SCR7 pyrazine

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

SCR7 是一种特异性 DNA 连接酶 IV 抑制剂，可阻断非同源末端连接 (NHEJ)。

SCR7 pyrazine is an inhibitor of nonhomologous end-joining (NHEJ), enhancing CRISPR-Cas9-mediated homology-directed repair (HDR) in vitro.

SCR7 pyrazine (20-100 μM; 24 hours; MCF7 cells) treatment interferes with NHEJ in cells, leading to accumulation of unrepaired double-strand breaks (DSBs).SCR7 pyrazine treatment shows a dose-dependent decrease in cell proliferation with IC50 values of 40 μM, 34 μM, 44 μM, 8.5 μM, 120 μM, 10 μM and 50 μM for MCF7, A549, HeLa, T47D, A2780, HT1080 and Nalm6 cells, respectively.In MCF7 cells, SCR7 pyrazine (20, 40 μM) treatment increases phosphorylation of ATM and activates p53, decreases MDM2, BCL2, resulting in activation of proapoptotic proteins, PUMA and BAX. And the shorter fragments of MCL1, PARP1, Caspase 3, and Caspase 9 cleavage are upregulated in a dose-dependent manner. Western Blot Analysis Cell Line:MCF7 cells Concentration:20 μM, 40 μM, 100 μM Incubation Time:24 hours Result:Showed an increase in levels of gH2AX foci and protein.

SCR7 pyrazine (10 mg/kg; intraperitoneal injection; six doses; BALB/c mice) treatment significantly reduces breast adenocarcinoma-induced tumor and increases lifespan. Animal Model:BALB/c mice injected with breast adenocarcinoma cells Dosage:10 mg/kg Administration:Intraperitoneal injection; on alternate days (0, 2, 4, 6, 8, and 10)Result:Significantly reduced breast adenocarcinoma-induced tumor and increased lifespan.

SCR7 pyrazine | SCR-7 pyrazine | SCR 7 pyrazine

Endocrinology/Hormones

CaMK

DNALigase IV

Cancer

——

14892-97-8

332.38

C18H12N4OS

>98% (HPLC)

In Vitro:?DMSO : 100 mg/mL (300.86 mM)

O=c1[nH]c(=S)[nH]c2c1nc(c1ccccc1)c(n2)c1ccccc1

2,3-Dihydro-6,7-diphenyl-2-thioxo-4(1H)-pteridinone

(-20℃)

With Ice Pack

≥ 2 years