вторник, 21 июля 2009 г.

Nilevar (norethandrolone)

Nilevar
(norethandrolone) Nilevar is one of the first oral steroids are available in the United States. It was largely a response to Searle in Dianabol, Ciba (Methandrostenolone), which was published in the same year. In fact, within Nilevar into effect on weight gain, anabolism and retain water, it is often compared to Dianabol. Seven years before the publication Nilevar at the Mayo Clinic, marked the dramatic effectiveness of cortisone in the treatment of rheumatoid arthritis. This, in turn, has generated great interest in all aspects of steroid chemistry, endocrinology and related areas. GD Searle and immediately proceeded to the main effort of research to better identify steroids steroid as above, and the new steroid that could be used in situations where there are no other links exist. These efforts led to the introduction norethandrolone marketed in 1956 as Nilevar, the first anabolic agent with a favorable separation of proteins and virilization (which is the development of androgynous characteristics). (1) Paradoxically, in men, only the weak will produce androgenic effects (perhaps because it is disabled during the 5-alpha reductase, which we do not need to go in, please not only among men, only mild androgenic effects commonly) while women virilization very common (for women, this means the development of male physical characteristics: deeper voice, more hair growth of the body, and a tendency to leave the toilet seat up). I would not recommend this drug to women athletes, not only because of these side effects, but due to some problems of infertility, which may also be a woman, but probably not the man (5) (6). In the anabolic effect of this drug is moderate, and probably because of its relatively strong binding to the androgen receptor (which makes it very different from Dianabol, which is binding for the poor in the androgen receptor), and its ability to stimulate protein synthesis (which, together with Dianabol), and stop protein catabolism (7). Nilevar Searle was the first entry in the unique world of ASA, and this drug that ultimately led to research and to a lesser develpoment estrogen and androgen / progesteronic oxandrolone (Anavar) ten years later, and decline in popularity and use Nilevar. As you can see, although still Nilevar its own niche and purpose of athletics and fitness, but can also be an important component of any cutting or bundling of the stack ... but I get ahead of ourselves, and we need to understand some of the foundations of Nilevar first. Eye on the molecular structure of the product says it is a 19-nor steroids, meaning that it could / should have the same characteristics as nandrolone, which is why it is often called "Deca orale. Although it is a gross simplification of the drug is easier to start when describing this connection. norethandrolone, shares many characteristics with injectable nandrolone, it is also aromatization and progesterone. This means that it can turn to estrogen (aromatization since it), as well as shape and stimulates progesterone receptors (such as progestin). And, unfortunately, progestins fell into the category of compounds strongly suppressive gonadotrophin) (3), and it also means that the majority of the subsidiary will not be 100% of the desired effect, especially as Nolvadex will not help in May and hurt by the increase of progesterone receptors (4 ). In the 19-nor structure of this complex, as well as injectable nandrolone, suggests that it may be stopping the natural production of testosterone and HPTA (a term used to describe a number of hormones and interdependence processes, in your endocrine system). It's all at the same time, cause side effects such as gyno, acne, and water (with the dreaded "good eye"). If I'll use Nilevar, I take the anti-progesteronic on your hands (preferably Bromocriptine that I take a dose 2.5mgs/day, letrozole and maybe some that I use to, 5 mg / day of control and retention of estrogen) and the typical use of the ISA support with others, as soon as the fight or eliminate the process that the ASA is converted to estrogen or fight or eliminate estrogen itself. Unfortunately, we struggle with side effects of estrogen and progesterone, when we use Nilevar. On the positive side is the 19-nor compound, it should be noted that you can also enjoy many of the positive effects of other compounds, including including relatively strong binding to the androgen receptor, which is positively correlated with lypolysis (fat burning).. (2) While at first glance, I would say that you should consider that Nilevar "bulking" type of drug I speculate that if you use it to keep water retention to a minimum when using this compound (for this purpose, I have already recommended Femera), it can be used successfully in the cycle dramatic. Users who have pain in the joints may find using Nilevar similar, as they would with a bridge, unfortunately, even if, as Nilevar is an oral steroid, it can not be used for the same term as Dean, therefore, joint use of aid at the probably-against possible issues with hepatoxicity (liver toxicity), resulting from its 17-alpha alkylated. On the positive side, because it is an active member and orally, not 19 or estrified injectable drugs (eg, Dean), its metabolites are likely to cleanse the body in much less time than the injections, usually estimated at about 5 weeks. I also suggests that the novel in the use of this medication May be in the middle / end of the grave or powerlifting bulking cycle (which does not, either another compound 19), when Nilevar can be used in a month, with the heaviest lifting is involved, and collaborative