Cerestat

Pricing Availability   Qty
说明: Potent and noncompetitive NMDA antagonist
别名: CNS 1102
化学名: N-(3-Ethylphenyl)-N-methyl-N'-1-naphthalenylguanidine hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献
评论
文献 (5)

生物活性 for Cerestat

Cerestat is a potent and noncompetitive NMDA receptor antagonist (IC50 = 36 nM). Exhibits >70-fold selectivity for NMDA receptor over σ receptor. Neuroprotective in a rat model of focal ischemia.

技术数据 for Cerestat

分子量 339.86
公式 C20H21N3.HCl
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 137160-11-3
PubChem ID 60839
InChI Key CKAKVKWRMCAYJD-UHFFFAOYSA-N
Smiles N=C(N(C)C3=CC=CC(CC)=C3)NC1=C2C(C=CC=C2)=CC=C1.Cl

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.

溶解性数据 for Cerestat

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
water 16.99 50
DMSO 33.99 100

制备储备液 for Cerestat

以下数据基于产品分子量 339.86。 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.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.94 mL 14.71 mL 29.42 mL
5 mM 0.59 mL 2.94 mL 5.88 mL
10 mM 0.29 mL 1.47 mL 2.94 mL
50 mM 0.06 mL 0.29 mL 0.59 mL

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参考文献 for Cerestat

参考文献是支持产品生物活性的出版物。

Reddy et al (1994) Synthesis and structure-activity studies of N,N'-diarylguanidine derivatives. N-(1-naphthyl)-N'-(3-ethylphenyl)-N'-methylguanidine: a new, selective noncompetitive NMDA receptor antagonist. J.Med.Chem. 37 260 PMID: 8295213

Schäbitz et al (2000) The N-MthD.-aspartate antagonist CNS 1102 protects cerebral gray and white matter from ischemic injury following temporary focal ischemia in rats. Stroke 31 1709 PMID: 10884477


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查看全部 NMDA Receptor Antagonists

关键词: Cerestat, Cerestat supplier, CNS1102, potent, noncompetitive, NMDA, receptors, antagonists, selective, neuroprotection, neuroprotective, ischemia, stroke, CNS, 1102, Receptors, 4492, Tocris Bioscience

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该领域的文献

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。


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