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ChemicalBook--->CAS DataBase List--->54845-95-3

54845-95-3

54845-95-3 Structure

54845-95-3 Structure
IdentificationBack Directory
[Name]

15(S)-HETE
[CAS]

54845-95-3
[Synonyms]

C04742
AL12959
AL-12959
AL 12959
Icomucret
15(S)-HETE
(S)-15-HETE
JSFATNQSLKRBCI-VAEKSGALSA-N
15(S)-HETE MaxSpec Standard
15(S)-HETE Lipid Maps MS Standard
15(S)-HYDROXYEICOSA-5Z,8Z,11Z,13E-TETRAENOIC ACID
15(S)-HYDROXY-(5Z,8Z,11Z,13E)-EICOSATETRAENOIC ACID
(15s,5z,8z,11z,13e)-15-hydroxyeicosatetraenoic acid
(15S)-15-Hydroxy-5,8,11-cis-13-trans-icosatetraenoate
(15S)-15-Hydroxy-5,8,11-cis-13-trans-eicosatetraenoate
(5Z,8Z,11Z,13E,15S)-15-hydroxyicosa-5,8,11,13-tetraenoic acid
(5Z,8Z,11Z,13E,15S)-15-Hydroxy-5,8,11,13-icosatetraenoic acid
5,8,11,13-Eicosatetraenoic acid, 15-hydroxy-, (5Z,8Z,11Z,13E,15S)-
[Molecular Formula]

C20H32O3
[MDL Number]

MFCD00063590
[MOL File]

54845-95-3.mol
[Molecular Weight]

320.47
Chemical PropertiesBack Directory
[Boiling point ]

487.7±45.0 °C(Predicted)
[density ]

0.984±0.06 g/cm3(Predicted)
[Fp ]

14℃
[storage temp. ]

-20°C
[solubility ]

0.1 M Na2CO3: 2 mg/ml; DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS (pH 7.2): 0.8 mg/ml
[form ]

Liquid.
[pka]

4.75±0.10(Predicted)
[BRN ]

2470466
Safety DataBack Directory
[Hazard Codes ]

F,Xi
[Risk Statements ]

11-36/37/38
[Safety Statements ]

7-16-26-36
[RIDADR ]

UN 1170 3/PG 2
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway. In mammals, 15(S)-HETE is synthesized in the respiratory epithelium, leukocytes, and reticulocytes. 15(S)-HETE is present in μg/ml concentrations in the nasal secretions of allergic rhinitis.
[Uses]

15(S)-HETE is a major arachidonic acid metabolite from the 15-lipoxygenase pathway. In mammals, 15(S)-HETE is synthesized in the respiratory epithelium, leukocytes, and reticulocytes. 15(S)-HETE is present in μg/ml concentrations in the nasal secretions of allergic rhinitis.
[Uses]

15(S)-HETE is an arachidonic acid metabolite with immunosuppressive activity.
[Definition]

ChEBI: An optically active form of 15-HETE having 15(S)-configuration..
[General Description]

15(S)-HETE is a product of the arachidonic acid pathway. It is synthesized by the human lungs and airway epithelial cells. 15(S)-HETE is a potent mucosecretagogue in human airways. It is a metabolite of 15-lipoxygenase. 15(S)-HETE is an endogenous ligand for peroxisome proliferator-activated receptor γ (PPARγ).
[Biochem/physiol Actions]

Metabolite of arachidonic acid via the 15-lipoxygenase pathway that may be involved in pulmonary anti-inflammatory responses through the inhibition of 5-lipoxygenase. 15(S)-HETE suppresses the incorporation of thymidine and biosynthesis of prostaglandin E2 in tumor cell cultures. Treatment of colon cancer cells with 15(S)-HETE inhibited cell proliferation and induced apoptosis, which was preceded by an increase in TGF-beta-inducible early gene (TIEG) and a decrease in Bcl-2.
[storage]

Store at -20°C
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