chemical-categories

 

Pharmaceutical Human Growth Hormone Peptide TB-500 Anti Inflammatory

 

TB 500 Basic Info.:

 

Product Name: TB 500 

Synonyms:TB 500;TB500;Thymosin Beta 500

TB500 Appearance: White powder

TB500 CAS No.: 77591-33-4

TB500 MF: C212H350N56O78S

TB500 MW: 4963.49

TB500 Specification: 2mg/vial,10vials/kit

TB500 Purity (HPLC): 95%min

TB500 Amino Acid Composition: ± 10% of theoretical

TB500 Peptide Content (N%): ≥ 80.0%

TB500 Water Content(Karl Fischer): ≤ 5.0%

TB500 Acetate Content (HPIC): ≤ 15.0%

TB500 Single Impurity (HPLC): 2.0%max

TB500 MS(ESI): Consistent

 

TB 500 Description:

 

TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human 

and animal cells. The main purpose of this peptide is to promote healing. It also promotes creation 

of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons,

ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher 

concentration where tissue has been damaged. This peptide is also a very potent anti-inflamatory 

agent. 

 

TB-500 is different from other repair factors (growth hormone, IGF-1), because it promotes 

endothelial and keratinocyte migration. It also does not bind to the extracellular matrix and has 

a very low molecular weight. Because of this it can travel long distances through the tissues in the 

human body. 

 

One of TB-500 key mechanisms of action is its ability to regulate the cell-building protein - Actin. 

Of the thousands of proteins present within human cells, actin represents roughly 10% of the total.

It is thus a vital component of cell structure and movement.

 

TB-500 was identified as a gene that was up-regulated four-to-six fold during early blood vessel

formation and found to promote the growth of new blood cells from the existing vessels. This peptide is present in wound fluid and when administered subcutaneously, it promotes wound healing, muscle building and speeds up recovery time of muscles fibres and their cells. An additional key factor of

TB-500 is that it promotes cell migration through a specific interaction with actin in the cell cytoskeleton.

It has been demonstrated that a central small amino acid long-actin binding domain has both blood cell reproduction and wound healing characteristics. These characteristics are uncovered by accelerating

the migration of endothelial cells and keratinocytes. It also increases the production of extracellular matrix-degrading enzymes.

 

TB 500 Application:

 

TB-500 is different from other repair factors because it promotes endothelial and keratinocyte migration. It also does not bind to the extracellular matrix and has a very low molecular weight.Because of this it can travel long distances through the tissues in the human body. 

 

TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human and animal cells. The main purpose of this peptide is to promote healing. It also promotes creation of new blood and muscle cells. The healing effects of TB-500 have been observed in tendons, ligaments, muscle, skin, heart, and the eyes. Thymosin beta-4 is naturally produced in higher concentration where tissue has been damaged. This peptide is also a very potent anti-inflamatory agent.

 

 

Pharmaceutical Raw Material Flutamide For Cancer Treament 13311-84-7

 

Flutamide Basic Info.:

 

Product Name: Flutamide 

Synonyms: Timtec-bb sbb006930;Flutamide;Aurora ka-860

CAS: 13311-84-7 

MF: C11H11F3N2O3 

MW: 276.21 

EINECS: 236-341-9 

Chemical Properties: Light Yellow Solid 

Standard: Enterprise Standard 

Packing: foil bag or as required

Product Categories: Antitumors for Research and Experimental Use;Biochemistry;Amines;Aromatics;Pharmaceutical raw material 

 

Flutamide Usage:

 

Neuroleptic, Flutamide is a nonsteroidal antiandrogen drug, antineoplastic (hormonal). 

 

Flutamide Features:

 

For prostate cancer or benign prostatic hypertrophy. This product with bright prolyl Lee Teuk combination (should also start and at the same time, the continued use of) for the treatment of metastatic prostate

cancer, can significantly increase the efficacy.

 

 

Steroid Hormone Nandrolone Phenylpropionate For Bodybuilding 62-90-8

Pharmaceutical Material Nandrolone Phenylpropionate 62-90-8

 

Nandrolone Phenylpropionate Basic Info.

 

Product Name: Nandrolone Phenylpropionate

CAS No.: 62-90-8

Molecular Formula: C27H34O3

Molecular weight: 406.56

EINECS: 200-551-9

Assay: 98%

Packing: Foil bag or tin.

Delivery: Express courier.

MOQ: 10 grams.

Appearance: White or almost white crystalline powder; Soluble in ethanol, slightly soluble in vegetable oil; Practically insoluble in water MP: 93~99

Usage: Pharmaceutical material, Steroid hormone, Anabolin. As a male hormone and anabolic hormones.

