Stereochemistry of leukotriene B4 metabolites formed by the reductase pathway in porcine polymorphonuclear leukocytes: inversion of stereochemistry of the 12-hydroxyl group
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00457a013
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Dehydrogenase reductase 9 (SDR9C4) and related homologs recognize a broad spectrum of lipid mediator oxylipins as substrates;Journal of Biological Chemistry;2022-01
2. The medicinal chemistry of stable synthetic leukotriene B3 and B4 analogues;Future Medicinal Chemistry;2012-05
3. Formation of cis, trans Conjugated Olefin Possessing a Hydroxyl Group Next to the cis Olefin End and Synthesis of Biologically Active Molecules with This Functionality.;Journal of Synthetic Organic Chemistry, Japan;2002
4. The Metabolism of Leukotriene B4in Lewis Lung Carcinoma Porcine Kidney Cells;American Journal of Respiratory and Critical Care Medicine;2000-02
5. Synthesis of 10,11-Dihydroleukotriene B4 Metabolites via a Nickel-Catalyzed Coupling Reaction of cis-Bromides and trans-Alkenyl Borates;The Journal of Organic Chemistry;2000-01-20
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