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JayDiesel
05-21-2011, 11:36 PM
By: Big Cat

Metribolone


Pharmaceutical Name: Methyltrienolone
Chemical structure: 17-methylestra-4,9,11-trien-3-one,17b-ol
Molecular weight of base: 284.3974


Effective dose: 5-15 mg / day
Average Street-price: Only available for research purposes.
Available Doses: None

Brands & Products: Originally produced by Negma, but never approved for production.

Characteristics:

Methyltrienolone is structurally similar to trenbolone (Parabolan/Finaplix), a well-liked and powerful androgen that does not aromatize to estrogen. The difference is the attachment of a 17-alpha-methyl group for oral activity. So one could refer to methyltrienolone as oral trenbolone. It was first explored quite some time ago by Negma in France, the same company that marketed Parabolan (trenbolone). But the drug was never approved by the French government and was hence never produced. The reason was extreme hepatoxicity. Bill Roberts, the biochemist, once commented that taking methyltrienolone made taking insane doses of anadrol and Halotestin together look mild on the liver. While I was unable to find anything in the literature that describes the extent of the liver toxicity, it's a generally accepted fact. That's also why, to the dissapointment of many, you will never find a commercially marketed methyltrienolone product. Its only sold in bulk to labs and universities for research studies involving androgens.

Mainly because (and those who wish it was available will wish so even more now) its such a potent androgen. There is some conflicting information in that regard however. Organic chemist Patrick Arnold, head of LPJ research, once stated that methyltrienolone was the most powerful steroid ever, and that statement has been blown out of proportion and taken on a life of its own. While androgenically a very potent steroid, methyltrienolone is still basically trenbolone with a 17-alpha-methyl group. A group that has the tendency to actually reduce the androgenic potency. So it may actually be somewhat milder than trenbolone, on the contrary to what many pseudo steroid guru's are now claiming after reading Pat Arnold's statement. I can't find any other documented effects of the 17-alpha-alkylation influencing androgen binding in a positive way. It's a potent androgen, with more binding than even DHT2, but the study that claims that is mild at the very best about quantifications, whereas people have used the term 1000 times more powerful than testosterone, which is surely exaggerated.

What is interesting is that it seems to show nearly no binding for sex-hormone binding proteins, which makes it a popular choice in androgen receptor studies3, since it will demonstrate equal binding in all tissues regardless of the presence and amount of these proteins. No doubt this plays a role in its supposed binding capacity. In this instance the 17-alpha-alkylation may have played a key role, since it has been demonstrated a multitude of times that 17-alpha-methyl groups decrease the binding for sex-hormone binding proteins as well as most other structures, and due to its triple double bond, trenbolone really didn't bind well to these to begin with.

One of the findings made in clinical tests with methyltrienolone was the discovery of high amounts of the DHT-deactivating enzyme 3alpha-hydroxysteroid dehydrogenase in muscle tissue4. Once again proof that God meant to keep us humans weak. Hurray for science. Follow-up studies then went on to show that DHT nonetheless showed similar binding in the prostate, and showing little or no presence of the deactivating enzyme. So God would rather have us all die of prostate cancer than gain a few ounces of muscle. It's a comforting thought, no?

What methyltrienolone, despite its amazing capacity, still doesn't overcome are the basic problems with any 19Nor compound. First of all its effects on libido. Methyltrienolone still seems to affect our sex drive in such a potent manner that the dreaded Deca Dick (temporary impotence) is a very real threat5. Another is that it still binds almost equipotently to the progesterone receptor3. The latter would be of little concern as long as no circulating estrogen is present since methyltrienolone does not aromatize, but could cause problems such as aggravating water retention and gyno (growth of breast tissue in men) if combined with an aromatizing androgen or an estrogen.

While many may wish that an incredibly strong androgenic, non-aromatizing compound as this was available for daily use, its not. And if the indications are true, its probably best. I've warned many people for the toxicity of fluoxymesterone, and everything points to it that methyltrienolone makes fluoxymesterone look like Tums tablets in terms of liver toxicity.

