). "Steroid structural requirements for high affinity binding to human sex steroid binding protein (SBP)". Steroids. 38 (3): 243–62. doi:10.1016/0039-128X(81)90061-1. PMID 7197818. S2CID 2702353.
- ^ a b Bursi R, Grootenhuis A, van der Louw J, Verhagen J, de Gooyer M, Jacobs P, Leysen D (March 2003). "Structure-activity relationship study of human liver microsomes-catalyzed hydrolysis rate of ester prodrugs of MENT by comparative molecular field analysis (CoMFA)". Steroids. 68 (3): 213–220. doi:10.1016/S0039-128X(02)00186-1. PMID 12628684. S2CID 32309966.
ERTooltip Estrogen receptor |
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GPERTooltip G protein-coupled estrogen receptor |
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PRTooltip Progesterone receptor |
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mPRTooltip Membrane progesterone receptor (PAQRTooltip Progestin and adipoQ receptor) |
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