Anabolic Steroids Profile
Myagen
Basically what we have here is DiMethyltestosterone, or Methyltestosterone with an added methyl group (hence "dimethyl") at the C7 position. I think, any further comparison to Methyltestosterone (except perhaps with regards to hepatoxicity) wouldn´t really be warranted.
It needs to be noted that a lot of what I´m going to tell you about this drug is basically speculation for now, although I suspect that since we´ve seen the reemergence of several drugs which wear gone for decades (Mitolan, OT, etc& ), this one isn´t far behind. Why would this stuff reappear on the market? Well, by taking a look at its androgenic/anabolic ratio, you should see why. It´s three times as androgenic as testosterone and almost six times as anabolic! This makes it one of the most powerful oral anabolic steroids ever made.
While writing this book, I contacted several underground labs to see if they could produce this drug, for me to test out on myself (as I have done with several experimental compounds already). Unfortunately, nobody seemed to know where to get this stuff from.
Bolasterone or Dimethyltestosterone Profile[7-ALPHA,17-ALPHA-DIMETHYLTESTOSTERONE] Active Life: 6 hours Androgenic/ Anabolic Ratio: 300:575
References:
CLINICAL EVALUATION OF A NEW ANABOLIC AGENT 7-ALPHA,17-ALPHA-DIMETHYLTESTOSTERONE (BOLASTERONE). Clin Pharmacol Ther. 1963 Nov-Dec;30:734-9.
Wednesday, October 17, 2007
Monday, October 15, 2007
Winstrol (Injectable)
Winstrol (Injectable) Buy Winstrol (Injectable) The injection form of stanozolol is a water based injectable steroid that is a derivative of DHT. Both oral and injectable forms are c17-alfa-alkylated chemicals. This of course makes the injectable form moderately liver toxic and the oral form liver toxic in high dosages. Before going on let me make it clear that the injectable form is the same as the oral. For this reason the injectable form has frequently been used as an oral also. Why would anyone have done that? Well, all c17-alfa-alkylated AAS, when passing through the liver for deactivation, cause a distinct elevation in IGF-1 production. (*Please see IGF-1). This is why 30-mg of Dianabol orals daily (210-mg weekly total) has been revered as more effective for mass and strength gains than 400-mg of testosterone enanthate. The injectable stanozolol has been much cheaper than oral stanozolol, so some athletes opted to utilize it as an oral. Winstrol Depot is one of the most commonly used versions of winstrol Stanozolol is a high anabolic /moderate androgenic that causes a significant elevation in protein synthesis and an improved nitrogen retention. Since it does not aromatize to estrogen, water retention, gyno, and female pattern fat deposits do not occur. A high protein diet of 1.5-2-g of protein per LB of bodyweight daily was necessary to obtain the best results. This was not noted as a steroid for rapid weight gains but was commonly affirmed as ideal for a continuous slow gain in very high quality lean muscle mass that was well retained after discontinuance. Many who compete utilized Winstrol off-season with testosterone in a Max Androgen Phase for its anabolic value. Many used Winstrol (stanozolol) as a pre-contest drug because it provided a continuously harder appearance. When 50-100mg every 1-2 days was stacked with 76- mg of Parabolan every 2-3 days, the results were quite impressive. Many also added Masteron, Equipoise, or Testosterone Propionate/ Testosterone Suspension with the addition of anti-estrogens for water retention and aromatization control. Women often reported use of Winstrol Depot. "Usually" those who reported 25mg 2-3 times weekly or a single weekly 50-mg injection use reported no virilization effects. (I have known many women who have utilized 50-100mg daily of this drug) Stacked with Oxandrolone and/or Durabolin, women achieved excellent quality lean mass gains. Winstrol tabs were often thought to be a better choice at a dosage of 10-20-mg daily, or about 1/4 -1/2ml of the injectable taken orally due to results realized. The method often employed for the injection product used as an oral was to mix 1ml of Stanozolol with 9 ml of water. Each ml=5-mg. (Duh!) Since Stanozolol produced a surprising increase in strength, it has been used as a part of a mass cycle as well. Novices and older males made very impressive "second cycle" gains stacking 50mg of Stanozolol every other day with 50-100mg of Primobolan Depot every 2-3 days, or with 200-400mg of Deca-Durabolin weekly. Many hard-core males reported serious strength and mass gains using 50-100mg stanozolol with 50- 100mg Testosterone Suspension daily. This was a fairly high weekly dosage and was hopefully considered for advanced athletes..if at all. Winstrol is another AAS that was commonly used in a site-injection protocol for lagging body parts. *I have been impressed with the results I have seen, but this method requires careful location. Hitting a vein would end any Mr. "O" dream real quick. Some black market Winstrol is testosterone suspension, so if gyno was reported
Wednesday, October 10, 2007
Arimidex (liquidex)
Arimidex
Arimidex is an aromatase inhibitor (sometimes called an AI). It is usually provided in 1MG tabs or in liquid form. The drug works in a non-steroid form by inhibiting the aromatase enzyme which convertstestosterone and other androgens into estrogen. This means that there is less estrogen tocause female pattern fat deposits, gyno, and water retention. In medicine, Arimidex isutilized to treat prostate cancer. In sports chemistry, the drug has been employed as ameans of preventing excessive estrogenic side effects during AAS use and to aid increating a harder appearing m
usculature for competitive bodybuilders. Unlike Nolvadex,which simply block estrogen receptor-sites, this drug prevents or reduces estrogenproduction. Though some estrogen presence is noted as necessary for AAS to reach fulleffectiveness, too much can cause a layer of fat, water retention, and breast tissue growthpotentially with tumors called gynecomastia or bitch tits. Arimidex has a 75-85%aromatization inhibition rate.
