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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6

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Safety Pure Amino Acid 3,5-Diiodo-L-Thyronine T2 Powder 1041-01-6
 
3,5-Diiodo-L-Thyronine Basic Information:
 
Product Name: 3,5-Diiodo-L-Thyronine
Synonyms: T2;Diiodothyronine;3,5-Diiodo-L-Thyronine;3,5-Diiodothyronine;
CAS: 1041-01-6
MF: C15H13I2NO4
MW: 525.08
EINECS: 213-867-7
Melting point: 255-260°C (dec.)
Storage temp.: 2-8°C
Chemical Properties: Off-White Solid
Product Categories: Medicine intermediate;Amino Acids 13C, 2H, 15N;Amino Acids & Derivatives;Intermediates;Labeling and Diagnostics Reagents
Usage: Of interest for the early detection and treatment of congenital or drug-induced hypothyroidism.
 

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White Crystalline Powder Treat Breast Cancer Trilostane 13647-35-3

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White Crystalline Powder Treat Breast Cancer Trilostane 13647-35-3
 
Trilostane Basic Info.
 
Product Name: Trilostane
Synonym: Trilostane;Vetoryl;Modrenal
CAS: 13647-35-3
Molecular Formula: C20H27NO3
Molecular Weight: 329.43
Einecs No.: 237-133-0
Assay: 99%
Melting point: 264 °C
Storage temp.: -20°C Freezer
Storage: Shading, confined preservation
Grade: Pharmaceutical Grade
Appearance: White crystalline powder
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Inhibitor;FULVICIN.
Usage: 
(1)Trilostane can inhibit cortical hormone in the process of synthesis of 3 beta dehydrogenase, make the cortisol, aldosterone synthesis decreased;
(2)Clinically used in the treatment of Cushing syndrome (hypercortisolism) and primary aldosteronism. 
(3)Trilostane also had significantly effect to decreased serum testosterone level.
 
Trilostane Description:
 
Trilostane is used in the treatment of Cushing's syndrome. It is normally used in short-term treatment until permanent therapy is possible. Trilostane blocks an enzyme involved in the production of several steroids including cortisol. Inhibiting this enzyme inhibits the production of cortisol. In Cushing's syndrome, the adrenal gland overproduces steroids. Although steroids are important for various functions of the body, too much can cause problems. Trilostane reduces the amount of steroids produced by the adrenal gland.
Trilostane produces suppression of the adrenal cortex by inhibiting enzymatic conversion of steroids by 3-beta-hydroxysteroid dehydrogenase/delta 5,4 ketosteroid isomerase, thus blocking synthesis of adrenal steroids.
 
Side effect:Symptoms of overdose include darkening of skin, drowsiness or tiredness, loss of appetite, mental depression, skin rash, and/or vomiting.
 
Trilostane Application:
 
Trilostane can suppress cortical hormone synthesis process of 3 beta dehydrogenase, make cortisol, aldosterone synthesis reduce, clinical used in the treatment of Cushing syndrome(cortisol increase disease) and primary aldosteronism,the effect is not good than testosterone metyrapone. This product has significantly reduced blood testosterone level role, may relevant to its inhibit synthetic.
 

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99% Benzocione Local Anesthetic Benzocaine For Anti-Paining 94-09-7

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99% Benzocione Local Anesthetic Benzocaine For Anti-Paining 94-09-7
 
Benzocaine Basic Info.:
 
Product Name: Benzocaine
Synonyms: Aethoform;Anesthesin;Akos Bbs-00003658;4-Aminobenzoic Acid Ethyl Ester;Labotest-Bb Ltbb000527;H-4-Abz-Oet;Ethyl 4-Aminobenzoate;Ethyl P-Aminobenzoate
CAS: 94-09-7
Molecular Formula: C9H11NO2
Molecular Weight: 166.1965
EINECS number: 202-303-5
Purity: 99%
Size: 40 mesh and 200 mesh
Melting point: 88-90°C
Boiling point: 172°C (12.7517 mmHg)
Density: 1.17
Flash Point: 164.2°C
Vapor Pressure: 0.000589mmHg at 25 °C
Fp: 172°C/13mm
Storage temp.: 0-6°C
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
Chemical Properties: White odourless crystals.
Product Categories: Aromatic Esters;C8 to C9;Carbonyl Compounds;Esters;Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Research Chemical;Pharmaceutical intermediate;API;Pharma materials;Intermediate of Tetracaine hydrochloride.
Uses: 
(1)The goods are used to relieve pain for the local anesthetic, wounds, ulcers and hemorrhoids facial, also are cough suppressants retreat intermediates.
(2)Used in cosmetic ultraviolet absorption, local anesthetics and used to relieve pain in the wound, ulcer surface and Hemorrhoids.
 
Product Description Of Benzocaine:
 
Benzocaine is used to relieve pain and itching caused by conditions such as sunburn or other minor burns, insect bites or stings, poison ivy, poison oak, poison sumac, minor cuts, or scratches.
 
Benzocaine belongs to a group of medicines known as topical local anesthetics. It deadens the nerve endings in the skin. This medicine does not cause unconsciousness like general anesthetics do when used for surgery.
 
This medicine is available without a prescription; However, your doctor may have special instructions on the proper use and dose for your medical condition.
 
Fat soluble surface anaesthetic. It's for the local anesthetic for wound, pain, ulcer and hemorrhoids, as well as cough suppressants retreat Benzocaine intermediates. Also can be used for ultraviolet absorption in cosmetic. Related product: Lidocaine. 
 
Benzocaine Applications: 
 
Benzocaine is a topical analgesic (meaning it is to be used on the body surface or in the mouth but should not be swallowed) that has a number of different uses in over-the-counter (OTC) medicines. Depending on the dose and form, the active ingredient benzocaine can be used to relieve throat and mouth pain; To alleviate external vaginal itching and burning; To stop pain and itching due to hemorrhoids; Or to relieve minor skin irritations, pain, and itching. Because benzocaine is available in different doses and forms, it is very important to read the Drug Facts label carefully to determine whether the medicine is intended to be used for the symptoms you are experiencing. 
 
Benzocaine can be the only active ingredient in oral treatments that relieve sore throat or address mouth pain caused by cold sores, canker sores, teething, and other issues. It also can be combined with other active ingredients in oral treatments that not only relieve mouth and throat pain, but also protect irritated areas, provide a soothing coating, or relieve dryness. 
 
While oral discomfort treatments containing benzocaine are intended to be used in and around the mouth, there are other topical benzocaine medicines that should only be used externally, or on the outer surface of the body (not near or in the mouth). For example, benzocaine can be found in vaginal medicines that contain more than one external analgesic ingredient or in single active ingredient hemorrhoid treatments. Benzocaine also is available in topical pain relievers that not only relieve skin irritations, pain, and itching, but also contain other active ingredients that kill germs and help prevent infection. 
 
Benzocaine is approved by the U. S. Food and Drug Administration (FDA) and is safe and effective when used according to label directions. Some oral discomfort treatments can be used to temporarily relieve pain due to toothaches; However, these medicines are not intended for long-term treatment. If your toothache pain is severe or lasts for more than seven days, you should talk to your dentist.
 
Benzocaine may not be contained in all products sold under these brands. Please read the OTC Drug Facts label carefully for active ingredient information for specific products.
 

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Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3

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Progestogen Hormonal Gestodene Female Anabolic Steroids 60282-87-3 
 
Gestodene Basic Info.:
 
Product name: Gestodene
Other names: Gestinol;13-Ethyl-17-hydroxy-18,19-dinor-17alpha-pregna-4,15-dien-20-yn-3-one;SHB 331;Gestodeno.
CAS: 60282-87-3
EINECS: 262-145-8
Molecular Formula: C21H26O2
Molecular Weight: 310.43
Melting point: 190-192 degree centigrade
Boiling Point: 462.7 degree centigrade at 760 mmHg
Flash Point: 196.9 degree centigrade
Refractive index:1.588
Density: 1.15 g/cm3
Vapour pressure: 1.66E-10mmHg at 25 degree centigrade
Appearance: White crystalline solid. 
Function: Used as resisting pregnant hormone pills.
 
Gestodene Description:
 
Gestodene is a synthetic version of a female sex hormone. When combined with other synthetic hormones, it interferes with a woman's menstrual cycle, decreasing the symptoms of severe menstruation and preventing pregnancy. Used correctly, it is more than 99% effective at preventing unwanted pregnancies.
 
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect. Oral absorption quickly and completely, after 1 to 2 hours of peak blood concentration, bioavailability 100%, eliminating t1 / 28 hours. Clinical and ethinyl estradiol or a composite sheet consisting of three photo used for short-acting oral contraceptives. Due to its reliable contraceptive effect, good cycle control, on lipid metabolism can produce beneficial effects, improve hdl, it is the most ideal one oral contraceptives.
 