Stacking and Use:

Obviously this section is mostly useless, as any who would use, let alone stack methyltrienolone for any decent period of time, wouldn't really be around long enough to tell us how well it worked. Ideally one would use it alone, while dieting or for the purpose of gaining lean mass. The androgenic potency is slightly higher than that of trenbolone, so the risk for aggravated hair loss, acne, prostate hypertrophy and deepening of voice is not only realistic, but almost likely. If one were to use it, you would probably have to use every trick in the book to protect your liver and stay alive: Alpha Lipoic Acid, Milk thistle, dessicated liver and Vitamin B6. The blood pressure raise would not be mild either. So something to lower blood pressure is advised as well.

Of course the best advice is to refrain from using such a compound, although for 99% of the population that is not a problem, and I would assume that the 1% that does have access would know better.

Dbolli
05-22-2011, 02:58 AM
Eww. tren and my body does not get along. We hate each other. Its to bad because its a good drug.

sebaco2011
05-27-2011, 03:39 AM
hehehe I finally got my 2 packets of GP Oral Tren ill be starting them in about 2-3 weeks , cant wait , from the reading iv done it seems to be good for strength and especially good for mental tear shit up in the gym attitude, but not to much in terms of the inj tren for the shredding abilities, guess we will find out :) going to run it with test prop and Tren E .

JayDiesel
05-27-2011, 07:35 PM
Let us know how it works out and everything. Its something im interested in just hear its soooo bad for the liver even more so than Halo.

tcastle
06-03-2011, 04:43 AM
Well, you hard wrong.
It's not good for the liver, but rumours about the toxicity are overdone.

At the moment i'm running methyl tren for the 3th time.
int the past i always dosed between 2-4 mg for 3 weeks
currently @2mg for 5 weeks

As long as you don't dose it too high or too long, damage isn't that big. I've had check ups after previous cycles and my liver values were all slightly elevated,
prolly the same as they would be from diana

Silver Back
06-03-2011, 08:56 AM
I will eventually run GP's oral tren. It looks bad ass. Their ace is sick.

DiscoDino247
06-13-2011, 06:41 PM
I took 100 mgs of Winny for 6 weeks and switched over to the oral Tren last week. Started off at 2 mgs/ day (8 pills @ 0.25mcgs each) last week and decided to up it to 2.5 mgs or 10 tabs per day this week. I am impressed so far with the strength gains and endurance, but I've been getting really lightheaded and short of breath in between sets, not to mention that I haven't stopped sweating since I started w/ the tren last week.

sebaco2011
06-13-2011, 10:17 PM
Wow disco! I only planned on using 3 tabs during the 4-6 weeks and maybe 4 pills MAX but WOWWW 10 tabs a day ? Crazy stuff , were you not getting enough results on 3 tabs ? Hehe I did GP oral winny at 50 mg for about 6 weeks also it was okay nothing special just made muscles harder but no other notable effects. Same with you though tcastle 2mg wowee

JayDiesel
06-14-2011, 05:31 AM
I took 100 mgs of Winny for 6 weeks and switched over to the oral Tren last week. Started off at 2 mgs/ day (8 pills @ 0.25mcgs each) last week and decided to up it to 2.5 mgs or 10 tabs per day this week. I am impressed so far with the strength gains and endurance, but I've been getting really lightheaded and short of breath in between sets, not to mention that I haven't stopped sweating since I started w/ the tren last week.

I believe you would get those effects bro thats alot! Yeah i was thinking 4 max if i do decide to run this

sam1976
06-16-2011, 11:27 AM
yea, disco, that is a pretty large dose. i know a national level super heavy weight who uses under 2 mg and i thought that was a lot! i can hardly deal with 1 mg after awhile.

