یکشنبه 27 مرداد 1398  05:58 ب.ظ

Apple offers $1 million reward to anyone who can hack an iPhone

It almost sounds too good to be true — Apple is offering up a $1 million reward to anyone who can hack an iPhone. Its an expansion of the tech giant's bug bounty program, but the reward has never been higher.
The bug bounty program, which previously offered rewards of up to $200,000 for finding problems in iOS devices, first launched in 2016. Apple head of security Ivan Krstić announced major changes to the program on stage at the Black Hat conference in Las Vegas Thursday, CNET reports.
Starting this fall, the reward will be increased to $1 million for the first time. It will also expand to include all of Apple's platforms — iOS, iCloud, tvOS, iPadOS, watchOS and macOS.All a hacker needs to do to get the million dollars is gain full control of an Apple device remotely, without the owner of the device ever interacting with it.
"This is an unprecedented fully Apple supported iOS security research platform," Krstić said at the conference. Finding other device vulnerabilities result in smaller rewards of up to $500,000. The program is now open to anyone who wants to participate. It's no longer invite-only.
Apple will also start offering special iPhones specifically for qualified security researchers. They are easier to hack than traditional iPhones, meant for developers to find security flaws so Apple can fix them before a new product launch.
Bug bounty programs are now commonplace among tech companies. Hackers search for security flaws missed by internal teams, and instead of exploiting the bugs, they submit them back to the programs for financial rewards.
"It is important for companies, especially those dealing with mounds of sensitive personal data, to have a public-facing way to report bugs and vulnerabilities," Marten Mickos, CEO of the bug bounty platform HackerOne, said in a statement.
The announcement comes as data breaches become increasingly common in tech and financial industries.Last month, Capital One said a hacker got access to the personal information of over 100 million individuals applying for credit. And Equifax will pay up to $700 million over the massive 2017 data breach that exposed the private data of nearly 150 million people.
Last October, Google's troubled social network Google Plus shut down following the discovery of a software glitch this past spring that may have exposed the user information of up to 500,000 customers between 2015 and 2018. https://www.ttspy.com/how-to-hack-into-someones-iphone.html

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یکشنبه 27 مرداد 1398  05:49 ب.ظ

Take a Closer Look at What Could Be the YEEZY Boost 350 V3

Highsnobiety aims to provide our readers with the latest updates in the sneaker world. However, we cannot verify the reliability of any unauthorized leaks or rumors unless this information is provided directly by the brands themselves.

After Kanye West was spotted in Los Angeles wearing what appeared to be an update of the adidas Originals YEEZY Boost 350, a mockup of the shoe and rumored release information have now appeared online. Rumors suggest the YEEZY Boost 350 V3 will drop sometime in late 2019 or early 2020 and will cost $230, making it the most expensive YEEZY Boost 350 yet.

The mockup (below) shows how the rubber midsole rises higher around the heel than on other versions, almost mimicking the design of the YEEZY basketball sneaker West has worn and teased previously. The ankle collar almost rises to a mid-top level, with the side stripe shortened and modified slightly.get Yeezy Boost Shoes,more order with big discount

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یکشنبه 27 مرداد 1398  05:41 ب.ظ

The Adidas Yeezy Boost 350 V3 Is Reportedly Releasing Soon

Kanye West has hundreds of Yeezy prototypes that may never see the light of day, but every so often he steps out in a never-before-seen design. According to Yeezy Mafia, the latest pair spotted on Yeezus could be the Yeezy Boost 350 V3.

Adidas has been consistently dropping colorways of the V2 since its debut back in 2016. Now, it appears that the Three Stripes might finally be ready to retire the second iteration of the popular silhouette. While the jump from the original 350 to the 350 V2 was fairly drastic, the rumored V3 remains almost identical in appearance to its predecessor. The main differences include a new Primeknit pattern covering the upper, elimination of the lateral side stripe from the V2, and a bulkier midsole.

While no official release information is available at the moment, check out an initial look at the white and grey "Alien" Adidas Yeezy Boost 350 V3 below.

