guardianactual
MuscleChemistry Registered Member
I used MENT in pill form @ 100mg ED it was pretty good.. I used it as a test base for my last cycle which included dienolone ace.. It was very similar to testosterone very strong sex drive water weight was higher than test & I ran asin instead of adex but gains were w/in 2 weeks and it kicked in w/ in 5 days
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</br> I would love the injections I'm sure, but imo 10mg ED is way too low.. injections r done @ 50mg ED typically and it's described as superdeca! MENT is to deca as Methyl tren is 2 tren ace from what users say.. I've never used tren or deca so I cannot compare BUT MENT did help my joints very well.
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</br>Pharmaceutical Name: Trestolone, MENT, 7MENT (as acetate) Chemical structure: 7-alpha-19Nor-androst-4-en-3-one,17b-ol Molecular weight of base: 288.429 Molecular weight of ester: 60.0524 (acetic acid, 2 carbons)
</br>
</br> Effective dose: 10-50 mg every day Average Street-price: Only available through chemical wholesale. Available Doses: None known. But Schering has been conducting extensive research into use for MENT both as a male contraceptive and as a means of hormonal replacement.
</br>
</br> Characteristics:
</br>
</br> I MENT has always been my favourite steroid, and that's just from reading the studies and looking at the structure of it. Thinking of what MENT can do should make every steroid user drool. This stuff is nearly as strong as its 17-alpha-alkylated counterpart mibolerone (cheque drops) but without the mad liver toxicity. It's a 19Nor substance, a nandrolone derivative. Its very much like nandrolone, except it has a 7-alpha-methyl attachment. This attachment stops it from being 5-alpha-reduced1. Now as you know, 5-alpha-reduction makes nandrolone, otherwise a very potent hormone, much weaker. A nandrolone derivative without 5-alpha-reduction for example is trenbolone (Parabolan/Finaplix), a very strong and potent androgen. But because of trenbolone's triple double bond structure, it also does not aromatize. But MENT on the other hand is still capable of aromatizing2 (which would not be the case with a 4 or 5 methylation), so you still have the benefits of estrogen : extra strength, better glycogen use, upgrading of androgen receptor, increased GH output and more IGF1. Its estrogenic potency may in fact be slightly larger because 7-alpha-methyl-estradiol (the product of MENT aromatization) may show less affinity to binding proteins as well. It is in fact suggested that part of MENT's actions may be the result of this potent estrogen1.
</br>
</br> This stuff should literally and in all aspects be stronger than testosterone. Its androgenic character will be like trenbolone (same risk of hair loss, prostate hypertrophy, acne, deepening of voice) and its estrogenic character will be like that of nandrolone (same risk of gyno, bloating and fat gain). But its hypertrophic ability should be much higher than either of these, or even testosterone.
</br>
</br> One question begs to be asked however: why on earth would they make it an acetate ester? In depot shots that means daily injections. This is after all the same company that is looking to market injectable testosterone undecanoate for shots once every 10 weeks. Well, so far two uses have been found for MENT in the medical community. Sundaram, who is probably the leading researcher where nandrolone and its derivatives are concerned, found it to be of perfect use for both replacment therapy for men, as well as for male contraception3 (Which would suggest it at least doesn't suffer from the libido suppressing drawback that nandrolone does). And from what the latest research in the matter seems to suggest, it looks like Schering is planning on making it in implant pellets4 that would release the drug over time, with 4 pellets delivering no more than 1.3 mg/day ! Assuming most of us do not want to use 40-50 pellets that could pose a problem for the use of MENT for enhancement purposes, lest there are some black market knock-offs. But take it from one who had looked, currently none of the wholesalers seem to have access to MENT. So the pending release of MENT may not be such joyful news after all (except for Schering who stands to profit nonetheless).
</br>
</br> There is one study5 in particular that documented the exact effects of MENT very well, although it was carried out on castrated mice so these effects may not be transcribed to humans. MENT was capable of restoring sexual behaviour and seminal vesicle weights to intact levels as good as testosterone but at 1/3rd of the dose ! What was also interesting was that MENT did not seem to stimulate aggressive behaviour at all. Compared to a control group of castrated mice, there levels of aggression did not nominally increase at all. This could be positive news for all those roid ragers out there giving the steroid community a bad name.