JacobS
06-17-2011, 12:24 AM
Healthy diet and good training exercise will keep you physically fit while aiming for the body of your dreams.
You need to work its out naturally. :)

ODB
06-17-2011, 01:07 AM
Healthy diet and good training exercise will keep you physically fit while aiming for the body of your dreams.
You need to work its out naturally. :)

while u r 80% correct, You do realize that u r on JUICEDMUSCLE.COM? not a ton of natural guys here. :cool:

JayDiesel
06-17-2011, 03:06 AM
Healthy diet and good training exercise will keep you physically fit while aiming for the body of your dreams.
You need to work its out naturally. :)

True AAS are for plateus! lol

DiscoDino247
06-17-2011, 04:15 AM
Healthy diet and good training exercise will keep you physically fit while aiming for the body of your dreams.
You need to work its out naturally. :)

Thanks JacobS and great first post, not really (btw hope you're kidding, and if not don't be "that guy"and come on here preaching about being natural.) I have been "physically fit" my entire life, I started training in HS and now that I'm older I DO have the body of my dreams thanks to a healthy diet, great routine and AAS.

JayDiesel
06-17-2011, 04:50 AM
Thanks JacobS and great first post, not really (btw hope you're kidding, and if not don't be "that guy"and come on here preaching about being natural.) I have been "physically fit" my entire life, I started training in HS and now that I'm older I DO have the body of my dreams thanks to a healthy diet, great routine and AAS.

Tell him brother!

DiscoDino247
07-21-2011, 03:30 PM
Tell him brother!

That's how I roll Jay.... C'mon tho seriously, that's really his (JacobS) first and only post?? Some people are just clowns!

jk703
07-18-2012, 08:34 AM
dude i dropped 63lbs with oral tren 3 tabs a day for 3 weeks. i was doing p90x and mma cardio. i went back to college in the fall and people were stunned. it will give your muscles more tone too. do not exceed 3 tabs a day and do not exceed 3 weeks of use without equal time off. my liver never spiked but everyone is different. GP ORAL TREN is my favorite oral in the world lol. i currently have some in the mail somewhere.

RonnyT
08-22-2012, 02:16 PM
Posted in the blog on MT better take it subQ .. or very cautious dosing

methan
08-23-2012, 07:51 AM
did hcl still produce oral mt

siberiantiger
08-26-2012, 02:01 PM
Posted in the blog on MT better take it subQ .. or very cautious dosing3858this is my recommendation

siberiantiger
08-26-2012, 02:26 PM
This month I thought it would be interesting to introduce readers to a new, underground steroid circulating on the black market. It’s called dimethylnandrolone (DMN) and as its name suggest, it’s a cousin to the popular drug Deca Durabolin (nandrolone decanoate), so highly favoured by athletes for its strong anabolic and mildly androgenic properties. Dimethylnandrolone or DMN for short, is an interesting analogue of nandrolone, displaying high relative potency and favourable estrogenic and androgenic characteristics. Although its emergence on the underground is fairly recent, it’s quickly gaining attention and favourable reviews. With this in mind, I figured a thorough examination was warranted. So, without further fanfare let’s find out what this new “designer” steroid is all about.



Dimethylnandrolone is a generic term that could refer to any number of different nandrolone-derived steroids. It really only tells us that this is a nandrolone with two additional methyl groups. In this case, the exact DMN we’re looking at is 7-alpha, 11-beta dimethylnandrolone. Steroidphiles will recognize that this steroid is very close in structure to MENT (7- alpha- methylnortestosterone), an anabolic steroid currently under commercial development by Schering- Plough. MENT (which had been given the conventional name “Trestolone”) is being examined as a new form of male contraception and androgen replacement therapy. The drug effectively supports male libido and suppresses spermatogenesis while simultaneously lacking a stimulatory effect on prostate volume (due to a reduced relative androgenic nature compared to testosterone). Given its similar structure, DMN shares many of the same qualities of MENT, although it’s indeed a unique steroid in its own right. One of its most striking traits, in fact, is its extreme level of activity compared to most other steroids.

