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Lose Stubborn Belly Fat Peptide Anabolic Peptide Cjc-1295 Without Dac 863288-34-0
Lose Stubborn Belly Fat Peptide Anabolic Peptide Cjc-1295 Without Dac 863288-34-0

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Lose Stubborn Belly Fat Peptide Anabolic Peptide Cjc-1295 Without Dac 863288-34-0
 
Basic Information For CJC-1295 Without DAC:
 
Product Name: 
Synonyms: CJC1295; CJC-1295 Acetate; CJC-1295 without DAC; CJC 1295 w/o DAC; MOD GRF 1-29; Neorelin; Modified Sermorelin
CAS: 863288-34-0
MF: C159H258N46O45
MW: 0
Density: 1.45
Molar Mass: 3368.7
Peptide purity: >98.0%
Appearance: White lyophilized powder
Related substance: Total Impurities (%) ≤ 2.0%
Acetate content: ≤ 15.0%
Bacterial Endotoxins: ≤5 IU/mg
Sequence: Tyr-d-ALA-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg-NH2
Source: Chemical Synthesis
Reconstitution: To follow best practice guidelines for reconstituting CJC-1295 without DAC, reconstitute in sterile, bacteriostatic, distilled water, with light sonication if necessary.
Storage for MOD GRF 1-29: Lyophilized MOD GRF 1-29 is 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 reconstitution, may be stored for a maximum of 14 days in a refrigerator at 2°C - 8°C. Store vials in an upright position. Store MOD GRF-129 refrigerated between temperatures 2°C - 8°C. Keep in the outer carton in order to protect from light. For one month can be stored at room temperature.
Shelf life: One year from dispatch.
 
What is CJC-1295 without DAC and used for?
 
Modified GRF 1-29 is also known as Mod GRF 1-29, but even more commonly known as CJC-1295 without DAC. It is a protein that is 29 amino acids long and it is a GHRH analogue. CJC-1295 without DAC acts on receptors at the pituitary gland to stimulate the release of Human Growth Hormone.
 
CJC-1295 without DAC could be referred to more properly as a second generation derivative of GHRH. GHRH is modified to create what is known as Releasing Factor (GRF) 1-29, also known as Sermorelin. GRF 1-29 is then further modified to create Mod GRF 1-29 which is CJC-1295 without DAC.
 
Application & More information for CJC-1295 without DAC:
 
Releasing Hormone (GHRH), which is the endogenously secreted GHRH by the arcuate nucleus of the hypothalamus of the human body, is 44 amino acids long. It was discovered, however, that only the first 29 amino acids of the protein were equally as effective in binding to receptors on the pituitary gland as the full 44 amino acid structure. The first 29 amino acids in its protein structure were then isolated, which was then called GRF 1-29, but the problem with this derivative of GHRH was the fact that it was rapidly metabolized and cleared from the body by enzymes. Studies have reported that GRF 1-29's half-life is less than 10 minutes and as little as 5 minutes. This was obviously not enough time to ensure a maximized and sustained release of HGH from the pituitary gland, as studies have demonstrated that the full potential of an HGH pulse from the pituitary requires at least 30 minutes as evidenced by the fact that much higher HGH levels (50 times greater) were observed 15 - 30 minutes into subcutaneous administration of GHRH analogues.
 
Therefore, the solution to this was to modify GRF 1-29 by replacing various amino acids in its structure with other amino acids that would provide a greater resistance to breakdown and cleavage by enzymes. There were many modified analogues developed, and Mod GRF 1-29 (CJC-1295 without DAC) was eventually selected for use, which demonstrated the most promising effects. Mod GRF 1-29 is a modification of GRF 1-29, specifically at amino acids #2, #8, #15, and #27. The result is an extended half-life to that of at least 30 minutes.
 
Mod GRF 1-29 acts upon receptors located in the anterior pituitary gland, and signals the pituitary gland to increase Human  production and cause a release of massive quantities of Human Hormone in a pulsatile manner. The effects of Mod GRF 1-29 are very similar from what would be expected from synthetic HGH administration over the long term, although the amount of time that the released human growth hormone will remain in circulation is of a far less amount of time than synthetic Human Growth Hormone does. Therefore, multiple applications of Mod GRF 1-29 is recommended throughout the day in order to simulate Human Growth Hormone levels that remain high on a constant basis. Mod GRF 1-29 (CJC-1295 without DAC) is commonly combined with a Ghrelin mimetic (also known as a GHRP - Releasing Hexapeptide), such as GHRP-6, GHRP-2, Hexarelin, or Ipamorelin in order to initiate and amplify a greater pulse from the pituitary compared to Mod GRF 1-29 used solitarily on its own.
 

