CAS 942069-11-6
:(5Z,8Z,11Z,14Z)-20-Hydroxy-N-(2-hydroxyethyl)-5,8,11,14-eicosatetraenamide
Description:
The chemical substance known as "(5Z,8Z,11Z,14Z)-20-Hydroxy-N-(2-hydroxyethyl)-5,8,11,14-eicosatetraenamide," with the CAS number 942069-11-6, is a synthetic derivative of arachidonic acid, characterized by its multiple double bonds and hydroxyl groups. This compound features a long hydrocarbon chain, specifically an eicosatetraene backbone, which contributes to its amphiphilic nature, allowing it to interact with both hydrophilic and hydrophobic environments. The presence of the hydroxyl group at the 20th position and the N-(2-hydroxyethyl) substituent enhances its solubility in polar solvents and may influence its biological activity. Such compounds are often studied for their potential roles in signaling pathways, particularly in relation to inflammation and cellular responses. The specific stereochemistry indicated by the Z configurations suggests that the double bonds are in the cis configuration, which is crucial for the compound's biological function and interaction with cellular membranes. Overall, this substance is of interest in biochemical research, particularly in the context of lipid signaling and pharmacology.
Formula:C22H37NO3
InChI:InChI=1S/C22H37NO3/c24-20-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-22(26)23-19-21-25/h1,3-4,6-7,9-10,12,24-25H,2,5,8,11,13-21H2,(H,23,26)/b3-1-,6-4-,9-7-,12-10-
InChI key:InChIKey=QRMZDMUHHZLRMH-DTLRTWKJSA-N
SMILES:C(C/C=C\C/C=C\C/C=C\C/C=C\CCCCCO)CC(NCCO)=O
Synonyms:- (5Z,8Z,11Z,14Z)-20-Hydroxy-N-(2-hydroxyethyl)-5,8,11,14-eicosatetraenamide
- 5,8,11,14-Eicosatetraenamide, 20-hydroxy-N-(2-hydroxyethyl)-, (5Z,8Z,11Z,14Z)-
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Found 2 products.
20-hydroxy-N-(2-hydroxyethyl)-5(Z),8(Z),11(Z),14(Z)-eicosatetraenamide
CAS:Formula:C22H37NO3Purity:>98%Color and Shape:In solution, EthanolMolecular weight:363.5320-Hydroxy-N-(2-hydroxyethyl)-5(Z),8(Z),11(Z),14(Z)-eicosatetraenamide
CAS:<p>20-Hydroxy-N-(2-hydroxyethyl)-5(Z),8(Z),11(Z),14(Z)-eicosatetraenamide is a specialized bioactive lipid, which is synthesized from arachidonic acid via enzymatic processes in the body. It functions primarily by modulating inflammatory pathways, and it acts as an endogenous mediator with significant roles in cellular signaling. Through its binding to specific receptors, it can influence immune responses and cellular homeostasis, exhibiting potent anti-inflammatory effects.</p>Formula:C22H37NO3Purity:Min. 95%Molecular weight:363.5 g/mol

