Raw Peptide Powder Triptorelin Acetate

Product Name: Triptorelin Acetate
Alias: GnRH,Decapeptyl,Triptorelin
CAS: 57773-63-4
MF: C64H82N18O13
MW: 1311.45
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18 dec. Upon reconstitution of the peptide it should be stored at 4 dec. between 2-21 days and for future use below -18 dec.

Triptorelin, a decapeptide,is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction. It is also used as therapy in cases of gender dysphoria. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals). In the United States, it is sold by Watson Pharmaceuticals as Trelstar. In Iran Triptorelin is marketed under the brand name Variopeptyl.

Raw Peptide Powder Tesamorelin

Product Name: Tesamorelin
Alias: Egrifta
CAS: 218949-48-5
MF: C221H366N72O67S
MW: 5135.9
Grade: Pharmaceutical Grade
Appearance: White Powder

Tesamorelin (INN) (trade name Egrifta) is a synthetic form of growth-hormone-releasing hormone (GHRH) which is used in the treatment of HIV-associated lipodystrophy. It is produced and developed by Theratechnologies, Inc. of Canada.

Tesamorelin is a synthetic peptide consisting of all 44 amino acids of human GHRH with the addition of a trans-3-hexenoic acid group.

Tesamorelin is used for Reducing excess stomach fat in certain HIV-infected patients.

Tesamorelin is a human growth hormone-releasing factor (GRF) analog. It works by stimulating the pituitary gland to release growth hormone (GH). This causes the breakdown of excess stomach fat.

Do Not Use Tesamorelin If:

you are allergic to any ingredient in tesamorelin or to mannitol
you are pregnant
you have cancer, an underactive pituitary gland, or a pituitary gland tumor
you have had your pituitary gland removed, pituitary gland surgery, radiation treatment of the head, or a head injury
Contact your doctor or health care provider right away if any of these apply to you.

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Before using tesamorelin:

Some medical conditions may interact with tesamorelin. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are planning to become pregnant or are breast-feeding
if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
if you have allergies to medicines, foods, or other substances
if you have a history of cancer, noncancerous growths, or diabetes
if you have severe breathing problems (eg, respiratory failure); a serious illness caused by complications from surgery, injury, or trauma; or kidney or liver problems

Some MEDICINES MAY INTERACT with tesamorelin. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticonvulsants (eg, phenytoin), corticosteroids (eg, prednisone), cyclosporine, or sex hormones (eg, estradiol, testosterone) because the risk of their side effects may be increased by tesamorelin.

This may not be a complete list of all interactions that may occur. Ask your health care provider if tesamorelin may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How To Use Tesamorelin

Use tesamorelin as directed by your doctor. Check the label on the medicine for exact dosing instructions.

An extra patient leaflet is available with tesamorelin. Talk to your pharmacist if you have questions about this information.

Tesamorelin is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using tesamorelin at home, a health care provider will teach you how to use it. Be sure you understand how to use tesamorelin. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

Do not use tesamorelin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

Use the proper technique taught to you by your doctor. Inject deep under the skin, NOT into a vein or muscle.

Be sure to rotate your injection site on the stomach area with each dose as directed. Do not inject tesamorelin into scar tissue, bruises, or the belly button.

Tesamorelin needs to be mixed before use. Follow how to mix as you were told by the doctor.

Do not prepare tesamorelin until you are ready to use it. After mixing, use tesamorelin right away and throw away any unused medicine. Do not store prepared doses for later use.

Keep this product, as well as syringes and needles, out of the reach of children and away from pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

If you miss a dose of tesamorelin, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use tesamorelin.

Important safety information:

The safety of long-term use of tesamorelin is not known. Contact your doctor if your condition does not improve while you use tesamorelin.
Tesamorelin is not intended to manage weight loss.

Tesamorelin may raise your blood sugar. High blood sugar may make you feel confused, drowsy, or thirsty. It can also make you flush, breathe faster, or have a fruit-like breath odor. If these symptoms occur, tell your doctor right away.

Diabetes patients - Tesamorelin may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

LAB TESTS, including IGF-I and blood sugar levels, may be performed while you use tesamorelin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Tesamorelin should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.

PREGNANCY and BREAST-FEEDING: Do not use tesamorelin if you are pregnant. It may cause harm to the fetus. Avoid becoming pregnant while you are taking it. If you become pregnant, stop taking tesamorelin and contact your doctor right away. It is not known if this medicine is found in breast milk. Mothers infected with HIV should not breast-feed. There is a risk of passing the HIV infection or tesamorelin to the baby.

Possible Side Effects Of Tesamorelin

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Nausea; night sweats; stomach upset; trouble sleeping; vomiting.

Seek medical attention right away if any of these SEVERE side effects occur:
Severe allergic reactions (rash; flushing; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue); arm, joint, leg, or muscle pain; burning, numbness, or tingling of the skin; decreased sense of touch; fainting or faintness; fast or irregular heartbeat; mental or mood changes (eg, depression); muscle or joint soreness or stiffness; numbness, pain, or weakness in your wrist, hand, or fingers; redness, swelling, itching, pain, irritation, rash, bleeding, or bruising at the injection site; shortness of breath or trouble breathing; swelling of the hands, ankles, or feet; symptoms of high blood sugar (eg, increased thirst, hunger, or urination; confusion; drowsiness; flushing; rapid breathing; fruit-like breath odor).

Raw Peptide Powder TB500

Product Name: TB500
Alias: Thymosin Beta 4 Acetate
CAS: 77591-33-4
MF: C212H350N56O78S
MW: 4963.50
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

TB500 Is Part Of Thymosin Beta 4 Acetate

TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human and animal cells. Thymosin beta-4 is a very large molecule. In fact, it is so large that it cannot fit entirely into the receptor. Different sections of the molecule have different activities. TB-500 is the part of thymosin beta-4 hormone which promotes the most useful effects (overall healing, repair, new blood and muscle cells). For medical applications it is more practical to use the TB-500 instead of the entire Thymosin Beta-4 protein.

Promote Healing

The main purpose of TB500 is to promote healing. It also promotes creation of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons, ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher concentration where tissue has been damaged.

TB-500 is specifically designed to help deal with injured athletes and bodybuilders,it is an injectable peptide drug which can be used to promote healing, enhance range of motion in cases of injury, or reduce pain in case of injury by reducing inflammation.This peptide is also a very potent anti-inflamatory agent.

