SML3622
CAY10444
≥98% (HPLC)
别名:
(4R)-2-Undecyl-4-thiazolidinecarboxylic acid, 2-Undecylthiazolidine-4(R)-carboxylic acid, BML 241, BML-241, BML241, CAY 10444, CAY-10444
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关于此项目
经验公式（希尔记法）:
C15H29NO2S
化学文摘社编号:
分子量:
287.46
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear (Warmed)
storage temp.
-10 to -25°C
Quality Level
Biochem/physiol Actions
CAY10444 is a selective sphingosine-1-phosphate (S1P) receptor 3 (S1P3; EDG3) antagonist that inhibits 1 µM S1P-induced calcium mobilization in HeLa transfectants that express S1P3 over those expressing S1P1/CD363/EDG1 (37.6% vs 6.92% inhibition by 10 µM CAY10444).
Selective sphingosine-1-phosphate (S1P) receptor 3 (S1P3; EDG3) antagonist.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Yuuki Koide et al.
Journal of medicinal chemistry, 45(21), 4629-4638 (2002-10-04)
Sphingosine-1-phosphate (S1P) is an intracellular second messenger and an extracellular mediator through endothelial differentiation gene (EDG) receptors, which are a novel class of G-protein-coupled receptors. Although EDG has attracted much attention because of its various roles, no selective agonists or
Inhibiting Sphingosine 1-Phosphate Receptor Subtype 3 Attenuates Brain Damage During Ischemia-Reperfusion Injury by Regulating nNOS/NO and Oxidative Stress
Frontiers in Neuroscience, 16, 838621-838621 (2022)
Alessandra Bigi et al.
The FEBS journal, 290(1), 112-133 (2022-07-20)
Soluble oligomers arising from the aggregation of the amyloid beta peptide (Aβ) have been identified as the main pathogenic agents in Alzheimer's disease (AD). Prefibrillar oligomers of the 42-residue form of Aβ (Aβ42 O) show membrane-binding capacity and trigger the
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