Synthetic androgens as designer supplements.

Anabolic androgenic steroids (AAS) are some of the most common performance enhancing drugs (PED) among society. Despite the broad spectrum of adverse effects and legal consequences, AAS are illicitly marketed and distributed in many countries. To circumvent existing laws, the chemical structure of AAS is modified and these designer steroids are sold as nutritional supplements mainly over the Internet. Several side effects are linked with AAS abuse. Only little is known about the pharmacological effects and metabolism of unapproved steroids due to the absence of clinical studies. The large number of designer steroid findings in dietary supplements and the detection of new compounds combined with legal loopholes for their distribution in many countries show that stricter regulations and better information policy are needed.

INTRODUCTION

The use of anabolic androgenic steroids is a widespread issue not only among athletes but also in recreational sports as well as in the general population. In elite sports, the use of anabolic agents is prohibited by the World Anti-Doping Agency (WADA). Its list of prohibited substances covers exogenous synthetic steroids as well as endogenous androgens and precursors of androgens [1]. The majority of adverse analytical findings in sports reported by WADA laboratories is associated with anabolic steroids [2]. An ever-increasing trend for attractive body appearance and better sports performance along with less effort is recognized in athletes and nonathletes. A large part of unapproved steroids is marketed as ‘dietary supplements’ in dubious stores or over the Internet. These products include common AAS, designer steroids and/or prohormones, often without proper labeling of the content. Even cross-contaminations of non-hormonal dietary supplements with steroids have been detected [3]. The illusion that these products have none or minimal side effects (or can be controlled by the users), along with the easy access of performance or image enhancing drugs, increases the willingness to take ‘pills for everything’ [4].

Data from the US suggest that 1-3 % of the inhabitants use anabolic steroids [5, 6]. The lifetime prevalence of AAS use in the US was estimated in a recent study with about 3-4 million [7], whereby also recently another study showed that AAS use is even prevalent in men >40 years [8], probably describing aging long-term user. A recent meta-analysis of 187 studies predicts for the first time a global lifetime prevalence with an estimated value of 3.3 % [9]. Pope et al. published an extensive review about performance enhancing drugs and their health consequences earlier this year [10]. This review focuses on the steroidal findings of androgens in dietary supplements.

STEROID HORMONES

Steroid hormones are lipophilic substances derived from cholesterol and are subgrouped based on their pharmacological profile and their receptor binding affinity as sex steroids (androgens, estrogens, gestagens) and corticosteroids (gluco-, and mineralocorticoids). After cleavage of the side chain of cholesterol by cytochrome P450 enzyme CYPscc pregnenolone represents the basic pregnane. Pregnenolone is the general precursor for the biosynthesis of androgens, estrogens and corticosteroids. Corticosteroids are mainly synthesized in the adrenal gland and regulate water and mineral transport (mineralcorticoids), energy metabolism and immune and stress response (glucocorticoids). The loss of C20/C21 from the molecule leads to the androgens and estrogens. The female sex steroids estrogens and gestagens are important for the development of female sex characteristics, the regulation of the menstrual cycle and maintenance of pregnancy. They also play a role in the regulation of spermatogenesis and sperm maturation in males [11]. Estrogens originate from androgens. The enzyme complex aromatase, CYP19, produces etradiol and estrone from testosterone and androstenedione respectively. Androgens represent the male sex steroids and are discussed in more detail below. In addition to the above mentioned functions, steroids play an important role in the brain: Peripheral steroids that are involved in brain functioning, so-called neuroactive steroids, and neurosteroids that are only synthesized within the central nervous system (Fig. ).

Androgens

The pharmacology of androgens and the androgen receptor has been extensively reviewed [12, 13]. Therefore, a very brief overview is given in here. Androgens are male sex hormones that promote androgenic and anabolic effects. Besides testosterone and its 5α-hydrogenated form, the more active metabolite 5α-dihydrostestosterone (5α-DHT), also other endogenous androgens like androstenedione, dehydro-epiandrosterone (DHEA) and its sulfate (DHEAS), and androstenediol play important roles in humans. In men, testosterone is mainly produced in the Leydig cells of the testis. The ovaries in women produce androstenedione and testosterone [14]. The biosynthesis of androgens in the testis and ovaries is regulated by the hypothalamic-pituitary-gonadal (HPG) axis. The anterior pituitary induces the production of testosterone through the secretion of luteinizing hormone (LH) after activation through gonadotropin releasing hormone (GnRH) by the hypothalamus. Negative feedback through testosterone is mediated through decreasing the release of GnRH by the hypothalamus as well as decreasing the sensitivity of the pituitary to GnRH. The weaker androgens are synthesized in both sexes in the adrenal cortex, regulated by adrenocorticotropic hormone (ACTH). In the bloodstream testosterone is predominantly bound to proteins like the sex hormone binding globulin (SHBG) or albumin. Transported to its target tissues, free testosterone mainly diffuses into the cells where it mediates its action itself by binding to the androgen receptor (AR) or is reduced by 5α-reductase to 5α-DHT or is aromatized by aromatase to estradiol.

Androgen Receptor Mediated Action

Androgens mainly exert their effects via the androgen receptor, a member of the nuclear receptor superfamily [15, 16]. AR’s are located in the cytosol stabilized by heat shock proteins (Hsp) and other chaperones (e.g. p23) [17]. After binding of an androgen this complex dissociates due to conformational changes within the receptor, which is then able to interact with coregulators that allow the AR to migrate into the cell nucleus and form a homodimer [13]. After dimerization the receptor complex binds to androgen response elements (AREs), specific promoter regions of the target genes and acts as a ligand dependent DNA-binding transcription factor. Heterodimers with ERα (estrogen receptor α) or orphan nuclear receptors are also possible but not so common and address different target genes [18]. AR action can be regulated by allosteric modulation or phosphorylation of the AR itself [19, 20] as well as by coregulators. These coregulators largely influence the androgen receptor and other steroid hormone receptors. Recent reviews summarized the importance of steroid receptor coregulators (SRC) [21, 22] acting as coactivators or corepressors by altering ligand selectivity, modification of DNA or histones, or acting as promoters [13, 23]. Differences in coregulator expression in androgen target tissues helps to understand the various effects of androgens.

Non-Classical Actions

Besides the classical, genomic mechanism of action, steroid hormones are reported to act via non-genomic pathways [24, 25]. It is known that estrogens can interfere with the orphan G-protein coupled receptor (GPCR) GPR30, an intracellular trans-membrane receptor, and cause rapid steroid hormone actions [26]. Effects of rapid estrogen action on the behavior in humans have been reviewed recently [27]. Progesterone and androgens have the ability to interact via non-genomic pathways as well [28, 29]. Non-classical testosterone actions were observed mediating their effects in several tissues (reproductive, cardiovascular, immune and musculoskeletal systems) [29, 30]. Signaling pathways via a SHBG receptor or interaction of androgens with tyrosine kinases which alter coregulator function by phosphorylation, as well as membrane associated ARs affecting intracellular Ca2+ levels or allosteric modulation of GABAA receptors are discussed [18, 31-33]. Recently, a group supported the assumption of rapid androgen signaling mediated via a membrane bound GPCR [34].

PHYSIOLOGICAL EFFECTS OF AAS

As the name implies, androgens play a key role in reproduction, sexual maturation and differentiation in males, but also have an important impact in normal human development and physiology in general. Reviewers showed the importance of the AR and androgen action in several tissues [35]. Depending on the target tissue, different androgens are the main endogenous ligand. The existence of 5α-reductase is a sign for effects mostly derived from 5α-DHT whereas aromatase activity is an indication that besides testosterone estrogens may play a role in signaling. Studies using AR knockout mice helped to discover the importance of estrogen action in androgen target tissues. Investigations using AR knockout mice (ARKO) have been reviewed by Chang et al. [36], showing many key roles and locations of AR and its significance in production and maturation of immune cells, bone mineralization, and muscle growth, regulation of insulin sensitivity and glucose homeostasis in brain and liver, cutaneous wound healing and cardiovascular diseases. As mentioned above the androgens testosterone and 5α-DHT regulate the development of the testis, spermatogenesis and differentiation of secondary male sex characteristics, whereby even the female sex steroid estrogen is involved in regulation of spermatogenesis and sperm maturation [11].

The anabolic effects of androgens are an increase of skeletal muscle mass and strength whereby the mechanism of action is not fully understood. AR mediated actions as well as AR independent pathways are suggested [37]. ARs are expressed in several cell types in human skeletal muscle, including satellite cells, fibroblasts, CD34+ precursor cells, vascular endothelial, smooth muscle cells, and mast cells [38]. In the skeletal muscle testosterone itself seems to be the acting hormone because no 5α-reductase activity is observed in these cells [12]. It induces hypertrophy of type 1 and 2 fibers and increases the number of muscle progenitor cells (satellite cells) and promotes their myogenic differentiation [38]. These changes in skeletal muscle lead to improved muscle strength and leg power [39, 40].

Besides AR both estrogen receptor isoforms ERα and ERβ are expressed in human skeletal muscle [41]. ERβ is also reported to mediate anabolic effects [42]. Another effect of androgens is the up-regulation of insulin-like growth factor-I receptor (IGF-IR) [43].

Additionally androgens affect bone maturation. Thereby AR action is important for trabecular and cortical bone maintenance, whereas for the latter estrogens play a part as well [44]. Evidence is emerging that androgens may protect men against osteoporosis via maintenance of cancellous bone mass and expansion of cortical bone. This effect was mediated by the AR and ERα [45, 46].

Recent epidemiological data showed a correlation between low testosterone levels in men and incidence of cardiovascular disease and stroke [47].

Behavioral effects of androgens include sexual behavior, cognitive abilities, aggression and mood [12, 48]. In adults, testosterone levels showed a positive correlation with good mood and negative correlations with anxiety and depression [12]. A clinical study in hypogonadal men showed a connection between testosterone administration and decrease in depressive symptoms [49]. High testosterone levels are often linked with aggressive behavior without resolved mechanism. A recent animal study with castrated macaques showed that androgens stimulated serotonin related gene expression [50], contradicting earlier studies that found low serotonin being one reason for androgen induced aggression [51]. Neuroprotective effects are currently discussed. The neural brain AR in rats increased remyelination, and aging men with low testosterone showed signs of Alzheimers disease [52, 53]. Other important target tissues of androgens are the liver, kidney, skin, and fat tissue. Adipose tissue has a considerable aromatase activity. Thereby the androgen testosterone is converted into estradiol. 5α-DHT is mostly inactivated due to 3α-hydroxy steroid dehydrogenase (3α-HSD) activity in adipose tissue [54]. An increase in androgen levels throughout gestation is likely to be important for establishment and maintenance of pregnancy and initiation of parturition [55].

ADVERSE EFFECTS

However, AAS abuse is associated with various adverse events in different androgen target tissues and has been reviewed extensively elsewhere [10, 56]. Pope et al. categorize adverse events in cardiovascular, neuroendocrine, neuropsychiatric, hepatic, musculoskeletal, kidney, immune and dermatologic effects. Common side effects of AAS abuse include virilization and menstrual irregularities in females, gynaecomastia mediated by an excess of estrogenic metabolites and decreased sperm count and testicle size in men, infertility, altered lipid metabolism, decreased glucose tolerance, hypertrophy of sebaceous gland, acne, hair loss and liver toxicity in both sexes. In adolescents an acceleration of bone maturation and premature closure of the epiphysis lead to cessation of the longitudinal growth.

