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Cannabidiol (CBD) is a chemical in the Cannabis sativa plant, also known as cannabis or hemp. One specific form of CBD is approved as a drug in the U.S. for seizures. Over 80 chemicals, known as cannabinoids, have been found in the Cannabis sativa plant. Delta-9-tetrahydrocannabinol (THC) is the most famous ingredient in cannabis. But CBD is obtained from hemp, a form of the Cannabis sativa plant that only contains small amounts of THC. CBD seems to have effects on some chemicals in the brain, but these are different than the effects of THC. Cannabidiol is a popular natural remedy used for many common ailments. Better known as CBD, it is one of more than 100 chemical compounds called cannabinoids that are found in the cannabis plant, Cannabis sativa (1Trusted Source). Tetrahydrocannabinol (THC) is the main psychoactive cannabinoid found in cannabis, which means it causes the sensation of getting high that’s often associated with cannabis. However, unlike THC, CBD is not psychoactive. This quality makes CBD an appealing option for those who are looking for relief from pain and other symptoms without the mind-altering effects of cannabis or other side effects related to some pharmaceutical drugs. CBD oil is made by extracting CBD from the cannabis plant and then diluting it with a carrier oil like coconut oil or hemp seed oil. CBD can be found in a variety of products online and in stores, including dietary supplements, bath soaks, drinks, and food. It continues to gain momentum in the health and wellness world, with some scientific studies finding that it may ease symptoms of conditions such as chronic pain and anxiety. But is it the right choice for you? This article covers 6 evidence-backed health benefits of CBD, as well as potential side effects and safety concerns related to CBD products.

cas: 29462-18-8 Bentazepam CBNumber: CB11178093 Chemical Name: Bentazepam Molecular Formula: C17H16N2OS Formula Weight: 296.39 CAS No.: 29462-18-8

CAS 317318-70-0 SARMS Raw Powder GW-501516 GW-501516 Muscle Building Endurobol Oral Steroids Cardarine Sarms Raw Powders Cardarine GW 501516 CAS 317318-70-0 Muscle Building Endurobol GW501516 is a selective agonist (activator) of the PPARδ receptor. It displays high affinity (Ki = 1 nM) and potency (EC50 = 1 nM) for PPARδ with > 1000 fold selectivity over PPARα and PPARγ. It activates the same pathways activated through exercise, including PPARδ and AMP-activated protein kinase. It had been investigated as a potential treatment for obesity, diabetes, dyslipidemia and cardiovascular disease. GW501516 has a synergistic effect when combined with AICAR: the combination has been shown to significantly increase exercise endurance in animal studies more than either compound alone. Product Name GW501516 Synonyms: Cardarine;2-[2-Methyl-4-[[[4-methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]methyl]thio]phenoxy]acetic Acid;Methyl-methyl-trifluoromethylphenyl -thiazolyl-methylsulfanyl-phenoxy-aceticAcid;2-(4-((2-(4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methylthio)-2-methylphenoxy)acetic acid;GSK-516 CAS Number 317318-70-0 Molecular Formula C21H18F3NO3S2 Molecular Weight 453.5 Assay 99%min HPLC Appearance White fine powder GW501516 Function: 1. GW-501516 & Liver Damage In contrast to popular belief, GW501516 doesn’t promote damage of liver cells. The chemical has actually been known to promote healthy liver function and faster healing properties to the skin and muscle tissue. In essence, you will not heal rapidly like Wolverine from the X Men movies, but you will shorten the your recovery time from scratches, blisters, and injured muscles by a significant amount. 2. GW-501516 & Cancer There has been many forum comments expressing the concerns of GW501516 and it’s relationship to cancer and tumor development. Since 2004 many experiments have been done to prove this hypothesis, but so far, all of them have been largely unsuccessful. Cardarine Dosage The half life of cardarine is 20-24 hours. This means that once a day dose is totally fine. Some athletes like to use all the 20 mg an hour before their workout session, and others will split the dose in half in the AM and PM. Cardarine Application: 1. Endurance: It is recommended stacking cardarine with AICAR and/or Equipoise. This is the ultimate endurance stack that will turn you into a race horse. 2. Fat loss: The best shredder stack would be stacking cardarine with S4 (Andarine). This is a well known potent ‘cutting’ stack. 3. Anabolic steroid stack: If you run moderate doses of anabolic steroids, or you run any harsh compound like trenbolone, then cardarine will aid in not only your lipids, but also with your ability to ‘catch your wind.’ Therefore, cardarine is a perfect stack for trenbolone, which makes many athletes lose their breath fast. 4. During PCT (post cycle therapy) or bridge: Since cardarine is not hormonal, it is in no way suppressive. Hence, you should not be scared of using it to keep fat off and improve your workouts between cycles during your bridge and PCT. 5. SARMs triple stack: If you want aato recomp, cardarine stacks beautifully with S4 and MK-2866. More Product Product name CASNo. Specification Ostarine(MK2866) 841205-47-8/1235370-13-4/1202044-20-9 99%min LGD-4033 1165910-22-4 98%min MK-677 159633-92-8 98%min Andarine(S-4) 401900-40-17 98%min GW 501516 317318-70-0 98%min AICAR 2627-69-2 98%min RAD140 1182367-47-0 98%min SR9009 1379686-30-2 98%min YK11 1370003-76-1 98%min