UPDATE (08/13): Yeezy Mafia has provided another update on the upcoming "Alien" Adidas Yeezy Boost 350 V3. The pair is expected to retail at $230. An exact release has yet to be announced. Take a look at some detailed shots of the pair's new midsole design below. Yeezy 350 Static online with hgih quality

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  05:32 ب.ظ

NSI-189 NOOTROPIC ≥98% CAS 1270138-40-3

NSI-189 Dosage: Neuralstem, Inc. is currently running clinical trials for its use in major depressive disorder, in addition to treating cognitive impairments, and brain degeneration. NSI-189 stimulates neurogenesis of the human hippocampus. NSI-189 dosage was 40 mg-80 mg daily for 12 weeks.NSi-189 powder
NSI-189 increases sociability interactions while enhancing confidence and improved life decisions that lead to elevated sexual enjoyment and quality of life.

NSI-189 review

NSI-189 stimulates neurogenesis of the human hippocampus.

Modern antidepressants focus on the monoamine neurotransmitter system. However, 66% of people treated for major depression disorder achieve clinically significant improvements.

Current antidepressants have long term side effects with negative consequences. Neuralstem Inc proposes that NSI-189 uses different pathways.

NSI-189 Benefits

Ability to control emotions that continue after cessation
Being fluent in speaking and writing.
Improved memory energy
Sharpness of vision
Logical and emotional difficulties resolve
Increased sexual enjoyment and quality of life.
Sociability and interactions are maintained with ease
Confidence while enhancing confidence and improved life decisions.
Reports indicate that suicidal tendencies disappear and personal relationships improve with a broad spectrum of reporting.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  05:25 ب.ظ


Propionyl-L-carnitine is a chemical. It is made in the body. Propionyl-L-carnitine is related to two other compounds called L-carnitine and acetyl-L-carnitine.

Propionyl-L-carnitine is commonly used for treating leg pain (intermittent claudication) due to poor blood circulation (peripheral vascular disease, PVD). PVD is often caused by diabetes or “hardening of the arteries” (atherosclerosis). Propionyl-L-carnitine is also used to treat congestive heart failure (CHF), chest pain (angina), and some bowel problems such as ulcerative colitis. A specific kind of propionyl-L-carnitine, called glycine propionyl-L-carnitine, is often used to improve athletic ability. There is limited scientific research that supports taking propionyl-L-carnitine by mouth for other uses..Glycine Propionyl-L-Carnitine powder

Healthcare providers may give propionyl-L-carnitine with a needle into the vein (by IV) for treating PVD and intermittent claudication; to improve wound healing in people with PVD; and to treat heart disease, including congestive heart failure, and chest pain (angina).

How does it work?
Propionyl-L-carnitine helps the body produce energy. It is important for heart function, muscle movement, and many other body processes. It also seems to help increase circulation.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  05:10 ب.ظ

Tryptamines, Beta-carbolines and You

Tryptamines and beta-carbolines are two classes of psychoactive indoles found in plants and animals (1). They have been implicated in a host of neurological functions and display a wide range of neurological activity, which is dependent on their molecular configurations (2). A subgroup of (beta)-carbolines found in some plants are known as the harmala alkaloids; e.g. harmaline in Peganum harmala or Banisteriopsis caapi. Some beta-carbolines have been detected in the tissues and fluids of mammals, including humans, where they are thought to be produced from endogenous tryptamines such as serotonin, 5-methoxy-tryptamine and tryptamine itself. Psychoactive methylated tryptamines such as dimethyltryptamine (DMT), 5-methoxy-dimethyltryptamine (5-MeO-DMT) and 5-hydroxy-dimethyltryptamine (bufotenine) and have been detected in normal human beings as well (3,4,5), though their biological purpose remains a mystery.beta carboline

