Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0489 |
Flutamide
SCH 13521,氟他胺 |
Androgen Receptor | Endocrinology/Hormones |
Flutamide (SCH 13521) 是一种抗雄激素化合物,在啮齿动物和犬科动物中的效力与环丙孕酮大致相同。 | |||
T7690 |
2-hydroxy Flutamide
|
Androgen Receptor | Endocrinology/Hormones |
2-hydroxy Flutamide 是 Flutamide 的活性代谢物,是雄激素受体拮抗剂,其 IC50值为700 nM。它可用于研究前列腺癌。 | |||
T0547 |
FlutaMide Related CoMpound B
|
Others | Others |
FlutaMide Related CoMpound B 用作医药中间体。 | |||
T69758 |
Flutamide-d7
|
||
Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo... | |||
T69757 |
PDDC inhibitor
|
||
PDDC is the first nSMase2 inhibitor that possesses both favorable pharmacodynamics and pharmacokinetic (PK) parameters, including substantial oral bioavailability, brain penetration, and significant inhibition of exosome release from the brain in vivo. |