cas: 159634-47-6 MK677 MK-677 Ibutamoren mesylate CBNumber: CB31178916 Chemical Name: Ibutamoren Molecular Formula: C27H36N4O5S Formula Weight: 528.66 CAS No.: 159634-47-6

cas: 159752-10-0 Increase Muscle MK677 MK-677 Capsules Ibutamoren Steroids Bulk Supply Sarms MK677 ibutamoren Capsule for Bodybuilding Cas159752-10-0 What is Ibutamoren MK677? Ibutamoren, also known as MK 677,is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. Studies have shown that this drug is highly potential in increasing bone turnover. When given to elderly subjects, It growth hormone secretagogue was seen to be efficiently improving the condition of bone turnover in them, based on elevations of biochemical markers of bone formation and resorption in them. All this was observed when this peptide was given to them orally. Product Name MK 677 Synonyms: MK677 Selective Androgen Receptor Modulators SARMs Bodybuilding CAS 159752-10-0;(R)-1'-(2-Methylalanyl-O-benzyl-D-seryl)-1-(Methylsulfonyl)-1,2-dihydrospiro[indole-3,4'-piperidine] Mesylate;Crescendo;IbutaMoren Mesylate(MK-677);MK-667;N-[1(R)-1,2-Dihydro-1-methanesulfonylspiro-3H-indole-3,4′-piperidin)-1′-yl]carbonyl-2-(phenylmethoxy)-ethyl-2-amino-2-methylpropanamide methanesulfonate;IBUTAMORIN;Ibutamoren mesylate, ≥98% CAS No 159752-10-0 Molecular Formula C27H36N4O5S.CH4O3S Molecular Weight 624.776 EINECS Number 1308068-626-2 Assay 99.5% Appearance White powder Ibutamoren and Growth Hormone: Ibutamoren is a strong and long-acting selective ghrelin receptor agonist . Ghrelin receptors – GHSRs (Growth hormone secretagogue receptors) naturally trigger the production of endogenous growth hormone . Ibutamoren stimulates the production of growth hormone essentially by mimicking the function and activity of another endogenous hormone – ghrelin: The action and binding of Ibutamorene MK-677 to Ghrelin receptors first results in the release GHRH (Growth-hormone-releasing hormone) from neurons in the Nucleus arcuatus (infundibular nucleus of the Hypothalamus), which is then transmitted by the hypothalamic-pituitary portal system to the anterior Pituitary, where by acting on GHRHR (Growth hormone-releasing hormone receptor (GHRH receptors)) stimulates the resulting growth hormone secretion pituitary gland. Ibutamoren– Benefits and Effects: Ibutamoren MK-677 strongly supports the growth of muscle mass and anabolic state of the body (helps maintain a positive nitrogen balance) Ibutamoren MK-677 has a strong anti-catabolic effect, effectively protects muscle mass from degradation Ibutamoren MK-677 improves performance and condition Ibutamoren MK-677 speeds up fat metabolism – helps burn excess body fat and prevent its re-storage Ibutamoren MK-677 brings very good and faster regeneration of muscles and the whole body, helps to heal old wounds and injuries Ibutamoren MK-677 significantly improves sleep quality at night, brings a very strong feeling of freshness, energy and vitality in the morning and during the day Ibutamoren MK-677 leads to a significant improvement in the condition and quality of the skin, helps to smooth out wrinkles Ibutamoren MK-677 has a strong anti-aging effect, rejuvenates the body, acts against aging MK677 Dosage: Optimal dose of Ibutamoren is 25-50 mg daily (1-2 tablets), max. 75 mg (max. 3 tablets a day, higher doses no longer represent a significant or linear increase in effects, but on the contrary – they can bring side effects). The usual period of use is 12 weeks. However, even with a long-term daily use of Ibutamoren No significant or dangerous side effects have been reported in medical studies for 12 or up to 24 months.