</br>
</br> Another interesting study6 more or less quantified the effects of MENT as compared to testosterone, and found that its androgenic character, based on the weights of ventral prostate and seminal vesicles, was 4 times greater than that of testosterone and that the hypertrophic nature was no less than 10 times greater, based on the weight increase in the levator ani muscle. More disturbing was the finding that the suppressive effect of MENT on HPTA was 12 times greater than that of testosterone, which is concerning at the least for a product with uses as a male contraceptive. The varying figures indicate that where a dose of testosterone that can maintain serum gonadotropin levels and muscle mass, can also maintain the prostate and seminal vesicles, where MENT cannot. This can easily be explained because the larger part of testosterones androgenic action stems from target specific conversion to a more androgenic form in the prostate and other androgen sensitive tissues, because these have a high concentration of 5-alpha-reductase. But MENT is not affected by 5-alpha-reductase. Because of its 7-alpha-methyl group, MENT also shows no significant binding to SHBG7 (sex hormone binding globuline). On the one hand that is why it is such a strong hormone compared to testosterone (estimated 3 times stronger), but also why its half-life is shorter (begging daily injections still with the acetate ester). So in conclusion we can state that this hormone is extremely powerful at what it does and could find more uses, both in the medical community (to treat wasting diseases and burns) and in the sports enhancement field. While its production is imminent and its safety record proven in both studies with humans and animals, it remains to be seen for what purpose and in what form it will be marketed by Schering. As things are now, it looks like it will be produced in a form that will only be useful in hormonal replacement therapy, and not in short term treatment of burns or wasting diseases, or for sports enhancement.
</br>
</br> Stacking and Use:
</br>
</br> This information is of course purely hypothetical and based on an injectable version of the aforementioned acetate ester of MENT. Given the short half life and the short ester, daily injections would be required. In most cycles we would inject around 75 mg per day of test (give or take, based on 500 mg/week). Similar results could be obtained with 25-50 mg per day of MENT. The drug does aromatize like nandrolone, and it aromatizes to 7-alpha-methyl-estradiol. In light of the low affinity of MENT for binding proteins, the same could be assumed of 7-alpha-methyl-estradiol, so this may be a quite potent estrogen. Combined with the progestagenic action of 19Nor steroids that could lead to a reasonable risk for gynocomastia. Especially those prone to estrogen should probably supplement with 1 mg per day of arimidex or 2.5 mg per day of letrozole to keep these effects at bay. If stacked with additional aromatizing or otherwise estrogenic hormones its best to keep Nolvadex on hand as well, and to remind yourself of the progestagenic action. RU486, the abortion drug, is the only known truly effective progestin blocker, but is hard to find and terribly expensive. Combining with Winstrol may help, as it does have some competitive progestagenic blocking abilities, but their extent is not quantified in any study. The androgenic effects may be quite strong, so acne probably will occur, and men prone to problems with male pattern hair loss or prostate problems should be cautious. Due to the 7-alpha-methyl group, MENT is not affected by 5-alpha-reductase, so treatments like Proscar will have no effect.
</br>
</br> When stacking this product, one will probably be looking to add mass to the frame. To that extent it could be stacked with testosterone (particularly powerful combo), Methandrostenolone (40 mg/day), Oxymetholone (100-150 mg/day) or Boldenone -(200-800 mg/week) (the latter would be my preference). It would not make a very good match for nandrolone, as nandrolone can be considered the weaker relative of MENT, with similar action but much less androgenic possibilities. Given the progestagenic nature, Stanazolol (50 mg/day) may be a good match for MENT as well.
</br>
</br> Keep in mind that there are very few real world results with MENT on humans, and there is no literal data on its hypertrophic ability, so a lot of this is hypothetical, based on the available studies and evidence. Extra:
</br>
</br> Researchers have found that 5a-dihydrotestosterone (DHT) has the same capability of myelin regeneration as testosterone while 17a-methyl-testosterone and epitestosterone have a weaker capacity for myelin regeneration. The most interesting finding was that Trestolone (7a-methyl-19-nortestosterone) which recently hit the market showed capability of myelin regeneration comparable to testosterone and 5a-DHT. Trestolone just gets better and better; it is 10x as potent as testosterone, has no action in the prostate, and it is capable of myelin regeneration. Although data on its ability to aromatize is not very concrete, in vitro testing shows Trestolone to aromatize significantly more than Nandrolone, but less than Testosterone.
</br>
</br>We sometimes forget the wide range of physiological effects the androgen receptor produces in our bodies. The androgen receptor is not limited to muscle tissue–it is expressed in many organs. It is expressed in our brains where it plays a role in sexual function and our CNS where it plays a role in physical strength. These neuronal androgen receptors help protect our neurons from myelin loss; improving our mood, sex drive, strength, and preventing demyelinating diseases. Check for yourself; see if you notice a little extra brain power next time you are on a cycle of Trestolone or Testosterone. Hussain R. et al. The neural androgen receptor: a therapeutic target for myelin repair in chronic demyelination. Brain: A Journal of Neurology.
