Leeyuan Huang - Concepedia

Author

Leeyuan Huang

Merck & Co., Inc., Rahway, NJ, USA (United States)

Also Known As

L Huang, L. HUANG, L. Huang, LEE-YUAN HUANG, LEEYUAN HUANG, Lee-Yuan Huang, Leeyuan Huang

Publications

770

Citations

H-Index

Concepts

All Affiliations

Merck & Co., Inc., Rahway, NJ, USA (United States)MSD (Spain)MSD K.K. (Japan)Merck (Japan)

About

Leeyuan Huang is an author at Merck & Co., Inc., Rahway, NJ, USA (United States) specializing in biochemistry, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	6	6	285
2	Medicine	5	5	227
3	Natural Sciences	4	4	190
4	Chemical Biology	3	3	170
5	Microbiology	2	2	74

Leeyuan Huang

Publications

767

Citations

H-Index

Page 1

	Year	Citations
Resorcylic Acid Lactones. Naturally Occurring Potent and Sclective Inbibitors. Annie Zhao, SEOK H. LEE, MARINA MOIENA, The Journal of Antibiotics	1999	112
D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent<i>in vitro</i>and<i>in vivo</i>antitumoral activity which involves DNA damage and ataxia telangiectasia–mutated nuclear protein kinase activation Shin‐Hun Juang, Chia-Chi Lung, Pi-Chen Hsu, Molecular Cancer Therapeutics	2007	65
Zaragozic Acids D and D<sub>2</sub>: Potent Inhibitors of Squalene Synthase and of Ras Farnesyl-Protein Transferase Claude Dufresne, Kenneth E. Wilson, Sheo B. Singh, Journal of Natural Products Pharmaceutical ScienceAltmetric Attention ScoreOrganic ChemistryChemical BiologyZaragozic Acids D	1993	60
L-652,469 - a dual receptor antagonist of platelet activating factor and dihydropyridines from Tussilago farfara L San-Bao Hwang, Michael N. Chang, Qui Qiu Han, European Journal of Pharmacology ThrombopoiesisThrombosisDual Receptor AntagonistBiochemistryBlood Platelet	1987	58
The isolation and structure elucidation of zaragozic acid C, a novel potent squalene synthase inhibitor. Claude Dufresne, Kenneth E. Wilson, Deborah L. Zink, Tetrahedron Medicinal ChemistryBiochemistryZaragozic Acid CNatural SciencesBiocatalysis	1992	58
Chaetomella acutiseta produces chaetomellic acids A and B which are reversible inhibitors of farnesyl-protien transferase R. B. Lingham, KeithC. Silverman, Gerald F. Bills, Applied Microbiology and Biotechnology Inhibitory ActivityFarnesyl-protien TransferaseBioorganic ChemistryBiochemistryChaetomella Acutiseta	1993	52
The Identification Of Fibrous Proteins In Fetal Rat Epidermis By Electrophoretic And Immunologic Techniques Beverly A. Dale, I. B. Stern, M Rabin, Journal of Investigative Dermatology	1976	46
Dihydrocompactin,a new potent inhibitor of 3-hydroxy-3-methylglutaryl coenzyme-A reductase from Penicillium citrinum. Y. K. TONY LAM, Vincent P. Gullo, Robert T. Goegelman, The Journal of Antibiotics	1981	45
Cochinmicins, novel and potent cyclodepsipeptide endothelin antagonists from a Microbispora sp. I. Production, isolation, and characterization. Y. K. TONY LAM, David L. Williams, J Sigmund, The Journal of Antibiotics	1992	41
Meridamycin: A novel nonimmunosuppressive FKBP12 ligand from streptomyces hygroscopicus Gino Salituro, Deborah L. Zink, Arlene Dahl, Tetrahedron Letters BiochemistryAntimicrobial ChemotherapyMicrobiologyStreptomyces HygroscopicusMedicine	1995	37

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