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Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2
Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2

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Pharmaceutical Intermediate Powder Peptide Lanreotide For Acromegaly 108736-35-2 
 
Lanreotide Basic Info.:
 
Product Name: Lanreotide
Synonyms: Lanreotide;Autogel;Bim-23014;Angiopeptin;Ipstyl 
CAS: 108736-35-2
MF: C54H69N11O10S2
MW: 1096.32
Storage temp.: −20°C
Chemical Properties: White to off-white lyophilised powder
Product Categories: hormones
 
Lanreotide Description:
 
Lanreotide (INN) is a medication used in the management of acromegaly and symptoms caused by neuroendocrine tumors, most notably carcinoid syndrome. It is a long-acting analogue of somatostatin, like octreotide. Its sequence is H-D-2Nal-Cys(1)-Tyr-D-Trp-Lys-Val-Cys(1)-Thr-NH2.
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas. In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma,a rare tumor of the pituitary gland which secretes TSH.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide Indications:
 
Lanreotide is used in the treatment of acromegaly, due to both pituitary and non-pituitary growth hormone-secreting tumors, and the management of symptoms caused by neuroendocrine tumors, particularly carcinoid tumors and VIPomas.  In the United States and Canada, lanreotide is only indicated for the treatment of acromegaly. In the United Kingdom, it is also indicated in the treatment of thyrotrophic adenoma, a rare tumor of the pituitary gland which secretes.
 
Lanreotide also shows activity against non-endocrine tumors, and, along with other somatostatin analogues, is being studied as a possible general antitumor agent.
 
Lanreotide ,In Dec 2014 the US FDA approved lanreotide for the treatment of patients with unresectable, well or moderately differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs).
 
Lanreotide Side Effects:
 
Lanreotide ,The main side effects of lanreotide treatment are mild to moderate pain at the injection site and gastrointestinal disturbances, such as diarrhea, nausea and vomiting. Isolated cases of gallstone formation have been associated with use of lanreotide, particularly over long periods of time.
 

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Steroid Hormone Powder DHT Stanolone For Muscle Building Androstanolone 521-18-6
Steroid Hormone Powder DHT Stanolone For Muscle Building Androstanolone 521-18-6

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Steroid Hormone Powder DHT Stanolone For Muscle Building Androstanolone 521-18-6 
 
Stanolone Basic Info.:
 
Product Name: Stanolone
Synonyms: Androstanolone;Stanolone;DHT
CAS: 521-18-6
MF: C19H30O2
MW: 290.44
EINECS: 208-307-3
Melting point: 178-183 °C
Assay: 99% min.
Storage temp.: Controlled Substance, -20°C Freezer
Chemical Properties: White Crystalline Solid
Usage: Anabolic steroid. Controlled substance
Product Categories: Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;Steroid and Hormone;API
 
Stanolone Description:
 
Androstanolone binds to and activates specific nuclear receptors. This agent may be used for testosterone replacement therapy in hypogonadal men, in HIV-wasting syndrome, and in other conditions in order to increase nitrogen retention and fat-free muscle mass.
 
The main androgen which is secreted by the testes is of course testosterone. However, in most of the body, the androgenic sign is not carried through by testosterone. In these tissues inluding brain (CNS), skin, genitals - practically everything but muscle - the active androgen is actually dihydrotestosterone (DHT). 
 
Stanolone Applications:
 
Use for chronic wasting disease, osteoporosis, severe infection and trauma, burn, etc caused by the negative nitrogen balance, promote the growth of premature infants and immature, etc. The fracture is not easy to heal, hypercholesterolemia and postpartum depression can also be used.
 

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99% Purity Hot Sale Ananbolic Steroid Hormone Powder Trenbolone Acetate 10161-34-9
99% Purity Hot Sale Ananbolic Steroid Hormone Powder Trenbolone Acetate 10161-34-9

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99% Purity Hot Sale Ananbolic Steroid Hormone Powder Trenbolone Acetate 10161-34-9
 
Trenbolone Acetate Basic Info.:
 
Product Name: Trenbolone Acetate
Synonym: Trenbolone Acetate; 
CAS No: 10161-34-9
Molecular formula: C20H24O
Molecular weight: 312.41
Assay: 99% min
Appearance: yellow or almost yellow crystalline powder
Place of origin: China
Quality standard: USP32
Effective Dose (Men): 200-600mgs/week
Effective Dose (Women):50-100mgs/week
Active life: 15 days
Detection Time: Up to 5 months
 
Product Description Of Trenbolone Acetate:
 
Trenbolone Acetate is an extremely powerful anabolic steroid and is considered the single greatest anabolic steroid by many performance enhancing athletes, it is much easier to maintain peaked and stable blood levels with this version.By carrying the Acetate ester, this gives Trenbolone an active half-life of approximately two days.
 
Trenbolone, whether as the acetate (Finaplix, Finajet), enanthate, or cyclohexylmethylcarbonate (Parabolan), should not be used as the sole anabolic in a steroid cycle. Mass gains are greatly limited when this is done. Instead, trenbolone should be stacked with Dianabol, Anadrol, or testosterone as the most common and highly suitable choices.
 
Application Of Trenbolone Acetate:
 
For bulking up, there may be no better steroid than Trenbolone Acetate also called Finaplix. Its anabolic effect is five times that of testosterone and it doesn't convert to estrogen, which makes it free from side effects like gynocomastia, water-retention, etc. Finaplix is not without its fair share of side effects, however. Testicular atrophy, hair loss, enlarged prostate and acne have been reported from using this drug. Finaplix will also shut down the body's natural testosterone production, which can lead to sexual dysfunction. Finaplix has a short-lived ester which means that it must be inject almost daily to maintain steady results. The good news for this is that the drug can be immediately stopped and the body can heal if adverse side effects appear.
 

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99.5% Purity USP Female Steroidal Progestin Hormone Megestrol Acetate CAS 595-33-5
99.5% Purity USP Female Steroidal Progestin Hormone Megestrol Acetate CAS 595-33-5

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99.5% Purity USP Female Steroidal Progestin Hormone Megestrol Acetate CAS 595-33-5
 
Megestrol Acetate Basic Info.:
 
Product Name: Megestrol acetate
CAS: 595-33-5
MF: C24H32O4
MW: 384.51
EINECS: 209-864-5
mp: 214°C
refractive index: 11°(C=2, CHCl3)
Chemical Properties: Crystalline Solid
Usage:Progestogen;Progesterone receptor agonist,Orally active progestogen; formerly used in combinations as oral contraceptive,treatment of endometrial hyperplasia.
 
Megestrol Acetate Description:
 
Megestrol acetate is used mainly as an appetite stimulant in a variety of conditions and as an antineoplastic agent in the treatment of breast, endometrial, and prostate cancers.
 
When given in relatively high doses, it can substantially increase appetite in most individuals, even those with advanced cancer, and is often used to boost appetite and induce weight gain in patients with cancer or HIV/AIDS-associated cachexia. It is also used as a contraceptive in combination with an estrogen at relatively low doses.
 
Megestrol Acetate Application:
 
Megestrol acetate is used mainly as an appetite stimulant in a variety of conditions and as an antineoplastic agent in the treatment of breast, endometrial, and prostate cancers. When given in relatively high doses, it can substantially increase appetite in most individuals, even those with advanced cancer, and is often used to boost appetite and induce weight gain in patients with cancer or HIV/AIDS-associated cachexia. It is also used as a contraceptive in combination with an estrogen at relatively low doses.
In addition to its use in humans, megestrol acetate has been used extensively in veterinary medicine in the treatment of medical conditions in cats and dogs.
 
Megestrol Acetate Usage:
 
Megestrol acetate is available as 5 mg, 20 mg and 40 mg tablets and in oral suspensions of 125 mg/ml and 40 mg/ml. It is used at a dose of 5 mg in combination with an estrogen for contraception. Appetite stimulation is achieved with doses ranging from 400 mg to 800 mg a day. Doses used to treat cancer usually range from 40 mg to 320 mg.
 

