DT204

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

DT204 (DT-204) 是一种新型 SCFSkp2 抑制剂，可减少 Skp2 与 Cullin-1 和 Commd1 的结合，协同增强 BTZ 诱导的细胞凋亡。

DT204 (DT-204) is a novel SCFSkp2 inhibitor that reduces Skp2 binding to Cullin-1 and Commd1, synergistically enhances BTZ-induced apoptosis; stablizes and increases p27 levels, does not increase the level of p53, demonstrates potential synergy with CI values of 0.7, 0.8 and 0.7 for RPMI8226, U266 and MM1.S respectively combined with 1 nM BTZ, co-treatment induces apoptosis in cells resistant to the proteasome inhibitors BTZ, carfilzomib or ixazomib; overcomes drug resistance and reduces the in vivo growth of myeloma tumors in murine models.

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DT-204 | DT 204

Proteasome/Ubiquitin

E3 Ubiquitin Ligase

E3 Ubiquitin Ligase

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428497-71-6

482.729

C19H13BrClNO5S

>98% (HPLC)

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O=C(O)COC1=CC=C(Br)C=C1/C=C(SC(N2CC3=CC=C(Cl)C=C3)=O)/C2=O

2-(4-bromo-2-((3-(4-chlorobenzyl)-2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)acetic acid

(-20℃)

With Ice Pack

≥ 2 years