Males who experienced excessive aromatization of AAS or who were extremelyestrogen sensitive usually utilized a dosage of 0.5-3.0 mg daily. In fact, most realizedexcellent estrogen control with only 0.5mg/d (mg daily). Women usually showedexcellent lean appearances (even in their legs) with 0.5-1.0 mg daily. Arimidex has a veryshort active-life so 0.5 mg dosages were often taken 2-6 times daily at equal intervals.Stacking 10-30 mg of Nolvadex with 1.0 mg of Arimidex has resulted in a near "0"estrogen activity situation regardless of the AAS protocol utilized. Directly following anAAS cycle, estrogen control has also become a problem (during periods intended for reestablishingHPTA function). In this case, the dosage was reduced from a higher startingdosage to a low dosage that was continued for 7-14 days after AAS discontinuance. Thisprotocol was considered necessary to assure clearing of AAS induced estrogen build-up.
Reported Characteristics
Active-Life: 4-6 hours Drug Class: Aromatase inhibitor (Oral) Average Reported Dosage: 0.5-3.0 mg daily Acne: No Water Retention: None Liver Toxic: Yes dosage dependent Decreases HPTA function: Increases it.
TRADE NAMES:
ARIMIDEX .25 MG TABS (International Pharmaceuticals) ARIMIDEX 1mg TABS (British Dragon)
Arimidex is an aromatase inhibitor (sometimes called an AI). It is usually provided in 1MG tabs or in liquid form. The drug works in a non-steroid form by inhibiting the aromatase enzyme which convertstestosterone and other androgens into estrogen. This means that there is less estrogen tocause female pattern fat deposits, gyno, and water retention. In medicine, Arimidex isutilized to treat prostate cancer. In sports chemistry, the drug has been employed as ameans of preventing excessive estrogenic side effects during AAS use and to aid increating a harder appearing m
usculature for competitive bodybuilders. Unlike Nolvadex,which simply block estrogen receptor-sites, this drug prevents or reduces estrogenproduction. Though some estrogen presence is noted as necessary for AAS to reach fulleffectiveness, too much can cause a layer of fat, water retention, and breast tissue growthpotentially with tumors called gynecomastia or bitch tits. Arimidex has a 75-85%aromatization inhibition rate.Males who experienced excessive aromatization of AAS or who were extremelyestrogen sensitive usually utilized a dosage of 0.5-3.0 mg daily. In fact, most realizedexcellent estrogen control with only 0.5mg/d (mg daily). Women usually showedexcellent lean appearances (even in their legs) with 0.5-1.0 mg daily. Arimidex has a veryshort active-life so 0.5 mg dosages were often taken 2-6 times daily at equal intervals.Stacking 10-30 mg of Nolvadex with 1.0 mg of Arimidex has resulted in a near "0"estrogen activity situation regardless of the AAS protocol utilized. Directly following anAAS cycle, estrogen control has also become a problem (during periods intended for reestablishingHPTA function). In this case, the dosage was reduced from a higher startingdosage to a low dosage that was continued for 7-14 days after AAS discontinuance. Thisprotocol was considered necessary to assure clearing of AAS induced estrogen build-up.
Reported Characteristics
Active-Life: 4-6 hours Drug Class: Aromatase inhibitor (Oral) Average Reported Dosage: 0.5-3.0 mg daily Acne: No Water Retention: None Liver Toxic: Yes dosage dependent Decreases HPTA function: Increases it.