TB500 is a synthetic peptide that has been directly linked to recovery as it is plays a vital role in building new blood vessels, new small muscle tissue fibers, cell migration and blood cell reproduction. If you are an injured athlete, all of these properties are something that becomes very desirable when looking to speed up the recovery process.

Dosage And Usage

TB500 is distributed as a lyophilized powder that should be kept out of the light and in a cool dry place.  Reconstitution is done with bacteriostatic water or sodium chloride meant for injection.  Doses range from 2-2.5mg twice weekly for 4-6 weeks (some user have reported success in dosing higher up to 8mg a week but how much more effective this is yet to be seen) .  Beyond that, one to two monthly injections of 2-2.5mg of TB500 can be further utilized to maintain rapid recovery and flexibility in strained areas.

For optimal recovery, a combination of TB500 with MK-2866 (Ostarine) should be used.  This combination allows the healing benefits of SARMS and peptides to delivery maximum results.

Side Effects

The positive attributes of TB500 include blood vessel and cell differentiation, growth of new blood cells from pre-existing vessels in dermal tissue, decreased inflammation and increase in flexibility.  The flu like symptoms or lethargy/head rush associated with most peptides does not seem to be widely reported with TB500.  Everybody is different, so always follow the suggested dosing protocols and practice sterile injection techniques.  This will cut down on environmental side effects associated with injections.

Raw Peptide Powder Sermorelin

Product Name: Sermorelin
Alias: Somatoliberin,Sermorelinum,Sermorelina,Sermoreline,GRF 1-29
CAS: 86168-78-7
MF: C149H246N44O42S
MW: 3357.96
Purity: 98.0%min
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

GRF 1-29

Sermorelin is actually known to us by the name GRF (1-29).  The original GFR (1-29) is, in fact, the root of the HGH molecule and that remaining peptide containing the first 29 amino acids is actually what is responsible for stimulating pituitary response.  The name Sermorelin is the prescription drug name and this alone is why it is so widely prescribed by hormone replacement therapy clinics (HRT).

In fact, anti-aging and hormone replacement clinics have been prescribing GRF 1-29 for years because it works as a clean GHRH.  The problem for the bodybuilder or athlete is that it has a very short half-life of about ten minutes.  This becomes an unattractive feature when compared to the half-life of MOD GRF (1-29) (CJC 1295 without DAC), which comes in around 30 minutes.  Despite its short window, it does bind quite effectively to the pituitary receptors.  The other main down side associated with its very short half life is that it is quickly broken down by blood enzymes within minutes.  This is why a GHRH peptide with a half life of 30 minutes or longer is desirable, since it will survive the blood enzyme death and allow it to circulate the body looking for hormone receptors to bind to.

HRT Function

So, why would bodybuilders or athletes want to utilize Sermorelin over other peptides that have longer half lives like MOD GRF (1-29) or CJC 1295 with DAC?  To put it simply, you could easily work this into a multi-dosing protocol along with you other long acting GHRH's and GHRP's. Let's look at Sermorelin's known positive effects like: increased lean body mass, reduced fat, increased strength, improved recovery, better sleep, strengthenining of the heart, enhancing of the immune system and increases IGF-1 production.  Yes, while the ability of Sermorelin to act is short, it still promotes all of these factors stated above. Not to mention it also has the ability to increase protein synthesis, promote growth of all internal organs with the exception of the brain and promote and increase in liver glucogenesis. Despite its tiny half life, Sermorelin's ability to increase IGF-1 in the blood stream will only further increase the function of the metabolism and the growth of new cells in muscles, bones and organs. Sermorelin is heavily pushed by HRT clinics and is often referred to as the anti-aging peptide since it is very good at reversing some of the effects of aging in adults.  The fact that doctors can legally prescribe this peptide helps HRT clinics further their legitimacy and also offer a viable and more cost effective solution to prescribing exogenous HGH.

Dosage And Usage

Sermorelin, along with the other peptides you will use, comes as a delicate lyophilized powder that should be kept out of the light and in a cool dry place.  Reconstitution is done with bacteriostatic water (BC water) or sodium chloride meant for injection.  Injections can be administered one hour before workout at a dose of 200mcg-300mcg.  Normally, Sermorelin injections are taken before bed at around 300mcgs. Of course, as with any GHRH, you will want to use this peptide alongside a GHRP like GHRP-2 or Ipamorelin for maximum release of growth hormone stores.  Ideally, though user could still benefit from using a GHRH like CJC 1295 with DAC and a GHRP like Ipamorelin throughout the day and then utilize Sermorelin as a pre-bed timed dose.  Do not discount Sermorelin as simply an anti-aging peptide.  It can still help promote the growth of lean body mass and increase the availability of IGF-1 in the blood stream.

Side Effects

Sermorelin is pretty mild in terms of side effects, but, like most peptides, it has the ability to bring on head rush, flush feeling, some swelling at injection site, dizziness, and nausea.  I could not find any cases where prolactin or cortisol levels were elevated by the use of Sermorelin. As always, listen to your body and follow a dosing protocol that is in tune with you goals.

Raw Peptide Powder Selank

Product Name: Selank
Synonyms: Selanc
Molar Mass: 751.8
Purity: 98.71%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 5mg/vial

Selank or selanc is a synthetic heptapeptide analog of the endogenous tetrapeptide tuftsin, with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. This synthetic variant of immunomodulatory tetrapeptide tuftsin possesses anxiolytic properties because of its mimic nature. Among this peptide's positive characteristics, are its ability to induce serotonin's metabolic processes and affect the concentration of specific monoamine neurotransmitters. Some scientists believe that Selank possesses such modulatory feature as influencing expression of brain-derived neurotropic factor.

Neuropeptide Selank is a synthetic derivative of the human body's naturally produced tetrapeptide Tuftsin. It is a hexapeptide whith a wide range of uses. Selank is used as an anxiolytic in the therapy of anxiety and phobic disorders, including generalized anxiety. Its action is similar to that of mild benzodiazepins but without the sedative effects. As a selective anxiolytic with a nootropic component, Selank can be used as treatment of depression, fear and general anxiety. It also reduces phsychic tension. This neuropeptide has passed all phases of clinical trials and is now being prepared for registration and mass production.

Selank is closely related to Semax, a hexapeptide previously invented by the same institute. Some consider Selank to be a more efficient alternative to Semax.

