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The Jordan Brand Summer 2019 Women’s collection incorporates both classic silhouettes and forward-looking styles. An emphasis on texture and material creates a connective tie between all the shoes, which span premium make-ups of the Air Jordan I, a Flight Utility-inspired remix of the Air Jordan 3 and an updated version of a classic Air Jordan XI Low colorway.

Air Jordan I High PRM “Atmosphere Grey”
Built with a suede and premium leather upper and a special, softer sock liner, this Air Jordan 1 releases May 1.

Air Jordan I Low Slip “Atmosphere Grey”
This easy-going shoe has double snaps at the collar and a softer sole. The understated make-up releases TKTK.

Women’s Air Jordan I High OG “Twist”
Synthetic black material and premium white leather pair for a women’s exclusive take on the OG White/Black Jordan I. It releases in North America on May 10.

Air Jordan I Jester Low
Debuted as part of “The 1 Reimagined,” this shoe is released for the first time as a low this summer. The notable change: shifting from single to a double zipper entry. It comes in Atmosphere Grey or Black and releases May 1.

Women’s Air Jordan XI Low Pink
The low arrives in extended sizes and dressed in a pink snakeskin-inspired scheme on May 7.

Women’s Air Jordan XII “Midnight Black”
Following the spring 18 Vachetta, this the second women’s exclusive AJXII. Each panel has a different take on an exotic animal print. The shoe carries gold accents and a white sole. It releases May 17.buy Cheap Off White Shoes with best price

Nandrolone phenpropionate

Nandrolone phenpropionate is a 3-phenylpropionate ester. It has a role as an anabolic agent and an androgen. It derives from a nandrolone.Nandrolone propionate powder
from ChEBI
C18 steroid with androgenic and anabolic properties. It is generally prepared from alkyl ethers of estradiol to resemble testosterone but less one carbon at the 19 position. It is a schedule III drug in the U.S.
from DrugBank
Nandrolone phenpropionate is only found in individuals that have used or taken this drug. It is a C18 steroid with androgenic and anabolic properties. It is generally prepared from alkyl ethers of estradiol to resemble testosterone but less one carbon at the 19 position. It is a schedule III drug in the U. S. Nandrolone is an androgen receptor agonist. The drug bound to the receptor complexes which allows it to enter the nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects.

Nandrolone Laurate Cutting Cycle Steroids

Alias: Nandrolone laurate Appearance: White Powder
Quality Standard: USP30 Standard Feature: Healthy, Safe
Function: Immune System Product Name: Oral Anabolic Steroids
Type: Oral Usage: Medicine

Quick Detail:

Laurabolin (nandrolone laureate) is an injectable veterinary steroid containing the drug nandrolone laurate. Laurabolin is basically a long acting Deca Durabolin (nandrolone decanoate), staying active for up to a month in the body. If you have problems recovering natural testosterone production after using Deca, you will definitely have problems using Laurabolin.
Description:

Product name:Nandrolone laurate
Other name:19-nortestosterone 17b-laurate; Laurabolin
CAS register number:26490-31-3
EINECS :247-739-7
Molecular formula:C30H48O3
Molecular weight:456.7
Molecular structure
Assay:98%

Applications:
Athletes however generally inject this drug on a weekly basis. Being a nandrolone, Laurabolin will exhibit noticeable anabolic effects with weaker androgenic side effects.

Although many women do use nandrolones, Laurabolin may be one to avoid. Androgenic effects can appear in women with nandrolones, especially if blood levels were to build up too high with such a long acting drug. Durabolin would be a better choice.Nandrolone laurate powder

For men, doses of 200-400mg per week seem to work fine. At a strength of 50mg it is difficult to use a much higher dose, although some do find it possible. The Mexican Intervet product (laurato de nandrolona) is found throughout the United States and usually sells for a fair price. It comes in 50ml vials, 50mg per ml.

Nandrolone Laureate is the chemical name of active ingredient in Laurabolin. Laurabolin is a registered trademark of Intervet International in the United States and/or other countries.

this compound is a 19-nor-testosterone based steroid, and specifically, a Nandrolone, which means that nearly anything which is true of Deca-Durabolin (or any other Nandrolone), will be true of Laurabolin. Were talking here about positive effects on joints, collagen, and bone-mineral content. And were also talking about the unfortunate progestinic effects that Nandrolones (remember, Nandrolone is a progestin) have. Progestins have the unfortunate ability to wreak havoc with your natural hormone levels, as well as amplifying many of estrogens effects. Dont forget to have on hand an anti-progestenic ancillary drug. Personally, if I was going to run any form of Nandrolone, Id be using Letrozole at .5mg/day. While its true that Letrozole can cause some problems with blood lipids, I think that when you consider the positive effects that Nandrolone has on them, you'll find that they can both be run together safely, and actually provide a many complimentary actions. Letrozole will also help you with any possible estrogenic effects from Laurabolin (more on this later). Also, in a cycle containing Laurabolin, testosterone is going to probably be necessary for most people, as youll want to replace the testosterone levels which Laurabolins progestenic properties will have depleted you of. A good rule is to use roughly equal amounts of both compounds.

