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  1. #11
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    Methylepitiostanol (Epistane)

    Chemical Name(s):
    2a,3a-epithio-17a-methyl-etioallocholan-17b-ol
    2a,3a-epithio-17a-methyl-5a-androstan-17b-ol

    Chemical Formula:
    C20H30OS

    Molecular Weight:
    320.5

    CAS:
    NA

    Q Qatio:
    12

    Anabolic #:
    1,100

    Androgenic #:
    91

    Oral Bioavailability:
    Estimated at 40%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    ~6 hours

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    40-50mg/day standalone
    10-20mg/day when stacked

    Average Cycle Length:
    4-6 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +3
    Strength Gain: +3
    Fat Gain (Negative Indicates Fat loss): -2
    Water Retention: -2
    Aggression: +1
    Libido: -2
    Acne: +1
    Hair Loss: +2
    Prostate Enlargement: +2
    Liver Toxicity: +3
    Lethargy +1

    Characteristics

    Methylepitiostanol is a methylated version of the steroid Epitiostanol. It is readily active and does not require conversion. Under the influence of heat methylepitiostanol readily breaks down to 17a-Methyl-androstan-2-en-17b-ol (DMT), a now illegal anabolic steroid.

    It does not aromatize, however it is possible that methylepitiostanol may offset estrogen and testosterone from SHBG thus increase the risk of gyno for certain individuals with high SHBG levels. Gyno symptoms from this compound may also be a result of this compounds inability to form a potent androgen such as DHT (to antagonize the effects of estrogen). However, in other cases methylepitiostanol can be used to prevent or reduce gynecomastia from an estrogenic steroid by acting as an aromatase inhibitor to keep estrogen down.

    It is a DHT derivative with a fairly moderate androgenic value so the chances of hair loss may be increased in certain sensitive users. Swelling of the prostate may also become an issue. The powerful estrogen suppressing action of this steroid and its 17aa stucture will cause it to negatively influence the cholesterol profile by lowering HDL and increasing LDL. It has also been reported to cause stiff joints, possibly related to its suppressive effect on estrogen levels.

    Anecdotal reports of appetite suppression and general fatigue would lead one to believe that the liver stress from this 17aa compound is rather severe. For this reason it is recommended to use a liver protecting supplement prior to and during the use of this steroid.

    Methylepitiostanol has a strong anabolic action that will lead to quick gains in lean muscle mass and strength with very little bloat. The gains will appear with minimal fat gain and increased vascularity.

    Because methylepitiostanol can negatively affect joint comfort it is recommended to be stacked with an aromatizing or progestational compound. However, it is not recommended to stack this steroid with another 17aa oral.

    Common Clones:

    Epistane by Innovative Body Enhancement (IBE)
    Havoc by Primaforce
    Havoc by Recomp Performance Nutrition (RPN)
    Epi-MAX by Anabolic Formulations
    M14-E by Purus Labs
    Methyl-E by Engineered Sports Technology (EST)
    E-Max by Juggernaut Nutrition
    E-Stane by Competitive Edge Labs (CEL)
    Hemaguno by Spectra Force Research
    Hemapolin by Starmark Labs
    Epi-Mass by Armour Nutrition

    References

    “2{alpha},3{alpha}-Epithio-5{alpha}-androstan-17ß-yl 1-Methoxycyclopentyl Ether in the Treatment of Advanced Breast Cancer —A Preliminary Clinical Trial”

    SOICHI KUMAOKA, M.D., OSAMU TAKATANI, M.D., MINORU YOSHIDA, M.D., SHIGETO MIURA, M.D., TETSUTO TAKAO, M.D., YÜJI HAMANAKA, M.D., MASARU IZUO, M.D. and TADAKAZU OKADA, M.D.
    Japanese Journal of Clinical Oncology 4:65-68 (1974)

    “Inhibited growth in vivo of a mouse pregnancy-dependent mammary tumor (TPDMT-4) by an antiestrogen, 2alpha, 3alpha-epithio-5alpha-androstan-17beta-ol (10275-S).”
    Matsuzawa A, Yamamoto T.Cancer Res. 1976 May;36(5):1598-606.

