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GW3965 hydrochloride ≥98%

2-(3-(3-((2-chloro-3-(trifluoromethyl)benzyl)(2,2-diphenylethyl)amino)propoxy)phenyl)acetic acid hydrochloride

源葉(MedMol)
S89028
405911-17-3
C33H31F3ClNO3.HCl
618.51
MFCD08276920
品牌 貨號 產品規(guī)格 價格(RMB) 庫存（上海） 北京 武漢 南京 購買數量
源葉(MedMol) S89028-5mg ≥98% ￥480.00元 >10 - - -
源葉(MedMol) S89028-10mg ≥98% ￥720.00元 8 - - -
源葉(MedMol) S89028-50mg ≥98% ￥2400.00元 4 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

GW3965 HCl is an effective and specific LXR agonist for hLXRα/β (EC50: 190/30 nM).
產品描述： GW3965 HCl is an effective and specific LXR agonist for hLXRα/β (EC50: 190/30 nM).
靶點： Liver X Receptor;LiverXReceptor
體外研究：
GW3965 recruits the steroid receptor coactivator 1 to human LXRα with EC50 of 125 nM in a cell-free ligand-sensing assay. GW3965 shows a potent antagonistic activity against hLXRα and hLXRβ in cell-based assays with EC50 of 190 nM and 30 nM, respectively. Besides, GW3965 also sows excellent selectivity over other nuclear receptors. In human islets, GW3965 (1 μM) reduces expression of selected pro-inflammatory cytokines including IL-8, monocyte chemotactic protein-1 and tissue factor.
體內研究：
In mice, GW3965 at a dose of 10 mg/kg upregulates ABCA1 expression 8-fold and raises circulating levels of HDL by 30% with Cmax of 12.7 μg/mL and t1/2 of 2 hours. GW3965 (10 mg/kg) induces expression of ABCA1 and ABCG1 and shows potent antiatherogenic activity in both LDLR/and apoE/mice. In male sprague-dawley rats, GW3965 reduces Ang II-mediated increases in blood pressure and decreases vascular Ang II receptor gene expression. In Glioblastoma mouse model, GW3965 results in inducible degrader of LDLR-mediated LDLR degradation, increased expression of the ABCA1 cholesterol efflux transporter, and thus potently promotes tumor cell death.
細胞實驗： Cells are seeded in 96 wells and are treated after 24 hours with different drugs indicated in each experiment in medium containing 1% FBS or lipoprotein deficient serum. Relative proliferation is determined using Cell Proliferation Assay Kit. Cells are incubated 1.5 hrs after adding tetrazolium salt WST-1 [2-(4-iodophenyl)-3- (4-nitrophenyl)-5-(2, 4-disulfo-phenyl)-2H-tetrazolium, monosodium salt] at 5% CO2, 37oC and the absorbance of the treated and untreated cells are measured using a microplate reader at 420 to 480 nm. Cells seeded in 12 well plates are counted using a hemocytometer, and dead cells are assessed using trypan blue exclusion assays.
參考文獻：
1. Guo D, et al. An LXR agonist promotes glioblastoma cell death through inhibition of an EGFR/AKT/SREBP-1/LDLR-dependent pathway. Cancer Discov. 2011, 1(5), 442-456. 2. Joseph SB, et al. Synthetic LXR ligand inhibits the development of atherosclerosis in mice. Proc Natl Acad Sci U S A. 2002, 99(11), 7604-7609. 3. Collins JL, et al. Identification of a nonsteroidal liver X receptor agonist through parallel array synthesis of tertiary amines. J Med Chem. 2002, 45(10), 1963-1966. 4. Scholz H, et al. The synthetic liver X receptor agonist GW3965 reduces tissue factor production and inflammatory responses in human islets in vitro. Diabetologia. 2009, 52(7), 1352-1362. 5. Leik CE, et al. GW3965, a synthetic liver X receptor (LXR) agonist, reduces angiotensin II-mediated pressor responses in Sprague-Dawley rats. Br J Pharmacol. 2007, 151(4), 450-456.
溶解性： Soluble  in  DMSO、Ethanol
保存條件： -20°C
配置溶液濃度參考：
1mg 5mg 10mg
1 mM 1.617 ml 8.084 ml 16.168 ml
5 mM 0.323 ml 1.617 ml 3.234 ml
10 mM 0.162 ml 0.808 ml 1.617 ml
50 mM 0.032 ml 0.162 ml 0.323 ml
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參考文獻

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