Binding studies show that DMN has an affinity for the cellular androgen receptor approximately twice that of DHT the most potent natural androgen in humans. A simple way to look at this is given equal concentration in the blood, you will find twice as much DMN bound to androgen receptors, compared to DHT. More binding usually means more activity. Compared to its (similarly) synthetic cousin MENT, DMN has about a 20 percent greater binding affinity. This is already some solid data, as DHT and MENT are no slackers as far as steroids are concerned. DMN is starting to look like it will be a fairly potent steroid. But it would be entirely misleading if we ended our examination here, as binding affinity is only one small part of the puzzle. Other primary factors effecting steroid potency include drug bioavailability, active half- life and binding affinity for constructive binding proteins. It may bind the androgen receptor well, but how long does it stick around in the body to do its job. Depending on how the compound fairs, pharmacologically speaking, it may be considerable stronger or weaker that relative binding affinity (RBA) alone would suggest (Dianabol and Winstrol are good examples of this).

A more accurate assessment of drug potency is made in vivo, or during experiments where the drug is administered to live animals (usually rats are used for the pre-human trials). Detailed in-vivo studies into DMN were published in 2005 and demonstrated a drug that was exceedingly potent. “During the investigation, animals were injected with DMN subcutaneously for seven days, after which the animals were sacrificed and analysed for muscle gain and androgenic activity according to the long-standard lavator any (LA), seminal vesicles (SV) and ventral prostate (VP) growth assays. Other steroids were also used , including testosterone and MENT. This result were quite remarkable for DMN, which turned out to be by far the most potent steroid of the group. Compared with testosterone, dimethylnandrolone displayed approximately 136 times greater anabolic activity. Yes, that was not a typographical error. It had 136 times, not 136 percent, greater anabolic activity. Its androgenic activity was shown to be 14-37 times greater than that of testosterone, making this not only an exceedingly potent steroid, but also one with a high ratio of anabolic to androgenic effect. Compared to MENT, DMN was five times more anabolic with two to five times more androgenic activity based on SV and VP assays, respectively.

While MENT maintains some moderate level of estrogenic activity, this does not appear to be the case with DMN. Studies with other 11 beta modified steroids like fluoxymesterone have shown that substitutions to this point on the steroid backbone inhibit estrogen conversion, which strongly suggests that DMN is a non-aromatizable nandrolone derivative. Furthermore, studies looking at the relative binding of this agent to the estrogen receptor have shown extremely weak binding affinity. As such, no appreciable intrinsic estrogenic activity appears to be present with this steroid. It seems reasonable to consider it a non-estrogenic drug. Similar to nandrolone and MENT, however, DMN maintains some moderate level of progestational activity. Which could mimic/intensify estrogen action in the body. This, however, is likely not going to be problematic unless high doses are taken, or the drug is administered in higher doses alongside other strongly aromatizable agent (obviously not the target clinical use for such a drug). Overall, it would appear the DMN is not only a strongly anabolic and mildly androgenic agent, but it’s also one not highly prone to causing estrogenic- type side effect such as gynecomastia, increased water retention or fat gain. Anecdotical report seem to support this conclusion as well. DMN does have one good thing going for it as far as safety is concerned. Unlike most of the recent “designer steroids” being released, it’s not a e-17 alpha alkylated substance. Although human studies are lacking in this regard, it seems reasonable to conclude that this drug displays relatively low hepatotoxity (liver toxicity). That is usually the case with non-17-methylated steroids, although at times even some of these drugs have been shown to cause elevated liver stress if taken into high a dosage or for too long a duration. Trenbolone, nandrolone and methenolone (Primabolan) have all displayed such liver toxicity in clinical reports, albeit isolated ones. Let’s therefore, not confuse “low toxity” with absolutely harmless. In a high enough dosage, you can likely run into trouble. The sheer potency of this drug suggest that daily doses below 1mg are going to be most commonly applied by bodybuilders. Doses well in excess of this are likewise discouraged. 17-methyllated steroids also tend to negatively affect lipids more so that their non-methylated analogs. This is one of the biggest drawbacks when it comes to the health risks of these drugs they legitimately and strongly affect a powerful factor in cardiovascular health. Without e-17 alpha methylation, DMN should have a less dramatic impact on your lipid. It’s still a potent, non estrogenic drug, however, and as such will still cause negative changes to HDL and LDL levels in most users when taken in an athletically sufficient dose. Proper monitoring of serum lipids is highly recommended with use, as would be suggested with nearly all cycles. Still, it should be better that something like winstrol or Dianabol. Overall, DMN seems to be potent and comparably less toxic new addition to the world of the underground designer steroids. One must always remember that this is a very potent drug, however, and while likely fairly safe when used responsibly, can be risky (as any steroid can) it abused.