    “Antitumor Effect of Two Oral Steroids, Mepitiostane and Fluoxymesterone, on a Pregnancy-dependent Mouse Mammary Tumor (TPDMT-4)1”
    Akio Matsuzawa and Tadashi Yamamoto
    Cancer Research 37, 4408-4415, December 1, 1977
    Epidrol by Genera Labs
    Methyl Freak by Rockhard Formulations
    Epistrong by Mrsupps

  2. #12
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    Methyl 1,4-AD

    Chemical Name(s):
    17a-methyl-1,4-androstadiene-3b,17b-diol
    17a-methyl-androst-1,4-diene-3b,17b-diol
    1,4-Methylandrostenedione

    Chemical Formula:
    C20H30O2

    Molecular Weight:
    302

    CAS:
    NA

    Q Qatio:
    NA

    Anabolic #:
    NA

    Androgenic #:
    NA

    Oral Bioavailability:
    Estimated at 40%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    NA

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    100-150mg/day standalone
    50-100mg/day with stacking

    Average Cycle Length:
    4 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +3
    Strength Gain: +3
    Fat Gain (Negative Indicates Fat loss): +2
    Water Retention: +3
    Aggression: 0
    Libido: +1
    Acne: +2
    Hair Loss: +2
    Prostate Enlargement: +3
    Liver Toxicity: +3
    Lethargy +2

    Characteristics

    Methyl-1,4AD is a 17aa pro-steroid that converts to the illegal anabolic steroid methandrostenolone (Dianabol) at a rate of about 15-20%. It takes one conversion with 3b-HSD to convert methyl-1,4AD to Dianabol which probably happens fairly rapidly in the liver.

    Since the average dose of Dianabol is generally 25-50mg/day with most steroid users, it is recommended to use this compound at 2-3x the dose for noticeable effects. While Methyl-1,4AD may have some activity on its own, it would be considered pretty weak until it makes the conversion to Dianabol.

    Although this compound does not appear to have any progestational effects, it can convert to estrogen (methylestradiol) at a fairly decent rate. If users are very sensitive to estrogenic side-effects then an aromatase inhibitor may be taken along with this compound. However, if one is using an anti-estrogen with this steroid it begs the question, “why chose this steroid to begin with?” Most of the weight and size gains from this compound come from its estrogen conversion, therefore using an AI would noticeably limit the gains from this compound.

    This compound has moderate androgenic effects, therefore users who are sensitive to hair loss should be careful with higher doses. The combined estrogenic and androgenic effects of this compound may lead to excessive prostate swelling, so frequent visits to the bathroom may become a problem. (although all steroids have this effect to degree)

    Since this compound readily converts to estrogen it will likely have a lubercative effect on joints, contrary to many modern designer steroids that do not convert to estrogen and tend to cause joint pains. This would make this compound a good choice for bulking cycles where joint comfort is important for heavy weight lifting.

    Because higher doses are needed with this compound, more stress is placed on the liver. As with any 17aa oral it is recommended to pre-condition the liver with a liver supporting supplement.

    Users who use this at higher doses will experience similar gains to Dianabol including rapid increases in strength and size. Side-effects may include rapid weight gain, increase in blood pressure, bloating, back pumps and acne.

    This compound could be used as a standalone for a bulking cycle, however users should be aware that much of the bloat and size gains from Methyl-1,4AD will be quickly lost after a cycle.

    Common Clones:

    M 1,4 ADD by Competitive Edge Labs (CEL)
    M14-E by Purus Labs
    M1, 4AD by Anabolic Formulation

    References

    Anabolic Pharmacology
    Seth Roberts (2009)

  3. #13
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    Furazabol THP

    Chemical Name(s):
    5a-androstano[2,3-c]furazan-17b-tetrahydropyranol ether

    Chemical Formula:
    C24H36N2O3

    Molecular Weight:
    401

    CAS:
    NA

    Q Qatio:
    NA

    Anabolic #:
    NA

    Androgenic #:
    NA

    Oral Bioavailability:
    Estimated at 15%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    2-4 hours

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    200-300mg/day standalone
    100-200mg/day when stacked

    Average Cycle Length:
    4-6 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +2
    Strength Gain: +2
    Fat Gain (Negative Indicates Fat loss): -1
    Water Retention: 0
    Aggression: 0
    Libido: 0
    Acne: +1
    Hair Loss: +2
    Prostate Enlargement: +1
    Liver Toxicity: +1
    Lethargy +1

    Characteristics

    Furazabol THP is the same compound as the illegal anabolic steroid furazabol except it is not 17aa methylated, and instead has a THP ether attached on the 17b position.

    Furazabol does not aromatize and also has very minimal bloat. It has a moderately potent androgenic activity, giving it a fairly low risk for gyno or negative effects on the libido. However its androgenic effects may pose a problem for users prone to androgenic related hair loss.

    Once the Furazabol THP reaches the stomach, most of the THP-ether is removed by the stomach acid to form the active Furazabol (the non-methylated version). Therefore, topical delivery of this compound is probably not worthwhile. Furazabol has a similar structure to the illegal anabolic steroid stanozolol (Winstrol). The only difference is the pyrazole ring has been replaced with a furazan ring. There is rumor that this compound has benefits for cholesterol levels. While some evidence proves that it can lower total cholesterol, it should be noted that the decrease in cholesterol is mostly due to a decrease in HDL. Therefore, your LDL/HDL ratio would become worse.

    Overall this compound produces mild gains, but the side-effects are very mild too. Noticeable gains in lean muscle mass and strength are likely not going to be achieved unless doses of at least 200mg/day are used. Furazabol is going to produce very little water retention, therefore it should produce a lean and vascular appearance. Big increases in weight are not likely to happen with this steroid either, so increased blood pressure and painful back pumps should not be a problem.

    The half-life of this compound is short, so dosages should be taken every few hours to keep blood levels stable. Although furazabol can successfully be used as a standalone it can be stacked with other compounds depending on the users goals.

    Common Clones:

    Furazadrol by Axis Labs
    FURUZA-A by Competitive Edge Labs (CEL)
    Orastan A by Competitive Edge Labs (CEL)
    Winadrol by CTD Labs
    Winabol by Generation X Labs
    Chlomadrol-50 by German American Technologies (G.A.T.)
    Furaguno by Spectra Force

    References

    “Enhancement of fibrinolytic and thrombolytic potential in the rat by treatment with an anabolic steroid, furazabol.”

    Kumada T, Abiko Y.
    Thromb Haemost. 1976 Nov 30;36(2):451-64.

  4. #14
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    Methyldrostanolone (Superdrol)

    Chemical Name(s):
    2a,17a-dimethyl-5a-androst-3-one-17b-ol
    2a,17a-dimethyl-etiocholan-3-one-17b-ol

    Chemical Formula:
    C21H34O2

    Molecular Weight:
    318

    CAS:
    NA

    Q Qatio:
    20

    Anabolic #:
    400

    Androgenic #:
    20

    Oral Bioavailability:
    Estimated at 50%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    High

    Half Life:
    ~8 hours

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    10-30mg/day standalone
    5-10mg/day when stacked

    Average Cycle Length:
    2-4 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +4
    Strength Gain: +5
    Fat Gain (Negative Indicates Fat loss): 0
    Water Retention: +2
    Aggression: +3
    Libido: -1
    Acne: +1
    Hair Loss: +1
    Prostate Enlargement: +2
    Liver Toxicity: +5
    Lethargy +2

    Characteristics

    Methyldrostanolone is a C-17 alpha alkylated steroid, originally developed by the American pharmaceutical company Syntex. This steroid is already active and does not require conversion. Methyldrostanolone is the 17aa version of the injectable steroid drostanolone (Masteron). This extra methylation makes this steroid about 3-4x more anabolic than Masteron, and slightly more anabolic than oxandrolone (Anavar). Due to the dimethylation, the toxicity of methyldrostanolone is greater than most other oral steroids. There have been many reported cases of heptatoxicity with this compound. (1-3)

    Despite the fact that methyldrostanolone is a DHT derivative and cannot convert to estrogen, some users have still reported gyno like symptoms during or after a cycle. This effect is likely related to the strong SHBG binding effect and increase in freely circulating estrogen (and testosterone) from SHBG. Gyno symptoms may also be related to the fact that methldrostanolone lacks a strong DHT metabolite to antagonize the effects of estrogen (while also having a relatively low intrinsic androgenic value).

    Having a fairly low androgenic value will mean that methyldrostanolone will be light on the hairline for most men. However those susceptible to male pattern baldness may still noticed accelerated hair loss during a cycle.