 

Nandrolone Phenylpropionate Description:

 

Nandrolone phenylpropionate is one of the most popular injectable steroids. It is basically Deca, with a shorter ester ( phenylpropionate instead of decanoate ester found in deca durabolin or nandrolone decanoate), resulting in quicker release into the bloodstream. Although its shorter ester means it will require more frequent injections than decanoate, the positive side is that the amount of effective nandrolone in the blood and its levels are more easilly contollable. It's popularity is likely due to the fact that nandrolone exhibits significant anabolic effects with minimal androgenic side effects.

 

Nandrolone Phenylpropionate Applications:

 

Use after surgery for chronic wasting disease, serious illness, and weak thin, infirm, osteoporosis, infantile dysplasia, aplastic anemia, etc.

In earlier years, the only pharmaceutical injectables that were both widely available to bodybuilders and economical. Estrogen control did not then exist. For this reason, Durabolin's low aromatizing properties were then quite useful. Durabolin therefore won wide popularity.

 

 

Cosmetic Peptide Argireline Anti-Aging Argreline Acetate 616204-22-9 

 

Argireline Basic Info.:

 

Product Name: Argreline Acetate (Argireline)

Specification: 5mg/vial

Synonyms: Argireline;Argireline Acetate;Argirelin Acetate(Acetyl Hexapeptide-3);Acetyl Hexapeptide;Acetyl Hexapeptide-8

CAS: 616204-22-9

MF: C{46}H{56}N{12}O{6}

MW: 888.99

Density: 1.54

Storage temp.: -20°C

Product Categories: Peptide;Cosmetic Peptide

 

 

High Purity Male Sex Hormones Sildenafil Mesylate For Male 131543-23-2

 

Sildenafil Mesylate Basic Info.:

 

Product Name: Sildenafil Mesylate

English name: Win 55,212-2 Mesylate

English Synonyms: Sildenafil Mesylate

CAS: 131543-23-2

MF: C28H30N2O6S

MW: 522.6126

Boiling point: 627.7 °C at 760 mmHg

Flash Point: 333.4 °C

Vapor Pressure: 1.14E-15mmHg at 25 °C

Properties:Solubility: 0.1 M HCl: 0.25 mg / mL

Appearance: White or white crystalline powder, odorless, bitter astringent taste, soluble in water and ethanol

Usage: Pharmaceutical raw materials, aphrodisiac It is medicine treatment raw material, indicated for the treatment of erectile dysfunction.

 

Sildenafil Mesylate Description:

 

Sildenafil Mesylate, same as Sildenafil is an inhibitor of type 5 -cGMP phosphodiesterase relaxing and smoothing muscle cells of the corpus cavernosum which leads to penile erection. This relaxation may be

mediated by nitric oxide via cyclic guanosine monophosphate.

 

pharmaceutical material, hormone. As a cyclic guanosine monophosphate (cGMP) specific phosphodiesterase type 5 (PDE5) selective inhibitor, penile smooth muscle relaxation allows rapid erection. Sildenafil is cheap, is the development and production of low-cost classes available kidney yang-like the perfect material for medicine and health products.

 

Sildenafil Mesylate Applications:

 

In 16 separate 4-24 week trials of men (over 18 years old) who suffered from impotence for longer than 6 months, dosages between 10-200 mgs were administered. Significant improvements in erectile function, including frequency of penetration as well as erection duration post penetration, were reported with Sildenfi* treatment compared to the placebo group.

Erections were improved in 72% of group verses 18% of the placebo group. In all cases effects were dependant upon dosage and improvement was the greatest when dosage exceeded 100 mgs. Responses were decreased by 40-60% in patients suffering from diabetes and prostatectomy, respectively. Withdrawal rates were less than 5% related to negative side effects and limited response rates

 

 

Peptides Alarelin Acetate For Ovulation And Endmometriosis 79561-22-1 

 

Alarelin Acetate Basic Info.:

 

Product Name: Alarelin Acetate

Synonyms: Des-Gly10,[D-Ala6]-Lh-Rh Ethylamide Acetate Salt.

CAS: 79561-22-1

MF: C56H78N16O12

MW: 1167.32

Storage temp.: −20°C

Form: Powder

Product Categories: Amino Acid Derivatives;Peptide;LH-RH;LH-RHPeptides for Cell Biology;Neuropeptides;Releasing Factors;API.

 

Alarelin Acetate (79561-22-1) Description:

 

Alarelin acetate is a gondatrophin releasing hormone. Natural forms of alarelin found in animals are used to induce ovulation. Synthetic versions of this product are created using an LH-RH antagonist which is commonly set in larger doses than the natural LH-RH that is typically found in the rat hypophyseal stimulation or the gondatoropin secretions in induced ovulation or in vitro.

 

This chemical is the acetate form of the natural hypothalamic peptide which is used by an animal’s body to release LH and FSH from the pituitary gland. The peptide alarelin acetate has a single non-glycosylated polypeptide structure that is made up of nine amino acids. This has a molecular mass of 1167.3.

