FASN-IN-5 (example 11), a FASN inhibitor, can be used for the research of TH17- or CSF1 -mediated disease or disorder such as cancer, immunological disorders, and obesity[1].
分子量
462.54
Formula
C29H26N4O2
CAS 号
1309805-49-9
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. David S. MILLAN, et al. Methods of using fasn inhibitors. WO2017189613A1.
FASN-IN-5 (example 11), a FASN inhibitor, can be used for the research of TH17- or CSF1 -mediated disease or disorder such as cancer, immunological disorders, and obesity[1].
分子量
462.54
Formula
C29H26N4O2
CAS 号
1309805-49-9
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. David S. MILLAN, et al. Methods of using fasn inhibitors. WO2017189613A1.
FASN-IN-5 (example 11), a FASN inhibitor, can be used for the research of TH17- or CSF1 -mediated disease or disorder such as cancer, immunological disorders, and obesity[1].
分子量
462.54
Formula
C29H26N4O2
CAS 号
1309805-49-9
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. David S. MILLAN, et al. Methods of using fasn inhibitors. WO2017189613A1.
FT113 is a potent and orally active fatty acid synthase (FASN) inhibitor, with an IC50 of 213 nM for full-length recombinant human FASN enzyme. In cell-based assay, FT113 blocks FASN activity in BT474 cells (IC50, 90 nM). FT113 shows anti-proliferative activity, and exhibits anti-cancer activity both in vitro and in vivo[1].
IC50 & Target
IC50: 213 nM (FASN), 90 nM (FASN, in BT474 cell)[1]
体外研究 (In Vitro)
FT113 shows anti-proliferative activity against PC3 and MV-411 cells with IC50s of 47 and 26 nM, respectively[1].
上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究 (In Vivo)
FT113 (5 mg/kg, p.o.) exhibits potent oral bioavailability of 95% and 84% in mice and rats, respectively[1]. FT113 (5, 25, or 50 mg/kg, p.o., twice daily for 16 days) increases malonyl-CoA concentration in tumors, inhibits tumor growth in a dose-dependent manner in mice[1].
上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Athymic nude mice bearing MV-411 cells[1]
Dosage:
5, 25, or 50 mg/kg
Administration:
P.O., twice daily for 16 days
Result:
Caused 32 % and 50% tumor growth inhibition at 25 and 50 mg/kg, respectively in mice.
分子量
409.41
Formula
C22H20FN3O4
CAS 号
1630808-89-7
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Martin MW, et al. Discovery and optimization of novel piperazines as potent inhibitors of fatty acid synthase (FASN). Bioorg Med Chem Lett. 2019 Apr 15;29(8):1001-1006.