Cas: 431579-34-9 YK11 YK-11 CBNumber: CB42756194 Chemical Name: YK11 Molecular Formula: C25H34O6 Formula Weight: 430.53386 CAS No.: 431579-34-9 YK11 is short for (17-alpha,20E) 17,20-[(1-methoxyethylidene)bis(oxy)] 3-oxo-19-norpregna-4,20-diene 21-carboxylic acid methyl ester. YK11 shows a lot of promise as an apt anabolic SARM. With the muscle growth potential it brings, it’s as effective as anabolic steroids and prohormones without the unwanted side effects connected to the latter. YK11 is a powerful SARM supplement promoting massive lean muscle gains which is a great benefit for those wanting to have an aesthetic and shredded physique.

CAS 1370003-76-1 YK11 YK-11 SARMS Raw PowderCapsule Hallucinate For Reduce Fat For Muscle Gainning Bodybuilding Muscle Building Best Price Bodybuilding muscles Sarms YK11 Powder Cas1370003-76-1 YK11 attaches itself to the AR (androgen receptor), but only inducts methods that lead to the traditional side effects of androgens such as growth of body hair and prostate and enhanced aggression – to a restricted degree. Most SARMS have quite limited androgenic side effects, but frequently only quite few anabolic effects when likened . Kanno tested C2C12 muscle cells and not lab animals or humans. It has been discovered that muscle cells produce more anabolic factors if exposed to 500 nmol (nanomoles) YK11 than if you expose the same muscle cells to 500 nmol DHT. YK11 induces muscle cells to make more follistatin (more than DHT does) – a strong myostatin inhibitor. YK11 works through the androgen receptor,with that said, YK11 can be as good as in terms of muscle Product Name YK11 Other Name YK-11 Purity 98%min CAS No. 1370003-76-1 M.W. 624.776 M.F. C27H36N4O5S.CH4O3S Appearance White powder The dosage of YK-11: 10 mg per day is a good start, and it is recommended to use the dosage separately, that is, take 5 mg in the morning and 5 mg in the evening. This SARM has a short half-life, so take it twice a day for best results. Of course, I have seen someone use the highest dose of 25 mg per day, and he also has a significant improvement in muscle mass. Weeks 1~4: 5 mg in the morning and 5 mg in the evening. Weeks 5-8: Increase the daily dose to 15mg, 5mg in the morning, 5mg for pre-exercise, and 5mg at night. Week 8-12 (optional): Increase the dose again to 20 mg per day. Take 5 mg in the morning, 10 mg before exercise, and 5 mg in the evening. Is YK-11 suitable for muscle gain (bulking) or fat loss (cutting)? One of the reasons why this SARM is popular is that it is very versatile and can be used for both purposes, but it is recommended to use a lower dose during fat loss, because your goal is to keep as much as possible while reducing fat. More muscle mass. If you are gaining muscle, you can evaluate your tolerance. If you feel comfortable, you can increase it to 20 mg per day. At the same time, many users also like to use it in combination with LGD 4033

cas: 1228078-65-6 PAR-4 Agonist Peptide,amide Chemical Name: PAR-4 Agonist Peptide, amide TFA Molecular Formula: C36H49F3N8O9 Formula Weight: 794.83 CAS No.: 1228078-65-6

