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法倔唑 /Fadrozole {[allProObj[0].p_purity_real_show]}

货号:A428094 同义名: CGS 16949A free base;(Rac)-FAD286 Ambeed 开学季,买赠积分,赢豪礼

Fadrozole is a selective aromatase inhibitor that has been introduced in Japan for the treatment of breast cancer.

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Fadrozole 化学结构 CAS号:102676-47-1
Fadrozole 化学结构
CAS号:102676-47-1
Fadrozole 3D分子结构
CAS号:102676-47-1
Fadrozole 化学结构 CAS号:102676-47-1
Fadrozole 3D分子结构 CAS号:102676-47-1
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Fadrozole 纯度/质量文件 产品仅供科研

货号:A428094 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Aromatase 其他靶点 纯度
Obacunone +

Aromatase, IC50: 28.4 μM

Nrf2 {[allProObj[0].p_purity_real_show]}
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Fadrozole 生物活性

描述 Estrogen is a sex hormone implicated in the progression of many diseases. Aromatase is a key enzyme responsible for the biosynthesis of estrogen. Fadrozole is a potent, selective, nonsteroidal inhibitor of aromatase that can be used for the treatment of estrogen-dependent diseases. Fadrozole inhibits aromatase at an IC50 value of 6.4nM. Fadrozole also inhibited the production of estrogen in hamster ovarian slices with an IC50 of 0.03μM. In immature female rats, orally administration of fadrozole inhibited aromatase-mediated, androstenedione-induced uterine hypertrophy with an ED50 value of 0.03mg/kg[2].

Fadrozole 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT00247663 Postmenopausal Women With Adva... 展开 >>nced Breast Cancer 收起 << Phase 2 Completed - Japan ... 展开 >> Novartis Investigative Site Kashiwa, Chiba, Japan, 277-8577 Novartis Investigative Site Amagasaki, Hyogo, Japan, 660-8511 Novartis Investigative Site Hamamatsu, Shizuoka, Japan, 430-8558 Novartis Investigative Site Chuo-Ku, Tokyo, Japan, 104-0045 Novartis Investigative Site Cyuo-ku, Tokyo, Japan, 104-8560 Novartis Investigative Site Shinjuku-ku, Tokyo, Japan, 160-8582 Novartis Investigative Site Fukuoka, Japan, 811-4395 Novartis Investigative Site Kumamoto, Japan, 862-0909 Novartis Investigative Site Nigata, Japan, 951-8566 Novartis Investigative Site Saitama, Japan, 338-8553 收起 <<
NCT03279289 Metastatic Colorectal Cancer Phase 2 Recruiting July 2021 Spain ... 展开 >> Spanish Cooperative Group for Digestive Tumour Therapy (TTD) Recruiting Madrid, Spain, 28046 Contact: Inmaculada Ruiz de Mena, PhD    0034 91 378 82 75    ttd@ttdgroup.org 收起 <<

Fadrozole 参考文献

[1]Minnaard-Huiban M, Emmen JM, et al. Fadrozole reverses cardiac fibrosis in spontaneously hypertensive heart failure rats: discordant enantioselectivity versus reduction of plasma aldosterone. Endocrinology. 2008 Jan;149(1):28-31.

[2]Browne LJ, Gude C, Rodriguez H, Steele RE, Bhatnager A. Fadrozole hydrochloride: a potent, selective, nonsteroidal inhibitor of aromatase for the treatment of estrogen-dependent disease. J Med Chem. 1991;34(2):725-736.

Fadrozole 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.48mL

0.90mL

0.45mL

22.39mL

4.48mL

2.24mL

44.79mL

8.96mL

4.48mL

Fadrozole 技术信息

CAS号102676-47-1
分子式C14H13N3
分子量 223.273
别名 CGS 16949A free base;(Rac)-FAD286;CGS16949A
运输蓝冰
存储条件

粉末 Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(470.28 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

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