Hormone drugs used in treating deficient hormone levels in body, thyroid problems, ovulation

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Bodybuilding Peptides Human Growth Hormones Fragment HGH 176-191

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Bodybuilding Peptides Human Growth Hormones Fragment HGH 176-191
 
HGH 176-191 Basic Info.
 
Product Name: HGH 176-191
Unit Size: 2 mg/vial 
Synonyms: Hgh Frag 176-191;Fragment 176 
Molecular Formula: C78H125N23O23S2 
Molecular Weight: 1817.1 
Sequence: H-Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe-OH 
Appearance: White Powder 
Purity: 98.14% 
Identity (ESI-MS): 1817.1±2.2 
Source: Chemical Synthesis 
Storage: Lyophilized Fragment 176-191 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 reconstituting Fragment 176-191 should be refrigerated at temperatures not to exceed 36 F. 
 
HGH 176-191 Description:
 
The HGH Fragment is a modified form of amino acids 176-191 at the C-terminal region of the human growth hormone (HGH). Studies have shown that it works by mimicking the way natural HGH regulates fat metabolism but without the adverse effects on insulin sensitivity (blood sugar) or cell proliferation (muscle growth) that is seen with unmodified HGH. Like unmodified GH, the HGH fragment 176-191 stimulates lipolysis (breaking down of fat) and inhibits lipogenesis (the formation of fatty acids and other lipids in the body).
 
HGH fragment 176-191 is meant to be 12.5 times stronger than human growth hormone (HGH) for weight loss than standard human growth hormone (HGH).
 
Of particular note is that in studies HGH fragment 176-191 had the ability to increase IGF-1 levels which translates into the fragments ability to give anti-aging effects.
 
Applications Of HGH 176-191:
 
How much Human Growth Hormone (HGH) Fragment 176-191 should be used?
In most studies favorable results have been shown with dosages between 400-600mcg or 4-6mcg/kg split into multiple dosages per day.
 
It has been shown that the fat-reducing effects of GH appear to be controlled by a small analog region of the C-terminus end of the GH molecule. This region consists of amino acids 176-191, thus the name. This peptide fragment works by mimicking the way natural hGH regulates fat metabolism but without the adverse effects on blood sugar or growth that is seen with unmodified hGH. Like unmodified GH, the HGH fragment 176-191 stimulates lipolysis and inhibits lipogenesis both en vivo/en vitro. Fragment 176-191 has shown no effect on growth or insulin resistance, unlike the full hGH molecule. This is the newest, most powerful hGH fragment on the market. Studies have shown sustained fatloss, aimed directly at adipose tissue.
 

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Nootropic Drugs Carphedon Phenylpiracetam Smart Drugs 77472-70-9

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Nootropic Drugs Carphedon Phenylpiracetam Smart Drugs 77472-70-9
 
Carphedon Basic information:
 
Product Name: Carphedon
Synonyms: 4-phenyl-2-pyrrolidone-1-acetamide;
CAS: 77472-70-9
MF: C12H14N2O2
MW: 218.25
EINECS: N/A
Apprarance: Off-white crystalline powder.
Product Categories: Pharmaceutical Intermediates; Nootropic Drug
Usage: Carphedone is a GABA derivative that exhibited apparent immunocorrection properties during immunosuppression induced by cyclophosphamide were studied.
 
Carphedon Dose:
 
As one of the strongest Racetam nootropics available, it is important that you precisely measure the dosage of your Carphedon powder.The suggested range of dosages for Carphedon is 100 mg to 250 mg taken a maximum of three times a day. You should experiment with different dosage levels to determine what works best for you. If this is your first time using nootropics, it is a good idea to start with a half dose and only build up to the full amount after a couple of weeks of experience.
 

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Best Price 99.9% Purity Vardenafil Fardenafil Hormone 224785-91-5

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Best Price 99.9% Purity Vardenafil Fardenafil Hormone 224785-91-5
 
Vardenafil Basic Info.:
 
Product Name: Vardenafil
Synonym: Fardenafil; Vardenafil 
CAS No: 224788-91-5
MF: C23H33ClN6O4S
MW: 525.06
Purity: 99%
Half life: 4-5 hours
Appearance: white powder, odorless, taste bitter and astringent soluble in water and alcohol.
Storage: in a cool and dry well-closed container and in ventilated area
  
Vardenafil Description:
 
Vardenafil (INN) is a PDE5 inhibitor used for treating erectile dysfunction. Vardenafil's indications and contra-indications are the same as with other PDE5 inhibitors; it is closely related in function to sildenafil citrate (Viagra) and tadalafil (Cialis). The difference between the vardenafil molecule and sildenafil citrate is a nitrogen atom's position and the change of sildenafil's piperazine ring methyl group to an ethyl group. Tadalafil is structurally different from both sildenafil and vardenafil. Vardenafil's relatively short effective time is comparable to but somewhat longer than sildenafil's.
  
