Synopsis of some recent tactical application of bioisosteres in drug design.
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Summary
In this Perspective, some contemporary themes exploring the role of isosteres in drug design are sampled, with an emphasis placed on tactical applications designed to solve the kinds of problems that impinge on compound optimization and the long-term success of drug candidates.
- Type
- article
- Published
- 2011-03-17
- Cited by
- 2,267
- References
- 347
- Access
- Open access
- OpenAlex
- https://openalex.org/W1975947882
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:26355203
Keywords
Citation, Phone, Computer science, Library science, Social media
References
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- Structure-based drug design of new leads for phosphatase research.
- Bioorganic and Medicinal Chemistry of Fluorine
- An approach to lipophilic nucleotide phosphate analogs: Synthesis of a lipophilic isostere of ATP
- The Weak Hydrogen Bond: In Structural Chemistry and Biology
- Observations on the strength of hydrogen bonding
- A novel synthesis of α- and γ- fluoroalkylphosphonates
- A possible mechanism of eighteen patient deaths caused by interactions of sorivudine, a new antiviral drug, with oral 5-fluorouracil prodrugs.
- Methoxy group nonplanarity in o-dimethoxybenzenes. Simple predictive models for conformations and rotational barriers in alkoxyaromatics
- Discovery and SAR of hydantoin TACE inhibitors.
- Design of a series of bicyclic HIV-1 integrase inhibitors. Part 1: selection of the scaffold.
- Toward Safe Genetically Modified Organisms through the Chemical Diversification of Nucleic Acids
- HYDROGEN-BOND BASICITY PKHB SCALE OF SIX-MEMBERED AROMATIC N-HETEROCYCLES
- The Magnitude of the Primary Kinetic Isotope Effect for Compounds of Hydrogen and Deuterium.
- (S)-(+)-2-(3'-carboxybicyclo[1.1.1]pentyl)-glycine, a structurally new group I metabotropic glutamate receptor antagonist.
- Design, synthesis, and evaluation of 3,4-dihydro-2H-[1,4]diazepino[6,7,1-hi]indol-1-ones as inhibitors of poly(ADP-ribose) polymerase.
Cited by
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- Synthesis and Anti‐Proliferative Activity of Sulfanyltriazolylnaphthalenols and Sulfanyltriazolylnaphthalene‐1,4‐diones
- Cu-Catalyzed Aminodifluoroalkylation of Alkynes and α-Bromodifluoroacetamides.
- PAd2-DalPhos Enables the Nickel-Catalyzed C-N Cross-Coupling of Primary Heteroarylamines and (Hetero)aryl Chlorides.
- Development of ligands for the validation of the lysophosphatidic acid receptor LPA
- Investigation of Candida albicans Prenyltransferases: Substrate Recognition and Enzyme Inhibition.
- Application of the guanidine–acylguanidine bioisosteric approach to NPY Y2 receptor antagonists: bivalent, radiolabeled and fluorescent pharmacological tools
- Synthesis and structure-activity relationships of inhibitors of bacterial hyaluronidase: An approach to obtain compounds with drug-like properties
- Practical strategies for small-molecule probe development in chemical biology.
- Shelf-stable electrophilic reagents for trifluoromethylthiolation.
- Dialkylzinc-mediated allylic polyfluoroarylation reaction
- Refining the chemical toolbox to be fit for educational and practical purpose for drug discovery in the 21st Century.
- Design, Synthesis, and Evaluation of Functionalized Chroman-4-one and Chromone Derivatives. Somatostatin receptor agonists and Sirt2 inhibitors
- Stereochemical properties of N-benzoylated carbazole derivatives
- 先导化合物结构优化策略(一)——改变代谢途径提高代谢稳定性
- Copper-Promoted Trifluoromethanesulfonylation and Trifluoromethylation of Arenediazonium Tetrafluoroborates with NaSO2CF3.
- Cytotoxicity of Thiazolidinedione-, Oxazolidinedione- and Pyrrolidinedione-Ring Containing Compounds in HepG2 Cells
- Palladium-Catalyzed Monofluoromethylation of Arylboronic Esters with Fluoromethyl Iodide.
- Selective synthesis of fluoroalkyl-containing multisubstituted benzenes through Co-mediated [2+2+2] cycloaddition reaction with fluoroalkylated alkynes
- 6-Arylpyrazine-2-carboxamides: A New Core for Trypanosoma brucei Inhibitors.
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