Literature DB >> 25499878

Isotope chemistry; a useful tool in the drug discovery arsenal.

Charles S Elmore1, Ryan A Bragg2.   

Abstract

As Medicinal Chemists are responsible for the synthesis and optimization of compounds, they often provide intermediates for use by isotope chemistry. Nevertheless, there is generally an incomplete understanding of the critical factors involved in the labeling of compounds. The remit of an Isotope Chemistry group varies from company to company, but often includes the synthesis of compounds labeled with radioisotopes, especially H-3 and C-14 and occasionally I-125, and stable isotopes, especially H-2, C-13, and N-15. Often the remit will also include the synthesis of drug metabolites. The methods used to prepare radiolabeled compounds by Isotope Chemists have been reviewed relatively recently. However, the organization and utilization of Isotope Chemistry has not been discussed recently and will be reviewed herein.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  C-14; Isotope chemistry; Isotopic labeling; Tritium

Mesh:

Substances:

Year:  2014        PMID: 25499878     DOI: 10.1016/j.bmcl.2014.11.051

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  22 in total

1.  Enabling Two-Electron Pathways with Iron and Cobalt: From Ligand Design to Catalytic Applications.

Authors:  Rebeca Arevalo; Paul J Chirik
Journal:  J Am Chem Soc       Date:  2019-05-28       Impact factor: 15.419

2.  Catalytic Deuterium Incorporation within Metabolically Stable β-Amino C-H Bonds of Drug Molecules.

Authors:  Yejin Chang; Ahmet Yesilcimen; Min Cao; Yuyang Zhang; Bochao Zhang; Jessica Z Chan; Masayuki Wasa
Journal:  J Am Chem Soc       Date:  2019-09-09       Impact factor: 15.419

3.  Photoredox-catalyzed deuteration and tritiation of pharmaceutical compounds.

Authors:  Yong Yao Loh; Kazunori Nagao; Andrew J Hoover; David Hesk; Nelo R Rivera; Steven L Colletti; Ian W Davies; David W C MacMillan
Journal:  Science       Date:  2017-11-09       Impact factor: 47.728

4.  B(C6F5)3-Catalyzed α-Deuteration of Bioactive Carbonyl Compounds with D2O.

Authors:  Yejin Chang; Tanner Myers; Masayuki Wasa
Journal:  Adv Synth Catal       Date:  2019-11-26       Impact factor: 5.837

5.  Site-Selective α-C-H Functionalization of Trialkylamines via Reversible Hydrogen Atom Transfer Catalysis.

Authors:  Yangyang Shen; Ignacio Funez-Ardoiz; Franziska Schoenebeck; Tomislav Rovis
Journal:  J Am Chem Soc       Date:  2021-11-05       Impact factor: 15.419

6.  Direct Carbon Isotope Exchange through Decarboxylative Carboxylation.

Authors:  Cian Kingston; Michael A Wallace; Alban J Allentoff; Justine N deGruyter; Jason S Chen; Sharon X Gong; Samuel Bonacorsi; Phil S Baran
Journal:  J Am Chem Soc       Date:  2019-01-03       Impact factor: 15.419

7.  Organophotocatalytic selective deuterodehalogenation of aryl or alkyl chlorides.

Authors:  Yanjun Li; Ziqi Ye; Yu-Mei Lin; Yan Liu; Yumeng Zhang; Lei Gong
Journal:  Nat Commun       Date:  2021-05-17       Impact factor: 14.919

8.  Formyl-selective deuteration of aldehydes with D2O via synergistic organic and photoredox catalysis.

Authors:  Jianyang Dong; Xiaochen Wang; Zhen Wang; Hongjian Song; Yuxiu Liu; Qingmin Wang
Journal:  Chem Sci       Date:  2019-12-04       Impact factor: 9.825

Review 9.  Six Decades of Research on Human Fetal Gonadal Steroids.

Authors:  Stéphane Connan-Perrot; Thibaut Léger; Pauline Lelandais; Christèle Desdoits-Lethimonier; Arthur David; Paul A Fowler; Séverine Mazaud-Guittot
Journal:  Int J Mol Sci       Date:  2021-06-22       Impact factor: 5.923

10.  Light-driven decarboxylative deuteration enabled by a divergently engineered photodecarboxylase.

Authors:  Jian Xu; Jiajie Fan; Yujiao Lou; Weihua Xu; Zhiguo Wang; Danyang Li; Haonan Zhou; Xianfu Lin; Qi Wu
Journal:  Nat Commun       Date:  2021-06-25       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.