Vardenafil Application:
 
Beyond its indications for erectile dysfunction, vardenafil may be effective in the treatment of premature ejaculation, where it may significantly increase the time from vaginal penetration to ejaculation.
Vardenafil, as with all PDE5 inhibitors, should not be used by men taking nitrate medications, because combining them with vardenafil might provoke potentially life-threatening hypotension (low blood pressure).
Further, Vardenafil causing lengthening of the QT interval. Therefore it should not be taken by men taking other medications that affect the QT interval (such as amiodarone).
 

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Factory Sell High Purity Nootropics Powder Phenibut CAS 1078-21-3

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Factory Sell High Purity Nootropics Powder Phenibut CAS 1078-21-3
 
Phenibut Basic information 
 
Product Name: Phenibut ( 4-Amino-3-phenylbutyric acid hydrochloride )
Product Name: 4-Amino-3-phenylbutyric acid hydrochloride
Synonyms: Phenibut;TIMTEC-BB SBB001567;PHENIBUT;4-amino-3-phenylbutanoicacid;4-amino-3-phenyl-butyricaci;beta-(aminomethyl)-benzenepropanoicaci;beta-(aminomethyl)benzenepropanoicacid;beta-(aminomethyl)hydrocinnamicacid;beta-phenyl-gamma-aminobutyrate
CAS: 1078-21-3
MF: C10H14ClNO2
MW: 215.68
EINECS: 214-079-6
Product Categories: Organic acids;Nutritions & Sterides;API;Inhibitors.
 

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Pharmaceutical Grade Raw Material Chitosan CAS 9012-76-4 For Food

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Pharmaceutical Grade Raw Material Chitosan CAS 9012-76-4 For Food
 
Chitosan Basic information
 
Product Name: Chitosan
Synonyms: POLY(BETA-(1,4)-2-AMINO-2-DEOXY-D-GLUCOSE);POLY(BETA-(1,4)-D-GLUCOSAMINE);POLY(D-GLUCOSAMINE);POLY-(1,4-BETA-D-GLUCOPYRANOSAMINE);POLY-[1->4]-BETA-D-GLUCOSAMINE;BETA-(1,4)-2-AMINO-2-DEOXY-D-GLUCOSE;DEACETYLATED CHITIN;CHITOSAN
CAS: 9012-76-4
MF: C6H11NO4X2
MW: 161.16
EINECS: 222-311-2
Storage temp.: room temp
Solubility: dilute aqueous acid (pH <6.5).: soluble
Stability: Stable. Incompatible with strong oxidizing agents.
Chemical Properties: faintly beige solid  (Coarse ground flakes and powder)
Product Categories: Miscellaneous Natural Products;Biochemistry;Polysaccharides;Sugars;Nutritional Supplements;Dextrins、Sugar & Carbohydrates;Activity Other;Carbohydrate adjuvants;Carbohydrates A-C;Chitosan and Chitin;Activity;and Substrates;Biochemicals and Reagents;Carbohydrates;Carbohydrates A to Z;Cell Culture;Chitosan;Enzyme Substrates;Enzymes;Inhibitors;Materials Science;Natural Polymers;Polymer Science;Polymers;Polysaccharide;Vaccine Adjuvants;Vaccine Production;Oligosaccharide,Biostimulate
Usage: Claimed to have the ability to retain fats and cholesterol in the stomach.
Properties: This product is non-toxic, odorless, off-white or slight yellow powder, and soluble in acid, insoluble in water and base or normal organic solutions.
 
Chitosan Description:
 
Chitosan is a linear polysaccharide composed of randomly distributed β-(1-4)-linked D-glucosamine (deacetylated unit) and N-acetyl-D-glucosamine (acetylated unit). It is made by treating shrimp and other crustacean shells with the alkali sodium hydroxide.
 
