Asymmetric synthesis of the stereoisomers of 11,12,15(S)-trihydroxyeicosa-5(Z),8(Z),13(E)-trienoic acid, a potent endothelium-derived vasodilator
- 4 October 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (19) , 4987-4990
- https://doi.org/10.1016/j.bmcl.2004.07.019
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Rabbit aorta converts 15-HPETE to trihydroxyeicosatrienoic acids: potential role of cytochrome P450Archives of Biochemistry and Biophysics, 2003
- Interleukin-13 Upregulates Vasodilatory 15-Lipoxygenase Eicosanoids in Rabbit AortaArteriosclerosis, Thrombosis, and Vascular Biology, 2003
- Lipids and endothelium‐dependent vasodilation—A reviewLipids, 2002
- The HepoxilinsPublished by Springer Nature ,1999
- Identification of the 11,14,15- and 11,12,15-Trihydroxyeicosatrienoic Acids as Endothelium-derived Relaxing Factors of Rabbit AortaJournal of Biological Chemistry, 1998
- Identification of Epoxyeicosatrienoic Acids as Endothelium-Derived Hyperpolarizing FactorsCirculation Research, 1996
- A novel potent vasoconstrictor peptide produced by vascular endothelial cellsNature, 1988
- Endothelium-derived relaxing factor produced and released from artery and vein is nitric oxide.Proceedings of the National Academy of Sciences, 1987
- The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholineNature, 1980
- An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregationNature, 1976