Description
LGD-3303 is a drug which acts as a selective androgen receptor modulator, with good oral bioavailability. It is a selective agonist for the androgen receptor, producing functional selectivity with effective dissociation of anabolic and androgenic effects, acting as a partial agonist for androgenic effects, but a full agonist for anabolic effects. It has been investigated as a possible treatment for osteoporosis, and was shown in animal studies to enhance the effectiveness of a bisphosphonate drug. Basic Info
| Chemical Name | LGD-3303 |
| Synonyms | 9-Chloro-2-ethyl-1-methyl-3-(2,2,2-trifluoroethyl)-3,6-dihydro-pyrrolo[3,2-f]quinolin-7-one |
| CAS No. | 917891-35-1 |
| Molecular Formula | C16H14ClF3N2O |
| Molecular Weight | 342.74300 |
| PSA | 37.79000 |
| LogP | 4.56930 |
Other SARMs
| Name | CAS NO. | Usage |
| AICAR | 2627-69-2 | acts by entering nucleoside pools, significantly increasing levels of adenosine
during periods of ATP breakdown |
| MK2866 | 841205-47-8 | medical prescription for prevention of cachexia, atrophy, and sarcopenia and
for Hormone or Testoserone Replacement Therapy. |
| MK-677 | 15972-10-0 | for the treatment of frailty in the elderly |
| LGD-4033 | 1165910-22-4 | pharmacological profile similar to that of enobosarm, Ostarine,MK-2866 |
| GW1516 | 317318-70-0 | For obesity, diabetes, dyslipidemia and cardiovascular disease |
| Andarine(S4) | 401900-40-0 | partial agonist, intended mainly for treatment of benign prostatic hypertrophy |
| SR9009 | 1379686-30-2 | under development at The Scripps Research Institute (TSRI),
increases the level of metabolic activity in skeletal muscles of mice |
| RAD140 | 1182367-47-0 | New generation for gaining mass and cutting edges |
| YK11 | 431579-34-9 | YK11: a SARM and myostatin inhibitor in one
|
| AC262356 | 870888-46-3 | New SARMS |
| SR9011 | 1379686-29-9 | New SARMS |
| S23 | 1010396-29-8 | New SARMS |
| GW0724 | 317318-84-6 | New SARMS |
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Product Categories : API Powder > N Isopropylbenzylamine
