Karen S. Anderson

Affiliations: 
Pharmacology Yale University School of Medicine, New Haven, CT 
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Deshmukh MG, Ippolito JA, Zhang CH, et al. (2021) Structure-guided design of a perampanel-derived pharmacophore targeting the SARS-CoV-2 main protease. Structure (London, England : 1993)
Zhang CH, Stone EA, Deshmukh M, et al. (2021) Potent Noncovalent Inhibitors of the Main Protease of SARS-CoV-2 from Molecular Sculpting of the Drug Perampanel Guided by Free Energy Perturbation Calculations. Acs Central Science. 7: 467-475
Ippolito JA, Niu H, Bertoletti N, et al. (2021) Covalent Inhibition of Wild-Type HIV-1 Reverse Transcriptase Using a Fluorosulfate Warhead. Acs Medicinal Chemistry Letters. 12: 249-255
Ghahremanpour MM, Tirado-Rives J, Deshmukh M, et al. (2020) Identification of 14 Known Drugs as Inhibitors of the Main Protease of SARS-CoV-2. Acs Medicinal Chemistry Letters. 11: 2526-2533
Ghahremanpour MM, Tirado-Rives J, Deshmukh M, et al. (2020) Identification of 14 Known Drugs as Inhibitors of the Main Protease of SARS-CoV-2. Biorxiv : the Preprint Server For Biology
Gannam ZTK, Min K, Shillingford SR, et al. (2020) An allosteric site on MKP5 reveals a strategy for small-molecule inhibition. Science Signaling. 13
Duong VN, Ippolito JA, Chan AH, et al. (2020) Structural Investigation of 2-Naphthyl Phenyl Ether Inhibitors Bound to WT and Y181C Reverse Transcriptase Highlights Key Features of the NNRTI Binding Site. Protein Science : a Publication of the Protein Society
Ruiz VG, Czyzyk DJ, Kumar VP, et al. (2020) Targeting the TS dimer interface in bifunctional Cryptosporidium hominis TS-DHFR from parasitic protozoa: Virtual screening identifies novel TS allosteric inhibitors. Bioorganic & Medicinal Chemistry Letters. 30: 127292
Newton AS, Faver JC, Micevic G, et al. (2020) Structure-Guided Identification of DNMT3B Inhibitors. Acs Medicinal Chemistry Letters. 11: 971-976
Sasaki T, Gannam ZTK, Kudalkar SN, et al. (2019) Molecular and cellular studies evaluating a potent 2-cyanoindolizine catechol diether NNRTI targeting wildtype and Y181C mutant HIV-1 reverse transcriptase. Bioorganic & Medicinal Chemistry Letters
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