Selank As A Nootropic

Recreationally Selank is used to improve one's ability to focus and concentrate, reduce mental fatigue, increase mental sharpness and increase memory and learning capacity. The first noticeable effect is usually stabilization of mood and general feeling of well-being.

Selank As An Antiviral Agent

Selank neuropeptide also expresses immunomodulatory effects. In 2009 a study by F. Ershov et all. has evaluated antiviral properties of Selank both in vitro and in vivo against the influenza virus strain A/Aichi 2/68 (H3N2). The pronounced antiviral effect of Selank was detected in both systems. The highest efficiency - completely supressed viral reproduction was shown when Selank was added to the cell culture 24 hours before inoculation.

Selank Effects

Improvement of learning and memory processes (reference, reference)
Increased sensory attention
Increased curiosity
Increased mental clarity
Restoration of balance of serotonergic and noradrenergic brain system activity (reference)
Anti-anxiety - inhibition of anxiety (reference)
Antiviral activity with no negative effects (reference)
Psychostimulant, anti-asthenic - increased mental energy (reference)
Stabilization of mood and overall feeling of wellbeing
Reversal of anhedonia (restoring the feeling of pleasure)
Potential restoration of catecholaminergic system functions after damage due to drug abuse reference

Raw Peptide Powder PT141

Product Name: PT141
Alias: Bremelanotide,Brmelanotice,BreMelanotide Acetate
CAS: 189691-06-3
MF: C50H69N15O10
MW: 1040.17736
Purity: 99%
Grade: Pharmceutical Grade
Appearance: White Powder

Developed From Melanotan II

Bremelanotide or PT-141, a research chemical and peptide, belongs to the classification known as melanocyte stimulating hormones (MSH).  It is a hexapeptide analog of alpha-MSH, and was originally developed from the MSH Melanotan II, a peptide agent that was reviewed in trials for sunless tanning but, unexpectedly, resulted in sexual arousal and sexual spontaneous erections in nine of ten test subjects.

Bremelanotide is a compound under drug as a treatment for female and male sexual dysfunction, hemorrhagic shock and reperfusion injury. 

Treatment Of Sexual Dysfunction

Bremelanotide or PT-141 is the generic term for a new research peptide for use in helping improve sexual dysfunction in men (erectile dysfunction or impotence) as well as helping improve sexual dysfunction in women (sexual arousal disorder).

PT-141 is a potential remedy for the treatment of sexual dysfunction; specifically, male erectile dysfunction.Bremelanotide, PT-141 does not act on the vascular system like the former compounds but it is known and has been shown to help increase sexual activity in both male and female mammals. Bremelanotide PT-141 allegedly works by activating melanocortin receptors in the brain, therefore helping increase ones sexual stimulation.

Bremelanotide is a novel treatment that could potentially change the face of treating sexual disorders, not only because of its effectiveness due to a unique mode of action, but also due to its safety and the fact it works synergistically with other ED/SAD treatments.

Bremelanotide is effective in its potential to treat sexual desire disorders as well as disorders that affect physical arousal. Bremelanotide induces lordosis in animal subjects, a sign of physical preparation for copulation. In males, it does not stimulate the vascular aspect of the penis, but instead acts to stimulate the central nervous system primarily via dopamine receptor activity to increase sexual desire and also demonstrates functionality in treating purely physical manifestations of ED/SAD, likely through improved signalling.

Co-Administration Pf PT-141 And Sildenafil

Bremelanotide also offers potential as a low-dose concurrent treatment with low-dose sildenafil.

The erectile response induced by co-administration of PT-141 and sildenafil was significantly greater than the response elicited by administration of sildenafil alone. Co-administration of PT-141 and sildenafil was safe and well-tolerated and did not result in new adverse events or adverse events that were increased in frequency or severity compared with monotherapy. Co-administration of intranasal PT-141 and a phosphodiesterase type 5 inhibitor may constitute a treatment alternative for patients in whom higher doses of a single therapy are not effective or well tolerated.

Raw Peptide Powder Pentadecapeptide BPC 157

Product Name: Pentadecapeptide BPC 157
Alias: Booly Protection Compound 15
CAS: 137525-51-0
MF: C62H98N16O22
MW: 1419.53552
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Pentadecapeptide BPC 157, composed of 15 amino acids, is a partial sequence of body protection compound (BPC) that is discovered in and isolated from human gastric juice. Experimentally it has been demonstrated to accelerate the healing of many different wounds, including transected rat Achilles tendon. This study was designed to investigate the potential mechanism of BPC 157 to enhance healing of injured tendon. The outgrowth of tendon fibroblasts from tendon explants cultured with or without BPC 157 was examined. Results showed that BPC 157 significantly accelerated the outgrowth of tendon explants. Cell proliferation of cultured tendon fibroblasts derived from rat Achilles tendon was not directly affected by BPC 157 as evaluated by MTT assay. However, the survival of BPC 157-treated cells was significantly increased under the H(2)O(2) stress. BPC 157 markedly increased the in vitro migration of tendon fibroblasts in a dose-dependent manner as revealed by transwell filter migration assay. BPC 157 also dose dependently accelerated the spreading of tendon fibroblasts on culture dishes. The F-actin formation as detected by FITC-phalloidin staining was induced in BPC 157-treated fibroblasts. The protein expression and activation of FAK and paxillin were determined by Western blot analysis, and the phosphorylation levels of both FAK and paxillin were dose dependently increased by BPC 157 while the total amounts of protein was unaltered. In conclusion, BPC 157 promotes the ex vivo outgrowth of tendon fibroblasts from tendon explants, cell survival under stress, and the in vitro migration of tendon fibroblasts, which is likely mediated by the activation of the FAK-paxillin pathway.

BPC 157 has a strong anti-inflammatory activity in both acute and chronic inflammation models. In fact, preliminary results in clinical trials suggest that BPC 157 may become an important therapeutic tool for the treatment of inflammatory bowel disease. BPC 157 was shown to accelerate wound healing and to have a marked angiogenic effect. In addition, it significantly facilitates the healing of bone fracture in rats. This peptide also exhibits an osteogenic effect significantly improving the healing of segmental bone defect. BPC 157 accelerates the healing of transected rat Achilles tendon and transected rat quadriceps muscle.