The psychoactive indoles are interesting not only for their exogenously induced effects on the human mind, but also for their natural occurrence in humans. In the early 1950's, Osmond and Smythies, in their transmethylation hypothesis, proposed endogenous 'schizotoxins' to be responsible for the symptoms characteristic of hallucinatory psychoses, and initiated an era of search for the chemical basis of undesirable states of mind (6). This search was later confounded by the fact that these substances were also found in otherwise normal humans, in addition to many of the other animals in the scientific barnyard. At that time, the psychedelics were commonly referred to as 'psychotomimetics' and 'models for psychosis', and it was difficult to rationalize a normal function for an endogenous psychedelic. Unfortunately, the idea of normal dreaming did not occur to the early pioneers as a possible function for the natural occurrence of endogenous psychedelic substances (7,8).

The Tryptamines Serotonin, melatonin, bufotenine, DMT, 5-MeO-DMT, and tryptamine are well known examples of this group. They primarily originate from tryptophan, an essential amino acid obtained through the diet. All of these tryptamines interact within the central nervous system. DMT is a very potent psychedelic chemical when smoked or injected, but is orally inactive. The onset of its effects are known to be extremely fast, brief and intense. One could say that DMT evokes a transient psychedelic test pattern, exploding with color imagery. 5-MeO-DMT shares similar properties, but is often devoid of visual imagery at effective doses. Its effects have been described as primarily emotive. Bufotenine shares similar properties with these two, especially in terms of a fast onset and short duration of intense action. However, at effective doses, any psychoactivity of interest is essentially lost in the physiological noise it elicits through the serotonergic system. Early reports on the effects of bufotenine in humans clearly indicate its psychoactivity (9), though its polar quality apparently hinders significant passage into the brain. Perhaps the psychoactivity of bufotenine is actually due to its enzymatic conversion to 5-MeO-DMT.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398

PeakNootropics Centrophenoxine Powder - 50 grams - Nootropic Supplement

Centrophenoxine is synthesized from DMAE. DMAE is a natural chemical that has been shown to improve areas of cognition and mood. DMAE’s exact method of action is slightly disputed. Some see it as a precursor to Acetylcholine but others contest this as choline molecules broken down from DMAE are not believed to cross the blood-brain-barrier efficiently.DMAE vs. CentrophenoxineIt is not clear how the method of action differs from DMAE to Centrophenoxine. One thing for sure is that Centrophenoxine is much stronger than DMAE as a nootropic. This is likely due to a higher bioavailability of Centrophenoxine or a difference in how it is metabolized in the liver. If you are taking DMAE as a choline source, consider switching to Centrophenoxine as it is known to be more powerful as a nootropic substance.Both substances are broken down in the liver. The liver metabolizes both substances and breaks them down into choline or phospholipid molecules.Centrophenoxine
DMAE has been suggested to have limited effectiveness because the choline molecules are charged and therefore have limited effectiveness in getting to the brain.Centrophenoxine Method of ActionCholine and certain phospholipids are converted into Acetylcholine. Acetylcholine is important and higher levels and receptor uptake will lead to better cognition. Not all choline will be converted into Acetylcholine and there are several processes that take place between the choline to Acetylcholine conversation. It seems as not all choline sources are created equal. Some sources will have much higher levels of Acetylcholine conversion.Centrophenoxine’s primary method of action is believed to be caused by increased levels of Acetylcholine. Whether this is from breakdown into choline or related phospholipids’ is unclear. There are several phospholipids that will also convert into Acetylcholine. This may be an area where Centrophenoxine is more superior to DMAE.
With this said, the general consensus is that Centrophenoxine supplementation leads to higher Acetylcholine levels and better cognition.Centrophenoxine also may have effects on other neurotransmitters in the brain. It has been suggested to help with mood.Claimed BenefitsCentrophenoxine has been marketed under trade names such as “Lucidril” in some countries. In medical science, Centrophenoxine has been tested for use in treating several cognitive disorders.Centrophenoxine is also an excellent antioxidant. It helps to reduce free radicals in the brain. It is more superior to DMAE as an antioxidant. For this reason, Centrophenoxine has been promoted to reduce “brain aging” and is marketed primarily as a powerful antioxidant.Side EffectsCentrophenoxine has been seen to be well tolerated.
Although this is true, side effects can still occur. These side effects are more likely in higher doses and when combined with other substances. If you are on prescription drugs you should speak with your doctor to assist in avoiding interactions with Centrophenoxine. Below are some common side effects of Centrophenoxine.HeadacheNauseaDizzinessGastronintesinal issuesJaw clenchingIrritabilityIf you do experience side effects it is recommended to discontinue use and speak to a doctor.Centrophenoxine vs. Alpha GPC vs. CDP CholineCentrophenoxine, like Alpha GPC and CDP Choline is an excellent Acetylcholine source. Comparing the three is very hard as it comes down to personal experimentation to find the best supplement for you. If you are using nootropics like racetams, an Acetylcholine source will often be added to potentiate effects. Centrophenoxine, Alpha GPC or CDP Choline may all be options for you. These three options are the best choices for choline supplementation.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  04:56 ب.ظ

Coluracetam Powder

Coluracetam is a nootropic in the racetam family. It shares the same 2-pyrrolidone base structure as all racetams. Coluracetam differs from the structure of piracetam by the addition of a bulky dimethyl-tetrahydrofuro-quinolinyl grouping. It has a molar mass of 341.404 g/mol and a molecular formula of C19H23N3O3.Coluracetam

CAS: 135463-81-9

IUPAC: N-(2,3-Dimethyl-5,6,7,8-tetrahydrofuro[2,3-b]quinolin-4-yl)-2-(2-oxo-1-pyrrolidinyl)acetamide

Product contains one jar of Coluracetam, in either .5g, 1g or 5g amounts.

Attention: All chemical compounds have risks. Please read the available research and understand the associated risks before handling. If you are uncertain of the appropriate handling methods, please consult a qualified professional. Misuse of this product may result in adverse reactions. This product is not approved by the FDA.
Ingredients: Coluracetam [2-(2-oxopyrrolidin-1-yl)-N-(2,3-dimethyl-5,6,7,8-tetrahydrofuro2,3-b quinolin-4-yl)acetoamide].

Ship code/Instructions: Ambient temperature only.

Storage Instructions: Coluracetam should not be refrigerated. Store at room temperature only.

Dosage Instructions: Coluracetam is known to be a somewhat fast-acting nootropic. It has been noted that neural tissues can detect it within 30 minutes of ingestion. The suggested dosage for Coluracetam is 48-480mcg/kg. For example, a person weighing 70kg should take between 3 and 33mg.

The Coluracetam nootropic stacks well with choline and the two are often taken together. The combination is used frequently for added memory and cognitive ability benefits. Those taking both Coluracetam and choline should take 300mg to 600mg of choline daily (if you are taking Alpha GPC) and 250mg to 750mg daily if using CDP Choline.

There is little information currently available on the toxicity of Coluracetam. Doses given at the above increments demonstrated no negative side-effects.

Side-effects: First time users of nootropics may develop headaches after use. This is common for people who have not used nootropics before. There is no reason for concern. When taking both Coluracetam and choline together, the risk of headaches will be reduced.

ATTENTION: This compound should be used for research purposes only. All chemical compounds have risks. Please consult your physician and understand the available research before consumption. This product is not intended to diagnose, treat, cure, or prevent any disease.

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یکشنبه 27 مرداد 1398  04:45 ب.ظ


Save 23% on 100 capsules, hot new analog CE-123 in stock.

Flmodafinil is the most potent legal eurogic known to man, it is a closely related smart drug to Modafinil Adrafinil, Fladrafinil, and Hydrafinil.Modafinil is a popular wakefulness drug prescribed to many CEO types of fortune 500 companies. CRL-40,940 powder

Yes, Flmodafinil capsules are legal to buy for research purposes only.Modafinil, Adrafinil, Hydrafinil, Fladrafinil (CRL-40,941) and Flmodafinil (CRL-40,940), come from the French "Laboratories Laflon".