Gestodene Applications:
 
Gestodene is asoral contraceptive. It mimics the naturally occurring female sex hormone progesterone, 
which is partially responsible for regulating the menstrual cycle. 
 
Gestodene as progestin far the strongest and one of the lowest dose of birth control pills. Its progestin activity is 2 times L norethindrone, there is no androgen and estrogen activity, there is an anti-estrogen effect.
 

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0

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17 Alpha-Estradiol / Estradiol For Skin Absorption Agent CAS 57-91-0
 
17 Alpha-Estradiol Basic Info.:
 
Product Name: 17 Alpha-Estradiol
Synonyms: Alpha-estradiol; 17A-estradiol 
CAS: 57-91-0 
EINECS: 200-354-8 
Molecular Formula: C18H24O2 
Molecular Weight: 272.39 
Appearance :hite or off-white crystalline powder 
Assay :99%min.
Melting range:216-224 oC 
Specific rotation:+52o to +60o 
Loss on drying :3.5%MAX
Monor impurity :0.2%MAX
Total impurities:1.0% max 
 
17 Alpha-Estradiol Description:
 
Estradiol (called α - estradiol or 17α - estradiol) for human breast cancer cells in tissue culture biologically active estrogen. Not part of the 17- and selective estrogen receptor (ER-X) traditional hormone / receptor of the endocrine system, but an important autocrine / paracrine function of the system is part of the growth in the adult brain. In menopause, and neurodegenerative diseases (eg Alzheimer's disease and ischemic stroke) treatment, 17- estradiol may have important implications for hormone replacement therapy thing. 
 
The development of secondary sex characteristics in women is driven by estrogens, to be specific, estradiol. These changes are initiated at the time of puberty, most are enhanced during the reproductive years, and become less pronounced with declining estradiol support after the menopause. Thus, estradiol enhances breast development, and is responsible for changes in the body shape, affecting bones, joints and fat deposition. Fat structure and skin composition are modified by estradiol. 
 
17 Alpha-Estradiol Applications: 
 
This medication is a female hormone. It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. 
Certain estrogen products may also be used by women after menopause to prevent bone loss (osteoporosis). However, there are other medications (such as bisphosphonates including alendronate) that are also effective in preventing bone loss and may be safer. These medications should be considered for use before estrogen treatment.
 

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Anabolic Steroid Powder Sunifiram For Memory Enhancement 314728-85-3

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Anabolic Steroid Powder Sunifiram For Memory Enhancement 314728-85-3
 
Sunifiram Basic Info:
 
Product Name: Sunifiram
Synonyms: Sunifiram;DM235;DM 235;
CAS: 314728-85-3
MF: C14H18N2O2
MW: 246.30492
Appearance: White powder
Purity: 99.32%
Shelf life: 2 years
Standard: In-house Standard
Usage: For the treatment of Alzheimers Dementia, Cognition Disorder, Neurologic Drugs, Senile Dementia, Acetylcholine Release Enhancers.
 
Product Description Of Sunifiram:
 
This compound is known as an AMPAkine due to exerting most of its actions via the AMPA receptor (one of the three main subsets of glutamate receptors, alongside NDMA and kainate). This enhancement of AMPA function seems to also rely on enhancing signalling via the Glycine binding site of NMDA receptors, although one minimal signalling goes through the NMDA receptor then the benefits on AMPA receptors seem dose-dependent.
 
Sunifiram (DM-235) is a piperazine derived ampakine drug which acts as a positive allosteric modulator of AMPA receptors, and has nootropic effects in animal studies with significantly higher potency than piracetam. A number of related compounds are known, the best known being unifiram (DM-232).
 
This enhancement by sunifiram is associated with an increase inphosphorylation of AMPAR through activation of protein kinase II(CaMKII) and an increase in phosphorylation of NMDAR through activation of protein kinase C α (PKCα). More specifically, sunifiram stimulates the glycine-binding site of NMDAR with concomitant PKCαactivation through Src kinase. Enhancement of PKCα activity triggers to potentiate hippocampal LTP through CaMKII activation.Sunifiram improves cognitive deficits via CaM kinase II andprotein kinase C activation.
 
Application Of Sunifiram:
 
For the treatment of Alzheimers Dementia, Cognition Disorder, Neurologic Drugs, Senile Dementia, Acetylcholine Release Enhancers.
 