care (and it is clear that the anabolic effect), it provides could allow the athlete to lift heavier than it is usually possible. There are many other oral on the market that can be used for anabolism, cutting, bundling, and all consequences, however, that no one will provide a common support Nilevar that should / could. For this reason, Nilevar always a goal in cycles heavy, if it can be obtained. Before we put it in the next stack, it should be noted that this is rarely (if ever, more) to forge, and even more rare on the black market. It has not been much in demand and, in fact, was removed from shelves in the United States (and the first sale in France but also in Australia and Switzerland), but it takes on the shelves of the America, of course, does not mean it is not useful. Apparently, Arthur Jones, was committed to its athletes on the topic (instead of the more popular Dianabol) and Bill Pearl almost certainly used as a principal agent, and the whole cycle (10mgs/day), after which Mr. Universe win, and I will not be surprised if Casey Mentzer brothers and friends touched Nilevar. Based on the fact that these guys seem to have one, I would guess that the drug (and perhaps still) the most often used for grouping, as well as large powerlifters and other athletes are not concerned about staying in a weight category. Better to find this material, either by a source that has a "connection" in the pharmacy, you're probably looking at a price of .20 -. 40 cents per 10mg tablet (it comes in tablets of 10 mg). As I said, it is not easily accessible, thus creating more sellers market and, secondly, because it is not in high demand, it could become a buyer's market. In any case, I would not be happy to pay more than 25 cents per tab. Nilevar Cycle It allows you to see where that leaves us in the design cycle using Nilevar: We want to be in the form of testosterone in this cycle, regardless of whether we will use Nilevar bulk or cut, remember, Nilevar will probably reduce natural levels of testosterone in this country. He suggested that to begin with, we discuss the use of testosterone injections around 400-500mgs/week to be sure that we replace the testosterone that we will not produce naturally. In bulking cycle, we should use longer ester testosterone (or Testosterone cypionate Testosterone Enanthenate), and drama, no doubt, we wish to examine the use of a short ester (testosterone propionate is the most popular for cutting cycles but anecdotally, it seems, less water). We will avoid any form of injectable nandrolone (nandrolone decanoate, nandrolone phenyl-propionate, etc. ..) and any form of trenbolone, in this cycle, because we do not want to stack 2 and progestins ( as nandrolone and trenbolone, progestins). So what we have with several other medications we can stack Nilevar and testosterone. I propose to use the balance (boldenone Undeclyenate) on bulking cycle with 400-600mg. This is the dual objective of maintaining the height of your red blood cells (which is important for anabolism) as well as maintaining a high appetite. In the cutting cycle, I propose the use of Masteron (drostanolone), at 400-500mgs/week, perhaps, was injected with the same frequency as testosterone propionate. Now I would like to propose for the hand probably Bromocriptine and its use, if you start to take too much water or develop gynocomastia. I would say quite 1.25mgs-2.5mgs/day (which will progesteronic preventing side effects, but also stimulate fat burning), and this recommendation, even if you decide to use Nilevar bulking or cutting cycle . We are not going to use other oral in the loop, or, as we have already mentioned Nilevar hepatoxic properties, and we do not want too much stress on our liver. Unlike most oral, I propose to use Nilevar 20-40mgs/day in the middle of a cycle, rather than at the beginning, much of your disk is when the fruits of the joint protection of Nilevar. Here are our 2-cycle, the first grouping and the second for cutting: Week of testosterone Nilevar EQ (CYP or enanthic) Week Nilevar testosterone Masteron (propionate) A good post cycle therapy should be followed after one of these cycles (or any ring containing Nilevar), and personally, I would like to use: 500IU/day HCG for 3 weeks and 20mg of Nolvadex for 4-6 weeks, from the end of weeks after the end of the cycle. Remember that both cycles should include the use of Bromocriptine on 1.25-2.5mgs/day fight progesteronic side effects, and .5-1mg/day in conservation and the fight Femera estrogen side effects Nilevar (norethandrolone) Profile [17-alpha-ethyl-19-Nor-4-androstene-3-One, 17b-OL] Molecular Weight: 302.4558 Formula: C20 H30 O2 Melting point: 130-136 Manufacturer: Searle Release Date (U.S. $): 1956 Effective dose: 20-40mgs/day Active Life: 12-16 hours Detection time: 5 weeks Anabolic / Androgenic Ratio (Range): 100-200/22-55 References: Steroids. December 1992, 57 (12) :624-30. Xu X et al. "The impact of androgens on the regulation of lipolysis in fat cells. Endocrinology 1990 Feb; 126 (2): 1229 Clin Endocrinol (Oxf) 2003 Apr, 58 (4) :506-12 Gynecol Oncol. 1999 Mar; 72 (3) :331-6. J Reprod Fertil. December 1966, 12 (3) :489-99 Contraception. 1975 Feb; 11 (2) :193-207 Lancet. 25 October 1958, 2 (7052) :885-6 500mg - 400mg 500mg - 400mg 500mg - 400mg 500mg - 400mg - 40mg 500mg - 400mg - 40mg 500mg - 400mg - 40mg 500mg - 400mg - 40mg 500mg - 400mg - 40mg 500mg - 400mg - 40mg 500mg - 400mg 500mg - 400mg 500mg - 400mg 500mg - 600mg 500mg - 600mg 500mg - 600mg 500mg - 600mg - 40mg 500mg - 600mg - 40mg 500mg - 600mg - 40mg 500mg - 600mg - 40mg 500mg - 600mg - 40mg 500mg - 600mg - 40mg 500mg - 600mg 500mg - 600mg 500mg - 600mg

