Blackstone Labs Brutal 4ce

Blackstone Labs Brutal 4ce

Rating: 9.6/10

Product Description:

Increases Lean Muscle Mass & Not Liver Toxic! Blackstone Labs is blazing the trail atop the supplement game once again with our new innovation, Brutal 4ce. As the saying goes, “It’s not what you do, it’s how you do it.” This is exactly why Brutal 4ce, 4-DHEA, will take the industry by storm. Brutal 4ce (4-DHEA) is a 2-step precursor, first converting to androstenediol, then to androstenedione, and then to testosterone. Conversion often gets interrupted in digestion, so we have implemented a highly scientific delivery method called Liposomal technology to remedy this. 4-DHEA has been around in the nutritional supplement industry for years, but never delivered in this way. We that are revolutionizing the game with this amazing compound. Through the groundbreaking, scientific liposomal delivery system, we have made 4-DHEA 99% bioavailable during the 2-step conversion process to testosterone. This makes Brutal 4ce extremely efficient compared to similar products from 10-15 years ago. LIPOSOMAL DELIVERY SYSTEM Liposomal technology has long been used in the medical field as a carrier for drugs, but only now has this innovation made its way into nutrition supplements. This new direction and employment of liposome science is in part due to the low absorption and bioavailability rates of older oral dietary and nutritional tablets and capsules. The low oral bioavailability and absorption of many nutrients is well-documented clinically. Being a hydrophobic (fat-soluble) molecule, 4-DHEA traditionally has been difficult to effectively get into the blood, which is hydrophilic(water-soluble). The natural encapsulation of hydrophobic nutrients within liposomes has made for a very effective method of bypassing the destructive elements of the and aiding the 4-DHEA to be delivered to the cells. Liposomes have a hydrophobic core with a hydrophilic shell, which simultaneously protects the molecule from degradation while allowing it be more soluble and get into the bloodstream. This is truly a breakthrough delivery technology that sets Brutal 4ce apart from other 4-DHEA products on the market. We have also attached esters to the compound in Brutal 4ce, creating an environment for sustained release of the 4-DHEA throughout the time of use. Esters are added to the molecule to control its release, which eliminates the need to be dosed throughout the day on a manually timed schedule. We included the undecanoate and caprylate esters, as well as the unesterified 4-DHEA to provide prolonged elevated levels with multiple peaks. A simple AM/PM dosing schedule is all you need for optimal results. No more setting your alarm to take pills. Brutal 4ce (4-DHEA) by design is non-methylated and does not affect the liver like most steroidal products have in the past. The liver contains the necessary enzyme needed to convert 4-DHEA into testosterone, but this process does not, in any way, harm liver function. You can expect a serious amount of muscle and strength to be added with Brutal 4ce. This is a serious compound for serious bodybuilders and athletes looking to pack on the mass on short notice. Just because the negative side-effects are non-existent, does not mean you won’t be experiencing some of the best results of your life. Huge pumps in the gym and adding weight to the bar each workout is not an overreach of expectations. Your GH and IGF-1 levels will be hitting new highs as well as your sex drive – a nice perk. Arguably, the best part about Brutal 4ce is that it is 100% legal!! In 2004, several anabolic precursors in nutritional supplements were banned by the American government. Among them were the precursors of testosterone. However, in the Anabolic Steroids Control Act almost no steroids with a C17 carbonyl group are mentioned. That means 4-DHEA is 100% above board!

Brutal 4CE

Blackstone Labs Chosen 1

Blackstone Labs Chosen 1

Rating: 9.2/10

Product Description:

Increase Muscle Mass With No bloating Or Water Retention! Just when you thought the testosterone game was over, Blackstone Labs has rewritten the playbook once again. Introducing Chosen 1 (1-DHEA), one of the two highest-powered proandros available anywhere in the world. Chosen 1 (1-DHEA) is not a steroid, however, it is a unique precursor to a powerful testosterone derivative known as 1-testosterone. It isn't the exact version of natural testosterone produced in the body, but differs from actual testosterone only by a double bond isomer. As a complex compound, they are both different, however 1-testosterone is considered much more potent. It has an anabolic:androgenic ratio of 1:2, meaning drier gains and more aggression in the gym. 1-DHEA has been around in the nutritional supplement industry for years, but never delivered in the way we that are revolutionizing this amazing compound. Through the groundbreaking scientific liposomal delivery system, we have made the 1-DHEA you’ll be ingesting 99% bioavailable during the 2-step conversion process from androstenediol, to androstenedione, and finally to 1-testosterone. This makes Chosen 1 extremely efficient compared to similar products from 10-15 years ago. LIPOSOMAL DELIVERY SYSTEM Liposomal technology has long been used in the medical field as a carrier for drugs, but only now has this innovation made its way into nutrition supplements. This new direction and employment of liposome science is in part due to the low absorption and bioavailability rates of older, oral dietary and nutritional tablets and capsules. The low oral bioavailability and absorption of many nutrients is clinically well-documented. Being a hydrophobic (fat-soluble) molecule, 1-DHEA traditionally it has been difficult to effective get into the blood, which is hydrophilic(water-soluble). Therefore, the natural encapsulation of hydrophobic nutrients within liposomes has made for a very effective method of bypassing the destructive elements of the gastric system and aiding the 1-DHEA to be delivered to the cells. Liposomes have a hydrophobic core with a hydrophilic shell, which simultaneously protects the molecule from degradation, while allowing it be more soluble to get into the bloodstream. This is truly breakthrough delivery technology that sets Chosen 1 apart from other 1-DHEA products on the market. We have attached esters to the compound in Chosen 1, creating an environment for sustained release of the 1-DHEA throughout the time of use. Esters are added to the molecule to control its release, which eliminates the need to be dosed throughout the day on a manually timed schedule. We included the undecanoate and caprylate esters, as well as the unesterified 1-DHEA to provide prolonged elevated levels with multiple peaks. A simple AM/PM dosing schedule is all you need for optimal results. No more setting your alarm to take pills. Chosen 1 (1-DHEA) is a derivative of DHT, which cannot aromatize into estrogen. Many other products formerly on the market did not have this luxury. As a result, the aesthetic side-effects, such as water retention and gynecomastia, are at a very low probability. Chosen 1 (1-DHEA), by design, is non-methylated and does not adversely affect the liver like most steroidal products have in the past. The liver contains the necessary enzyme needed to convert 1-DHEA into 1-testosterone, but this process does not in any way harm liver function. Arguably, the best part about Chosen 1 is that it is 100% legal!! In 2004, several anabolic precursors in nutritional supplements were banned by the American government. Among them were the precursors of testosterone. However, in the Anabolic Steroids Control Act almost no steroids with a C17 carbonyl group are mentioned. That means 1-DHEA is 100% above board!

Chosen 1

Test Force2 by E-Pharm

Test Force by E-Pharm

 

Rating: 9.7/10

Product Description:

Dual Action Natural Testosterone Elevator! TestForce2 contains the most soluble form of d-aspartic acid combined with another remarkable amino acid known as sarcosine. This combination provides results clearly superior to other d-aspartic acid product formulations. In case you aren't aware, d-aspartic acid is the hottest supplement ingredient on the market right now. It has more scientific literature supporting its ability to act as a natural regulator of anabolic hormone (i.e. testosterone, growth hormone) release in the body than any supplement ingredient EVER. And E-Pharm was the company to bring you the premium form of d-aspartic acid d-aspartate calcium chelate. This form is more than 75 times as water soluble as regular d-aspartic acid and soluble over a wide pH range. This ensures the most rapid and complete absorption possible. And now E-Pharm has taken the lead in d-aspartic acid technology again with the patent pending addition of the amino acid sarcosine. Why Sarcosine? Let's start with some background. When d-aspartic acid (DAA) is ingested it is absorbed into the body and taken up preferentially by endocrine tissues such as the hypothalamus, pituitary, and testicles. There it stimulates the activity of what are known as NMDA receptors. NMDA receptors are located on neurons and they regulate neuronal activity. DAA binds to a specific docking site (receptor) located on the NMDA receptor known as NMDA binding site. In the hypothalamus the stimulation of NMDA receptors leads to the production of gonadotropin releasing hormone (GnRH). GnRH then stimulates the pituitary gland to release luteinizing hormone (LH) and follicle stimulating hormone (FSH). LH and FSH then in turn travel to the testicles to initiate the process of steroidogenesis, which leads eventually to the release of testosterone into the blood stream. Stimulation of NMDA receptors in the hypothalamus also leads to the release of growth hormone releasing hormone (GHRH) which in turn promotes the release of growth hormone from the pituitary gland. So the key here is the NMDA receptor. The more you activate this receptor in the hypothalamus the greater the release of GnRH and GHRH, and ultimately testosterone and growth hormone. The NMDA receptor is somewhat unique in that it requires activation by two ligands (a ligand is like a key to a receptor). In the hypothalamus the main ligand for the NMDA receptor is d-aspartic acid. The secondary ligand (or co-activator) is the amino acid glycine. Both DAA and glycine have specific binding sites on the NMDA receptor. These sites are known as the NMDA binding site and the glycine binding site respectively. Think of it this way - just like how firing a nuclear missile requires two soldiers to turn two separate keys, so the NMDA receptor requires binding by two ligands to initiate its influence on the firing of a neuronal signal. So to review, administration of DAA leads to it's uptake into the hypothalamus and binding to the NMDA receptors there. And to activate the NMDA receptor you also require adequate levels of ligands that bind to the glycine site of the NMDA receptor. Now common sense would lead one to assume that by ingesting supplemental amounts of glycine would ensure that glycine site co-activation is ensured. However the scientific literature has shown that this method has limited efficacy. The reason that glycine administration is not very effective at stimulating NMDA activity is not completely straight forward, but one reason is because it is efficiently removed from the synapses by the reuptake regulator Glycine Transporter 1 (GT1). Interestingly, much of the science published on the subject of stimulation of NMDA receptor activity revolves around the theory that NMDA receptor hypo-activity is a causative factor in schizophrenia. For years scientists have been investigating ways to stimulate NMDA activity as a means for treating schizophrenic patients. One of the most effective strategies has been through targeting the GT1 protein. And one of the most efficient means to do this is actually through supplementation with sarcosine. Of course we aren't concerned about treating schizophrenia here, what we are concerned with is maximally stimulating natural production of testosterone (or growth hormone). But the mechanism in question is exactly the same for both purposes. By blocking the re-uptake of glycine you increase the concentration of glycine in neuronal synapses, and therefore increase the influence of NMDA upon nerve transmission. In essence this is the exact way some anti-depressants (such as SSRIs) work, except the goal there is to increase binding and activating of serotonin or dopamine receptors, not NMDA receptors. Blocking glycine reuptake is not the only mechanism through which sarcosine stimulates DAA activity. Sarcosine actually can itself bind to the glycine binding site of NMDA receptors. In fact, it binds with a higher affinity than even glycine. So basically it replaces glycine as well as serves as its own reuptake inhibitor. It totally solves the glycine co-activation issue in one shot. Knowing all these facts you can see why sarcosine produces a rather dramatic effect on NMDA neuronal transmission compared to glycine itself, or other endogenous ligands for the glycine receptor such as d-serine. test force2 Conclusion To summarize, for d-aspartic acid to work to its maximum potential it must be taken with an efficient stimulator of the glycine binding site on the NMDA receptor. The most efficient non-drug stimulator we know of is the natural amino acid sarcosine. TestForce2 contains 3 grams of d-aspartic acid (as d-aspartate calcium chelate) and 3 grams of sarcosine per serving. It also is flavored with a light fruit punch flavor and slightly sweetened to provide a very pleasurable taste experience. It dissolves almost instantly. So if you like d-aspartic acid you will love TestForce2. And if you were one of the few non-responders to d-aspartic acid then you will also love TestForce2 because you will no longer be a non-responder. You would be a fool to settle for any other d-aspartic acid supplement.

Test Force2 by E-Pharm