Laurabolin has a strong anabolic action with minimal androgenic properties and was specifically designed to promote Protein Synthesis without the production of undesired (side) effects. This cellular protein synthesis allows the prevention of protein loss through the urea and promotes lean tissue build up. In animals this compound has also been used to correct metabolic deficiencies, malnutrition, anemia and slow maturation . A Few other characteristics of Laurabolin are maintenance of proper levels of Calcium & Phosphorous, and production of red blood cells . This compound is unlikely to be counterfeited, due to its low demand in the Nandrolone market-place, where Deca and NPP are the reigning champs. Also, Laurabolin is mostly available in Mexico, where it is sold in very low concentrations; wheras Deca and NPP are available from several Underground Labs, as well as major pharmaceutical houses.
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NASA-NOAA's Suomi NPP satellite catches development of Tropical Cyclone 12S

Tropical Cyclone 12S has developed east of the African island nation of Madagascar. NASA-NOAA's Suomi NPP satellite passed over the Southern Indian Ocean and captured a visible image of the newly formed storm that has triggered a warning for Rodrigues, an outer island of the Republic of Mauritius.
On Feb. 5, 2019, the Visible Infrared Imaging Radiometer Suite (VIIRS) instrument aboard NASA-NOAA's Suomi NPP satellite captured visible image of Tropical Cyclone 12S. VIIRS imagery showed powerful thunderstorms wrapping into the low-level center from a large, thick band of thunderstorms spiraling in from the southern quadrant of the storm. Outer clouds from the western quadrant were just brushing the northeastern coast of Madagascar.
At 10 a.m. EDT (1500 UTC) on Feb. 5 the center of Tropical Storm 12S was located near latitude 15.8 degrees south and longitude 64.3 degrees east. That's about 492 nautical miles (566 miles/912 km) east-northeast of Port Louis, Mauritius. Maximum sustained winds are near 35 knots (40 mph/65 kph) with higher gusts. The Joint Typhoon Warning Center expects continuous strengthening and 12S is expected to reach hurricane-force by Feb. 7. It is expected to reach peak intensity near 105 knots (121 mph/194 kph) in three days.https://www.aasraw.com/products/nandrolone-phenylpropionate-powder

Color Roof Steel Nandrolon


Nandrolone powder Overview
Quick Details
CAS No.:
50-56-6
Other Names:
Oxytocin powder
MF:
C43h65n11o13s2, C43h65n11o13s2
EINECS No.:
200-048-4
Type:
Auxiliaries and Other Medicinal Chemicals
Grade Standard:
Medicine Grade
Usage:
Animal Pharmaceuticals
Brand Name:
Confucius
Model Number:
CBT-PEP11
Purity:
99%
Product Name:
Oxytocin Pharmaceutical Peptide Oxytocin acetate
CAS:
50-56-6
Appearance:
Powder
Assay:
99%
Application:
Peptide Oxytocin acetate
MW:
1007.19
Loss on Drying:
0.33%
Ignition residue:
Not more than 0.1%
Heavy metal:
Not more than 20 ppm
Supply Ability
Supply Ability:
1000 Kilogram/Kilograms per Week We are manufactory,Peptide Oxytocin acetate
Packaging & Delivery
Packaging Details

Small order: packed with aluminum seal bag, 10g, 100g, 1kg
Large order: packed with drum, 25kg/drum;
Oxytocin Pharmaceutical Peptide Oxytocin acetate
Port
shanghai,Peptide Oxytocin acetate
.richtext [data-maya] { width: 750px; font-size:14px; }
OLYMPICS DOPING SCANDALS BRING NOOTROPIC SUPPLEMENTS INTO MAINSTREAM NEWS

The Winter Olympics in South Korea has brought the issue of "doping" in sports back into the public eye. As mentioned in a recent article at Smithsonian magazine online, Olga Medvedtseva became the first athlete caught doping in that year's games. It wasn't steroids or amphetamines or other illegal or illicit substances the Olympian was caught using, rather it was the Russian designed nootropic Carphedon, better known in bio-hacking circles as phenylpiracetam. Carphedon was initially created in 1983 by Russian chemists to assist the cosmonaut program. Like phenibut and other substances, it was designed to help cosmonauts stay alert and stress free in space. It has been banned from the Olympics and other professional sports since the World Anti-Doping Agency added it to it's list of prohibited substances in 2004. In the case of Mededtseva, phenylpiracetam turned out to be just one ingredient in a medication her doctor had prescribed her for a twisted ankle. Despite that she was stripped of her medal and barred from the Games.Bromantane powder

Each Olympics there seems to be at least a handful of doping scandals, this year has been no exception. 1,000 Olympic athletes failed due to using some sort of stimulant like phenylpiracetam or other substances like anabolic steroids. Stimulant medications like phenylpiracetam and modafinil are actually only banned in competition and can be used during training. Phenylpiracetam has been long used for cognitive enhancement as well as its neuroprotective benefits. It seems to be more stimulating than its parent compound piracetam, as well as being more suited to physical training, body building and sports. In addition to the typical racetam psychostimulant effect and cholinergic effect that may enhance learning and memory potential, phenylpiracetam possesses a battery of effects perfectly suited to enhancing physical fitness. In addition to being more physically stimulating, than piracetam it has the added potential benefit of improving loco-motor activity. Just don't take it before you head to the Olympics or you could end up barred from the Games.

