LXR-623

LXR-623 (WAY 252623) 是一种LXRα部分激动剂和LXRβ完全激动剂,可透过血脑屏障,IC50分别为 179 nM 和 24 nM 。

CAS号

875787-07-8

分子式

C21H12ClF5N2

主要靶点

Liver X Receptor

仅限科研使用

Cat No : CM01070

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Synonyms

LXR623|WAY 252623



产品信息

LXR-623 (WAY 252623) is an orally bioavailable and highly specifical synthetic modulator of LXR.

CAS号 875787-07-8
分子式 C21H12ClF5N2
主要靶点 Liver X Receptor
主要通路 代谢
分子量 422.78
纯度 97.17%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 LXR623|WAY 252623

靶点活性

LXR-α:179 nM|LXR-β:24 nM

体内活性

LXR-623 is absorbed rapidly with peak concentrations (Cmax) achieved at approximately 2 hours. The Cmax and area under the concentration-time curve increases in a dose-proportional manner. The mean terminal disposition half-life is between 41 and 43 hours independently of dose. In a low-density lipoprotein (LDL) receptor, (LDLr) knockout mouse model of atherosclerosis, LXR-623 administered orally upregulates intestinal ABCG5 and ABCG8 and reduces atheroma burden without altering serum or hepatic cholesterol and trig-lycerides. LXR-623 shows brain penetration and causes tumor regression in a GBM(glioblastomas) mouse model, reducing cholesterol and inducing cell death[1].

体外活性

LXR-623 suppresses LDLR expression, increases expression of the ABCA1 efflux transporter, and induces substantial cell death in all of the GBM samples tested. The brain metastatic breast cancer cell line MDA-MB-361, which harbors ERBB2 amplification, is also highly sensitive to LXR-623- dependent cell death in a concentration-dependent manner. LXR-623 inhibits LDL uptake and induces cholesterol efflux in GBM cells, resulting in a significant reduction in cellular cholesterol content. Normal brain cell insensitivity to LXR-623 may be due to reliance on endogenous synthesis of cholesterol and intact negative feedback through synthesis of endogenous oxysterols[3].

溶解度

Ethanol:42.3 mg/mL (100 mM),DMSO:42.3 mg/mL (100 mM)

细胞实验

The purified PBMC are resuspended in culture medium (RPMI + 10% fetal calf serum + 1% penicillin/streptomycin with 1% L-glutamine), transferred to 6-well (9.5 cm2 each) tissue culture dishes at approximately 5 × 106 cells per well, and 2 μM LXR-623 or vehicle (DMSO) are added. After 18 hours of culture, RNA isolation and qPCR analysis for LXRα, LXRβ, ABCA1, ABCG1, and PLTP is performed.(Only for Reference)

参考文献

1.Katz A, et al. J Clin Pharmacol. 2009, 49(6):643-9.
2.Elizabeth A DiBlasio-Smith, et al. Journal of Translational Medicine. 2008, 6:59.
3.Villa GR, et al. Cancer Cell. 2016, 30(5):683-693.

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