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Encoded combinatorial chemistry.
Open accessAbstract
The diversity of chemical synthesis and the power of genetics are linked to provide a powerful, versatile method for drug screening. A process of alternating parallel combinatorial synthesis is used to encode individual members of a large library of chemicals with unique nucleotide sequences. After the chemical entity is bound to a target, the genetic tag can be amplified by replication and utilized for enrichment of the bound molecules by serial hybridization to a subset of the library. The nature of the chemical structure bound to the receptor is decoded by sequencing the nucleotide tag.
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“Originally conceived by Brenner and lerner, Dels are built through iterative chemical synthesis in which each small molecule is covalently linked to a unique DNA tag that enables the parallel screening of millions of pooled compounds (Brenner and lerner 1992).”
From From serendipity to strategy: molecular glue degraders in cancer therapeutics (2025) · cites this paper as Brenner and lerner 1992
Experimental — accuracy not yet measuredIn the citing paper
“Conceptualized by Brenner and Lerner, 170 DNA encoded libraries (DELs) are increasingly being adopted in drug discovery.”
From Chasing molecular glue degraders: screening approaches (2022) · cites this paper as [170]
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Cites
Tuerk, C., & Gold, L. (1990) · Science · doi:10.1126/science.2200121 · Cited by 10,421
In vitro selection of RNA molecules that bind specific ligands
Ellington, A. D., & Szostak, J. W. (1990) · Nature · doi:10.1038/346818a0 · Cited by 9,845
Light-Directed, Spatially Addressable Parallel Chemical Synthesis
Fodor, S. P. A., Read, J., Pirrung, M. C., Stryer, L., Lu, A. T., & Solas, D. W. (1991) · Science · doi:10.1126/science.1990438 · Cited by 2,697
Searching for Peptide Ligands with an Epitope Library
Scott, J. K., & Smith, G. P. (1990) · Science · doi:10.1126/science.1696028 · Cited by 2,087
A new type of synthetic peptide library for identifying ligand-binding activity
Lam, K. S., Salmon, S. E., Hersh, E. M., Hruby, V. J., Kazmierski, W. M., & Knapp, R. J. (1991) · Nature · doi:10.1038/354082a0 · Cited by 1,803
Geysen, H. M., Meloen, R. H., & Barteling, S. J. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.13.3998 · Cited by 1,478
Houghten, R. A., Pinilla, C., Blondelle, S. E., Appel, J. R., Dooley, C. T., & Cuervo, J. H. (1991) · Nature · doi:10.1038/354084a0 · Cited by 1,327
Peptides on phage: a vast library of peptides for identifying ligands.
Cwirla, S. E., Peters, E. A., Barrett, R. W., & Dower, W. J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6378 · Cited by 930
Crick, F. H. C., Griffith, J. S., & Orgel, L. E. (1957) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.43.5.416 · Cited by 333
Flagged first, then by citations
Research works printed but not linked: 4
- [2]Geysen, H. M., Meloen, R. H. & Barteling, S. J. (1984) Proc. Natl. Acad. Sci. USA 81, 3998–4002.
- [6]Cwirla, S. E., Peters, E. A., Barrett, R. W. & Dower, W. J. (1990) Proc. Natl. Acad. Sci. USA 87, 6378–6382.
- [9]Crick, F. H. C., Griffith, J. S. & Orgel, L. E. (1957) Proc. Natl. Acad. Sci. USA 43, 416–421.
- [10]Merrifield, B. (1984) Les Prix Nobel (Almqvist & Wiksell International, Stockholm), pp. 127–153.
Cited by
Sorted by citations
Items 501–600 of 1,000
Modular assembly and encoding strategies for dual-display DNA-encoded chemical libraries
Oehler, S., Plais, L., Bassi, G., Neri, D., & Scheuermann, J. (2021) · Chemical Communications · doi:10.1039/d1cc04306d · Cited by 17
DNA Compatible Oxidization and Amidation of Terminal Alkynes
Sun, Z., Zhang, J., Zhang, H., Cao, H., Xiao, L., Yang, K., & Hu, Y. J. (2022) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.2c00340 · Cited by 16
Combinatorial chemistry and high-throughput screening in drug discovery and development
Appell, K., Baldwin, J. J., & Egan, W. J. (2001) · Separation science and technology · doi:10.1016/s0149-6395(01)80004-0 · Cited by 16
Construction of DNA codes by using algebraic number theory
Hong, H., Wang, L., Ahmad, H., Li, J., Yang, Y., & Wu, C. (2015) · Finite Fields and Their Applications · doi:10.1016/j.ffa.2015.10.008 · Cited by 16
“DNA codes are also used for DNA computation [1,3,7–10,12,20,22], as probes in DNA microarray technologies [24] and as molecular barcodes for chemical libraries [5].”
