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: 210821-63-9 Org12962 HCl hydrochloride Org-12962 CBNumber: CB02473321 Chemical Name: Org 12962 HCl Molecular Formula: C10H11ClF3N3.ClH Formula Weight: 302.126 CAS No.: 210821-63-9 ORG-12962 is a pyridinylpiperazine drug developed by Organon, which acts as a potent and selective agonist for the 5-HT2 receptor family, with highest affinity at 5-HT2C and lowest at 5-HT2B subtypes. It was developed as a potential anti-anxiety drug, but was discontinued from human trials after tests in a public speaking challenge showed that its anti-anxiety effects were accompanied by side effects such as dizziness and a "spacey" feeling, which were attributed to poor selectivity in vivo over the hallucinogenic 5-HT2A receptor.

English Name:GSMTX-4 CAS:1209500-46-8 Assay:98%+ Molecular weight:0 Molecular formula: / Appearance: White powder Remarks: Only for research, not for human Packing specifications (powder): 1g, 10g, 100g,1kg Storage conditions: -20°C GsMTx4 is a spider venom peptide that selectively inhibits cationic mechanosensitive channels (MSCs) such as TRPC1 and TRPC6 and Piezo channels. GsMTx4 blocks stretch-activated cation channels in astrocytes, cardiac cells, and smooth and skeletal muscle cells. GsMTx4 also inhibits TACAN, a mechanosensitive ion channel involved in the pain response. GsMTx4 decreases the leptin-induced AMPK and MLC-2 phosphorylation in breast epithelial cells. GsMTx4 is neuroprotective and inhibits lysophosphatidylcholine-induced astrocyte toxicity in vivo in mice. GsMTx4 suppresses neurogenesis and enhances astrogenesis in human neural stem cells. GsMTx4 (GsMTx-4, M-theraphotoxin-Gr1a) has been isolated from the venom of the spider Grammostola rosea. This cationic hydrophobic polypeptide blocks selectively the gating of cation selective channels and mechanosensitive ion channels such as TRPC1 or TRPC6, without having any effect on whole-cell voltage-sensitive currents. This toxin acts by perturbing the interface between the channel and the lipid bilayer without necessarily being in physical contact with the channel. GsMTx4 also demonstrated to active TRPA1 channel at 1µM concentration and to inhibit Piezo1 currents.

cas: 95958-84-2 Etonitazepyne Protonitazene FIubromazepam BUTONITAZENE Butoxynitazene CBNumber: CB59001825 Chemical Name: 1H-Benzimidazole-1-ethanamine, N,N-diethyl-5-nitro-2-[(4-propoxyphenyl)methyl]- Molecular Formula: C23H30N4O3 Formula Weight: 410.51 CAS No.: 95958-84-2