 

Alarelin is commonly used in research settings both to better understand this peptide’s effects on an animal’s body and to induce conditions that may assist with reproductive research. Samples of this chemical intended for research settings are typically stable for around three weeks at room temperature, and will need to be stored at temperatures below -18 degrees Celsius for long term use.

 

Most versions of this chemical are shipped as a lyophilized powder that can be reconstituted at a sterile temperature. This chemical may remain stable for up to three weeks at room temperature if it is kept sealed when it is not in use. If this product will be used for long periods of time is should be kept in a freezer with a waterproof sea.

 

If the mixture has already been reconstituted it can be kept at 40 degrees Celsius for 2-7 days but should be kept at -180 degrees Celsius for longer periods of time. Do not continually refreeze and thaw the product.

 

 

Polypeptide Human Growth Powder Hormone Peptide Selank CAS 129954-34-3

 

Selank Basic Info.

 

Product Name: Selank

Alias: Selanc;Selank

Sequence: Thr-Lys-PRO-Arg-PRO-Gly-PRO

CAS: 129954-34-3

MF: C33H57N11O9

MW: 751.9

Purity: 99%

Specification: 5mg/vial

Appearance: White Lyophilized Powder

Place of Origin: China

Standard: USP

Certification: SGS

Method of Analysis: HPLC

Use: Reduce stress, relieve depression, insomnia quit. Of course, with Selank a puzzle-anxiolytic

 

Descriptions Of Selank:

 

Selank was developed by the Russian Academy of Sciences. anxiolytic peptide based drugs. Selank is a heptapeptide with the sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro. It is a synthetic analogue of a human tetrapeptide tuftsin.

 

it uses relief of anxiety and improved cognitive functioning alone. Selank used for : Stress reduction, the alleviation of depression, reversal of anhedonia, improvement in mood in emotionally stable individuals, and cessation of insomnia.

 

In fact,Selank more suitable for long-term use. for the large majority of researchers claiming that it is a "side effect free" compound. Some believe an overdose might cause fatigue.

 

Application Of Selank:

 

(1)Selank as a nootropic:

Recreationally Selank is used to improve one's ability to focus and concentrate, reduce mental fatigue, increase mental sharpness and increase memory and learning capacity. The first noticeable effect is usually stabilization of mood and general feeling of well-being.

 

(2)Selank as an antiviral agent:

Selank neuropeptide also expresses immunomodulatory effects. In 2009 a study by F. Ershov et all. has evaluated antiviral properties of Selank both in vitro and in vivo against the influenza virus strain A/Aichi 2/68 (H3N2). The pronounced antiviral effect of Selank was detected in both systems. The highest efficiency - completely supressed viral reproduction was shown when Selank was added to the cell culture 24 hours before inoculation.

 

 

Steroid Hormone Powder Eplerenone For Lowering Blood Press 107724-20-9

 

Eplerenone Basic Info.:

 

Product Name: Eplerenone

Chemical Name: Pregn-4-ene-7,21-dicarboxylic acid 9,11-epoxy-17-hydroxy-3-oxo gamma-

lactone methyl ester

CAS No.: 107724-20-9

Molecular Formula: C24H30O6

Molecular weight: 414.49

Appearance: white crystalline powder; slightly soluble in water.

Standard: Enterprise Standard

 

Eplerenone Description:

 

Eplerenone (INN) /plrnon/ is an aldosterone antagonist used as an adjunct in the management of chronic heart failure. It is similar to the diuretic spironolactone, though it is much more selective for the mineralocorticoid receptor in comparison (i.e., does not possess any antiandrogen, progestogen, or estrogenic effects), and is specifically marketed for reducing cardiovascular risk in patients following myocardial infarction. It was marketed byPfizer under the trade name Inspra but is now only available as a generic in every country except the United Kingdom. Eplerenone is a potassium-sparing diuretic, meaning that it helps the body get rid of water but still keep potassium.

 

Eplerenone Application:

 

Eplerenone is specifically indicated for the reduction of risk of cardiovascular death in people with heart failure andleft ventricular dysfunction within 3-14 days of an acute myocardial infarction, in combination with standard therapies and as treatment against hypertension. It appears equivalent to spironolactone but is much more expensive.

 

 

99% Pharmaceutical Sarms Powder Ostarine Enobosarm Mk-2866 1202044-20-9

 

MK-2866 (Ostarine) Basic Info.:

 

Product Name: MK-2866

Synonyms: Ostarine

CAS: 1202044-20-9

MF: C19H10D4F3N3O3

Product Categories: Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Hormone Drugs

Recommended maximum dose OSTARINE about 25 mg once a day for men, females and 12.5 mg. It has a half-life of 24 hours a day.Improve the minimum recommended dose aesthetic constitution (means) male is 12.5 mg. Low dose may produce little results notification clause or muscle growth, but it will help to health. Women's minimum recommended dose, and for those who seek to improve health, 5 mg per day, it should be noted that therapeutic doses as low as 3 mg a day have been reported in the gender is good.

