Tetrahydrodeoxycorticosterone (Synonyms: Tetrahydro-11-deoxycorticosterone)
目录号: PL02144 纯度: ≥98%
CAS No. :567-03-3
商品编号 规格 价格 会员价 是否有货 数量
PL02144-1mg 1mg ¥3696.00 请登录
PL02144-5mg 5mg ¥9322.00 请登录
PL02144-10mg 10mg 询价 询价
PL02144-50mg 50mg 询价 询价
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
Tetrahydrodeoxycorticosterone
中文别名
1-[2-氨基-1-(4-苄氧基苯基)乙基]环己醇盐酸盐;21-羟基孕烷醇酮;21-羟基孕烷醇酮标准品;21羟基孕烯醇酮
英文名称
Tetrahydrodeoxycorticosterone
英文别名
Pregnan-20-one,3,21-dihydroxy-, (3a,5b)-;Tetrahydro 11-Deoxycorticosterone;5B-PREGNAN-3A,21-DIOL-20-ONE;Tetrahydro 11-Deoxyc;TETRAHYDRODEOXYCORTICOSTERONE
Cas No.
567-03-3
分子式
C21H34O3
分子量
334.49
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
Tetrahydrodeoxycorticosterone 是一种神经类固醇,是一种有效的 GABAA 受体正变构调节剂 (PAM)。Tetrahydrodeoxycorticosterone 具有有效的神经抑制特性。
生物活性
Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABA A receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties.
性状
Solid
IC50 & Target[1][2]
Human Endogenous Metabolite
体外研究(In Vitro)
The endogenous neurosteroid Tetrahydrodeoxycorticosterone (THDOC) at physiological concentrations selectively enhances tonic currents mediated by αβδ receptors.
In hippocampus, 10 nM Tetrahydrodeoxycorticosterone reduces neuronal excitability by augmenting tonic αβδ receptor currents. In thalamocortical neurons, although 100 nM Tetrahydrodeoxycorticosterone enhances tonic currents, 10 nM Tetrahydrodeoxycorticosterone does not. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Concentrations of Tetrahydrodeoxycorticosterone (THDOC) in brain tissue from mice with hepatic encephalopathy (HE) resulting from toxic liver injury are sufficient to induce sedation in animals of the same species. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Hua-Jun Feng, et al. Comparison of αβδ and αβγ GABA A receptors: Allosteric modulation and identification of subunit arrangement by site-selective general anesthetics. Pharmacol Res. 2018 Jul;133:289-300.
[2]. Roger F Butterworth. Neurosteroids in hepatic encephalopathy: Novel insights and new therapeutic opportunities. J Steroid Biochem Mol Biol. 2016 Jun;160:94-7.
溶解度数据
In Vitro: DMSO : 100 mg/mL (298.96 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2