chris42393
New member
anybody know what Pheroplex is? i need some info on it. PLZ HELP
anybody know what Pheroplex is? i need some info on it. PLZ HELP
- Thread starter chris42393
- Start date
UnrealMachine
Well-known member
try typing it into google and reading
or try typing its scientific name into google and reading, it's called desoxymethyltestosterone
or try typing its scientific name into google and reading, it's called desoxymethyltestosterone
gamer2be08
Banned
Firstly, it is a prohormone (designer steroid). Secondly, it probably is a clone of Phera Plex, one that I have never heard of before. And as I browse through google, I cant find really any results. Are you sure you spelled it right? Another thing, even if you are only 5'6'', 125 is not a lot of weight and I dont think you would get what you want out of an anabolic if you dont have a solid baseline. What is your age and BF percentage? The gains you get out of a PH cycle at your size would probably be the same as the gains you could achieve naturally. I would hold off until you are at the least 150 for your height and even then it better be mostly lean body mass... Then look into a good mild prohormone like H-Drol, a great clone of Halodrol...
jbryand101b
Banned
jbryand101b
Banned
Pheraplex (steroid name "madol"
here ya go, straight from anabolics 2009. now, this is the last freebee, next your lazy ass needs to search, and find the right spelling of the steroid ur wanting to know about. got it? :twak:
--------------
Modol (desoxymethyltestosterone)
Androgenic 187
Anabolic 1,200
Standard Methyltestosterone (oraI)
Chemical Names 17a-methyl-17b-hydroxy-Saandrost-
2-ene Estrogenic Activity none Progestational Activity no data available
Description:
Madol (desoxymethyltestosterone; also known as DMT) is a potent synthetic oral anabolic steroid. Desoxymethyltestosterone is thought of as a cousin to methyltestosterone, although the association between the two steroids is very loose. The unique thing about desoxymethyltestosterone is that it is structurally a 2-ene compound, lacking the 3-keto group present on most commercial anabolic steroids. This lack of a 3-keto group, however, does not mean desoxymethyltestosterone is a weak compound. Quite the contrary, it is an exceedingly potent oral steroid. According to the standard rat assays, desoxymethyltestosterone exceeds methyltestosterone in oral potency by a factor of 12.588 At the same time, its androgenicity is recorded to be only 87% higher, giving desoxymethyltestosterone an extremely favorable anabolic to androgenic ratio (measured to be nearly 6.5:1). The resulting steroid is considerably different than methyltestosterone, a drug which is both significantly weaker mg for mg than desoxymethyltestosterone, and possesses a much more formidable androgenic component. .
History;
Desoxymethyltestosterone was first described in 1963.589 This agent was never made available as a commercial prescription drug product, and saw only limited investigation in animals during the mid-1960's before disappearing into research obscurity. This agent remained hidden in the library bookshelves for decades, until reemerging in 2005 as a new "designer steroid" of interest to international sports doping officials. This was due to the confiscation of a sample of DMT at the Canadian border in December of 2003, where it was found in the possession of Canadian sprinter Derek Dueck during a routine vehicle inspection. The DMT sample remained nameless in a Customs warehouse for over a year, until officials from the World Anti-Doping Agency (WADA) finally had it tested and identified. Desoxymethyltestosterone is only the third never commercially marketed anabolic steroid found to be in use by athletes, following norbolethone and THG.
Although at one point DMT could have been considered an effective and "invisible" designer steroid for use while competing in drug-tes~ed sports, this is no longer the case. The UCLA Olympic Laboratory was successful in its quest to outline methods for detecting desoxymethyltestosterone in the urine,and these methods have been made available to all Olympic drug-testing labs. They have also been published, and as such are available to any other agency that wants to take an interest in its detection as well. Any sport that has its athletes' urine samples analyzed at an accredited laboratory will likely be checking for DMT at this point. Still, it is an oral steroid, and likely most metabolites are cleared from the body within a few weeks of stopping its use (not unlike most oral steroids). This agent is likely still around in some competitive circles, taunting testing officials with its relatively rapid rate of clearance.
