Arthur F. Kluge - Concepedia

Author

Arthur F. Kluge

Also Known As

A. F. KLUGE, A. F. Kluge, A. Kluge, A.F. Kluge, ARTHUR F. KLUGE, Arthur F Kluge, Arthur F. Kluge, Arthur Kluge, Kluge, Anton

104

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Cornell University Aurigene Discovery Technologies (India)Astellas Pharma (Japan)IIT@MIT

About

Arthur F. Kluge is an author at Cornell University specializing in pharmacology, natural sciences, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	18	21	1.1K
2	Engineering	12	12	599
3	Medicine	11	14	1.5K
4	Public Health	3	3	97
5	Arts	2	2	52

Arthur F. Kluge

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Discovery of a selective catalytic p300/CBP inhibitor that targets lineage-specific tumours Loren Lasko, Clarissa G. Jakob, Rohinton Edalji, Nature Lineage-specific TumoursMedicineImmune Checkpoint InhibitorAnti-cancer AgentTumor Suppressor	2017	813
Targeted covalent drugs of the kinase family Juswinder Singh, Russell C. Petter, Arthur F. Kluge Current Opinion in Chemical Biology Medicinal ChemistryDrug TargetDrug TargetingMedicineReceptor Tyrosine Kinase	2010	175
Prostaglandins. X. Synthesis of prostaglandin models and prostaglandins by conjugage addition of a functionalized organocopper reagent Arthur F. Kluge, Karl G. Untch, John H. Fried Journal of the American Chemical Society Bioorganic ChemistryEngineeringChemical AnalysisProstaglandin ModelsAltmetric Attention Score	1972	161
A Three-Hybrid Approach to Scanning the Proteome for Targets of Small Molecule Kinase Inhibitors Frank Becker, Krishna K. Murthi, Chase C. Smith, Chemistry & Biology Molecular DockingThree-hybrid ApproachDrug TargetBiochemistryNatural Sciences	2004	136
Novel highly selective inhibitors of ubiquitin specific protease 30 (USP30) accelerate mitophagy Arthur F. Kluge, Bharat Lagu, Pranab Maiti, Bioorganic & Medicinal Chemistry Letters Protease InhibitorsCell AutophagyMitophagyMedicineAutophagy	2018	122
Synthesis and antihypertensive activity of 4'-substituted spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-ones Robin D. Clark, Joan M. Caroon, Arthur F. Kluge, Journal of Medicinal Chemistry Medicinal ChemistryHeterocyclicBiochemistryNatural SciencesAntihypertensive Activity	1983	81
Prostaglandins. XI. Synthesis of 13-cis-prostaglandins via a highly stereoselective conjugate addition with a functionalized organocopper reagent Arthur F. Kluge, Karl G. Untch, John H. Fried Journal of the American Chemical Society Stereoselective Conjugate AdditionEngineeringBiochemistryDonut IconNatural Sciences	1972	76
Phosphonate reagents for the synthesis of enol ethers and one-carbon homologation to aldehydes Arthur F. Kluge, Ian S. Cloudsdale The Journal of Organic Chemistry Novel OrganocatalystsMolecular SciencesEngineeringBiochemistryOne-carbon Homologation	1979	72
Discovery of Spiro Oxazolidinediones as Selective, Orally Bioavailable Inhibitors of p300/CBP Histone Acetyltransferases Michael R. Michaelides, Arthur F. Kluge, Michael A. Patane, ACS Medicinal Chemistry Letters	2017	72
Molecular spectra and conformations of conjugated dienones C. Peter Lillya, Arthur F. Kluge The Journal of Organic Chemistry HeterocyclicChemical AnalysisNatural SciencesConjugated DienonescAltmetric Attention Score	1971	65

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