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经验公式(希尔记法):
C26H26ClN2O3S2 · Na
化学文摘社编号:
分子量:
537.07
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.77
产品名称
MK571,钠盐, A selective, competitive antagonist of leukotriene D4 (LTD4) (Ki = 2.1 nM for inhibition of [³H]LTD4 binding to human lung membranes).
SMILES string
S(C(SCCC(=O)O)c1cc(ccc1)\C=C\c2nc3c(cc2)ccc(c3)Cl)CCC(=O)N(C)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
assay
≥90% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, desiccated
color
off-white
solubility
DMSO: 10 mg/mL, water: 200 mg/mL
storage temp.
−20°C
Quality Level
General description
白三烯D4 (LTD4)受体的选择性竞争性拮抗剂(Ki =2.1 nM,用于抑制[3H]LTD4与人肺膜的结合)。据报告还抑制多药耐药相关蛋白1(MRP1)。
Biochem/physiol Actions
主要靶标
白三烯D4(LTD4)的拮抗剂
白三烯D4(LTD4)的拮抗剂
靶标Ki:2.1 nM用于抑制[3H]LTD4与人肺膜的结合
Preparation Note
溶解后,等分并冷冻保存(-20°C)。贮备水溶液在-20°C下可稳定长达1周;DMSO贮备液在-20°C下可稳定长达6个月。酸性pH值和重金属会加速分解。
Other Notes
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.
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.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
毒性:标准处理(A)
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Gad D Vatine et al.
Cell stem cell, 20(6), 831-843 (2017-05-21)
Inactivating mutations in the thyroid hormone (TH) transporter Monocarboxylate transporter 8 (MCT8) cause severe psychomotor retardation in children. Animal models do not reflect the biology of the human disease. Using patient-specific induced pluripotent stem cells (iPSCs), we generated MCT8-deficient neural
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