MethodA Chemistry for Incorporation of Selenium into DNA‐Encoded Libraries
Xu, H., Gu, Y., Zhang, S., Xiong, H., Ma, F., Lu, F., Ji, Q., Liu, L., Ma, P., Hou, W., et al. (2020) · Angewandte Chemie · doi:10.1002/ange.202003595 · Cited by 16
Self-citationThe Yeast Two-hybrid System and Its Pharmaceutical Significance
Topcu, Z., & Borden, K. L. B. (2000) · Pharmaceutical Research · doi:10.1023/a:1026493310144 · Cited by 17
Binäre Codierung von Verbindungsbibliotheken
Eckes, P. (1994) · Angewandte Chemie · doi:10.1002/ange.19941061507 · Cited by 16
A Three‐Dimensional Array for Multiparallel Synthesis
Kozmin, S. A., & Wang, Y. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200390238 · Cited by 16
On-DNA C–H functionalization of electron-rich arenes for DNA-encoded libraries
Beato, E. D. P., Torkowski, L., Hartmann, P., Vogelsang, L., Dietz, K., & Ritter, T. (2025) · Nature Chemistry · doi:10.1038/s41557-025-01844-6 · Cited by 15
Multiplexed Small‐Molecule‐Ligand Binding Assays by Affinity Labeling and DNA Sequence Analysis**
Cai, B., & Krusemark, C. J. (2021) · Angewandte Chemie International Edition · doi:10.1002/anie.202113515 · Cited by 15
Biomacromolecule-Assisted Screening for Reaction Discovery and Catalyst Optimization
de Dios, S. M. R., Tiwari, V. K., McCune, C. D., Dhokale, R. A., & Berkowitz, D. B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00213 · Cited by 15
On-DNA Synthesis of Functionalized 4H-Pyran Scaffolds for Focused DNA-Encoded Chemical Libraries
Gao, Y., Sun, Y., Zhao, G., Zhang, G., Li, Y., & Li, Y. (2022) · Organic Letters · doi:10.1021/acs.orglett.2c02714 · Cited by 15
Isotope Ratio Encoding of Sequence-Defined Oligomers
Zwillinger, M., Fischer, L., Sályi, G., Szabó, S., Csékei, M., Huc, I., & Kotschy, A. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c08135 · Cited by 16
Discovery of hit compounds for methyl-lysine reader proteins from a target class DNA-encoded library
Shell, D. J., Rectenwald, J. M., Buttery, P. H., Johnson, R. L., Foley, C. A., Guduru, S. K. R., Uguen, M., Rubiano, J. S., Zhang, X., Li, F., et al. (2022) · SLAS DISCOVERY · doi:10.1016/j.slasd.2022.10.003 · Cited by 16
Chemistry on Nucleic Acid Templates
Berger, J., & Oberhuber, M. (2010) · Chemistry & Biodiversity · doi:10.1002/cbdv.201000108 · Cited by 15
Liang, Q., Zuo, H., Yang, T., Yin, J., Huang, X., Wang, J., Li, Q., Yin, G., & Zhao, X. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114212 · Cited by 15
Non‐binary Encoded Nucleic Acid Barcodes Directly Readable by a Nanopore
Yan, S., Wang, L., Wang, Y., Cao, Z., Zhang, S., Du, X., Fan, P., Zhang, P., Chen, H., & Huang, S. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202116482 · Cited by 16
Bellmann, L., Klein, R., & Rarey, M. (2022) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.2c00334 · Cited by 15
Development of a Micellar-Promoted Heck Reaction for the Synthesis of DNA-Encoded Libraries
Stanway‐Gordon, H. A., Odger, J. A., & Waring, M. J. (2023) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.3c00051 · Cited by 15
Lead Discovery and Lead Modification
Silverman, R. B., & Holladay, M. W. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-382030-3.00002-7 · Cited by 17
Le, A. T. H., Krylova, S. M., & Krylov, S. N. (2019) · Electrophoresis · doi:10.1002/elps.201900028 · Cited by 15
Wang, Q., Scheigetz, J., Roy, B., Ramachandran, C., & Gresser, M. J. (2002) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/s1570-9639(02)00412-0 · Cited by 15
Drug Discovery, Design, and Development
Silverman, R. B. (2004) · Elsevier eBooks · doi:10.1016/b978-0-08-051337-9.50007-9 · Cited by 15
Novel avidin and streptavidin binding sequences found in synthetic peptide libraries
Østergaard, S., Hansen, P. H., Olsen, M., & Holm, A. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00262-8 · Cited by 15
