BI-4924

BI-4924

B646378-5mg

5mg

≥99%

-20°C储存

超低温冰袋运输

BI-4924 is a lipophilic, highly plasma protein bound selective phosphoglycerate dehydrogenase ( PHGDH ) inhibitor ( IC 50 =3 nM) with excellent microsomal, as well as hepatocytic stability. Intracellular trapping of BI-4924 disrupts serine biosynthesis with an IC 50 of 2200 nM at 72 h In Vitro BI-4924 is a highly potent co-factor nicotinamide adenine dinucleotide (NADH/NAD + )-competitive PHGDH inhibitor. BI-4924 shows high selectivity against the majority of other dehydrogenase targets. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid IC50& Target:PHGDH

BI-4924 是一种亲脂性、与血浆蛋白高度结合的选择性磷酸甘油脱氢酶（PHGDH）抑制剂（IC 50 =3 nM），具有极佳的微粒体和肝细胞稳定性。BI-4924 的细胞内捕获作用可破坏丝氨酸的生物合成，并使丝氨酸在细胞内的浓度降低。

2244452-09-1

C21H20Cl2N2O6S

499.36 g/mol

O=C(O)CS(=O)(C1=CC=C([C@H](NC(C(N2C)=CC3=C2C=C(C)C(Cl)=C3Cl)=O)CO)C=C1)=O

DMSO : 125 mg/mL (250.32 mM; Need ultrasonic)