Hey Milton dont know the status of the google search engine but I think it would do wonders adding some key search words to put ology at the top
That is a great idea! SOOO here we go..... nonsteroidal.
ketosteroids.
holasteroida.
glucosteroid.
pygasteroida.
retrosteroid.
aminosteroid.
ecdysteroids.
A steroid is a organic compound, either natural or man-made, which has four cycloalkane rings in its structure. ... Steroid hormones are steroids which act as hormones in the body. Natural steroid hormones are usually made from cholesterol in the adrenal glands and gonads.
The common street (slang) names for anabolic steroids include arnolds, gym candy, pumpers, roids, stackers, weight trainers, and juice.
15 letter words containing steroid
steroidogenesis
steroidogeneses
corticosteroids
14 letter words containing steroid
corticosteroid
13 letter words containing steroid
steroidogenic
12 letter words containing steroid
nonsteroidal
ketosteroids
11 letter words containing steroid
ketosteroid
nonsteroids
10 letter words containing steroid
asteroidal
nonsteroid
9 letter words containing steroid
hysteroid
asteroids
steroidal
8 letter words containing steroid
asteroid
steroids
Steroid, any of a class of natural or synthetic organic compounds characterized by a molecular structure of 17 carbon atoms arranged in four rings. Steroids are important in biology, chemistry, and medicine. ... Many important physiological functions of vertebrates are controlled by steroid hormones.
19-Nortestosterone (nandrolone) derivatives
Compound Chemical name Marketed
Norclostebol 4-Chloro-19-nortestosterone ***10003;
Oxabolone 4-Hydroxy-19-nortestosterone ***10003;
Trenbolone (trienolone) 19-Nor-***948;9,11-testosterone ***10003;
Trestolone (MENT) 7***945;-Methyl-19-nortestosterone
This is a list of androgens/anabolic steroids (AAS) or testosterone derivatives. Esters are mostly not included in this list; for esters, see here instead. The major classes of testosterone derivatives include the following (as well as combinations thereof):
Testosterone derivatives: direct derivatives of testosterone not falling into the groups below
4,5***945;-Reduced/dihydrogenated testosterone derivatives: dihydrotestosterone (DHT) derivatives
19-Demethylated testosterone derivatives: 19-nortestosterone (nandrolone) derivatives
17***945;-Alkylated testosterone derivatives: methyltestosterone and ethyltestosterone derivatives
17***945;-Ethynylated/vinylated testosterone derivatives: ethynyltestosterone (ethisterone) and vinyltestosterone derivatives
The last group consists of progestins with mostly only very weak androgenic/anabolic activity.
This article pertains to steroidal androgens; nonsteroidal androgens like the selective androgen receptor modulators (SARMs) andarine and enobosarm (ostarine) are not included here.
Contents
1 Testosterone derivatives
2 Dihydrotestosterone derivatives
3 19-Nortestosterone (nandrolone) derivatives
4 17***945;-Alkylated testosterone derivatives
5 17***945;-Alkylated dihydrotestosterone derivatives
6 17***945;-Alkylated 19-nortestosterone derivatives
7 17***945;-Vinylated testosterone derivatives
8 17***945;-Ethynylated testosterone derivatives
9 See also
10 Notes
11 References
12 Further reading
Testosterone derivatives
Compound Chemical name Structure Marketed
Testosterone Androst-4-en-17***946;-ol-3-one Testosteron.svg ***10003;
4-Hydroxytestosterone 4-Hydroxytestosterone 4-hydroxytestosterone.png ***8211;
11-Ketotestosterone 11-Ketotestosterone 11-Ketotestosterone.svg ***8211;
Boldenone ***916;1-Testosterone Boldenone.png ***10003;