Discovery of Inhibitors of Protein-Protein Interactions from Combinatorial Libraries
Vicent, M. J., Pérez‐Payá, E., & Orzáez, M. (2006) · Current Topics in Medicinal Chemistry · doi:10.2174/156802607779318307 · Cited by 15
“identification techniques have been also developed, such as nucleotide- [45,46],”
MethodScreening Large Compound Collections
Hale, S. P. (2014) · doi:10.1002/9781118832738.ch13 · Cited by 15
DNA-encoded drug libraries come of age
Mullard, A. (2016) · Nature Biotechnology · doi:10.1038/nbt0516-450b · Cited by 15
Eine DNA‐kodierte Molekülbibliothek mit Elementen natürlicher Makrocyclen
Stress, C., Sauter, B., Schneider, L. A., Sharpe, T., & Gillingham, D. G. (2019) · Angewandte Chemie · doi:10.1002/ange.201902513 · Cited by 14
DNA-encoded libraries via late-stage functionalization strategies: a review
Sahu, R., Yadav, S., Nath, S., Banerjee, J., & Kapdi, A. R. (2023) · Chemical Communications · doi:10.1039/d3cc01075a · Cited by 14
Wang, Y., Fang, X., Liao, H., Zhang, G., Li, Y., & Li, Y. (2023) · Organic Letters · doi:10.1021/acs.orglett.3c01482 · Cited by 14
DNA‐Encoded Libraries and Their Application to RNA
Yang, X., Childs‐Disney, J. L., Paegel, M., & Disney, M. D. (2023) · Israel Journal of Chemistry · doi:10.1002/ijch.202300073 · Cited by 13
Building Block-Based Binding Predictions for DNA-Encoded Libraries
Zhang, C., Pitman, M., Dixit, A., Leelananda, S. P., Palacci, H., Lawler, M., Belyanskaya, S. L., Grady, L. C., Franklin, J., Tilmans, N., et al. (2023) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.3c00588 · Cited by 14
DNA-compatible functional group transformations via K 2 RuO 4 -mediated oxidation
He, P., Zhao, G., Zhu, M., Li, Y., Zhang, G., & Li, Y. (2024) · Organic Chemistry Frontiers · doi:10.1039/d4qo00203b · Cited by 14
Chemical Tools to Monitor and Manipulate the Adaptive Immune System
Kodadek, T. J. (2014) · Chemistry & Biology · doi:10.1016/j.chembiol.2014.07.009 · Cited by 14
“[PubMed: 21892506] Scheuermann J, Neri D. DNA-encoded chemical libraries: a tool for drug discovery and for chemical biology.”
BackgroundA Point of Inflection and Reflection on Systems Chemical Biology
Johnson, E. O., & Hung, D. T. (2019) · ACS Chemical Biology · doi:10.1021/acschembio.9b00714 · Cited by 15
A smart polymer for sequence-selective binding, pulldown, and release of DNA targets
Krieg, E., Gupta, K., Dahl, A., Lesche, M., Boye, S., Lederer, A., & Shih, W. M. (2020) · Communications Biology · doi:10.1038/s42003-020-1082-2 · Cited by 14
Visible Light Photochemical Reactions for Nucleic Acid-Based Technologies
Koo, B., Yoo, H., Choi, H. J., Kim, M., Kim, C., & Kim, K. T. (2021) · Molecules · doi:10.3390/molecules26030556 · Cited by 15
Liang, Q., Zhao, X., Fu, X., Wang, J., Li, Q., & Zhao, X. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2021.104986 · Cited by 14
Combinatorial technology revitalized by DNA‐encoding
Furka, Á. (2021) · MedComm · doi:10.1002/mco2.84 · Cited by 13
Identification and Validation of New Interleukin-2 Ligands Using DNA-Encoded Libraries
Gironda-Martínez, A., Gorre, É. M. D., Prati, L., Gosalbes, J.-F., Plaza, S. D., Cazzamalli, S., Samain, F., Donckèle, E. J., & Neri, D. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c01693 · Cited by 13
Development of on-DNA vinyl sulfone synthesis for DNA-encoded chemical libraries
Gao, Y., Yang, S., Fang, X., Zhao, G., Li, X., Zhang, G., Li, Y., & Li, Y. (2022) · Organic Chemistry Frontiers · doi:10.1039/d2qo00881e · Cited by 14
DNA Code Design Based on the Bloch Quantum Chaos Algorithm
Guo, Q., Wang, B., Zhou, C., Wei, X., & Zhang, Q. (2017) · IEEE Access · doi:10.1109/access.2017.2760882 · Cited by 14
“They are widely applied into DNA computing [1], DNA Microarray technology [2], Molecular bar codes for chemical libraries [3], image encryption [4], [5] and data storage [6].”