Dimethylnandrolone is currently available only as an underground steroid. No legitimate pharmaceutical company produces it, and it’s not approved for human use in any country. It’s being exclusively produced by a small number of clandestine labs that operate specifically to bring drugs to the black market for sale. The typical formulation of an underground DMN is that of an injectable solution containing 200mcg/mL (micrograms) of drug, although many variations are likely. Given that there’s no significant estrogenic component and relative androgenicity is reduced compared to the primary male androgen testosterone, one should expect that the drug would work like something along the lines of a strong Primabolan depot, with clean, solid gains, not bulk. It must be injected on a daily or every-other-day basis however, and as such would probably be more reminiscent of a stronger form of Primabolan Acetate.

The photo on the prior page is that of a blender product produced by HardCore labs, an underground lab based in Western Europe. This particular item, labelled MT-DMN, includes a hefty 3mg/mL dose of methyltrienolone , one of the most potent synthetic steroids known to man. While the addition of methyltrienolone present a strong added element of potentional hepatotoxicity, there’s little arguing with the results of such a powerful stack. Still more health-conscious individuals will likely stay far away from methyltrienolone and opt to find one of the handful of pure DMN product in circulation at this time.

Given the feedback on the product as of late, they are expected to greatly increase in popularity in the coming months (the fact that DMN is presently unknown to drug testing officials doesn’t hurt either). This steroid may indeed turn out to be a new, “serious player” among designer steroids.

siberiantiger
08-26-2012, 02:27 PM
The effect of 6 weeks MT-DMN on bloodvalues

This is the cycle of a man that has his own vision on using gear. After reading the article of William Llewellyn on MT-DMN he decided to give it a try and to have his bloodvalues checked before and after cycling. The article somewhat scared him off and because he was scared to ruin his body, he decided to inject MT-DMN and DMN on alternating weeks.It’s a shame that he hasn’t done his bloodwork immediately after his cycle, but waited until after his PCT.

I.m.o. he also used to little Testosterone, Sustanon isn’t meant to be shot every day, thus I would have prefered propionate for daily use, but even better a long estrificated Testosterone 700-1000 mg once a week. Beside that I’m convinced that DMN on its own is to weak, so I would prefer the use of just the MT-DMN. Thus first run two weeks of Testosterone enanthate/cypionate or decanoate and then 6 weeks of MT-DMN together with the Testosterone. Followed by 4-5 weeks on Nolvadex and Clomid. Personally I see no use for HCG post-cycle. The time of the post-cycle is because the effect of long-estrificated testosterone slowly declines.

Beside this the given bloodvalues show that a theorical idea often conflicts with the “in vivo” results. Probably because the MT-DMN is meant to be administerd sub-cutanously and therefore is less toxic for the organs and probably stronger in effect. And maybe all toxic effects are just "official" scaremongering.