TRADE NAMES:
ARIMIDEX .25 MG TABS (International Pharmaceuticals) ARIMIDEX 1mg TABS (British Dragon)
Tuesday, October 9, 2007
Testosterone propionate
Testosterone Propionate Testosterone propionate is a common oil-based injectable testosterone. The added propionate extends the activity of the testosterone but it is still comparatively much faster acting than other testosterone esters such as Cypionate and Enanthate. While cypionate and enanthate are injected weekly, propionate is most commonly injected at least every third day to keep blood levels steady. For strength and muscle mass gains, this drug is quite effective. With propionate, androgenic side effects seem somewhat less pronounced than with the other testosterones, probably due to the fact that blood levels do not build up as high. Users often report less gyno trouble, lower water retention and commonly claim to be harder on prop than with the others. This however is still a testosterone and, as with all testosterone products, androgenic side effects are unavoidable. It should also be noted that propionate is often a very painful injection. Users very regularly report swelling and noticeable pain for days after a shot. Package: Multiple dose vials of 10 ml or vials of 2ml. 100 mg per 1 ml. Usage: Average dose is 100-300 mg per week.
Saturday, October 6, 2007
Stanozolol (Winstrol Depot)
One obvious difference between Winstrol Depot and other injectables is that it is not esterified, being sold as aqueous stanozolol suspension. (It should not be called water-soluble: virtually none of it is dissolved in the water.) This means that it does not have a classical half-life, where at time x the level is ½ the starting level, at time 2 x the level is ¼, at time 3 x the level is 1/8, etc. Instead, the microcrystals slowly dissolve, and when they have all dissolved levels of the drug then fall very rapidly. For veterinary application, Upjohn claims that once-weekly doses supply constant levels. I am not sure if that is actually true or not – it might be true in terms of being clinically practical but not literally true. If true, then it may be that the observation of bodybuilders that frequent dosing is required has more to do with a significant dose being required, e.g. 350 mg/week, rather than an actual need for it to be injected daily. Unfortunately bodybuilders often make illogical comparisons, and will conclude that daily injections are needed, since a once a week injection of 50 mg did not do the job! Well, of course it didn’t: the dose was too low. For a future article, some urinalysis testing may be performed to come up with some more specific information on this matter, since it is of interest to many. In some cases, women have had virilization problems with oral Winstrol at only 2 mg/day. Thus, it cannot be assumed that even a single tab per day is necessarily safe for all women concerned about maintaining their natural voice, avoiding hirsutism, etc. Stanozolol has some unique biochemical properties which we will discuss in a later article. Trivial name Stanozolol Systematic name 2'H-Androst-2-eno(3,2-c)pyrazol-17-ol, 17-methyl-, (5alpha,17beta)- CAS number 10418-03-8 ATC code A14AA02 Merck Index Number 8873 Chemical formula C21H32N2O Molecular weight 328.497 g/mol Bioavailability Metabolism Hepatic Elimination half-life Excretion Renal: 84% Pregnancy category X Legal status Prescription only (US) Controlled substance Yes, DEA Schedule III (US) Routes of administration Oral, Intramuscular
Friday, October 5, 2007
Winstrol (Injectable)
Winstrol (Injectable) Buy Winstrol (Injectable) The injection form of stanozolol is a water based injectable steroid that is a derivative of DHT. Both oral and injectable forms are c17-alfa-alkylated chemicals. This of course makes the injectable form moderately liver toxic and the oral form liver toxic in high dosages. Before going on let me make it clear that the injectable form is the same as the oral. For this reason the injectable form has frequently been used as an oral also. Why would anyone have done that? Well, all c17-alfa-alkylated AAS, when passing through the liver for deactivation, cause a distinct elevation in IGF-1 production. (*Please see IGF-1). This is why 30-mg of Dianabol orals daily (210-mg weekly total) has been revered as more effective for mass and strength gains than 400-mg of testosterone enanthate. The injectable stanozolol has been much cheaper than oral stanozolol, so some athletes opted to utilize it as an oral. Winstrol Depot is one of the most commonly used versions of winstrol Stanozolol is a high anabolic /moderate androgenic that causes a significant elevation in protein synthesis and an improved nitrogen retention. Since it does not aromatize to estrogen, water retention, gyno, and female pattern fat deposits do not occur. A high protein diet of 1.5-2-g of protein per LB of bodyweight daily was necessary to obtain the best results. This was not noted as a steroid for rapid weight gains but was commonly affirmed as ideal for a continuous slow gain in very high quality lean muscle mass that was well retained after discontinuance. Many who compete utilized Winstrol off-season with testosterone in a Max Androgen Phase for its anabolic value. Many used Winstrol (stanozolol) as a pre-contest drug because it provided a continuously harder appearance. When 50-100mg every 1-2 days was stacked with 76- mg of Parabolan every 