Raw Peptide Powder PEG-MGF

Product Name: Pegylated Mechano Growth Factor,PEG MGF
Molecular Formula: C121H200N42O39
Purity (HPLC): 98.0%
Packing: 2mg/vial
Grade: Pharmarceutical Grade
Appearance: White powder

Longer half life of MGF

PEGylation is the act of attaching a Polyethylene glycol (PEG) structure to another larger molecule (in this case, MGF). The PEG acts as a protective coating and the theory here is that this will allow the MGF to be carried through the blood stream without being broken down.

MGF that's pegylated, which means it has the addition of Polyethylene glycol - a non toxic additive that increased the half life of MGF from minutes to hours.  This means its uses and versatility make it a tremendous addition to a bodybuilders arsenal.  I have found it most effective, as its effects are systematic, that means they have a whole body effect wherever muscle has been damaged or is diseased.

PEG MGF Benefits

When your muscle is damaged, your body releases a pulse of an MGF splice variant as I outlined above, followed by a less anabolic longer acting version from the liver.  Therefore, it seems a waste to inject MGF at this time as you will just blunt your body's own release, your not enhancing it.  So using PEG MGF on non workout days is actually the best route.  Since the muscle has been damaged, there are plenty of receptors for MGF, and the effects are systematic.  All muscles will be aided in recovery through increased nitrogen retention, protein turnover, and satellite cell activation.  Recovery is just going to sky rocket.  Doing this means you're increasing the length of your body's own mechanism for muscle repair and growth, and you're opening up the anabolic window.

When you are working out, you are breaking muscles down and the real growth happens when the muscle heals and cells are able to grow and increase in size.  This is where PEG MGF can be utilized as an incredible recovery tool.  PEG MGF can be ran as a standalone peptide post workout, but it's especially useful on recovery days.  By injecting 200mcg bilaterally (subcutaneously or intramuscularly) PEG MGF will bind to receptors and actually help recover damaged muscle tissue better than IGF-1. PEG MGF has also shown to signal satellite cells close to the damaged muscle tissue to grow just as if they were a part of the damaged tissue cells.  This means that damaged cells are going to grow larger and faster, but also it is going to grow cells near the damaged tissue.  In simple terms, this means you're creating new muscle tissue while recovering the already-existing muscles.  This is extremely helpful, considering that as you get older the ability to proliferate satellite cell regeneration decreases drastically.  This leads to age related muscle loss, as you aren't able to create new muscle cells.  This is where MGF comes in!  Mechano growth factor directly increases the availability of muscle cell production; therefore, recovery times from damaged muscle tissue are going to decrease and muscle size is, in turn, increased.

Doses and Usage

Using PEG MGF on cycle or off cycle, you are going to experience recovery that is far superior to any generic peptide available.  Just like normal peptides, remember that PEG MGF comes in the form of a white delicate powder that needs to be reconstituted with bacteriostatic water and kept in the refrigerator.

PEG MGF does not need to be systematically administered because of its long half-life (several days).  It will circulate your body binding to the receptors where muscle tissue damage has taken place.  Administration should be timed post workout or on recovery days when you plan on resting.  Since mechano growth factor is a variant of IGF-1, you do not want to use MGF pre-workout because it will have to fight for position with IGF-1 as they both try to bind to the same receptor.  IGF-1 has a much stronger affinity to bind then MGF.

Rest days are the best way to get the most use out of PEG MGF, as you will have lower level of IGF-1 and the long lasting PEG MGF will have the ability to run the course of the body while you focus on recovery. I have personally ran PEG MGF and administered into the quad regions after very long sessions where my quads were ripped to shreds.  The recovery time and muscle growth in those areas was noticed after one week of use.  Duly noted was the recovery time after a 100+ mile ride. On the recovery day, I administered 200mcg of PEG MGF and rested.  The following day muscles felt recovered and soreness was not present for the next training ride.

An insulin syringe needs to be used to inject subcutaneously or intramuscularly with a dose around 200-400mcg.  Bilateral dosing can be used, but a single site administration will work just as well.

Raw Peptide Powder Oxytocin

Product Name: Oxytocin
Alias: Atonin,,Orasthin,Oxytocinum,Partocon,Pitocin,Piton,Pitupartin,Utedrin
CAS: 50-56-6
EINECS: 200-048-4
MF: C43H66N12O12S2
MW: 1007.19
Purity: 98.0%min
Grade: Pharmaceutical Grade
Appearance: White Powder

Usage: For induction of labor, postpartum oxytocin, and abortion due to uterine atony or retraction caused by the bad uterus bleeding; understand the placental function reserve (oxytocin challenge test); nasal drops can promote milk ejection.

Oxytocin (Oxt) is a mammalian neurohypophysial hormone. Produced by the hypothalamus and stored and secreted by the posterior pituitary gland, oxytocin acts primarily as a neuromodulator in the brain.
Oxytocin plays an important role in the neuroanatomy of intimacy, specifically in sexual reproduction of both sexes, in particular during and after childbirth; its name, meaning "swift childbirth", comes from Greek, oksys "swift" and , tokos "birth". It is released in large amounts after distension of the cervix and uterus during labor, facilitating birth, maternal bonding, and, after stimulation of the nipples, lactation. Both childbirth and milk ejection result from positive feedback mechanisms.

Application

Injected oxytocin analogues are used for labor induction and to support labor in case of difficult parturition. It has largely replaced ergometrine as the principal agent to increase uterine tone in acute postpartum hemorrhage. Oxytocin is also used in veterinary medicine to facilitate birth and to stimulate milk release. The tocolyticagent atosiban (Tractocile) acts as an antagonist of oxytocin receptors; this drug is registered in many countries to suppress premature labor between 24 and 33 weeks of gestation. It has fewer side effects than drugs previously used for this purpose (ritodrine, salbutamol, and terbutaline).

Usage And Dosage

Odinopoeia or oxytocin intravenous drip, once the 2.5 - 5 units, with Sodium Chloride Injection diluted to each 1ml contains 0.01 units. Intravenous drip of the beginning of every minute of not more than 0.001 to 0.002 units, each 15 - 30 minutes increased 0.001 to 0.002 units, to achieve the contractions and normal childbirth is similar, the fastest per minute of not more than 0.02 units, usually 0.002 to 0.005 units per minute.