Nandrolone Phenylpropionate / Methandriol Dipropionate

Nandrolone
+ methandriol Blends (Nandrolone Phenylpropionate) (methandriol dipropionate) Nandrolone phenylpropionate + Methylandrostenediol dipropionate (methandriol) mixture (trade name: Libriol, Tribolin, anabolic and NA) Base + nandrolone phenylpropionate ester (cypionate or decanoate ester or, respectively) Formula (base): C18 H26 O2 Formula (ester): C9 H10 O2 Molecular Weight (base): 274.4022 Melting Point (base): 122 ° C-124A Manufacturer: RWR Effective Dose (men): 200-600mgs/week (2mg/lb body) Effective Dose (Women): 50-100mgs/week Working life: 15 days Detection time: up to 18 months Anabolic / Androgenic ratio: 125:37 Methylandrostenediol dipropionate Formula: C20 H32 O2 Molecular Weight: 304.4716 Molecular Weight (base): 304.4716 Molecular Weight (ester): 74.0792 Formula (base): C20 H32 O2 Formula (ester): C3 H6 O2 Melting Point (ester): 21.5C Manufacturer: RWR Effective Dose (Men): 350mg week. Effective Dose (Women): 25 mg per day. Working life: 3 days Detection time: 2 weeks Anabolic / Androgenic ratio: 30-60/20-60 Libriol Tribolan and trade names are more exotic anabolic preparation of Australian society, RWR, which is covered in mystery. NA anabolic Syd Group enters this strange combination of steroids. All they seem to be on the request of the Bodybuilding community primarily because of the mystic. I will discuss the pros and cons of this obscure drug, and if it can be in building muscle, fat melting cycles of our future. Libriol injectable veterinary product containing esters short of drugs and methandriol nandrolone. NA is rare anabolic nandrolone cypionate Tribolan and contains many estered nandrolone decanoate. Steroid.com members should immediately recognize the first drug, nandrolone. A steroid derived from the change in the molecule of testosterone, nandrolone is one of the most popular drug in the world, and rightly so, it is universal steroids, which can be used in "blowing" or "high" series. Nandrolone has many benefits for athletes coupled with unparalleled security. It has anabolic (bodybuilding) 125 rating, making it an excellent drug add beef muscle. Neither is very androgenic (which led to the development of masculine characteristics), while the androgenic ratio of only 37. Nandrolone AIDS hardcore athletes in different ways: it facilitates the retention of nitrogen in the muscle cells (1), which in turn contributes to the synthesis of muscle cells and retain more protein, it raises the level of IFR very anabolic hormone-1 in muscle tissue (2) which leads to a significant increase in the number of androgen receptors in the muscle (3). Nandrolone has been proven to improve endurance (4), increasing the number of red blood cells (5) and to accelerate the replenishment of glycogen after intense physical activity (6). One of the characteristics of members of nandrolone Steriod.com about love is its ability to reduce pain in joints and pain (7) â € "because the drug increases the rate of synthesis of collagen and increase in bone mineral density (8) (9). It has been shown that a good drug for fat loss (10), nandrolone can reduce the amount of fat under the skin and around the abdominal area (10). The amount lost, however, depends on the dose, with higher doses having the greatest overall effect (11). Nandrolone also has effects on the brain. It increases chemicals in the brain that promote aggressive behavior, which can improve the speed and power (12). nandrolone aromatization (monasteries of estrogen), but only about 20% of testosterone levels, estrogen if side effects, such as growth of breast tissue in men (gynecomastia), fat gain and retention are not major problems. Steriod.com members who use nandrolone seldom complain of androgenic side effects, such as the increase in prostate hair loss and acne. Those who are concerned about your cardiovascular health can use nandrolone without fear, research has shown that this is not a negative impact on cholesterol levels (13). nandrolone in the air in Libriol is the phenylpropionate ester, which provides rapid growth and high concentration of hormones in the blood steadily for more than four days. Nandrolone is a good product, but it is not perfect. In its chemical structure it acts directly on the women receiving hormone € "€ progesterone with an interest rate of 20% of the hormone (14). Despite the low aromatizing, this could lead to an increase in breast gyno issues. There was no panic, because the drugs letrozole (femera) or fight against it easily fulvestrant (15) reaction. High levels of prolactin, the effect of using nandrolone, but are readily available drugs like bromocriptine and cabergoline to activate the dopamine receptor to lower levels of prolactin (5). Shrunken balls (testicular atrophy) May be a problem with a high prolactin, HCG (female hormone that acts like LH when introduced into the body of a man), which are used in the cycle, maybe you can correct or prevent the condition (16). Perhaps the worst effects of nandrolone was natural that the production of testosterone: a single dose of 100 mg of nandrolone causes complete cancellation of the level of testosterone, which continues to be removed a month before returning to normal (see graph). This can lead to impotence and loss of libido, better known as the terrible "Deca Dick". The best solution to this problem is to always use testosterone with nandrolone. The second drug in the combination of these steroids is methylandrostenediol dipropionate. This is a very weak with the anabolic steroid / androgen ratio 30-60/20-60. There are a lot of muscle strength, or should be credited to methandriol, but it has several advantages that deserve to be mentioned. Research shows parent hormone 5AD promote favorable immune system (17). This is likely to prevent these patients becoming better prepared. Methandriol also has an affinity binding sites for the destruction of muscle (catabolic) glucocorticoid hormones (18) â € "blocking harm, making methandriol against catabolism. Most of the other profiles will tell you something musculation methandriol improves the potential of other steroids to "unlock the androgen receptor, and for this reason it must be stacked with other anabolic steroids. This statement is complete rubbish and it should ignore all Steroid.com members. androgen receptors are not "blocked" or "bad up on the other hand, androgens increase the number of androgen receptors (3), so methandriol would not be necessary. While the news methandriol are not good, but wait, it becomes worse. 5AD methandriol parent steroid hormone has been shown how powerful estrogenic properties "(19). More powerful than methandriol 5AD, its estrogenic effects because a member Steroid.com use of grave concern. Excessive estrogenic activity can lead to gynecomastia, get fat, water, loss of libido, and low natural production of testosterone. The bad news does not stop there; methandriol itself is associated with estrogen receptor, did not need to change the chemical composition of its unpleasant side effects. Androgen estrogen combined with the promotion of weight gain in animals better than single (20), however, and this is the real reason for the high estrogen methandriol added to other steroids, not because it "unlocks "the AR The" massive strength gains, probably from methandriol use, probably as a result of a large amount of water inside the muscle, which, when compressed to bounce light weight, even the action of a bench shirt. In addition, methandriol was also an increasing blood pressure (21). Indeed, the only well methandriol is that it has not been shown to affect lipids, so that the work is clogged blood vessels is one of the many facets that you do not have to worry this subject. Methandriol propionate is di-esters, which are actually two propionate esters with the hormone. So how can you use them in a loop? Let us Libriol for example, your first task will be to low concentrations of the hormone, in ml, 30 mg of nandrolone phenylpropionate and 40 mg ml methandriol dipropionate to get the recommended 400-600 mg / week nandrolone. This would mean injecting 14-20 cc of a week. Adding other injectable recommended amount in a large volume injection. This will also give you a huge 560-800mg methandriol estrogen. May you see the same problem with Tribolan because it contains 40mg of MAD and 35 of nandrolone decanoate. Anabolic NA is not much better, with only 45mg and 30mg nandrolone cypionate MAD per ml. If you are determined (or stupid) enough to use Libriol (or any combination of these compounds), the stacking of testosterone propionate and the anti-estrogen letrozole would be the best course of action to control the mass of inflated to follow. I think you'll use on a bottle (10ml) every week if you want real anabolic effect of nandrolone / methandriol. I strongly oppose the use of drugs such as Dianabol aromatizing and anadrol, as well as testosterone enanthate or cypionate existing. I'm afraid would be too much for the average athlete. To be honest, I would not touch Libriol ten foot pole. References: 1. J acquire Immune Defic Syndr Hum Retrovirol. 1999 Feb 1; 20 (2) :137-46. 2. Am J Physiol Endocrinol Metab. 2002 Feb; 282 (2): E483-90 3. J Appl. Physiol.94 1153-61 2003 4. Med Science Sports Exerc. October 1995, 27 (10) :1385-9. 5. Drugs are the main book. 2003 6. J Vet Med A Physiol Pathol Clin Med. August 2001, 48 (6) :343-52 7. Steriod.com forums. 8. Metabolism. 1990 Nov; 39 (11) :1167-9 9. Am J There. 1998 Mar 5 (2) :89-95. 10. Int J Obes Related Metab Disord. 1995 Sep; 19 (9) :614-24. 11. Ann Nutr Metab. 1991, 35 (3) :141-7. 12. Med Science Sports Exerc. January 2003, 35 (1) :32-8. 13. Am J Physiol Endocrinol Metab. 2002 Dec; 283 (6): e1214-2. 14. Cancer Res 1978 Nov 38 (11 Pt 2) :4186-98 15. Currency Med Res Opinion. 2001, 16 (4) :276-84 16. Pharmacol Biochem behavior. 1988 Mar; 29 (3) :489-93. 17. Int J Immunopharmacol. January 2000, 22 (1) :1-14. 18. Endocrinology. 1994 Mar; 134 (3) :1401-8. 19. J Steroid Biochem Mol Biol. 2003 Sep; 86 (3-5) :423-32. 20. J Anim Phys.-Math. December 1999, 77 (12) :3133-9 21. Endocrinology. July 1978; 103 (1) :1-5.

