LGD-3303
CAS: 917891-35-1
Kemijsko ime: 9-kloro-2-etil-1-metil-3-(2,2,2-trifluoroetil)-6H-pirolo[3,2-f]kinolin-7-on
Sopomenke: LGD-3303, UNII-7N4E1X2RJM, 7N4E1X2RJM, 917891-35-1, SCHEMBL4130914, LGD3303, OMXGOGXEWUCLFI-UHFFFAOYSA-N, EX-A1672, LGD 3303, 1196133-39-7, 9-kloro-2-etil-1-metil-3-(2,2,2-trifluoroetil)-3h-pirolo(3,2-f)kinolin-7(6h)-eno, 9-kloro-2-etil-1-metil-3-(2,2,2-trifluoroetil)-6H-pirolo[3,2-f]kinolin-7-on, 7H-pirolo(3,2-F)kinolin-7-on, 9-kloro-2-etil-3,6-dihidro-1-metil-3-(2,2,2-trifluoroetil)- 9-kloro-2-etil-1-metil-3-(2,2,2-trifluoroetil)-3,6-dihidro-7H-pirolo[3,2-f]kinolin-7-on
Molekularna teža: 342.75
Kemijska formula: C16H14ClF3N2O
Videz: Off-White to Pale yellow fine powder
Shranjevanje: Hraniti pri sobni temperaturi, tesno zaprta, stran od vročine, svetloba in vlaga.
Topnost: PEG400, Etanol
Aplikacija: Selektivni modulator androgenih receptorjev( SARM)
LGD-3303 is a drug with a selective androgen receptor modulator (SARM) with good oral bioavailability. It is a selective agonist of androgen receptors that produces functional selectivity and is effective in isolating anabolic and androgenic effects, acting as an agonist of partial androgenic effects, but as a full agonist of anabolic effects. It has been studied as a possible treatment for osteoporosis and has been shown to improve the effectiveness of bisphosphonate drugs in animal studies.
Lgd3303 - Most anabolic SARMs powder? This video is about lgd3303. About lgd3303 is the growth hormone secretagogue Anamorelin, also known as lgd3033 instead of lgd3303, there has been a lot of confusion. After doing our own research and learning from our personal experience, we decided to make this video as detailed as possible about lgd3303. Lgd3303 is not Anamurin. This is the most effective SARM we have seen so far! We are happy to see what happens with more information, but from our experience we are impressed with the potential of muscle building.
LGD-3303 is a drug which acts as a selective androgen receptor modulator (SARM), 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.
