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117690-79-6

中文名称 1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
英文名称 1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
CAS 117690-79-6
分子式 C19H28N4O3
分子量 360.45
MOL 文件 117690-79-6.mol
更新日期 2023/03/20 15:41:27
117690-79-6 结构式 117690-79-6 结构式

基本信息

中文别名
化合物LY 255283
英文别名
LY 255283
CGS 23356
5'-Ethyl-2'-hydroxy-4'-[6-methyl-6-(1H-tetrazol-5-yl)heptyloxy]acetophenone
1-[5-ethyl-2-hydroxy-4-[6-methyl-6-(2H-tetrazol-5-yl)heptoxy]phenyl]ethanone
1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOLE-5-YL)HEPTYL]OXY]PHENYL]-ETHANONE
Ethanone, 1-[5-ethyl-2-hydroxy-4-[[6-methyl-6-(2H-tetrazol-5-yl)heptyl]oxy]phenyl]-

物理化学性质

熔点160-162 °C
沸点573.4±60.0 °C(Predicted)
密度1.157±0.06 g/cm3(Predicted)
储存条件Store at +4°C
溶解度二甲基亚砜:>20mg/mL
酸度系数(pKa)5.11±0.10(Predicted)
形态粉末
颜色灰白色至淡黄色

安全数据

WGK Germany2

常见问题列表

生物活性
LY255283 是一种 leukotriene B4 (LTB4) receptor (BLT2) 的拮抗剂,可将 [3H]LTB4 从其在肺膜上的结合位点置换,pKi为7.0。
靶点
TargetValue
BLT2
(Cell-free assay)
7.0(pKi)
体外研究

LY255283 competitively reduces conlractilc responses of lung parcnchyma to LTB, (pA 2 = 7.2).
LY255283 (10 μM, 7 days) significantly suppresses the invasiveness of highly aggressive 253 J-BV bladder cancer cells.

Cell Viability Assay

Cell Line: 253 J-BV cells.
Concentration: 5 or 10 μM.
Incubation Time: 7 days.
Result: Inhibition of BLT2 signaling attenuates aggressive migration by 253 J-BV cells.
体内研究

LY255283 (3, 30 mg/kg) ameliorates lipopolysaccharide-induced ARDS in pigs, possibly by blocking the recruitment of activated PMNs into alveoli in a dose-dependent fashion.
LY255283 (2.5 mg/kg, ip) inhibits transitional cell carcinoma metastasis in mice models. The result suggests that a BLT2–Nox–ROS–NF–κB cascade plays a critical role in bladder cancer invasion and metastasis.

Animal Model: Mice (253 J-BV cells injected).
Dosage: 2.5 mg/kg.
Administration: IP injected 3 and 5 days after injection of cells.
Result: By 12 weeks after injection, in mice treated with LY255283 only 0-3 nodules formed per lung, and histological analysis confirmed that the number of micrometastatic lesions was markedly reduced.
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