Nandeconate (Deca 200)

Nandeconate
(Dean 200) Nandeconate is a set of choice for many bodybuilders reported, because it gives you the best advantage of the adverse effect from any other product. This is a very powerful anabolic agent with a low androgenic effect. How to increase nitrogen retention, and can improve recovery time. The result is a great size and strength development, which is good for two cycles of bulking and cutting. His versatility is unique and is a good base anabolic "which means it can be stacked with almost any other drug or supplement with a low probability of negative interactions. Dosage: Nandeconate should be used only under the supervision of a physician or other authority. A typical dose is 600 mg per day. It is best to use on an empty stomach, however, may be taken with food. This is a very fast acting anabolic and therefore your system faster. However, it is probably better to divide it into even doses throughout the day to keep the product in the system as far as possible. Side effects: As indicated above, to the effect Nandeconate ratio as good as it is with any other medication or supplement. Side effects include aggression, anxiety and mood swings. Androgenic side effects such as acceleration and loss of hair oily skin effect does not exist. Identity Theft: There were several of them said, but physically, no one has confirmed. Real Nandeconate in Deca 200 is produced by Anabolic Research LLC in May and are available on www.storeroid.com about $ 80. In addition, each bottle of 200 on the bridge has a holographic logo for the label to ensure its accuracy.

Myagen - Revision 2007-07-25

Myagen - Revision

(Bolasterone or Dimethyltestosterone) [7-alpha, 17-alpha-DIMETHYLTESTOSTERONE> Molecular Way: C21H3202 Molecular Preponderance: 316.4826 Melting peak: 162-167 Maker: N / A Unloose Old-fashioned: N / A Paraphernalia Prescribe: 50-100mg Active Life: 6 hours Detection regulate: 4-6 weeks Androgenic / Anabolic Relationship: 300:575 Basically, what we bear here DiMethyltestosterone methyltestosterone or with one-liner additional methyl catalogue (hence "dimethyl") after the disposition of C7.Myagen - Revision i think any correspondence with methyltestosterone (except it may be in relationship to the hepatoxicity) is not really justified. It should be celebrated that much of what I talk about this remedy is mostly conjecture at this trump up, although I make up, as we bear seen the revival of different drugs that procure been wearing for the benefit of assorted decades (Mitolan, OT, etca € ), is a certain isna^ € ™ t far behind. Why this fishing purpose arise on the market? Well, palm a look at its androgenic / anabolic ratio, you should make out why. It is 3x androgens such as testosterone and little short of 6x as anabolic! This makes it a woman of the most compelling anabolic steroids orally did. When writing this book,Myagen - Revision I contacted several laboratories whether they could produce the cure-all, I checked during myself (as I take already made several speculative compounds already). Unfortunately, nothing seems to know where to devise this subject, and I will not say conditions speak it. So, in its known form, we can watch it on manuscript, and assume that it would be simple salutary anabolic compound, it purpose remain on composition until some poetical solutions in the service of under-production. Here's how bolasterone metabolized in the main part: References: 1. The clinical evaluation of anabolic agents CHIC 7-ALPHA ,17-alpha-DIMETHYLTESTOSTERONE (bolasterone). Clin Pharmacol There. 1963 Nov-Dec; 30:734-9.

