(±)16-HETE
- Product Name
- (±)16-HETE
- CAS No.
- 128914-46-5
- Chemical Name
- (±)16-HETE
- Synonyms
- (±)16-HETE;JEKNPVYFNMZRJG-UFINWASNSA-N;(±)16-HETE, CAS 128914-46-5;16-hydroxy-5(Z),8(Z),11(Z),14(Z)-ETA;16-hydroxy-5(Z),8(Z),11(Z),14(Z)-eicosatetraenoic acid;5,8,11,14-Eicosatetraenoic acid, 16-hydroxy-, (5Z,8Z,11Z,14Z)-
- CBNumber
- CB02589794
- Molecular Formula
- C20H32O3
- Formula Weight
- 320.47
- MOL File
- 128914-46-5.mol
(±)16-HETE Property
- 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
N-Bromosuccinimide Price
- Product number
- 10010635
- Product name
- (±)16-HETE
- Purity
- ≥98%
- Packaging
- 25μg
- Price
- $146
- Updated
- 2024/03/01
- Product number
- 10010635
- Product name
- (±)16-HETE
- Purity
- ≥98%
- Packaging
- 50μg
- Price
- $278
- Updated
- 2024/03/01
- Product number
- 10010635
- Product name
- (±)16-HETE
- Purity
- ≥98%
- Packaging
- 100μg
- Price
- $525
- Updated
- 2024/03/01
(±)16-HETE Chemical Properties,Usage,Production
Description
Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. (±)16-
Uses
16-HETE is arachidonic acid metabolite through subterminal hydroxylation by cytochrome P-450. 16-HETE exhibits vasodilatory and PMN inhibitory effects and serves as biomarker for early stages of non-alcoholic fatty liver disease[1][2][3].
Definition
ChEBI: A HETE that consists of arachidonic acid bearing an additional hydroxy substituent at position 16.
in vivo
16-HETE (1-20 μg, i.a.) is stereospecificially involved in vasodilation, regulation of renal perfusion and in mechanisms of tubular transport with S- enantiomer in New Zealand white rabbit[2].
16-HETE (1 μg/kg/min) suppresses the increase of intracranial pressure (ICP) in a rabbit model of thromboembolic stroke[1].
| Animal Model: | New Zealand White rabbit[2] |
| Dosage: | 1-20 μg |
| Administration: | injection into artery |
| Result: | 16S inhibited 60% ATPase activity at the concentration of 2 μM, while 16R enantiomer remained inactive. |
| Animal Model: | New Zealand White rabbit[1] |
| Dosage: | 1 μg/kg/min |
| Administration: | 6 hours constant infusion from Hours 1 to 2 after autologous clot embolization |
| Result: | Reduced infarction area and less increased ICP. |
References
[1] Bednar MM, et al., 16(R)-hydroxyeicosatetraenoic acid, a novel cytochrome P450 product of arachidonic acid, suppresses activation of human polymorphonuclear leukocyte and reduces intracranial pressure in a rabbit model of thromboembolic stroke. Neurosurgery. 2000 Dec;47(6):1410-8; discussion 1418-9. PMID:11126912
[2] Carroll MA, e al., Cytochrome P-450-dependent HETEs: profile of biological activity and stimulation by vasoactive peptides. Am J Physiol. 1996 Oct;271(4 Pt 2):R863-9. DOI:10.1152/ajpregu.1996.271.4.R863
[3] Maciejewska D, et al., Metabolites of arachidonic acid and linoleic acid in early stages of non-alcoholic fatty liver disease--A pilot study. Prostaglandins Other Lipid Mediat. 2015 Sep;121(Pt B):184-9. DOI:10.1016/j.prostaglandins.2015.09.003
(±)16-HETE Preparation Products And Raw materials
Raw materials
Preparation Products
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