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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEVER-82576Cat. No.: HY-10942CAS No.: 847559-80-2Synonyms: NVP-BEP800分式: CHClNOS分量: 480.41作靶点: HSP作通路: Cell Cycle/DNA Damage; Metabolic Enzyme/Protease储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性数据体外实验

2、 DMSO : 6.2 mg/mL (12.91 mM; Need ultrasonic)Mass Solvent1 mg 5 mg 10 mg Concentration制备储备液1 mM 2.0816 mL 10.4078 mL 20.8156 mL5 mM 0.4163 mL 2.0816 mL 4.1631 mL10 mM 0.2082 mL 1.0408 mL 2.0816 mL请根据产品在不同溶剂中的溶解度,选择合适的溶剂配制储备液,并请注意储备液的保存式和期限。BIOLOGICAL ACTIVITY物活性 VER-82576 (NVP-BEP800)种有效的,可服的,选择性的 H

3、sp90 抑制剂,对 Hsp90 的 IC50 值为 58nM;VER-82576 同时可较弱地抑制 Grp94 和 Trap-1 的活性,IC50 值分别为 4.1 和 5.5 M。IC50 & Target HSP90 GRP94 TRAP-158 nM (IC50) 4.1 M (IC50) 5.5 M (IC50)1/3 Master of Small Molecules 您边的抑制剂师www.MedChemE体外研究 VER-82576 (NVP-BEP800) is a potent and selective Hsp90 inhibitor, with an IC50 of 58

4、 nM for Hsp90 andis 70-fold selective against Grp94 and Trap-1, with IC50s of 4.1 1.1 and 5.5 0.48 M. VER-82576potently inhibits the proliferation of tumor cells, with GI50s ranging from 38 nM in A375 cells to 1050 nM inPC3 cells, with an average GI50 of 245 nM. VER-82576 (250-1250 nM) depletes clie

5、nt proteins in humancancer cell lines in vitro 1. VER-82576 (NVP-BEP800; 200 nM) shows no significant effect on the ionizingradiation (IR) dose-response curves of A549 cells, and is less toxic to SNB19 cells. VER-82576 incombination with IR results in more severe DNA damage in both A549 and SNB19 ce

6、ll lines than eachtreatment alone and also protracts the kinetics of DNA damage repair in SNB19 cells 2. VER-82576 (NVP-BEP800; 0.05, 0.1 or 0.2 M) dose-dependently decreases the viability and induces apoptosis ofglioblastoma cells. VER-82576 (0.2 M) suppresses the expression of IKK protein but does

7、 not alter thelevels of IKK mRNA in T98G cells. VER-82576 (0.2 M) suppresses the expression of heat shock protein 703.体内研究 VER-82576 (NVP-BEP800; 15 or 30 mg/kg, p.o.) shows antitumor activities in A375 cancer xenografts andBT-474 xenograft-bearing mice 1.PROTOCOLCell Assay 3 Prior to treatments, th

8、e cells are placed into 6-well plates in medium at a density of 1 105 cells/well, threewells per treatment group and cultured for 24 h. The cells are divided into treatment groups and treatedaccordingly for 40 h: vehicle control (DMSO, 0.016%, v/v), VER-82576 (0.05, 0.1 or 0.2 M), irradiation (10Gy)

9、, or VER-82576 (0.05, 0.1 or 0.2 M) in combination with irradiation (10 Gy). Upon completion of thetreatment, all cells are incubated with 0.5 mg/ml MTT for 3 h. The relative viability of the treated cells to theuntreated control cells is measured. The absorbance is measured at 490 nm on a microplat

10、e reader 3.MCE has not independently confirmed the accuracy of these methods. They are for reference only.Animal The estrogen receptor (ER)-positive, ErbB2-overexpressing cell line BT-474 is grown in DMEM high glucoseAdministration 1 (4.5 g/L) supplemented with 10% FCS, 200 mM l-glutamine, and 1% so

11、dium pyruvate (BioConcept). Two or3 d before cell inoculation, each mouse is s.c. implanted on the upper dorsal side with a 17-estradiol pellet(25 g/d; 90-d release) using a trocar needle. BT-474 cells (5 106) are injected in 200 L Matrigel/HBSS(1:1 volume) s.c. in the right flank. The A375 cell lin

12、e expresses mutant B-Raf (V600E). The cells are grownin RPMI 1640 supplemented with 10% FCS and 200 mM l-glutamine. To establish tumors, 5 106 A375 cellsare injected s.c. in 200 L PBS in the right flank. The animals are kept under optimized hygienic conditionswith a 12-h dark, 12-h light cycle. The

13、animals are fed food and water ad libitum. Tumor growth and bodyweights are monitored at regular intervals. The xenograft tumor sizes are measured manually with calipers,and the tumor volume is estimated using the following formula: (W L H /6), where width (W), length(L), and height (H) are the thre

14、e largest diameters. Treatment with VER-82576 is initiated when the averagetumor volume reaches 100 to 300 mm3 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only.REFERENCES2/3 Master of Small Molecules 您边的抑制剂师www.MedChemE1. Massey AJ, et al. Preclinical

15、antitumor activity of the orally available heat shock protein 90 inhibitor NVP-BEP800. Mol Cancer Ther.2010 Apr;9(4):906-19.2. Niewidok N, et al. Hsp90 Inhibitors NVP-AUY922 and NVP-BEP800 May Exert a Significant Radiosensitization on Tumor Cells alongwith a Cell Type-Specific Cytotoxicity. Transl Oncol. 2012 Oct;5(5):356-69. Epub 2012 Oct 1.3. Wu J, et al. Irradiation facilitates the inhibitory effect of the heat shock protein 90 inhibitor NVP-BEP800 on the proliferation of malignantglioblastoma cells through attenuation of the upregulation of heat shock protein 70. Exp Ther Med.

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