FPTQ B

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

FPTQ 是一种有效的 mGluR1 拮抗剂，抑制人和鼠的 IC50 值分别为 6 nM 和 1.4 nM。FPTQ 具有抗氧化、抗炎作用。

FPTQ is potent mGluR1 antagonist with IC50 values of 6 nM and 1.4 nM for human and mouse mGluR1 respectively. FPTQ has anti-oxidant and anti-inflammatory effects in vitro and in vivo.

FPTQ (0.5-10 μM) does not shows any cytotoxicity was not observed at 0.5, 1, 5, and 10 μM in RAW264.7 macrophage cells.FPTQ (1-20 μM; 24 hours) reduces LPS-induced NO production at > 1 μM FPTQ, and at 10 μM, FPTQ treatment causes a 31% anti-oxidant effect in RAW264.7 macrophage cells.FPTQ (1-20 μM; 24 hours) dramaticly decreases LPS-induced expression levels of IL-1β and Il-6. At a concentration of 10 μM, FPTQ causes a 27% and 44% reduction in the mRNA expression of IL-1β and Il-6, respectively in RAW264.7 macrophage cells.RT-PCR Cell Line:RAW264.7 macrophage cells Concentration:1, 10, or 20 μM Incubation Time:24 hours Result:Decreased IL-1β and IL-6 mRNA expression

FPTQ (5-20 μM) decreases the number of neutrophils migrating to the amputation site in zebrafish larvae by tail amputation. In the tailfin wound method, the number of neutrophils collecting at the wound site also decreases in a dose-dependent manner in zebrafish.In a LPS-induced inflammation zebrafish model, LPS solution is injected into the yolks of Tg(mpx:EGFP)i114 zebrafish larvae and exposed the zebrafish larvae immediately to FPTQ treatment.FPTQ (20 μM; 4 hours) significantly decreases the fluorescent neutrophils after yolk injection and has an anti-inflammatory effect during the early phase of inflammation.

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Neuroscience

GluR

GluR

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864863-72-9

305.31

C17H12FN5

>98% (HPLC)

In Vitro:?DMSO 中的溶解度 : 33.33 mg/mL (109.17 mM; 超声助溶 )

Cc1c(nnn1-c1cccnc1F)-c1ccc2ncccc2c1

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(-20℃)

With Ice Pack

≥ 2 years