Clostebol 4-Chlorotestosterone Clostebol.svg ***10003;
Prohormone-like
Compound Chemical name Structure Marketed
4-Androstenediol 4-Androstenediol 4-Androstenediol.svg ***8211;
4-Dehydroepiandrosterone (4-DHEA) 4-Dehydroepiandrosterone 3beta-Hydroxyandrost-4-en-17-one.png ***8211;
5-Androstenedione 5-Androstenedione 5-Androstenedione.svg ***8211;
5-Dehydroandrosterone (5-DHA) 5-Dehydroandrosterone Dehydroandrosterone.svg ***8211;
11***946;-Hydroxyandrostenedione (11***946;-OHA4) 11***946;-Hydroxy-4-androstenedione 11***946;-Hydroxyandrostenedione.svg ***8211;
Adrenosterone (11-ketoandrostenedione, 11-KA4) 11-Keto-4-androstenedione Adrenosterone.png ***8211;
Androstenediol (5-androstenediol, A5) 5-Androstenediol 5-Androstenediol.png ***8211;
Androstenedione (4-androstenedione, A4) 4-Androstenedione Androstendion.svg ***8211;
Atamestane 1-Methyl-***948;1-4-androstenedione Atamestane.svg ***8211;
Boldione (1,4-androstadienedione) ***948;1-4-Androstenedione Boldione.png ***8211;
Dehydroepiandrosterone (DHEA, 5-DHEA; prasterone, androstenolone) 5-Dehydroepiandrosterone Dehydroepiandrosteron.svg ***10003;
Exemestane 6-Methylidene-***948;1-4-androstenedione Exemestane.svg ***10003;
Formestane 4-Hydroxy-4-androstenedione Formestane.svg ***10003;
Plomestane 10-Propargyl-4-androstenedione Plomestane.svg ***8211;
Prodrugs
Ethers
Compound Chemical name Structure Marketed
Cloxotestosterone Testosterone 17-chloral hemiacetal ether Cloxotestosterone.svg ***10003;
Quinbolone ***916;1-Testosterone 17***946;-cyclopentenyl enol ether Quinbolone.png ***10003;
Silandrone Testosterone 17***946;-trimethylsilyl ether Silandrone.png ***8211;
Dihydrotestosterone derivatives
Compound Chemical name Structure Marketed
Dihydrotestosterone (DHT); androstanolone, stanolone) 4,5***945;-Dihydrotestosterone Androstanolone.svg ***10003;
1-Testosterone (dihydro-1-testosterone, dihydroboldenone) 4,5***945;-Dihydro-***948;1-testosterone 1-testosterone.png ***8211;
11-Ketodihydrotestosterone (11-KDHT) 11-Keto-4,5***945;-dihydrotestosterone 11-Ketodihydrotestosterone.svg ***8211;
Drostanolone 2***945;-Methyl-4,5***945;-dihydrotestosterone Drostanolone New-And-Improved.png ***10003;
Epitiostanol (epithioandrostanol) 2***945;,3***945;-Epithio-3-deketo-4,5***945;-dihydrotestosterone Epitiostanol.png ***10003;
Mesterolone 1***945;-Methyl-4,5***945;-dihydrotestosterone Mesterolone.svg ***10003;
Metenolone (methenolone, methylandrostenolone) 1-Methyl-4,5***945;-dihydro-***948;1-testosterone Metenolone.svg ***10003;
Nisterime 2***945;-Chloro-4,5***945;-dihydrotestosterone 3-O-(p-nitrophenyl)oxime Nisterime.svg ***8211;
Stenbolone 2-Methyl-4,5***945;-dihydro-***948;1-testosterone Stenbolone.svg ***10003;
Prohormone-like
Compound Chemical name Structure Marketed
1-Androsterone (1-Andro, 1-DHEA) 1-Dehydroepiandrosterone 1-Androsterone.svg ***8211;
1-Androstenediol (dihydro-1-androstenediol) 1-Androstenediol (4,5***945;-dihydro-***948;1-4-androstenediol) 1-Androstenediol.svg ***8211;
1-Androstenedione (dihydro-1-androstenedione) 1-Androstenedione (4,5***945;-dihydro-***948;1-4-androstenedione) 1-Androstenedione.svg ***8211;
5***945;-Androst-2-en-17-one 3-Deketo-2-androstenedione (3-deketo-4,5***945;-dihydro-***948;2-4-androstenedione) 5alpha-androst-2-ene-17-one.svg ***8211;
Androsterone Androsterone Androsterone.png ***8211;
Epiandrosterone Epiandrosterone Epiandrosterone.png ***8211;
Prodrugs
Ethers
Compound Chemical name Structure Marketed
Mepitiostane 2***945;,3***945;-Epithio-3-deketo-4,5***945;-dihydrotestosterone 17***946;-(1-methoxycyclopentane) ether Mepitiostane.png ***10003;