Control postpartum hemorrhage per minute intravenous drip of 0.02 - 0.04 units, expulsion of the placenta after intramuscular injection of 5 to 10 units.
Lactogenic just before a 2 - 3 minutes, with nasal drops a 3 drop, drop into one side or both sides of the nostril.

Preparation and specification : oxytocin injection (1) 0.5ml:2.5 units (2) 1ml:5 (3) 1ml units 10 units;

Oxytocin nasal drops 1ml:40 units. The induction of labor or prenatal uterine atony: in 2.5-5 units in 500ml 5% glucose for intravenous drip slowly (10-30 drops / minute), maximum time 20 units. (2). Prevention of postpartum hemorrhage: intramuscular injection of 5-10 on each unit, or 5% glucose solution for intravenous drip.

The main contraindication, heart disease, a caesarean history and more than three fetal maternal disable.

Raw Peptide Powder MGF

Product Name: MGF
Alias: Mechano Growth Factor
MF: C121H200N42O39
MW: 2888.16
Purity: 99%
Grade: Pharmarceutical Grade
Appearance: White Powder
Specification: 2mg/vial

2 Kinds Of MGF Splice Variants Of IGF

Mechano Growth Factor (MGF) also known as IGF-1Ec is a growth factor/repair factor that is derived from exercised or damaged muscle tissue.  It's called MGF as IGF-IEa is a bit of a mouthful and harder to identify amongst the other IGF variants.

IGF-1Ec: This is the first phase release igf splice variant and it appears to stimulate satellite cells into activation, This is the closest variant to synthetic MGF.When mechanical overload is introduced to a muscle (as by weight training), the IGF-1 gene released and is differentially spliced during the bodies response. Initially, it it is spliced to produce predominantly IGF-1Ec (called the MGF splice variant of IGF-1). This early splicing stimulates satellite cells into activation. Which in turn allows the activation of extra undamaged nuclei to grow new muscle fiber and tissue. The appearance of MGF also initiates the upregulation of new protein synthesis.

IGF-1Ea: After this initial splicing of IGF-1 into MGF, production then switches towards producing a systemic release of IGF-1Ea from the liver, which also upregulates protein synthesis as well. It is the secondary release of igf from the liver, and its far less anabolic and shorter acting.

The expression of IGF-1 splice variants, over the course of the healing and regrowth phase of muscle repair is thought to be the primary anabolic mechanism by which the body produces new muscle. MGF is available as an injectable peptide, and it has been anecdotally shown that injecting it will cause a response in the area resulting in localized muscle growth.

MGF Benefits

MGF is a splice variant of the IGF gene which increases stem cell count in the muscle and allows for muscle fibers to fuse and mature. This is a process required for growth of adult muscle. Natural MGF is made locally and does not travel into the bloodstream. Synthetic MGF is water based and when administered intramuscularly, travels into the bloodstream. MGF is only stable in the blood stream for only a few minutes.

In bodybuilding this drug is used to accelerate muscle growth. Other effects of the drug include decrease of fat mass of the body, endurance increase, improvement of immune defenceand skin, bone strengthening, lowering of cholesterol level, accelerated recovery. Those who administered MGF declared that they experienced no side effects, which frequently occur with the use of other drugs for gaining body mass.

Muscle Repair Factor

When you train, what happens to your muscles is they break down, the cells are damaged, muscle tissue needs to be repaired and your body produces 2 forms of MGF splice variant. The first initial release of the above mentioned number 1 variant from the liver helps muscle cell recovery, if there is no MGF then muscle cells die.

As muscle is a post-mitotic tissue and as such cell replacement is not a means of tissue repair, if the cells are not repaired they die and your muscles get smaller and weaker.  In muscle tissue, the pool of these stem cells is apparently replenished by the action of MGF, which is produced as a pulse following damage.

Now, with synthetic injections of MGF you can increase the pulse and so speed up recovery, and increase the muscle tissue cells by stimulating satellite cells into full maturity. In terms of dosages, 200mcg bi-laterally is the very best choice of dosing in muscles trained.

Raw Peptide Powder Melanotan II

Bodybuilding Peptide Melanotan II

Product Name: Melanotan II
Alias: MT-2
CAS: 121062-08-6
MF: C50H69N15O9
MW: 1024.180
Purity: 98%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 10mg/vial

Many in the bodybuilding community have already heard of Melanotan II (M2) and its amazing ability to promote darker skin pigmentation.  What many bodybuilders don't realize is that Melanotan II also comes with other added benefits that would be of great interests to those on and off cycle.   These can include weight loss, increased libido and lean body mass.

For a bodybuilder planning to compete on stage, there is a considerable amount of time and attention to detail committed before they are ready to compete.  Being muscled up and defined is only accentuated by a nice tan to make lines and definitions pop out and become more evident to viewers and judges.  Enter the heptapeptide Melanotan II, now bodybuilders can actually protect themselves from over exposure to the sun while boosting melanin.  This results in a darker and more tanned complexion.   When Melanotan II is added to a peptide protocol leading up to a show, it will boost melanin levels, resulting in tanner skin; in addition, it will increase fat loss and muscle hardness.

In addition, central application of the MC3/4-R agonist melanotan-II decreases body fat (increases lipolysis) beyond that accounted for by its ability to decrease food intake.

Dosages And Usage

Like every peptide we have discussed thus far, please remember that peptides come in the form of a white delicate powder and should be stored out of light in a cool dry place.  All peptides need to be reconstituted with bacteriostatic water or sodium chloride specifically used for injections.  In order to use Melanotan II effectively, you need to understand your skin type.  To keep things simple, we can go ahead and break skin types into three categories.

Skin Type 1:  Very fair skin, never tans.  Dosages: 50-60mgs or 5-6vials.
Skin Type 2:  Fair skin, burns but sometimes tans.  Dosages: 30-40mgs or 3-4 vials.
Skin Type 3:  Medium skin, sometimes burns and always tans.  Dosages: 20mgs or 2 vials.
Beyond that, if your pigmentation is already naturally olive or darker, you will need to use less Meanotan II for your tanning needs.  The tan results coupled with exposure to sunlight and UV rays should last a user all summer or through a season.

Daily Dosages vary depending on your needs:

For Erectile Dysfunction (ED): average dose is around 0.025 mgs/kg (1kg = 2.2 lbs)
For Tanning (skin pigmentation): average dose is 0.025-0.030 mgs/kg (1kg = 2.2 lbs)

Side Effects

The side effects associated with Melanotan II are similar to other peptides:  flushed face, headache, feeling dizzy, lethargy, nausea, white patches and possible soreness or redness at site of injection.  The benefits users get from Melanotan II are: darker skin pigmentation, appetite suppression, fat loss, lean body mass, increased libido and frequency of erections.

