Pharmaceutical raw materials used in synthesizing new medications

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Similar to calgizzarin; similar to PID:g3115349 (40-49) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Similar to calgizzarin; similar to PID:g3115349 (40-49).http://www.creative-peptides.com/product/similar-to-calgizzarin-similar-to-pid-g3115349-item-ta-154-9887.html

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Small subunit processome component 20 homolog (626-634) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply Small subunit processome component 20 homolog (626-634).http://www.creative-peptides.com/product/small-subunit-processome-component-homolog-item-ta-061-1996.html

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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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4-cprc 4cprc 4c-prc high purity,high quality CAS NO.63547-13-7 CP >99%

4CPRC 4-CPRC crystal

CAS No: 63547-13-7.

Formula : C15H20ClND

IUPAC Name : 1-(4-Chloro-phenyl)-2-pyrrolidin-1-yl-pentan-1-one.

Appearance: White crystal

Purity: >99%

Package: 1kg/Aluminum foil bag

Application: For chemical research

Production Capacity: 500 Kilogram/Month

Storage: Kept in a cool,dry and ventilated place

Payment: Bitcoin, bank transfer(T/T), Western Union, MoneyGram

Shipment: TNT, UPS, DHL, FEDEX, EMS and Client's request.

Please let me know if you are interested in our products.

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5,6-dihydroxyindole-2-carboxylic acid oxidase (alt. ORF) LAB GRADE 97%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We supply 5,6-dihydroxyindole-2-carboxylic acid oxidase (alt. ORF).http://www.creative-peptides.com/product/dihydroxyindole-carboxylic-acid-oxidase-alt-orf-item-ta-287-17592.html

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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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Biotinyl-Tau Peptide (306-336) (Repeat 3 Domain) (human) LAB GRADE 98%

Creative peptides is specialized in the process development and the manufacturing of bioactive peptides. We offer custom peptide synthesis, process development, GMP manufacturing as well as catalog products. We provide Biotinyl-Tau Peptide (306-336) (Repeat 3 Domain) (human). More information please visit the website:http://www.creative-peptides.com/product/biotinyl-tau-peptide-repeat-domain-human-item-cad-066-33790.html

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Factory Supply 99.9% Purity Polyethylene Glycol / PEG CAS 25322-68-3

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Factory Supply 99.9% Purity Polyethylene Glycol / PEG CAS 25322-68-3
 
Poly Ethylene Glycol Basic Info.:
 
Product Name: Poly Ethylene Glycol
Synonym: AlkoxE 130;1,2-ethanediol,homopolymer;Alcox E 30;alcoxe30;alkapolpeg-200;alkapolpeg-300;alkapolpeg-600
InChI:InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2
CAS No.: 25322-68-3
EINECS No.: 200-849-9
MF: (C2H4O)H2O
MW: 44.0526
Density: 1.125
Melting Point: -65ºC
Boiling Point: 250ºC
Refractive Index: 1.458-1.461
Flash Point: 171ºC
Solubility: H2O: 50 mg/mL, clear, colorless.
Appearance: Clear colorless viscous liquid.
Grade: Cosmetic Grade, Food Grade, Medicine Grade
Storage: This product is non-toxic, flame retardant, as a general shipments of chemicals, sealed and stored in dry place.
 
Poly Ethylene Glycol Usage:
 
Used in conjunction with carbon black to form a conductive composite. 1 Polymer nanospheres of poly(ethylene glycol) were used for drug delivery
 
Poly Ethylene Glycol Applications:
 
Polyethylene glycol 400 is suited to prepare for the soft capsule most. The polyethylene glycol 400 is a liquid and has a broad compatibility with various solvents, so it is a good solvent and solubilizer and is widely used in liquid preparations, such as the oral solution, eye drops and so on.
 
When the vegetable oil is not suitable for a co-active ingredient carrier material, the polyethylene glycol is the preferred substitute material because the polyethylene glycol is stable and non-perishable. Besides, the injections containing polyethylene glycol are very safe and stable as long as it has been heated to 150 degrees Celsius. In addition, it can blend with PEG with high molecular weight and the mixture has a good solubility and drug compatibility.
 