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Muscle Growth Steriods Polypeptide Hormone Oxytocin 50-56-6 For Hasten Parturition
Muscle Growth Steriods Polypeptide Hormone Oxytocin 50-56-6 For Hasten Parturition

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Muscle Growth Steriods Polypeptide Hormone Oxytocin 50-56-6 For Hasten Parturition
 
Oxytocin Basic Info.:
 
Product Name: Oxytocin
Synonyms: Oxytocin Acetate Salt Hydrate;Ocytocinum;Alpha-Hypophamine 
Unit Size: 2 mg/vial 
Unit Quantity: 1 Vial 
CAS NO.: 50-56-6 
Molecular Formula: C43H66N12O12S2 
Molecular Mass: 1,007.19    
Appearance: White Powder 
Purity: 98.2%  
Source: Chemical Synthesis 
Storage: Lyophilized Oxytocin is stable at room temperature for 90 days,however it should be stored in a freezer below -8C for any extended period of time. After reconstituting Oxytocin should be refrigerated at temperatures not to exceed 36 F.
 
Oxytocin Description:
 
Oxytocin is a hormone that is made in the brain, in the hypothalamus, and it is transported to, and secreted by, the pituitary gland, which is located at the base of the brain.
 
Chemically it is known as a nonapeptide (a peptide containing nine amino acids), and biologically, as a neuropeptide. It acts both as a hormone and as a brain neurotransmitter.
In both men and women, sexual intercourse stimulates the release of oxytocin, which has a role in erection and orgasm. The reason for this is not fully understood, although in women, it has been proposed that the increased uterine motility may help sperm to reach their destination.
 
The research to uncover oxytocin's "anxiolytic and pro-social influences, beneficial to relief, reproduction, and love" is what has led scientists to describe it as a one of the "most promising neuromodulator/neurotransmitter systems of the brain for psychotherapeutic intervention and treatment of numerous psychiatric illnesses, for example social phobia, autism, and postpartum depression.
 
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.
 
Oxytocin 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).
 

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Sex Enhancement Medicine Avanafil For Treating Male Sexual Dysfunction 330784-47-9
Sex Enhancement Medicine Avanafil For Treating Male Sexual Dysfunction 330784-47-9

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Sex Enhancement Medicine Avanafil For Treating Male Sexual Dysfunction 330784-47-9
 
Avanafil Basic Info:
 
Product Name: Avanafil
CAS: 330784-47-9
Molecular Formula: C23H26ClN7O3
Molecular Weight: 483.9506
Character: White to Off-White Cyrstalline Solid.
Assay: 99% min.
Store: Store at room temperature away from moisture, heat, and light.
Product Categories: Aromatics;Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitor;Avanafil;Inhibitors
Usage: Used for the treatment of erectile dysfunction. A phosphodiesterase 5 inhibitor.
 
Avanafil Description:
 
Avanafil is a PDE5 inhibitor approved for erectile dysfunction by the FDA and EMA,it acts by inhibiting a specific phosphodiesterase type 5 enzyme which is found in various body tissues, but primarily in the corpus cavernosum penis and retina.Avanafil works the same way as the three other ED drugs currently on the market: Viagra, Cialis, and Levitra. All these drugs target an enzyme called PDE5,and avanafil appears to inhibit this enzyme more selectively than the other. It is absorbed quickly, reaching a maximum concentration in about 30-45 minutes. About two-thirds of the participants were able to engage in sexual activity within 15 minutes.Avanafil's most frequent side effect was headache, and the other common side effects included flushing and nasal congestion,this new drug may have fewer side effects.
 
Avanafil Application:
 
Avanafil is used to treat male sexual function problems such as impotence or erectile dysfunction,it is in a class of medications called phosphodiesterase inhibitors.Avanafil works by increasing blood flow to the penis to help a man get and keep an erection.This drug does not protect against sexually transmitted diseases such as HIV, gonorrhea and syphilis.To decrease your risk of infection, always use an effective barrier method during all sexual activity.
 