There is a serious anecdotal note about Melanotan II, some users have experienced serious nausea after using M2.  This is variable from user to user, but has to be a concern.  You need to feel out your dosages and start slow before you go head long into using this peptide.

Raw Peptide Powder Melanotan I

Product Name: Melanotan I
Alias: Afamelanotide,Melanotan,Melanotropin
CAS: 75921-69-6
MF: C78H111N21O19
MW: 1646.845
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White Powder

Usage

Melanotan 1 (also referred to as Afamelanotide) is a synthetic peptide variant of a peptide hormone, called alpha-Melanocyte stimulating hormone or MSH that is naturally produced in the body and is responsible for stimulating melanogenesis, a peptide process for pigmentation of the skin. Alpha-MSH activates certain melanocortin receptors in the process of exerting its effects. Indeed, MSH also exerts potent influence over lipid metabolism, appetite, and sexual libido via these melanocortin receptors. As a result, Melanotan-1 sunless skin tanning effects. While Melanotan 2 and PT-141 have been studied at length as a potential remedies for the treatment of sexual dysfunction, Melanotan-1 has been researched extensively for use in protecting against the harmful effects of ultraviolet radiation from sunlight due to its melanogenesis-stimulating properties.

Both Melanotan-1 and Melanotan 2 are analogs of the peptide hormone alpha-melanocyte stimulating hormone (α -MSH) that tend to induce skin tanning. Unlike Melanotan 1, Melanotan 2 has been shown to have aphrodisiac properties, the additional effect of increasing libido. Melanotan-1 is a non selective agonist of the melanocortin receptors (MC1R, MC3-5R). As an analogue of α -MSH, its mechanism of action is biomimicry of the natural mammalian tanning process.

Raw Peptide Powder Ipamorelin

Product Name: Ipamorelin
CAS: 170851-70-4
MF: C38H49N9O5
MW: 711.853
Purity: 99%min
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Ipamorelin Is A Kind Of GHRP

Ipamorelin is a peptidic, selective agonist of the ghrelin/growth hormone secretagogue receptor (GHS) and a growth hormone secretagogue.It is a pentapeptide with the amino acid sequence Aib-His-D-2-Nal-D-Phe-Lys-NH2 that was derived from GHRP-1.

Ipamorelin or NNC 26-0161, a polypeptide hormone, is a growth hormone secretagogue and ghrelin mimetic and analog.  Ipamorelin belongs to the most recent generation of GHRPs and causes significant release of growth hormone by itself, due both to its suppression of somatostatin (an antagonist to GHRH) and stimulation of release of GH from the anterior pituitary, similar to GHRP-2 and GHRP-6 which are compounds from the same class (growth hormone releasing peptides).  The cells that produce and release GH are known as somatotropes. Ipamorelin acts synergistically when applied during a native GHRH (growth-hormone releasing hormone) pulse or when co-administered with GHRH or a GHRH analog such as Sermorelin or GRF 1-29 (growth releasing factor, aminos 1-29).

The synergy comes both due to the suppression of somatostatin and the fact that ipamorelin increases GH release per-somatotrope, while GHRH increases the number of somatotropes releasing GH. There is also a secondary effect of neuronal excitation in the hypothalamus caused by ipamorelin, which lasts for approximately 3 hours after application, similar to GHRP-2 and GHRP-6.

Compared To GHRP-2 And GHRP-6

Ipamorelin significantly increases plasma growth hormone (GH) levels in both animals and humans.In addition, ipamorelin stimulates body weight gain in animals.Like pralmorelin and GHRP-6, ipamorelin does not affect prolactin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), or thyroid-stimulating hormone (TSH) levels.

However, unlike pralmorelin (GHRP-2) and GHRP-6, but similarly to growth hormone-releasing hormone (GHRH), ipamorelin does not stimulate the secretion of adrenocorticotropic hormone (ACTH) or cortisol, and is highly selective for inducing the secretion only of GH.

Ipamorelin has a unique property among the GHRP class of peptides.  That property is known as selectiveness.  Whereas GHRP-6 and GHRP-2 cause a release and increase in cortisol and prolactin levels, ipamorelin only selectively releases GH at any dose.  Further, a mega-dose of ipamorelin results in a concomitant mega-release of GH (up to the entire amount present in the pituitary), whereas GHRP-2 and GHRP-6 have limits of approximately 1mcg/kg in humans for their maximal GH release.

Ipamorelin Function

Increased energy
Improved sleep and mood
Increased lean muscle mass
Decreased body fat
Increased healing ability
Increased collagen production
No marked effects on FSH, LH, or TSH plasma levels

Raw Peptide Powder IGF-1 LR3

Product Name: IGF-1 LR3
Specification: 0.1mg/vial
CAS: 946870-92-4
Molecular Formula: C400H625N111O115S9
Molecular Weight: 9117.5
Purity: 99%
Grade: Pharmaceutical Grade
Appearance: White cystalline powder

Long arginine 3-IGF-1, abbreviated as IGF-1lr3 or LR3-IGF-1, is a synthetic protein and lengthened analogue of human insulin-like growth factor 1 (IGF-1).It differs from native IGF-1 in that it possesses an arginine instead of a glutamic acid at the third position in its amino acid sequence ("arginine 3"), and also has an additional 13 amino acids at its N-terminus (MFPAMPLLSLFVN) ("long"), for a total of 83 amino acids (relative to the 70 of IGF-1).The consequences of these modifications are that IGF-1lr3 retains the pharmacological activity of IGF-1 as an agonist of the IGF-1 receptor, has very low affinity for the insulin-like growth factor-binding proteins (IGFBPs), and has improved metabolic stability.As a result, it is approximately three times more potent than IGF-1,and possesses a significantly longer half-life of about 20-30 hours (relative to IGF-1's half-life of about 12-15 hours).

IGF-1 is basically a polypeptide hormone that has the same some of the same molecular properties as insulin. IGF-1 dose actually stand for insulin-like growth factor. IGF-1 is mainly responsible for long bone growth in children and it also affects muscle growth and repair of adults. Long R3 IGF-1 is a more potent version of IGF-1. It's chemically altered i like to think "enhanced" to prevent deactivation by IGF-1 binding proteins in the bloodstream. This results in a longer half-life of 20-30 hours instead of 20 min... So that means a far more effective version than the short chain we we re perhaps more familiar with.

