| Identification | Back Directory | [Name]
(17R,5Z,8Z,11Z,14Z)-17-HYDROXY-5,8,11,14-EICOSATETRAENOIC ACID | [CAS]
183509-24-2 | [Synonyms]
17(R)-HETE
OPPIPPRXLIDJKN-DWUYYRGZSA-N
17(R)-hydroxy-5(Z),8(Z),11(Z),14(Z)-eicosatetraenoic acid
(17R,5Z,8Z,11Z,14Z)-17-HYDROXY-5,8,11,14-EICOSATETRAENOIC ACID
(17R,5Z,8Z,11Z,14Z)-17-hydroxyeicosa-5,8,11,14-tetraenoic acid | [Molecular Formula]
C20H32O3 | [MDL Number]
MFCD11113136 | [MOL File]
183509-24-2.mol | [Molecular Weight]
320.47 |
| Chemical Properties | Back Directory | [Boiling point ]
477.3±33.0 °C(Predicted) | [density ]
0.984±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
0.1 M Na2CO3: 2 mg/ml; DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS (pH 7.2): 0.8 mg/ml | [pka]
4.75±0.10(Predicted) |
| Hazard Information | Back Directory | [Description]
Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 17-HETE is a cytochrome P450 (CYP450) metabolite of arachidonic acid that has stereospecific effects on sodium transport in the kidney. 17(R)-HETE is an inactive isomer of 17-HETE, whereas the (S) enantiomer can inhibit proximal tubule ATPase activity at a concentration of 2 μM. 1 | [Uses]
17R-HETE is an arachidonic acid metabolite through cytochrome P-450 pathways. 17R-HETE exhibits efficacy in inducing cardic hypertrophy with less efficiency with compared to 17S-HETE[1][2]. | [storage]
Store at -20°C | [References]
1. Carroll, M.A., Balazy, M., Margiotta, P., et al. Cytochrome P-450-dependent HETEs: Profile of biological activity and stimulation by vasoactive peptides Am. J. Physiol. 271(4 Pt 2),R863-R869(1996). |
|
|