cas: 352017-71-1 AY-NH2 PAR-4 Agonist Peptide,amide Chemical Name: H-ALA-TYR-PRO-GLY-LYS-PHE-NH2 Molecular Formula: C34H48N8O7 Formula Weight: 680.79 CAS No.: 352017-71-1

cas: 129186-29-4 gidazepam factory lab laboratory manufacturer supplier wholesale CBNumber: CB41364172 Chemical Name: gidazepam factory lab laboratory manufacturer supplier wholesale Molecular Formula: C17H15BrN4O2 Formula Weight: 387.236 CAS No.: 129186-29-4

cas: 197250-15-0 GAP26 Gap-26 Molecular Formula: C70H107N19O19S Formula Weight: 1550.78 CAS No.: 197250-15-0

cas: 115150-59-9 Antagonist G Molecular Formula: C49H66N12O6S Formula Weight: 951.19 CAS No.: 115150-59-9

cas: 110590-60-8 Laminin Nonapeptide Molecular Formula: C40H62N12O14S Formula Weight: 967.06 CAS No.: 110590-60-8 Laminin Nonapeptide, amide, contains an active cell-binding site, consisting of human Laminin beta1 residue 970 to 978. It has been shown to inhibit both angiogenesis and solid tumor growth.

cas: 1313730-19-6 TFLLR-NH2(TFA) CBNumber: CB94713833 Chemical Name: TFLLR-NH2(TFA) Molecular Formula: C33H54F3N9O8 Formula Weight: 761.85 CAS No.: 1313730-19-6

cas: 197794-83-5 TFLLR-NH2CBNumber: CB9464681 Chemical Name: TFLLR-NH2 Molecular Formula: C31H53N9O6 Formula Weight: 647.81 CAS No.: 197794-83-5

cas: 86408-36-8 polymyxin B nonapeptide CBNumber: CB4668435 Chemical Name: POLYMYXIN B NONAPEPTIDE HYDROCHLORIDE Molecular Formula: C43H74N14O11 Formula Weight: 963.13 CAS No.: 86408-36-8

cas: 5746-86-1 (±)-Nornicotine s-nornicotine CBNumber: CB4385206 Chemical Name: 3-(2-Pyrrolidinyl)pyridine Molecular Formula: C9H12N2 Formula Weight: 148.21 CAS No.: 5746-86-1 Nornicotine is an alkaloid found in various plants including Nicotiana, the tobacco plant. It is chemically similar to nicotine, but does not contain a methyl group. It is a precursor to the carcinogen N-nitrosonornicotine that is produced during the curing and processing of tobacco. Nornicotine can react in human saliva to form N-nitrosonornicotine, a known type 1 carcinogen Nornicotine is a secondary tobacco alkaloid that is produced by the N-demethylation of nicotine. Nornicotine production and accumulation in tobacco are undesirable because nornicotine serves as the precursor in the synthesis of the well characterized carcinogen N′-nitrosonornicotine during the curing and processing of tobacco. Although nornicotine is typically a minor alkaloid in tobacco plants, in many tobacco populations a high percentage of individuals can be found that convert a substantial proportion of the nicotine to nornicotine during leaf senescence and curing. We used a microarray-based strategy to identify genes that are differentially regulated between closely related tobacco lines that accumulate either nicotine (nonconverters) or nornicotine (converters) as the predominant alkaloid in the cured leaf. These experiments led to the identification of a small number of closely related cytochrome P450 genes, designated the CYP82E2 family, whose collective transcript levels were consistently higher in converter versus nonconverter tobacco lines. RNA interference-induced silencing of the CYP82E2 gene family suppressed the synthesis of nornicotine in strong converter plants to levels similar to that observed in nonconverter individuals. Although each of the six identified members of the P450 family share >90% nucleotide sequence identity, sense expression of three selected isoforms revealed that only one (CYP82E4v1) was involved in the conversion of nicotine to nornicotine. Yeast expression analysis revealed that CYP82E4v1 functions as a nicotine demethylase.