IGF-1lr3 What does it do?

IGF-1lr3 greatly boosts muscle mass by inducing a state of muscle hyperplasia (increase in number of new muscle cells) in the MUSCLE WHERE ITS INJECTED!  So think of it as muscle cell proliferation, or even the splitting of the cell so 1 becomes 2... That's why its perfect on cycle when you get increased muscle cell growth too.  But why is IGF-1 better than HGH? The reason being is HGH causes IGF-1 levels to rise in the liver first, then then the muscle, Whereas IGF-LR3 causes localized IGF-1 levels to rocket.

IGF-1lr3 As you all know is the long acting version of Igf-1, Taking its active potential up towards 20 hours, But along with its ability to stimulate the growth of satellite muscle cells and helping them to mature into new muscle fibers it holds the ability to increase the uptake of many supplements we currently use, And it can cause the enhanced recovery of testicle size, and prevent muscle loss even in PCT.  Plus another reason its so potent is because of the decreased binding of Long R3 IGF-1 to all known IGF-1 binding proteins. These binding proteins normally inhibit the biological actions of IGF-1. not so with this long acting version.

Dosage

it is 83 AA analog of IGF-1 and 13 AA extension>It needs to be shot PWO. bilaterally into muscle. Best used in conjunction with other AAS. Inject twice a day due to short half life. No more than 100mcg per day. and for no more than five weeks. Users got great results from 60mcg per day.

Dsage should not exceed 4-5 weeks, and an OFF period should be about the same. Daily dosages work best (split up into 2 seems to make little difference in the Long R3 version) Most people see results at about 40mcg/day, some use as low as 30mcg/day, and some folks even use 80-100mcg. I SUGGEST to ALL first time users no matter what level, to start at about 40-50mcg/day.

Raw Peptide Powder HGH Fragment 176-191

Product Name: HGH Fragment 176-191
Alias: Growth Hormone Peptide Fragment
Purity: 98%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

Fragment 176-191 As An Active HGH Truncated Peptide

HGH Fragment 176-191 is an analog of the growth hormone-releasing factor (GRF) which signals the effects of growth hormone. It is a 15-mer peptide residue of the C-terminus of HGH to which tyrosine is added at the N-terminal end. This synthetically produced hormone is very common to weightlifters and bodybuilders because of a number of physical benefits. Studies claimed that it actually acts on the reduction of excessive adipose tissues such as those in the abdominal area, increase in muscle mass, and enhances the lipid content of the body.

Fat Loss

HGH Frag 176-191 is a fragment of the HGH peptide. Scientists found that if they truncated the peptide at the C terminal region they could isolate the fat loss attributes associated with HGH. Taking this fragment from HGH, including the peptide bonds from 176-191, they found they had developed a peptide that regulated fat loss 12.5 times better than regular HGH.

There is no question as to why bodybuilders of the modern era utilize human growth hormone.  Its ability to regulate fat loss, pack on size and increase IGF-1 levels is just a few of the many attributes that many seek. HGH Frag 171-191 was developed so that bodybuilders and athletes not looking for the growth properties from HGH could still reap all the results of its amazing fat loss properties.

The hgH fragment released fat specifically from obese fat cells but not from lean ones, reduced new fat accumulation in all fat cells, enhanced the burning of fat. In rodents (rats and mice), hgH fragment reduced body fat in obese animals but, enhanced fat burning without changing food consumption or inducing growth (as it does not increase IGF levels) or any other unwanted Growth Hormone effect.

The (hgH fragment 176-191) exhibits the ability to burn through stubborn adipose tissue, while increasing energy expenditure, muscle mass, and fat oxidation. All studies have pointed to the fact that the fragment is an effective treatment for obesity and fat loss, and much safer than its Human Growth Hormone counterpart.

How It Works

Growth Hormone peptide fragment 176-191, also known as HGH Frag 176-191, is a modified form of amino acids 176-191 of the GH polypeptide. The fat-reducing effects of GH appear to be controlled by a small region near one end of the Growth Hormone molecule. This region, which consists of amino acids 176-191, is less than 10% of the total size of the GH molecule and appears to have no effect on growth or insulin resistance. It works by mimicking the way natural Growth Hormone regulates fat metabolism but without the adverse effects on blood sugar or growth that is seen with unmodified Growth Hormone. Like Growth Hormone, the hgH fragment 176-191 stimulates lipolysis (the breakdown or destruction of fat) and inhibits lipogenesis (the transformation of nonfat food materials into body fat) both in animals and humans.

Dosage And Usage

HGH Frag is like all of the other peptides we have covered and come as a delicate lyophilized powder that should be kept out of the light and in a cool dry place. Reconstitution is done with bacteriostatic water or sodium chloride meant for injection. In order to reap the benefits of HGH Frag, users will need to dose around 500mcgs per day.  This can be done by dosing 250mcgs in the morning pre-workout, and 250mcgs before lunch or 250mcgs before bed.  Users will also want to take note of the timing of injections and their diet at that time. It is optimal to inject HGH Frag 176-191 on an empty stomach or with just protein in the stomach. Like other peptides, HGH Frag has been noted to not work as effectively in the presence of carbohydrates and sugars.

Raw Peptide Powder Hexarelin

Product Name: Hexarelin
Alias: Examorelin,HEX,Hexarelin Acetate
CAS: 140703-51-1
MF: C47H58N12O6
MW: 887.04022
Purity: 98%
Grade: Pharmaceutical Grade
Appearance: White Powder
Specification: 2mg/vial

The Strongest Pulse From A GHRP

Hexarelin (HEX) is a peptide GH secretagogue, structurally similar to GHRP-6, in the growth factor family which stimulates the release of growth hormone (GH). It can be used medically to treat GH deficiency.

Hexarelin is another hexapeptide like GHRP-6.For starters Hexarelin is not your average GHRP. The structure of the amino acid is that of a hexapeptide known to help promote the release of growth hormone (GH). Hexarelin has the ability to act both on the pituitary gland and the hypothalamus.  It is known to give the largest release of GH than any other GHRP.