Search for ancient patterns in protein sequences
Thode, G., Ranea, J. A. G., & Jiménez, J. (1996) · Journal of Molecular Evolution · doi:10.1007/bf02198848 · Cited by 14
“It is remarkable, however, that some significant patterns can be identified in the randomized sequences, too, It has been shown that combinatorial libraries, consisting of six-residue peptide sequences, permit the identification of antigenic determinants and the development of biologically active antimicrobial peptide…”
BackgroundA combinatorial method for constructing libraries of long peptides displayed by filamentous phage
Haaparanta, T., & Huse, W. D. (1995) · Molecular Diversity · doi:10.1007/bf01715808 · Cited by 14
Kombinatorische Chemie ‐ Revolution in der Pharmaforschung?
Weber, L. T. (1994) · Nachrichten aus Chemie Technik und Laboratorium · doi:10.1002/nadc.19940420708 · Cited by 14
Zhou, W., Wang, Y., Zhang, S., Zhang, C., Pang, J., Hou, S., Li, J., Yao, Y., Su, A., Ma, P., et al. (2025) · Chemical Science · doi:10.1039/d5sc05512a · Cited by 13
Rama-Garda, R., Amigo, J., Priego, J., Molina‐Martín, M., Cano, L., Domínguez, E., Loza, M. I., Rivera‐Sagredo, A., & de Blas, J. (2021) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2021.116178 · Cited by 13
Gurav, R., Gurav, A. P., Salunke‐Gawali, S., Jadhav, S. A., Choudhari, P. B., Sankpal, S., & Hangirgekar, S. (2022) · Applied Organometallic Chemistry · doi:10.1002/aoc.6547 · Cited by 13
Impact of DNA-Encoded Chemical Library Technology on Drug Discovery
Keller, M., Schira, K., & Scheuermann, J. (2022) · CHIMIA International Journal for Chemistry · doi:10.2533/chimia.2022.388 · Cited by 13
Using DNA-encoded libraries of fragments for hit discovery of challenging therapeutic targets
Zhao, G., Zhu, M., Li, Y., Zhang, G., & Li, Y. (2024) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2024.2354287 · Cited by 13
“The concept of DEL was initially proposed by Brenner and Lerner in 1992 [27].”
BackgroundDNA-encoded chemical libraries on stage
Gloger, A., & Scheuermann, J. (2024) · Nature Chemical Biology · doi:10.1038/s41589-024-01791-2 · Cited by 13
Reflections on DNA-encoded chemical libraries
Lerner, R. A., & Neri, D. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.04.080 · Cited by 13
Self-citationEde, S., Schenk, M., Bierer, D. E., Weinmann, H., & Graham, K. (2021) · Molecules · doi:10.3390/molecules26061790 · Cited by 14
“This complete process has been excellently reviewed and described previously [1–5].”
N‐Alkyl Linkers for DNA‐Encoded Chemical Libraries
Sun, Z., Yang, S., Xue, L., Zhang, J., Yang, K., & Hu, Y. J. (2022) · Chemistry - An Asian Journal · doi:10.1002/asia.202200016 · Cited by 13
Xu, H., Wang, Y., Dong, H., Zhang, Y., Gu, Y., Zhang, S., Yu, M., Li, J., Shi, X. J., Ji, Q., et al. (2022) · Angewandte Chemie · doi:10.1002/ange.202206516 · Cited by 13
On-DNA hydroalkylation of N -vinyl heterocycles via photoinduced EDA-complex activation
Sharique, M., Matsuo, B. T., Granados, A., Kim, S., Arshad, M., Oh, H., Wu, V. E., Huang, M., Csakai, A., Marcaurelle, L. A., et al. (2023) · Chemical Science · doi:10.1039/d3sc03731b · Cited by 14
Randomized fast design of short DNA words
Kao, M., Sanghi, M., & Schweller, R. (2009) · ACM Transactions on Algorithms · doi:10.1145/1597036.1597047 · Cited by 13
“DNA words can be used to store information at the molecular level [Brenner 1997], act as molecular bar codes for identifying molecules in complex libraries [Brenner and Lerner 1992; Brenner 1997; Shoemaker et al. 1996], or implement DNA arrays [Ben-Dor et al.”