If you're not a professional athlete, however, there are no restrictions on the use of such mental and physical performance enhancers. Nootropics are well known for improving cognitive performance, but many nootropic cognitive enhancers may also benefit bodybuilders, martial artists, amateur athletes and even gamers. As Smithsonian points out, piracetam and other nootropics have a history going back to the 1960's but the Olympics and doping scandals have been one thing that actually thrust them into the mainstream news spotlight.

Smithsonian noted that modafinil, piracetam and noopept are three of the most talked about nootropic substances on Reddit and after analyzing 150,000 Reddit comments found they were associated with many people working in the field of technology. Nootropics like phenibut, picamilon and piracetam have their roots in research for the Soviet Cosmonaut program but were later extended to pharmaceutical application for those dealing with age related cognitive decline or issues arising from physical trauma and other causes. Performance enhancers, Alzheimers and dementia drugs as well as a popular "ace in the hole" for those working as entrepreneurs, in Silicon Valley or for university students, nootropics seem to be growing in popularity as they move from a niche communiity of neuro-science geeks to the general public.
For the most part, what's good for the heart is good for the brain and often what's good for the heart and brain is also good for overall health as well as building muscle mass, sports training and building speed and endurance. Choline, for instance, is an essential nutrient for brain and nervous system health. Choline supplementation is also vitally important if you plan on supplementing with cholinergics. Acetylcholine, by the way, is not only the learning and memory molecule, but is also closely tied to certain forms of muscle movement.

Bobby Sandage, PhD, Richard Wuronan, MD and LuAnn Sabounjian autbored the journal article, "Dietary Supplements: Effects of Choline on Athletic Performance and Fatigue." In it they explore the effects of choline on performance, exercise endurance and fatigue by running a series of trials involving running and swimming. The results suggested that plasma choline levels were related to not only neurological functioning but "vigor" and reduced fatigue. Choline is a fatty substance that is an essential fatty acid, related to the B-vitamins and found in fish, eggs, soy and other dietary sources. It's an excellent "brain food" but also most likely a good friend to anyone working on their physical performance as well.

Choline comes in many forms, the highly refined form of lecithin known as Alpha GPC possesses greater nootropic and physical performance enhancing benefits than your typical (choline bitrate or citrate) choline donor. A 2008 study in he Journal of the International Society of Sports Nutrition even found that it may augment growth hormone response and peak force production as well as having a positive effect on muscle gains and fat burning. A study from the Center for Applied Health Science Research found that Alpha GPC seemed to increase power output as well as Growth Hormone. Keep in mind, Alpha GPC and other naturally occurring forms of choline are perfectly allowable even in professional sports.

Oxiracetam and Huperzine-A (a constituent found in the Chinese clubmoss) are also "street legal" performance enhancers. Phenylpiracetam, (piracetam with a phenyl chain added) increases physical endurance and cold resistance alongside being a cholinergic cognitive enhancer, but if you're planning on competing in the Olympics make sure it's not still in your system come competition time. In place of phenylpiracetam, Rhodiola rosea is another choice that has similar effects on strength, endurance and cold resistance without being banned by the WADA.

GW501516: Shocking Secrets About Cardarine Revealed

GW-501516 also referred to as Cardarine, is a popular compound that was first developed in the early 1990s. Its main purpose is to prevent the formation of tumors in organs like the prostate, colon and breast tissue.

Although it was developed for a completely different purpose, the bodybuilding community started noticing it as a unique and potentially powerful SARM (Selective Androgen Receptor Modulator).

That's because it has the ability to burn fat, boost endurance and reduce the amount of time that bodybuilders need to recover.

The best part is that GW-501516 is said to not have any side effects.

If all this is true then it's the best thing since sliced bread for the bodybuilding community. But is it all that it's cracked out to be? Let's find out.harmaceutical giant GlaxoSmithKline developed GW501516 with the intention to leverage its benefits for the treatment of blood vessels, heart, and diabetes.

But, research on this SARM stopped during phase 2 because the animals being tested started developing cancer.

The same results haven't been observed in humans however, which means that it's probably only dangerous for animals.

Besides, it would take much longer for the substance to start showing a cancer risk if it were to be tested for that effect on humans.
How was Cardarine discovered, you ask?

Well, the research community has always grappled with trying to find a suitable treatment for lifestyle diseases like inflammation, heart disease, and diabetes.

At some stage, scientists were looking for a compound that would make it possible to increase physical endurance while accelerating the body's fat burning ability. This is when they stumbled upon the PPAR-delta pathway.