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Top Quality White Steroid Hormone Powder Triamcinolone Acetonide Acetate 3870-07-3
Top Quality White Steroid Hormone Powder Triamcinolone Acetonide Acetate 3870-07-3

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Top Quality White Steroid Hormone Powder Triamcinolone Acetonide Acetate 3870-07-3
 
Triamcinolone Acetonide Acetate Basic Info.:
 
Product Name: Triamcinolone Acetonide 21-acetate
Synonyms: Triamcinolone Aceton;20-dione 21-acetate
CAS: 3870-07-3
MF: C26H33FO7
MW: 476.5344232
EINECS: 223-388-5
Purity: 99%  
Density: 1.314g/cm3    
Boiling point: 589.398 C at 760 mmHg
Refractive index: 1.57    
Flash point:310.257 C    
Vapour Pressur: 0mmHg at 25C
Apprarance: White or almost white crystalline powder
Solubility: Slightly soluble in water, ethanol and acetone and soluble in chloroform
Place of Origin: China (Mainland)    
Grade Standard: Medicine Grade
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids;Steroid and Hormone
Usage: Derivative of Triamcinolone Acetonide, a glucocorticoid, antiasthmatic (inhalant); antiallergic (nasal).
 
Description Of Triamcinolone Acetonide Acetate:
 
The glucocorticoid triamcinolone acetonide is clinically used for the treatment of suppression of inflammation in chronic inflammatory diseases such as asthma, rheumatiod arthritis, inflammatory bowel disease and autoimmune diseases (Barnes, 1998; Buttgereit, 2000; Uckermann et al., 2005). Triamcinolone acetonide acetate is another derivatives of triamcinolone, which has been used in therapy for several decades. Despite its great importance, no crystal structures of the title compound has been reported. But crystal structure of it's analogue compounds, triamcinolone diacetate chloroform solvate and triamcinole acetonide methanol solvate have been reported (Suitchlmezian et al., 2006 & Jess et al., 2006). In the title compound, the bond lengths and angles are in agreement with those reported for other triamcinolone derivatives (Suitchlmezian et al., 2006; Jess et al., 2006). and are within the expected ranges. The molecular framework consists of five condensed rings, including three six-membered rings and two five-membered rings.
 
Application Of Triamcinolone Acetonide Acetate:
 
Triamcinolone acetonide is a synthetic corticosteroid used to treat various skin conditions, to relieve the discomfort of mouth sores, and in nasal spray form, to treat allergic rhinitis. It is a more potent derivative of triamcinolone, and is about eight times as potent as prednisone.
It is also known under the brand names Kenalog (topical) and Volon A as an injection, to treat allergies, arthritis, eye diseases, intestinal problems, and skin diseases. In 2014, the FDA made triamcinolone acetonide an over-the-counter drug in the USA in nasal spray form under the brand name Nasacort.
 
Triamcinolone acetonide as an intra-articular injectable has been used to treat a variety of musculoskeletal conditions. When applied as a topical ointment, it is used for blistering from poison ivy, oak, and sumac, applied to the skin, avoiding eyes, mouth, and genital area. It provides relatively immediate relief and is used before using oral prednisone. Oral and dental paste preparations are used for treating aphthous ulcers.
 
As an intravitreal injection, triamcinolone acetonide has been used to treat various eye diseases and has been found useful in reducing macular edema. Drug trials have found it to be as efficient as anti-VEGF drugs in eyes with artificial lenses over a two-year period.
Uncommonly, intramuscular injection of triamcinolone acetonide may be indicated for the control of severe or incapacitating allergic states for which conventional treatments have failed, such as asthma, atopic dermatitis, contact dermatitis, perennial or seasonal allergic rhinitis, serum sickness, and transfusion and drug hypersensitivity reactions.
 
Triamcinolone acetonide is also used in veterinary medicine as an ingredient in topical ointments and in topical sprays for control of pruritus in dogs. A series of injections with triamcinolone acetonide or another corticosteroid may reduce keloid size and irritation. It is also used as a preinductor and/or inductor of birth in cows.
 
Many drugs have been demonstrated to increase triamcinolone acetonide concentration in the blood to well above the intended level. Patients should inform doctors about any other drugs they are taking.Triamcinolone acetonide should not be used by those with tuberculosis or untreated fungal, bacterial, systemic viral or herpes simplex infections without consulting a doctor first.
 