Sunifiram (DM-235) is a synthetic derivative of Piracetam, although due to breaking the pyrrolidone backbone it is no longer in the Racetam class of drugs (yet by being derived from them, it is still commonly associated with this class).
 
Sunifiram has mechanisms similar to Nefiracetam in the hippocampus, and similar to that drug sunifiram shows anti-amnesiac properties and is potentially a cognitive enhancer. Its anti-amnesiac activity is several orders of magnitude greater than piracetam on a per weight basis, and preliminary evidence suggest it has a similarly low toxicity profile.
 
Function Of Sunifiram:
 
Sunifiram increases energy levels, allowing users to feel more motivated and eliminate
Sunifiram increase Levels of concentration increase, and users feel less distracted by external stimuli
Sunifiram also enhances long-term potentiation, which is the forming of new connections regarding memory storage.
Sunifiram has some anxiolytic benefits. Feeling more relaxed is beneficial when trying to focus.
 

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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5

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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5
 
Androstenediol Basic information:
 
Product Name: Androstenediol
Synonyms: Hermaphrodiol;5-Androstenediol;Androstenediol
CAS: 521-17-5
MF: C19H30O2
MW: 290.44
EINECS: 208-306-8
Product Categories: Steroids;API
Melting point: 178-182°C
Alpha: -52.2 º (c=0.4,2-propanol)
Storage temp.: 2-8°C
 
Androstenediol Description:
 
Androstenediol, commonly referred to simply as , and also known as androst-5-ene-3β,17β-diol, is an endogenous androgen and estrogen steroid hormone and intermediate in the biosynthesis of testosteronefrom dehydroepiandrosterone.
Androstenediol is a direct metabolite of the most abundant steroid produced by the human adrenal cortex. It is less androgenicthan the related compound, Δ4-androstenediol, and has been found to stimulate the immune system. When administered to rats, Δ5-diol, in vivo, has approximately 1.4% of the androgenicity , 0.54% of the androgenicity of androstenedione, and 0.21% of the androgenicity of testosterone.
 
1.People Use Androstenediol For:
 Orally, 5-Androstenediol is used to increase endogenous testosterone production to increase energy, enhance recovery and growth from exercise, heighten sexual arousal and function, and to promote a greater sense of well being.
 
2.Mechanism of Action:  
5-Androstenediol, a prohormone, is a weak steroid hormone and is a direct precursor of testosterone . Androstenediol can be converted to estradiol, estrone, dehydroepiandrosterone (DHEA), and testosterone; and may increase levels of these hormones. 
 

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9
 
Clomiphene Citrate Basic Info.:
 
Product Name: Clomiphene Citrate
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene.
 
Clomiphene Citrate Description:
 
Clomiphene Citrateis a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, putsClomiphene Citratein a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. As for women, the only real use for Clomiphene Citrate is the possible management of endogenous estrogen levels near contest time. This can increase fat loss and muscularity, particularly in female trouble areas such as this HIPS and thighs. Clomiphene Citrate however often produces troubling side effects in women (discussed below), and is likewise not in very high demand among this group of athletes. Clomid are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time.
 
Clomiphene Citrate Application:
 
As for toxicity and side effects, Clomiphene Citrateis considered a very safe drug. Bodybuilders seldom report any problems, but listed possible side effects do include hot flashes, nausea, dizziness, headaches and temporarily blurred vision. Clomifene citrate is a drug treatment that stimulates your ovaries to release eggs. Ovulation stimulation using clomifene citrate is a well-established, effective treatment. Clomifene citrate is the most widely used of all fertility drugs. Other drugs that may be used to treat ovulation disorders include metformin and bromocriptin.
 

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New Trestolone Decanoate Effective Yellow Liquid For Muscle Building

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New Trestolone Decanoate Effective Yellow Liquid For Muscle Building
 
Trestolone Decanoate Basic Info.:
 
Product Name: Trestolone Decanoate
Synonyms: Trest Deca
Assay: 99%
Standard: USP/BP
Appearance: Light Yellow Liquid
Suitable for: Adult
Usage: A synthetic, anabolic steroid. Used to promote muscle growth and combat involuntary weight loss. It has also been used to treat cases of osteoporosis.
 
