Amy M. Quinn, Ph.D.
Affiliations: | 2008 | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Pharmacology, ToxicologyGoogle:
"Amy Quinn"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Trevor M. Penning | grad student | 2008 | Penn | |
| (Role of aldo -keto reductase enzymes in polycyclic aromatic hydrocarbon trans-dihydrodiol activation in human lung cells.) | ||||
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| Kallander LS, Washburn D, Hilfiker MA, et al. (2018) Reverse Hydroxamate Inhibitors of Bone Morphogenetic Protein 1. Acs Medicinal Chemistry Letters. 9: 736-740 |
| Wang L, Chang J, Varghese D, et al. (2013) A small molecule modulates Jumonji histone demethylase activity and selectively inhibits cancer growth. Nature Communications. 4: 2035 |
| Wang L, Chang J, Varghese D, et al. (2013) Erratum: A small molecule modulates Jumonji histone demethylase activity and selectively inhibits cancer growth Nature Communications. 4 |
| Lu Q, Quinn AM, Patel MP, et al. (2012) Perspectives on the discovery of small-molecule modulators for epigenetic processes. Journal of Biomolecular Screening. 17: 555-71 |
| Quinn AM, Simeonov A. (2011) Methods for Activity Analysis of the Proteins that Regulate Histone Methylation. Current Chemical Genomics. 5: 95-105 |
| Shultz CA, Quinn AM, Park JH, et al. (2011) Specificity of human aldo-keto reductases, NAD(P)H:quinone oxidoreductase, and carbonyl reductases to redox-cycle polycyclic aromatic hydrocarbon diones and 4-hydroxyequilenin-o-quinone. Chemical Research in Toxicology. 24: 2153-66 |
| King ON, Li XS, Sakurai M, et al. (2010) Quantitative high-throughput screening identifies 8-hydroxyquinolines as cell-active histone demethylase inhibitors. Plos One. 5: e15535 |
| Liu F, Chen X, Allali-Hassani A, et al. (2010) Protein lysine methyltransferase G9a inhibitors: design, synthesis, and structure activity relationships of 2,4-diamino-7-aminoalkoxy-quinazolines. Journal of Medicinal Chemistry. 53: 5844-57 |
| Quinn AM, Allali-Hassani A, Vedadi M, et al. (2010) A chemiluminescence-based method for identification of histone lysine methyltransferase inhibitors. Molecular Biosystems. 6: 782-8 |
| Boxer MB, Quinn AM, Shen M, et al. (2010) A highly potent and selective caspase 1 inhibitor that utilizes a key 3-cyanopropanoic acid moiety. Chemmedchem. 5: 730-8 |