Edmond J. LaVoie - Concepedia

Author

Edmond J. LaVoie

Rutgers, The State University of New Jersey ORCID

Also Known As

E J LaVoie, E J Lavoie, E LaVoie, E. J. LAVOIE, E. J. LaVoie, E. LAVOIE, E.J. LaVoie, EDMOND J. LAVOIE, Edmond J LaVoie, Edmond J. LaVoie

219

Publications

7.9K

Citations

H-Index

106

Concepts

All Affiliations

Rutgers, The State University of New Jersey Rutgers Cancer Institute Institute for Cancer Prevention Dana (United States)National Institutes of Health

About

Edmond J. LaVoie is an author at Rutgers, The State University of New Jersey specializing in medicine, pharmacology, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	85	4.2K
2	Natural Sciences	27	42	1.9K
3	Engineering	12	12	364
4	Health Sciences	5	5	112
5	Public Health	3	3	88

Edmond J. LaVoie

148

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
Antioxidative Phenolic Compounds from Sage (<i>Salvia officinalis</i>) Mingfu Wang, Jiangang Li, Meera Rangarajan, Journal of Agricultural and Food Chemistry Phenolic CompoundsSage ExtractsMedicineBioactive CompoundsPhytochemical	1998	613
Substituted 2,5‘-Bi-1<i>H</i>-benzimidazoles: Topoisomerase I Inhibition and Cytotoxicity Jung Sun Kim, Barbara Gatto, Chiang Yu, Journal of Medicinal Chemistry	1996	229
Antibacterial activity of quinoxalines, quinazolines, and 1,5-naphthyridines Ajit K. Parhi, Yong‐Zheng Zhang, Kurt W. Saionz, Bioorganic & Medicinal Chemistry Letters Bioorganic ChemistryAntibioticsMedicineAntibacterial ActivityAntibacterial Agent	2013	157
Stimulation of Topoisomerase II-Mediated DNA Damage via a Mechanism Involving Protein Thiolation Huimin Wang, Yong Mao, Allan Y. Chen, Biochemistry Thiol-reactive QuinonesChromatinGenome InstabilityBreakage/reunion ReactionDna Damage	2001	154
Minor Groove-Directed and Intercalative Ligand−DNA Interactions in the Poisoning of Human DNA Topoisomerase I by Protoberberine Analogs Daniel S. Pilch, Chiang Yu, Darshan Makhey, Biochemistry	1997	110
5-(2-Aminoethyl)dibenzo[<i>c</i>,<i>h</i>][1,6]naphthyridin-6-ones: Variation of <i>N</i>-Alkyl Substituents Modulates Sensitivity to Efflux Transporters Associated with Multidrug Resistance Alexander L. Ruchelman, Peter J. Houghton, Nai Zhou, Journal of Medicinal Chemistry Pharmaceutical ScienceMultidrug ResistancePharmacotherapyChemical BiologyPharmaceutical Chemistry	2005	110
5H-Dibenzo[c,h]1,6-naphthyridin-6-ones: novel topoisomerase I-Targeting anticancer agents with potent cytotoxic activity Alexander L. Ruchelman, Sudhir Singh, Abhijit Ray, Bioorganic & Medicinal Chemistry Medicinal ChemistryDrug TargetingMedicineAnti-cancer AgentDrug Development	2003	109
TXA709, an FtsZ-Targeting Benzamide Prodrug with Improved Pharmacokinetics and Enhanced <i>In Vivo</i> Efficacy against Methicillin-Resistant Staphylococcus aureus Malvika Kaul, Lilly Mark, Yongzheng Zhang, Antimicrobial Agents and Chemotherapy Antimicrobial ChemotherapyPharmaceutical ChemistryDrug ResistanceMedicinal ChemistryFtsz-targeting Benzamide Prodrug	2015	108
Structure-activity relationships of benzimidazoles and related heterocycles as topoisomerase I poisons Jung Sun Kim, Qun Sun, Barbara Gatto, Bioorganic & Medicinal Chemistry Combinatorial ChemistryHeterocyclicBiochemistryAntiparasitic AgentNatural Sciences	1996	96
Determination of the Predominant Catechins in <i>Acacia catechu</i> by Liquid Chromatography/Electrospray Ionization−Mass Spectrometry Diandian Shen, Qingli Wu, Mingfu Wang, Journal of Agricultural and Food Chemistry	2006	96

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