chemical-categories

 

Amino Acid Derivatives Angiotensin 1407-47-2

 

Angiotensin Basic Info.:

 

Product Name: Angiotensin

Synonyms: Angiotensin;Angiotensinii;Hypertensin

CAS: 1407-47-2

MF: C62H89N17O14

MW: 1296.49

EINECS: 215-804-9

Purity: 1407-47-2

Product Categories: Amino Acid Derivatives;Enzyme

 

 

Human Growth Peptides IGF-1 IGF1 Human Des1-3

 

IGF-1 Basic Info.

 

Product Name: IGF1 Human Des1-3 (IGF-1)

Molar Mass: 7,372 Da

Synonyms: IGF-1Des(1-3); Des1-3; Des 1-3; Des (1-3)

Compound: Thr-Leu-Cys-Gly-Ala.

Purity: 99.21%

 

IGF-1 IGF-1DES Dose:

 

DES IGF-1 can be dosed at 50-150mcg multiple times a day (prior to training) into specific target areas. since DES has such a short half life (20-30 minutes), desensitization was not noticed at all . Injection sites should be localized; preferably, at the muscle group you want to grow. In simple terms, if you want to grow your biceps, inject IGF-1DES right into your bicep.

 

IGF-1 IGF-1DES Half-life:

 

DES IGF-1 is the shorter version of the IGF-1 chain. It is five (5) times more powerful than IGF-1LR3 and ten (10) times more powerful than regular base IGF-1. The half-life for DES is about 20-30 minutes, which means this is a very delicate chain. Therefore, administration should only be done at the site where you want to see muscle growth. DES has the ability to stimulate muscle hyperplasia better than LR3. In simple terms, it's best used for site injections, rather than overall growth.

In addition, DES is known to bind to receptors that have been deformed by lactic acid, which is often present during workouts. This allows the DES to attach itself to a mutated receptor and signal tissue growth during training. DES can be used longer and more frequently than LR3.

 

 

Human Growth SR9009 Powder SR-9009 1379686-30-2

 

SR 9009 Basic Info.

 

Product Name: SR 9009

SR9009 Prohormone Steroids SARMS

CAS: 1379686-30-2

MF: C20H24ClN3O4S

MW: 437.94

Purity: 99%

Appearance: White powder

Solubility: DMSO

Application: SR9009 increase exercise endurance and loss weight.

 

SR 9009 Description:

 

SR9009 also known as Stenabolic,is a synthetic Rev-Erb ligand and PPAR alpha modifier drug,which is taken orally.This is a very unique compound. By stimulating the Rev-Erb protein, SR9009 has the ability to greatly influence a lot of regulatory mechanisms in the human body.it can affect the circadian rhythms, lipid and glucose metabolism, fat-storing cells, as well as macrophages. SR9009 will allow the user to lose fat and drastically increase endurance, both of which are very desirable effects for an athlete.

 

How SR 9009 Works?

 

By binding and activating the Rev-Erb protein, Stenabolic triggers a very wide range of processes in the body. The most prominent being the increase of mitochondria count in the muscles and an enhanced metabolism.That causes a drastic improvement in endurance and muscle strength.And thanks to the increase in number of macrophages, defective mitochondria are removed from the muscles and replaced with new ones.

 

Furthermore, the change in metabolic rates increases energy expenditure by 5% even when the user is resting.It burns excess calories and doesn’t allow them to convert into fat.Coupled with enhanced metabolism of glucose, helps effectively burn fat, which makes the body act is if it were in a constant state of exercise.

 

This means that less fat is stored, less cholesterol is developed by the liver, and more fat and glucose is burned in the muscles.

 

 

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－triiodothyronine 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.

 

 

Injectable Anabolic Steroids Peptide CJC-1295 DAC

 

CjC 1295 DAC Basic Info.

 

Product Name: CjC 1295 DAC

Other name: CJC1295dac, CJC1295 with DAC

Product Description: CJC-1295 2mg/Vial

Type: Immune Function Agents

Grade

Standard: Medicine Grad

Classification: Brassinosteroid

CAS: 863288-34-0

MF: C165H271N47O46

Molecular Weight: 3649.30

Purity (HPLC): 98.0%

Appearance: White powder

Single Impurity(HPLC): 1.0%

Amino Acid Composition: 10% of theoretical

Peptide Content(N%): 80%(by %N)

Water Content(Karl Fischer): 6.0%

Acetate Content(HPIC): 15.0%

Mass Balance: 95.0~105.0%

 

CjC 1295 DAC Description:

 

CJC 1295 with DAC is a powerful growth hormone releasing hormone that can be effectively used with a GHRP in order to maximize the greatest endogenous growth hormone release bodybuilders and athletes are looking for. Even though CJC 1295 with DAC may be a bit more expensive than MOD GRF 1-29 (CJC 1295 without DAC), it is still the preferred and more powerful GHRH component in your peptide protocol.

 

Know more about CJC1295 with DAC:

 

The original GRF (1-29) has a half-life of about 30 minutes. Half-life means the time within which half of the hormone administered will be destroyed within the body. This short half-life is due to the fact that the compound is highly unstable and breaks down soon. To increase its stability and to make it last longer, it was modified by adding 4 amino acids in its structure. This gave it the name Modified GRF (1-29) or Mod GRF 1-29. It was originally invented by DatBtrue. The portion of the molecule that actually stimulates the growth hormone secretion is found in the chain of 29 amino acids, so it is named GRF (1-29). This chemical also produces slow-wave sleep.

 

However, both the original GRF (1-29) and the Mod GRF 1-29 required frequent dosages. So a new compound called CJC-1295 was created which was far more stable. This compound was made by adding Lysine - which is a non-peptide, and is also called Drug Affinity Complex or DAC. Since the original Mod GRF 1-29 does not contain DAC, it is named as CJC-1295 without DAC. However, the actual CJC-1295 is not only difficult, but also very expensive to produce. This is why it is not produced or used extensively. The Mod GRF 1-29 is far easier and cheaper to produce.

 

 

99% Oxandrolone Anavar Bodybuilding Powder 53-39-4

 

Oxandrolone Basic Info.:

 

Product Name: Oxandrolone

Alias: Anavar

CAS No: 53-39-4

Einecs No: 200-172-9

MF: C19H30O3

MW: 306.44

Purity: 99%

Appearance: White crystalloid powder.

Anabolic Oral Steroid Hormone Powder Oxandr Anavar

 

Oxandrolone Description:

 

Anavar, also called Lonavar, Oxandrin, Vasorome, its chemical name is 17beta-Hydroxy-17-methyl-2-oxa-5alpha-androstan-3-one. Anavar is a kind of oral testosterone drugs synthetised by actively metabolizing anabolic. It researched that 20mg Oxandrolone daily dose has an effect on weight gaining and rehabilitation muscle for who encounters large area burnt.

Anavar, which comes out of androgenic character, can cause retention of nitrogen, potassium and phosphorus, and promote anabolism and inhibit excessive catabolism. Anavar is widely used for boys who come across abnormal growth and late puberty, and also girls who encounter congenital ovarian hypoplasia.

 

Anavar absorbed rapidly according to intestines and stomach. Its metabolites and unchanged oxandrolone excreted by the kidneys, and small amount exclude from gastrointestine.

 

Oxandrolone Applications:

 

Anavar has often been called a weak steroid. Part of the reason for this is that use of a Class I steroid alone never is maximally effective. The other cause is that bodybuilders and authors in the field sometimes make unfortunate and unreasonable comparisons when judging anabolic steroids. 

 

Oxanabol(Anavar, Oxanabol) has given optimistic consequences in taking care of anemia and hereditary angioedema. Proven studies though have given links linking expanded use of the medicine and problems of liver toxicity like to those found with additional 17α-alkylated steroids. Yet in little dosages, numerous patients shown gastro-intestinal troubles such as bloating, nausea, and diarrhea. Oxanabol(Anavar, Oxanabol)`s specificity targeting the androgen receptor predestined that, unlike lot other steroids, it had not been seen to give stunted development in teens people, as well at usual measure not often observed clear masculinising reactions external of stimulating strength growth. Oxanaboldoes not aromatize at any measure, and is not without problems ingested into DHT or estrogen. As such, a typical dose of 20-30 mg offered eminent androgen levels for up to eight hours. To enlarge use, bodybuilders classical "stacked" the Oxanabol(Anavar, Oxanabol) with others such as , advance enhancing corp power increase. 

