Arachidonic acid - 90%

CAS : 506-32-1

Ref. 3D-FA164836

Informations sur le produit

• Nom: Arachidonic acid - 90%
• Synonymes: (5E,8E,11E,14E)-icosa-5,8,11,14-tetraenoic acid, (5Z,8Z,11Z,14Z)-5,8,11,14-Eicosatetraenoic acid, (5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraenoic acid, (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoic acid, (all-Z)-5,8,11,14-Eicosatetraenoic acid, 20:4N-6, 5,8,11,14-Eicosatetraenoic Acid, 5,8,11,14-Eicosatetraenoic Acid (7CI,8CI,9CI), 5,8,11,14-Eicosatetraenoic acid, (5Z,8Z,11Z,14Z)-, 5,8,11,14-Eicosatetraenoic acid, (all-Z)-, 5,8,11,14-all-cis-Eicosatetraenoic acid, 5-cis,8-cis,11-cis,14-cis-Eicosatetraenoic acid, 5Z,8Z,11Z,14Z-Eicosatetraenoic acid, A 0871, ARA, Acide Icosa-5,8,11,14-Tetraenoique, Acido Icosa-5,8,11,14-Tetraenoico, Arachidonate, Icosa-5,8,11,14-Tetraenoic Acid, Icosa-5,8,11,14-tetraensaure, Immunocytophyt, Immunocytophyte, Vevodar, all-cis-5,8,11,14-Eicosatetraenoic acid, cis-Δ5,8,11,14-Eicosatetraenoic acid, cis-Δ^5,8,11,14-Eicosatetraenoic acid
• CAS: 506-32-1

Description

Arachidonic acid is a type of omega-6 fatty acid that belongs to the class of eicosanoids. It is metabolized by cyclooxygenase and lipoxygenase, which are enzymes that synthesize this compound from arachidonic acid. Arachidonic acid is involved in the inflammatory response and can be used for the treatment of infectious diseases. This agent has been shown to be effective against bowel disease, as well as other diseases such as Crohn's disease, ulcerative colitis, and rheumatoid arthritis. Arachidonic acid also has anti-inflammatory properties, which may be due to its ability to inhibit signal pathways in human polymorphonuclear leukocytes.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 304.47 g/mol
• Formule: C₂₀H₃₂O₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C20H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-19H2,1H3,(H,21,22)/b7-6-,10-9-,13-12-,16-15-
• Code InChI: InChIKey=YZXBAPSDXZZRGB-DOFZRALJSA-N
• SMILES: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O