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http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_35/101021ja072777z/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_15/101021jm800136b/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_17/101021jm800555h/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_6/101021jm049614v/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_10/101021jm0601147/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_4/101021ja039671y/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_30/101021ja0526416/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_14/101021jm061414r/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_4/101021jm701210y/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_51/101021ja038672n/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_23/101021jo035119f/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_1/101021ja038162t/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_36/101021ja0632862/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_49/101021ja064228j/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_45/101021ja073989z/authorship/10
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_49/101021ja075398e/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_43/101021ja064522b/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_5/101021jm0611509/authorship/3
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Optimization of the Central Heterocycle of α-Ketoheterocycle Inhibitors of Fatty Acid Amide Hydrolase
Asymmetric Synthesis of Inhibitors of Glycinamide Ribonucleotide Transformylase
Total Synthesis and Examination of Three Key Analogues of Ramoplanin:A Lipoglycodepsipeptide with Potent Antibiotic Activity
Fundamental Role of the Fostriecin Unsaturated Lactone and Implications forSelective Protein Phosphatase Inhibition
Total Synthesis of Piericidin A1 and B1 and Key Analogues
A Unique Class of Duocarmycin and CC-1065 AnaloguesSubject to Reductive Activation
Delineation of a Fundamental α-Ketoheterocycle Substituent Effect for Use inthe Design of Enzyme Inhibitors
Synthesis and Evaluation of Duocarmycin and CC-1065 AnaloguesIncorporating the1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]-3-azaindol-4-one (CBA)Alkylation Subunit
Total Synthesis of Ningalin D
Discovery of a Potent, Nonpolyglutamatable Inhibitor of Glycinamide RibonucleotideTransformylase
Systematic Exploration of the Structural Features ofYatakemycin Impacting DNA Alkylation and Biological Activity
Potent and Selective α-Ketoheterocycle-Based Inhibitors of the Anandamide and OleamideCatabolizing Enzyme, Fatty Acid Amide Hydrolase
Establishing the Parabolic Relationship between Reactivity and Activity forDerivatives and Analogues of the Duocarmycin and CC-1065 AlkylationSubunits
Rational Design, Synthesis, and Evaluation of Key Analoguesof CC-1065 and the Duocarmycins
Asymmetric Total Synthesis of (+)- and ent-(−)-Yatakemycinand Duocarmycin SA: Evaluation of Yatakemycin Key PartialStructures and Its Unnatural Enantiomer
Discovery of a Potent, Selective, and Efficacious Class of Reversibleα-Ketoheterocycle Inhibitors of Fatty Acid Amide Hydrolase Effective asAnalgesics
Optimization of α-Ketooxazole Inhibitors of Fatty Acid Amide Hydrolase
Structure−Activity Relationships of α-Ketooxazole Inhibitors of Fatty Acid Amide Hydrolase
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