Synthesis of a Phosphoserine Mimetic Prodrug with Potent 14-3-3 Protein Inhibitory Activity-Reference-Cited by-同舟云学术

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Synthesis of a Phosphoserine Mimetic Prodrug with Potent 14-3-3 Protein Inhibitory Activity

Published:2012-06 Issue:6 Volume:19 Page:764-771
ISSN:1074-5521
Container-title:Chemistry & Biology
language:en
Short-container-title:Chemistry & Biology

Author:

Arrendale Allison,Kim Keunho,Choi Jun Young,Li Wei,Geahlen Robert L.,Borch Richard F.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry

Reference36 articles.

1. 14-3-3 proteins: a historic overview;Aitken;Semin. Cancer Biol.,2006

2. Formation of scalemic aziridines via the nucleophilic opening of aziridines;Bergmeier;J. Org. Chem.,1997

3. Synthesis of the (α,α-difluoroalkyl)phosphonate analogue of phosphoserine;Berkowitz;Tetrahedron Lett.,1994

4. Ready access to fluorinated phosphonate mimics of secondary phosphates. synthesis of the (α,α-difluoroalkyl)phosphonate analogues of L-phosphoserine, L-phosphoallothreonine, and L-phosphothreonine;Berkowitz;J. Org. Chem.,1996

5. Synthesis and cell-based activity of a potent and selective protein tyrosine phosphatase 1B inhibitor prodrug;Boutselis;J. Med. Chem.,2007

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1. 14‐3‐3 Family of Proteins: Biological Implications, Molecular Interactions, and Potential Intervention in Cancer, Virus and Neurodegeneration Disorders;Journal of Cellular Biochemistry;2024-06-30

2. Genetic Encoding of Phosphorylated Amino Acids into Proteins;Chemical Reviews;2024-05-01

3. Usnic Acid Targets 14-3-3 Proteins and Suppresses Cancer Progression by Blocking Substrate Interaction;JACS Au;2024-04-11

4. Access to mixed difluoromethylphosphonates by alkylation of phosphonamidates;Journal of Fluorine Chemistry;2022-09

5. Chiral Organophosphorus Compounds in Asymmetric Synthesis;Chiral Building Blocks in Asymmetric Synthesis;2022-08-12

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