I cycled 6 weeks with 2 weeks post-cycle. Alternating each week with MT-DMN or DMN. Every day: 1 / 10 of an insulin syringe of MT-DMN or DMN and 25 mg Sustanon. 4 iu growth hormone Post cycle therapy: Pregnyl / GH / Nolvadex. Before the cycle: 45.9 hematocrit (blood viscosity) creatinine 0.83 (kidneys) e-GFR (MDRD) 90 (kidneys) GOT 25 (liver) LH 2.6 (hormones) testosterone 4.68 (hormones) After the cycle: hematocrit 53.2 (should not exceed 53) creatinine 1.30 (should not exceed 1.10) e-GFR (MDRD) 59 (must be greater than 60) GOT 39 (must not exceed 37) LH 11.4 (should be less than 8.8) Testosterone 11.66 (may not exceed 11) A few values where very slightly elevated. Cholesterol, was not checked by the doctor. LH and testosterone were mildly elevated. (Actually they should be reduced after a treatment.) The increase is probably due to the 2 weeks post-cycle (usage of growth hormone and Pregnyl 5000iu plus Nolvadex) The rest of the blood counts were all ok (simular to the values before the cycle)

Underneath the complete bloodvalues.

The text is in the Dutch language because the tests where done in Belgium > Date: Mon, 2 Aug 2010 21:20:01 +0200

> H E M A T O L O G I E

>

> ERYTHROCYTEN 4.59 4.84 4.75 4.2-5.5

> LEUKOCYTEN 6000 * 4170 4610 4300-11000

> LEUKOC. FORMULE St 0.0 0.0 0.0 < 1

> Neutr 55.4 46.9 52.5 50-65

> Eosin 1.9 1.7 1.1 0-6

> Basof 0.4 0.8 0.6 0-2

> Lymfo 34.5 40.3 36.1 25-45

> Monoc 7.8 * 10.3 9.7 3-10

> LYMFOCYTEN (ABSOL.) 2070 1680 1664 1200-3500

> GRANULOCYTEN (ABSOL.) 3324 * 1955 2420 2100-7000

> HEMOGLOBINE 15.1 16.0 15.4 13-17

> HEMATOCRIET 44.8 46.6 46.0 39-50

> M C V 98 96 97 81-99

> M C H 33 33 32 27-34

> M C H C 34 34 33 32-36

> THROMBOCYTEN 1.97 1.83 2.06 1.5-4.0

> IJZER 148 83 55-180

> IJZERBINDING TIBC 370 322 250-400

> IJZERVERZADIGING 40 26 20-50

> FERRITINE 34 66 85 20-360

> VITAMINE B12 978 1059 300-960

> FOLIUMZUUR ERYTHR. 812.0 871.0 > 280

>

> B I O C H E M I E

>

> HbA1c (DCCT) 5.4 5.4 4-6 (T<7)

> CREATININE 1.06 0.78 < 1.2

> URINEZUUR 4.2 4.1 3.5-7.6

> CLEARANCE MDRD (eGFR) 74.3 106.2 > 60

> GPT (ALT) 26 20 < 39

> Y GT 10 10 10-49

> TRIGLYCERIDEN 50 79 < 150

> CHOLESTEROL * 194 * 238 < 190

> HDL-CHOLESTEROL 75 67 > 40

> LDL-CHOLESTEROL 109 * 155 < 115

> RISICOFACT. CHOL/HDL 2.6 3.6 < 5

> LDL-SUBFRAKTIES .