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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5

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Highly Effective Steroids 5-Androstenediol For Bodybuilding 521-17-5
 
Androstenediol Basic information:
 
Product Name: Androstenediol
Synonyms: Hermaphrodiol;5-Androstenediol;Androstenediol
CAS: 521-17-5
MF: C19H30O2
MW: 290.44
EINECS: 208-306-8
Product Categories: Steroids;API
Melting point: 178-182°C
Alpha: -52.2 º (c=0.4,2-propanol)
Storage temp.: 2-8°C
 
Androstenediol Description:
 
Androstenediol, commonly referred to simply as , and also known as androst-5-ene-3β,17β-diol, is an endogenous androgen and estrogen steroid hormone and intermediate in the biosynthesis of testosteronefrom dehydroepiandrosterone.
Androstenediol is a direct metabolite of the most abundant steroid produced by the human adrenal cortex. It is less androgenicthan the related compound, Δ4-androstenediol, and has been found to stimulate the immune system. When administered to rats, Δ5-diol, in vivo, has approximately 1.4% of the androgenicity , 0.54% of the androgenicity of androstenedione, and 0.21% of the androgenicity of testosterone.
 
1.People Use Androstenediol For:
 Orally, 5-Androstenediol is used to increase endogenous testosterone production to increase energy, enhance recovery and growth from exercise, heighten sexual arousal and function, and to promote a greater sense of well being.
 
2.Mechanism of Action:  
5-Androstenediol, a prohormone, is a weak steroid hormone and is a direct precursor of testosterone . Androstenediol can be converted to estradiol, estrone, dehydroepiandrosterone (DHEA), and testosterone; and may increase levels of these hormones. 
 

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9

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Hot Selling 99% Purity Steroid Raw Powder Clomiphene Citrate 50-41-9
 
Clomiphene Citrate Basic Info.:
 
Product Name: Clomiphene Citrate
Alias: Clomid;Clomifen;Clomiphene;Clomiphene Citrate;Serophene;Pergotime;Clomphid;Clomiphene Citrate Salt.
CAS No: 50-41-9
MF: C32H36ClNO8
MW: 598.09
Einecs No: 200-035-3
Purity: 99%
Melting point: 116.5-118°C
Storage temp.: 2-8°C
Appearance: Crystalline Solid; Odourless.
Product Categories: API;Intermediates & Fine Chemicals;Pharmaceuticals;Amines;Aromatics;Peptides;CLOMID
Usage:
(1)An unducer of ovulation. A gonad-stimulating principle
(2)Synthetic estrogen agonist-antagonist. Gonad-stimulating principle.
(3)A selective estrogen receptor modulator
Male Anti Estrogenic Clomid for Steroid Cycle Clomiphene.
 
Clomiphene Citrate Description:
 
Clomiphene Citrateis a mixed estrogen agonist/antagonist (activator/blocker) which, when bound to the estrogen receptor, putsClomiphene Citratein a somewhat different conformation (shape) than does estradiol. The estrogen receptor requires binding of an estrogen or drug at its binding site and also the binding of any of several cofactors at different sites. As for women, the only real use for Clomiphene Citrate is the possible management of endogenous estrogen levels near contest time. This can increase fat loss and muscularity, particularly in female trouble areas such as this HIPS and thighs. Clomiphene Citrate however often produces troubling side effects in women (discussed below), and is likewise not in very high demand among this group of athletes. Clomid are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time.
 
Clomiphene Citrate Application:
 
As for toxicity and side effects, Clomiphene Citrateis considered a very safe drug. Bodybuilders seldom report any problems, but listed possible side effects do include hot flashes, nausea, dizziness, headaches and temporarily blurred vision. Clomifene citrate is a drug treatment that stimulates your ovaries to release eggs. Ovulation stimulation using clomifene citrate is a well-established, effective treatment. Clomifene citrate is the most widely used of all fertility drugs. Other drugs that may be used to treat ovulation disorders include metformin and bromocriptin.
 

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