Literature DB >> 34413951

The Growing Importance of Chirality in 3D Chemical Space Exploration and Modern Drug Discovery Approaches for Hit-ID: Topical Innovations.

Ilaria Proietti Silvestri1, Paul J J Colbon1.   

Abstract

Modern-day drug discovery is now blessed with a wide range of high-throughput hit identification (hit-ID) strategies that have been successfully validated in recent years, with particular success coming from high-throughput screening, fragment-based lead discovery, and DNA-encoded library screening. As screening efficiency and throughput increases, this enables the viable exploration of increasingly complex three-dimensional (3D) chemical structure space, with a realistic chance of identifying highly specific hit ligands with increased target specificity and reduced attrition rates in preclinical and clinical development. This minireview will explore the impact of an improved design of multifunctionalized, sp3-rich, stereodefined scaffolds on the (virtual) exploration of 3D chemical space and the specific requirements for different hit-ID technologies.
© 2021 American Chemical Society.

Entities:  

Year:  2021        PMID: 34413951      PMCID: PMC8366003          DOI: 10.1021/acsmedchemlett.1c00251

Source DB:  PubMed          Journal:  ACS Med Chem Lett        ISSN: 1948-5875            Impact factor:   4.632


  61 in total

Review 1.  Designing screens: how to make your hits a hit.

Authors:  W Patrick Walters; Mark Namchuk
Journal:  Nat Rev Drug Discov       Date:  2003-04       Impact factor: 84.694

Review 2.  SPR-based fragment screening: advantages and applications.

Authors:  T Neumann; H-D Junker; K Schmidt; R Sekul
Journal:  Curr Top Med Chem       Date:  2007       Impact factor: 3.295

Review 3.  Improvement in aqueous solubility in small molecule drug discovery programs by disruption of molecular planarity and symmetry.

Authors:  Minoru Ishikawa; Yuichi Hashimoto
Journal:  J Med Chem       Date:  2011-02-23       Impact factor: 7.446

4.  A Photoaffinity-Based Fragment-Screening Platform for Efficient Identification of Protein Ligands.

Authors:  Emma K Grant; David J Fallon; Michael M Hann; Ken G M Fantom; Chad Quinn; Francesca Zappacosta; Roland S Annan; Chun-Wa Chung; Paul Bamborough; David P Dixon; Peter Stacey; David House; Vipulkumar K Patel; Nicholas C O Tomkinson; Jacob T Bush
Journal:  Angew Chem Int Ed Engl       Date:  2020-09-07       Impact factor: 15.336

5.  Escaping from Flatland: Substituted Bridged Pyrrolidine Fragments with Inherent Three-Dimensional Character.

Authors:  Brian Cox; Victor Zdorichenko; Philip B Cox; Kevin I Booker-Milburn; Romain Paumier; Luke D Elliott; Michael Robertson-Ralph; Graham Bloomfield
Journal:  ACS Med Chem Lett       Date:  2020-03-27       Impact factor: 4.345

6.  Synthesis of Enantiomerically Pure 6-Substituted-Piperazine-2-Acetic Acid Esters as Intermediates for Library Production.

Authors:  Srinivas Chamakuri; Prashi Jain; Shiva Krishna Reddy Guduru; J Winston Arney; Kevin R MacKenzie; Conrad Santini; Damian W Young
Journal:  J Org Chem       Date:  2018-06-06       Impact factor: 4.354

Review 7.  Fragment-based drug discovery using NMR spectroscopy.

Authors:  Mary J Harner; Andreas O Frank; Stephen W Fesik
Journal:  J Biomol NMR       Date:  2013-05-18       Impact factor: 2.835

8.  Discovering Drugs with DNA-Encoded Library Technology: From Concept to Clinic with an Inhibitor of Soluble Epoxide Hydrolase.

Authors:  Svetlana L Belyanskaya; Yun Ding; James F Callahan; Aili L Lazaar; David I Israel
Journal:  Chembiochem       Date:  2017-03-24       Impact factor: 3.164

9.  A yoctoliter-scale DNA reactor for small-molecule evolution.

Authors:  Margit Haahr Hansen; Peter Blakskjaer; Lars Kolster Petersen; Tara Heitner Hansen; Jonas Westergaard Højfeldt; Kurt Vesterager Gothelf; Nils Jakob Vest Hansen
Journal:  J Am Chem Soc       Date:  2009-01-28       Impact factor: 15.419

10.  Cycloaddition Strategies for the Synthesis of Diverse Heterocyclic Spirocycles for Fragment-Based Drug Discovery.

Authors:  Thomas A King; Hannah L Stewart; Kim T Mortensen; Andrew J P North; Hannah F Sore; David R Spring
Journal:  European J Org Chem       Date:  2019-07-29
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  2 in total

1.  Catalytic Enantioselective Birch-Heck Sequence for the Synthesis of Phenanthridinone Derivatives with an All-Carbon Quaternary Stereocenter.

Authors:  Mary Sexton; William P Malachowski; Glenn P A Yap; Diana Rachii; Greg Feldman; Andrew T Krasley; Zhilin Chen; My Anh Tran; Kalyn Wiley; Alexandra Matei; Samantha Petersen; Sabrina Tran Tien
Journal:  J Org Chem       Date:  2022-01-05       Impact factor: 4.198

2.  Stereocontrolled Synthesis of Fluorinated Isochromans via Iodine(I)/Iodine(III) Catalysis.

Authors:  Joel Häfliger; Olga O Sokolova; Madina Lenz; Constantin G Daniliuc; Ryan Gilmour
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-13       Impact factor: 16.823

  2 in total

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