Robert C. Rizzo, Ph.D.
Affiliations: | 2001 | Yale University, New Haven, CT |
Area:
computational chemistry and molecular designGoogle:
"Robert Rizzo"Mean distance: 8.16 | S | N | B | C | P |
Parents
Sign in to add mentorWilliam L. Jorgensen | grad student | 2001 | Yale | |
(Computational advances in structure based drug design with applications to HIV -1 reverse transcriptase.) |
Children
Sign in to add traineeLauren E Prentis | grad student | SUNY Stony Brook | |
Guilherme Duarte Ramos Matos | post-doc | 2019- | SUNY - Stonybrook |
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Publications
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Duarte Ramos Matos G, Pak S, Rizzo RC. (2023) Descriptor-Driven de Novo Design Algorithms for DOCK6 Using RDKit. Journal of Chemical Information and Modeling. 63: 5803-5822 |
Coant N, Bickel JD, Rahaim R, et al. (2023) Neutral ceramidase-active site inhibitor chemotypes and binding modes. Bioorganic Chemistry. 139: 106747 |
Prentis LE, Singleton CD, Bickel JD, et al. (2022) A molecular evolution algorithm for ligand design in DOCK. Journal of Computational Chemistry |
Telehany S, Humby M, McGee TD, et al. (2020) Identification of Zika Virus Inhibitors Using Homology Modeling and Similarity-based Screening to Target Glycoprotein E. Biochemistry |
Zhou Y, Elmes MW, Sweeney J, et al. (2019) Identification of Fatty Acid Binding Protein 5 Inhibitors Through Similarity-based Screening. Biochemistry |
Kim J, Bogdan DM, Elmes MW, et al. (2019) Incarvillateine produces antinociceptive and motor suppressive effects via adenosine receptor activation. Plos One. 14: e0218619 |
Elmes MW, Prentis LE, McGoldrick LL, et al. (2019) FABP1 controls hepatic transport and biotransformation of Δ-THC. Scientific Reports. 9: 7588 |
Singleton CD, Humby MS, Yi HA, et al. (2019) Identification of Ebola Virus Inhibitors Targeting GP2 using Principles of Molecular Mimicry. Journal of Virology |
Guo J, Collins S, Miller WT, et al. (2018) Identification of a water-coordinating HER2 inhibitor by virtual screening using similarity-based scoring. Biochemistry |
Yan S, Elmes MW, Tong S, et al. (2018) SAR studies on truxillic acid mono esters as a new class of antinociceptive agents targeting fatty acid binding proteins. European Journal of Medicinal Chemistry. 154: 233-252 |