PEPTIDES

CJC-1295 W/ DAC
CJC 1295 W/DAC is a synthetically produced peptide that can dramatically increase your plasma
growth hormone levels.

CJC 1295 can increase IGF-1 levels and GH (growth hormone) levels in humans and in animals. DAC
is added to this peptide in order to increase the half-life of CJC-1295. Initially CJC 1295 was developed
to treat diseases and medical conditions for patients who had muscle disorders, diseases, and burn
victims. CJC 1295 has drawn many individuals like athletes from around the globe for its incredible
benefits and minimal side effects to enhance their performance on the field, and in the gym.

EFFECTS: Numerous studies have shown that CJC-1295 builds muscle mass, decreases body fat, and
otherwise benefits adult users by improving sleep quality and elevating ones own endogenous levels of
HGH.

DOSING GUIDELINES: For best effects, CJC-1295 should be administered three times per week.
Dosing ranges vary between 200mcg-300mcg per dose. A typical dosing schedule would be Monday,
Wednesday and Friday, dosed in the evening approximately two to three hours after your last meal. CJC-
1295 can be dosed subcutaneously or intra-muscularly.
STACKING: CJC-1295 W/DAC is in a family of peptides known as a GHRH (Growth Hormone
Releasing Hormone). To reap the optimal benefits of CJC-1295 it is common to stack it with a GHRP
(Growth Hormone Releasing Peptide) such as GHRP2 or GHRP6. The two peptide families work
synergistically to promote optimal GH secretion, muscle building and fat loss.
 HGH FRAGMENT 176-191
HGH Fragment 176-191 is a modified form of amino acids 176-191 at the C-terminal region of the human growth hormone (HGH).
Studies have shown that it works by mimicking the way natural HGH regulates fat metabolism but without the adverse effects on
insulin sensitivity (blood sugar) or cell proliferation (muscle growth) that is seen with unmodified HGH. Like unmodified GH, the
HGH fragment 176-191 stimulates lipolysis (breaking down of fat) and inhibits lipogenesis (the formation of fatty acids and other
lipids in the body).
EFFECTS: HGH fragment 176-191 is meant to be 12.5 times stronger than human growth hormone (HGH) for weight loss than
standard human growth hormone (HGH). Of particular note is that in studies HGH fragment 176-191 had the ability to increase IGF-1
levels which translates into the fragments ability to give anti-aging and MUSCLE SPARING EFFECTS during periods of caloric
restriction such as contest prep or dieting for a special event.
DOSING GUIDELINES: HGH Fragment can be dosed at 500mcg twice per day AM/PM on an empty stomach or three times per day at
300mcg for similar effects. For best effects, one of the daily doses should be administered 30 minutes prior to exercise. HGH Fragment should
be administered subcutaneously.
COUPLING: HGH Fragment 176-191 can be stacked with HGH for dramatically increased fat loss effects. A typical coupling dose would be
300mcg of HGH Fragment with 1-1.5iu of HGH three times per day or 500mcg of HGH Fragment and 2iu of HGH twice per day. HGH
Fragment can also be combined with Helios and T5 for even more increased effect.
 GHRP2
GHRP-2 is a Growth Hormone Releasing Peptide (GHRP) that does not affect appetite or induce a hunger
effect. It is a single chain of six amino acids that can stimulate release of ghrelin or can replace low levels
of growth hormone in the body. It is a hormone that can help with fighting anti-aging problems.

EFFECTS: Decreased body fat, increase lean body mass, improved sleep, increase in IGF-1 production,
increase in bone density and increase in cellular repair. GHRP-2 injections are beneficial for bodybuilders
and athletes seeking to increase muscle mass, shed fat and improve performance.

DOSING GUIDELINES: GHRP-2 should be used around 100mcg-300mcg per injection. GHRP-2
should be used only up to 2-3 times a day.