Chitosan has a number of commercial and possible biomedical uses. It can be used in agriculture as a seed treatment and biopesticide, helping plants to fight off fungal infections. In winemaking it can be used as a fining agent, also helping to prevent spoilage. In industry, it can be used in a self-healing polyurethane paint coating. In medicine, it may be useful in bandages to reduce bleeding and as an antibacterial agent; it can also be used to help deliver drugs through the skin.
 
More controversially, chitosan has been asserted to have use in limiting fat absorption, which would make it useful for dieting, but there is evidence against this.
 
Other uses of chitosan that have been researched include use as a soluble dietary fiber.
 
Chitosan is extracted from chitin, insoluble in water but soluble in dilute acid and absorbed by human body. As the firdt derivate, it's chemical constitution is macromolecule alkalescent polysaccharide polymer with cation. It has peculiar physical, chemical properties and bioactive function.
 
Chitosan is listed as follows:
A. High Density Chitosan
B. High Viscosity Chitosan
C. Industrial Grade Chitosan
D. Food Grade Chitosan
E. Medical Grade Chitosan
F. Low Molecular Weight Chitosan
G. Aroxymethyl Chitosan
H. Chitosan Oligosaccharide
 
Chitosan Applications:
 
1)Food Field:
Used as food additives, thickeners, preservatives fruits and vegetables, fruit juice clarifying agent, forming agent, adsorbent, and health food.
2)Medicine, health care products field:
As the chitosan non-toxic,has anti-bacterial, anti-inflammatory, hemostatic, and immune function, can be used as artificial skin, self-absorption of surgical sutures, medical dressing Branch, bone, tissue engineering scaffolds, enhance liver function, improve digestive function, blood fat, lowering blood sugar, inhibiting tumor metastasis, and adsorption and complexation of heavy metals and can be excreted, and so on, was vigorously applied to health food and drug additives.
3)Environmental protection field:
Chitosan and its derivatives is a good flocculant for wastewater treatment and metal recovery from metal-containing waste water; in textile field: as a mordant, health care fabric, sizing agents, printing and dyeing
4).Agricultural field:
As growth promoters, bio-pesticides, feed additives, seeds, etc.
5)Field of tobacco
Tobacco sheet used as adhesives, low-tar filter and so on.
 
Chitosan is refined from deacetylation of chitin which is extracted from deep-sea Alaska crab cods. As the only basic polysaccharide among natural polysaccharides, this product has many physical and chemical characteristics and physiological activities. Precisely, this product can control cholesterol, inhibit bacterial activity, prevent and control high blood pressure, absorb and excrete heavy metals, maintain humidity and strengthen immunity. In food industry, this product can be used as antibacterial agent, fruit and vegetable preservative and antioxidant. There are many special functional groups in molecular chain, so the chitosan can be manufactured into many products according to different reactions on functional groups, such as acylation, sulfation and oxidation, grafting and crosslinking, hydroxyethylation and hydroxymethylation. These products can be used in many fields, including medicine, food, chemical, cosmetic, water treatment, metal extraction and recovery, biochemical and biomedical engineering. There are many types of chitosan, including GS-chitosan oligosaccharide, high density type, special molecular weight type, medical/food / industrial grade type, water soluble type and specialized type.
Chitosan can inhibit growth and reproduction of fungi, bacteria, and virus. When this product is used as coating preservation, it can inhibit respiratory metabolism and water loss of fruits and vegetables, thus slowing their aging process of organization and structure and effectively extending their postharvest life. This product can also be used as antioxidant. In heating process, free iron ions are released from meat hemoglobin and they form chelates with chitosan, thus their catalytic activity is inhibited.
 
Chitosan Usage:
 
Agricultural and horticultural use
The agricultural and horticultural uses for chitosan, primarily for plant defense and yield increase, are based on how this glucosamine polymer influences the biochemistry and molecular biology of the plant cell. The cellular targets are the plasma membrane and nuclear chromatin. Subsequent changes occur in cell membranes, chromatin, DNA, calcium, MAP Kinase, oxidative burst, reactive oxygen species, callose pathogenesis-related (PR) genes and phytoalexins.
 
Natural biocontrol and elicitor
In agriculture, chitosan is used primarily as a natural seed treatment and plant growth enhancer, and as an ecologically friendly biopesticide substance that boosts the innate ability of plants to defend themselves against fungal infections. The natural biocontrol active ingredients, chitin/chitosan, are found in the shells of crustaceans, such as lobsters, crabs, and shrimp, and many other organisms, including insects and fungi. It is one of the most abundant biodegradable materials in the world.
 

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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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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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