Hoe‐Sup Byun

Biochemistry, Genetics and Molecular Biology · Life Sciences

28h-index2.4kcitations73works0.02yr avg
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Research Topics

Sphingolipid Metabolism and Signaling(30), Carbohydrate Chemistry and Synthesis(19), Synthetic Organic Chemistry Methods(13), Lipid Membrane Structure and Behavior(12), Chemical Synthesis and Analysis(9)

Publications73 total

Chemical Preparation of Sphingosine and Sphingolipids
2018· 2 cited
Effect of ether glycerol lipids on interleukin-1β release and experimental autoimmune encephalomyelitis
Chemistry and Physics of Lipids·2015· 6 cited
A Fluorescent Alkyllysophospholipid Analog Exhibits Selective Cytotoxicity Against the Hormone-Insensitive Prostate Cancer Cell Line PC3
Anti-Cancer Agents in Medicinal Chemistry·2014· 2 cited
Novel sphingosine-containing analogues selectively inhibit sphingosine kinase (SK) isozymes, induce SK1 proteasomal degradation and reduce DNA synthesis in human pulmonary arterial smooth muscle cells
MedChemComm·2013· 58 citedOpen Access
Practical multigram-scale synthesis of 4,6- and 4,8-sphingadienes, chemopreventive sphingoid bases
Chemistry and Physics of Lipids·2012· 4 citedOpen Access
The sphingolipid degradation product trans-2-hexadecenal forms adducts with DNA
Biochemical and Biophysical Research Communications·2012· 28 citedOpen Access
Chemopreventive sphingadienes downregulate Wnt signaling via a PP2A/Akt/GSK3β pathway in colon cancer
Carcinogenesis·2012· 68 citedOpen Access
An active endocytosis pathway is required for the cytotoxic effects of glycosylated antitumor ether lipids.
PubMed·2011· 15 cited
NKT TCR Recognition of CD1d-α-<i>C</i>-Galactosylceramide
The Journal of Immunology·2011· 55 citedOpen Access
Total Synthesis of α-1<i>C</i>-Galactosylceramide, an Immunostimulatory <i>C</i>-Glycosphingolipid, and Confirmation of the Stereochemistry in the First-Generation Synthesis
The Journal of Organic Chemistry·2011· 23 cited
Corrigendum to “The sphingolipid degradation product trans-2-hexadecenal induces cytoskeletal reorganization and apoptosis in a JNK-dependent manner” [Cell. Signal. 23(7) (2011) 1144-1152]
Cellular Signalling·2011· 1 cited
The sphingolipid degradation product trans-2-hexadecenal induces cytoskeletal reorganization and apoptosis in a JNK-dependent manner
Cellular Signalling·2011· 105 citedOpen Access
Selective deuterium labeling of the sphingoid backbone: facile syntheses of 3,4,5-trideuterio-d-erythro-sphingosine and 3-deuterio-d-erythro-sphingomyelin
Chemistry and Physics of Lipids·2010· 10 citedOpen Access
Characterization of sphingosine-1-phosphate lyase activity by electrospray ionization–liquid chromatography/tandem mass spectrometry quantitation of (2E)-hexadecenal
Analytical Biochemistry·2010· 38 citedOpen Access
ChemInform Abstract: An Improved Two‐Step Synthetic Route to Primary Allylic Alcohols from Aldehydes.
ChemInform·2010
Synthesis and Antitumor Activity of Ether Glycerophospholipids Bearing a Carbamate Moiety at the <i>sn</i>‐2 Position: Selective Sensitivity Against Prostate Cancer Cell Lines
ChemMedChem·2010· 9 cited
Asymmetric Synthesis of <scp>d</scp>-<i>ribo</i>-Phytosphingosine from 1-Tetradecyne and (4-Methoxyphenoxy)acetaldehyde
The Journal of Organic Chemistry·2010· 23 cited
Synthesis of Immunostimulatory α-<i>C</i>-Galactosylceramide Glycolipids via Sonogashira Coupling, Asymmetric Epoxidation, and Trichloroacetimidate-Mediated Epoxide Opening
Organic Letters·2010· 38 cited
An improved two-step synthetic route to primary allylic alcohols from aldehydes
New Journal of Chemistry·2010· 25 cited
A glycosylated antitumor ether lipid kills cells via paraptosis-like cell death
Biochemistry and Cell Biology·2009· 29 cited
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Frequent Co-authors

Robert Bittman(49), Linli He(9), Jiong Chun(7), Gilbert Arthur(6), Zheng Liu(5), Pranati Samadder(5), Ning Zhong(4), Ashok Kumar(3), Julie D. Saba(3), Kasireddy Chandraprakash Reddy(3), Daniel L. Baker(2), Glenn D. Prestwich(2), Gábor Tigyi(2), Rhoderick E. Brown(2), Richard W. Franck(2), Xuequan Lu(2), Meni Wanunu(2), Ravi Kumar Erukulla(2), Erukulla Ravi Kumar(2), Peter Mattjus(2)