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Testosterone USP 99%

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Muscle Body Building Anabolic Steroids Powder Testosterone Base 58-22-0
 
Testosterone Base Basic Info:
 
Chemical name: Testosterone Base
Synonyms: Testosterones;Testosteron;Testred;Testex;Testoderm;Orquisteron;Oreton;Primoteston;Test Base 
CAS: 58-22-0
MF: C19H28O2
MW: 288.43
EINECS: 200-370-5
Assay: 99%
Packing: foil bag or tin.
Appearance: white or off-white crystalline powder
Product Categories: MI;TPI;Steroids;Intermediates & Fine Chemicals;Pharmaceuticals; Intracellular receptor; Steroid and Hormone; API; testosterone; TESTIM; Inhibitors.
Usage: to promote the development of male genitalia and maintain their normal function, for disease-free Testosterones replacement therapy, male menopause syndrome, impotence and other diseases Treatment, but also for women of functional uterine bleeding, dysmenorrhea, menorrhagia, aplastic anemia embolism.
 
Testosterone Base Description:
 
Testosterones base is the undisputed king of steroids mainly because it is safe, elicits rapid mass and strength gains while maintaining libido, a sense of well being and energy. It's not uncommon for a first time user to gain 15-20lbs of LBM in a standard Testosterones cycle. Pure Testosterones comes in a water based aqueous form (Suspension) and also in a solvent/oil based form (Test Base).
 
Suspensions have tiny particles that are visible with the naked eye. If left on the shelf for a few days many times the particles will sink to the bottom leaving the clear solvents and water on the top. Depending on the manufacturer, particle sizes vary meaning some Suspension preparations can clog a 22 gauge needle. Ultra micronized Suspension can pass through a 25 gauge needle making injections more comfortable. Shake the suspension preparation vigorously before injecting.
 
Testosterones Base is the most common anabolic hormone that there is and is also considered the most basic. Due to this, bodybuilders often consider it the base steroid to most all cycles. Testosterones Base is both anabolic and androgenic in nature. Users of this steroid will notice a dramatic gain in muscle size and strength, as well as an overall sense of well being and increases libido and sex drive.
 
Testosterone Base Applications:
 
Testosterones Suspension is an injectable Testosterones hormone in a water base that was developed and used for decades, and is actually the first anabolic androgenic steroid made. For the purpose of building mass, Testosterones Suspension has never been surpassed since it was first developed in the 1930s. Many underground labs also suspend this product in propylene glycol or oil as well (which makes for a very painful injection). It has no ester attached; therefore no ester is calculated into the weight.
 

 

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Thrombopoietin

Thrombopoietin is a glycoprotein hormone produced mainly by the liver and the kidney that regulates the production of platelets by the bone marrow. It stimulates the production and differentiation of megakaryocytes, the bone marrow cells that fragment into large numbers of platelets.Thrombopoietin is produced primarily in liver parenchymal cells with much smaller amounts being made in the kidney and bone marrow.It is synthesized as a 353 amino acid precursor protein with a molecular weight of 36 kDa.It has an unusual structure in that the first 153 amino acids of the mature protein are 23% homologous with human erythropoietin.

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Thromboxane

Thromboxane is a member of the family of lipids known as eicosanoids. The two major thromboxanes are thromboxane A2 and thromboxane B2. Thromboxane acts by binding to any of the thromboxane receptors, G-protein-coupled receptors coupled to the G protein Gq. Thromboxanes are formed from endoperoxides, cause constriction of vascular and bronchial smooth muscle, and promote blood clotting. Thromboxane is a vasoconstrictor and a potent hypertensive agent, and it facilitates platelet aggregation. It is in homeostatic balance in the circulatory system with prostacyclin, a related compound.

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Thymosin Alpha1 Acetate

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Thyroid Hormone L-Liothyronine Powders 6893-02-3

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Thyroid Hormone L-Liothyronine Powders 6893-02-3
 
L-Liothyronine Basic Info.
 
Product Name: L-Liothyronine
Synonyms: T3;O-(4-Hydroxy-3-iodophenyl)-3,5-diiodo-L-tyrosine;Cytomel;L-Liothyronine
CAS: 6893-02-3
MF: C15H12I3NO4
MW: 650.97
EINECS: 229-999-3
Purity: 99%
Melting point: 234-238 °C(lit.)
Alpha: 23°(c=2 in ethanol)
Storage temp.: −20°C
Chemical Properties: Off-White Solid
Product Categories: Amino Acids & Derivatives;Intermediates & Fine Chemicals;Labeling and Diagnostics Reagents;Pharmaceuticals;Inhibitors;Stable Isotopes.
Usage: One of the hormones produced by the thyroid gland that is involved in the maintenance of metabolic homeostasis. Also produced in peripheral tissues as the active metabolite of Thyroxine.
 
L-Liothyronine Description :
 
Triiodothyronine, also known as T3, is a thyroid hormone. It affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate.
 
Production of T3 and its prohormone thyroxine (T4) is activated by thyroid-stimulating hormone (TSH), which is released from the pituitary gland. This pathway is regulated via a closed-loop feedback process: Elevated concentrations of T3, and T4 in the blood plasma inhibit the production of TSH in the pituitary gland. As concentrations of these hormones decrease, the pituitary gland increases production of TSH, and by these processes, a feedback control system is set up to regulate the amount of thyroid hormones that are in the bloodstream.
 
As the true hormone, the effects of T3 on target tissues are roughly four times more potent than those of T4.Of the thyroid hormone that is produced, just about 20% is T3, whereas 80% is produced as T4. Roughly 85% of the circulating T3 is later formed in the thyroid by removal of the iodine atom from the carbon atom number five of the outer ring of T4. In any case, the concentration of T3 in the human blood plasma is about one-fortieth that of T4. This is observed in fact because of the short half-life of T3, which is only 2.5 days.This compares with the half-life of T4, which is about 6.5 days.
 
L-Liothyronine Application:
 
High Purity Liothyronine sodium/Cytomel T3/3,3',5´╝Źtriiodothyronine sodium/CAS No: 55-06-1 200-223-5 Weight Loss Powders
Liothyronine is the most potent form of thyroid hormone. Chemically, it is nearly identical to triiodothyronine (T3). As such, it acts on the body to increase the basal metabolic rate, affect protein synthesis and increase the body's sensitivity to catecholamines (such as adrenaline) by permissiveness. The thyroid hormones are essential to proper development and differentiation of all cells of the human body. These hormones also regulate protein, fat, and carbohydrate metabolism, affecting how human cells use energetic compounds.
In comparison to levothyroxine (T4), liothyronine has a faster onset of action as well as a shorter biological half-life, which may be due to less plasma protein binding to thyroxine-binding globulin and transthyretin.
 
Physicians can use this instead of or in addition to levothyroxine (T4) for patients undergoing thyroid withdrawal. When a patient has thyroid cancer or Graves' disease, ablation therapy with radioactive iodine can be used to remove any trace thyroid tissue. For 131I therapy to be effective, the trace thyroid tissue must be avid to iodine. The best method is to starve the tissue of iodine but this can lead to hypothyroid symptoms for the patient. Withdrawal from levothyroxine can be done but it takes six weeks of withdrawal for the remaining thyroid tissue to be completely starved. Six weeks is needed owing to levothyroxine's long half life. Six weeks can be inconvenient for the patient and delay treatment. Liothyronine instead can be taken and withdrawn from for two weeks to starve the thyroid tissue. This is much safer and more convenient than levothyroxine.
 

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Top Quality Loss Weight Peptide Adipotide For Fat Burn

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Top Quality Loss Weight Peptide Adipotide For Fat Burn
 
Adipotide Basic Info.:
 
Product Name: Adipotide
Place of origin: China
Routine use of Storage: 2-8°C
Molecular Formula: C111H204N36O28S2
Molar Mass: 2555.22 g/mol
Appearance: White powder
Purity: 99%+
Lead time: Customized
Mini Order: 2mg
Usage: The King of Weight Loss
Brand Name: KaFen
 
Adipotide Description:
 
What is Adipotide?
Aditpotide is an experimental weight loss peptidomimetic with the amino acid sequence CKGGRAKDC-GG-D(KLAKLAK)2, which has been developed by researchers in the United States in an effort to fight obesity. Peptidomimetics are small protein-like chains designed to mimic a peptide. The peptide called Adipotide has been developed by U.S. researchers in the fight against the obesity . This experimental treatment has reduced by 11% the weight of the treated monkeys by reducing fatty tissue, the BMI, and waist circumference.
 
For Anti-Obesity
Pathological studies have shown that obesity serves a risk factor for a myriad of diseases such as cancer, hypertension, endocrine disorders (such as diabetes mellitus, hyperlipidemias and metabolic syndrome), cardiovascular disease (such as stroke and myocardial infarctions) and degenerative diseases (such as osteoarthritis). Moreover, aberrant accumulation of white adipocytes predisposes the affected individual to lipoma and lipomatosis. It is well known that abdominal adiposity is mainly caused by white adipocytes, and this form of adiposity is the most lipolytically active, thus requiring a steady blood supply. Any interference with the blood supply causes it to activate the apoptotic process.
 

