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Submit ReviewGanaxolone is a potent positive allosteric modulator of GABAA receptors. Enhances GABA-evoked chloride currents in Xenopus oocytes expressing GABAA receptors (EC50 values are 94, 122 and 213 nM for α2β1γ2L, α3β1γ2L and α1β1γ2L receptors respectively). Exerts anticonvulsive effects in a broad range of animal seizure models.
分子量 | 332.53 |
公式 | C22H36O2 |
储存 | Store at +4°C |
CAS Number | 38398-32-2 |
PubChem ID | 6918305 |
InChI Key | PGTVWKLGGCQMBR-FLBATMFCSA-N |
Smiles | O[C@]1(C)CC[C@@]2(C)[C@](CC[C@]3([H])[C@@]([H])2CC[C@@]4(C)[C@]([H])3CC[C@@H]4[C@](C)=O)([H])C1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 3.33 | 10 温和加热 | |
ethanol | 6.65 | 20 |
以下数据基于产品分子量 332.53。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.2 mM | 15.04 mL | 75.18 mL | 150.36 mL |
1 mM | 3.01 mL | 15.04 mL | 30.07 mL |
2 mM | 1.5 mL | 7.52 mL | 15.04 mL |
10 mM | 0.3 mL | 1.5 mL | 3.01 mL |
参考文献是支持产品生物活性的出版物。
Carter et al (1997) Characterization of the anticonvulsive properties of ganaxolone (CCD 1044; 3α-hydroxy-3β-methyl-5α-pregnan-20-one), a selective, high affinity, steroid modulator of the γ-aminobutyric acidA receptor. J.Pharmacol.Exp.Ther. 280 1284 PMID: 9067315
Lyden et al (2000) Effect of ganaxolone in a rodent model of cerebral hematoma. Stroke 31 169 PMID: 10625734
Ungard et al (2000) Modification of behavioral effects of drugs in mice by neuroactive steroids. Psychopharmacology 148 336 PMID: 10928304
If you know of a relevant reference for Ganaxolone, please let us know.
关键词: Ganaxolone, Ganaxolone supplier, Potent, positive, allosteric, modulators, GABAA, receptors, Receptors, CCD1042, PAM, CCD, 1042, 2531, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Ganaxolone 的部分引用包括:
Asiedu et al (2012) Modulation of spinal GABAergic analgesia by inhibition of chloride extrusion capacity in mice. J Pain 13 546 PMID: 22537560
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
Written by Ian Martin, Norman Bowery and Susan Dunn, this review provides a history of the GABA receptor, as well as discussing the structure and function of the various subtypes and the clinical potential of receptor modulators; compounds available from Tocris are listed.
The key feature of drug addiction is the inability to stop using a drug despite clear evidence of harm. This poster describes the brain circuits associated with addiction, and provides an overview of the main classes of addictive drugs and the neurotransmitter systems that they target.