AbMole|MDV3100 恩杂鲁胺;恩扎卢胺(CAS号915087-33-1;目录号 M1839)

Enzalutamide (MDV3100)是一种雄激素受体(AR)拮抗剂,IC50为36 nM。可用于前列腺癌的相关研究。

MDV3100结构式

生物活性

恩杂鲁胺 Enzalutamide (MDV3100)是一种雄激素受体(AR)拮抗剂,IC50为36 nM。Enzalutamide是雄激素受体(AR)拮抗剂,IC50为36 nM。在加入16β-[18F]氟-5α-DHT (18-FDHT)的竞争性实验中发现作用于AR时Enzalutamide比bicalutamide具有更高的亲和力。而Enzalutamide作用于LNCaP/AR(AR-过量表达)前列腺细胞时没有效果。

 

实验参考
体外实验*
细胞系VCaP cell line
方法Proliferation assays Trypsinized VCaP cells were adjusted to a concentration of 100,000 cells per mL in phenol-red-free RPMI 1640 (with 5% CSS), and dispensed in 16 µL aliquots into CellBIND 384 well plates (Corning, Lowell, MA). Cells were incubated for 48 hours, after which ligand was added in a 16 µL volume to the RPMI culture medium. For the antagonist mode assay, the ligands were diluted in culture medium also containing 30 pM R1881 (final [R1881] = 15 pM). After 7 days’ incubation, 16 µL of CellTiter-Glo Luminescent Cell Viability Assay (Promega, Madison, WI) was added and Relative Luminescence Units (RLUs) measured.  In the agonist mode assay, percent viability of the samples was calculated as: % viability=[RLU sample-RLU medium without cells]/[RLU DMSO treated cells-RLU medium without cells]. In the antagonist mode assay, the percent viability of the samples was calculated as: % viability=[RLU sample-RLU VCaP without R1881]/[RLU R1881-treated cells - RLU VCaP without R1881].
浓度0~10µM
处理时间48h

*上述方法来自公开文献,仅供相同目的实验参考。如实验目的、材料、方法不同,请参考其他文献。

体内实验*
动物模型LNCaP/AR(cs) xenograft model in mice
配制prepared in 18% PEG-400, 1% Tween-80 and 1% povidone, and were formulated for dosing in 15% Vitamin E-TPGS and 65% of a 0.5% w/v CMC solution in 20 mM citrate buffer (pH 4.0).
剂量100mg/kg
给药处理oral gavage

*上述方法来自公开文献,仅供相同目的实验参考。如实验目的、材料、方法不同,请参考其他文献。

化学性质
分子量464.44
分子式C21H16F4N4O2S
CAS号915087-33-1
溶解性(25°C)DMSO 60 mg/mL
储存条件粉末型式       -20°C   3年;4°C   2年
溶于溶剂       -80°C   6个月;-20°C   1个月
运输方式冰袋运输,根据产品的不同,可能会有相应调整。
储备液配制

*下述溶液配置方法仅为基于分子量计算出的理论值。不同产品在配置溶液前,需考虑其在不同溶剂中的溶解度限制。

Concentration / Solvent Volume / Mass1 mg5 mg10 mg
1 mM2.1531 mL10.7657 mL21.5313 mL
5 mM0.4306 mL2.1531 mL4.3063 mL
10 mM0.2153 mL1.0766 mL2.1531 mL

 参考文献

[1] Kohli et al. Adv Urol. Biomarker-based targeting of the androgen-androgen receptor axis in advanced prostate cancer.

[2] Scher et al. N Engl J Med. Increased Survival with Enzalutamide in Prostate Cancer after Chemotherapy.

[3] Schweizer et al. Ther Adv Urol. Abiraterone and other novel androgen-directed strategies for the treatment of prostate cancer: a new era of hormonal therapies is born.

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