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Aniracetam Capsules and Powder Reviews & Information

Aniracetam powder is a compound in the group of racetams due to its common pyrrolidone structure. It is one of the more common Racetamic structures. It is fat-soluble and thus needs to be ingested with fatty acids. Additionally, Aniracetam is cholinergic

Aniracetam acts as a positive modulator of some excitatory receptors known as AMPA receptors and decreases the rate of receptor desensitization. This typically manifests as a controlled and prolonged neurological stimulation effect. Since AMPA receptors differ in structure across the brain, different AMPA modulators affect the brain in different ways.

Anecdotally, Aniracetam has been know to aid in ‘collective and holistic thinking’, or putting the pieces of the puzzle together. It also increases blood flow and activity in the area of the brain known for this action, the association cortex.

Aniracetam, as an AMPA modulator, is currently being studied for usage in depression and other CNS disorders such as Alzheimer’s disease.

Oct 4 '19 · 0 comments

Emoxypine (2-ethyl-6-methyl-3-hydroxypyridine), also known as Mexidol or Mexifin when used as the succinate salt, is an antioxidant manufactured in Russia by Pharmasoft Pharmaceuticals. Its chemical structure resembles that of pyridoxine (a type of vitamin B6).Emoxypine powder

Puhopharma specializes in controling the quality and reducing the impurities of Mexidol Base.Our Mexidol Base is with the best quality and the most competitive price in China.

Magnetite nanoparticles (NPs) are studied as agents for magnetic resonance imaging, hyperthermia of malignant tumors, targeted drug delivery as well as anti-anemic action. One of the main problems of such NPs is their aggregation that requires creation of methods for magnetite NPs stabilization during preparation of liquid medicinal forms on their basis. The present work is devoted to the possibility of mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate) use for solubilization of magnetite NPs in hydrophilic medium. For this purpose, the condensate produced by electron-beam evaporation and condensation, with magnetite particles of size 5-8 nm deposited into the crystals of sodium chloride were used in conjunction with substance of mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate), and low molecular weight polyvinylpyrrolidone (PVP).
The NP condensate was dispersed in distilled water or PVP or mexidol solutions. NPs size distribution in the liquid phase of the systems was determined by photon correlation spectroscopy, iron (Fe) concentration was evaluated by atomic emission spectrometry. It is shown that in the dispersion prepared in distilled water, the major amount of NPs was of 13-120 nm in size, in mexidol solution – 270-1700 nm, in PVP solution – 30-900 nm. In the fluid containing magnetite NPs together with mexidol and PVP, the main fraction (99.9%) was characterized by the NPs size of 14-75 nm with maximum of 25 nm. This system had the highest iron concentration: it was similar to that in the sample with mexidol solution and 6.6-7.3 times higher than the concentration in the samples with distilled water or PVP. Thus, in the preparation of aqueous dispersions based on magnetite NPs condensate, mexidol provides a transition of Fe to the liquid phase in amount necessary to achieve its biological activity, and PVP stabilizes such modified NPs.

Oct 4 '19 · 0 comments

99% Purity Idra-21 Powder China Factory Direct Supply Safe Ship

IDRA-21 is an ampakine drug derived from aniracetam, IDRA-21 shows nootropic effects in animal studies
While more research is needed for this relatively new compound, it has taken the nootropic community by storm.
This means it is able to improve focus and attention as well as promote learning and memory.

In comparison to the benzoylpiperidine derived ampakine drugs, IDRA-21 was more potent than CX-516, but less potent than CX-546.Newer benzothiadiazide derivatives with greatly increased potency compared to IDRA-21 have been developed, but these have not been researched to the same extent, with the benzoylpiperidine and benzoylpyrrolidine CX-series of drugs being favoured for clinical development, most likely due to more favourable toxicity profiles at high doses.
Studies conducted to evaluate effects of NSI-189 revealed that 40 to 80 mg daily is effective in treating depression and cognitive symptoms amongst healthy patients.
In these trials, there are no serious adverse events recorded. Generally, NSI-189 is well tolerated and safe for human use.

Function
1.Increases in cognitionIncreased Task Accuracy.
2.Increases in Short Term Memory.
3.Potential Therapeutic Effects On Schizophrenia.
4.Potental Therapeutic Effects On Depression.
5.Neuroprotection.
6.Benefits Against Alp-induced Cognitive Deficit.

Oct 4 '19 · 0 comments

IIDRA-21 is an ampakine drug derived from aniracetam, IDRA-21 shows nootropic effects in animal studies
While more research is needed for this relatively new compound, it has taken the nootropic community by storm.
This means it is able to improve focus and attention as well as promote learning and memory.Nootropics Powder

In comparison to the benzoylpiperidine derived ampakine drugs, IDRA-21 was more potent than CX-516, but less potent than CX-546.Newer benzothiadiazide derivatives with greatly increased potency compared to IDRA-21 have been developed, but these have not been researched to the same extent, with the benzoylpiperidine and benzoylpyrrolidine CX-series of drugs being favoured for clinical development, most likely due to more favourable toxicity profiles at high doses.
Studies conducted to evaluate effects of NSI-189 revealed that 40 to 80 mg daily is effective in treating depression and cognitive symptoms amongst healthy patients.
In these trials, there are no serious adverse events recorded. Generally, NSI-189 is well tolerated and safe for human use.
Function
1.Increases in cognitionIncreased Task Accuracy.
2.Increases in Short Term Memory.
3.Potential Therapeutic Effects On Schizophrenia.
4.Potental Therapeutic Effects On Depression.
5.Neuroprotection.
6.Benefits Against Alp-induced Cognitive Deficit.

Oct 4 '19 · 0 comments
Product Description of FASORACETAM
Product Name: Fasoracetam powder
Synonyms: FASORACETAM;(5R)-5-(piperidine-1-carbonyl)-2-pyrrolidone;(5R)-5-(piperidine-1-carbonyl)pyrrolidin-2-one;(5R)-5-piperidin-1-ylcarbonylpyrrolidin-2-one;2-Pyrrolidinone, 5-(1-piperidinylcarbonyl)-, (5R)-;(5R)-5-(Piperidine-1-Carbonyl)Pyrrolidin-2-One (5R)-5-[Oxo-(1-Piperidyl)Methyl”>-2-Pyrrolidinone;aka NS-105;LAM-105)
CAS: 110958-19-5
MF: C10H16N2O2
MW: 196.248
FASORACETAM Descriptions:
Fasoracetam is a research compound and member of the racetam family of nootropics,primarily known for their cognitive enhancing abilities.Fasoracetam is also an axiolytic 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.
Fasoracetam Usage :
Through the stimulation of metabotropic glutamate receptors play a role in enhancing memory
Fasoracetam How Does Fasoracetam Work?
There is no conclusive evidence as to how fasoracetam works to improve cognition, but theories suggest it interacts with the cholinergic system and receptors of GABA and glutamate.
Fasoracetam Dosage
There is no standardized dose of fasoracetam for humans yet. The anecdotal evidence suggests smaller doses range around 10 – 15 mg with larger doses in the 30 – 50 mg per serving three times per day.
The latter heavy dose was used by someone who tried using GABA up-regulation to resolve phenibut withdrawal symptoms, however.
Oct 4 '19 · 0 comments

To reconstitute, the peptide the technician adds 1ml of Bacteriostatic water to the vial. Once dissolved in the solution proceed to draw 5iu as referenced on an insulin syringe, equaling to a 250mcg GHRP-6 dose for research purposes only.GHRP-6 powder,GHRP 6 powder

GHRP-2 or 6 peptides activate the Growth Hormone Secretagogue Receptor (GHS-R) in the pituitary gland. Both Ghrelin and all of the synthetic compounds such as GHRP’s are called growth hormone secretagogues.

GHRP-2 vs GHRP-6

The main difference is growth hormone releasing peptide-6 gives a considerable increase in appetite being synthetic ghrelin; it is exceptionally potent in this regard.Ghrelin is a peptide that is released naturally in the lining of the stomach that increases gastric emptying and hunger. IGF-1 boosts the body’s ability to build muscle and burn fat.

GHRP-2 & 6 both increase levels of circulating growth hormone and may cause the liver to secrete the hormone IGF-1.

GHRP-6 Results

Being the first growth hormone releasing hexapeptide to be developed, leading to new peptide synthesis and design. The primary synthetic growth hormone-releasing hormone (GHRH) was manufactured in 1982.

Additional, studies soon showed that growth hormone GH Release Peptides acted synergistically with the natural hormone growth hormone-releasing hormone (GHRH), resulting in substantial increases in growth hormone GH from growth hormone secretagogues.

Growth hormone releasing peptides are new potent stimulators of the ghrelin receptor. The synthetic met-enkephalin amino acid chains lack opioid activity and may be useful for gaining muscle mass.

Oct 4 '19 · 0 comments

Because of the way in which BPC 157 powder inherent mechanics operate in conjunction with an animal test subject’s digestive tract, scientific studies have produced several hypothetical ways in which the peptide could provide aid regarding specific functions pertaining to the gastro-intestinal tract. For instance, it is thought that the peptide’s wound-healing and anti-inflammatory properties could provide aid in the treatment to various inflammatory bowel diseases such as Chron’s disease and ulcerative colitis. The anti-inflammatory properties have also allowed the peptide to be linked to conceivable quelling the effects of periodontitis around the teeth.

