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EPI-001
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
EPI-001图片
CAS NO:227947-06-0
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)394.89
FormulaC21H27ClO5
CAS No.227947-06-0
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 79 mg/mL (200.1 mM)
Water: <1 mg/mL
Ethanol: 79 mg/mL (200.1 mM)
Other infoChemical Name: 3-[4-[1-[4-(3-chloro-2-hydroxypropoxy)phenyl]-1-methylethyl]phenoxy]-1,2-propanediol
InChi Key: HDTYUHNZRYZEEB-UHFFFAOYSA-N
InChi Code: InChI=1S/C21H27ClO5/c1-21(2,15-3-7-19(8-4-15)26-13-17(24)11-22)16-5-9-20(10-6-16)27-14-18(25)12-23/h3-10,17-18,23-25H,11-14H2,1-2H3
SMILES Code: OCC(O)COC1=CC=C(C(C)(C2=CC=C(OCC(O)CCl)C=C2)C)C=C1
SynonymsEPI-001; EPI 001; EPI001
实验参考方法
In Vitro

In vitro activity: EPI-001 blocks transactivation of the AR NTD, interacts with the AF-1 region, inhibits protein-protein interactions with AR, and reduces AR interaction with androgen-response elements on target genes. In LNCaP cells, EPI-001 inhibits both androgen-dependent and androgen-independent (OCM-induced) cell proliferation. In LNCaP cells, EPI-001 also acts as a PPAR-gamma modulator to result in inhibition of androgen receptor expression and activity, which inhibits prostate cancer growth.


Cell Assay: LNCaP cells are treated with bicalutamide (BIC) or EPI-001 for 1 hr before the addition of R1881 (0.1 nM) for 4 days. LNCaP cells are treated with OCM (50%) with, or without, EPI-001 for 3 days (serum-free, androgen-free, phenol red-free conditions).

In VivoIn male mice bearing CRPC LNCaP s.c. xenografts, EPI-001 (50 mg/kg, i.v.) blocks the androgen-axis and inhibits androgen-dependent tumor growth by reducing proliferation and increasing apoptosis.
Animal modelMale mice bearing LNCaP s.c. xenografts
Formulation & DosageDissolved in DMSO; 50 mg/kg; i.v. injection
ReferencesCancer Cell. 2010 Jun 15;17(6):535-46; Oncotarget. 2015 Feb 28;6(6):3811-24.