> LDL-1 Cholesterol * 70.4 < 57

> LDL-2 Cholesterol * 30.7 < 30

> LDL-3 Cholesterol 3.1 < 5

> LDL-4 Cholesterol 0.0 < 1

> LDL-5 Cholesterol 0.0 < 1

> LDL-6 Cholesterol 0.0 < 1

> LDL-7 Cholesterol 0.0 < 1

> IDL-A 22.8 < 26.1

> IDL-B 11.9 < 17.1

> IDL-C 23.6 < 24.1

> LDL MEAN PART. SIZE 271.4 > 268.0

> GEOXIDEERD LDL AL 126 < 500

> OMEGA-3-INDEX 6.8 4-7 T > 7

> Lp(a) * 93 * 79 < 30

> MAGNESIUM BLOED 2.90 2.77 2.40-3.7

> 25(OH) VIT D 73.0 62.9 50-120

> VITAMINE E 15.4 14.1 6.9-19.3

> GAMMA-TOCOFEROL 0.41 0.44 0.4-1.6

> HOMOCYSTEINE 10.1 10.5 < 16

> ZINK BLOED 715.0 475-770

> SELENIUM BLOED 113 145 80-234

> UBIQUINONE Coenzym Q10 * 2.1 * 2.0 0.6 - 1.8

> GLUTATHION (GSH) 829 600-1600

> PSA 2.30 2.03 < 4

> VRIJ PSA 0.47

> VRIJ PSA RATIO 23.2 > 16

> CRP < 0.1 0.1 < 0.8

> FIBRINOGEEN 299.0 200-440

>

> T H Y R O I D

>

> TSH 1.12 1.44 0.2 - 4.0

>

> H O R M O N E N

>

> TOTAAL TESTOSTERON 771 529 634 250-1100

> VRIJ TESTOSTERON 22.2 10.3 11.6 6 - 25

> DHEA SULFAAT 231 258 100-440

> S H B G 31.9 12-60

>

> T O X I C O L O G I E

>

> LOOD IN BLOED 3.3 2.4 < 15 MPV 30

> UITZICHT SERUM Licht hemolytisch,Licht troebel

> Normaal Normaal

> VETZUREN-CHROMATOGRAM

> OMEGA 3 . .

> 18:3 alfa-linoleenzuur 0.12 * 0.09 0.1-0.16

> 20:5 eicosapentaeenzuur * 1.66 1.18 0.53-1.43

> 22:5 docosapentaeenzuur 2.42 2.42 2.09-2.66

> 22:6 docosahexaeenzuur * 5.09 4.49 3.17-4.83

> OMEGA 6 . .

> 18:2 linolzuur * 8.90 * 9.40 6.98-8.64

> 18:3 gammalinoleenzuur * 0.01 * 0.01 0.03-0.06

> 20:3 dihomogammalinoleenz 1.27 1.24 1.03-1.51

> 20:4 arachidonzuur * 10.33 * 9.36 10.6-12.9

> OMEGA 9 . .

> 18:1 oleinezuur 9.69 * 10.92 9.5-10.7

> 20:1 eicoseenzuur * 0.29 * 0.24 0.18-0.23

> VERZADIGDE VETZUREN . .

> 14:0 myristinezuur * 0.43 * 0.45 0.20-0.28

> 16:0 palmitinezuur * 17.00 * 17.01 17.3-18.7

> 16:1 palmitoleinezuur * 0.12 * 0.13 0.14-0.30

> 18:0 stearinezuur 13.85 14.05 13.4-14.5

> 20:0 arachidinezuur 0.34 0.36 0.34-0.43

> 22:0 docosaanzuur 1.57 1.80 1.56-1.82

> 24:0 tetracosaanzuur 4.71 * 5.37 4.36-5.00

> VERHOUDINGEN . .

> LA/DGLA * 7.01 * 7.58 < 7.00

> DGLA/AA 0.12 0.13 > 0.10

> OMEGA-6/OMEGA-3 2.21 2.45 2.18-3.71

siberiantiger
09-01-2012, 10:27 AM
A few more products of HCL38703869386838673866

RonnyT
10-07-2012, 02:24 PM
Yo Siberian how do you post these large pictures on here I can't

HCL now is testing Methasterone injectable on bloodvalues. As SuperDrol it was known to distroy livers and kidneys.
They also sell Metribolone at 25 mg/ml In my opinion better subq then oral

phatdaddy77
02-12-2013, 07:04 PM
Whats up sam when you took oral tren how long did it take to start feeling its magic?