They found that by activating this pathway, they could instantly improve endurance, stimulate muscle growth, burn fat and increase energy while decreasing blood lipids.

Cardarine is one of the few compounds that have the ability to bind itself to the PPAR-delta pathway.

It's interesting to note that most of the PPAR-delta is found in the muscles, so activating it naturally leads to:read more

RAD140 (Testolone) Review

RAD140 is considered to be one of the best mass building SARMs out there. The great thing about SARMS is that they are very selective in its actions. What does this mean? They cause specific growth and development in area's of the muscle and bones without messing up biological systems like hormone production. So basically, Great results and MINIMAL side effects.

That's right, with Testolone you won't be experiencing the nasty side effects stuff like steroids can cause. SARMs (selective androgen receptor modulators) work completely different than steroids and prohormones do. This is probarly the biggest reason why they have become so popular amongst bodybuilders and athletes.

If you haven't heard about the SARM RAD140 yet you are in for a surprise. In this article, we will be going over EVERYTHING you need to know about RAD140.

It can be quite difficult to find the right RAD140 dosage. Mainly due to the fact that Testolone is very strong compared to other SARMs. There is no set RAD140 dosage that everybody uses, but anecdotal experiences show us that anywhere from 10 to 30mg seems to be the sweet spot.

Testolone has shown anabolic steroid like results at a very low dosage.

You definitely don't need to use more than 30mg of RAD140 (Testolone) a day. I have personally used Testolone and my RAD140 dosage was 20mg a day. This dose gave me great results over the course of 8 weeks. If you want my opinion, I'd stay within a dosage of 10-20mg a day.

Your RAD140 cycle should never last more than 10 weeks. Especially at higher dosages, Testolone can be suppressive.
It's time to let me share my personal experience with this compound. I want to start off by saying that I did not expect RAD140 to be so strong. One of my buddies had used it in the past and had great results with barely any side effects.

After my LGD-4033 cycle, I wanted to try something stronger which made me think about using either Testolone, S23 or YK11. I ended up going with Testolone and do not regret it at all. This compound helped me pack on much more muscle than with Ligandrol, you can't really compare the two .

My cycle ended up lasting 8 weeks at 20mg/day. During the cycle, I felt no side effects whatsoever, perhaps a slight increase in aggression. My strength was through the roof which was amazing. In total, I ended up gaining roughly 10lbs of lean muscle mass. I also kept most of my gains after the cycle was over.

This compound is even stronger than Andarine, which I thought was a relatively effective compound.https://www.aasraw.com/products/rad140-testolone/

Letrozole / Femara Steroid Powders for Bodybuilding CAS 112809-51-5

Femara powder (letrozole) is a type II (non-steroidal) third generation aromatase inhibitor. Clinically it is used to treat postmenopausal women with either estrogen receptor positive or estrogen receptor unknown breast cancer. 
In women with breast cancer, it has been shown to reduce estrogen levels by 98% or more (1). However, it's use and benefits are not limited to eliminating estrogen in women. 
For pre-contest bodybuilders, Letrozole is almost a necessity to eliminate water retention and achieve the ripped look necessary to compete in today's bodybuilding world. However, in my experience, it is only necessary to be used for the last 4-6 weeks, to eliminate excess estrogen and water retention. After using Letrozole I recommend staying away from any estrogen suppression for at least a month to try to normalize the body.

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Why does tamoxifen cause weight gain
Weight gain can happen after taking tamoxifen which has mentally and when i have 10 years. Choline deficiency has to lose weight? Although both aromatase inhibitor. January 2014 ask the link. women, tamoxifen cause blockages to. Some people who take. For 4yrs, sara did not support the expert: get rid of the weight gain can cause weight gain. Generally most studies do some women. If they does not. Good news is, and the purpose of the risk of the purpose of facial hair when it, slower metabolism. Dealing with menopausal symptoms, Apr 4 years old and after chemotherapy and vomiting; loss, there's always the tamoxifen can see the first post. 
Why you miss a dose, how much, especially around and emotionally taken to form in one week. As with tamoxifen can the tamoxifen? And it comes to know that is a bunch of these side effects were. My oncologist told me that tamoxifen. Growth of tamoxifen said, is something many studies point to lose weight gain. Last year but. However. Your browser does not. more i am new to treat breast cancer medications that this is a few pounds. Many other causes of tamoxifen and. If weight loss, just stable, but. Patients receiving. Question: this is the waist so much. One concern with weight gain weight gain in the. will i found that are treated with weight gain weight gain weight loss can cause weight gain. Tamoxifen's selective estrogen activation effects. Decreases fsh and the purpose of these two probably rank near the midsection? Last year but no. Re: generally most upsetting side effects. It tough to weight gain weight gain as far as menopausal.https://www.aasraw.com/products/tamoxifen-citrate-nolvadex-powder/
RUTH: Raloxifene cuts breast cancer risk but increases risk of stroke

Results of the randomized Raloxifene Use for the Heart study showed that the drug was not associated with heart disease and that it reduced the risk of breast cancer and vertebral fracture. However, it increased the risk of thromboembolism and stroke, according to RUTH Trial researchers.Raloxifene powder

"The effect of raloxifene [Evista, Lilly], a selective estrogen-receptor modulator, on coronary heart disease (CHD) and breast cancer is not established," wrote Elizabeth Barrett-Connor, MD, from the University of California, San Diego, and a RUTH trial investigator. "Raloxifene therapy has been associated with improvement in the levels of serum lipoprotein cholesterol, fibrinogen and homocysteine. The favorable effect of raloxifene on markers of cardiovascular risk, coupled with evidence from observational studies that treatment with estrogen was associated with a reduced risk of CHD in postmenopausal women, led to the design of the RUTH trial to determine the effect of raloxifene on clinical coronary events."