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99% Antiestrogen Steroid Hormones Toremifene Citrate For Cancer Patients 89778-27-8
99% Antiestrogen Steroid Hormones Toremifene Citrate For Cancer Patients 89778-27-8

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99% Antiestrogen Steroid Hormones Toremifene Citrate For Cancer Patients 89778-27-8

Toremifene Citrate Basic Info.

Product Name: Toremifene Citrate

Synonyms: FC 1157a; Fareston; NK 622; NSC 613680

CAS: 89778-27-8

Molecular Formula: C32H36ClNO8

Molecular Weight: 598.08

Melting point: 160-162°C

Boiling point: 146-148C

Density: 1,045g/cm

Refractive index: 1,416-1,418

Storage temp.: -20°C Freezer

Appearance: White or almost white powder

Toremifene Citrate Descriptions:

Fareston will display both estrogen antagonist / agonist properties in the body. This puts Fareston in the same category as Nolvadex and Clomid, the two most popular drugs in Farestons category. FARESTON is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors.

Toremifene administration for a period of 3 months in men with idiopathic oligozoospermia is associated with significant improvements of sperm count, motility, and morphology, mediated by increased gonadotropin secretion and possibly a direct beneficial effect of toremifene on the testes. The above findings are also indicative of a better testicular exocrine (improved sperm parameters) response to treatment in men whose partners achieved pregnancy compared with those who did not. Further randomized, placebo-controlled trials should be conducted to determine whether this particular selective estrogen receptor modulator can be useful as an initial approach in men with oligozoospermia.

Toremifene Citrate Applications:

Toremifene Citrate improved lipid profiles, particularly as an enhancer of high density lipoprotein cholesterol. it improved low density lipoprotein cholesterol levels.Both fareston and tamoxifen selective estrogen receptor modulators and equivalent treatments for metastatic breast cancer.No significant differences were found between treatment with either tamoxifen or fareston Treatment of HR-positive patients with either tamoxifen or toremifene is appropriate.In treating idiopathic oligozoospermia, tamoxifen and fareston are roughly equally effective but raloxifene is not.The antiestrogenic effects of SERMs at the hypothalamic level result in a statistically significant increase of gonadotropin levels, which is more marked for tamoxifen and fareston compared with raloxifene.

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99% Purity Muscle Building Steroids Peptide Powder Sermorelin For Alduts 86168-78-7
99% Purity Muscle Building Steroids Peptide Powder Sermorelin For Alduts 86168-78-7

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99% Purity Muscle Building Steroids Peptide Powder Sermorelin For Alduts 86168-78-7
 
Sermorelin Description:
 
Product Name: Sermorelin
Alias: GRF 1-29 NH2, Sermorelin Acetate Hydrate
Sequence: H-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2
CAS: 86168-78-7
MF: C149H246N44O42S
MW: 3357.96
Purity: 99%
Specification: 2mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18°C. Upon reconstitution of the peptide it should be stored at 4°C between 2-21 days and for future use below -18°C.
 
Sermorelin Details:
 
Sermorelin acetate is a recently synthesized (man-made) peptide analogue of growth hormone releasing hormone (GHRH) a naturally occurring hormone that is produced in the hypothalamus and stimulates and controls the production of growth hormone (GH) within the pituitary gland. GHRH, which is necessary for growth and development, was first described by Nobel Laureates R. Guilleman and A Shalley. In the 1970s one of their students, William Wehrenberg, began studying which part of the GHRH molecule was essential in stimulating the pituitary gland.
 
By removing individual amino acids from the GHRH molecule, Wehrenberg found that only the first 29 amino acids were essential for the stimulation of GH production in the pituitary gland. Semorelin is therefore only comprised of these 29 essential amino acids, forming a short polypeptide chain that is considered one of the shortest functional fragments of the GHRH molecule. It was first developed with a one-step chromatographic method capable of separating all isomers of polyethylene glycol (PEG) from naturally occurring GHRH.
 
Sermorelin Effect:
 
Sermorelin has a wide range of positive effects. Due to its nature as a GHRH, sermorelin only increases the body's ability to produce more growth hormone; it is not an injection of growth hormone itself. In both a performance enhancing and general well-being sense, sermorelin has a wide array of benefits that make it a powerful and valuable substance.
 

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