Additionally, adverse cardiovascular effects after AAS abuse are widely reported [57-60]. Recent studies repeatedly confirmed this. A forensic study in polydrug abusing AAS users showed an obvious number of cardiovascular diseases [61]. Again, case reports revealed the connection between myocardial infarction [62], myocardial hypertrophy and hypertension with AAS abuse [63]. A group postulated possible subclinical markers for these cardiac effects. They associated long-term supraphysiological doses of AAS with higher values of intra- and interatrial electrochemical delay in healthy young bodybuilders [64]. Another research group confirmed in a cross-sectional study increased markers of cardiovascular risk and endothelial dysfunction [65]. To investigate how endothelial dysfunction might arise after AAS use, a supraphysiological dose of testosterone was administered to 17 young males. Decreased urinary nitric oxide levels and decreased antioxidative capacity were detected as well as lower expression of endothelial NO synthase in a cell model [66]. A mechanism how AAS may influence cardiovascular health was postulated recently. In this study, the androgen fluoxymesterone has shown to inhibit 11β-hydroxysteroid dehydrogenase, which may lead to decreased glucocorticoid inactivation and therefore to cortisol-induced mineralcorticoid receptor activation ending up in electrolyte disturbances. This could cause possible hypertension [67]. A recent study in recreational sports was conducted in 17 men given either the prohormone 3β-hydroxy-5α-androst-1-en-17-one or placebo where the treated group showed negative effects on cardiovascular and liver parameters [68].

The central nervous system is another important target for AAS side effects. There are several studies describing psychiatric symptoms after AAS abuse like major mood disorders, aggressive behavior, dependence syndrome, or cognitive effects [51, 69]. Neuroprotective as well as neurotoxic effects of testosterone are discussed. Apoptotic effects of AAS are present in several cell culture models regarding different cell types [70, 71]. Neurotoxic effects due to apoptotic mechanisms are emerging [72]. A study using neuronal cells treated with testosterone or AAS showed neurotoxic effects via a genomic as well as a non-genomic pathway with a membrane-bound AR being the more potent target [73]. The administration of supraphysiological doses of metandienone and 17α-methyltestosterone promotes apoptotic pathways in AR expressing neuron cells only [74]. Cognitive deficits in a human study after long-term high-dose AAS exposure were investigated recently [75]. Increased sensitivity towards psychopathological disorders has been reviewed in regard of pubertal AAS use in preclinical models and humans [76].

Major mood disorders are connected with AAS use as is shown in humans [77] and animals. An animal study in rats showed that nandrolone and stanozolol administration resulted in pathophysiological signs of major depressive disorder like decreased levels of brain-derived neurotrophic factor (BDNF), lowered expression of glucocorticoid receptors, and an increase in corticosterone levels (the stress hormone in rodents) whereas the antidepressant chlorimipramine antagonized these effects [78]. Investigations of depressive but not anxious symptoms linked to changes in dopaminergic, serotonergic and noradrenergic neurotransmission of nandrolone exposed rats [79] are partly inconsistent with a recent study describing serotonergic and noradrenergic changes in neurotransmission as well as depressive and anxious behavior in rats [80].

Observations of aggressive behavior caused by AAS use are described in human and animal studies [81, 82]. Aggression might be linked with anxiety in animals and involves several brain circuits that are affected by AAS [83]. Animal studies showed impact on the glutamate, the GABAergic, the serotonergic and dopaminergic system as well as on tachykinin and encephalin pathways [84-88]. A recent controlled study in healthy young males investigated the potential of testosterone towards aggressive behavior. A testosterone baseline was established after administering a GnRH antagonist (cetrorelix acetate). Physiological doses of testosterone rapidly increased the response of neural circuits mediating threat processing and aggressive behavior, probably via non-genomic pathways [89].

Steroid dependence is another severe and perhaps underestimated adverse event of AAS abuse. Data from the Anabolic 500 survey showed that almost one quarter of AAS users were dependent on these drugs [90]. The relatively high prevalence of AAS use in the US (about 4 mio.) is accompanied by roughly 1 million users who might have experienced AAS dependence [7].

