全部分类
  • Lumula
Lumula的可视化放大

Lumula

A hybrid eicosanoid analog

此产品仅用于科学研究,我们不为任何个人用途提供产品和服务

Lumula的二维码
  • 库存: 现货
可选规格
  • 包装
    价格
    促销价
    数量
  • 1mg
    ¥1175.00
    940.00
    - +
  • 5mg
    ¥5162.00
    4130.00
    - +
  • 10mg
    ¥9200.00
    7360.00
    - +
已选 0 0
金额: ¥0.00
首页 收藏
  • 货号: ajcx18640
  • CAS: N/A
  • 别名: Maxeyprost, Unoprostone Nethyl amide
  • 分子式: C24H43NO4
  • 分子量: 409.6
  • 纯度: >98%
  • 溶解度: DMF: 30 mg/ml,DMSO: 25 mg/ml,Ethanol: 50 mg/ml,Ethanol:PBS (pH 7.2): miscible
  • 储存: Store at -20°C
  • 库存: 现货

Background

There are currently four prostaglandin (PG) derivatives which have been approved for human clinical use for the treatment of glaucoma. The names of the PGs and the concentrations of the approved doses are: travoprost (40 µg/ml), latanoprost (50 µg/ml), bimatoprost (300 µg/ml), and unoprostone (1,500 µg/ml). All of these compounds are modified at C-1 in order to act as lipophilic prodrugs in the eye. All have also been postulated to function via activation of the prostanoid FP receptor. Unoprostone and bimatoprost stand out in this class due to their lack of potency. Both are also claimed to have "alternate" mechanisms of actions: as a "docosanoid" in the case of unoprostone and as a "prostamide" in the case of bimatoprost. Lumula is a hybrid eicosanoid analog which incorporates the "docosanoid" features of unoprostone as well as the "prostamide" features of bimatoprost. Based on classical structure-activity relationships which have been established for prostanoid receptors, one would predict very low activity for lumula. The N-ethyl amide prodrug moiety which it inherits from bimatoprost is slow to hydrolyze, and the lower side chain modifications inherited from unoprostone interfere with FP receptor binding. Lumula is therefore a good tool for testing the validity of the alternate mechanism theories.

温馨提示 ×
商品已成功加入购物车!
购物车共 0 件商品
去购物车结算