STACKING: GHRP-2 Can be stacked with a GHRH (Growth Hormone Releasing Hormone) such as
CJC-1295 W/DAC, Mod GRF (CJC-1295 no DAC) or Sermorelin for enhanced effects.
 GHRP-6
• GHRP-6 is a Growth Hormone Releasing Peptide (GHRP) like GHRP-2, but it targets the pituitary
to secrete the growth hormone that you have stored. GHRP-6 can increase hunger after injection by
increasing the amount of the hormone ghrelin, which is produced in the stomch and signals the
feeling of hunger or empty stomch, GHRP-6 not only works in releasing stored growth hormones,
but also regulates appetite, promotes fat loss through nutrient repartitioning, builds and repairs
muscle tissues and helps in healing damaged tendons.
• EFFECTS: GHRP-6 will aid in body fat reduction, appetite, muscle growth and quality of sleep. It
is also effective in recovery protocols in healing sports related injures such as minor sprains and tears

• DOSING GUIDELINES: GHRP-6 should be dosed at 100mcg 20-30 minutes after each meal up to
three times per day.

• STACKING: For optimal effects, GHRP-6 should be paired with a GHRH such as CJC 1295 or
Sermorelin.
 HEXARELIN
Hexarelin is a synthetic growth hormone secretagogue. It is derived from GHRP-6 and has effects similar to
ghrelin. The primary function of hexarelin is to increase plasma levels of growth hormone and promote the
development of lean body mass. Indirectly, hexarelin has been shown to improve cardiac function, lower lipid
levels, and protect against the effects of certain chemotherapeutic agents. The peptide is currently under
investigation for its ability to mitigate the effects of certain metabolic diseases, such as diabetes.

EFFECTS: Like GHRP-6, hexarelin causes substantial, dose-dependent increases in growth hormone. In fact,
hexarelin causes more substantial increases in growth hormone than naturally secreted growth hormone releasing
hormone.

DOSING GUIDELINES: Hexarelin is most commonly dosed at 200-300mcg once per week for a duration of no
more than six weeks before taking a 2-3 week break. Hexarelin is best used at lower doses and in combination with
milder GHRP’s such as GHRP-2 and or Ipamorelin.

RESEARCHERS CAN EXPECT Modest increases in lean body mass, improved sleep, increased fat loss. This
peptide is very commonly used in calorie restricted situations to preserve lean muscle such as contest preparation or
short term, extreme dieting in preparation for a photo shoot or other special event.

 
 IPAMORELIN
Ipamorelin is a penta-peptide hormone, a growth hormone secretagogue and a small molecule
ghrelin mimetic. Ipamorelin belongs to the most recent generation of GHRPs and causes significant
release of growth hormone. Similar to GHRP-6 and GHRP-2, it suppresses somatostatin and
increases the stimulation and release of Growth Hormone (GH) from the anterior pituitary. It acts
very similarly to GHRP-6 without the increase in appetite.

EFFECTS: Increases in lean body mass, decreased body fat, anti-aging properties (faster recovery),
Improved sleep and mood elevation. This peptide is very mild and perfect for researchers new to
peptides.

DOSING GUIDELINES: Dosing for Ipamorelin is 200-300mcg two to three times daily. Twelve
week cycles are quite normal. Ipamorelin is best when stacked with a GHRH. Cabergoline or
Pramipexole should be kept on hand in the event prolactin issues arise as well Aromasin and or
Letrozole if estrogenic side effects are experienced. Ipamorelin is administered subcutaneously.
 ACE-031
Ace-031, also known as ACVR2B, is a soluble form of activin type IIB receptor, which is an
inhibitor of myostatin and other naturally occurring proteins that limit muscle growth.  This
compound was genetically developed to bind to myostatin before it can attach to its receptor and halt
muscle growth.

EFFECTS: Pronounced increase in lean body mass, increased fat loss, increased bone density.

DOSING GUIDELINES: Initial research used doses of 1-3mg per kilogram of bodyweight, once
per month. Common practices however seem to be doses of 1-3mg per month regardless of
bodyweight, which, when used as a part of a comprehensive approach utilizing GHRP’s and
GHRH’s still yields respectable results at an affordable cost. ACE can be administered
subcutaneously or intramuscularly based on individual preference.
 FOLLISTATIN 344
• Follistatin 344 is a protein used in order to increase muscle mass through the suppression of
myostatin. Scientists discovered it while they observed the porcine follicular fluid in the ovaries.
This protein can be found in the skeletal muscle of humans and other mammals, containing
carbohydrates attached to it. Follistatin 344 was the first autocrine glycoprotein supplement to
become popular in search of the increased tissue mass

• EFFECTS: Pronounced increase in lean body mass. Notable strength increase.

• DOSING GUIDELINES: Doses of 100mcg per day for cycles ranging from 10-30 days. Like all
myostatin inhibitors, best results are achieved when used in combination with GHRP’s, GHRH’s
and Growth Factors such as PEG-MGF, IGF-1 DES and IGF-1LR3. Follistatin can be
administered subcutaneously or intramuscularly based on individual preference.
 AOD-9604
HGH Fragment 176-191 Evolved
AOD-9604 (Advanced Obesity Drug) also known as Lipotropin is a drug used in obesity treatment. It is
a peptide derived from amino acids 176-191 of the GH polypeptide, which enhances fat reducing effects.
One of the advantages of this drug is the absence of adverse effects on blood sugar and insulin resistance.
AOD-9604 has shown potential effects to repair cartilage and muscle, and it is often used in the
treatment of osteoarthritis.

EFFECTS: Enhanced fat burning, increased lean body mass, enhanced recovery and joint health.

DOSING GUIDELINES: Typically dosed in the vicinity of 300mcg at bedtime. This peptide works
extremely well when incorporated into a comprehensive weight/fat loss program utilizing stimulatory
compounds during waking hours and AOD being administered in the evening to keep lipolysis on-going
during sleep. AOD is administered subcutaneously for best effect.
 DSIP
DELTA SLEEP INDUCING PEPTIDE
• DSIP (Delta Sleep-Inducing Peptide) is a neuropeptide that induces sleep. It induces the
spindle and delta EEG activity and reduces motor activities. DSIP is classified as an
amphiphilic peptide, which represents a chemical compound possessing both hydrophilic
and lipophilic properties. This substance has been found in the hypothalamus, limbic
system, pituitary and in other organs such tissues and body fluids. This peptide is found
abundantly in the gut secretory cells and in the pancreas.

• EFFECTS: Creates a general feeling of relaxation and increases ones ability to fall asleep
and stay asleep. Deceases cortisol levels, Stimulates the release of luteinizing hormone
(LH), Increases the release of Growth Hormone Releasing Hormone(GHRH), Normalizes
blood pressure, may improve body composition as a result of decreased cortisol levels.

• DOSING GUIDELINES: DSIP is typically dosed between 200-300mcg 30-45 minutes before
bed time. Researchers will have to determine their own individual “sweet spot” but it is
generally between 200-300mcg.
 FTPP (ADIPOTIDE)
FAT TARGETED PROAPOPTIC PEPTIDE
• FTPP (Adipotide) is designed to target the specific blood vessels supplying
adipose tissue with blood. By denying fat cells an adequate blood supply, FTPP is
able to kill fat cells thereby causing a decrease in the volume and mass of
subcutaneous fat. Adipotide is able to kill the adipocytes (fat cells) by selectively
causing programmed cell death (apoptosis) of the blood vessels supplying the
adipocytes. 
• EFFECTS: Significant reduction in body fat (most notably in the typical “trouble
areas” of both men and women), increased insulin sensitivity.
• DOSING GUIDELINES: Research has determined that the most effective dose
of this peptide is 43-45mcg per kg of body weight, administered once daily. FTPP
is administered subcutaneously.
 TB-500
(Thymosin Beta 4)
TB500 (Thymosin Beta 4) is a muscle recovery drug. It is present in the body and is commonly found
in the skeletal muscles and all muscles of the body. Many bodybuilders inject TB-500 into their body to
increase the healing process of their naturally occurring TB-500. It has a vital role in building new
blood vessels, new small muscle tissue fibers, cell migration and blood cell reproduction. The main
focus of using TB-500 is to increase the production of Actin in the body that is associated with muscle
repair.