DESIGNER ANDROGENS

Androgenic anabolic steroids are derived from the endogenous androgens testosterone and 5α-DHT. Chemical modifications of these molecules aimed towards more selective anabolic properties, higher oral bioavailability, optimized pharmacokinetics and minimized estrogenic side effects. Attempts to separate androgenic from anabolic activity entirely failed. However, there are some AAS with a relatively high anabolic-androgenic index (e.g. stanozolol, nandrolone), which means the anabolic effects exceed the androgenic effects but are still inseparable. 17α-Methylation enables oral administration by decreasing inactivation during first pass metabolism however liver toxicity increases at the same time [56]. Reduction of estrogen-related side effects can be achieved by elimination of the C19-methyl group, introduction of a 1,2-double bond or methylation at C2, not allowing the aromatase enzyme complex for aromatization of the A-ring, but still cannot be avoided completely [91-94]. Further modifications include methylation, halogenation or hydroxylation at C-1, C-2, C-4, C-6, C-7, or C-11, or introduction of additional double bonds in ring A, B and/or C, as well as attachment of an additional ring at C-2/C-3 [12, 95] (Fig. ).

Precursors of active hormones with only little intrinsic effects are often called prohormones. Today, this term is mainly used for prohormones of anabolic androgenic steroids with testosterone or nortestosterone being the corresponding active hormones (e.g. 19-norandrostenedione, 4-androstenediol).

The inhibition of the enzyme complex aromatase is therapeutically used in estrogen depending cancer [96]. In combination with anabolic steroids they are administered in order to reduce side effects like gynocomastia resulting from estrogenic metabolites [91]. Additionally, they are discussed to increase endogenous testosterone levels by reducing its metabolic conversion and thereby leading to muscle hypertrophy [97]. Aromatase inhibitors (as well as other anti-estrogens) are prohibited substances in sports according to regulations of the World Anti-Doping Agency [1], and can be subgrouped into steroidal (type-I, e.g. exemestane) and non-steroidal (type-II, e.g. anastrozole) inhibitors [98, 99]. Several steroids appeared on the dietary supplement market, that are advertised to result in aromatase inhibition (e.g. formestane, androst-4-ene-3,6,17-trione, androsta-1,4,6-triene-3,17-dione, and 6α-methylandrost-4-ene-3,17-dione) [100-102]. The chemical structures of steroidal aromatase inhibitors are closely related to those of anabolic androgenic steroids.

More recently so-called selective androgen receptor modulators (SARMs, examples in Fig. ) got the attraction of the pharmaceutical industry. They promote full agonistic action in muscles and bones while only partial or antagonistic effects in the prostate [103]. Like aromatase inhibitors, they are divided in steroidal (e.g. 7α-methyl-19-nortestosterone) and non-steroidal (e.g. Andarine) types. A recent review updates the developments of SARMs [104]. Some clinical trials involving non-steroidal SARMs are currently ongoing but approved drugs are still missing. Nevertheless they are listed on the WADA prohibited list and adverse analytical findings in doping control already occurred (S-4, Andarine) [105]. Positive findings of Andarine (S4) as well as MENT (7α-methyl-19-nortestosterone) and its prodrug 7α-methyl-19-norandrost-4-ene-3,17-dione in ‘dietary supplements’ were also reported recently [106, 107].

DESIGNER SUPPLEMENTS

To avoid legal consequences with regard to trading or using androgenic anabolic steroids, chemical modifications of existing approved or prohibited substances have been realized [95]. Only testosterone, nortestosterone, dihydrochlormethyltestosterone (DHCMT), metenolon, metandienone, methyltestosterone, oxandrolone, fluoxymesterone, stanozolol, formestane, 5α-DHT, and DHEA, have ever been approved for therapeutical use in humans. Aside from these substances any institution has never approved other steroids, and therefore their effects, side effects or metabolism are not well investigated. In addition to the above mentioned effects and side effects of AR agonists the designer steroids may also display side effects related to an activation of other steroid receptors, e.g. the glucocorticoid receptor (GR) in case of tetrahydro-gestrinone [108]. The first designer steroid that has never been marketed as approved drug before was DHCMT, which has been used in regard to doping purposes by athletes. In the early 2000s norbolethone, tetrahydrogestrinone (THG, ‘The Clear’) and desoxymethyltestosterone (madol, DMT) were marketed as ‘undedectable’ steroids by the US ‘nutritional supplement’ company BALCO whereby the identification of their structures started in 2002 [109-112]. Since then, an increasing number of designer steroids appeared, mainly marketed as supplements (Table ). Only recently methylstenbolone was discovered as a new designer steroid [113].

The legal status of designer steroids differs from country to country. In most countries, they are regarded as controlled substances. In the US most anabolic steroids are classified as schedule III controlled substances, which means that already possession is classified as offense [114]. In 2005 prohormones were also included in the list of controlled substances by the ‘Anabolic Steroid Control Act’ [115]. By the term ‘chemically and pharmacologically related to testosterone (other than estrogens, progestins, corticosteroids, and dehydroepiandrosterone)’ designer steroids may also be regarded as controlled substances. Recent developments in updating the legal status of designer steroids are ongoing. A new version of the designer steroid control act was introduced to the US senate in 2014 literally naming 27 new steroids [116].

The legal status of dietary supplements is also not clear in several countries. In the United States, the ’Dietary Supplement Health and Education Act’ (DSHEA) classifies dietary supplements as a subcategory of food, allowing manufacturers to distribute their products without submitting proof of safety or efficacy to the Food and Drug Administration (FDA). Potential ingredients are vitamins, minerals, botanicals, amino acids, concentrates, metabolites, extracts, etc. Therefore it is possible to sell AAS containing supplements until the FDA or another administrative agency classifies otherwise. In the European Union, the European Food Safety Authority (EFSA) defines dietary supplements as ‚concentrated sources of nutrients or other substances with a nutritional or physiological effect, alone or in combination, marketed in dose form, namely forms such as capsules, pastilles, tablets, pills and other similar forms, sachets of powder, ampoules of liquids, drop dispensing bottles, and other similar forms of liquids and powders designed to be taken in measured small unit quantities’ [117]. Medicinal products are defined as ‚any substance or combination of substances presented as having properties for treating or preventing disease in human beings; or any substance or combination of substance which may be used in or administered to human beings either with a view to restoring, correcting or modifying physiological functions by exerting a pharmacological, immunological or metabolic action, or to making a medical diagnosis’ [118, 119]. Hence, dietary supplements are categorized as foodstuff in almost every country and a strict discrimination from pharmaceuticals remains complex. Often, the difficulty in classifying these products exists not because of the ingredients but of its presentation [120].

Several investigators showed the presence of designer steroids, prohormones, aromatase inhibitors, and SARMs in products marketed as dietary supplements (Table ). Probably due to insufficient quality control procedures during the production of steroid containing preparations cross-contaminations have been detected in non-hormonal dietary supplements as well [3, 121]. Only recently contaminated nutritional supplements appeared where vitamin B capsules contained the designer steroids methylstenbolone and methasterone [122]. Supplements containing steroids that are not or falsely labelled have also been identified [123]. Dimethazine (17β-hydroxy-2α,17β-dimethyl-5α-androstan-3-one-azine), a steroid dimer consisting of two methasterone (17β-hydroxy-2α,17α-dimethyl-5a-androstan-3-one) molecules linked with an azine group, was detected in a dietary supplement [124]. A case report shows severe adverse events in connection with this steroid [125]. Phytoecdysteroids show anabolic effects with very little androgenic action and may therefore represent a new therapeutical as well as a doping alternative [126]. Effects on skeletal muscle seem to be mediated via ERβ [127]. Like aromatase inhibitors, selective estrogen receptor modulators (SERMs) are administered by AAS user to reduce androgenic side effects. For instance tamoxifen was found recently in a dietary supplement [128].

The detection of designer steroids remains a challenging task because often reference material is hardly commercially available.

CONCLUSION

The large number of positive findings of designer steroids in dietary supplements together with the discovery of new structures shows the importance of further research in this field. The easy access of designer steroids and readiness of many users to take supplements with often unknown content needs to be stricter regulated by authorities. Immense health risks may arise from the ingestion of underinvestigated ingredients. The complex production and trade of dietary supplements needs collaborative international intervention.