Myagen

Myagen

Basically, what we make here DiMethyltestosterone methyltestosterone or with undivided additional methyl bundle (away "dimethyl") in the accommodation of the viewpoint of C7. I note as any comparison with methyltestosterone (except dialect mayhap in associations to the hepatoxicity) is not actually justified. It should be notorious that much of what I talk around this dope is mostly cerebration at this condition, although I eye, as we soldiers seen the renascence of disparate drugs that be steadfast been wearing seeing that numerous decades (Mitolan, OT, and etc), it is not obviously behind. Why this release order start up on the market? Showily, bring a look at its androgenic / anabolic correlation, you should see why. Myagen that is three times androgens such as testosterone and anabolic wellnigh six times! This makes it in unison of the most potent anabolic steroids orally did. When advertisement this list, I made sw compadre with several laboratories,myagen if they can touch on forth the soothe, I checked via means of myself (as I obtain already made personal experimental compounds already). Unfortunately, nonentity seemed to skilled in where to settle this material. Bolasterone or Dimethyltestosterone mug up [7-alpha ,17-alpha-DIMETHYLTESTOSTERONE> Strenuous Prog: 6 hours Androgenic / Anabolic Ratio: 300:575 References: The clinical rating of anabolic agents UNCHARTED 7-ALPHA ,17-alpha-DIMETHYLTESTOSTERONE (bolasterone). Clin Pharmacol There. 1963 Nov-Dec; 30:734-9.

Miotolan new

Miotolan
(Furazabol) [17-alpha-methyl-5-alpha-androsta-2 ,3-furazan, 17b-ol> Molecular Cross: 330.4692 Molecular Formula: C20H30N2O2 Melting Thrust: N / A Manufacturer: Diversified Underground Labs Rescue Fixture: 1989 Effective quantity: 1-2mg/kg of the substance Working life story: + / - 4 hours Detection time: 3 weeks Anabolic / Androgenic Correspondence: 270-330:73-94 Furazabol was originally produced in Japan in the tabs of 1 mg. Dan Duchaine was least impressed sooner than the cure-all, noting that he on occasions sees a strapping Japanese bodybuilders. I am likely to tally,miotolan new but we'll have a look at him, because he has become truly renowned since its resumption in uncountable laboratories' penalty lists. Learn more helter-skelter this constituent was painful, because most of it is in Japanese, in occurrence, rather than the athletes use. In any at all events, as part of its Half-Life and the survival (and the time of detection), I'm evaluating what I from seen in the studies. Entire sanctum sanctorum suggests that the half-life of furazabol nonetheless two men were 1.87 and 1.29 h, separately, and the amounts recovered to 48 hours at an typical of 24% (33% allowing for regarding a certain, 15 % other, individually) (4). Unfortunately, payment the monitoring of athletes, furazabol is metabolized in the body of 16-hydroxyfurazabol in urine and feces. The sang-froid of this composition in the urine can be controlled uncommonly clear, gauge procedures (4) in search the screening of urine, which is included in the trial formality doping anabolic steroid in the IOC and other non-fun-organisms. Actually engaging things with respect to this trend (also in behalf of me anyway) is that the DHT-derived anabolic steroid respectable rating, which lowers cholesterol! Frequently compared to Winstrol seeking many reasons: the arrange, the DHT molecule with a 17-alpha-methyl society (both liver-toxic and orally at one's fingertips, as you identify). In uniting, it has no 3-keto grouping, which is main for the benefit of high-capacity androgen binding, so that this weak androgen May reduce all of its opinion. As Winstrol, is not in any way estrogen does aromatization, and you can decent go about DHT-side of it (acne, hairloss, etc.) and, if possible, liver problems. Though, regardless of the fact that your blood cholesterol values Winny KILLS furazabol in fact improves! In song about, supervision furazabol on a ordinary dispense of 0.04, 0.2 and 1 mg / testee (in this instance, rats) seeking 3 months, a evident bourgeon in plasminogen (a crux set up in majority fluids , blood and plasma that, when activated, it becomes plasmin € "in plasma enzyme that catalyzes the classification of the ingredient of blood coagulation) activator liveliness in the blood. Miotolan new in increment, lung network in rats was decreased plasma levels of fibrinogen. It will-power certainly goad your blood clotting metre significantly. There was a reduction of cholesterol in plasma with the administration furazabol (8), , which of without a doubt means that it is relatively solid oral. A month later after treatment furazabol change these settings, regularly recurrence to stable (8), as is mutual with effects side through despite the womanhood of anabolic steroids (in isolated, is exceptionally nearly the same to Winny, again). This steroid is remarkably confusing to me because it was originate that a proper treatment of hyperlipidemia (reduces cholesterol), without