BackgroundDNA-Compatible Copper-Catalyzed Oxidative Amidation of Aldehydes with Non-Nucleophilic Arylamines
Li, K., Qu, Y., An, Y., Breinlinger, E. C., Webster, M. P., Wen, H., Ding, D., Zhao, M. Q., Shi, X., Wang, J., et al. (2020) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.0c00392 · Cited by 13
Multifunctional Peptide Synthetases Required for Nonribosomal Biosynthesis of Peptide Antibiotics
Rajendran, N., & Marahiel, M. A. (1999) · Elsevier eBooks · doi:10.1016/b978-0-08-091283-7.00094-1 · Cited by 13
Neilly, J. P., & Hochlowski, J. E. (1999) · Applied Spectroscopy · doi:10.1366/0003702991945245 · Cited by 13
Hypertension care at a Cape Town community health centre.
Lunt, D., Edwards, P. R., Steyn, K., Lombard, C. J., & Fehrsen, G. S. (1998) · PubMed · Cited by 13
Wang, S., & Leblanc, R. M. (1999) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(99)00079-6 · Cited by 13
Felder, E. R., Heizmann, G., Matthews, I. T. W., Rink, H., & Spieser, E. (1996) · Molecular Diversity · doi:10.1007/bf01721325 · Cited by 13
Carell, T., Wintner, E. A., & REBEK, J. J. (1994) · Angewandte Chemie · doi:10.1002/ange.19941062014 · Cited by 13
Effective heuristic methods for DNA strand design
Tulpan, D. (2010) · cIRcle (University of British Columbia) · doi:10.14288/1.0051756 · Cited by 13
Micelle‐Promoted Reductive Amination of DNA‐Conjugated Amines for DNA‐Encoded Library Synthesis
Anderson, M. J., Carton, T. P., Salvini, C. L. A., Crawford, J. J., Pairaudeau, G., & Waring, M. J. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202400239 · Cited by 12
DNA-Compatible Cyclization Reaction to Access 1,3,4-Oxadiazoles and 1,2,4-Triazoles
Wang, G., Tan, Y., Zou, H., Sui, X., Wang, Z., Satz, A. L., Kuai, L., Su, W., & Zhang, Q. (2024) · Organic Letters · doi:10.1021/acs.orglett.3c04240 · Cited by 12
Bräse, S. (2024) · Digital Discovery · doi:10.1039/d4dd00130c · Cited by 15
On-DNA Mannich Reaction for DNA-Encoded Library Synthesis
Ryzhikh, D., Seo, H., Lee, J., Lee, J., Nam, M. H., Song, M., & Hwang, G. T. (2024) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.4c02098 · Cited by 12
Synthesis of 5-Arylidene Thiohydantoin Derivatives via DNA-Compatible Knoevenagel Condensation
Fang, X., Ju, Y., Nie, Q., Fan, X., Wang, H., Li, Y., Zhang, G., & Li, Y. (2025) · 化学学报 · doi:10.6023/a25050155 · Cited by 13
Isocyanides: Promising Functionalities in Bioorthogonal Labeling of Biomolecules
Zhu, Y., Liao, J., & Qian, L. (2021) · Frontiers in Chemistry · doi:10.3389/fchem.2021.670751 · Cited by 12
“As early as 1992, Brenner and Lerner proposed the concept of adding a DNA barcode to chemically synthesized molecules to form DNAencoded libraries (Brenner and Lerner, 1992).”
BackgroundMaximizing the integration of virtual and experimental screening in hit discovery
Bajusz, D., & Keserű, G. M. (2022) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2022.2085685 · Cited by 11
“First conceptualized in 1992 [99], the DEL technology has reached its maturity in the past decade, with the advent of the necessary technological advances [100].”