Dr. Michel Jouvet uncovered these eurogics in the 1970s.Laflon Lab scientists made a crucial observation in their patent applications.

"In man, particularly old people, it was observed that ... CRL-40,940 ... administered in the form of gel capsules or tablets – each containing 100 to 200 mg of the active ingredient, at the rate of 1 to 3 capsules as arousing medicaments.Flmodafinil dosage in clinical studies was in the range of 100 mg to 600 mg Daily. It is considered safer than caffeine and lacks addictive properties.

In 2015 a new patent was filed under a new name Lauflumide a derivative of modafinil.(2-((bis(4-fluorophenyl)methane)sulfinyl)acetamide) Lauflumide is more effective than adrafinil or modafinil with fewer side effects. It was made very clear in the application that CRL-40,940 lacks any resemblance to amphetamines in effect or structure.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398

Gender-Related Effect of Sodium Dichloroacetate on the Number of Hassall’s Corpuscles

Department of Histology and Embryology, Medical Academy, Lithuanian University of Health Sciences, Kaunas, LT 44307, Lithuania
2Institute of Cardiology of Lithuanian University of Health Sciences, Kaunas, LT 50009, Lithuania
3Laboratory of Molecular Oncology, National Cancer Institute, LT 08660 Vilnius, Lithuania
4Biological Research Center, Lithuanian University of Health Sciences, Kaunas, LT 47181, Lithuania

Received 24 July 2018; Revised 26 February 2019; Accepted 8 April 2019; Published 24 April 2019

Copyright © 2019 Jūratė Stanevičiūtė et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.Testosterone Dichloroacetate
The aim was to investigate the effect of dichloroacetate (DCA) on thymus weight, Hassall’s corpuscle number (HCs), and NKCC1 RNA expression in Wistar rats aged 4–5 weeks. They were investigated in the controls and DCA-treated gonad-intact and castrated males and females. The treatment lasted 4 weeks with DCA 200 mg/kg/day. At the end of the experiment, rat thymus was weighted, and its lobe was taken for the expression of NKCC1 RNA determined by the PCR method and of Hassall’s corpuscles by immunohistochemistry. DCA caused a thymus weight decrease in DCA-treated gonad-intact rats of both genders as compared with their controls (p < 0.05), and no such impact was found in castrated DCA-treated males and females. DCA caused an increase of the HCs in gonad-intact males (p < 0.05), and no such increase in the DCA-treated gonad-intact females was found. There was gender-related difference in the HCs when comparing DCA-treated gonad-intact males and females: males showed significantly higher HCs (p < 0.05); no gender-related differences were found in the castrated DCA-treated groups. The Slc12a2 gene RNA expression level was found to be significantly decreased only in gonad-intact and in castrated DCA-treated males. The authors discuss the gender-related DCA effects on the thymus.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  04:30 ب.ظ

Aniracetam Powder

Aniracetam (chemical name 1-[(4-methoxybenzoyl)]- 2-pyrrolidinone) is purported to be much more potent that piracetam so you need to take significantly less of it to achieve a similar effect. Unlike piracetam, aniracetam is fat soluable and therefore should be taken with a meal.Aniracetam

Nootropics, also known as smart drugs, are a group of health supplements which are purported to increase cognitive ability, intelligence, memory, and general brain function.

Aniracetam is an ampakine and nootropic of the Racetam family. This supplement is used for and improving reaction time and mental focus.

As an analogue to piracetam, it is considered that aniracetam is virtually non-toxic, non addictive, has very few side effects, and enhances verbal memory. Nonetheless, unlike piracetam there have been fewer clinical trials and research into the affects of aniracetam, however it is widely considered to be considerably more potent than piracetam, and users of aniracetam generally report that it increases alertless, cognitive ability, attention span, and learning ability.

