LY2828360
目录号: PL13533 纯度: ≥98%
CAS No. :1231220-79-3
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PL13533-5mg 5mg ¥3375.00 请登录
PL13533-10mg 10mg ¥5464.00 请登录
PL13533-25mg 25mg ¥10929.00 请登录
PL13533-50mg 50mg ¥15269.00 请登录
PL13533-100mg 100mg 询价 询价
PL13533-10mM*1mLinDMSO 10mM*1mLinDMSO ¥3712.00 请登录
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中文名称
LY2828360
英文名称
LY2828360
英文别名
LY2828360;8-(2-Chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(tetrahydro-2H-pyran-4-yl)-9H-purine;8-(2-chloro-phenyl)-2-methyl-6-(4-methyl-piperazin-1-yl)-9-(tetrahydro-pyran-4-yl)-9h-purine;O12H7VFU6P;BCP29625;BDBM50006250;SB17392;8-(2-chlorophenyl)-2-methyl-6-(4-methylpiperazin-1-yl)-9-(oxan-4-yl)purine;2-Methyl-6-(4-methyl-1-piperazinyl)-8-(2-chlorophenyl)-9-(tetrahydro-2H-pyra
Cas No.
1231220-79-3
分子式
C22H27ClN6O
分子量
426.94
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
LY2828360 是一个作用缓慢但很有效的 G 蛋白偏倚的大麻素受体 2 (CB2) 激动剂,能够抑制 cAMP 的积累并激活 ERK1/2 通路。
生物活性
LY2828360 is a slowly acting but efficacious G protein-biased cannabinoid (CB 2 ) agonist, inhibiting cAMP accumulation and activating ERK1/2 signaling.
性状
Solid
IC50 & Target[1][2]
CB2.
体内研究(In Vivo)
In WT mice, acute systemic administration of LY2828360 suppresses paclitaxel-induced mechanical and cold allodynia in a dose-dependent manner. LY2828360 produces time-dependent suppressions of paclitaxel-evoked mechanical and cold hypersensitivities and suppression of allodynia is maintained for at least 4.5 h post-injection relative to drug pre-injection levels. At 24 h post-injection, paclitaxel-induced mechanical allodynia has returned to drug pre-injection levels of hypersensitivity. Residual suppression of cold allodynia was absent by 72 h post LY2828360 treatment. Previously chronic administration of LY2828360 blocks the development of tolerance to the antiallodynic effects of morphine in WT but not in CB 2 KO mice. Chronic LY2828360 treatment suppresses paclitaxel-induced mechanical and cold allodynia in WT mice but not in CB 2 KO mice previously rende
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Lin X, et al. Slowly Signaling G Protein-Biased CB2 Cannabinoid Receptor Agonist LY2828360 Suppresses Neuropathic Pain with Sustained Efficacy and Attenuates Morphine Tolerance and Dependence. Mol Pharmacol. 2018 Feb;93(2):49-62.
溶解度数据
In Vitro: DMSO : 20.83 mg/mL (48.79 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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