475874-M

MK571, Sodium Salt

A selective, competitive antagonist of leukotriene D4 (LTD4) (K_i = 2.1 nM for inhibition of [³H]LTD4 binding to human lung membranes).

• 別名: MK571, Sodium Salt, L 660711, Sodium Salt, (E)-3-[[[3-[2-(7-Chloro-2-quinolinyl)ethenyl]phenyl]-[[3-dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid, Sodium Salt
• 実験式（ヒル表記法）: C₂₆H₂₆ClN₂O₃S₂ · Na
• CAS番号: 115104-28-4
• 分子量: 537.07
• UNSPSCコード: 12352211

特性

• 品質水準: 100
• アッセイ: ≥90% (HPLC)
• 形状: solid
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; desiccated
• 色: off-white
• 溶解性: DMSO: 10 mg/mL; water: 200 mg/mL
• 保管温度: −20°C
• InChI: 1S/C26H27ClN2O3S2/c1-29(2)24(30)12-14-33-26(34-15-13-25(31)32)20-5-3-4-18(16-20)6-10-22-11-8-19-7-9-21(27)17-23(19)28-22/h3-11,16-17,26H,12-15H2,1-2H3,(H,31,32)/b10-6+
• InChI Key: AXUZQJFHDNNPFG-UXBLZVDNSA-N

詳細

詳細

A selective, competitive antagonist of leukotriene D₄ (LTD₄) (K_i = 2.1 nM for inhibition of [³H]LTD₄ binding to human lung membranes). Also inhibits multidrug resistance-associated protein 1 (MRP1).

A selective, competitive antagonist of leukotriene D₄ (LTD₄) receptor (K_i = 2.1 nM for inhibition of [³H]LTD₄ binding to human lung membranes). Also reported to inhibit multidrug resistance-associated protein 1 (MRP1).

生物化学的／生理学的作用

Primary Target
Antagonist of leukotriene D4 (LTD4)

Target K_i: 2.1 nM for inhibition of [3H]LTD4 binding to human lung membranes

警告

Toxicity: Standard Handling (A)

再構成

Following reconstitution, aliquot and freeze (-20°C). Aqueous stock solutions in are stable for up to 1 week at -20°C; DMSO stock solutions are stable for up to 6 months at -20°C. Acidic pH and heavy metals will accelerate decomposition.

その他情報

Olson, D.P., et al. 2001. Cytometry46, 105.
Van der Kolk, D.M., et al. 1998. Clin. Cancer Res.4, 1727.
Jones, T.R., et al. 1989. Can. J. Physiol. Pharmacol.67, 17.

法的情報

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

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 1
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable