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Alprostadil
本半岛bd体育手机客户端 不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Alprostadil图片
CAS NO: 745-65-3
包装与价格:
包装 价格(元)
10mM (in 1mL DMSO) 电议
10mg 电议
50mg 电议

半岛bd体育手机客户端 介绍

化学性质

Physical Appearance A solid
Storage Store at -20°C
M.Wt 354.48
Cas No. 745-65-3
Formula C20H34O5
Solubility insoluble in H2O; ≥13.4 mg/mL in DMSO; ≥47.1 mg/mL in EtOH
Chemical Name 7-[(1R,2R,3R)-3-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid
Canonical SMILES CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O
运输条件 蓝冰运输或根据您的需求运输。
一般建议 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。不同厂家不同批次半岛bd体育手机客户端 溶解度各有差异,仅做参考。若实验所需浓度过大至半岛bd体育手机客户端 溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

Prostaglandin E1 (Alprostadil) is a prostaglandin, which is used in the treatment of erectile dysfunction and has vasodilatory properties.

试验操作

Cell experiment:[1]

Cell lines

Human umbilical vein endothelial cells (HUVECs)

Reaction Conditions

0 ~ 10 μM alprostadil

Applications

Alprostadil (1 nM ~ 10 μM; 48 h) concentration-dependently reduced HUVEC proliferation (up to 100% inhibition) in the presence of 20 ng/mL vascular endothelial growth factor (VEGF), with an IC50 of 400 nM. Alprostadil (0.01 ~ 10 μM; 6 h) also inhibited VEGF-induced HUVEC migration in a concentration dependent manner, with an IC50 of 500 nM.

Animal experiment:[1]

Animal models

Female C57/bl6 mice, 6 ~ 8 weeks of age

Dosage form

20 ng

Administered subcutaneously for 4 days

Applications

Alprostadil treatment (20 ng/animal/day; 4 days) significantly inhibited the fibroblast growth factor (FGF)-induced angiogenesis in mice. Alprostadil could be useful for diseases that require anti-angiogenic therapy, such as diabetic retinopathy and solid tumors.

Note

The technical data provided above is for reference only.

References:

1. Cattaneo MG, Pola S, Dehò V, et al. Alprostadil suppresses angiogenesis in vitro and in vivo in the murine Matrigel plug assay. British Journal of Pharmacology, 2003, 138(2): 377-385.

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