Trestolone Decanoate Applications:
 
Trestolone Decanoate is intended for research purposes only and, is not to be used for any other purposes, including but not limited to, in vitro diagnostic purposes, in foods, drugs, medical devices, or cosmetics for humans or animals or for commercial purposes. Trestolone Decanoate has not been tested for safety and efficacy in food, drug, and medical device, cosmetic, commercial or any other use.  Under no circumstances shouldTrestolone Decanoate be used as or be considered to be foods, drugs, medical devices or cosmeticsThis product is intended for laboratory/hobbyist research use only. There are risks involved with consumption or distribution of this product. 
 
Trestolone Decanoate is NOT intended to use as food additives,drugs, cosmetics, household chemicals or other inappropriate applications. The listing, purchase and/or distribution of this material does not constitute a license to its use in infringement of any patent.  Trestolone Decanoate should be handled only by qualified and properly trained professionals.  
 
Trestolone Decanoate Function:
 
Trestolone Decanoate in pure Grapeseed Oil is for research use only. This product is NOT for human use and can be harmful if ingested. Trestolone Decanoate is for research/laboratory use only. Trestolone Decanoate is in a sterile solution BUT is NOT to be injected. Trestolone Decanoate should only be handled by licensed, qualified professionals.Trestolone Decanoate is not a drug, food, or cosmetic and should not be misbranded, misused or mislabeled as a drug, food or cosmetic.
 

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain
 
Ipamorelin Basic Info.:
 
Product Name: Ipamorelin
Synonyms: IpoMarelin;IpaMorelin Acetate;Aib-His-D-2-Nal-D-Phe-Lys-NH2
Unit Size: 2 mg/vial
Unit Quantity: 1 Vial
CAS NO.: 170851-70-4
Molecular Formula: C38H49N9O5
Molecular Weight: 711.85
Sequence: H-Aib-His-D-2-Nal-D-Phe-Lys-NH2
Appearance: White Powder
Purity: 98.49%
Identity (ESI-MS) 711.85±0.5
Source Chemical Synthesis
Storage: Stable at room temperature for 90 days,however it should be stored in a freezer below -8°C for any extended period of time. After reconstituting Ipamorelin should be refrigerated at temperatures not to exceed 36°F.
 
Ipamorelin Description:
 
Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. It is a synthetic peptide that has powerful Growth Hormon releasing properties. And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat.
 
Ipamorelin is a penta-peptide. (Aib-His-D-2-Nal-D- Phe-Lys-NH2) And, the strength it displays may very well make regular old Growth Hormon (GH) obsolete. But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other GHRP peptides?
 
Athletes are taking Ipamorelin in a 200mcg -300mcg dosage, two or three times daily, using a tiny insulin needle to inject. They usually start with the lower dose since side effects can include headaches or what feels like a head-rush. Ipamorelin can be taken at anytime but taking it about 30-45 minutes before a workout would seem ideal because of the pulse in Growth Hormon (GH) it creates allowing for maximum growth.
 
Studies on the effects of Ipamorelin on bone growth, body weight, and GH release showed some interesting conclusions.In one experiment, various doses were administered over the course of 15 days to test the group's reactions.
 
There was a distinct and dose-dependent effect on body weight gain however, the treatment group did not show a change in total IGF-I levels. Nor did the treatment group produce serum markers of bone development. For example, the number of cells in the wide portion of the tibia (the shinbone) did not change significantly. This is a good thing because it suggests muscle growth with less potential for deformity of bone or cartilage.
 
Ipamorelin in theory may increase Acetylchloine or Cortisol when used in higher dosages. However, and increase in Acetylchloine or Cortisol is even more likely with GHRP-2 and GHRP-6. In fact, in the case of Ipamorelin, there was little to no rise in Acetylcholine and Cortisol blood plasma levels even at injections more than 200 times higher than the effective dosage for comparable GH release.
 
Ipamorelin Applications:
 
Ipamorelin is a selective growth hormon secretagogue and agonist of the ghrelin receptor. In pentobarbital anaesthetised rats, ipamorelin released GH with a potency and efficacy comparable to GHRP-6 (ED50 = 80±42 nmol/kg and Emax = 1545±250 ng GH/ml vs 115±36nmol/kg and 1167±120ng GH/ml). In conscious swine, ipamorelin released GH with an ED50 = 2.3±0.03 nmol/kg and an Emax = 65±0.2 ng GH/ml plasma. Again, this was very similar to GHRP-6 (ED50 = 3.9±1.4 nmol/kg and Emax = 74±7ng GH/ml plasma). GHRP-2 displayed higher potency but lower efficacy (ED50 = 0.6 nmol/kg and Emax = 56±6 ng GH/ml plasma). The specificity for GH release was studied in swine.
 

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