</br>
</br> I would love the injections I'm sure, but imo 10mg ED is way too low.. injections r done @ 50mg ED typically and it's described as superdeca! MENT is to deca as Methyl tren is 2 tren ace from what users say.. I've never used tren or deca so I cannot compare BUT MENT did help my joints very well.
</br>
</br>
</br>
</br>Pharmaceutical Name: Trestolone, MENT, 7MENT (as acetate) Chemical structure: 7-alpha-19Nor-androst-4-en-3-one,17b-ol Molecular weight of base: 288.429 Molecular weight of ester: 60.0524 (acetic acid, 2 carbons)
</br>
</br> Effective dose: 10-50 mg every day Average Street-price: Only available through chemical wholesale. Available Doses: None known. But Schering has been conducting extensive research into use for MENT both as a male contraceptive and as a means of hormonal replacement.
</br>
</br> Characteristics:
</br>
</br> I MENT has always been my favourite steroid, and that's just from reading the studies and looking at the structure of it. Thinking of what MENT can do should make every steroid user drool. This stuff is nearly as strong as its 17-alpha-alkylated counterpart mibolerone (cheque drops) but without the mad liver toxicity. It's a 19Nor substance, a nandrolone derivative. Its very much like nandrolone, except it has a 7-alpha-methyl attachment. This attachment stops it from being 5-alpha-reduced1. Now as you know, 5-alpha-reduction makes nandrolone, otherwise a very potent hormone, much weaker. A nandrolone derivative without 5-alpha-reduction for example is trenbolone (Parabolan/Finaplix), a very strong and potent androgen. But because of trenbolone's triple double bond structure, it also does not aromatize. But MENT on the other hand is still capable of aromatizing2 (which would not be the case with a 4 or 5 methylation), so you still have the benefits of estrogen : extra strength, better glycogen use, upgrading of androgen receptor, increased GH output and more IGF1. Its estrogenic potency may in fact be slightly larger because 7-alpha-methyl-estradiol (the product of MENT aromatization) may show less affinity to binding proteins as well. It is in fact suggested that part of MENT's actions may be the result of this potent estrogen1.
</br>
</br> This stuff should literally and in all aspects be stronger than testosterone. Its androgenic character will be like trenbolone (same risk of hair loss, prostate hypertrophy, acne, deepening of voice) and its estrogenic character will be like that of nandrolone (same risk of gyno, bloating and fat gain). But its hypertrophic ability should be much higher than either of these, or even testosterone.
</br>
</br> One question begs to be asked however: why on earth would they make it an acetate ester? In depot shots that means daily injections. This is after all the same company that is looking to market injectable testosterone undecanoate for shots once every 10 weeks. Well, so far two uses have been found for MENT in the medical community. Sundaram, who is probably the leading researcher where nandrolone and its derivatives are concerned, found it to be of perfect use for both replacment therapy for men, as well as for male contraception3 (Which would suggest it at least doesn't suffer from the libido suppressing drawback that nandrolone does). And from what the latest research in the matter seems to suggest, it looks like Schering is planning on making it in implant pellets4 that would release the drug over time, with 4 pellets delivering no more than 1.3 mg/day ! Assuming most of us do not want to use 40-50 pellets that could pose a problem for the use of MENT for enhancement purposes, lest there are some black market knock-offs. But take it from one who had looked, currently none of the wholesalers seem to have access to MENT. So the pending release of MENT may not be such joyful news after all (except for Schering who stands to profit nonetheless).
</br>
</br> There is one study5 in particular that documented the exact effects of MENT very well, although it was carried out on castrated mice so these effects may not be transcribed to humans. MENT was capable of restoring sexual behaviour and seminal vesicle weights to intact levels as good as testosterone but at 1/3rd of the dose ! What was also interesting was that MENT did not seem to stimulate aggressive behaviour at all. Compared to a control group of castrated mice, there levels of aggression did not nominally increase at all. This could be positive news for all those roid ragers out there giving the steroid community a bad name.