 

 

Legal Hormone Adrenaline For Body Building 51-43-4

 

Adrenaline Basic Info.

 

Product Name: Adrenaline

Synonyms: Adrenaline, L-Epinephrine

CAS: 51-43-4

MF: C9H13NO3

MW: 183.2

EINECS: 200-098-7

Purity: 99%

Melting point: 215 °C (dec.)(lit.)

Alpha: -51.5 º (c=4, 1M HCl, dry sub)

Refractive index: -51.5 ° (C=4, 1mol/L HCl)

Storage temp.: 2-8°C

Water Solubility: <0.01 g/100 mL at 18 ºC

Sensitive: Air & Light Sensitive

Stability: Stable. Incompatible with acids, acid chlorides, acid anhydrides, oxidizing agents. Light sensitive.

Chemical Properties: Off-white powder

Product Categories: Medical Fabric;Standards - 13C & 2H for GC-Mass Spectrometry;Non-steroidal hormone drugs;Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitors.

Usage: 

(1)Endogenous catcholamine with combined α-and β-agonist activity. Principal sympathomimetic hormone produced by the adrenal medulla. Bronchodilator; cardiostimulant; mydriatic; antiglaucoma.

(2)L-Adrenaline (Epinephrine) belongs to a group of the compounds known as catecholamines, which play an important role in the regulation of physiological process in living organisms. The antioxidant activity and antioxidant mechanism of L-adrenaline was cla.

(3)Gibberellic Acid-3 (GA-3) is a plant growth regulator.

 

What is Adrenaline?

 

Adrenaline is produced in the medulla in the adrenal glands as well as some of the central nervous system's neurons. Within a couple of minutes during a stressful situation, adrenaline is quickly released into the blood, sending impulses to organs to create a specific response.

 

What is the Function of Adrenaline?

 

Adrenaline triggers the body's fight-or-flight response. This reaction causes air passages to dilate to provide the muscles with the oxygen they need to either fight danger or flee.

 

Adrenaline also triggers the blood vessels to contract to re-direct blood toward major muscle groups, including the heart and lungs. The body's ability to feel pain also decreases as a result of adrenaline, which is why you can continue running from or fighting danger even when injured.

 

Adrenaline causes a noticeable increase in strength and performance, as well as heightened awareness, in stressful times. After the stress has subsided, adrenaline’s effect can last for up to an hour.

 

 

High Purity Nootropic Powder Fasoracetam 110958-19-5

 

Fasoracetam Basic Info.:

 

Product Name: Fasoracetam

Synonyms: Fasoracetam; Aka NS-105; LAM-105

CAS: 110958-19-5

MF: C10H16N2O2

MW: 196.248

EINECS: N/A

Product Categories: Pharmaceutical Intermediates; Nootropic Drug

 

Fasoracetam description:

 

Fasoracetam is a research compound and member of the racetam family of nootropics,primarily known for their cognitive enhancing abilities. Fasoracetam is also an anxiolytic and may be able to improve mood as well. This racetam works by affecting three receptors within the brain: acetylcholine,GABA and glutamate, all of three of which are involved in the creation and retention of memories.

 

it is now a nootropic smart drug which portrays itself in one of the most powerful racetams in the nootropic universe. Made from a class of compounds called the racetams, and acting on not only acetylcholine but also GABA receptors in the brain, this has the ability of activating both cholinergic and glutamate receptors of the cerebral cortex, and is a revolutionary racetam drug due to its extremely unique mechanism of action. Fasoracetam currently also shows benefits as an anti-depressant, ADHD stimulant, and an anxiolytic, it also, as proven in laboratories across the nation, helps with the formation and retention of new memories.

 

Fasoracetam has also been observed to block the amnestic effects of scopolamine in a rat model of cholinergic dysfunction, which was noted as an increase of both ACh release in the cerebral cortex, as well as HACU enhancement in both the cerebral cortex and hippocampus. ChAT activity remained unaffected. In the same study, Fasoracetam was able to reverse baclofen-induced memory disruption, thus suggesting a blocking role at the GABAB receptor.