EFFECTS: This peptide speeds injury repair, increases joint mobility and encourages tissue repair.
Improved athletic performance and body composition have also been associated with TB500.

DOSING GUIDELINES: Dosing of TB500 consists of two phases. A repair phase where doses of 2-
2.5mg are administered subcutaneously twice per week for 4-6 weeks, followed by a maintenance
phase of 4-6 months consisting of once monthly doses of 2.5mg.

STACKING: TB-500 can be stacked with BPC-157 for super-human, mutant-like healing abilities like
Wolverine
 BPC-157
BPC-157 (pentadecapeptide) is an injectable peptide developed for alleviating stomach
ulcers. It is characterized by its ability to accelerate the healing of a huge variety of wounds
such as skin, cornea, muscle, colon, bone defects and tendons.

EFFECTS: BCP-157 has shown impressive results with regards to healing. Some injuries
that take more time to recover are those related to muscles and ligaments. This protein allows
faster healing process bringing an excellent advantage to injured athletes to achieve their
recovery in less time.

DOSING GUIDELINES: Dosages of 250mcg twice per day have been reported to yield
exceptional results.

STACKING: BPC-157: Can be stacked with TB-500 for super-human, mutant-like healing
abilities like Wolverine.
 PT-141
(The Libido Peptide)
PT-141 or Bremelanotide is the generic term for a research peptide being studied for its possible use
in helping to improve sexual dysfunction in both men (erectile dysfunction or impotence) and
women (sexual arousal disorder). PT-141 was developed from the tanning peptide Melanotan 2.

EFFECTS: Improved erectile quality in men and increased vaginal moisture in women. Causes a
noticeable increase in arousal in BOTH SEXES. Onset of effects generally occurs about four hours
after administration. * may cause slight nausea and flushing of the face, neck and shoulders within 2-
3 minutes after administration but symptoms quickly dissipate within a few minutes.

DOSING GUIDELINES: PT-141 is generally dosed between 1mg -2mg approximately four hours
prior to sexual activity. PT does require increased dosing with more frequent usage. PT-141 is
administered subcutaneously.
 TRIPTORELIN
Triptorelin is a GnRH (Gonadotropin Releasing Hormone). GnRH is a chemical that is sent from our brain to the
pituitary to tell it to produce both FSH and LH. When a small pulsed dose of GnRH is injected, your pituitary
receives that signal to start producing. This will result in both an increase in testosterone serum (as a result from
the LH stimulation) and an increase in sperm (or egg in a female case) count. The result may be an effective
jumpstart to our reproductive system for steroid users.

EFFECTS: Triptorelin is typically used as a “one shot” alternative to the time tested, 10 day, 1000iu HCG
protocol used by AAS users prior to beginning Post Cycle Therapy (PCT). It is also used to kick start the
reproductive system in female AAS users after a cycle to restore normal menstrual function and fertility as well as
restore virility in males after a particularly suppressive cycle.

DOSING GUIDELINES:1 single 100mcg dose administered subcutaneously after all esters have cleared the
body. *If normal pituitary function is not restored after the 100mcg dose, DO NOT, UNDER ANY
CIRCUMSTANCES, ADMINISTER ANOTHER DOSE. At doses exceeding 100mcg, pituitary function and
FSH/LH production can be permanently and irreversibly damaged (at doses of 1000mcg this drug is used as a
chemical castration method through over-stimulation of the pituitary gland) THIS PEPTIDE SHOULD NOT BE
USED MORE THAN FOUR TIMES PER YEAR.