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Xeno Laboratories
Buy Metribolone by Xeno Labs at XSteroids. The pack holds oral methyltrienolone tablets, the compound written about in the sport as oral tren. This page explains what the molecule is, why it was abandoned as a medicine before it ever reached a pharmacy, how it behaves at the androgen receptor, why every serious reference measures it in micrograms and limits the block to a fortnight, and where the liver conversation becomes the whole conversation.
Methyltrienolone is a research reference compound first and a bodybuilding curiosity second. It is the standard labelled ligand in laboratory work on androgen receptors, and it is sold here as a Xeno Labs research item rather than a medicine. Nothing below was measured on this batch.
A sealed pack of oral methyltrienolone tablets. The official brand page for this product prints the packing, 50 tablets, but leaves the strength field blank, and no independent assay of the batch has been published. The description therefore does not invent a milligram figure; it sets out how the compound is used in the literature instead.
The chemistry places it in the trenbolone family. Methyltrienolone is trenbolone carrying a methyl group at the 17-alpha position, which makes it orally active and, in the same stroke, one of the most demanding oral steroids described anywhere. It was examined in early research, showed potency that interested investigators, showed liver injury that did not, and was never brought to market.
The 17-alpha-methyl group allows the tablet to survive the first pass through the liver, so an effective amount reaches the bloodstream after swallowing. Its affinity for the androgen receptor is higher than testosterone's, and it also binds the progesterone receptor while barely interacting with sex hormone binding globulin, so almost all of what circulates is free and immediately active.
That combination is why the compound is so visible in the laboratory. R1881, as it is catalogued in research, is used as the reference ligand in receptor binding assays precisely because it attaches so strongly and so specifically. The same strength that makes it a good scientific tool makes it a poor choice for anything resembling a normal cycle.
Once bound, it increases protein synthesis and nitrogen retention with unusual force and produces no estradiol at all, since there is no aromatisation pathway available to it. The effect appears fast and ends fast.
Users who write about this compound describe a change measured in days rather than weeks: hardness, density and a sharp rise in strength, with an appearance that looks almost dry to the point of flatness. Total weight gain is modest, and the look is not soft in any way.
What follows is the part that matters. Appetite usually collapses within the first week or two, energy drops, and the drug is widely described as making ordinary life unpleasant. Symptoms that point at the liver, including nausea, dark urine and pain under the right ribs, are treated as stop signals rather than side effects to tolerate.
The third expectation is that nothing here is sustainable. No reference material presents a long methyltrienolone block as a reasonable idea, and the compound is generally discussed as a last experiment rather than a plan.
Every serious source measures this drug in micrograms, not milligrams, because of how tightly it binds the receptor. Reported amounts sit in the hundreds of micrograms per day, and the block is measured in days to about two weeks rather than weeks to months.
The liver carries the dose. Enzyme elevation on this compound is not a rare footnote; it is the expected response, and published discussion of the molecule centres on hepatocellular injury. Extending the block past roughly a fortnight means accepting liver stress that no amount of training justifies.
Liver enzymes before, during and after; the lipid panel; blood pressure; and a clear list of anything else the user is taking, since alcohol or a second oral steroid alongside methyltrienolone stacks the hepatic load directly. Any laboratory result outside the normal range is a reason to stop, not to adjust.
The honest recommendation is not to stack it at all. Adding another 17-alpha-alkylated oral multiplies liver stress without adding a result, and the compound is potent enough on its own that extra anabolics contribute little. Where a base is used out of necessity, it should be an injectable and a modest one: Testosterone Esters from Xeno Labs at replacement-level dosing rather than a heavy cycle.
Anyone looking for a comparable hardening effect without the hepatic risk is better served by a different molecule entirely. Trenbolone Esters from Xeno Labs deliver the trenbolone effect by injection and skip the oral liver burden, while Drostanolone and Anavar (oxandrolone) cover hardening and lean tissue at a fraction of the risk.
Suppression is severe, and the axis does not restart by itself. Because the compound clears within days, a SERM can begin soon after the final tablet, but the recovery period should be planned as generously as possible given how hard the run was on the whole system.
Either Tamox (tamoxifen) or Clomiphene from the Xeno range can carry the restart, usually for four to six weeks. Liver values need their own repeat test after the block, separately from the hormone panel, and training should stay light until both have settled.
This is the single most hepatotoxic oral steroid in common circulation, and there is no way to write around that. The 17-alpha-methyl group forces the liver to process the molecule on every pass, the dose is concentrated, and the injury described in the medical literature is serious rather than cosmetic. Elevated transaminases are expected; more severe damage has been reported.
Nothing about this product is a first experience, a summer experiment or a beginner option. Methyltrienolone was never a licensed medicine, it is banned in sport under the WADA S1 class, and it is supplied here strictly as a research reference. The page is informational and is not medical advice. Anyone with existing liver disease, regular alcohol intake or a second oral steroid in the plan should not be considering it at all.
Keep the pack closed in a dry cupboard at room temperature, away from direct light and away from the humidity of kitchens and bathrooms. Read the batch and expiry printing before the first tablet, keep the tablets in their blister, and discard any that have softened or discoloured. Because the block is so short, no opened pack should ever be left half used for months.
Metribolone can be found in the Xeno Labs range on this site, beside the safer compounds most users end up choosing instead and the recovery products a short block still requires. Checkout is encrypted; a parcel usually reaches a US address in three to six days and an international one in twelve to twenty-six. The related cards below contrast this tablet with the compounds normally chosen in its place.
It is a pack of oral methyltrienolone tablets sold by Xeno Labs as a research product. The molecule is a methylated form of trenbolone that binds the androgen receptor more tightly than testosterone, does not aromatise, and was abandoned in early research because of severe liver toxicity. Its catalogue name in science is R1881.
Because it binds the androgen receptor far more strongly than testosterone and circulates almost entirely unbound, since it barely attaches to sex hormone binding globulin. Reported amounts sit in the hundreds of micrograms per day rather than in milligrams. That potency is also the reason the liver burden rises so quickly.
Days to roughly two weeks, and no longer. Enzyme elevation is an expected response rather than an occasional one, and the medical discussion of the compound centres on liver injury. Reference material treats the drug as a very short exposure at a microgram dose, never as a conventional multi-week oral cycle.
Yes, and that is its defining characteristic. It is widely described as the most hepatotoxic oral anabolic in circulation. Transaminase elevation is expected within a short block, and more serious injury has been documented. Alcohol, another oral steroid or existing liver disease make the risk substantially worse, and any abnormal result is a reason to stop.
It binds the androgen receptor with higher affinity than testosterone and also binds the progesterone receptor, while showing almost no affinity for sex hormone binding globulin. That profile is why the compound is used as the reference labelled ligand, R1881, in laboratory receptor binding studies rather than as a therapeutic drug.
Yes, but it has to be planned. The compound clears within days, so a SERM such as tamoxifen or clomiphene can start shortly after the last tablet and run for four to six weeks. Liver values are repeated separately, training stays light until they normalise, and another oral steroid should not follow soon afterwards.
You can buy Metribolone by Xeno Labs online at XSteroids, direct from the brand catalogue. Add the 50 tablet pack to the cart on this page and complete checkout securely. US domestic shipping takes three to six days and international delivery twelve to twenty-six days.
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