SRS11-92

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

SRS11-92 (SRS 11-92) 是一种 Ferroptosis 的小分子抑制剂，也是 Ferrostatin-1 (Fer-1) 的衍生物。

SRS11-92 (SRS 11-92) is a small molecule inhibitor of Ferroptosis and a derivative of Ferrostatin-1 (Fer-1), inhibits ferroptotic cell death induced by erastin in HT-1080 human fibrosarcoma cells with EC50 of 6 nM; inhibits iron-induced cell death in isolated mouse kidney proximal tubules at 2 uM, and fully protects rat oligodendrocytes from cystine deprivation-induced cell death in an in vitro model of periventricular leukomalacia when used at a concentration of 100 nM; also increases survival of medium spiny neurons in rat corticostriatal brain slices in an in vitro model of Huntington’s disease in a concentration-dependent manner.

SRS11-92 fully protects oligodendrocytes (OLs) from cystine deprivation when tested at 100 nM. SRS11-92 rescues primary human fibroblasts from death induced by frataxin knock-down.

SRS11-92, used at 500 nM, is efficacious in protecting human and mouse cellular models of Friedreich ataxia (FRDA)treatedwith ferricammoniumcitrate (FAC) andaninhibitorofglutathione synthesis (BSO), whereas caspase-3 inhibitors fail to show significant biological activity.

SRS 11-92

Apoptosis

Ferroptosis

Ferroptosis

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1467047-25-1

352.478

C22H28N2O2

>98% (HPLC)

In Vitro:?DMSO : 250 mg/mL (709.28 mM)

CCOC(=O)C1=CC(=C(C=C1)NC2CCCCC2)NCC3=CC=CC=C3

4-(cyclohexylamino)-3-[(phenylmethyl)amino]-benzoic acid, ethyl ester

(-20℃)

With Ice Pack

≥ 2 years