HE-3235
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | ¥2654.00 | 10-15工作日发货 | |
| 10mg | ¥4170.00 | 10-15工作日发货 | |
| 25mg | ¥7962.00 | 10-15工作日发货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
HE-3235 is a novel antagonist of androgen receptor.
Androgen receptor (AR) is an adrenal hormone belongs to the steroid hormone receptor family of molecules. AR is responsible for mediating the physiologic effects of androgens by binding to specific DNA sequences that influence transcription of androgen-responsive genes. Variations in the AR gene may lead to genetic predisposition to prostate cancer development and severity [2].
In vitro: In LNCaP cells expressing a mutated androgen receptor, HE3235 significantly inhibited activity for AED-stimulated LNCaP proliferation. This inhibitory activity is accompanied by an increase in the number of apoptotic cells [1].
In vivo: Animal studies have confirmed the cytoreductive activity of HE3235 on LNCaP tumours. The results suggest that this compound may be of clinical use in castration-resistant prostate cancer. In castrated male mice implanted subcutaneously with LuCaP35V CaP xenografts, treatment with HE3235 significantly prolonged the tumor doubling time of LuCaP35V, decreased androgen receptor expression, and lowered levels of intratumoral testosterone by 89% and dihydrotestosterone by 63% in both the presence and the absence of AED. HE3235 inhibited tumor growth in the bone environment. HE3235 inhibited the growth of subcutaneous CRPC as well as CRPC in the bone environment. HE3235 exhibited a wide range of effects, including alteration of androgen receptor signaling and reductions in levels of intratumoral androgens. Weights of tumored tibiae of HE3235-treated animals were lower than those of control [3].
References:
[1] Trauger R, Corey E, Bell D, et al. Inhibition of androstenediol-dependent LNCaP tumour growth by 17α-ethynyl-5α-androstane-3α, 17β-diol (HE3235)[J]. British journal of cancer, 2009, 100(7): 1068-1072.
[2] Gelmann E P. Molecular biology of the androgen receptor[J]. Journal of Clinical Oncology, 2002, 20(13): 3001-3015.
[3 Gelmann E P. Molecular biology of the androgen receptor[J]. Journal of Clinical Oncology, 2002, 20(13): 3001-3015.] Koreckij T D, Trauger R J, Montgomery R B, et al. HE3235 inhibits growth of castration-resistant prostate cancer[J]. Neoplasia, 2009, 11(11): 1216IN22-1225IN23.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 183387-50-0 |
| 分子式 | C21H32O2 |
| 分子量 | 316.5 |
| 化学名称 | (3α,5α,17α)-pregn-20-yne-3,17-diol |
| 溶解度 | ≤10mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in dimethyl formamide |
| SMILES | C[C@](CC1)([C@@H](CC2)[C@H](CC3)[C@H]1[C@@](C)(CC1)[C@@H]3C[C@@H]1O)[C@@]2(C#C)O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | Apoptone 是 3beta-androstanediol 的合成类似物,是一种口服生物可用抗癌剂。Apoptone 在前列腺癌和乳腺癌的啮齿动物模型中具有活性。 |




沪公网安备 31011002003500