BPC 157 Basic Info.
Alias: Booly Protection Compound 15, Pentadecapeptide, BPC 157
CAS: 137525-51-0
Sequence: Gly-Glu-Pro-Pro-Pro-Gly- Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val
MF: C62H98N16O22
MW: 1419.53552
Purity: 99%
Specification: 2mg/vial
Appearance: White Lyophilized Powder
Place of Origin: China
Standard: USP
Certification: SGS
Method of Analysis: HPLC
Storage: Lyophilized peptides although stable at room temperature for 3 months, should be stored desiccated below -18° C. Upon reconstitution of the peptide it should be stored at 4° C between 2-21 days and for future use below -18° C

Oct 4 '19 · 0 comments

Teriparatide Acetate Peptide Pharmaceutical Intermediate

Teriparatide Acetate powder is a recombinant form of parathyroid hormone consisting of the first (N-terminus) 34 amino acids, which is the bioactive portion of the hormone. It is an effective anabolic(i.e., bone growing) agent used in the treatment of some forms of osteoporosis. It is also occasionally used off-label to speed fracture healing. Teriparatide is identical to a portion of human parathyroid hormone (PTH) and intermittent use activates osteoblasts more than osteoclasts, which leads to an overall increase in bone.
Teriparatide is the only anabolic (i.e., bone growing) agent indicated for use in postmenopausal women with osteoporosis at a high risk for fracture or with a history of osteoporotic fracture, patients with multiple risk factors for fracture, and for patients who have failed or are intolerant to other available osteoporosis therapy. It has been FDA-approved since 2002. It is effective in growing bone (e.g., 8% increase in bone density in the spine after one year)[6] and reducing the risk of fragility fractures. Osteoporosis medications are generally safe, but some side effects of teriparatide include headache, nausea, dizziness, and limb pain.
Our process:
The quality control process
1)Purchasing
Thorough market research, understand the price of raw materials and performance.To the procurement source to understand fully, and fully guarantee the quality of the procurement of raw materials.
2) Inspection
Four steps: sampling, sample pretreatment, measuring and data processing.
3) Producing
a)Each operator must do self-inspection of producs and make the corresponding inspection records.
b)Full-time inspectors through check the operator self-inspection, and review and sign in the corresponding record. Full-time inspection is responsible for inspection of finished product, and make the finished product incoming inspection records.
4) Before selling
Test result can be provided before selling.
Third-party detection institution is allowed if you are not satisfied with test results.
Our advantages:
1. Quality:
Our company is a professional production of hormone intermediates for many years, our products have exported to Germany,Spain, UK, USA, Australia, Middle East, and so on other country, and we have got very good feedback from our customers, you can trust us.
And we are the manufactory, so no problem for us to control the quality.
2.Payment method: Western Union,TT.
3.Service: Best service with after-sales service to all clients.
4.Delivery:
Sample Order :P ackage will be shipped with 3days after payment. We can send it via UP, EMS, HK Air Post, DHL or othermethod. We have a professional and stable logistics, and we can deliver the package smoothly around 3 to 5 days.

Oct 4 '19 · 0 comments

Hot Sale High Quality Teriparatide Acetate with GMP

Teriparatide Acetate powder is a recombinant form of parathyroid hormone consisting of a first (N-terminal) 34 amino acid, which is a biologically active part of the hormone. It is an effective anabolic (ie, bone) agent for the treatment of certain forms of osteoporosis. And sometimes use de-labeling to accelerate fracture healing. Trepipril is identical to a part of human parathyroid hormone (PTH), which is used intermittently to activate osteoblasts than osteoclasts, resulting in an overall increase in bones.
Usage
A fragment of human parathyroid hormone (hPTH) peptide sequence containing the 34 N-terminal residues of hPTH. This fragment was also found to be an agonist at PTH1 and PTH2 receptors.Recombinant parathyroid hormone, treatment of osteoporosis.
Quack Details:

Name: Teriparatide Acetate
Sequence Ser-Val-Ser-Glu-Ile-Gln-Leu-Met-His-Asn-Leu-Gly-Lys-His-Leu-Asn-Ser-Met-Glu-Arg-Val-Glu-Trp-Leu-Arg-Lys-Lys-Leu-Gln-Asp-Val-His-Asn-Phe-OH
Cas No:
52232-67-4
Molecular Formula: C181h291n55o51s2
Purity (HPLC): 98% Min
Molecular Weight: 41177.72
Appearance : White powder

Oct 4 '19 · 0 comments

Top Grade &Freeze-Dried Injection Peptides Triptorelin Acetate Powder with 99% Purity

Triptorelin Acetate powder, a decapeptide (pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-Pro-Gly-NH2), is a gonado-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts.

Triptorelin raises test levels by causing constant stimulation of the pituitary, it decreases pituitary secretion of gonado luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction.

Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals). In the United States, it is sold by Watson as Trelstar.In Iran Triptorelin is marketed under the brand name Variopeptyl (Varian Darou Pajooh).
Triptorelin Application:
Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, estrogen-dependent conditions (such as endometriosis or uterine fibroids), and in assisted reproduction. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl . In the United States, it is sold by Watson as Trelstar.In Iran Triptorelin is marketed under the brand name Variopeptyl (Varian Darou Pajooh). In India, Dr. Reddy’s Laboratories has launched recently Triptorelin under the brand name “Pamorelin LA”. In men a reduction of serum levels into the range normally seen after surgical castration occurs approximately two to four weeks after initiation of therapy.

Oct 4 '19 · 0 comments
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