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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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Treatment Receptor Metastatic Drug Fulvestrant / Faslodex 129453-61-8 Anti Cancer Steroids Raw Powder

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Treatment Receptor Metastatic Drug Fulvestrant / Faslodex 129453-61-8 Anti Cancer Steroids Raw Powder
 
Fulvestrant Basic Info.:
 
Product Name: Fulvestrant
Synonyms: Faslodex
Chemical Name: (7a,17b)-7-[9-[(4,4,5,5,5-Pentafluoropentyl)sulfinyl]nonyl]estra-1,3,5(10)-triene-3,17-diol
CAS: 129453-61-8
Molecular Fomular: C32H47F5O3S
Molecular Weight: 606.77
Purity: 99%
Appearance: White powder
Density: 1.201 g/cm3
Melting Point: 104-106°C
Boiling Point: 674.8 °C at 760 mmHg
Package: 10g/foil bag
Usage: To treat estrogen receptor positive metastatic breast cancer in postmenopausal women, with disease progression following antiestrogen therapy.
 
Fulvestrant Description:
 
Fulvestrant also called Faslodex or AstraZeneca,is is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It works by blocking the actions of estrogen in the body. Fulvestrant is a complete estrogen receptor antagonist with no agonist effects, which in addition, accelerates the proteasomal degradation of the estrogen receptor. The drug has poor oral bioavailability, and is administered monthly via intramuscular injection.Certain types of breast cancer use estrogen to grow and multiply in the body.do not use fulvestrant if you are allergic to any ingredient in fulvestrant ,and Contact your doctor or health care provider right away if any of these apply to you.
 
Fulvestrant Applications:
 
Many breast cancers are stimulated to grow by the female sex hormones oestrogen and progesterone. These breast cancers are called hormone sensitive or hormone receptor positive. Drugs that block the effects of these hormones can slow or stop the growth of the breast cancer cells. Fulvestrant stops oestrogen getting to the cancer cells by blocking oestrogen receptors and reducing the number of receptors the cancer cell has.
 
Fulvestrant Acetate (Faslodex, AstraZeneca) is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It is an estrogen receptor antagonist with no agonist effects, which works by down-regulating the estrogen receptor.
 
Fulvestrant Acetate is a selective estrogen receptor down-regulator (SERD). Fulvestrant is indicated for the treatment of hormone receptor positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. The dosing schedule for fulvestrant remains under investigation in an attempt to optimize its effectiveness.
 

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Triiodothyronine

Triiodothyronine is a thyroid hormone. It is metabolically active hormone that is produced from T4. It affects almost every physiological process in the body, including growth and development, metabolism, body temperature, and heart rate, increases the basal metabolic rate and, thus, increases the body's oxygen and energy consumption, stimulates the production of RNA Polymerase I and II, potentiates the effects of the b-adrenergic receptors on the metabolism of glucose, stimulates the breakdown of cholesterol and increases the number of LDL receptors. It affects the lungs and influences the postnatal growth of the central nervous system. It stimulates the production of myelin, the production of neurotransmitters, and the growth of axons. It is also important in the linear growth of bones, may increase serotonin in the brain, in particular in the cerebral cortex, and down-regulate 5HT-2 receptors, used to treat Wilson's syndrome.

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USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9

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USP Grade Pharmaceutical Raw Materials 99%Min Idebenone For Cerebral Infarction 58186-27-9
 
Idebenone Basic Info.:
 
Product Name: Idebenone
CAS: 58186-27-9
Chemical name: 6-(10-Hydroxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone
Molecular formula: C19H30O5
Molecular weight: 338.44
Melting point: (52- 55 °C )
Loss on drying: ≤ 0.5%
Relevant impurities(HPLC ): ≤ 0.8%
Content(HPLC ): ≥ 99.5%
Packing specification: 5Kg / tin, 25Kg / tin
Storage: Sealed and stored at room temperature.
Executive standard:Enterprise standard
Appearance: Orange yellow or orange crystalline powder, odorless, flavorless.
Property: This product is orange yellow or orange crystalline powder, soluble in methanol, ethanol, insoluble in water, odorless, flavorless.
Used for cerebral infarction, cerebral hemorrhage and cerebral artery sclerosis associated with depression, such as language barriers and intelligence impairment, etc.
 
Idebenone Introduction:
 
Idebenone is a kind of new drug for treating senile dementia and improving mental symptom. Also, it is a better antioxidant in cosmetics and health care than Coenzyme Q10 and Vitamin.
 
Idebenone is a modified version of coenzyme Q10 (CoQ10), which is absolutely crucial for metabolic function. Without it, the electron respiratory chain breaks and cells cannot produce energy. It is also the only lipid-soluble antioxidant that is synthesized in our bodies. Natural levels of CoQ10 begin to decrease after age 30.
 
CoQ10 would be a perfect supplement for athletes that expend excessive energy or push the anaerobic envelope were it not for one important detail: under hypoxic conditions (like going anaerobic), CoQ10 becomes pro-oxidative and creates a powerful free radical that can damage DNA, mitochondria, and lipid membranes.
 
There is a synthetic variation of CoQ10 called ubiquinol, also known as idebenone. It has been formulated to have all the advantages of CoQ10 without the pro-oxidative drawback.
 

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