Desoxymethyltestosterone was never sold as a commercial prescription anabolic steroid; however, it did appear on the sports nutrition market in 2005 under the brand name ErgoMax LMG (Lean Mass Generator), and subsequently other brand names. This drug is in sort of a grey area legally. It is not yet listed on any State or Federal law as an anaboHc steroid, and is not subject to criminal possession laws. But at the same time, it is clearly synthetic, and therefore not legal to sell as a dietary supplement. The FDA had acknowledged the presence of DMT in the supplement market in late 2005, and claimed they were investigating the issue and planning to take action. This resulted in the voluntary withdrawal of desoxymethyltestosterone-containing products from the
U.S. marketplace. Today, desoxymethyltestosterone is scarcely available, with residual stock and a very small number of clone products being traded overseas.
a should be noted that manufacture of this steroid is not extremely easy. The first hints of this came from the World ~nti-Doping Agency, who reported that the confiscated iample of OMT was shown to be very impure upon lnalysis. It was principally comprised of four different teroidal components: OMT, its unmethylated analog, and pomers of these two steroids bearing a 3-ene structure nstead of 2-ene. DMT is likely the only highly effective I!lnabolic steroid in the group, making it obvious the blend IS an issue of manufacturing contamination and not functionality. The same issue appeared again when Don Catlin and his staff at the UCLA Olympic Analytical Laboratory began working on methods for detecting DMT lin urine. The procedure required they obtain samples of IOMT to work with, which was accomplished by chemically imodifying the available starting materiaI5-alpha-androst2-ene-17-one. Even the laboratory material they had to work with was shown to be a mixture of both 2-ene and 3ene isomers (in approximately a 4:1 ratio) upon analysis, an unexpected but now consistent result. Although marketed as such, the existence of pure OMT products has not been independently confirmed. The same purity lissues may apply to other (perhaps all) DMT-containing Iproducts.
How Supplied:
desoxymethyltestosterone is not available as a rescription drug product.
structural caracterlistics:
desoxymethyltestosterone is a modified form of dihydrotestosterone. It differs by 1) the addition of a rethyl group at carbon 17-alpha,which helps protect the pormone during oral administration, 2) the introduction bf a double bond between carbons 2 and 3 (2-ene) and 3)
the removal of the 3-keto group (des-oxy). The latter two modifications greatly enhance the anabolic and relative biological activity of the steroid, partly by preventing the reduction of DMT to inactive 3-hydroxysteroid metabolites.
Side Effects (Estrogenic):
desoxymethyltestosterone is not aromatized by the body, and is not known to be measurably estrogenic. An anti-strogen should not be necessary when using this steroid. since estrogen is the usual culprit with water retention, !his steroid instead tends to produces a lean, quality look t0 the physique for most users. This makes it a favorable feroid to use during cutting cycles, when water and fat retention are major concerns. Note that some sensitive individuals do report estrogen-like side effects from this Irteroid, which suggests that it may have some low level of estrogen or progesterone receptor binding.
Side Effects (Androgenic):
Although desoxymethyltestosterone is classified as an anabolic steroid, androgenic side effects are still possible with this substance. These may include bouts of oily skin, acne, and body/facial hair growth. Higher doses are more likely to cause such side effects. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are additionally warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Desoxymethyltestosterone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.
Side Effects (Hepatotoxicity):
Oesoxymethyltestosterone is a c17-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances lifethreatening
dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain.
The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.
Side Effects (Cardiovascular):
Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HOL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Desoxymethyltestosterone has a strong effect on the hepatic management of cholesterol due to its nonaromatizable
nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction.
To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.
Side EffectsTestosterone Suppression):
All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.
The above side effects are not inclusive. For more detailed discussion ofpotential side effects/see the Steroid Side Effects section ofthis book.
Administration (General):
Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability.59o This is caused by the fat-soluble nature of steroid hormones, which can allow some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization, this steroid should be taken on an empty stomach.
Administration (Men):
Desoxymethyltestosterone was never approved for use in humans; actual prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall in the range of 5-15 mg, taken in cycles lasting no more than 6-8 weeks to minimize hepatotoxicity. This level is sufficient for measurable increases in lean muscle mass and strength. Note that a dosage of 5-15 mg per day could relate ~o as much as 10-30 mg when using an impure "supplement" product containing a mixture of DMT and its isomers. Desoxymethyltestosterone is considered a very versatile steroid, and while it is most ideally used during cutting phases of training, is potent enough to stack with other agents for bulking purposes as well.
