Literature DB >> 32663408

The Most Common Functional Groups in Bioactive Molecules and How Their Popularity Has Evolved over Time.

Peter Ertl1, Eva Altmann1, Jeffrey M McKenna2.   

Abstract

The concept of functional groups (FGs), sets of connected atoms that can determine the intrinsic reactivity of the parent molecule and in part are responsible for the overall properties of the molecule, form a foundation within modern medicinal chemistry. In this Article, we analyze the occurrence of various FGs in molecules described in the medicinal chemistry literature over the last 40 years and show how their development and utilization over time has varied. The popularity of various FGs has not evolved randomly, but instead, clear patterns of use are evident. Various factors influencing these patterns, including the introduction of new synthetic methods, novel techniques, and strategies applied in drug discovery and the better knowledge of molecular properties affecting the success of candidate development, are discussed.

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Year:  2020        PMID: 32663408     DOI: 10.1021/acs.jmedchem.0c00754

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  16 in total

1.  Chemoselective Transamidation of Thioamides by Transition-Metal-Free N-C(S) Transacylation.

Authors:  Guangchen Li; Yangyang Xing; Hui Zhao; Jin Zhang; Xin Hong; Michal Szostak
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-23       Impact factor: 15.336

2.  Ti-Catalyzed and -Mediated Oxidative Amination Reactions.

Authors:  Ian A Tonks
Journal:  Acc Chem Res       Date:  2021-08-22       Impact factor: 24.466

3.  Forging C-S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides.

Authors:  Chengwei Liu; Michal Szostak
Journal:  ChemCatChem       Date:  2021-09-25       Impact factor: 5.497

4.  Bioisostere Effects on the EPSA of Common Permeability-Limiting Groups.

Authors:  Andrew K Ecker; Dorothy A Levorse; Daniel A Victor; Matthew J Mitcheltree
Journal:  ACS Med Chem Lett       Date:  2022-05-23       Impact factor: 4.632

Review 5.  Replacement of Less-Preferred Dipolar Aprotic and Ethereal Solvents in Synthetic Organic Chemistry with More Sustainable Alternatives.

Authors:  Andrew Jordan; Callum G J Hall; Lee R Thorp; Helen F Sneddon
Journal:  Chem Rev       Date:  2022-02-24       Impact factor: 72.087

6.  Amino-oxetanes as amide isosteres by an alternative defluorosulfonylative coupling of sulfonyl fluorides.

Authors:  Juan J Rojas; Rosemary A Croft; Alistair J Sterling; Edward L Briggs; Daniele Antermite; Daniel C Schmitt; Luka Blagojevic; Peter Haycock; Andrew J P White; Fernanda Duarte; Chulho Choi; James J Mousseau; James A Bull
Journal:  Nat Chem       Date:  2022-01-27       Impact factor: 24.274

7.  Decatungstate-Catalyzed C(sp3)-H Sulfinylation: Rapid Access to Diverse Organosulfur Functionality.

Authors:  Patrick J Sarver; Noah B Bissonnette; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2021-06-23       Impact factor: 15.419

8.  Overview of the SAMPL6 pKa challenge: evaluating small molecule microscopic and macroscopic pKa predictions.

Authors:  Mehtap Işık; Ariën S Rustenburg; Andrea Rizzi; M R Gunner; David L Mobley; John D Chodera
Journal:  J Comput Aided Mol Des       Date:  2021-01-04       Impact factor: 3.686

9.  R-group replacement database for medicinal chemistry.

Authors:  Kosuke Takeuchi; Ryo Kunimoto; Jürgen Bajorath
Journal:  Future Sci OA       Date:  2021-06-30

10.  Nickel-Catalyzed Deaminative Cyanation: Nitriles and One-Carbon Homologation from Alkyl Amines.

Authors:  Jianyu Xu; J Cameron Twitty; Mary P Watson
Journal:  Org Lett       Date:  2021-07-30       Impact factor: 6.072

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