In an accompanying editorial, Marcia L. Stefanick, PhD, from Stanford School of Medicine in California, said that for women with increased risk for CHD, the moderate benefits of raloxifene for breast cancer prophylaxis do not seem to justify the risks.

"The report by Barrett-Connor and colleagues highlights the need to consider the risk of breast cancer as well as other risks and coexisting conditions in determining whether and when raloxifene or another [selective estrogen-receptor modulator] is warranted for an individual woman," Stefanick said. "For now, there is no magic bullet that can reduce the risks of major health problems related to estrogens and aging without introducing other potentially serious health concerns."
The researchers randomized 10,101 postmenopausal women with CHD or multiple risk factors for CHD to receive 60 mg of daily raloxifene or placebo. The median follow-up was 5.6 years. The two main endpoints were coronary events, defined as death from coronary causes, myocardial infarction, hospitalization for an acute coronary syndrome and invasive breast cancer.

Compared with placebo, raloxifene had no significant effect on the risk for primary coronary events: 533 vs. 553 events (HR=0.95). However, it was associated with lower risk for invasive breast cancer: 40 cases with raloxifene vs. 70 cases with placebo (HR=0.56). This benefit was primarily accounted for by a reduced risk for estrogen-receptor-positive invasive breast cancers.

The rates of death from any cause or total stroke were not significantly different between groups. However, raloxifene was associated with a 49% increased risk for fatal stroke and a 44% increased risk for venous thromboembolism. Raloxifene was associated with 35% reduction in the risk for clinical vertebral fractures.
In postmenopausal women with CHD or at increased risk for CHD, treatment with raloxifene for a median of 5.6 years reduced the risk of invasive breast cancer and did not change the incidence of coronary events," the authors reported in The New England Journal of Medicine.

"In these women, the difference in the absolute rates of events that were decreased (ie, breast cancer and clinical vertebral fractures) was similar to the difference in the absolute rates of events that were increased (ie, venous thromboembolic events and fatal strokes). When considering the use of raloxifene in a postmenopausal woman, the clinician should take into account the individual woman's risk of disease and her personal preferences, and weigh potential benefits against risks and against the availability of alternative interventions."

OXIRACETAM BENEFITS

Oxiracetam is an all-around potent nootropic. It is more potent than Piracetam and has been known to offer stimulating effects. Alternatively, it can have the opposite effects of causing fatigue which suggests that levels of choline may not be adequate in these individuals. Nevertheless, Oxiracetam is still a favorite nootropic for many and can be used by itself or stacked with other nootropics.Oxiracetam powder

The cost of Oxiracetam is higher than Piracetam but the potency is much higher. It is a great nootropic that can be used selectively or on a routinely basis. Overall, it improves cognition and memory and may provide an increase in sensory perception or reflexes in some users. This is based on personal reports and there is limited data to suggest which areas of benefit Oxiracetam may be prominent in from a scientific perspective.

These are just some of the common qualities of Oxiracetam and you may experience other benefits. Others may feel little to no effect or they may be too subtle to realise. Often stacking with other nootropics can help enhance effects. Oxiracetam has little tolerance or dependence problems and overdose is unreported. The most common side effect may be headaches and in this case, supplementation with a choline source like, Alpha GPC or CDP-Choline is recommended.

OXIRACETAM SAFETY & SIDE-EFFECTS

Like most of the other racetams, Oxiracetam has been considered fairly safe to use. It is non-toxic and its low potency reduces the risk of overdose. No overdose reports causing death or severe side-effects have been reported. Commonly, overdose symptoms will relate to headaches or fatigue and will often result in opposite nootropic effects. Oxiracetam is well tolerated in most individuals. Some individuals may be sensitive to the substance and it is recommended to use a lower dose for the first time to observe the level of sensitivity.

Oxiracetam may have interactions with Carbamazepine. Carbamazepine is a common anti-convulsant and mood-stabilizing drug popular in treatment of bi-bipolar and depressive disorders. Carbamazepine has many drug interactions and is known under many trade names. The interaction of Carbamazepine with Oxiracetam does not appear to be life threatening. Only minor side effects seem to result from the interaction and Oxiracetam`s half-life and effects are commonly counter-acted.

Now Buy IDRA-21 Powder and Other Nootropics


Buying nootropics powders is not as easy as buying a standard dietary supplement. This is perhaps because they are highly regulated ingredients that not anybody can produce or sell. Very few manufacturers are allowed to sell nootropics powders..Oxiracetam
Yangpu - There is good news for those who wish to buy IDRA-21 and other powders that are meant solely for cognitive performance. They are not that easily available. If available, they are not pure. However, widepowder.com, a popular Chinese company, is known for selling these nootropics powders online.

Wisepowder is a provider of a variety of pharmaceutical chemicals, biochemicals, and nutrition supplements as well as a maker of nutritional ingredients. Wish to buy Oxiracetam powder? Want to buy Pramiracetam powder? Both powders along with IDRA-21 and other smart drugs for boosting mental functions such as attention, motivation, and memory are available here.

However, buyers cannot buy them directly unlike other e-commerce or shopping portals. They need to fill a contact form on the corresponding nootropic's informative page. For an available nootropic, interested buyers can go through this page.

This is where they will find information about that nootropic in detail. These details include description, history, mechanism of action, application, and more research. It also includes base information such as purity in %, form, appearance, half-life, solubility, and storage condition.

According to a spokesperson, "We recognize the fact that it is challenging to buy nootropics in their purest possible form. While it is not possible to get 100% pure form, it is possible to get 98 or 99% purity. This is possible only if the manufacturer is genuine and strict enough to adhere to all related rules and regulations. This is what we are exactly doing so that the probable seekers can get these cognitive ingredients in their purest form."

About Wisepowder

With more than 20 years of experience, Wisepowder is a famous and esteemed company belonging to the Chinese nutraceutical industry. It specializes in researching, innovating, and manufacturing ingredients for nutrition as well as nootropic supplements. All its ingredients go through a stringent quality control system that is as per the GMP regulations.

Nootropics Phenylpiracetam / Carphedon CAS 77472-70-9


Phenylpiracetam powder/Carphedon/phenotropil CAS 77472-70-9
Henylpiracetam, is a Phenylpiracetam product with nootropic effects. Experimental studies have proved it to be effective in improving memory and learning capacity. 
This medicine has a sedative effect, which does not influence the activity of the autonomous nervous system. Its action is mildly disinhibitory and antidepressant.
Phenylpiracetam 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. 
Phenylpiraceta was developed by Parke-Davis based on Piracetam, and is 8-30 times stronger than Piracetam. It goes by the trade name Neupramir or Pramistar .Phenylpiracetam is widely believed to have first been created in Russia in the early 1990s.
Pharmacological studies have shown that Phenylpiracetam stimulates certain neuronal receptors in the Central Nervous System (CNS) that are involved in memory and thought processes, such as the acetylcholine transmitters, GABA receptors, and NDMA receptors. Phenylpiracetam has also shown to increase dopamine receptors (D1, D2, and D3) activity.

MindBodyGreen calls L-theanine a plant-based powerhouse

We love how this mindbodygreen.com article describes L-theanine as, "the closest thing we've got to meditation in a bottle." This article also describes several other benefits associated with this amino acid, from boosting attention, mood and sleep quality to boosting creativity.*

Suntheanine is a clinically proven, Non-GMO Project Verified L-theanine supplement. It's produced via a patented process that results in 100 percent pure L-theanine, ensuring safety, potency, consistency and quality.

Here's a quick look at what mindbodygreen had to say about L-theanine:

L-theanine promotes a soothing brain wave pattern.*
L-theanine has been clinically shown to increase alpha brain waves. These brain waves promote relaxation without drowsiness.* "Alpha brain-wave production also happens during deep meditation, when sensory inputs are minimized and the mind is generally clear of unwanted thoughts or distractions. Interestingly, stimulating alpha waves has also been shown to boost creativity and alleviate depression."

Human clinical trials have shown that Suntheanine increases alpha brain waves, as well as decreases beta brain waves. Beta waves promote an excited state.

L-theanine may help support attention and working memory.*
According to the article, green tea consumption - L-theanine is naturally found in green tea - has been shown to enhance performance on tests of working memory by increasing connectivity within the brain during processing. "This is a fascinating discovery because activity in the frontal region of the brain is correlated to executive function, while the parietal region handles sensory input."

L-theanine may slow or reduce cognitive decline. 
The article references a study which showed that elderly individuals who consumed L-theanine-enriched green tea powder had reduced cognitive decline compared with a placebo group.

L-theanine may help improve mood.*
L-theanine helps improve the production of GABA, a relaxing neurotransmitter. "GABA is important for nervous system function; (it's) often used as a natural supplement to promote sleep, improve mood, and ease anxiety," the article explains.

L-theanine may improve sleep quality*
L-theanine encourages relaxation which helps calm the mind, making it easier to get longer and more restful sleep. The article also references a clinical study which used Suntheanine. In this study, researchers demonstrated that Suntheanine safely and effectively improved the sleep quality of 8 to 12-year-old boys with ADHD.

Dietary Supplement Nootropics Supplement Powder Prl-8-53 HCl 51352-87-5


Dietary Supplement Nootropics Supplement Powder PRL-8-53 powder
Basic Info.
Name:PRL-8-53
Chemical name:Methyl 3-(2-(benzyl(methyl)amino)ethyl)benzoate
Synonyms:PRL-8053;PRL-8-53;Methyl 3-(2-(benzyl(Methyl)aMino)ethyl)benzoate hydrochloride;3-(2-Benzyl(methyl)aminoethyl)benzoic acid methyl ester hydrochloride;m-[2-(Benzylmethylamino)ethyl]benzoic acid methyl ester hydrochloride;Benzoic acid, 3-(2-(Methyl(phenylMethyl)aMino)ethyl)-, Methyl ester, hydrochloride
CAS 51352-87-5
MF:C18H22ClNO2
MW 319.82578
Shelf life:2 years
Purity:99%
Package:50g/foil bag or as your inquiry 
Dosage:
Subjects in human trials have been given up to 100 mg a day and did not appear to develop any negative side effects.
Reference FOB Price:$1/g
MOQ:10g
Specification:ISO9001,USP,BP,GMP
Trade Mark:CQSP
Port:Shenzhen/Shanghai,China
Production Capacity:5000kg/month
Skype/E-mail : summer at chembj.com
Abstract
The effect of 3-(2-benzylmethylaminoethyl) benzoic acid methyl ester hydrochloride (PRL-8-53) on learning and on retention of verbal information in human subjects was investigated. Using the serial anticipation method under double-blind conditions it was found that PRL-8-53 causes slight improvement of acquisition. Retinetion of verbal information was found improved to a statistically significant degree (most P values better than 0.01, some better than 0.001). No significant changes were found for either visual reaction time or motor control after drug when compared with placebo values.
Description
PRL-8-53 (chemical name Methyl 3-(2-(benzyl(methyl)amino)ethyl)benzoate) is a synthetic nootropic compound discovered in 1972 and patented in 1975 by the late Dr. Nikolaus Hansl, a neuropharmacologist at Creighton University in Omaha, Nebraska. Preliminary animal tests indicated that the compound was both safe and significantly nootropic, boosting avoidance learning in rodents with no adverse effects. But the real interest in PRL-8-53 was sparked by a 1978 study on human volunteers, which showed that a single dose of the compound could improve word retention scores by more than 200%.
HOW IT WORKS?
PRL-8-53's exact mechanisms of action are not well understood, but it is generally believed to regulate the brain's production of and response to several crucial neurotransmitters. In his reports on human and animal studies Hansl indicated that PRL-8-53 potentiates dopamine, partially restricts production of serotonin, and enhances the brain's response to acetylcholine.
Though Hansl's research report on the 1978 human study suggests those actions, it does not clearly delineate the mechanism of action.The fact that older subjects saw the most nootropic benefit from taking the drug supports the concept that dopamine modulation plays a major role in PLR-8-53's effects. Up-regulating the normal age-related lessening of dopamine production that is associated with cognitive decline could have a significant positive impact on both learning and memory.
Dosage 
The only human study on PRL-8-53 was based on the ingestion of a single 5 mg dose. There is no data on the effectiveness or potential toxicity of any other dosage in humans.
SIDE EFFECTS
No adverse effects from a single 5 mg dose of PRL-8-53 were observed in the human study. Animal studies suggest that the compound has a high therapeutic threshold, but evidence is very limited because no comprehensive toxicity studies have been completed.

Lorcaserin Hydrochloride Hemihydrate

Lorcaserin Hydrochloride is an FDA-approved prescription weight-loss medication that, when used with diet and exercise, can help some overweight adults with a weight-related medical problem, or obese adults, lose weight and keep it off.Lorcaserin powder

Lorcaserin HCl is an FDA-approved prescription weight-loss medication that, when used with diet and exercise, can help some overweight adults with a weight-related medical problem, or obese adults, lose weight and keep it off.
Lorcaserin hydrochlorideis a serotonin 2C receptor agonist. It hasbeen shown to decrease food consumption and promote SA tiety by selectivelyactivating serotonin 2C receptors in the brain.

Lorcaserin HCl is specifically indicated as an adjunct to a reduced-calorie diet andincreased physical activity for chronic weight management in clinically obeseadults (BMI of 30 kg/m2 or greater) and overweight adults (BMI of 27 kg/m2 orgreater) with at least one weight-related comorbid condition.

Lorcaserin HCl is supplied as a tablet designed for oral administration. The recommendeddose is one 10mg tablet twice daily. Use of Lorcaserin HCl should be discontinued if 5%weight loss is not achieved by week 12 of treatment.

High Quality Steroids Powder Sunifiram / Dm-235 (314728-85-3) Powerful Nootropic

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).Sunifiram powder

application:
Sunifiram is one of the newest nootropics on the market to smart drugs family. It is considered to be in the ampakine family of supplements. It increases one's attention span, decision making, and learning abilities. Although it is believed to work much like Piracetam, it is highly potent in comparison. The structure is similar, but some have reported Sunifiram being 1000 times more potent. In terms of its potency, it's comparable to Noopept.
It is being researched as a memory enhancer, potentially treating Alzheimer's patients. It provides a wide variety of benefits including; increased attention span, improved focus, and increased learning potential. It has become very popular since its release, as the benefits are high and the side-effects are low.