It is suggested that aniracetam affects the Corpus Callosum in the same way as piracetam, which is the part of the brain which connects the left (logical) and right (creative) hemispheres of the brain. It is suggested that by increasing the linkages between the left and right hemispheres of the brain, piracetam users benefit from greater cognitive potential.

Aniracetam has also been shown to have a more potent affect on the AMPA receptor than piracetam, which results in enhanced focus and concentration.

As with all of our racetams, racetam is very popular among students, sufferers of Alzheimer's and dementia, those recovering from alcoholism, and life extension enthusiasts.

As with most all racetams, aniracetam should be taken with a choline source such as choline bitartrate. It is also often ‘stacked’ with other racetams as well as with supplements such as GABA, and L-Tyrosine, and L-Phenylananine.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  04:22 ب.ظ

Weight-loss drug lorcaserin’s glycemic effects revealed

BERLIN – Lower rates of incident type 2 diabetes mellitus (T2DM) and improved glycemic control were two of the metabolic effects seen with the appetite-suppressant drug lorcaserin versus placebo on top of existing lifestyle management measures in a large-scale trial of more than 12,000 overweight or obese individuals with established cardiovascular disease or T2DM and other cardiovascular risk factors.Lorcaserin HCL

In the CAMELLIA-TIMI 61 trial, treatment with a twice-daily, 10-mg dose of lorcaserin for a median of 3.3 years was associated with a significant 19% reduction in the risk of incident T2DM in participants with prediabetes, compared with placebo (8.5% vs. 10.3%; hazard ratio, 0.81; 95% confidence interval, 0.66-0.99; P = .038). The reduction in the risk of incident T2DM was even greater (23%) in people without diabetes at baseline (6.7% lorcaserin vs. 8.4% placebo; HR, 0.77; 95% CI, 0.63-0.94; P = .012).

Furthermore, in patients with T2DM who had a mean baseline glycated hemoglobin (HbA1c) of 7%, an absolute 0.33% reduction was seen at 1 year between the lorcaserin and placebo groups, with more modest but still significant between-group reductions (–0.09% and –0.08%) in individuals with prediabetes or normoglycemia (all P less than .0001). When baseline HbA1c levels were higher in patients with T2DM (8%), greater net reductions (0.52%) versus placebo were seen (P less than .0001).

These were some of the metabolic findings, published online in the Lancet to coincide with their presentation at the annual meeting of the European Association for the Study of Diabetes, that add to those already released from the CAMELLIA-TIMI 61 trial on cardiovascular safety, lead author and TIMI (Thrombolysis in Myocardial Infarction) group investigator Erin A. Bohula May, MD, observed during a press conference.

The cardiovascular safety data were presented at the 2018 annual congress of the European Society for Cardiology in August and published in the New England Journal of Medicine. These showed no increase with lorcaserin versus placebo in the risk of achieving a major cardiovascular endpoint (MACE) of cardiovascular death, MI, or stroke (HR, 0.99; 95% CI, 0.85-1.14; P less than .001 for noninferiority). There was also no difference between groups in the cumulative incidence of MACE+, which included heart failure, hospitalization for unstable angina, and the need for coronary revascularization (HR, 0.97; 95% CI, 0.87-1.07; P = .55 for superiority).

“We know that weight loss can improve cardiovascular and glycemic risk factors, but it’s difficult to achieve and maintain, and weight-loss agents are guideline-recommended adjuncts to lifestyle modification,” said Dr. Bohula May, who is a cardiovascular medicine and critical care specialist at Brigham and Women’s Hospital in Boston.

“However, prior to this study no agent had convincingly demonstrated cardiovascular safety in a rigorous clinical outcomes study,” she said, noting that several agents, such as the now-withdrawn rimonabant (Acomplia/Zimulti) and sibutramine (Meridia), had been shown to precipitate cardiovascular or psychiatric events, which led the Food and Drug Administration to mandate that all weight-loss drugs be assessed for cardiovascular safety. Lorcaserin (Belviq) is a centrally acting 5-HT2C agonist that works by decreasing appetite and was approved by the FDA in 2012 but is not currently available in Europe.

Long-term data on the effects of weight-loss agents on glycemic parameters were limited, hence the remit of the CAMELLIA-TIMI 61 trial was to assess both the cardiovascular and metabolic safety of lorcaserin. The drug was used on a background of lifestyle modification in 6,000 obese or overweight individuals at high risk of cardiovascular events. A further 6,000 individuals received placebo.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  04:14 ب.ظ

Testosterone Decanoate Powder

Testosterone Decanoate Mechanism of action
Testosterone Decanoate will cause an increase in IGF-1 levels, Red Blood Cell count. Testosterone Decanoate is subject to aromatization as well as 5alpha-reduction, which are the pathways through which testosterone is converted to estrogen and dihydrotestosterone respectively.Tadalafil powder

Testosterone Decanoate (active half-life 12-14 days)
Testosterone Decanoate is well-known as part of the very popular form of testosterone known as sustanon. It is ideal for TRT or HRT users as well as to be stacked with a much longer ester steroid like deca durabolin for less frequent injection schedules. Decanoate can be injected once a week and maintain stable test levels. A 100mg Decanoate shot yields approximately 62 mg of actual testosterone.

Dosages and Uses

Testo sterone can be dosed from little as 100mg per week for therapeutic use, to as much as 1,000mg per week for hardcore bodybuilders looking for the ultimate stack. Some professional bodybuilders have been reported as using as much as 2,000mg of testo sterone per week.

Most bodybuilders whom are just beginning to dabble with testo sterone will opt for doing a testo sterone-only cycle as their very first run. Dosages of 500mg per week are enough to put on considerable mass and size on any bodybuilder who is training hard and eating properly during their cycle.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  03:22 ب.ظ

Testosterone Decanoate Powder

We supply Testosterone decanoate is a steroid hormone from the androgen and is found in mammals and other vertebrates, testosterone decanoate is primarily secreted in the tests of mails and the ovaries of female, testosterone decanoate is the principle male sex hormone and an anabolic steroid.Testosterone Decanoate powder

Detail Information:
Neotest 250 was a veterinarian grade product manufactured by Loeffler out of Mexico. Loeffler is one of the well-known companies that felt a brunt of the blow during the DEA’s Operation Gear Grinder, which would lead to the end of the Neotest 250 product. From this time, Testosterone Decanoate has typically only been found in testosterone blends. You may find an underground lab that manufactures a Testosterone Decanoate product and you may even find one who now uses the Neotest 250 name, but it is unlikely and is not the original. With the right lab, long-term customers may even be able to have a lab specially manufacture the compound for them, but there is really no need due to Testosterone Cypionate and Testosterone Enanthate being so readily available. For your single large ester testosterone compound needs, both of those aforementioned compounds will get the job done.

As a testosterone hormone, Neotest 250 could be used to treat a low testosterone condition. Although a synthetic version of the primary male androgen, once in the body the body will make no distinguishing difference. However, Testosterone Decanoate is not a prescribed testosterone for this purpose with certain testosterone blends being the exception. Both Sustanon 250 and Omnadren carry the Decanoate ester, and in both cases, both compounds were developed for testosterone replacement therapy. Originally, Omnadren carried the Caproate ester, but Testosterone Decanoate has since replaced it.

Modern Day Omnadren And Sustanon 250 Are Both Mixed As Follows In A Single 1ml Ampule Giving A Total 250mg Dose:
30mg Testosterone Propionate
60mg Testosterone Phenylpropionate
60mg Testosterone Isocaproate
100mg Testosterone Decanoate
Despite Testosterone Decanoate appearing in testosterone blends designed for testosterone replacement therapy the Neotest 250 compound was primarily used for performance enhancement purposes. Although a veterinarian grade compound, the very reason it came under DEA fire was due to who the company was pushing it to. Despite it no longer existing, the functions and traits of Neotest 250 represent the primary functions and traits desired by all performance enhancing athletes.

Effects Of Neotest 250:
By understanding the functions and traits of Neotest 250 we have already begun to grasp a good understanding of the compound. However, we want to look at the effects of Neotest 250 in a more practical manner so that you know what to expect.
For the low testosterone patient, the effects of Neotest 250 are fairly straightforward. You suffer from low testosterone, your body is no longer producing enough of this essential hormone and that can occur for a number of reasons.

  • آخرین ویرایش:یکشنبه 27 مرداد 1398
یکشنبه 27 مرداد 1398  03:15 ب.ظ

Testosterone Undecanoate Powder

Testosterone undecanoate capsules, prescription drugs, are exogenous androgen drug preparations and are oral natural testosterone that can be stored for three years at room temperature.testosterone undecanoate powder
Testosterone is the androgen secreted by the male testicles and is the most important substance that determines the characteristics of males. Once the secretion is below normal levels, it will have an impact on the psychology and physiology of males. Studies have shown that after reaching the age of 40, men's testosterone levels gradually decline, triggering the above series of characterization, medically known as delayed hypogonadism (LOH), according to statistics, currently nearly 40 percent of Chinese 40-year-old All of the above men suffer from LOH. Testosterone supplementation therapy is a safe and effective treatment for this disease. It is supplemented by the use of exogenous androgenic drug preparations, Antel®, to relieve physiological changes and clinical symptoms caused by partial testosterone deficiency.
At present, testosterone undecanoate capsules have been used by the International Association of Male Science (ISA), the International Society of Older Men (ISSAM), the European Society of Urology (EAU), the European Academy of Urology (EAA) and the American College of Male Science (ASA). The joint recommendation is for the treatment of male late onset hypogonadism (LOH).

Testosterone Undecanoate Powder Dosage
Orally, it must be used under the guidance of a specialist. The starting dose is 120-160 mg daily, and the dose of 40-120 mg daily is maintained after two weeks of administration. Two times sooner or later, after meals, oral administration, if the daily capsules taken into the singular, you can take more than 1 capsule in the morning, or as directed.
In general, the dosage should be adjusted or prescribed according to each patient's response to the drug. The usual starting dose is 120-160 mg daily for 2-3 weeks, followed by a maintenance dose of 40-120 mg daily.
This product should be taken at meal time. If necessary, a small amount of water can be swallowed. The entire capsule must be swallowed and cannot be crunched. The daily dose can be divided into two equal portions, one serving in the morning and one serving in the evening.

Testosterone Undecanoate Powder Warning
a.Puberty and preadolescent boys should be careful to use androgen to avoid premature osteoporosis and precocious puberty.
b.Patients with occult or dominant heart failure, renal insufficiency, hypertension, epilepsy, migraine (or a history of the above) should be checked regularly because androgens may occasionally induce fluid retention.
c.It is recommended that patients undergo long-term treatment for liver function tests.
d.Use caution in patients with liver damage.
e.In male patients with benign prostatic hyperplasia, complaints related to prostate disorders may increase.
f.Hypercalcemia and hyperuricemia may be aggravated in patients with bone metastases. It is recommended that these patients regularly monitor serum concentratioAns.
g.All patients should undergo a detailed physical examination to rule out the possibility of prostate cancer before starting treatment with this product.
Since testosterone may promote the growth of subclinical prostate cancer, the prostate must be examined every year during the course of treatment according to the doctor's recommended protocol (rectal rectal examination and PSA assessment), elderly patients and high-risk groups (patients with clinical or family genetic factors) Should be checked twice a year.

It has been reported that the use of testosterone esters may cause sleep apnea in some men, particularly those with risk factors such as obesity or chronic lung disease.
If androgen-related adverse reactions occur, the drug should be discontinued immediately. After the symptoms disappear, take a lower dose.
Athletes please note that the ingredients contained in this product may make the test of stimulants positive.So far, this product has not been found to have an impact on the ability to drive and operate the machine.
Please keep out of reach of children.
Do not use expired.
This product contains sunset yellow and may cause allergic reactions

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