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17(S)-HDHA-d5
本产品不向个人销售,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。
17(S)-HDHA-d5图片
规格:98%
分子量:349.5
包装与价格:
包装价格(元)
25ug询价
50ug询价
100ug询价

A neuropeptide with diverse biological activities
货号:ajcx20454
CAS:N/A
分子式:C22H27D5O3
分子量:349.5
溶解度:DMF: miscible,DMSO: miscible,Ethanol: miscible,PBS (pH 7.2): 0.8 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

17(S)-HDHA-d5 is intended for use as an internal standard for the quantification of 17(S)-HDHA by GC- or LC-MS. 17(S)-HDHA is a hydroxy fatty acid formed from docosahexaenoic acid by 15-lipoxygenase (15-LO) and is a precursor to 17(S)-resolvins.1,2 17(S)-HDHA inhibits platelet 12-LO (IC50 = 0.4 μM).1 It inhibits TNF-α-induced expression of IL1B in a human glial cell line (IC50 = ~0.5 nM).2 17(S)-HDHA (100 nM) inhibits NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome formation induced by homocysteine in podocytes.3


|1. Mitchell, P.D., Hallam, C., Hemsley, P.E., et al. Inhibition of platelet 12-lipoxygenase by hydroxy-fatty acids. Biochem. Soc. Trans. 12, 839-841 (1984).|2. Hong, S., Gronert, K., Devchand, P.R., et al. Novel docosatrienes and 17S-resolvins generated from docosahexaenoic acid in murine brain, human blood, and glial cells. Autacoids in anti-inflammation. J. Biol. Chem. 278(17), 14677-14687 (2003).|3. Li, G., Chen, Z., Bhat, O.M., et al. NLRP3 inflammasome as a novel target for docosahexaenoic acid metabolites to abrogate glomerular injury. J. Lipid Res. 58(6), 1080-1090 (2017).

 
 
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