    Because of the di-methylation, methlydrostanolone is considerably more resistant to breakdown, thus more potent per mg than most other steroids. However this makes it more liver toxic than other single methylated 17aa orals. Negative effects on the liver generally manifest as a condition known as reversible cholestasis. This is essentially a slowing or complete blockage of bile acids from the liver. Immediate signs of compromised liver function included reduced appetite and general sickness, which will soon be accompanied by yellowing of the eyes (jaundice), excessive itchiness and very dark urine. If these effects are noticed, methyldrostanolone should be discontinued immediately.

    Because the effects on the liver it is very important to use a liver protecting supplement during any methyldrostanolone cycle. If not using a supplement to protect your liver, methyldrostanolone should never be used any longer than 2 weeks, with a maximum cycle length of 4 weeks with liver protection.

    Other reversible side effects from methyldrostanolone may include increased blood pressure, reduced HDL cholesterol and lower back pumps.

    Results wise, users should expect extreme strength increases and weight gain in a relatively short 2-4 week period. Weight gain upwards of 20lbs in 4 weeks is not unheard of with this incredibly potent compound. Although subcutaneous water gain would be minimal, intramuscular water retention should be expected. This is due to inhibition of 11b-hydroxylase and build-up of mineralcorticoids which encourage salt and water retention within the muscles. The most obvious physical effects will be improved vascularity, aggressive muscular pumps, and oily skin.

    While methyldrostanolone can stack well with most other steroids, it should never be stacked with another methylated (17aa) steroid.

    Common Clones:


    Oxodrol 12 by IDS
    Superdrol by Anabolic Xtreme
    M-Drol by Competitive Edge Labs (CEL)
    SD-1 by Performance Design
    Methyl VOL by Engineered Sports Technology (EST)
    Revenge SDX by Bioscience Technologies
    S-Drol by Nutracoastal
    E-Pol by Purus Labs
    MethaDROL by IForce
    Straight-DROL by Black China Labs
    MethylDX3 by Physical Enhancing Industries
    Oxevol (same as Dianevol) by Evolution Labs
    Beastdrol by Mrsupps

    References


    Cholestatic Jaundice and IgA Nephropathy Induced by OTC Muscle Building Agent Superdrol.

    Beata Jasiurkowski MD, et al.
    The American Journal of Gastroenterology (2006) 101, 2659-2662;

    Severe Cholestasis and Renal Failure Associated with the Use of the Designer Steroid Superdrol (Methasteron): A Case Report and Literature Review
    John Nasr and Jawad Ahmad
    Digestive Diseases and Sciences

    Methasteron-Associated Cholestatic Liver Injury: Clinicopathologic Findings in 5 Cases”
    Neeral L. et al.
    Clinical Gastroenterology and Hepatology, Volume 6, Issue 2, February 2008, Pages 255-258

    Identification of drostanolone and 17-methyldrostanolone metabolites produced by cryopreserved human hepatocytes”
    Julie Gauthier, Danielle Goudreault, Donald Poirier and Christiane Ayotte
    Steroids; Volume 74, Issue 3, March 2009, Pages 306-314

  5. #15
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    Formestane

    Chemical Name(s):
    4-Hydroxyandrost-4-ene-3, 17-dione
    4-hydroxy-4-androstene-3,17-dione
    4-Hydroxyandrostenedione

    Chemical Formula:
    C19H26O3

    Molecular Weight:
    302

    CAS:
    NA

    Q Qatio:
    NA

    Anabolic #:
    NA

    Androgenic #:
    NA

    Oral Bioavailability:
    Estimated at 4%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    2-3 hours oral, Transdermal: Varies by matrix

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    Aromatase inhibition
    100-200mg/day (transdermal)
    150-250mg/day (oral)
    Anabolic effects
    800-1000mg/day (oral)

    Average Cycle Length:
    4-8 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +1
    Strength Gain: 0
    Fat Gain (Negative Indicates Fat loss): -1
    Water Retention: +1
    Aggression: 0
    Libido: -1
    Acne: 1
    Hair Loss: 0
    Prostate Enlargement: 0
    Liver Toxicity: 0
    Lethargy 0

    Characteristics

    Formestane is a steroidal aromatase inhibitor, known as a suicidal inhibitor because it permanently binds to the aromatase enzyme.

    Formestane was originally used as an injectable for breast cancer patients, but due to its possible androgenic effects it has largely been replaced by non-steroidial AIs in the medical community. Most of its use is now is limited to the bodybuilding community since it is available as a legal dietary supplement for reducing estrogen and increasing testosterone production.

    Although formestane can effectively reduce estrogen through oral consumption, its low oral bioavailability has lead to the development of several transdermal based products (which appear to offer higher efficacy at a lower dose).

    Relative to 6-oxo and ATD, Formestane is a more potent aromatase inhibitor, which appears to effectively reduce natural estrogen levels by as much as 50% within several days (while higher doses may further suppress estrogen). Because of formestanes potent ability at reducing estrogen it will tend to reduce HDL levels, while increasing LDL levels, thus harming the cholesterol profile. For this reason, it is recommended to limit cycles of formestane to 8 weeks max.

    Because formestane also has a strong affinity for the 5a-reductase enzyme it will reduce DHT levels in the body by effectively competing with testosterone for the 5a-reductase.

    Formestane converts to the active androgen 4-hydroxytestosterone which has about half the anabolic potency, and about 25% of the androgenic potency as testosterone. This would suggest that fairly high doses of formestane (800-1000mg/day) could lead to some level of anabolic enhancement (although the amount required for this would surely lead to undesirably low estrogen levels).

    Formestane is successfully used as a standalone during re-composition cycles to help reduce “bloat” and fat storage. It can also be used as an anti-estrogen to counter aromatization of aromatizing steroids.

    Common Clones:

    Formestane by Primordial Performance
    Formex by Innovative Body Enhancement (IBE)
    Formestane by Competitive Edge Labs (CEL)
    Formadex by BCS LABS

    References

    Anabolic Pharmacology
    Seth Roberts (2009)

  6. #16
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    Halodrol

    Chemical Name(s):
    4-chloro-17a-methyl-androst-1,4-diene-3b,17b-diol

    Chemical Formula:
    C20H29C1O2

    Molecular Weight:
    337

    CAS:
    NA

    Q Qatio:
    2.6

    Anabolic #:
    74

    Androgenic #:
    28

    Oral Bioavailability:
    Estimated at 40%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    ~16 hours

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    100-150mg/day standalone
    50-100mg/day when stacking

    Average Cycle Length:
    4-6 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +3
    Strength Gain: +3
    Fat Gain (Negative Indicates Fat loss): -1
    Water Retention: +1
    Aggression: +1
    Libido: -1
    Acne: 0
    Hair Loss: +1
    Prostate Enlargement: +1
    Liver Toxicity: +3
    Lethargy +0

    Characteristics

    Halodrol is a 17aa steroid that converts to the steroid oral Turinabol after interaction with 3b-HSD at an estimated rate of about 5%.

    Because of this low conversion, doses must be higher than other 17aa pro-steroids. However, it is suspected that Halodrol has decent potency without conversion as good results are seen despite the relatively low conversion to Turinabol. Based on Vida’s data Halodrol appears to be about as potent as testosterone, and significantly less androgenic.

    Because of the 4-chloro group, halodrol has no progestational effects, it cannot interact with the aromatase enzyme, and it produces inactive 4-chloro-DHT metabolites. This makes androgenic side-effects such as hair loss, high blood pressure, acne and prostate enlargement less likely. Anecdotal reports would also have us believe that side-effects with this compound are fairly mild.

    Although caution would still need to be had, the low androgenic value of this compound would also make it one of the more appropriate anabolic steroids for women wishing increase lean mass yet avoid a deeper voice, increased hair growth, acne and clitoral growth. (Oral Turinabol was actually the preferred steroid for Olympic female athletes in East Germany)

    The lack of androgenic potency might be expected to create problems with gyno, however the low SHBG binding affinity has minimal interference with SHBG levels and/or freely circuiting estrogen and testosterone. It does not appear that halodrol has a significant gyno risk.

    Because halodrol must be used at such a high dose to see noticeable effects, liver toxicity may become an issue. Therefore it is recommended to use a liver protecting supplement before and during halodrol cycles.

    Gains from Halodrol generally take a few weeks to notice, but users can expect solid increases in strength, lean muscle mass, improved vascularity and minimal water retention. This allows some of the gains to be kept after the cycle if good diet and training are continued. Quick dramatic gains in size and strength are not generally noticed with Halodrol.

    It is used successfully as a standalone, but would be expected to stack well with most other steroids, except 17aa oral due to liver toxicity concerns.

    Common Clones:

    Halo-MASS by Anabolic Formulations
    HD-1 by Performance Design
    H-Drol by Competitive Edge Labs (CEL)
    Halovar by Purus Labs
    Hemadrol by Engineered Sports Technology (EST)
    Halodrol-50 by Gaspari Nutrition
    Oral Turinadrol by Juggernaut Nutrition
    Super Halo by Black China Labs
    H-Drol by Nutracoastal
    Helladrol by Mrsupps

    References

    “Hepatotoxicity Associated With Dietary Supplements Containing Anabolic Steroids”

    Michel I. Kafrouni, Robert A. Anders and Sumita Verma
    Clinical Gastroenterology and Hepatology; Volume 5, Issue 7, July 2007, Pages 809-812

  7. #17
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    4-DHEA

    Chemical Name(s):
    1-androsten-3b-ol-17-one
    4-Dehydroepiandrosterone

    Chemical Formula:
    C19H28O2

    Molecular Weight:
    288

    CAS:
    NA

    Q Qatio:
    NA

    Anabolic #:
    NA

    Androgenic #:
    NA

    Oral Bioavailability:
    Estimated at 4%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    NA

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    500-1000mg/day standalone
    200-500mg/day when stacked

    Average Cycle Length:
    4-6 weeks

    Characteristics

    4-DHEA is a naturally occurring non-methylated (non-17aa) pro-steroid.

    4-DHEA, like DHEA, requires a 2 step conversion process involving 3b-HSD and 17b-HSD to convert it to Androstenedione/androstenediol, and then testosterone. What makes 4-DHEA slightly different from DHEA is a double bond in the 4th position rather than the 5th. This makes 4-DHEA less estrogenic by not acting directly upon the estrogen receptor like DHEA has been found to do.

    Although 4-DHEA can aromatize to estrogen it is probably not enough to cause high estrogen related side-effects.

    Overall results will be similar to or the original 4-AD banned back in 2004. Higher doses of this compound will produce fairly lean gains in muscle mass, with moderate improvements in strength. This product may produce some bloat from the estrogen conversion, which could be countered by administering an aromatase inhibitor, but this will largely defeat the purpose of using this compound to begin with.

    Since this compound is naturally occurring and non-methylated overall side-effects will be fairly mild. However, high doses may also lead to oily skin, acne and increased blood pressure. Because this steroid is non-17aa there should be less concern about it negatively affecting the HDL/LDL ratio.

    Because this compound can convert to testosterone it can also convert to DHT and other 5a-reduced metabolites. This can serve as a good stack with progestational or relatively non-androgenic compounds that may create problems with libido or gyno because of lacking androgenic potency.

    Although this compound is relatively safe and moderately effective, its high cost has probably been the reason for its lack of popularity.

    Common Clones:

    4-AD UTT by Advanced Muscle Science (AMS)

    References

    Anabolic Pharmacology
    Seth Roberts (2009)

  8. #18
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    Dimethazine

    Chemical Name(s):
    17beta-hydroxy 2alpha,17alpha-dimethyl 5alpha-androstan 3-one azine

    Chemical Formula:
    C42H68N2O2

    Molecular Weight:
    632

    CAS:
    NA

    Q Qatio:
    2.2

    Anabolic #:
    210

    Androgenic #:
    95

    Oral Bioavailability:
    Estimated at 40%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    NA

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    20-40mg/day standalone
    10-20mg/day when stacked

    Average Cycle Length:
    2-4 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +4
    Strength Gain: +4
    Fat Gain (Negative Indicates Fat loss): 0
    Water Retention: +1
    Aggression: +2
    Libido: 0
    Acne: +1
    Hair Loss: +2
    Prostate Enlargement: +2
    Liver Toxicity: +5
    Lethargy +1

    Characteristics


    Dimethazine is actually two steroid molecules bound together by a nitrogen atom. Upon ingestion, stomach acid separates the two steroid molecules that closely resemble methyldrostanolone (Superdrol).

    Although dimethazine appears very similar to methyldrostanolone, the presence of a nitrogen at the 3rd position appears to increase its androgenic potency relative to its anabolic potency (210/95 compared to 400/20 for methyldrostanolone). Therefore, dimethazine could be considered a slightly weaker form of methyldrostanolone, but perhaps less likely to cause gyno related issues because of its higher relative androgenic value (and ability to antagonize estrogenic effects).

    Otherwise, all side-effects and benefits could be considered relatively the same as methyldrostanolone. Liver toxicity and its associated side-effects of general sickness should still be expected, especially if the liver becomes compromised. Using a liver protecting supplement prior to and during a cycle of Dimethazine would be very important.

    The quick gains in size and strength will likely be accompanied by increases in intense back pumps, high blood pressure, shortness of breath and oily skin. Vascularity would also be expected to improve with this compound due to the increase in extra-cellar water and possible decrease in subcutaneous water weight.

    Because this compound is a 17aa oral, it is not recommended to be stacked with other 17aa oral steroids.

    Common Clones:

    Dymethazine by IForce

    References

    “Oral administration of an anabolic-androgenic steroid dimethazine increases the growth and food conversion efficiency and brings changes in molecular growth responses of carp (Cyprinus carpio) tissues”

    LONE K. P. (1) ; MATTY A. J. ;
    Nutrition reports international

    “Contribution to the study of the proteoanabolic effects of dimethazine. (Clinical research)”
    CEI C, ANSELMI G.
    Gazz Med Ital. 1963 Feb;122:57-61

    “A new steroid having proteo-anabolic action: dimethazine.”
    DE RUGGIERI P, MATSCHER R, GANDOLFI C, CHIARAMONTI D, LUPO C, PIETRA E, CAVALLI R.Arch Sci Biol (Bologna). 1963 Jan-Mar;47:1-19.

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    Desoxymethyltestosterone (Pheraplex, DMT, Madol)

    Chemical Name(s):
    17a-methyl-etioallocholan-2-ene-17b-ol
    17a-methyl-5a-androst-2-ene-17b-ol

    Chemical Formula:
    C20H32O

    Molecular Weight:
    288

    CAS:
    NA

    Q Qatio:
    6.5

    Anabolic #:
    1200

    Androgenic #:
    187

    Oral Bioavailability:
    Estimated at 40%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    ~9 hours

    Legal Status (US):
    Listed as a controlled substance

    Average Dose:
    40-60mg/day standalone
    10-30mg/day when stacked

    Average Cycle Length:
    4 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +4
    Strength Gain: +3
    Fat Gain (Negative Indicates Fat loss): +1
    Water Retention: +2
    Aggression: +2
    Libido: 0
    Acne: +1
    Hair Loss: +1
    Prostate Enlargement: +1
    Liver Toxicity: +3
    Lethargy +2

    Characteristics

    Desoxymethyltestosterone (DMT) is a 17aa steroid with equal toxicity as other 17aa oral steroids. While nearly all anabolic steroid molecules have a 3-keto group, Desoxymethyltestosterone lacks it, and has a 2-ene structure. This compound is readily active and does not require conversion.

    DMT does not aromatize, nor does it appear to have any progestational activity, yet some users still experience gyno symptoms and bloat from this compound. This is likely related to the lack of androgenic potency from this compound (to antagonize the effect of estrogen). DMT may also contribute to gyno by displacing estrogen (and testosterone) from SHBG. It has also been proposed that DMT can inhibit 11b-hydroxylase and thus increase intracellular sodium and water retention by building up mineralcorticoid levels.

    Depending on where you look, DMT has been reported to be 2-12 times more anabolic and 0.4-2 times as androgenic as methyltestosterone. It has been proposed that DMT is a naturally occurring substance because it has an almost identical structure to delta 2-androstenol, a naturally occurring pheromone in mammals. However, being a 17aa steroid hormone makes it synthetically altered and not naturally occurring. Either way, it is now a controlled substance in the United States.

    Users should expect significant strength increases, weight gain, and bloat. Weight gains upwards of 20lbs in 4-6 weeks are not unheard of with this compound. The most obvious physical side effects will be strong muscular pumps, shortness of breath, high blood pressure, oily skin, and bloating. If users wanted to minimize toxic effect on the liver or other side effects, DMT could be used at doses as low as 10mg/day for a decent effect.