2-3 days, the results were quite impressive. Many also added Masteron, Equipoise, or Testosterone Propionate/ Testosterone Suspension with the addition of anti-estrogens for water retention and aromatization control. Women often reported use of Winstrol Depot. "Usually" those who reported 25mg 2-3 times weekly or a single weekly 50-mg injection use reported no virilization effects. (I have known many women who have utilized 50-100mg daily of this drug) Stacked with Oxandrolone and/or Durabolin, women achieved excellent quality lean mass gains. Winstrol tabs were often thought to be a better choice at a dosage of 10-20-mg daily, or about 1/4 -1/2ml of the injectable taken orally due to results realized. The method often employed for the injection product used as an oral was to mix 1ml of Stanozolol with 9 ml of water. Each ml=5-mg. (Duh!) Since Stanozolol produced a surprising increase in strength, it has been used as a part of a mass cycle as well. Novices and older males made very impressive "second cycle" gains stacking 50mg of Stanozolol every other day with 50-100mg of Primobolan Depot every 2-3 days, or with 200-400mg of Deca-Durabolin weekly. Many hard-core males reported serious strength and mass gains using 50-100mg stanozolol with 50- 100mg Testosterone Suspension daily. This was a fairly high weekly dosage and was hopefully considered for advanced athletes..if at all. Winstrol is another AAS that was commonly used in a site-injection protocol for lagging body parts. *I have been impressed with the results I have seen, but this method requires careful location. Hitting a vein would end any Mr. "O" dream real quick. Some black market Winstrol is testosterone suspension, so if gyno was reported
Thursday, October 4, 2007
EPO (ErythropoietinErythropoietin)
EPO
ErythropoietinErythropoietin (EPO) gained notoriety in 1998 when a bunch of cyclists in the Tour de France got caught in possession of it.
EPO increases RBC in the blood. This will basically raise your energy levels (Cancer. 2003 Sep 1;98(5):1072-9), and thus will improve recovery, etc... A50 was developed for a very similar purpose as EPO, and I suspect that a lot of the muscle enhancing effects/potency of A50 (increased muscle fullness, etc...) can be attributed to the much of same mechanisms which are at work in EPO. Its worth noting that EPO increases protein synthesis, just like A50 as well. Primarily, though, its effect is to increase RBCs.
Having more RBCs, thus having more oxygen delivered to muscle tissues is directly associated with a substantial improvement in athletic performance, i.e speed, endurance, strength, etc...(Sports Med. 2003;33(3):187-212.). EPO is associated with improved bodyweight, exercise capacity, oxygen uptake, respiration, whole body metabolism and energy efficiency (Semin Oncol. 2002 Jun;29(3 Suppl 8):69-74) In addition, cognitive function (learning, etc...)is also improved with EPO(Clin Breast Cancer. 2002 Dec;3 Suppl 3:S116-20).
Ok... so how much do you take? I´d say you´ll need about 8,000-10,000IU for 2 weeks. That´s it. You take it all at once over 2 weeks (maybe a little over 1,000IU or so per day for 14 days) and then that´s it. Then, sometime in week 3, you´ll start feeling the results...which will last...for 3-6 months! Yeah, you read that right.
Watch your BP, and don´t let it get out of hand, because that could mean your hematocrit is getting too high... and remember to keep well hydrated to avoid any possible issues with clotting & keep some aspirin on hand just in case you find that you need to thin your blood out a bit
ErythropoietinErythropoietin (EPO) gained notoriety in 1998 when a bunch of cyclists in the Tour de France got caught in possession of it.
EPO increases RBC in the blood. This will basically raise your energy levels (Cancer. 2003 Sep 1;98(5):1072-9), and thus will improve recovery, etc... A50 was developed for a very similar purpose as EPO, and I suspect that a lot of the muscle enhancing effects/potency of A50 (increased muscle fullness, etc...) can be attributed to the much of same mechanisms which are at work in EPO. Its worth noting that EPO increases protein synthesis, just like A50 as well. Primarily, though, its effect is to increase RBCs.
Having more RBCs, thus having more oxygen delivered to muscle tissues is directly associated with a substantial improvement in athletic performance, i.e speed, endurance, strength, etc...(Sports Med. 2003;33(3):187-212.). EPO is associated with improved bodyweight, exercise capacity, oxygen uptake, respiration, whole body metabolism and energy efficiency (Semin Oncol. 2002 Jun;29(3 Suppl 8):69-74) In addition, cognitive function (learning, etc...)is also improved with EPO(Clin Breast Cancer. 2002 Dec;3 Suppl 3:S116-20).
Ok... so how much do you take? I´d say you´ll need about 8,000-10,000IU for 2 weeks. That´s it. You take it all at once over 2 weeks (maybe a little over 1,000IU or so per day for 14 days) and then that´s it. Then, sometime in week 3, you´ll start feeling the results...which will last...for 3-6 months! Yeah, you read that right.
Watch your BP, and don´t let it get out of hand, because that could mean your hematocrit is getting too high... and remember to keep well hydrated to avoid any possible issues with clotting & keep some aspirin on hand just in case you find that you need to thin your blood out a bit
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