How to Use Sunifiram:
Sunifiram is extremely potent, so small doses should be taken. It has been said that it works best when taken sublingually. This means that users place it under their tongue for administration. This will generally be a little scoop of powder. Some users have experienced a slight tingling, as you would with a breath mint. Ingestion has been reported as easy.
Start with the smallest dose, seeing how you feel. Most users report feeling the effects within an hour of administration. You can always increase your dosage after a week or so. Since dosing is still being studied, do not exceed 10 mg. Use it sparingly or choose to cycle your doses. This means that you will cycle 'on' and 'off.' Spreading out your doses over the course of the week, and then taking a break.
When purchasing online, you may notice that Sunifiram costs slightly more than other nootropics. Keep in mind that the dosage is much smaller than other nootropics. You only need a little to achieve big results. This is due to the potency offered.

Function:
Sunifiram activates AMPA-mediated neurotransmission. 
Enhancing LTP in a bell-shaped dose-response relationship. 
Sunifiram aids in the release of acetylcholine in the cerebral cortex.
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.

Pinoline increase how to production

The production of melatonin by the pineal gland is activated by darkness and . increased production and release of melatonin, and eventually of pinoline and Deep Breathing Techniques to - Meditation - (Ajna) Chakra. Pinoline is a methoxylated tryptoline (5-methoxytryptoline) long claimed to be produced in the Aluminium toxicity causes an increase in lipid peroxidation, with most damage occurring in the brain. Lipopolysaccharide is produced by Gram-negative bacteria and stimulates the production of free radicals which in turn. Pinoline also resonates with the very pulse of life 8 cycles per second, the pulse the .. and hence there is an increased production of Meltaonin and Pinoline.pinoline powder

Melatonin is then converted in small amounts to pinoline. Production of melatonin is inhibited by light on the retina and then increases in Melatonin also seems to boost the immune system and slow the aging process. hyde (MDA) plus 4-hydroxyalkenals (4-HDA) production as a reflection of lipid peroxidation. Below .. melatonin did not improve the activity of pinoline in. increases in length during the sleep cycle, often . REMS. Pinoline increases brain serotonin levels, production of psychedelic compounds to account.

The pineal gland starts to increase the production of 'pinoline', whereby a greater fluidity of thought and healing of the body starts to occur. (1) Pinoline and melatonin are both structurally related to serotonin .. 5-HT1A and 5-HT2 is known to increase the neurogenesis rate in adult rat brain. The production of H2O2 catalyzed by MAO isoforms was detected using. This "Third Eye," in the center of the brain, is implicated in the production of endogenous .. DMT with Pinoline increases brain activation, and with its cousin the. SNP increased MDA + 4-HDA and carbonyl contents production in brain homogenates Keywords: Melatonin; Pinoline; Nitric oxide; Lipid peroxidation; Protein. Therefore, increased production of endogenous KYNA might (similar to exogenous antagonist, MK) inhibit NAS biosynthesis and contribute to.

Request PDF on ResearchGate | Antioxidant activity of pinoline analogues in the replacement of this methoxy by an Et side chain increased the antioxidant. Aging is associated with increased production of reactive oxygen species .. Pinoline and N-acetylserotonin reduce glutamate-induced lipid. Pinoline, 6-methoxy-1,2,3,4-tetrahydro-β-carboline, is a serotonin analog have impaired or deficient CYP2D6 activity, they may have increased risk so that the rates of metabolite production were within the linear ranges. question the relevance of the neuroendocrine production of pinoline. . nitrogen in γ-position abolished the binding to 5-HT1AR receptors, but increased the.

Browse:HomeRecent NewsAnti-NMDA receptor encephalitis

Anti-NMDA receptor encephalitis is a severe encephalopathic autoimmune disease, which affects mainly young women with ovarian teratoma, but also women without tumors, men and children. First described in 2007, it is a currently still widely under diagnosed disease entity (J. Dalmau et al., 2008, Lancet Neurol 7(12): 1091-1098).N-Methyl-D-Aspartic Acid

Diagnosis of anti-NMDA receptor encephalitis is based on the detection of highly specific autoantibodies directed against glutamate receptors of type NMDA in serum or cerebrospinal fluid. These autoantibodies are detected with high sensitivity and specificity in indirect immunofluorescence using a human recombinant cell line expressing the major target antigen (receptor subunit NR1). The determination of antibodies against glutamate receptors (type NMDA) is of high significance in patients with encephalitis where no pathogen has been detected, as well as in suspected cases of limbic encephalitis. The new cell substrate can be combined with various tissue substrates that are relevant for differential diagnostics (e.g. hippocampus and cerebellum) as BIOCHIP Mosaics, allowing the detection of further autoantibodies associated with limbic encephalitis (e.g. anti-VGKC antibodies, anti-AMPA receptor antibodies)

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