Mesabolone 4,5***945;-Dihydro-***948;1-testosterone 17***946;-(1-methoxycyclohexane) ether Mesabolone.png ***8211;
Prostanozol 2'H-5***945;-Androst-2-eno[3,2-c]pyrazol-17***946;-ol 17***946;-tetrahydropyran ether Prostanozol.png ***8211;
Azine dimers
Compound Chemical name Structure Marketed
Bolazine (di(drostanolone) azine) 3,3-[(1E,2E)-1,2-Hydrazinediylidene]di(2***945;-methyl-5***945;-androstan-17***946;-ol)? Bolazine.png ***10003;
19-Nortestosterone (nandrolone) derivatives
Compound Chemical name Structure Marketed
Nandrolone (nortestosterone) 19-Nortestosterone Nandrolone.svg ***10003;
11***946;-Methyl-19-nortestosterone (11***946;-MNT) 11***946;-Methyl-19-nortestosterone 11***946;-Methyl-19-nortestosterone.svg ***8211;
Dienolone 19-Nor-***948;9-testosterone Dienolone structure.png ***8211;
Dimethandrolone 7***945;,11***946;-Dimethyl-19-nortestosterone Dimethandrolone structure.svg ***8211;
Norclostebol 4-Chloro-19-nortestosterone Norclostebol.svg ***10003;
Oxabolone 4-Hydroxy-19-nortestosterone Oxabolone.svg ***10003;
Trenbolone (trienolone) 19-Nor-***948;9,11-testosterone Trenbolone.svg ***10003;
Trestolone (MENT) 7***945;-Methyl-19-nortestosterone Trestolone structure.svg ***8211;
Prohormone-like
Compound Chemical name Structure Marketed
7***945;-Methyl-19-nor-4-androstenedione (MENT dione, trestione) 7***945;-Methyl-19-nor-4-androstenedione 7***945;-Methyl-19-norandrostenedione.svg ***8211;
19-Nor-5-androstenediol 19-Nor-5-androstenediol 19-Nor-5-androstenediol.svg ***8211;
19-Nor-5-androstenedione 19-Nor-5-androstenedione 19-Nor-5-androstenedione.svg ***8211;
19-Nordehydroepiandrosterone 19-Nor-5-dehydroepiandrosterone 19-Nordehydroepiandrosterone.svg ***8211;
Bolandiol (nor-4-androstenediol) 19-Nor-4-androstenediol Bolandiol.svg ***10003;
Bolandione (nor-4-androstenedione) 19-Nor-4-androstenedione 19-norandrostenedione.png ***8211;
Dienedione (nor-4,9-androstadienedione) 19-Nor-***948;9-4-androstenedione Dienedione.svg ***8211;
Methoxydienone (methoxygonadiene) 18-Methyl-19-nor-***948;2,5(10)-epiandrosterone 3-methyl ether Methoxydienone.svg ***8211;
Trendione (nor-4,9,11-androstatrienedione) 19-Nor-***948;9,11-4-androstenedione Trendione.svg ***8211;
Prodrugs
Esters
Compound Chemical name Structure Marketed
Bolmantalate (nandrolone adamantoate) 19-Nortestosterone 17***946;-adamantoate Bolmantalate.svg ***10003;
17***945;-Alkylated testosterone derivatives
See also: 17***945;-Alkylated anabolic steroid
Compound Chemical name Structure Marketed
Bolasterone 7***945;,17***945;-Dimethyltestosterone Bolasterone.png ***10003;
Calusterone 7***946;,17***945;-Dimethyltestosterone Calusterone.svg ***10003;
Chlorodehydromethyltestosterone (CDMT) 4-Chloro-17***945;-methyl-***948;1-testosterone 4-Chlorodehydromethyltestosterone.png ***10003;
Enestebol 4-Hydroxy-17***945;-methyl-***948;1-testosterone Enestebol.png ***8211;
Ethyltestosterone 17***945;-Ethyltestosterone Ethyltestosterone structure.png ***8211;
Fluoxymesterone 9***945;-Fluoro-11***946;-hydroxy-17***945;-methyltestosterone Fluoxymesterone structure.svg ***10003;
Formebolone 2-Formyl-11***945;-hydroxy-17***945;-methyl-***948;1-testosterone Formebolone.png ***10003;
Hydroxystenozole 17***945;-Methyl-2'H-androsta-2,4-dieno[3,2-c]pyrazol-17***946;-ol Hydroxystenozole.png ***8211;
Metandienone (methandienone, methandrostenolone) 17***945;-Methyl-***948;1-testosterone Metandienone.svg ***10003;
Methylclostebol (chloromethyltestosterone) 4-Chloro-17***945;-methyltestosterone Methylclostebol.svg ***8211;
Methyltestosterone 17***945;-Methyltestosterone Methyltestosterone.svg ***10003;
Oxymesterone 4-Hydroxy-17***945;-methyltestosterone Oxymesterone.png ***10003;