here ya go, straight from anabolics 2009. now, this is the last freebee, next your lazy ass needs to search, and find the right spelling of the steroid ur wanting to know about. got it? :twak:
--------------
Modol (desoxymethyltestosterone)
Androgenic 187
Anabolic 1,200
Standard Methyltestosterone (oraI)
Chemical Names 17a-methyl-17b-hydroxy-Saandrost-
2-ene Estrogenic Activity none Progestational Activity no data available
Description:
Madol (desoxymethyltestosterone; also known as DMT) is a potent synthetic oral anabolic steroid. Desoxymethyltestosterone is thought of as a cousin to methyltestosterone, although the association between the two steroids is very loose. The unique thing about desoxymethyltestosterone is that it is structurally a 2-ene compound, lacking the 3-keto group present on most commercial anabolic steroids. This lack of a 3-keto group, however, does not mean desoxymethyltestosterone is a weak compound. Quite the contrary, it is an exceedingly potent oral steroid. According to the standard rat assays, desoxymethyltestosterone exceeds methyltestosterone in oral potency by a factor of 12.588 At the same time, its androgenicity is recorded to be only 87% higher, giving desoxymethyltestosterone an extremely favorable anabolic to androgenic ratio (measured to be nearly 6.5:1). The resulting steroid is considerably different than methyltestosterone, a drug which is both significantly weaker mg for mg than desoxymethyltestosterone, and possesses a much more formidable androgenic component. .
History;
Desoxymethyltestosterone was first described in 1963.589 This agent was never made available as a commercial prescription drug product, and saw only limited investigation in animals during the mid-1960's before disappearing into research obscurity. This agent remained hidden in the library bookshelves for decades, until reemerging in 2005 as a new "designer steroid" of interest to international sports doping officials. This was due to the confiscation of a sample of DMT at the Canadian border in December of 2003, where it was found in the possession of Canadian sprinter Derek Dueck during a routine vehicle inspection. The DMT sample remained nameless in a Customs warehouse for over a year, until officials from the World Anti-Doping Agency (WADA) finally had it tested and identified. Desoxymethyltestosterone is only the third never commercially marketed anabolic steroid found to be in use by athletes, following norbolethone and THG.
Although at one point DMT could have been considered an effective and "invisible" designer steroid for use while competing in drug-tes~ed sports, this is no longer the case. The UCLA Olympic Laboratory was successful in its quest to outline methods for detecting desoxymethyltestosterone in the urine,and these methods have been made available to all Olympic drug-testing labs. They have also been published, and as such are available to any other agency that wants to take an interest in its detection as well. Any sport that has its athletes' urine samples analyzed at an accredited laboratory will likely be checking for DMT at this point. Still, it is an oral steroid, and likely most metabolites are cleared from the body within a few weeks of stopping its use (not unlike most oral steroids). This agent is likely still around in some competitive circles, taunting testing officials with its relatively rapid rate of clearance.
Desoxymethyltestosterone was never sold as a commercial prescription anabolic steroid; however, it did appear on the sports nutrition market in 2005 under the brand name ErgoMax LMG (Lean Mass Generator), and subsequently other brand names. This drug is in sort of a grey area legally. It is not yet listed on any State or Federal law as an anaboHc steroid, and is not subject to criminal possession laws. But at the same time, it is clearly synthetic, and therefore not legal to sell as a dietary supplement. The FDA had acknowledged the presence of DMT in the supplement market in late 2005, and claimed they were investigating the issue and planning to take action. This resulted in the voluntary withdrawal of desoxymethyltestosterone-containing products from the
U.S. marketplace. Today, desoxymethyltestosterone is scarcely available, with residual stock and a very small number of clone products being traded overseas.
a should be noted that manufacture of this steroid is not extremely easy. The first hints of this came from the World ~nti-Doping Agency, who reported that the confiscated iample of OMT was shown to be very impure upon lnalysis. It was principally comprised of four different teroidal components: OMT, its unmethylated analog, and pomers of these two steroids bearing a 3-ene structure nstead of 2-ene. DMT is likely the only highly effective I!lnabolic steroid in the group, making it obvious the blend IS an issue of manufacturing contamination and not functionality. The same issue appeared again when Don Catlin and his staff at the UCLA Olympic Analytical Laboratory began working on methods for detecting DMT lin urine. The procedure required they obtain samples of IOMT to work with, which was accomplished by chemically imodifying the available starting materiaI5-alpha-androst2-ene-17-one. Even the laboratory material they had to work with was shown to be a mixture of both 2-ene and 3ene isomers (in approximately a 4:1 ratio) upon analysis, an unexpected but now consistent result. Although marketed as such, the existence of pure OMT products has not been independently confirmed. The same purity lissues may apply to other (perhaps all) DMT-containing Iproducts.
How Supplied:
desoxymethyltestosterone is not available as a rescription drug product.
structural caracterlistics:
desoxymethyltestosterone is a modified form of dihydrotestosterone. It differs by 1) the addition of a rethyl group at carbon 17-alpha,which helps protect the pormone during oral administration, 2) the introduction bf a double bond between carbons 2 and 3 (2-ene) and 3)
the removal of the 3-keto group (des-oxy). The latter two modifications greatly enhance the anabolic and relative biological activity of the steroid, partly by preventing the reduction of DMT to inactive 3-hydroxysteroid metabolites.
Side Effects (Estrogenic):
desoxymethyltestosterone is not aromatized by the body, and is not known to be measurably estrogenic. An anti-strogen should not be necessary when using this steroid. since estrogen is the usual culprit with water retention, !his steroid instead tends to produces a lean, quality look t0 the physique for most users. This makes it a favorable feroid to use during cutting cycles, when water and fat retention are major concerns. Note that some sensitive individuals do report estrogen-like side effects from this Irteroid, which suggests that it may have some low level of estrogen or progesterone receptor binding.
Side Effects (Androgenic):
Although desoxymethyltestosterone is classified as an anabolic steroid, androgenic side effects are still possible with this substance. These may include bouts of oily skin, acne, and body/facial hair growth. Higher doses are more likely to cause such side effects. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are additionally warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Desoxymethyltestosterone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.
Side Effects (Hepatotoxicity):
Oesoxymethyltestosterone is a c17-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances lifethreatening
dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain.
The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.
Side Effects (Cardiovascular):
Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HOL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Desoxymethyltestosterone has a strong effect on the hepatic management of cholesterol due to its nonaromatizable
nature, structural resistance to liver breakdown, and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction.
To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.
Side EffectsTestosterone Suppression):
All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.
The above side effects are not inclusive. For more detailed discussion ofpotential side effects/see the Steroid Side Effects section ofthis book.
Administration (General):
Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability.59o This is caused by the fat-soluble nature of steroid hormones, which can allow some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization, this steroid should be taken on an empty stomach.
Administration (Men):
Desoxymethyltestosterone was never approved for use in humans; actual prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall in the range of 5-15 mg, taken in cycles lasting no more than 6-8 weeks to minimize hepatotoxicity. This level is sufficient for measurable increases in lean muscle mass and strength. Note that a dosage of 5-15 mg per day could relate ~o as much as 10-30 mg when using an impure "supplement" product containing a mixture of DMT and its isomers. Desoxymethyltestosterone is considered a very versatile steroid, and while it is most ideally used during cutting phases of training, is potent enough to stack with other agents for bulking purposes as well.
gamer2be08
Banned
im shure he spellid it rite.
Actually, he spelled it as Pheroplex.. The real name is Phera Plex, which is Madol. Now, the clone may be called Phero-Plex....
jbryand101b
Banned
Reely? are yu shure???? durrr, uh, i donta know about dat won.....:icon_lol:
:flowers1:
***edit*** guess closed this thread. lol
UnrealMachine
Well-known member
It's way better when people have already started inject cycles and can't spell what they're injecting and have no clue what the esters mean
Stuff like "Hey guyz i've bin injecting sustinon for 4 days why don't i feel it yet?"
-----------SLAP
dpfisher
Guest
Nolanaf67
Member
Uuummm.........wow that just isn't smart.
UnrealMachine
Well-known member
It shouldn't differ at all. That's what a "CLONE" is
I used PPlex and it worked for me
I used PPlex and it worked for me
gamer2be08
Banned
Thats right, key word "shouldnt" is used.. We all know some supposed clones dont do jack ****....
dpfisher
Guest
CEL is legit, the only thing some people have complained about is a couple Mdrol batches.
Libertarian
Active member
Reading through this guy's post history... He is a real fool when it comes to steroids and shouldn't be anywhere near them.
Also his favorite phrase, is "plz help", which he puts in the title of almost all his threads. F*ckin' annoying.
He says he's 22 but I'm guessing 16 tops.
Also his favorite phrase, is "plz help", which he puts in the title of almost all his threads. F*ckin' annoying.
He says he's 22 but I'm guessing 16 tops.