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-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE

中文名称1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
中文同义词化合物LY 255283;LY255283游离态;1-(5-乙基-2-羟基-4-((6-甲基-6-(2H-四唑-5-基)庚基)氧基)苯基)乙-1-酮;LY255283,BLT2受体拮抗剂;LY255283,BLT2 RECEPTOR拮抗剂;化合物LY 255283,10 MM DMSO 溶液;LY255283 ,S2959
英文名称1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
英文同义词LY 255283;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;5'-Ethyl-2'-hydroxy-4'-[6-methyl-6-(1H-tetrazol-5-yl)heptyloxy]acetophenone;CGS 23356;1-[5-ethyl-2-hydroxy-4-[6-methyl-6-(2H-tetrazol-5-yl)heptoxy]phenyl]ethanone;Ethanone, 1-[5-ethyl-2-hydroxy-4-[[6-methyl-6-(2H-tetrazol-5-yl)heptyl]oxy]phenyl]-;1-(5-Ethyl-2-hydroxy-4-((6-methyl-6-(2H-tetrazol-5-yl)heptyl)oxy)phenyl)ethan-1-one
CAS号117690-79-6
分子式C19H28N4O3
分子量360.45
EINECS号
相关类别Prostanoid receptor and related
Mol文件117690-79-6.mol
结构式1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE 结构式

1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE 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
形态粉末
酸度系数(pKa)5.11±0.10(Predicted)
颜色灰白色至浅黄色
InChI1S/C19H28N4O3/c1-5-14-11-15(13(2)24)16(25)12-17(14)26-10-8-6-7-9-19(3,4)18-20-22-23-21-18/h11-12,25H,5-10H2,1-4H3,(H,20,21,22,23)
InChIKeyWCGXJPFHTHQNJL-UHFFFAOYSA-N
SMILESCCc1cc(C(C)=O)c(O)cc1OCCCCCC(C)(C)c2nnn[nH]2

1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE 用途与合成方法

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。
TargetValue
BLT2
(Cell-free assay)
7.0(pKi)

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.

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.

安全信息

WGK Germany2
存储类别11 - 可燃固体

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2026/06/05HY-15744LY255283117690-79-61 mg550元
2026/06/05HY-157441-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE
LY255283
117690-79-65mg1200元

1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE 上下游产品信息

"1-[5-ETHYL-2-HYDROXY-4-[[6-METHYL-6-(1H-TETRAZOL-5-YL)HEPTYL]OXY]PHENYL]ETHANONE"相关产品信息
CS-2822 13,14-二氢前列腺素E1 LY294002/PI3K抑制剂 (1R,4S,5S,6S)-4-氨基-2-硫杂双环[3.1.0]己烷-4,6-二甲酸2,2-二氧化物 化合物LY3143921HYDRATE 5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈 CS-1087 LY2109761 前列腺素A1 硫前列酮 前列腺素B1 氟前列醇 地诺前列素 前列腺素D2 PGF1Α 拉坦前列腺素 米索前列醇酸
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