Tiomesterone (thiomesterone) 1***945;,7***945;-Diacetylthio-17***945;-methyltestosterone Tiomesterone structure.svg ***10003;
Prohormone-like
Compound Chemical name Structure Marketed
Chlorodehydromethylandrostenediol (CDMA) 4-Chloro-17***945;-methyl-***948;1-4-androstenediol Halodrol.svg ***8211;
Chloromethylandrostenediol (CMA) 4-Chloro-17***945;-methyl-4-androstenediol Chloromethylandrostenediol.svg ***8211;
Methandriol (methylandrostenediol) 17***945;-Methyl-5-androstenediol Methandriol.svg ***10003;
Prodrugs
Ethers
Compound Chemical name Structure Marketed
Methyltestosterone 3-hexyl ether 17***945;-Methyl-4-hydro-***948;3,5-testosterone 3-hexyl ether? Methyltestosterone 3-hexyl ether.svg ***10003;
Penmesterol (penmestrol) 17***945;-Methyl-4-hydro-***948;3,5-testosterone 3-cyclopentyl ether? Penmesterol.svg ***10003;
17***945;-Alkylated dihydrotestosterone derivatives
Compound Chemical name Structure Marketed
Androisoxazole 17***945;-Methyl-5***945;-androstano[3,2-c]isoxazol-17***946;-ol Androisoxazole.png ***10003;
Desoxymethyltestosterone 3-Deketo-17***945;-methyl-4,5***945;-dihydro-***948;2-testosterone Desoxymethyltestosterone.png ***8211;
Furazabol 17***945;-Methyl-5***945;-androstano[2,3-c][1,2,5]oxadiazol-17***946;-ol Furazabol.png ***10003;
Mestanolone (methyl-DHT) 17***945;-Methyl-4,5***945;-dihydrotestosterone Mestanolone.png ***10003;
Methasterone (methyldrostanolone) 2***945;,17***945;-Dimethyl-4,5***945;-dihydrotestosterone Methasterone.png ***8211;
Methyl-1-testosterone (methyldihydro-1-testosterone) 17***945;-Methyl-4,5***945;-dihydro-***948;1-testosterone Methyl-1-testosterone.svg ***8211;
Methyldiazinol 3-Azi-17***945;-methyl-4,5***945;-dihydrotestosterone Methyldiazirinol.svg ***8211;
Methylepitiostanol 2***945;,3***945;-Epithio-3-deketo-17***945;-methyl-4,5***945;-dihydrotestosterone Methylepitiostanol.svg ***8211;
Methylstenbolone 2,17***945;-Dimethyl-4,5***945;-dihydro-***948;1-testosterone Methylstenbolone.svg ***8211;
Oxandrolone 2-Oxa-17***945;-methyl-4,5***945;-dihydrotestosterone Oxandrolone.svg ***10003;
Oxymetholone 2-Hydroxymethylene-4,5***945;-dihydro-17***945;-methyltestosterone Oxymetholone.svg ***10003;
Stanozolol 17***945;-Methyl-2'H-5***945;-androst-2-eno[3,2-c]pyrazol-17***946;-ol Stanozolol.svg ***10003;
Prodrugs
Azine dimers
Compound Chemical name Structure Marketed
Mebolazine (dimethazine, di(methasterone) azine) 3,3-[(1E,2E)-1,2-Hydrazinediylidene]di(2***945;,17***945;-dimethyl-5***945;-androstan-17***946;-ol)? Mebolazine.png ***10003;
17***945;-Alkylated 19-nortestosterone derivatives
Compound Chemical name Structure Marketed
Dimethyltrienolone (7***945;,17***945;-dimethyltrenbolone) 7***945;,17***945;-Dimethyl-19-nor-***948;9,11-testosterone 7a17a-dimethyltrenbolone.png ***8211;
Dimethyldienolone (7***945;,17***945;-dimethyldienolone) 7***945;,17***945;-Dimethyl-19-nor-***948;9-testosterone Dimethyldienolone.svg ***8211;
Ethyldienolone 17***945;-Ethyl-19-nor-***948;9-testosterone Ethyldienolone.png ***8211;
Ethylestrenol (ethylnandrol) 17***945;-Ethyl-3-deketo-19-nortestosterone Ethylestrenol.svg ***10003;
Methyldienolone 17***945;-Methyl-19-nor-***948;9-testosterone Methyldienolone.svg ***8211;
Methylhydroxynandrolone (MOHN, MHN) 4-Hydroxy-17***945;-methyl-19-nortestosterone Methylhydroxynandrolone.svg ***8211;
Metribolone (methyltrienolone, R-1881) 17***945;-Methyl-19-nor-***948;9,11-testosterone Metribolone.png ***8211;
Mibolerone 7***945;,17***945;-Dimethyl-19-nortestosterone Mibolerone structure.png ***10003;
Norboletone 17***945;-Ethyl-18-methyl-19-nortestosterone Norboletone.svg ***8211;
Norethandrolone (ethylnandrolone, ethylestrenolone) 17***945;-Ethyl-19-nortestosterone Norethandrolone structure.png ***10003;
Normethandrone (methylestrenolone, normethisterone) 17***945;-Methyl-19-nortestosterone Methylestrenolone.png ***10003;
RU-2309 (18-methymetribolone, 17***945;-methyl-THG) 17***945;,18-Dimethyl-19-nor-***948;9,11-testosterone RU-2309.svg ***8211;
Tetrahydrogestrinone (THG) 17***945;-Ethyl-18-methyl-19-nor-***948;9,11-testosterone Tetrahydrogestrinone.png ***8211;
Prohormone-like
Compound Chemical name Structure Marketed
Bolenol (ethylnorandrostenol) 3-Deketo-17***945;-ethyl-19-nor-5-androstenediol Bolenol.png ***8211;
Prodrugs
Esters
Compound Chemical name Structure Marketed
Propetandrol 17***945;-Ethyl-19-nortestosterone 3-propionate Propetandrol.png ***10003;
17***945;-Vinylated testosterone derivatives
Compound Chemical name Structure Marketed
Vinyltestosterone 17***945;-Ethenyltestosterone 17a-vinyltestosterone structure.png ***8211;
17***945;-Vinylated 19-nortestosterone derivatives
Compound Chemical name Structure Marketed
Norvinisterone (vinylnortestosterone) 17***945;-Ethenyl-19-nortestosterone Norvinisterone.svg ***10003;
Commentary
The 17***945;-ethenylated (vinylated) testosterone derivative norvinisterone (vinylnortestosterone) is much more potent as an AAS than the 17***945;-ethynylated testosterone derivatives and is intermediate in potency between the 17***945;-ethynylated progestins and conventional AAS, with approximately one-third and one-fifth of the respective androgenic and anabolic activity of nandrolone in animal bioassays.[1]
Vinyltestosterone has been described as a weak AAS, though stronger than its 17***945;-ethynylated analogue ethisterone.[2]
17***945;-Ethynylated testosterone derivatives
Compound Chemical name Structure Marketed
Ethisterone (ethinyltestosterone) 17***945;-Ethynyltestosterone Ethisterone.svg ***10003;
Danazol (2,3-isoxazolethisterone) 2,3-Isoxazol-17***945;-ethynyltestosterone Danazol.svg ***10003;
17***945;-Ethynylated 19-nortestosterone derivatives
Compound Chemical name Structure Marketed
Norethisterone (norethindrone) 17***945;-Ethynyl-19-nortestosterone Norethisterone.svg ***10003;
Etynodiol (ethynodiol, 3***946;-hydroxynorethisterone) 17***945;-Ethynyl-3-deketo-3***946;-hydroxy-19-nortestosterone Etynodiol.svg ***8211;
Gestrinone (ethylnorgestrienone, R-2323) 17***945;-Ethynyl-18-methyl-19-nor-***948;9,11-testosterone Gestrinone.svg ***10003;
Levonorgestrel ((***8722
-norgestrel) (***8722
-17***945;-Ethynyl-18-methyl-19-nortestosterone Levonorgestrel.svg ***10003;
Lynestrenol (3-deketonorethisterone) 17***945;-Ethynyl-3-deketo-19-nortestosterone Lynestrenol.svg ***10003;
Norgestrel (18-methylnorethisterone) 17***945;-Ethynyl-18-methyl-19-nortestosterone Levonorgestrel.svgDextronorgestrel.svg ***10003;
Norgestrienone (ethynyltrenbolone) 17***945;-Ethynyl-19-nor-***948;9,11-testosterone Norgestrienone.svg ***10003;
Tibolone (7***945;-methylnoretynodrel) 7***945;-Methyl-17***945;-ethynyl-19-nor-***948;5(10)-testosterone Tibolone.svg ***10003;
Prodrugs
Ethers
Compound Chemical name Structure Marketed
Quingestanol 4-Hydro-19-nor-***948;3,5-testosterone 3-cyclopentyl ether? Quingestanol structure.svg ***8211;
Esters
Compound Chemical name Structure Marketed
Etynodiol diacetate (ethynodiol diacetate) 17***945;-Ethynyl-3-deketo-3***946;-hydroxy-19-nortestosterone 3***946;,17***946;-diacetate Ethynodiol diacetate.svg ***10003;
Norethisterone acetate (norethindrone acetate) 17***945;-Ethynyl-19-nortestosterone 17***946;-acetate Norethisterone acetate.svg ***10003;
