Creation of a S1P Lyase bacterial surrogate for structure-based drug design
- Authors:
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1358847
- Grant/Contract Number:
- AC02-06CH11357
- Resource Type:
- Publisher's Accepted Manuscript
- Journal Name:
- Bioorganic and Medicinal Chemistry Letters
- Additional Journal Information:
- Journal Name: Bioorganic and Medicinal Chemistry Letters Journal Volume: 26 Journal Issue: 9; Journal ID: ISSN 0960-894X
- Publisher:
- Elsevier
- Country of Publication:
- United Kingdom
- Language:
- English
Citation Formats
Argiriadi, Maria A., Banach, David, Radziejewska, Elzbieta, Marchie, Susan, DiMauro, Jennifer, Dinges, Jurgen, Dominguez, Eric, Hutchins, Charles, Judge, Russell A., Queeney, Kara, Wallace, Grier, and Harris, Christopher M. Creation of a S1P Lyase bacterial surrogate for structure-based drug design. United Kingdom: N. p., 2016.
Web. doi:10.1016/j.bmcl.2016.02.084.
Argiriadi, Maria A., Banach, David, Radziejewska, Elzbieta, Marchie, Susan, DiMauro, Jennifer, Dinges, Jurgen, Dominguez, Eric, Hutchins, Charles, Judge, Russell A., Queeney, Kara, Wallace, Grier, & Harris, Christopher M. Creation of a S1P Lyase bacterial surrogate for structure-based drug design. United Kingdom. https://doi.org/10.1016/j.bmcl.2016.02.084
Argiriadi, Maria A., Banach, David, Radziejewska, Elzbieta, Marchie, Susan, DiMauro, Jennifer, Dinges, Jurgen, Dominguez, Eric, Hutchins, Charles, Judge, Russell A., Queeney, Kara, Wallace, Grier, and Harris, Christopher M. Sun .
"Creation of a S1P Lyase bacterial surrogate for structure-based drug design". United Kingdom. https://doi.org/10.1016/j.bmcl.2016.02.084.
@article{osti_1358847,
title = {Creation of a S1P Lyase bacterial surrogate for structure-based drug design},
author = {Argiriadi, Maria A. and Banach, David and Radziejewska, Elzbieta and Marchie, Susan and DiMauro, Jennifer and Dinges, Jurgen and Dominguez, Eric and Hutchins, Charles and Judge, Russell A. and Queeney, Kara and Wallace, Grier and Harris, Christopher M.},
abstractNote = {},
doi = {10.1016/j.bmcl.2016.02.084},
journal = {Bioorganic and Medicinal Chemistry Letters},
number = 9,
volume = 26,
place = {United Kingdom},
year = {Sun May 01 00:00:00 EDT 2016},
month = {Sun May 01 00:00:00 EDT 2016}
}
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1016/j.bmcl.2016.02.084
https://doi.org/10.1016/j.bmcl.2016.02.084
Other availability
Cited by: 9 works
Citation information provided by
Web of Science
Web of Science
Save to My Library
You must Sign In or Create an Account in order to save documents to your library.
Works referenced in this record:
Synthesis of a Fluorogenic Analogue of Sphingosine-1-Phosphate and Its Use to Determine Sphingosine-1-Phosphate Lyase Activity
journal, March 2009
- Bedia, Carmen; Camacho, Luz; Casas, Josefina
- ChemBioChem, Vol. 10, Issue 5
Inhibition of Sphingosine-1-Phosphate Lyase for the Treatment of Autoimmune Disorders
journal, July 2009
- Bagdanoff, Jeffrey T.; Donoviel, Michael S.; Nouraldeen, Amr
- Journal of Medicinal Chemistry, Vol. 52, Issue 13
Incomplete Inhibition of Sphingosine 1-Phosphate Lyase Modulates Immune System Function yet Prevents Early Lethality and Non-Lymphoid Lesions
journal, January 2009
- Vogel, Peter; Donoviel, Michael S.; Read, Robert
- PLoS ONE, Vol. 4, Issue 1
Structure and Function of Sphingosine-1-Phosphate Lyase, a Key Enzyme of Sphingolipid Metabolism
journal, August 2010
- Bourquin, Florence; Riezman, Howard; Capitani, Guido
- Structure, Vol. 18, Issue 8
Lymphocyte Sequestration Through S1P Lyase Inhibition and Disruption of S1P Gradients
journal, September 2005
- Schwab, S. R.
- Science, Vol. 309, Issue 5741
Orally Active 7-Substituted (4-Benzylphthalazin-1-yl)-2-methylpiperazin-1-yl]nicotinonitriles as Active-Site Inhibitors of Sphingosine 1-Phosphate Lyase for the Treatment of Multiple Sclerosis
journal, May 2014
- Weiler, Sven; Braendlin, Nadine; Beerli, Christian
- Journal of Medicinal Chemistry, Vol. 57, Issue 12