| Description | BLT-1 is a scavenger receptor BI (SR-BI)inhibitor. |
| In vitro | BLT-1对ldlA[mSR-BI]细胞中DiI-HDL和[3H]CE-HDL的摄取具有IC50值分别为60 nM和110 nM[1]。BLT-1能够抑制mSR-BI-t1含有的脂质体在细胞和脂质体中从[3H]CE-HDL选择性摄取[3H]CE，其IC50值分别为0.057 μM和0.098 μM[2]。在HeLa和BSC-1细胞中，BLT-1（50 μM；3小时）不会引起依赖或不依赖clathrin的胞内膜运输过程中的一般缺陷[1]。 |
| molecular weight | 241.4 |
| Molecular formula | C12H23N3S |
| CAS | 321673-30-7 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
| Solubility | DMSO: 38.67 mg/mL (160.19 mM), Sonication is recommended. |
| References | 1. Nieland TJ, et al. Discovery of chemical inhibitors of the selective transfer of lipids mediated by the HDL receptorSR-BI. Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15422-7. 2. Nieland TJ, et al. Identification of the molecular target of small molecule inhibitors of HDL receptor SR-BI activity. Biochemistry. 2008 Jan 8;47(1):460-72. 3. Raldúa D, et al. BLT-1, a specific inhibitor of the HDL receptor SR-BI, induces a copper-dependent phenotype during zebrafish development. Toxicol Lett. 2007 Dec 10;175(1-3):1-7. Epub 2007 Aug 22. |