TLB150Benzoate;TLB-150,RAD-150;Benzonitrile,4-[[(1R,2S)-2-(benzoyloxy)-1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]propyl]amino]-2-chloro-3-methyl-;RAD140replacementTLBChemicalbook150benzoatepowder;TLB150;TestoloneAcetate;RAD-140Acetate;(1R,2S)-1-(3-Chloro-4-cyano-2-methylphenylamino)-1-(5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl)propan-2-ylbenzoate

RAD140;RAD140Whitepowder99%;Testolone;OralSARMSMuscleBuildingRad140/TestoloneForIncreasingMuscleMass;LowestpriceofRAD140CASNO.1182367-47-0;2-Chloro-Chemicalbook4-[[(1R,2S)-1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl]amino]-3-methylbenzonitrile;SARMRAD-140Powderwhnohe_carolin(at)163.com;CS-2554

YK11 can inhibit myostatin production in muscles by attaching androgen receptors. It may induce muscles to produce more folliclestatin, which in turn limits myostatin levels, allowing for increased muscle growth beyond genetic ability. YK-11 inhibits myostatistatin (MyostatiChemicalbookn), which means that

ACP-105;ACP105;ACP105;APC-105;Benzonitrile,2-chloro-4-[(3-endo)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methyl-;PharmaceuticalGradeAChemicalbookCP-105;HotSellingACP105;PharmaceuticalChemicalACP105;2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]octan-8-yl]-3-methylbenzonitrile

Myocardial infarction is one of the most deadly cardiovascular diseases. Myocardial infarction is caused by coronary artery stenosis or spasm, resulting in acute or persistent ischemia and hypoxia of the heart muscle, and cardiac cell death. Several pro-inflammatory cytokines such as interleukin-1β (IL-1β)

SR9009 has a lethal effect on cancer cells and oncogene-induced senescent cells, including melanocyte nevus, but has no effect on the viability of normal cells and tissues. SR9009 regulates autophagy and lipid regeneration, which plays a key role in inducing apoptotic responses in malignant cells. Treatment of

Ligandrol (LGD-4033, VK-5211) is a novel, non-steroidal, orally selective androgen receptor regulator with high affinity (Kd of about 1 nM) and high selectivity for androgen receptors.

Sarmspowder;S-23Sarms;S-23/S23,CASNO1010396-29-8NewSarmsPowdermuslcebuilding;S23S23S-23;(S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide;S-23;(S)Chemicalbook-3-(4-Chloro-3-fluorophenoxy)-N-(4-cyano-3-trifluoromethylphenyl)-2-hydroxy-2-methylpropionamide;(2S)-3-(4-Chloro-3-fluorophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2-hydroxy-2-methylpropanamide

In vivo,Andarine has potent anabolic activity and stimulates the growth of the prostate, seminal vesicle, and levator anal muscle with ED50 of 0.43mg/day,0.55mg/day, and 0.14mg/day, respectively, in a dose-dependent manner. In addition,Andarine acts on FSH, has no effect on some physiological changes caused

Ostarine binds to the androgen receptor (AR) and has the highest affinity for SARMs with a Ki value of 3.8nM. Ostarine acted on CV-1 cells cotransfected with human AR expression vector, luciferase reporter vector and β-galactosidase control vector when the concentration of Chemicalbook10nM to regulate AR

Ibumolan mesylate has been shown to increase the release and produce sustained increases in plasma levels of several hormones including gh and insulin-like growth factor 1(igf-1), but does not affect cortisol levels. Potential treatments are currently being developed to reduce the levels of these stimulants, such

N-[(R)-[(1,2-Dihydro-1-methanesulfonylspiro[3H-indoole-3,4'-piperidin]-1'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-[(1,1-dimethyl-ethoxy)carbonyl]amino-2-methyl-propanamide;Carbamicacid,N-[2-[[(1R)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3H-indole-3,4'-piperidin]-1'-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]amino]-1,1-dimethyl-2-oxoethyl]-,1,1-dimethylethylesteChemicalbookr;TC6N;Tc6nPowder;tert-butyl(R)-(1-((3-(benzyloxy)-1-(1-(methylsulfonyl)spiro[indoline-3,4'-piperidin]-1'-yl)-1-oxopropan-2-yl)amino)-2-methyl-1-oxopropan-2-yl)carbamate;-[(R)-[(1,2-Dihydro-1-methanesulfonylspiro[3H-indole-3,4'-piperidin]-1'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-[(1,1-dimethyl-ethoxy)carbonyl]amino-2-methyl-propanamide;ibutamoren(NewMK-677)

GW501516isshowntobethemostpotentandselectivePPARαagonistsknownwithanEC50of1.1nMagainstPPARαand1000-foldselectivityovertheotherhumansubtypes,PPARαand-γ.GW501516exerChemicalbooktsanti-inflammatoryeffectsinmouseculturedproximaltubular(mProx)cells.GW501516inhibitspalmitate-andTNFα-inducedincreasesinMCP-1mRNAexpressioninadose-dependentmanner.

GW0742 is a small molecule agonist of human peroxisome proliferator-activated receptor δ (PPARδ). It showed an EC50 of 1.1 nM for PPARδ, which is 100 times more selective than other human subtypes.

Sildenafil citrate is a selective 5-phosphodiesterase inhibitor, which enhances nitric oxide dependence and pulmonary vasodilation mediated by cyclic guanosine phosphate by inhibiting the breakdown of guanosine phosphate. In addition to the direct dilation of pulmonary blood vessels, it can also prevent or

Dihydroxyacetone is a naturally occurring ketose that is biodegradable, edible, and non-toxic to humans and the environment. It is a multifunctional additive that can be used in the cosmetics, pharmaceutical and food industries. dihydroxyacetone (DHA), chemically known as 1, 3-dihydroxy-2-acetone, is a

6.Pregabalin is a non-γ-aminobutyric acid (GABA) receptor agonist or antagonist. It is a new calcium channel regulator, which can block voltage-dependent calcium channels and reduce the release of neurotransmitters. Clinically, it is mainly used for neuralgia related to diabetic Chemicalbook peripheral neuropathy,

Methyl piperonyl epoxide propionate can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development process and pharmaceutical chemical production process.

Intermediates in organic synthesis. Production method: The anhydrous ethanol, which is co-steamed with diethyl phthalate and sodium metal, is added to the mixture of diethyl malonate, carbon tetrachloride and magnesium. The reaction is heated to start, and the temperature is controlled to smooth the reaction.

2-methyl-3-phenyl epoxy-ethane-2-carboxylic acid can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development process and pharmaceutical chemical production process.