Examorelin releases more GH than does growth hormone-releasing hormone (GHRH) in humans,and produces synergistic effects on GH release in combination with GHRH, resulting in "massive" increases in plasma GH levels even with only low doses of examorelin.Pre-administration of GH blunts the GH-releasing effect of examorelin, while, in contrast, fully abolishing the effect of GHRH.Pre-treatment with IGF-1 also blunts the GH-elevating effect of examorelin.Testosterone, testosterone enanthate, and ethinyl estradiol, though not oxandrolone, have been found to significantly potentiate the GH-releasing effects of examorelin in humans.In accordance, likely due to increases in sex steroid levels, puberty has also been found to significantly augment the GH-elevating actions of examorelin in humans.

Benefits Of Hexarelin

Like other peptides, hexarelin has the ability to help promote more production of natural growth hormone, and it will not shut down the production of the body's ability to produce GH.It also has benefits as below:

The strongest pulse from a GHRP.
Increase LBM (lean body mass).
Help with fat reduction.
Increase bone density.
Anti aging properties heals skin.
Heart protective properties shown to heal heart tissue.

How Does It Work?

When Hexarelin is given as a subcutaneous injection, it activates the pituitary via a pulse, just like GHRP-6, and helps circulate growth hormone in the body.  Unlike GHRP-6, it does not induce any hunger side effects.  Hexarelin has the ability to not only raise the level of GH in the body but to also suppress somatostatin, which is the main culprit that inhibits GH from being released.  This means that there will be more GH in abundance. In addition, hexarelin is the strongest GHRP available, so users should notice that desensitization can come much quicker than other GHRP's. This makes it less ideal for long term use, but with hexarelin's ability to raise healthy levels of IGF-1 and GH it can work perfect as a PCT tool for those coming off a synthetic GH/IGF-1 cycle. The potency of this peptide should not be underestimated and it comes with an increase in cortisol production as well as prolactin.  Nothing close to what might be seen in elevated levels from steroid use, but compared to other GHRP's it has the strongest affinity to raise cortisol/prolactin.

Dosage And Usage

Hexarelin comes in a freeze dried powder just like the other GHRP peptides and storage should be done in a cool dry place until reconstituted and placed in a refrigerator. Bacteriostatic water is used to reconstitute the powder and an insulin syringe is the preferred method for administering subcutaneous injections of hexarelin. Users will notice 200mcgs is the saturation dose for hexarelin and over a few weeks of use total desensitization may begin to take place.

Raw Peptide Powder Gonadorelin

Product Name: Gonadorelin
Alias: Gonadorelin Diacetate,Man Diacetate Salt
CAS: 34973-08-5
MF: C55H75N17O13
MW: 1182.29
Purity: 99.6%
Grade: Pharmaceutical Grade
Appearance: White Powder

Desctiprion

Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. 
GnRH is available as gonadorelin hydrochloride and gonadorelin diacetate tetrahydrate for injectable use. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. It is also used in veterinary medicine as a treatment for cattle with cystic ovarian disease.

Raw Peptide Powder GHRP-6

Product Name: GHRP-6
CAS: 87616-84-0
MF: C46H56N12O6
MW: 873.01
Purity: 98.0%min
Grade: Pharmaceutical Grade
Appearance: White Powder
Specifications: 5mg/vial,10mg/vial

General Information

GHRP-6 is basically a hgH secretagoue, which has the potential to facilitate the effective increase the levels of natural secretion of hgH in our body. At the same time, this compound can also facilitate a sudden increase in body mass and bring about a massive reduction in body fat. GHRP-6 also includes artificial d-amino acids which lead the body to release growth hormones as well. GHRP-6 is not known to work well with GHRH, so it works at the Ghrelin's receptor in place of that receptor.

GHRP-6 is a compound with a unique chain consisting of 6 amino acids which is responsible for telling our body when it has to start releasing the HGH secretions. GHRP-6 also blocks out somatostatin, a hormone which is primarily responsible for stopping HGH secretions from releasing.

The main use of GHRP-6 is promoting food consumption by initiating the feeling of hunger and to improve a person's energy metabolism. This compound has also been extensively used to treat the deficiency of growth hormone along with other complications like cachexia, obesity, and eating disorders.

Although, GHRP-6 is relatively new in the market it has become quite the rage as performance enhancer. It is being made available the market by a few research companies.

How Does It Work?

GHRP-6 directly stimulates the anterior pituitary gland which subsequently leads to an increase in the release of growth hormones in the body. As GHRP-6 directly affects the feedback loop which triggers changes in inhibition of the release of Growth Hormones, it can be used to restore the natural manufacturing of the Growth Hormone if natural secretion has been impaired because of long term artificial use. GHRP-6 also reportedly has an impact on our nervous system. They are potentially capable of protecting neurons and increasing the strength of a person. The functioning of GHRP-6 is strikingly similar to the working of several steroids in the DHT family.

Benefits Of GHRP-6

As discussed earlier, GHRP-6 is a newer drug in the market, but it has caught on the fancy of many who are looking for a shortcut to performance enhancement. The following benefits come after GHRP-6 administration:

Lowers body fat: GHRP-6 administration has the reputation of lowering fat, making it a good option for bodybuilders in their cutting cycles. It is also extremely attractive to those people who are weight conscious and are looking to shed those extra pounds without working hard at the gym.
Increase muscle: GHRP-6 administration also has the reputation of facilitating an increase and development in muscles.
Increase stamina: Those users who are vouching for the drug claim improvement in stamina levels post the administration of GHRP-6.
Protective and anti-inflammatory: GHRP-6 administration initiates better protection of the muscles and acts as an anti-inflammatory agent which is crucial in the muscle recovery process and synthesis.
GHRP-6 also ensures that the liver is working to initiate IGF-1 secretions helping you lose fat quicker and gain strength as the time passes by.

Dosing And Usage

Despite it being third in class as far as strength of GH release, GHRP-6 is still a potent GHRP and can be taken 2-3 times per day. Though there is a slight issue, GHRP-6 has been shown to not be as effective in the presence of elevated blood glucose levels. As a result, I believe the best practice for GHRP-6 dosing is to dose 2 hours after your last meal and 30 minutes before you take in any food, so that no interactions weaken the effect of GHRP-6. Taking this into consideration, GHRP-6 can be taken 2-3 times a day (approximately 3 hours in between injections) for maximum effectiveness with a range of 100mcg-200mcg per dose.