5.04596

TCN-201

• 別名: TCN-201, 3-Chloro-4-fluoro-N-[(4-{[2-(phenylcarbonyl)hydrazino]carbonyl}phenyl)methyl]benzenesulfonamide, NMDA Antagonist X
• 実験式（ヒル表記法）: C₂₁H₁₇ClFN₃O₄S
• CAS番号: 852918-02-6
• 分子量: 461.89
• MDL番号: MFCD06683895
• UNSPSCコード: 12352200

特性

• アッセイ: ≥98% (HPLC)
• 品質水準: 100
• フォーム: powder
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; protect from light
• 色: white
• 溶解性: DMSO: 5 mg/mL
• 保管温度: 2-8°C
• InChI: 1S/C21H17ClFN3O4S/c22-18-12-17(10-11-19(18)23)31(29,30)24-13-14-6-8-16(9-7-14)21(28)26-25-20(27)15-4-2-1-3-5-15/h1-12,24H,13H2,(H,25,27)(H,26,28)
• InChI Key: FYIBXBFDXNPBSF-UHFFFAOYSA-N

詳細

詳細

A negative allosteric modulator selective for NR2A containing NMDA receptors (pIC₅₀ = 6.8 and <4.3 µM for NR2A and NR2B, respectively). No effect on NR2B-containing NMDA receptors with concentrations less than 50 mM. Inhibition on NR2A containing NMDA receptors is glycine (or D-serine)-binding, but not glutamate-binding, dependent.

生物化学的／生理学的作用

Primary Target
NMDA receptors

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

その他情報

Bettini. E., et al. 2010. J. Pharm. Exp. Ther.335, 644.
Shin, A., et al. 2011. Br. J. Pharmacol.166, 1002.
Edman, S., et al. 2012. Neuropharmacology63, 441.
Hansen, K., et al. 2012. J. Neurosci.32, 6197.

法的情報

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

安全性情報

• ピクトグラム: GHS07
• シグナルワード: Warning
• 危険有害性情報: H315 - H319 - H335 - H336
• 注意書き: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• 危険有害性の分類: Eye Irrit. 2 - Skin Irrit. 2
• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable