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Topilutamide (BP766) Sale

(Synonyms: BP766; Fluridil) 目录号 : GC33122

Topilutamide (BP766) 是一种局部非甾体抗雄激素 (NSAA)。

Topilutamide (BP766) Chemical Structure

Cas No.:260980-89-0

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥1,485.00
现货
5mg
¥1,350.00
现货
10mg
¥2,250.00
现货
50mg
¥8,550.00
现货
100mg
¥14,850.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

Topilutamide is a topical nonsteroidal antiandrogen (NSAA).

Prostate cancer is the most common cancer and one of the leading causes of cancer deaths in men. One of the commonly used approaches to treat metastatic prostate cancer is via first-generation nonsteroidal anti-androgens (NSAAs), namely Flutamide, Nilutamide, Bicalutamide and Topilutamide[1].

[1]. Suresh PS, et al. Review of HPLC and LC-MS/MS assays for the determination of various nonsteroidal anti-androgens used in the treatment of prostate cancer. Biomed Chromatogr. 2017 Jun 21.

Chemical Properties

Cas No. 260980-89-0 SDF
别名 BP766; Fluridil
Canonical SMILES O=C(NC1=CC=C([N+]([O-])=O)C(C(F)(F)F)=C1)C(C)(O)CNC(C(F)(F)F)=O
分子式 C13H11F6N3O5 分子量 403.23
溶解度 DMSO : 150 mg/mL (372.00 mM) 储存条件 Store at -20°C
General tips 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;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.48 mL 12.3999 mL 24.7997 mL
5 mM 0.496 mL 2.48 mL 4.9599 mL
10 mM 0.248 mL 1.24 mL 2.48 mL
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Research Update

Review of HPLC and LC-MS/MS assays for the determination of various nonsteroidal anti-androgens used in the treatment of prostate cancer

Biomed Chromatogr 2018 Jan;32(1).PMID:28636139DOI:10.1002/bmc.4034

Prostate cancer is the most common cancer and one of the leading causes of cancer deaths in men. One of the commonly used approaches to treat metastatic prostate cancer was via first-generation nonsteroidal anti-androgens (NSAAs), namely flutamide, nilutamide, bicalutamide and Topilutamide. Most prostate cancer patients who are initially responsive develop the most aggressive form of disease called castration-resistant prostate cancer. Second-generation NSAA receptor antagonists (enzalutamide, apalutamide and darolutamide) are emerging as additional new options to treat castration-resistant prostate cancer. The objective of this work was to review the literature on the bioanalytical methods for the quantification of first- and second-generation NSAA inhibitors in clinical (human plasma) and preclinical (mouse plasma, rat plasma, urine and tissue homogenates etc.) studies along with relevant case studies for some chosen drugs. Based on the review, it was concluded that the published methodologies using either HPLC or LC-MS/MS are well suited for the quantification of NSAA inhibitors in various biological fluids to delineate pharmacokinetic data.