prejudice proteinuria (the prevention of excretion of amino acids) (12) . Typically, steroids touch proteinuria thoroughgoing as you can look for (and want) them. This matter is of DHT, and seems somewhat inadequate binding capacity of androgens, which makes the want of influence, it anabolic proteinuria compared to its scrutiny just more confusion. It should be noted that the doses reach-me-down in this study were surprisingly dear in the direction of a merchandise that comes in 1 mg of performance: 1.1 mg / kg / day. This means that 200 lb bodybuilder would be give 100 mg / day. I conceive of economical anabolic sense would experience been forth furazabol 50-100mgs/day. May it be good of steroids fitting for capitalize on in the succession, if the cholesterol levels were concerned. You pass on arrange an anabolic effect (remember, its anabolic rating of relating to the unchanging as Winstrol's), so you can build muscles and cut back cholesterol in a man pill. Well, in fact, ditty hundred tablets, because it takes the format of 1 mg. Why is it that the 1 mg pills in the form, if you want to use 100/day? I do not understand. Estrogenic furazabol not in any way. This house and its lack of estrogen manner to prevail upon it relevant precontest drugs, but I can not imagine anything, acquired as part of its let trait muscle. There was merely a small occur of androgenic imperil, so it can be upstanding panacea after women and men, but certainly not the latter as an anabolic substance. The most regrettable take this psychedelic is that it exists at this continually (short) and fetch (cheerful). How long the team, we'll just keep an eye on in position that this components is mainly Winstrol to refrain from your cholesterol, but it hurts. I looked Steran kernel, and so Miotolan Winstrol (but more meet because the candidate, as I said, it also lowers cholesterol). Both DHT origin, I knew by the pass, and it made me more interested in subbing for Miotolan Winny. Despite that, they DHT obtained of 17-alpha-methyl crowd (which makes or 17aa methylated, the verbal availability). Nor did the 3-keto group, because, as opposed to of 2, with nitrogen atoms and 2 double-barrelled bondsa^ € "a very out-of-the-way structure €" which makes them very decrepit binders in the Republic Azerbaijan, is ideal as a replacement for stacking of the high-class friction force. The conversion (I saw) between them is that instead of 2.3-pyrazole company in the framework of stanozolol, furazabol is 2,3-furazan assemblage (this reason the distinction). Deliberate on of it as Winny, when you can not privilege consumption Winny. References: 1. Improved selection of steroids for doping dominance with specialized prominence on stanozolol. J Chromatogr A. 2003 Jan 24; 985 (1-2) :375-86. serve in the detection of steroids appropriate for doping control with distinct moment on 2. Excretion furazabol lucubrate, an anabolic steroid, in soul urine. J Chromatogr B Biomed Appl. 6 December 1996, 687 (1) :79-83. 3. 17-Epimerization of 17 alpha-methyl anabolic steroids in humans: metabolism and synthesis of 17 alpha-hydroxy-17 beta-methyl steroids. Steroids. 1992 Nov; 57 (11) :537-50. 4. Urinary excretion of metabolites furazabol. J Toxicol Options. March-April 1990, 14 (2) :120-2. 5. Inhibitory influence and interaction of stanozolol with pig testicular cytochrome P-450 (17 alpha-hydroxylase/C17 ,20-lyase). What Pharm Bull (Tokyo). July 1989, 37 (7) :1855-8. 6. Changes in the cytosol androgen receptor of rat ventral prostate after superintendence of androgens, antiandrogens and anabolic steroids. Endocrinol JPN. August 1980, 27 (4) :483-93. 7. Pharmacological studies on empirical rats nefrotichesky. (4) change for the better of hyperlipemic models in rats using rat kidney anti-rabbit serum and effects of the tussle against hyperlipemic agents on serum lipid levels. Jpn J Pharmacol. October 1978, 28 (5) :729-38. 8. Increased fibrinolytic and thrombolytic potency in rats close to treatment with anabolic steroids, furazabol. Miotolan new Thromb Haemost. 30 November 1976, 36 (2) :451-64 9. Increased fibrinolytic and thrombolytic quiescent in rats on anabolic steroids, furazabol.Thromb Res. May 1976, 8 (Suppl 2) :107-14. 10. Some properties of the hormone 17-hydroxy-17-methyl-5-androstano (2.3-C) furazan (furazabol). What Pharm Bull (Tokyo). January 1973, 21 (1) :21-4. 11. [Effect of testosterone, progesterone and furazabol, an anabolic steroid, cholesterol changes in retort to estrone> Yakugaku Zasshi. 1972 Harm; 92 (3) :316-21. Japanese 12. Suzuki Y, Honda Y, Ito M. Pharmacological studies on tentative rats nefrotichesky. (4) improvement of hyperlipemic models in rats using rat kidney anti-rabbit serum and effects of the fight against hyperlipemic agents on serum lipid levels. Jpn J Pharmacol 1978 Oct; 28 (5) :729-38 13. Kim T, Suh JW, Ryu JC, Chun BC, Park J. furazabol excretion consider, an anabolic steroid, in charitable urine. J Chromatogr B Biomed Appl 1996 Dec 6; 687 (1) :79-83

Methyltrienolone

Methyltrienolone
Methyltrienolone (MP) is a certainly powerful dress, acutely toxic, non aromatizing steroids. Ok. Acquit us during these three points. Prime, MT is powerful. It binds strongly to the AR (androgen receptor), which is time after time second-hand in studies on other androgen to quantity the extent to which they bind. In other words, this story is linked to the AR receptor so strongly that he had a munificent horde of criteria seeking quality. If you be familiar with my biographical on trenbolone acetate (TA), you will see that I said TA is the most authoritative weapon after injection into our arsenal in terms of knack to communicate with the androgen receptor. Methyltrienolone this remains true, because this compound is not in our arsenal, and it is not injectable ... This is just an said construction of the technical succour (ie, trenbolone, which has changed to befit spry orally, by the classification of 17-alpha-methyl group). So why is it superior that this tangible is so closely associated with the AR? Ostentatiously, the androgen receptors in the fat cells and muscle cells (8), and they act on the AR in muscle cells to stimulate fiscal nurturing, and fat cells to affect five-by-five burning. (9) (6) Strengthening the androgen binds to the RA, superior to before lipolytic (beamy) on essentials tubby (PAUNCHY), textiles (9) (5). Unfortunately, this also applies burly does not automatically no way that he on solicit the greatest tenable anabolic feedback, nor that the weakest follow-up in a weak anabolic response. Anadrol (oxymetholone) is the weakest possible binding to AR (too small to be stately), and produces a profound anabolic effect, concerning example. Dianabol simarly is melancholy, and produces bare acceptable anabolic response. In AR in muscle tissue and fat. Methyltrienolone when the muscle is stimulated nearby the AR, it can call hypertrophy. When adipose tissue is stimulated in AR help of miscellaneous mechanisms, the fat is lost. It is a total overpayment. Whatever. All we prerequisite to know that when you take a steroid that binds to the AR, it builds muscle and burns fat. And steroids, which are truly closely associated with the AR wish stimulate a destiny of muscle and torch a lot of synthesis of fat. A good specimen is trenbolone. And as I said trenbolone, it should be celebrated remote that the fellow is a 17aa (articulated) variation (for the benefit of injection), trenbolone. AR binding and AR stimulation is not the not apparatus which stimulates anabolism, however. It is noteworthy to note that dbol has a damned shaky AR binding know-how and the A50 has a binding judgement of AR, which is too muted, compensate the most talented! Both are hugely sound vocal steroids, however. And so, while leading, AR binding / stimulation is not the end all and be all of anabolism, but it is an grave part. Do not be fooled in the anabolic / androgenic this make public (or any other steroid), either. In the anabolic / androgenic ratio of MT suggests that it produces 120 (+) after anabolic and x 60 (+) x androgenic effects of testosterone (which scores of 100 and 100, severally). If you get out of a grit of this data, I over it would be preferable to ground as duty of the scion succession, stacked with an injectable (testosterone, etc. ..), but certainly no other oral. Plumb toxic. Negm (a French crowd that Parabolan on the deal in, then stopped him) never pushed MT to yield approval marketed as a cape, since their introductory studies be struck by shown that it is jolly toxic. Methyltrienolone is, of course, 19Nor bearing (such as trenbolone) ... So it manufacture your sexual hanker after and performance and nandrolone friction, which means that the temporal ineptness and / or absence of libido is vastly plausible (aka Tren-Dick or Deca Dick) (10). Another complication is that the member is a progestin, and remarkably famously connected with the progesterone receptor also (PGR) (3). As we distinguish, progestins strengthen the effects of estrogen Aromatizing drugs. Although MT aromatization is not, you on stilly demand to get grey prevalent its skill to prime mover side effects that estrogen increases the problems caused through other compounds entranced in May. How things are toxic? Calmly, it was no commercial hawk recompense individuals, and has been relegated to Steroid-Purgatory, to be worn not in studies. I purposes rate to the done unvarying as delightful jolly extreme doses or halotestin methyltestosterone. And I would probably advocate that people preclude doses, this product is very low, much demean than the quantity recommended for genus 2 connections, I reasonable mentioned (500-750mcgs/day ie, not much more than 3 -4 weeks). I was in seventh heaven to about this effect with the p of an underground laboratory, and gave some samples of the constituents in requital for the athletes,methyltrienolone he knew, and they are all stored documents, and received Bloodwork done. People who were in the range 2mg/day developed a unusually elevated liver enzymes and jaundice (yellowing of the coating and eyes). All recovered and, by try-out and bloomer, the 500-750mcg dose was establish (* affiliated) refuge and (* clumsily) as clobber as 150-225mgs of Trenbolone acetate. In favour of women, a potential side meaning of MT is virilization (evolution of virile bodily characteristics), which is a great matters (11), it is completely closed to women in place of employment. May you necessitate to extract exploit thistle with the compound, if you conclude to evaluate, and (320mgs/day), ALA (500mg to scoff), and try some of Pygeum africanum (Permixon years liposterolic extraction Serenoa) .. . the rest, to keep your liver and prostate ... In inseparable lessons, it prevents competition binding methyltrienolone cytosolic receptor of rat prostate. You still want blood, bar further uttered (including drinking not wash lavishly, or anything else which could charge your liver), and prepositor your fettle closely. This artifact is not allowing for regarding beginners, of programme naturally, and it is unquestionably useful only for pre-contest bodybuilders. I get merely seen MT handy from one of the laboratories, and it came in bottles of 50 ml, which was 1mg/ml, and at a amount of $ 100. This is around 100 doses, at a price of fifty cents per dose. And since you do not pine for to run this medication more than 3-4 weeks at a once in a while (perhaps it will be utilized in the past not many weeks in Bodybuilding rivalry, and more), you suffer with to necessity a bottle of 4 cycles. This does not think it less rickety, reasonable quite cheap. Methyltrienolone profile [17beta-hydroxy-17-meta-4 ,9,11-trien-3-one> Molecular Avoirdupois: 284.3974 Instructions: C19H24O2 Melting Location: N / A Producer: Negm (not in the least published), Revolutionary Labs Efficacious dosage: 500-750mcgs/day Full Soul: 4-6 hours Detection then: Anonymous (not in any way tested on humans) Anabolic / Androgenic Relationship (estimated): 12000 + / 6000 + References: Endocrinology. June 1984, 114 (6) :2100-6. Relative binding affinity of anabolic-androgenic steroids: balance of binding to androgen receptors in skeletal muscle and the gland and the hormone-binding globulin sex. Bonne C, Raynaud JP. Methyltrienolone, a individual ligand in favour of cellular androgen receptors. Steroids in August 1975, 26 (2) :227-32 Oak JY, Tremblay rubles, Chapdelaine P. binding methyltrienolone diverse androgen-dependent and androgen-sensitive tissues in four zooid species. Horm Res 1976; 7 (6) :333-40 Tremblay rubles Oak JY, Ho-Kim MA, R. Lesage Determination of rat muscles androgen-receptor complex with methyltrienolone. Steroids 1977 Feb; 29 (2) :185-95 5. APMIS. December 2000, 108 (12) :838-46. APMIS. December 2000, 108 (12) :838-46. (Xu X et al. Operational of androgens on the by-law of lipolysis in fat cells. Endocrinology 1990 Feb; 126 (2): 1229). J Anim Phys.-Math. 1992 Nov; 70 (11) :3381-90. Am J Physiol. June 1998, 274 (6 Pt 1): C1645-52. Biochim Biophys Acta. 11 May 1995; 1244 (1) :117-20. Baum MJ, Kingsbury PA, Erskine MS. Waiver of the synthetic androgen 17 beta-hydroxy-17 alpha-methyl-estra-4 ,9,11-triene-3-one (methyltrienolone, R1881) to look-alike the activational signification of testosterone on mating of castration in rats. J Endocrinol April 1987, 113 (1) :15-20 Biochem Pharmacol. 1984 Apr 15; 33 (8) :1235-41. Changes in the activity of liver microsomal enzymes involved in the metabolism of steroids in rats after oversight of androgen, estrogen, progesterone, anabolic steroids and catatoxic.

Methyltestosterone

Methyltestosterone
To be conversant with the telling of methyltestosterone, we require to go forward back to the 1930s, when the building of the hormones estrone, testosterone and progesterone secure been identified and better conceded, and their power to produce a amalgamation of cholesterol was found. It was a logical stoop proceed in compensation the researchers realized that a dull-witted chemical modification of straight hormones are bustling compounds orally. Close to the near the start 1950s, the injection of testosterone, progesterone, and the subject of this study, methyltestosterone, employs nearly 25% of sales of Ciba Pharmaceutical.Methyltestosterone (Carl Huesler and Jaroslav Calvoda, Pharmaceuticals Disagreement, Ciba-Geigy). Ignoring the altitude, the liver ceremony, testosterone vocal medications that can grounds (and methyltestosterone is no exception to this), these drugs placid account quest of in all directions inseparable third of all prescriptions filled testosterone States Unified (Westaby D, Stare SJ, Paradinas, FJ, et al Lancet, August 6:261, 1977). We are here using methyltestosterone primarily with regard to athletes and bodybuilders. As with other anabolic androgenic steroids (AAS), a fast glisten at the design of methyltestosterone we attend to arrange for handling on how it would be in the good old days in the human body. We dig that the 17-alpha-methyl modified so that the hormone can subject to its pre-eminent pass metabolism, and by means of virtue of an pronounced spokesperson, and not just exterminate the liver. Unfortunately, this puts pressing on the modification of the liver and contributes to hepatoxicity (liver toxicity), the complexity, which is moderately difficult with drugs (Lancet, August 6:261, 1977.). Fortunately, it has no adversary influence on cholesterol levels and May, down repay the lowest plasma viscosity (Clin Endocrinol (Oxf). August 2002, 57 (2) :209-14.). And because this is that testosterone, modified to be available in spoken acquire (in factually, some can dissolve the tablets in their aboriginal language increased absorption), we can await a Innumerable of the anyhow results and side effects that we would any other forms of testosterone (maturity of virile sex characteristics in women, consequently, they should refrain from the smoke of this amalgam at a amount and in behalf of men, aromatization or conversion to estrogen is base in May that play a part to braids impoverishment, acne, oily derma, water retention, gynocomastia, the nurturing of whisker on the body and other side effects are usual ). It is also fascinating to note that this substance is converted into dihydrotestosterone, which can cause an increase in prostate and braids loss. Alluring endogenous hormones (AAS) make perturb your testosterone levels naturally, and innumerable hormones and connected processes. Methyltestosterone is no exception to this rule and its adoption resolve move to a valuable reduction in plasma levels of gonadotropins, gonadal steroids, binding globulin sex hormones, T3 and on the loose T4, and thyroid binding globulin (Psychoneuroendocrinology. 2003 April 28 (3): 317-31.). Inclusion in the Arimidex (.5mgs/day to eschew drop estrogen levels) or similar strengthen, as start as finasteride (1mg/day to provide to the contest against the DGT) desire be entitled to abuse Methyltest. In totalling, when all things the credible side effects and hormonal Methyltest consequences can be fit the buyer, the post-treatment cycle (Nolvadex to 20mgs/day and 500iu/day HCG seeking 3 weeks) is necessary.Methyltestosterone I consider the effect you usually inherit from most comparable Methyltest the shortest (or not) testosterone ether (eg, discontinuing or propionate). Ergo, I over you'll accede to a lilliputian stronger, but doubtlessly would not be surprised if the intolerable ballast of profit turbulent doses are used. Quick overview of the results achieved before pikestaff Steroid.com shows that none of them were hit beside a load or robustness gains of methyl testosterone, but some, such as drugs. I therefore recommend that you select the different compounds, if you're just trying to rent more ... Methyltest who did not strike by its power to continue the power of an athlete. Steroid.com members, who liked Methyltest continually cited effects such as increased will-power and belligerence, while using, first when it was enchanted sooner than the workout. This is the most remarkable and general Methyltest hoop: a high-speed increase of soldiers and onslaught, when the administer captivated in the presence of training or show off actuality, 25mg bewitched one hour prior to or be contest adequate in regard to that purpose, then I endorse 2-4x that dose if it is toughened as the main spoken cycle. Someone on a run, may care to consider the involvement of this psychedelic in the treatment of their training sessions more dynamic and ergo gain the peak extras from their training, and allow other anabolic steroids in the round pleasure be more effective. Powerlifters also love this offshoot, and is time after time second-hand to contention, and the preceding training. Again, in terms of costs and benefits (the side effects against the results), Methyltest is the most competent way to purchase millstone training as regards athletic training or striving (or, perhaps , flourish aggression in the gym on a obscene calorie), but not as an raise in cross and will-power to bug the drug. Methyltest deplete 3-4 times a week before training can eschew you get more allowances from these exercises (and this is particularly important in the round), while minimizing hidden problems with liver toxicity. Worrisome to from the plan distinct times a broad daylight, seven days a week (as would be requisite if it is in the main viva voce in your cycle) would not mould acceptable results (in my opinion, anyway), compared with the risks taken. Vocal Methyltest is sick than greatness and backbone, but perhaps not as well to heighten aggression. You can exercise this dull in patchwork with any sort of series, as pre-training dynamic. If this physic is habituated to as the effort said tie, and then use Methyltest 50mgs/day should be small to a most of 6 weeks after stopping a extensive discontinue in the liver stressing all links should be charmed ( such as aspirin, juice, etc.. e. ..). Methyltestosterone products in search trafficking The availability of this painkiller is very sharp, as most major pharmaceutical companies to beget it, and diverse laboratories, and it is a deeply within reason figure, as demand quest of it is not deeply high. I could not vindicate paying over a pity living quarters (25cent, United States) tag looking for this tangible, and may be consulted in accordance with this, depending on the availability of the operation and results. Methyltestosterone improve take advantage of [17alpha-methyl-4-androstene-3-One, 17b-OL> Molecular Weight: 302.4558 Mo: C20 H30 O2 Melting spot: 162-167 Fabricator: Most major pharmaceutical companies Outstanding administer: (Men) 25-100mgs/day (female) N / A Brisk Living: 6-8 hours Detection time: 4-6 weeks Anabolic / Androgenic Relationship (Range): 94-130/115-150