 

 

Polypeptide Hormone Follistatin 315 Antibody Fst-315

 

Follistatin 315 Basic Info.

 

Product Name: Follistatin 315 / Fst-315

Specification: 1mg/vial

Purity: 85%+

Appearance: White powder

Specific Optical Rotation (c=0.5,10% HAc): -50.0~-60.0°

Water Content(Karl Fischer): ≤5.0%

Acetate Content(by HPLC): ≤15.0%

Amino Acid Composition: ±10% of theoretical

Purity (by HPLC): ≥98.0%

Single Impurity(by HPLC): ≤1.0%

Peptide Content(by %N): ≥80%

Assay(By Anhydrous, Acetic Acid-free ) :95.0~105.0%

Bacterial Endotoxins: ≤5EU/mg

Storage/Stability: Stored at -20 °C if preferred. Storage in frost-free freezers is not recommended.

Note: This product is furnished for LABORATORY RESEARCH USE ONLY. Not for diagnostic or therapeutic use.

 

Description of Follistatin 315:

 

Follistatin is being studied for its role in regulation of muscle growth in mice, as an antagonist to myostatin (also known as GDF-8, a TGF superfamily member) which inhibits excessive muscle growth. Lee & McPherron demonstrated that inhibition of GDF-8, either by genetic elimination (knockout mice) or by increasing the amount of follistatin, resulted in greatly increased muscle mass.In 2009, research with macaque monkeys demonstrated that regulating follistatin via gene therapy also resulted in muscle growth and increases in strength. This research paves the way for human clinical trials, which are hoped to begin in the summer of 2010 on Inclusion body myositis.

A study has also shown that increased levels of follistatin, by leading to increased muscle mass of certain core muscular groups, can increase life expectancy in cases of spinal muscular atrophy (SMA) in animal models.

It is also being investigated for its involvement in polycystic ovary syndrome (PCOS), though there is debate as to its direct role in this infertility disease.

 

Follistatin 315 Application:

 

Follistatin 315 primary function is the binding and bioneutralization of members of the TGF-β superfamily, with a particular focus on activin, a paracrine hormone.

 

Storage Instruction

Store at +4°C or at -20°C if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.

 

 

Budesonide Powder Inhalation Antiasthmatic 51333-22-3

 

Budesonide Basic Info.:

 

Product Name: Budesonide

Synonyms: Dexbudesonide;TriaMcinolone-D5;Preferid;Pulmicort;Spirocort;S-1320;Rhinocort;Bidien;Cortivent.

CAS: 51333-22-3

MF: C25H34O6

MW: 430.5339

EINECS: 257-139-7

Assay: 99.5%

Density: 1.27g / cm3

Boiling point: 599.7 °C at 760 mmHg

Flash Point: 201.8 °C

Melting point: 221-232°C (dec.)

Storage temp.: Store at RT, Ventilated, low-temperature ,dry storeroom.

Appearance: White Solid

Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Steroids

Usage: 

(1)A non-halogenated glucocorticoid related to triamcinolone hexacetonide. Used as an antiinflammatory agent

(2)laxative, antineoplastic

(3)The oral capsule is used for the treatment of mild to moderate active Crohn's disease. The oral tablet is used for induction of remission in patients with active, mild to moderate ulcerative colitis. The oral inhalation formulation is used for the treatme.

 

Budesonide Attribute:

 

Budesonide is a glucocorticoid steroid for the treatment of asthma, COPD and non-infectious rhinitis (including hay fever and other allergies), and for treatment and prevention of nasal polyposis. In addition, it is used for inflammatory bowel disease. It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.

 

Budesonide Effect:

 

Budesonide is nebulized for maintenance and prophylactic treatment of asthma. also for treatment and prevention of nasal polyposis. maintenance of remission (for up to 3 months) of Crohn's disease (mild-to-moderate) involving the ileum and/or ascending colon. Budesonide assists in the induction of remission in patients with active ulcerative colitis.