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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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Kin of IRRE-like protein 3 isoform 2 precursor (402-419) 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 Kin of IRRE-like protein 3 isoform 2 precursor (402-419).http://www.creative-peptides.com/product/kin-of-irre-like-protein-isoform-precursor-item-ta-181-12516.html

 

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New Trestolone Decanoate Effective Yellow Liquid For Muscle Building

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New Trestolone Decanoate Effective Yellow Liquid For Muscle Building
 
Trestolone Decanoate Basic Info.:
 
Product Name: Trestolone Decanoate
Synonyms: Trest Deca
Assay: 99%
Standard: USP/BP
Appearance: Light Yellow Liquid
Suitable for: Adult
Usage: A synthetic, anabolic steroid. Used to promote muscle growth and combat involuntary weight loss. It has also been used to treat cases of osteoporosis.
 
Trestolone Decanoate Applications:
 
Trestolone Decanoate is intended for research purposes only and, is not to be used for any other purposes, including but not limited to, in vitro diagnostic purposes, in foods, drugs, medical devices, or cosmetics for humans or animals or for commercial purposes. Trestolone Decanoate has not been tested for safety and efficacy in food, drug, and medical device, cosmetic, commercial or any other use.  Under no circumstances shouldTrestolone Decanoate be used as or be considered to be foods, drugs, medical devices or cosmeticsThis product is intended for laboratory/hobbyist research use only. There are risks involved with consumption or distribution of this product. 
 
Trestolone Decanoate is NOT intended to use as food additives,drugs, cosmetics, household chemicals or other inappropriate applications. The listing, purchase and/or distribution of this material does not constitute a license to its use in infringement of any patent.  Trestolone Decanoate should be handled only by qualified and properly trained professionals.  
 
Trestolone Decanoate Function:
 
Trestolone Decanoate in pure Grapeseed Oil is for research use only. This product is NOT for human use and can be harmful if ingested. Trestolone Decanoate is for research/laboratory use only. Trestolone Decanoate is in a sterile solution BUT is NOT to be injected. Trestolone Decanoate should only be handled by licensed, qualified professionals.Trestolone Decanoate is not a drug, food, or cosmetic and should not be misbranded, misused or mislabeled as a drug, food or cosmetic.
 

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain

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Peptides 170851-70-4 Weight Loss Steroids Ipamorelin For Muscle Gain
 
Ipamorelin Basic Info.:
 
Product Name: Ipamorelin
Synonyms: IpoMarelin;IpaMorelin Acetate;Aib-His-D-2-Nal-D-Phe-Lys-NH2
Unit Size: 2 mg/vial
Unit Quantity: 1 Vial
CAS NO.: 170851-70-4
Molecular Formula: C38H49N9O5
Molecular Weight: 711.85
Sequence: H-Aib-His-D-2-Nal-D-Phe-Lys-NH2
Appearance: White Powder
Purity: 98.49%
Identity (ESI-MS) 711.85±0.5
Source Chemical Synthesis
Storage: 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 Ipamorelin should be refrigerated at temperatures not to exceed 36°F.
 
Ipamorelin Description:
 
Ipamorelin is a fascinating new muscle building discovery that is getting a lot of attention in the bodybuilding world. It is a synthetic peptide that has powerful Growth Hormon releasing properties. And these GH releasing properties are what is of interest to athletes and bodybuilders since they can make a tremendous difference in the amount of muscle you can grow and how quickly you burn fat.
 
Ipamorelin is a penta-peptide. (Aib-His-D-2-Nal-D- Phe-Lys-NH2) And, the strength it displays may very well make regular old Growth Hormon (GH) obsolete. But what athletes and bodybuilders really want to know is what is this wonder peptide capable of doing, how is it used, and how does it compare to the other GHRP peptides?
 
Athletes are taking Ipamorelin in a 200mcg -300mcg dosage, two or three times daily, using a tiny insulin needle to inject. They usually start with the lower dose since side effects can include headaches or what feels like a head-rush. Ipamorelin can be taken at anytime but taking it about 30-45 minutes before a workout would seem ideal because of the pulse in Growth Hormon (GH) it creates allowing for maximum growth.
 
Studies on the effects of Ipamorelin on bone growth, body weight, and GH release showed some interesting conclusions.In one experiment, various doses were administered over the course of 15 days to test the group's reactions.
 
There was a distinct and dose-dependent effect on body weight gain however, the treatment group did not show a change in total IGF-I levels. Nor did the treatment group produce serum markers of bone development. For example, the number of cells in the wide portion of the tibia (the shinbone) did not change significantly. This is a good thing because it suggests muscle growth with less potential for deformity of bone or cartilage.
 
Ipamorelin in theory may increase Acetylchloine or Cortisol when used in higher dosages. However, and increase in Acetylchloine or Cortisol is even more likely with GHRP-2 and GHRP-6. In fact, in the case of Ipamorelin, there was little to no rise in Acetylcholine and Cortisol blood plasma levels even at injections more than 200 times higher than the effective dosage for comparable GH release.
 
Ipamorelin Applications:
 
Ipamorelin is a selective growth hormon secretagogue and agonist of the ghrelin receptor. In pentobarbital anaesthetised rats, ipamorelin released GH with a potency and efficacy comparable to GHRP-6 (ED50 = 80±42 nmol/kg and Emax = 1545±250 ng GH/ml vs 115±36nmol/kg and 1167±120ng GH/ml). In conscious swine, ipamorelin released GH with an ED50 = 2.3±0.03 nmol/kg and an Emax = 65±0.2 ng GH/ml plasma. Again, this was very similar to GHRP-6 (ED50 = 3.9±1.4 nmol/kg and Emax = 74±7ng GH/ml plasma). GHRP-2 displayed higher potency but lower efficacy (ED50 = 0.6 nmol/kg and Emax = 56±6 ng GH/ml plasma). The specificity for GH release was studied in swine.
 

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Pharmaceutical Human Growth Hormone Peptide TB-500 Anti Inflammatory

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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.
 

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

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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.
 

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