 

MK-2866 (Ostarine) Description:

 

Ostarine (MK-2866) is a SARM developed by GTx for the prevention and treatment of muscle wasting. It may eventually be a medical prescription for the prevention of cachexia, atrophy and sarcopenia as well as for Hormone or Testosterone Replacement Therapy.

As a research chemical, Ostarine belongs to a class of chemicals know as SARMS or selective androgen receptor modulators. SARMS create selective anabolic activity at certain androgen receptors. In comparison to testosterone and other anabolic steroids, the advantage of SARMS, is they do not have androgenic activity in non-skeletal muscle tissues. Ostarine is effective in maintaining and increasing lean body mass.

Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.

 

MK-2866 (Ostarine) Application:

 

Selective androgen receptor modulators may be used by athletes to assist in training and increase physical stamina and fitness, potentially producing effects similar to anabolic steroids.

Ostarine is a potent and tissue-selective androgen receptor modulator (SARM) for treatment of conditions such as muscle wasting and osteoporosis. These patent products for research purposes only use. Ostarine (GTx-024, MK-2866, Enobosarm, S-22) is an orally bioavailable nonsteroidal selective androgen receptor modulator. Therefore, ostarine can be used for treatment of conditions such as muscle wasting and osteoporosis.

 

MK-2866 (Ostarine) Function:

 

1.Enobosarm (Ostarine, MK-2866, GTx-024) - affects both muscle and bone, intended mainly for osteoporosis but also general treatment for andropause and reversing muscle sarcopenia in the elderly and for cachexia in cancer patients

2.Nonsteroidal selective androgen receptor modulator (SARM) used in the treatment of osteoporosis and muscle wasting in animal models. A potential compound for the treatment of hypoactive sexual desire disorder.

 

 

99% Purity Cancer Treatment Steroids Formestane For Breast CAS 566-48-3

 

Formestane Basic Info.:

 

Product name: Formestane

Other name: Formestane; Lentaron; Formestqne; Hydroxyandrostenedione

CAS Registry Number: 566-48-3

Assay: 98%Packing: 1kg/aluminum foil bag

Molecular Formula: C19H26O3

Molecular Weight: 302.41

Appearance: White crystalline powder

 

Product Description Of Formestane:

 

Formestane was the first selective, type I, steroidal aromatase inhibitor used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. Formestane suppresses estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosterone, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor. It is listed as a prohibited substance by the World Anti-Doping Agency for use in athletes. 

 

Formestane has poor oral bioavailability, and thus must be administered forthnightly (bi-weekly) by intramuscular injection. Some clinical data has suggested that the clinically recommended dose of 250mg was too low. With the discovery of newer, non-steroidal and steroidal, aromatase inhibitors which were orally active and less expensive than formestane, formestane lost popularity. 

 

Currently, formestane (categorized as an anti-estrogenic agent) is prohibited from use in sports in accordance to the regulations of the World Anti-Doping Agency. It is not US FDA approved, and the intramuscular injection form of formestane (Lentaron) which was approved in Europe has been withdrawn. 

 

Formestane (Lentaron) is a type I, steroidal aromatase inhibitor. It is used in the treatment of estrogen-receptor positive breast cancer in post-menopausal women. It is available as an intramuscular depot injection.

 

Formestane is often used to suppress estrogen production from anabolic steroids or prohormones. It also acts as a prohormone to 4-hydroxytestosteron, an active steroid which displays weak androgenic activity in addition to acting as a mild aromatase inhibitor.

 

Formestane has poor oral bioavailability and as such is no longer popular as many orally active aromatase inhibitors have been identified.

 

Formestane Applications:

 

Formestane is a second generation, irreversible, steroidal aromatase inhibitor. It inhibits the aromatase enzyme responsible for converting androgens to estrogens, thereby preventing estrogen production. Breast cancer may be estrogen sensitive or insensitive. A majority of breast cancers are estrogen sensitive. Estrogen sensitive breast cancer cells depend on estrogen for viability. Thus removal of estrogen from the body can be an effective treatment for hormone sensitive breast cancers. Formestane has been targeted specifically for the treatment of postmenopausal women. Unlike premenopausal women who produce most estrogen in the ovaries, postmenopausal women produce most estrogen in peripheral tissues with the help of the aromatase enzyme. Formestane, an aromatase inhibitor, can thus help to decrease the local production of estrogen by blocking the aromatase enzyme in peripheral tissues (ie. Adispose tissue of the breast) to treat hormone sensitive breast cancer.