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Sofiya Leshchenko
Observed names:
S. Leshchenko,
Sofiya Leshchenko-Yashchuk
Observed institutions:
University of Debrecen,
Georgia State University,
Rosalind Franklin University of Medicine and Science,
Purdue University West Lafayette,
University of Illinois Chicago,
National Cancer Institute,
Kumamoto University
show all 7
OpenAlex ID:
A5082575233
High Resolution Crystal Structures of HIV-1 Protease with a Potent Non-peptide Inhibitor (UIC-94017) Active Against Multi-drug-resistant Clinical Strains
2004
·
Yunfeng Tie
, Peter I. Boross
, et al.
·
Journal of Molecular Biology
·
230
Structure-Based Design of Novel HIV-1 Protease Inhibitors To Combat Drug Resistance
2006
·
Arun K. Ghosh
, Perali Ramu Sridhar
, et al.
·
Journal of Medicinal Chemistry
·
155
Ultra-high Resolution Crystal Structure of HIV-1 Protease Mutant Reveals Two Binding Sites for Clinical Inhibitor TMC114
2006
·
Andrey Y. Kovalevsky
, Fengling Liu
, et al.
·
Journal of Molecular Biology
·
147
Effectiveness of Nonpeptide Clinical Inhibitor TMC-114 on HIV-1 Protease with Highly Drug Resistant Mutations D30N, I50V, and L90M
2006
·
Andrey Yu. Kovalevsky
, Yunfeng Tie
, et al.
·
Journal of Medicinal Chemistry
·
140
Stereoselective Photochemical 1,3-Dioxolane Addition to 5-Alkoxymethyl-2(5H)-furanone: Synthesis of Bis-tetrahydrofuranyl Ligand for HIV Protease Inhibitor UIC-94017 (TMC-114)
2004
·
Arun K. Ghosh
, Sofiya Leshchenko
, et al.
·
The Journal of Organic Chemistry
·
135
Design and synthesis of novel HIV-1 protease inhibitors incorporating oxyindoles as the P 2 ′ -ligands
2006
·
Arun K. Ghosh
, Gary Schiltz
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
109
In Vitro Selection of Highly Darunavir-Resistant and Replication-Competent HIV-1 Variants by Using a Mixture of Clinical HIV-1 Isolates Resistant to Multiple Conventional Protease Inhibitors
2010
·
Yasuhiro Koh
, Masayuki Amano
, et al.
·
Journal of Virology
·
95
Design of HIV-1 Protease Inhibitors with Pyrrolidinones and Oxazolidinones as Novel P1′-Ligands To Enhance Backbone-Binding Interactions with Protease: Synthesis, Biological Evaluation, and Protein−Ligand X-ray Studies
2009
·
Arun K. Ghosh
, Sofiya Leshchenko-Yashchuk
, et al.
·
Journal of Medicinal Chemistry
·
65
Structure-Based Design: Synthesis and Biological Evaluation of a Series of Novel Cycloamide-Derived HIV-1 Protease Inhibitors
2005
·
Arun K. Ghosh
, Lisa M. Swanson
, et al.
·
Journal of Medicinal Chemistry
·
64
Potent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein–ligand X-ray studies
2008
·
Arun K. Ghosh
, Sandra Gemma
, et al.
·
Organic & Biomolecular Chemistry
·
16
Corrigendum to “Ultra-high Resolution Crystal Structure of HIV-1 Protease Mutant Reveals Two Binding Sites for Clinical Inhibitor TMC114” [J. Mol. Biol. 363 (2006) 161–173]
2006
·
Andrey Y. Kovalevsky
, Fengling Liu
, et al.
·
Journal of Molecular Biology
Design and Synthesis of Novel HIV‐1 Protease Inhibitors Incorporating Oxyindoles as the P2′‐Ligands.
2006
·
Arun K. Ghosh
, Gary Schiltz
, et al.
·
ChemInform
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Works count:
16
Citation count:
1,156
H-index:
10
I10-index:
10
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