CONFLICT OF INTEREST

The authors confirm that this article content has no conflict of interest.

Table 1

Findings of caffeine effects on main neurodegenerative diseases.

Chemical Name (IUPAC)	Trivial Name	References
17β -Hydroxy-2α ,17α -dimethyl-5a-androstan-3-one 2)	Methasterone	[122,129-134]
17β -Hydroxy-17α -methyl-5α -androst-1-en-3-one 1)		[131]
4,17β -Dihydroxyandrost-4-en-3-one 1)	4-Hydroxytestosterone	[135,136]
5α -Androstane-3β ,17α -diol		[137]
Androst-4-ene-3β ,17α -diol		[137]
5β -Androst-1-ene-3β ,17β -diol		[137]
5β -Androst-1-ene-3α ,17β -diol		[137]
17β -Hydroxy-5α -androstano-[3,2-c]-pyrazol 2)	Prostanozol	[130]
6α -Methylandrost-4-ene-3,17-dione 2)		[102, 130, 132]
3β -Hydroxy-5β -androstan-17-one	Epietiocholanolone	[132]
17β -Hydroxy-17α -methyl-5β -androstan-3-one	5β -Mestanolone	[132]
17α -Methyl-5α -androst-2-en-17β -ol	Desoxymethyltestosterone, DMT, Madol	[132, 138, 139]
4-Chloro-17α -methylandrost-4-ene-3α ,17β -diol		[133]
Androst-4-ene-3,6,17-trione	6-Oxoandrostenedione, 6-Oxo	[140, 141]
Androsta-1,4,6-triene-3,17-dione 2)	Androstatrienedione	[142-144]
3β -Hydroxyandrost-4-ene-7,17-dione	7-Keto-DHEA	[145]
6α /β -Bromoandrost-4-ene-3,17-dione	6-Bromandrostenedione	[139, 146]
Estra-4,9-diene-3,17-dione	Trenbolox	[123, 139, 147]
17β -Acetoxy-17α -methylandrost-5-ene-3β ,7β -diol	MbAEt	[139]
3β -Hydroxy-5β -androstan-17-one	Epiandrosterone	[139]
2α ,3α -Epithio-17α -methylandrostan-17β -ol 2)	2a,3a-Epithio-17a-methyletiocholanol	[123, 139]
3-Tetrahydropyranoloandrost-4-ene-6,17-dione	6-KetoDHEA	[139]
Androsta-1,4-diene-3,17-dione	Boldione	[139]
3α -Acetoxy-5α -androstan-17-one	Androsterone acetate	[139]
5α -Androst-1-ene-3β ,17β -diol 1)		[139]
17β -Hydroxy-17α -methyl-5á-androstan-3-oxime 2)	Mestanolon-oxim	[139]
5α -Androstane-3,17-dione-bis-oxim		[139]
17β -Hydroxy-5α -androstano-[3,2-c]-isoxazol 2)		[123, 139, 147-149]
17β -Hydroxy-5α -androstano-[2,3-d]-isoxazol 2)		[123, 139, 147-149]
6ξ-Hydroxyandrost-4-ene-3,17-dione		[123, 142]
3ξ-Hydroxyandrost-4-ene-6,17-dione	6,17-Keto-etiocholeve-3-ol-tetrahydropyranol	[144]
4,17α -Dimethylestra-1,3,5-trien-17β -ol	M1,4ADD (Methyl-1,4-androstadiene-3,17-diol)	[150]
17β -Hydroxy-17α -methylandrosta-4,6-dien-3-one	Jungle Warfare	[123, 139, 151]
3β -Hydroxy-5α -androst-1-en-17-one	1-Androsterone, 1-DHEA	[139, 152, 153]

listed in the ‘Anabolic Steroid Control Act’, 2listed in the ‘Designer Anabolic Steroid Control Act 2014’.