Full Catalog

Albuterol Albuterol is a Beta-2 agonist also known internationally as salbutamol, similar to clenbuterol but shorter-acting.  Therapeutic uses of B2 agonists include treatment of bronchial asthma.  This class of drug has also been demonstrated to lower C-reactive proteins, an important ..

Anastrozole Anastrozole  belongs to a class of compounds known as aromatase inhibitors (AIs).  An enzyme known as aromatase is responsible in the human body for producing estrogen by converting androgens into estrogen. Aromatase inhibitors like Anastrozole  prevent aromatase from f..

DAC CJC 1295 DAC conjugated CJC 1295 (Receptor Grade) is an hGH secretogue that is unique by way of an additional lysine molecule that is added to facilitate the DAC complex. This conjugation makes for a much longer half-life.  DAC CJC 1295 tends to have a very limited availability everywher..

CJC-1293 Modified GRF (1-29) In the healthy human body, large amounts of growth hormone are stored in the pituitary.  The cells within the pituitary release growth hormone in response to signaling by GHRH (Growth Hormone Releasing Hormone), Ghrelin (of which GHRPs - Growth Hormone Releasing ..

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Clomiphene Clomiphene citrate (USA trade name Clomid) is a selective estrogen receptor modulator (SERM) that increases production of the body's gonadotropins via disruption of the natural negative feedback system in the hypothalamus.  Clomiphene consists of two bioactive isomers, zuclomi..

D-CLOPROSTENOL: PGF2a Super-Agonist - 50mcg / ml, 60ml D-cloprostenol, also called (+)-cloprostenol sodium, is a highly potent prostaglandin F2-alpha analog with selective agonistic activity at the FP receptor.  It binds to the prostaglandin FP receptor with two-hundred-fold greater ..

      Exemestane       Exemestane, sold as Aromasin, is a steroidal aromatase inhibitor (AI) primarily administered in the adjuvant treatment of hormonally responsive breast cancer in postmenopausal women. In that type of cancer, higher estrogen lev..

Ghrelex   5mg / vial   D-Lys-GHRP6 or Ghrelex is an ghrelin antagonist, meaning it is a peptide with opposite effects of ghrelin.  When D-Lys-GHRP6 is administered in mammals, it has the effect of inhibiting the effects of ghrelin within the body. Ghrelin is secreted mainl..

GHRP-6 GHRP-6, a polypeptide hormone, is a growth hormone secretagogue and ghrelin mimetic and analog.  GHRP-6 is from the first generation of GHRPs and causes significant release of growth hormone by itself, due both to its suppression of somatostatin (an antagonist to GHRH) and stimul..

GW1516   GW1516, also written GW 50516, is a drug and research chemical developed by pharmaceutical client GlaxoSmithKline, which acts as a PPARδ (peroxisome proliferator activated receptor delta) modulator and selective agonist.[1][2] GW1516 activates AMP-K (5' adenosine monoph..

DES(1-3)IGF   DES(1-3)IGF is a truncated form of IGF-1 with the tri-peptide structure Glycine-Proline-Glutamine cleaved from the N-terminus.  It has been isolated from and detected in numerous in vivo sources, including the human brain, bovine colostrum, and porcine uterus.[2]  ..

      IGF1-LR3   The insulin-like growth factors (IGFs) are peptides with sequence similarities to insulin. IGF-1 is mainly secreted by the liver via stimulation of GH (growth hormone); this is the primary mechanism of what is known as the IGF/GH axis.. IGF-1 plays..

IGF-2 This is a bulk discount for 10 vials of IGF-2 Lr3 (receptor grade) 10 vials (total 1200mg). IGF-2 is a protein hormone/peptide that is endogenous to the human body and, like IGF-1 and relaxin, shares structural and functional similarities to insulin.[4][5]  The IGF-2 gene is genetic..

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Meclofenoxate   Meclofenoxate, also known by the name centrophenoxine or the commercial name Lucidril, is used to treat symptoms of senile dementia in the elderly and Alzheimer's Disease.[1] It is compounded from two distinct biochemical sources: dimethylaminoethanol (DMAE) and parach..

Melanotan II   Classification, Actions, Mechanisms: Melanotan II belongs to a group of peptides called the melanotropin peptides.  Other peptides belonging to this group are ACTH (adrenocortropic hormone) and the melanocyte-stimulating hormones (MSH).   The MSHs contrib..

In Stock Now! Ostarine / MK-2866 Ostarine or MK-2866 (CAS# 1235370-13-4) is a research chemical developed originally by Merck Inc. and now owned by GTx Inc.  It is undergoing trials for Phase II (human) research.  MK-2688 belongs to a class of chemicals known as SARMs or selective an..

Pramipexole Pramipexole is a dopamine receptor agonist with affinity for D2S, D2L, D3, and D4 receptors.[1,2]  Officially pramipexole is indicated for prescription to treat Parkinson's disease and Restless Legs Syndrome.[3]  Pramipexole has also been used off-label with reported success..

PT-141 (Bremelanotide)   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 ..

SARMs S4 SARMs, Selective Androgen Receptor Modulators, are a relatively new class of research chemicals that have selective androgenic activity in a given area of the body.[1]  The specific activity is determined by which androgen receptors are activated and in what tissue.[1]  The cli..

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T4   Thyroxine, also known as tetraiodothyronine or “T4” for short is an endogenous prohormone released from the follicular cells of the thyroid gland.  T4 is converted into the more potent T3 (triiodothyronine) by enzymes called deiodinases.  T4 is active on its own..

Tesamorelin 5 vials, 2mg / vial, 10mg total weight Tesamorelin Tesamorelin is an analogue of GHRH (growth hormone releasing hormone, a naturally-occurring peptide released from the hypothalamus) that was recently approved by the FDA for treatment (reduction) of HIV-induced lipodystrophy-re..

Toremifene Citrate Toremifene citrate is a selective estrogen receptor modulator (SERM), a class of research chemicals that exhibits affinity for estrogen  receptors but does not have estrogenic activity at the receptor, thereby limiting many of the physiological effects of estrogen..Toremif..

    Vardenafil  Vardenafil is a PDE5 inhibitor that is comparable in effect and indication to sildenafil and tadalafil.  Its primary use is in assisting men who experience erectile dysfunction (ED) regain the ability to have penile erections and thus better cope with o..