| Year |
Citation |
Score |
| 2023 |
Nag A, Mafi A, Das S, Yu MB, Alvarez-Villalonga B, Kim SK, Su Y, Goddard WA, Heath JR. Stereochemical engineering yields a multifunctional peptide macrocycle inhibitor of Akt2 by fine-tuning macrocycle-cell membrane interactions. Communications Chemistry. 6: 95. PMID 37202473 DOI: 10.1038/s42004-023-00890-w |
0.809 |
|
| 2022 |
Borges A, Nguyen C, Letendre M, Onasenko I, Kandler R, Nguyen NK, Chen J, Allakhverdova T, Atkinson E, DiChiara B, Wang C, Petler N, Patel H, Nanavati D, Das S, ... Nag A, et al. Facile de novo sequencing of tetrazine-cyclized peptides through UV-induced ring-opening and cleavage from solid phase. Chembiochem : a European Journal of Chemical Biology. PMID 36471561 DOI: 10.1002/cbic.202200590 |
0.427 |
|
| 2022 |
Borges A, Onasenko I, Nag A. Binding Characterization of Cyclic PeptideĀ Ligands to Target Proteins and Chemical Epitopes Using ELISA and Fluorescence Polarization Assays. Methods in Molecular Biology (Clifton, N.J.). 2371: 335-354. PMID 34596857 DOI: 10.1007/978-1-0716-1689-5_18 |
0.517 |
|
| 2021 |
Kandler R, Das S, Nag A. Copper-ligand clusters dictate size of cyclized peptide formed during alkyne-azide cycloaddition on solid support. Rsc Advances. 11: 4842-4852. PMID 34377440 DOI: 10.1039/D0RA07491H |
0.459 |
|
| 2018 |
Farrow B, Wong M, Malette J, Lai B, Deyle KM, Das S, Nag A, Agnew HD, Heath JR. Corrigendum: Epitope Targeting of Tertiary Protein Structure Enables Target-Guided Synthesis of a Potent In-Cell Inhibitor of Botulinum Neurotoxin. Angewandte Chemie (International Ed. in English). 57: 1439. PMID 29377421 DOI: 10.1002/anie.201712967 |
0.772 |
|
| 2016 |
Henning RK, Varghese JO, Das S, Nag A, Tang G, Tang K, Sutherland AM, Heath JR. Degradation of Akt using protein-catalyzed capture agents. Journal of Peptide Science : An Official Publication of the European Peptide Society. PMID 26880702 DOI: 10.1002/Psc.2858 |
0.682 |
|
| 2016 |
Nag A. Abstract 2172: Circle Akt in: Epitope catalyzed assembly of macrocyclic therapeutics against phosphorylated Akt Cancer Research. 76: 2172-2172. DOI: 10.1158/1538-7445.Am2016-2172 |
0.659 |
|
| 2016 |
Liang J, Nag A, Das S, Bunck D, McCarthy A, Mishra A, Heath JE, Villalonga B, Heath JR. Detection of a Geographically Diverse Malarial Biomarker via Multi-Epitope Targeted Screening Biophysical Journal. 110: 519a. DOI: 10.1016/J.Bpj.2015.11.2774 |
0.797 |
|
| 2015 |
Das S, Nag A, Liang J, Bunck DN, Umeda A, Farrow B, Coppock MB, Sarkes DA, Finch AS, Agnew HD, Pitram S, Lai B, Yu MB, Museth AK, Deyle KM, et al. A General Synthetic Approach for Designing Epitope Targeted Macrocyclic Peptide Ligands. Angewandte Chemie (International Ed. in English). PMID 26377818 DOI: 10.1002/Anie.201505243 |
0.713 |
|
| 2015 |
Farrow B, Wong M, Malette J, Lai B, Deyle KM, Das S, Nag A, Agnew HD, Heath JR. Epitope targeting of tertiary protein structure enables target-guided synthesis of a potent in-cell inhibitor of botulinum neurotoxin. Angewandte Chemie (International Ed. in English). 54: 7114-9. PMID 25925721 DOI: 10.1002/Anie.201502451 |
0.802 |
|
| 2015 |
Deyle KM, Farrow B, Qiao Hee Y, Work J, Wong M, Lai B, Umeda A, Millward SW, Nag A, Das S, Heath JR. A protein-targeting strategy used to develop a selective inhibitor of the E17K point mutation in the PH domain of Akt1. Nature Chemistry. 7: 455-62. PMID 25901825 DOI: 10.1038/Nchem.2223 |
0.79 |
|
| 2013 |
Nag A, Das S, Yu MB, Deyle KM, Millward SW, Heath JR. A chemical epitope-targeting strategy for protein capture agents: the serine 474 epitope of the kinase Akt2. Angewandte Chemie (International Ed. in English). 52: 13975-9. PMID 24254999 DOI: 10.1002/Anie.201305882 |
0.838 |
|
| 2013 |
Millward SW, Agnew HD, Lai B, Lee SS, Lim J, Nag A, Pitram S, Rohde R, Heath JR. In situ click chemistry: from small molecule discovery to synthetic antibodies. Integrative Biology : Quantitative Biosciences From Nano to Macro. 5: 87-95. PMID 22836343 DOI: 10.1039/C2Ib20110K |
0.851 |
|
| 2011 |
Millward SW, Henning RK, Kwong GA, Pitram S, Agnew HD, Deyle KM, Nag A, Hein J, Lee SS, Lim J, Pfeilsticker JA, Sharpless KB, Heath JR. Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1. Journal of the American Chemical Society. 133: 18280-8. PMID 21962254 DOI: 10.1021/Ja2064389 |
0.755 |
|
| 2009 |
Agnew HD, Rohde RD, Millward SW, Nag A, Yeo WS, Hein JE, Pitram SM, Tariq AA, Burns VM, Krom RJ, Fokin VV, Sharpless KB, Heath JR. Iterative in situ click chemistry creates antibody-like protein-capture agents. Angewandte Chemie (International Ed. in English). 48: 4944-8. PMID 19301344 DOI: 10.1002/Anie.200900488 |
0.814 |
|
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