U-51605，PGI2 and TXA2 synthase抑制剂(ab120908)
Key features and details
- Selective PGI2 and TXA2 synthase inhibitor. PGH2 analog.
- CAS Number: 64192-56-9
- Purity: > 98%
- Supplied in methyl acetate (5 mg/ml)
- Form / State: Liquid
- Source: Synthetic
概述
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产品名称
U-51605，PGI2 and TXA2 synthase抑制剂 -
描述
Selective PGI2 and TXA2 synthase抑制剂. PGH2 analog. -
纯度
> 98% -
CAS编号
64192-56-9 -
化学结构
性能
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化学名称
9α,11α-Azoprosta-5Z,13E-dien-1-oic acid -
分子量
332.49 -
分子式
C20H32N2O2 -
存放说明
Store at -80°C. Store under desiccating conditions. -
溶解度概述
Supplied in methyl acetate (5 mg/ml) -
处理
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 12 months. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Refer to SDS for further information.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES
CCCCCC/C=C/[C@H]1C2N=NC(C2)C1C/C=CCCCC(=O)O -
来源
Synthetic
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研究领域
图片
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Chemical Structure - U-51605, PGI2 and TXA2 synthase inhibitor (ab120908)2D chemical structure image of ab120908, U-51605, PGI2 and TXA2 synthase inhibitor
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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SDS download
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Datasheet download
文献 (1)
ab120908 被引用在 1 文献中.
- Totoson P et al. Activation of endothelial TrkB receptors induces relaxation of resistance arteries. Vascul Pharmacol 106:46-53 (2018). PubMed: 29471140