E. Sudbeck
Publications by Year
Research Areas
Crystallization and Solubility Studies, X-ray Diffraction in Crystallography, HIV/AIDS drug development and treatment, HIV Research and Treatment, Crystallography and molecular interactions
Most-Cited Works
- → Rational Design and Synthesis of a Novel Anti-leukemic Agent Targeting Bruton′s Tyrosine Kinase (BTK), LFM-A13 [α-Cyano-β-Hydroxy-β-Methyl-N-(2,5-Dibromophenyl)Propenamide](1999)189 cited
- Structure-based design of specific inhibitors of Janus kinase 3 as apoptosis-inducing antileukemic agents.(1999)
- → Synthesis, X-ray structure, and anti-leukemic activity of oxovanadium(IV) complexes(2000)120 cited
- → Anti-HIV activity of aromatic and heterocyclic Thiazolyl Thiourea compounds(2001)87 cited
- → Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reverse transcriptase(1998)79 cited
- → Dye solubilization in polyelectrolyte—micelle complexes(1991)61 cited
- → Structure-based drug design of non-nucleoside inhibitors for wild-type and drug-resistant HIV reverse transcriptase(2000)59 cited
- → Potent Inhibition of Influenza Sialidase by a Benzoic Acid Containing a 2-Pyrrolidinone Substituent(1999)59 cited
- → Complexes of Lysine, Histidine, and Arginine with Sulfonated Azo Dyes: Model Systems for Understanding the Biomolecular Recognition of Glycosaminoglycans by Proteins(1996)59 cited
- → Structure-based design of N-[2-(1-piperidinylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N′-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase(1998)55 cited