BackgroundWu, X., Chen, Y., Lu, W., Jin, R., & Lu, X. (2022) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.2c00421 · Cited by 12
Encoding microcarriers for biomedicine
Wei, X., Shang, Y., Zhu, Y., Gu, Z., & Zhang, D. (2023) · Smart Medicine · doi:10.1002/smmd.20220009 · Cited by 12
Development of the Inverse Sonogashira Reaction for DEL Synthesis
Luo, A., Zhou, H., Hua, Q., An, Y., Ma, H., Zhao, X., Yang, K., & Hu, Y. J. (2023) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.2c00477 · Cited by 12
Wen, X., Zhang, M., Duan, Z., Suo, Y., Lu, W., Jin, R., Mu, B., Li, K., Zhang, X., Meng, L., et al. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c02129 · Cited by 12
Autonome Entdeckung in den chemischen Wissenschaften, Teil I: Fortschritt
Coley, C. W., Eyke, N. S., & Jensen, K. F. (2019) · Angewandte Chemie · doi:10.1002/ange.201909987 · Cited by 12
Zhang, Y., Luo, H., Ma, H., Wan, J., Ji, Y., Shaginian, A., Li, J., Deng, Y., & Liu, G. (2021) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.1c00346 · Cited by 12
Oligonucleotide-conjugated beads for transdominant genetic experiments
Feldhaus, M. J. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.2.534 · Cited by 12
Microarray Generation of Thousand-Member Oligonucleotide Libraries
Svensen, N., Díaz‐Mochon, J. J., & Bradley, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024906 · Cited by 12
“There are many examples of where DNA has been used as an encoding device for peptides or small molecules, enabling the high-throughput screening of peptide/small molecule interactions with a range of biological targets [1–10].”
BackgroundCombinatorial chemistry: A conservative perspective
Lyttle, M. H. (1995) · Drug Development Research · doi:10.1002/ddr.430350404 · Cited by 12
Speeding Up a Chemical Game of Chance
Amato, I. (1992) · Science · doi:10.1126/science.1631554 · Cited by 12
Edgington, S. M. (1993) · Nature Biotechnology · doi:10.1038/nbt0393-285 · Cited by 12
Pan, K., Meng, W., Yao, Y., Bi, W., Yang, G., & Xu, H. (2025) · Organic Letters · doi:10.1021/acs.orglett.5c03695 · Cited by 11
Zhang, Y., Lan, Y., Fan, R., Feng, L., Wang, G., Wu, X., Wen, L., Duan, Z., Xia, Y., Wang, X., et al. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c14634 · Cited by 13
sp3‐Rich Heterocycle Synthesis on DNA: Application to DNA‐Encoded Library Production
Gruber, F., McDonagh, A. W., Rose, V. E., Hunter, J. H., Guasch, L., Martin, R. E., Geigle, S. N., & Britton, R. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202319836 · Cited by 11
Advanced technologies for screening and identifying covalent inhibitors
Guo, Y., Wen, S., Tong, A., & Wang, Y. (2024) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2024.117833 · Cited by 11
Suo, Y., Xu, Q., Xiong, Z., Liu, X., Wang, C., Mu, B., Wu, X., Lu, W., Cui, M., Liu, J., et al. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c01416 · Cited by 11
Lee, K., Wang, H. M., Kim, M., Park, J., Kim, J., Jang, S., Im, D., Goh, B., Shin, M. H., Shim, J. H., et al. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.4c13487 · Cited by 10
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“First proposed by Brenner & Lerner in 1992, the emergence of next-generation sequencing technology may have fostered their renaissance [12].”
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Metadata
- Authors
- Brenner, S., & Lerner, R. A.
- Affiliations
- Scripps Research Institute (US)
- ORCID
- Lerner, R A
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1992-06-15
- Volume
- 89
- Issue
- 12
- Pages
- 5381-5383
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC49295
- OpenAlex
- W2017423606
- Cited by
- 1,014
- References
- 9
- Citations by year
- 2026: 60 · 2025: 77 · 2024: 71 · 2023: 73 · 2022: 87 · 2021: 72 · 2020: 52 · 2019: 55 · 2018: 30 · 2017: 32 · 2016: 25 · 2015: 24 · 2014: 13 · 2013: 9 · 2012: 8
- FWCI
- 8.46
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
- Physical Sciences › Chemistry › Organic Chemistry › Click Chemistry and Applications
- Keywords
- drug screening, gene tagging, ligand-receptor binding
- MeSH terms
- Amino Acid Sequence, Base Sequence, Molecular Sequence Data, Peptides, Restriction Mapping, Drug Design, Polymerase Chain Reaction, Databases, Factual
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