Norethisterone enanthate (norethindrone enanthate) 17***945;-Ethynyl-19-nortestosterone 17***946;-enanthate Norethindrone enanthate.svg ***10003;
Ethers and esters
Compound Chemical name Structure Marketed
Quingestanol acetate 4-Hydro-17***945;-ethynyl-19-nor-***948;3,5-testosterone 3-cyclopentyl ether 17***946;-acetate? Quingestanol acetate.svg ***10003;
Commentary
17***945;-Ethynylated testosterone derivatives are potent progestins with only very weak androgenic/anabolic activity and are used as oral contraceptives or for the treatment of gynecological conditions in women. They are invariably classified as progestins rather than as AAS. However, these progestins are testosterone derivatives and do have significant androgenic/anabolic activity, sometimes producing acne and other mild androgenic effects in women. Conversely, in men, these drugs may actually have functional antiandrogen effects due to their potent progestogenic and hence antigonadotropic activity and capacity to suppress gonadal testosterone production.[3]
See also
List of steroids
List of designer drugs § Androgens
List of androgens/anabolic steroids available in the United States
Notes
? = Chemical names that are unverified.
References
Saunders, Francis J.; Drill, Victor A. (1956). "The Myotrophic and Androgenic Effects of 17-Ethyl-19-Nortestosterone and Related Compounds". Endocrinology. 58 (5): 567***8211;572. doi:10.1210/endo-58-5-567. ISSN 0013-7227. PMID 13317831.
LEWIS RA, DeMAJO S, ROSEMBERG E (1949). "The effects of 17-vinyl testosterone upon the rat adrenal". Endocrinology. 45 (6): 564***8211;70. doi:10.1210/endo-45-6-564. PMID 15402199.
Paulsen, C. Alvin; Leach, Robert B.; Lanman, John; Goldston, Norman; Maddock, W. O.; Heller, Carl G. (1962). "Inherent Estrogenicity of Norethindrone and Norethynodrel: Comparison with Other Synthetic Progestins and Progesterone1". The Journal of Clinical Endocrinology & Metabolism. 22 (10): 1033***8211;1039. doi:10.1210/jcem-22-10-1033. ISSN 0021-972X. PMID 13942007. "Androgenic effects were absent for each of the compounds in the doses administered as judged by: (a) marked decrease in libido and sexual potentia in each of 21 normal male subjects receiving norethynodrel, norethindrone and norethandrolone; (b) failure to increase libido and sexual potentia in each of four hypogonadotrophic eunuchoidal men receiving norethandrolone (each had previously responded to testosterone administration); (c) no virilization of 14 of 15 postmenopausal women receiving the three progestins (one who was taking norethandrolone at the dose level of 30 mg daily noted lowering in the pitch of her voice during the second month of therapy)."
Further reading
Kicman, A T (2008). "Pharmacology of anabolic steroids". British Journal of Pharmacology. 154 (3): 502***8211;521. doi:10.1038/bjp.2008.165. ISSN 0007-1188. PMC 2439524. PMID 18500378.
Fragkaki AG, Angelis YS, Koupparis M, Tsantili-Kakoulidou A, Kokotos G, Georgakopoulos C (2009). "Structural characteristics of anabolic androgenic steroids contributing to binding to the androgen receptor and to their anabolic and androgenic activities. Applied modifications in the steroidal structure". Steroids. 74 (2): 172***8211;97. doi:10.1016/j.steroids.2008.10.016. PMID 19028512. S2CID 41356223.
McRobb L, Handelsman DJ, Kazlauskas R, Wilkinson S, McLeod MD, Heather AK (2008). "Structure-activity relationships of synthetic progestins in a yeast-based in vitro androgen bioassay". J. Steroid Biochem. Mol. Biol. 110 (1***8211;2): 39***8211;47. doi:10.1016/j.jsbmb.2007.10.008. PMID 18395441. S2CID 5612000.
