Drug Chemistry Chemical Biology Peptide Drugs Glycochemistry
Development of Oligomeric Mannose-6-phosphonate Conjugates for Targeted Protein Degradation, Stevens, C. M.; Zhou, Y.; Teng, P.; Rault, L. N.; Liao, Y.; Tang, W., 2023
Small molecular mimetics of antimicrobial peptides as a promising therapy to combat bacterial resistance, Teng, P.; Shao, H.; Huang, B.; Xie, J.; Cui, S.; Wang, K.; Cai, J., 2023
Progress and medicinal applications of bioorthogonal reactions, Wen, Q.; Luo, J.; Shao, H.; Deng, Z.; Teng, P., 2022
Using proteomimetics to switch angiogenic signaling, Teng, P.; Cai, J., 2022
The folding propensity of α/sulfono-γ-AA peptidic foldamers with both left- and right-handedness, Teng, P.; Zheng, M. M.; Cerrato, D. C.; Shi, Y.; Zhou, M.; Xue, S.; Jiang, W.; Wojtas, L.; Ming, L.-J.; Hu, Y.; Cai, J., 2021
Development of triantennary N‑acetylgalactosamine conjugates as degraders for extracellular proteins, Zhou, Y.; Teng, P.; Montgomery, N. T.; Li, X.; Tang, W., 2021
Development of MDM2 degraders based on ligands derived from Ugi reactions: Lessons and discoveries, Wang, B.; Liu, J.; Tandon, I.; Wu, S.; Teng, P.; Liao, J.; Tang, W., 2021
Lipidated α/Sulfono-α-AA heterogeneous peptides as antimicrobial agents for MRSA, Singh, S.; Wang, M.; Gao, R.; Teng, P.; Odom, T.; Zhang, E.; Xu, H.; Cai, J., 2020
Orthogonal halogen bonding driven 3D supramolecular assembly of right-handed synthetic helical peptides, Teng, P.; Gray, G. M.; Zheng, M.; Singh, S.; Li, X.; Wojtas, L.; Van der Vaart, A.; Cai, J., 2019
Development of EGFR-targeted Evodiamine-loaded poly(amino acid)s nanoparticles for the treatment of colorectal cancer, Li, C.; Cai, G.; Song, D.; Gao, R.; Teng, P.; Zhou, L.; Ji, Q.; Sui, H.; Cai, J.; Li, Q.; Wang, Y., 2019
Structural basis of resistance of mutant RET protein-tyrosine kinase to its inhibitors nintedanib and vandetanib, Terzyan, S.; Shen, T.; Liu, X.; Huang, Q.; Teng, P.; Zhou, M.; Hilberg, F.; Cai, J.; Mooers, B. H. M.; Wu, J., 2019
Molecular architecture and charging effects enhance the in vitro and in vivo performance of multi-arm antimicrobial agents based on star-shaped poly(L-lysine), Lu, C.; Quan, G.; Su, M.; Nimmagadda, A.; Chen, W.; Pan, M.; Teng, P.; Yu, F.; Liu, X.; Jiang, L.; Du, W.; Hu, W.; Yao, F.; Pan, X.; Wu, C.; Liu, D.; Cai, J., 2019
Hydrogen-bonding-driven 3D supramolecular assembly of peptidomimetic zipper, Teng, P.; Niu, Z.; She, F.; Zhou, M.; Sang, P.; Gray, G. M.; Verma, G.; Wojtas, L.; Van der Vaart, A.; Ma, S.; Cai, J., 2018
Facilely accessible quinoline derivatives as potent antibacterial agents, Teng, P.; Li, C.; Peng, Z.; Vanderschouw, A. M.; Nimmagadda, A.; Su, M.; Li, Y.; Sun, X.; Cai, J., 2018
De novo left-handed synthetic peptidomimetic foldamers, She, F.; Teng, P.; Ma, N.; Gray, G. M.; Odom, T.; Zhou, M.; Van der Vaart, A.; Wojtas, L.; Cai, J., 2018
Bis‐cyclic guanidines as a novel class of compounds potent against Clostridium difficile, Li, C.; Teng, P.; Peng, Z.; Sang, P.; Sun, X.; Cai, J., 2018
Selective inhibition of leukemia-associated SHP2E69K mutant by the allosteric SHP2 inhibitor SHP099, Sun, X.; Ren, Y.; Gunawan, S.; Teng, P.; Lawrence, H.; Cai, J.; Lawrence N. J.; Wu, J., 2018
Small antimicrobial agents encapsulated in poly(epsilon-caprolactone)-poly(ethylene glycol) nanoparticles for treatment of S. aureus-infected wounds, Hua, J.; Teng, P.; Zou, Y.; Zhang, C.; Shen, X.; Cai, J.; Hu, Y., 2018
Nano-sized lipidated dendrimer as potent and broad spectrum antibacterial agents, Gide, M.; Nimmagadda, A.; Su, M.; Wang, M.; Teng, P.; Li, C.; Gao, R.; Xu, H.; Li, Q.; Cai, J., 2018
Lipidated α/α-AA heterogeneous peptides as antimicrobial agents, Singh, S.; Nimmagadda, A.; Su, M.; Wang, M.; Teng, P.; Cai, J., 2018
Synthesis of antimicrobial poly(guanylurea)s, Ahmed, M. S.; Annamalai, T.; Li, X.; Seddek, A.; Teng, P.; Tse-Dinh, Y.-C.; Moon, J. H., 2018
Right-handed helical foldamers consisting of de novo D-AApeptides, Teng, P.; Ma, N.; Cerrato, D. C.; She, F.; Odom, T.; Wang, X.; Ming, L-J.; Van der Vaart, A.; Wojtas, L.; Xu, H.; Cai, J., 2017
Membrane-active hydantoin derivatives as antibiotic agents, Su, M.; Xia, D.; Teng, P.; Nimmagadda, A.; Zhang, C.; Odom, T.; Cao, A. Hu, Y.; Cai, J., 2017
Novel bis-cyclic guanidines as potent membrane-active antibacterial agents with therapeutic potential, Teng, P.; Nimmagadda, A.; Su, M.; Hong, Y.; Shen, N.; Li, C.; Tsai, L.-Y.; Cao, J.; Li, Q.; Cai, J., 2017
Modulation of lipid membrane structural and mechanical properties by a peptidomimetic derived from reduced amide scaffold, Khadka, N. K.; Teng, P.; Cai, J.; Pan J., 2017
One-bead−two-compound thioether bridged macrocyclic γ‑AApeptide screening library against EphA2, Shi, Y.; Challa, S.; Sang, P.; She, F.; Li, C.; Gray, G. M.; Nimmagadda, A.; Teng, P.; Odom, T.; Wang, Y.; Van der Vaart, A.; Li, Q.; Cai, J., 2017
Membrane disruption mechanism of a prion peptide (106-126) investigated by atomic force microscopy, Raman and electron paramagnetic resonance spectroscopy, Pan, J.; Sahoo, P. K.; Dalzini, A.; Hayati, Z.; Aryal, C. M.; Teng, P.; Cai, J.; Humberto Rodriguez Gutierrez, and Likai Song, 2017
Polycarbonates with potent and selective antimicrobial activity toward Gram-positive bacteria, Nimmagadda, A.; Liu, X.; Teng, P.; Su, M.; Li, Y.; Qiao, Q.; Khadka, N. K.; Sun, X.; Pan, J.; Xu, H.; Li, Q.; Cai, J., 2017
