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CAS NO:68497-62-1
EINECS No.:N/A
Molecular Formula:C14H27N3O2
MW:269.38
Category:API
Appearance:White Powder
Form: white powder
Specification: 98%
Test Method : HPLC
99% Pramiracetam powder cas 68497-62-1 buy pramiracetam powder pramiracetam bulk powder
Density:1.036g/cm3
Boiling Point:461°C at 760 mmHg
Flash Point:232.6°C
Extraction Method: Water/ Grain Alcohol
Usage:Animal Pharmaceuticals
Storage Situation: Stored in a cool and dry well-closed container. Keep away from moisture and strong light/heat.
Synonyms:N-[2-(dipropan-2-ylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide sulfate (1:1); N-[2-(dipropan-2-ylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
Pramiracetam is a nootropic drug derived from piracetam, and is more potent (i.e. lower dosage is used). It belongs to the racetam family of nootropics, and goes by the trade name Remen (Parke-Davis), Neupramir (Lusofarmaco) or Pramistar (Firma). Pramiracetam is used off-label for a wide range of applications.
2) Specification:99%
3) Appearance:White powder
4) Introduction:Tianeptine sodium salt is a salt of Tianeptine. Tianeptine sodium salt, a tricyclic compound, is a selective facilitator of 5-HT (serotonin; sc-201146) uptake in vitro and in vivo. Additionally, Tianeptine is reported to act as a selective inhibitor of dopamine uptake . Tianeptine does not have a noted effect on monoamine uptake. In a study utilizing purified synaptosomes from rat brain, Tianeptine was reported to enhance serotonin uptake in selective brain regions. Purified synaptosomes were obtained from rats and incubated with tritium-labeled 5-HT and Tianeptine in vitro . The synaptosomes were then analyzed for uptake and release of 5-HT via a liquid scintillation.
Tianeptine is a drug used primarily in the treatment of major depressive disorder, although it may also be used to treat asthma or irritable bowel syndrome. Chemically it is a tricyclic antidepressant (TCA), but it has different pharmacological properties than typical TCAs as recent research suggests that tianeptine produces its antidepressant effects through indirect alteration of glutamate receptor activity (i.e., AMPA receptors and NMDA receptors) and release of BDNF, in turn affecting neural plasticity.
Tianeptine has antidepressant and anxiolytic (anti-anxiety) properties with a relative lack of sedative, anticholinergic and cardiovascular adverse effects, thus suggesting it is particularly suitable for use in the elderly and in those following alcohol withdrawal; such persons can be more sensitive to the adverse effects of psychotropic drugs. Recent results indicate possible anticonvulsant (anti-seizure) and analgesic (painkilling) activity of tianeptine via immediate or downstream modulation of adenosine A1 receptors (as the effects could be experimentally blocked by antagonists of this receptor).
Phenibut powder, also known as “4-Amino-3-Phenylbutyric Acid,” Phenibut is a non-prescription pharmaceutical that is actually a GABA molecule with the addition of a phenyl group. Russian researchers discovered that by changing GABA into 4-Amino-3-Phenylbutyric Acid, it was able to cross more easily into the nervous system & across the blood-brain barrier. Since it is a GABA, an inhibitory neurotransmitter, derivative, Phenibut increases GABA levels.
Phenibut is a white crystalline powder and the taste is very sour. It is readily soluble in water, soluble in alcohol, and the pH of a 2.5% water solution is between about 2.3 and 2.7.
1. Phenibut powder is a derivative of the naturally occurring inhibitory neurotransmitter GABA.
2. Phenibut powder is used by bodybuilders to reduce fatigue and improve neurological functions.
3. Phenibut powder has been and is still used medically to treat stress, relieve tension, improve sleep, and as a potentiate for other medications.
Nutritional supplement, nutrition enhancer, dietary supplements, heatlh food additives, pharmaceutical raw material. sport supplements, sport nutrtional supplements, bodybuilding supplement.
1. It's a kind of nutritional supplement.
2. It can improve the aerobic metabolism of the muscle and greatly enhance muscle strength and endurance from diet alone.
3. It can be used as nutrition enhancer.
4. It's one of the most popular and effective nutritional supplements as well as the indispensable product for bodybuilders.
5. It is also widely used by other athletes, such as football players, basketball players and so on.
Product Name: Phenethyl caffeate
Purity: 99%
Appearance: White powder
Source: Propolis
Molecular Formula: C17H16O4
CAS Registry Number: 104594-70-9
Funcation: Anti-inflammatory
The chemical composition of propolis is very complicated. Since the
functional components of propolis have not affected the application of
propolis in modern medicine for a long time, CAPE has been identified as
one of the main components in propolis, and it has a wide range of
pharmacological activities. Because of its strong anti-inflammatory and
anti-oxidant activity, it can play an anti-tumor role, so CAPE has broad
application prospects in medicine.
The CAPE structure contains a
catechol structure and is a strong antioxidant. The Sudina experiment
demonstrated that CAPE completely blocked the production of active
oxidants in neutrophils at 10 μM and blocked the xanthine oxidase
system. Moreover, it was found that the propolis containing CAPE has
stronger antioxidant activity than CAPE. The activity of CAPE is
stronger than that of another important component in propolis,
indicating that CAPE is an important component of antioxidant activity.
Anti-inflammatory effect
Studies have shown that propolis ethanol
extract containing CAPE can inhibit carrageenan-induced adjuvant
arthritis, pleurisy and rat foot swelling, and extracts without CAPE do
not have this activity, indicating that CAPE is anti-inflammatory. The
main component of the action.
Anti-tumor effect
Among the propolis, CAPE, quercetin,
isoprenate, rhamnosin, homocodant, and terpenoids, polysaccharides and
other substances have anticancer activity, can inhibit tumor cell
proliferation, and have a certain poisoning effect on cancer cells. And
CAPE has a specific lethal effect on tumor cells.
Our acridine orange staining and LC3 II expression results suggest that PCBL induces autophagosomes in WiDr cells. The levels of LC3 II expression we observed after co-treatment of PCBL with bafilomycin A1 and the reductions in p62 expression we observed after PCBL treatment in WiDr cells demonstrate increased autophagic flux, a reliable indicator of autophagic induction. The increased Beclin 1 expression in PCBL-treated cells and the incapacity of PCBL to induce LC3 II in 3-methyladenine (3-MA)-treated cells we observed suggests that PCBL-induced autophagy is class III PI3-kinase dependent. Nootropics Powder
PCBL did not alter phosphorylation of the mTOR substrate p70 S6 kinase, indicating that PCBL-induced autophagy was not mTOR regulated. Two autophagy related proteins, Atg5 and Atg12, also remained uninduced during PCBL treatment. The increased caspase activity and expression levels of LC3 II and p62 we observed in response to PCBL treatment in primary glioma cells demonstrates that PCBL-induced apoptosis and autophagy were not cell line specific. Pharmacological inhibition of autophagy did not alter the antitumor efficacy of PCBL in WiDr cells. This attests to the bystander nature of PCBL-induced autophagy (in terms of cell death). In toto, these data suggest that PCBL induces a class III kinase dependent, but mTOR independent, bystander mode of autophagy in WiDr cells.
High purity Exenatide acetate powder with bottom price
Exenatide acetate powder,Exenatide powder is a glucagon-like peptide-1 agonist (GLP-1 agonist) medication, belonging to the group of incretin mimetics, approved in April 2005 for the treatment of diabetes mellitus type 2. Exenatide in its Byetta form is administered as a subcutaneous injection (under the skin) of the abdomen, thigh, or arm, any time within the 60 minutes before the first and last meal of the day.A once-weekly injection has been approved as of January 27, 2012 under the trademark Bydureon. It is manufactured by Amylin Pharmaceuticals and commercialized by Astrazeneca
Exenatide is believed to facilitate glucose control in at least five ways:
1. Exenatide augments pancreas response and more appropriate amount of insulin that helps lower the rise in blood sugar from eating.
2. Exenatide also suppresses pancreatic release of glucagon, which prevents hyperglycemia (high blood sugar levels).
3. Exenatide helps slow down gastric emptying and thus decreases the rate at which meal-derived glucose appears in the bloodstream.
4. Exenatide has a subtle yet prolonged effect to reduce appetite, promote satiety via hypothalamic receptors.
5. Exenatide reduces liver fat content. Fat accumulation in the liver or nonalcoholic fatty liver disease (NAFLD) is strongly related with several metabolic disorders.
Factory Pharmaceutical triptoreli powder peptide Triptorelin gnrh triptorelin
Triptorelin powder is used to suppress spontaneous ovulation which is the required element in vitro fertilization (IVF). Increase in FSH triggers an oocyte release which results in the likelihood of pregnancy opportunities. When this peptide stimulates the production of LH and FSH from the pituitary, it leads to an increase in testosterone serum and an increase of sperm count.
Benefits:
Triptorelin acetate is mainly used for fertility. This
peptide can manage dependent estrogen disorders such as menorrhagia
(menstrual period abnormality), endometriosis (the growth of uterine
tissue outside the uterus), adenomyosis (the growth of ectopic
endometrial tissue inside the myometrium), or uterine fibroids (smooth
muscle tumors of the uterus).
Triptorelin delays the adverse effects
of puberty in the reduction of height potential and other lifelong
health and psychological risks.
Triptorelin is useful in the treatment of congenital adrenal hyperplasia that entails abnormal production of sex steroids that cause nausea, ambiguous genitalia, early childhood pubic hair, early and delayed puberty, menstrual inconsistency, infertility and an expanded clitoris, just to mention a few.
Triptorelin is also successful in the treatment of hormonally sensitive cancers especially prostate cancer and breast cancer. A curable stage in prostate cancer happens only when the disease is still located in the affected organs, but the time it gets to the bones, it loses its potency. People using Triptorelin peptide for prostate cancer treatment should be aware of the risk of heart problems. When it comes to breast cancer, hormonal inhibiting therapy reduces the production of estrogen that allows the growth of cancer.
Factory price cjc 1295 with without dac peptide Powder
CJC1295 Without DAC powder,CJC without DAC powder is basically a peptide hormone that acts similar to growth hormone releasing hormones (GHRH). It achieves this by preventing degradation of its amino acids. With a single dose, it can remain in the body for quite a few days and can cause the growth hormone to be released many times per day. This reduces the frequency of injections needed.
CJC-1295 increases the production of growth hormone as well as IGF-1 – which has good effects in adults. However, it does not increase the levels of prolactin – high levels of which can create impotence and mental health problems in men. By increasing these two hormones, it enhances protein production in the body, which in turn, boosts muscle mass. It also induces lipolysis – the breakdown of fat tissue, boosts recovery from injuries, increases bone density, and also reduces aging factors like skin wrinkles. It can also stimulate cell growth, due to which it can be used to treat withered tissue or organs.
Cjc 1295
Alias: CJC-1295 Acetate; CJC1295
Item: CJC1295
CAS No.: 863288-34-0
Molecular Formula: C165H271N47O46
Molecular Weight: 3649.30
Purity (HPLC): 98.0%
Appearance: White crystalline powder
Single Impurity(HPLC): 1.0%
mino Acid Composition: 10% of theoretical
Peptide Content(N%): 80%(by %N)
Water Content(Karl Fischer): 6.0%
Acetate Content(HPIC): 15.0%
Identity (ESI-MS):3367.97±3.0
Mass Balance: 95.0~105.0%
Type: Immune Function AgentsGrade
Standard: Medicine Grade
Storage: Lyophilized CJC1295 Without DAC powder,CJC without DAC powder is stable at room temperature for 90 days, however it should be stored in a freezer below -8C for any extended period of time. After reconstituting CJC1295 W/O DAC should be refrigerated at temperatures not to exceed 36 F.
CJC-1295 DAC has shown some amazing results as a growth hormone
releasing hormone (GHRH) analog. Not only has CJC-1295 shown the ability
to increase growth hormone and IGF-I secretion and its benefits, but it
has been able to do so in very large amounts. Recent research studies
have shown that CJC - 1295 stimulates GH and IGF-1 Secretion, and will
keep a steady increase of HGH and IGF-1 with no increase in prolactin,
leading to intense fat loss, and increases protein synthesis.
CJC-1295 is a long acting Growth Hormone Releasing Hormone, which causes
the anterior pituitary to release more growth hormone. GHRH is released
in pulses in the body, which alternate with corresponding pulses of
somatostatin (growth-hormone inhibiting-hormone). Clinical Research was
first conducted for CJC-1295 during the mid-2000s. The objective of the
peptide was to treat visceral fat deposits in obese AIDS patients, as
increased levels of exogenous hgH are presumed to increase lipolysis
(fat loss). The clinical research was ultimately successful for most
research subjects. Ghrelin, released from the gut, which circulates and
acts as a hunger hormone, has synergistic activity in the body with GHRH
and also suppresses somatostatin to make way for the GHRH pulse.
Studies shows that combining a GHRP-6 with CJC 1295 DAC, significantly
increase the release of GH and IGF-1 production without an increase in
prolactin. An example of a GHRP (GH Releasing Peptide) is Hexarelin or
GHRP-2. CJC 1295 DAC is a exceptionally designed peptide and is known
for being the finest of the hGH secretogues. The DAC (Drug Affinity
Complex) portion increases the half-life by binding with serum albumin
and protects the CJC-1295 DAC peptide from degradation. This was formed
when a lysine link was bounded to DACs to a reactive chemical called
maleimidoproprionic acid (MPA).
What is Terlipressin Acetate?
Terlipressin Acetate powder,Terlipressin powder
is an analogue of vasopressin used as a vasoactive drug in the
management of low blood pressure. It has been found to be effective when
norepinephrine does not help.
Indications for use include norepinephrine-resistant septic shock and hepatorenal syndrome. In addition, it is used to treat bleeding esophageal varices.
Pharmacodynamics
Terlipressin is a medicine similar to a naturally occurring hormone present in the body, known as antidiuretic hormone (ADH) or vasopressin. ADH has two main effects in the body. Firstly, it causes narrowing of blood vessels (vasoconstriction), thereby limiting blood flow to a particular area of the body. It also acts on receptors in the kidney to retain water in the body, which helps to prevent excessive loss of water in the urine.
