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Author Details

Yaroslav Bilokin
OTAVA LTD
1999
8
6
Jake Y. Chen (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
33850196Vitamin D and lumisterol derivatives can act on liver X receptors (LXRs).Sci Rep2021
33850196Vitamin D and lumisterol derivatives can act on liver X receptors (LXRs).Sci Rep2021
32683178Flavone inspired discovery of benzylidenebenzofuran-3(2H)-ones (aurones) as potent inhibitors of human protein kinase CK2.Bioorg Chem2020
32683178Flavone inspired discovery of benzylidenebenzofuran-3(2H)-ones (aurones) as potent inhibitors of human protein kinase CK2.Bioorg Chem2020
24533775In vitro Activation of heme oxygenase-2 by menadione and its analogs.Med Gas Res2014
24533775In vitro Activation of heme oxygenase-2 by menadione and its analogs.Med Gas Res2014
22178909Electrochemical screening of the indole/quinolone derivatives as potential protein kinase CK2 inhibitors.Anal Biochem2012
23127989Discovery of new scaffolds for rational design of HCV NS5B polymerase inhibitors.Eur J Med Chem2012
22178909Electrochemical screening of the indole/quinolone derivatives as potential protein kinase CK2 inhibitors.Anal Biochem2012
23127989Discovery of new scaffolds for rational design of HCV NS5B polymerase inhibitors.Eur J Med Chem2012
14995181Efficient stereoselective alkenylation through a homolytic domino reaction involving a 1,5 sulfur-to-carbon translocation.J Am Chem Soc2004
14995181Efficient stereoselective alkenylation through a homolytic domino reaction involving a 1,5 sulfur-to-carbon translocation.J Am Chem Soc2004
12126403Approach toward the total synthesis of orevactaene. 2. Convergent and stereoselective synthesis of the C18-C31 domain of orevactaene. Evidence for the relative configuration of the side chain.J Org Chem2002
12126403Approach toward the total synthesis of orevactaene. 2. Convergent and stereoselective synthesis of the C18-C31 domain of orevactaene. Evidence for the relative configuration of the side chain.J Org Chem2002
10889323Synthesis and anti-inflammatory activity of N-substituted 2-oxo-2H-1-benzopyran-3-carboxamides and their 2-iminoanalogues.Eur J Med Chem1999
10889323Synthesis and anti-inflammatory activity of N-substituted 2-oxo-2H-1-benzopyran-3-carboxamides and their 2-iminoanalogues.Eur J Med Chem1999
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Collaborators

Andriy G Golub
OTAVA LTD
Co-authored papers 4
Yuwei Song
Anyang Institute of Technology
Co-authored papers 1
David K Crossman
University of Alabama at Birmingham
Co-authored papers 1
Shariq Qayyum
University of Alabama at Birmingham
Co-authored papers 1
Zorica Janjetovic
University of Alabama at Birmingham
Co-authored papers 1
Venkatram R Atigadda
Heersink School of Medicine, University of Alabama at Birmingham
Co-authored papers 1
Anton M Jetten
National Institutes of Health
Co-authored papers 1
Radomir M Slominski
University of Alabama at Birmingham
Co-authored papers 1
Carlos A Mier-Aguilar
University of Alabama at Birmingham
Co-authored papers 1
Jake Y Chen
Co-authored papers 1
Jake Y. Chen (CM4AI)
University of Alabama at Birmingham
Co-authored papers 1
Tae-Kang Kim
University of Alabama at Birmingham
Co-authored papers 1
Allen S W Oak
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 1
Edith K Y Tang
The University of Western Australia
Co-authored papers 1
Andrzej T Slominski
University of Alabama at Birmingham
Co-authored papers 1
Chander Raman
University of Alabama at Birmingham
Co-authored papers 1
Robert C Tuckey
The University of Western Australia
Co-authored papers 1
Joanna Stefan
University of Alabama at Birmingham, 1670 University Blvd
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Yuhua Song
The University of Alabama at Birmingham
Co-authored papers 1
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