</br>
</br> Another interesting study6 more or less quantified the effects of MENT as compared to testosterone, and found that its androgenic character, based on the weights of ventral prostate and seminal vesicles, was 4 times greater than that of testosterone and that the hypertrophic nature was no less than 10 times greater, based on the weight increase in the levator ani muscle. More disturbing was the finding that the suppressive effect of MENT on HPTA was 12 times greater than that of testosterone, which is concerning at the least for a product with uses as a male contraceptive. The varying figures indicate that where a dose of testosterone that can maintain serum gonadotropin levels and muscle mass, can also maintain the prostate and seminal vesicles, where MENT cannot. This can easily be explained because the larger part of testosterones androgenic action stems from target specific conversion to a more androgenic form in the prostate and other androgen sensitive tissues, because these have a high concentration of 5-alpha-reductase. But MENT is not affected by 5-alpha-reductase. Because of its 7-alpha-methyl group, MENT also shows no significant binding to SHBG7 (sex hormone binding globuline). On the one hand that is why it is such a strong hormone compared to testosterone (estimated 3 times stronger), but also why its half-life is shorter (begging daily injections still with the acetate ester). So in conclusion we can state that this hormone is extremely powerful at what it does and could find more uses, both in the medical community (to treat wasting diseases and burns) and in the sports enhancement field. While its production is imminent and its safety record proven in both studies with humans and animals, it remains to be seen for what purpose and in what form it will be marketed by Schering. As things are now, it looks like it will be produced in a form that will only be useful in hormonal replacement therapy, and not in short term treatment of burns or wasting diseases, or for sports enhancement.
</br>
</br> Stacking and Use:
</br>
</br> This information is of course purely hypothetical and based on an injectable version of the aforementioned acetate ester of MENT. Given the short half life and the short ester, daily injections would be required. In most cycles we would inject around 75 mg per day of test (give or take, based on 500 mg/week). Similar results could be obtained with 25-50 mg per day of MENT. The drug does aromatize like nandrolone, and it aromatizes to 7-alpha-methyl-estradiol. In light of the low affinity of MENT for binding proteins, the same could be assumed of 7-alpha-methyl-estradiol, so this may be a quite potent estrogen. Combined with the progestagenic action of 19Nor steroids that could lead to a reasonable risk for gynocomastia. Especially those prone to estrogen should probably supplement with 1 mg per day of arimidex or 2.5 mg per day of letrozole to keep these effects at bay. If stacked with additional aromatizing or otherwise estrogenic hormones its best to keep Nolvadex on hand as well, and to remind yourself of the progestagenic action. RU486, the abortion drug, is the only known truly effective progestin blocker, but is hard to find and terribly expensive. Combining with Winstrol may help, as it does have some competitive progestagenic blocking abilities, but their extent is not quantified in any study. The androgenic effects may be quite strong, so acne probably will occur, and men prone to problems with male pattern hair loss or prostate problems should be cautious. Due to the 7-alpha-methyl group, MENT is not affected by 5-alpha-reductase, so treatments like Proscar will have no effect.
</br>
</br> When stacking this product, one will probably be looking to add mass to the frame. To that extent it could be stacked with testosterone (particularly powerful combo), Methandrostenolone (40 mg/day), Oxymetholone (100-150 mg/day) or Boldenone -(200-800 mg/week) (the latter would be my preference). It would not make a very good match for nandrolone, as nandrolone can be considered the weaker relative of MENT, with similar action but much less androgenic possibilities. Given the progestagenic nature, Stanazolol (50 mg/day) may be a good match for MENT as well.
</br>
</br> Keep in mind that there are very few real world results with MENT on humans, and there is no literal data on its hypertrophic ability, so a lot of this is hypothetical, based on the available studies and evidence. Extra:
</br>
</br> Researchers have found that 5a-dihydrotestosterone (DHT) has the same capability of myelin regeneration as testosterone while 17a-methyl-testosterone and epitestosterone have a weaker capacity for myelin regeneration. The most interesting finding was that Trestolone (7a-methyl-19-nortestosterone) which recently hit the market showed capability of myelin regeneration comparable to testosterone and 5a-DHT. Trestolone just gets better and better; it is 10x as potent as testosterone, has no action in the prostate, and it is capable of myelin regeneration. Although data on its ability to aromatize is not very concrete, in vitro testing shows Trestolone to aromatize significantly more than Nandrolone, but less than Testosterone.
</br>
</br>We sometimes forget the wide range of physiological effects the androgen receptor produces in our bodies. The androgen receptor is not limited to muscle tissue–it is expressed in many organs. It is expressed in our brains where it plays a role in sexual function and our CNS where it plays a role in physical strength. These neuronal androgen receptors help protect our neurons from myelin loss; improving our mood, sex drive, strength, and preventing demyelinating diseases. Check for yourself; see if you notice a little extra brain power next time you are on a cycle of Trestolone or Testosterone. Hussain R. et al. The neural androgen receptor: a therapeutic target for myelin repair in chronic demyelination. Brain: A Journal of Neurology.