    Being that this compound is methylated, it should not be stacked with other methylated compounds. Having moderately low androgenic activity, DMT may negatively affect the libido and erectile function. This side effect could be offset by stacking DMT with testosterone or one of its non-aromatizing metabolites to preserve DHT levels.

    Common Clones:

    P-Plex by Competitive Edge Labs (CEL)
    Phera-Plex by Anabolic Xtreme
    Nasty Mass by Purus Labs
    Phera-VOL by Engineered Sports Technology (EST)
    PheraFLEX by IForce
    D-Stianozol by Nutracoastal
    Pheradrol by PH Design
    P-Max by Growth Labs
    Phera-MAX by Generic Labs
    Phera-BOL by Juggernaut Nutrition
    Phera-Mass by Kilo Sports
    Straight Phlexed by Black China Labs

    References


    “Characterisation of the pharmacological profile of desoxymethyltestosterone (Madol), a steroid misused for doping”

    P. Diel, A. Friedel, H. Geyer, M. Kamber, U. Laudenbach-Leschowsky, W. Schänzer, M.
    Thevis, G. Vollmer and O. Zierau
    Toxicology Letters; Volume 169, Issue 1, 28 February 2007, Pages 64-71

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    norDHEA

    Chemical Name(s):
    5-estren-3b-ol-17-one
    Nordehydroepiandrosterone

    Chemical Formula:
    C18H26O2

    Molecular Weight:
    274

    CAS:
    NA

    Q Qatio:
    NA

    Anabolic #:
    NA

    Androgenic #:
    NA

    Oral Bioavailability:
    Estimated at 4%

    AR Binding Affinity:
    NA

    SHBG Binding Affinity:
    NA

    Half Life:
    NA

    Legal Status (US):
    Not listed as a controlled substance

    Average Dose:
    300-600mg/day standalone
    200-300mg/day when stacked

    Average Cycle Length:
    4-6 weeks

    Ratings (On Scale of -5 to +5):

    Muscle Gain: +2
    Strength Gain: +1
    Fat Gain (Negative Indicates Fat loss): 0
    Water Retention: +1
    Aggression: +1
    Libido: -2
    Acne: +1
    Hair Loss: 0
    Prostate Enlargement: 0
    Liver Toxicity: 0
    Lethargy +1

    Characteristics

    norDHEA is a non-methylated (non-17aa) pro-steroid. (naturally occurring in trace amounts in humans)

    norDHEA can convert to the illegal anabolic steroid nandrolone by converting to norandrostenediol/norandrostenedione, and then to nandrolone. Nandrolone is known to have stronger anabolic effects than testosterone, yet weaker androgenic effects.

    norDHEA will aromatize to estrogen less than regular DHEA, but because it is a nor compound it lacks strong androgenic metabolites. For instance, after nandrolone interacts with 5a-reductase, the metabolite dihydronandrolone (DHN) is formed, which is a weaker nor-version of DHT.

    Ironically, the lack of estrogen conversion from norDHEA is probably balanced by the lack of androgenic potency and progestational effects, which makes the possibility of bloating and experiencing gyno about as likely as with regular DHEA.

    One difference between norDHEA and DHEA that should be considered is the fact that norDHEA will have less androgenic effects, which may pose less risk of androgenic related hair loss and/or acne. This may be a smart choice for some men, and a decent choice for women looking for a moderately anabolic compound without much androgenic effect. (to avoid masculinizing side-effects)

    Because of the low bio-availability, high doses must be used to notice gains in lean muscle mass and strength. Even with higher doses, the gains will be mild to moderate. Some bloat should be expected from the estrogenic and progestational effects of the nor-steroids. Because this steroid is non-17aa there should be less concern about it negatively affecting the HDL/LDL ratio.

    Like the other DHEA derivatives, norDHEA would be useful in a transdermal application since the enzymes needed for the conversions to more powerful metabolites are concentrated in the skin and absorption through the skin using a good transdermal delivery cream could allow for 5-10x higher absorption than oral.

    This compound would stack well with almost any other steroid, except those with progestational activity.


    Common Clones:

    Decavol by Advanced Muscle Science (AMS)

    References

    Anabolic Pharmacology
    Seth Roberts (2009)

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