Literature DB >> 20214568

Aminophosphonic acids and derivatives. Synthesis and biological applications.

F Orsini1, G Sello, M Sisti.   

Abstract

In recent years, phosphonic acids and their derivatives have received increasing attention as analogues of a series of naturally occurring phosphates and as "bio-isosteric phosphorus analogues" of amino acids. Unlike a phosphate group, the phosphonate moiety is not readily hydrolyzed, in a biological environment, by the enzymes involved in the phosphate cleavage. This feature makes these compounds extremely useful in several applications, in metabolic regulation, in enhancement or inhibition studies, in the development of potential drugs against several metabolic disorders. The great potential of these compounds in biological applications resulted in an intense effort directed to the development of efficient synthetic methods for their preparation, with particular attention to stereoselective synthesis. The purpose of this review is to give an up-to-date account of the chemistry, the synthesis and the biological activity of aminophosphonic acids and their derivatives.

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Year:  2010        PMID: 20214568     DOI: 10.2174/092986710790149729

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  23 in total

1.  New approaches towards the synthesis of 1,2,3,4-tetrahydro isoquinoline-3-phosphonic acid (TicP).

Authors:  José Luis Viveros-Ceballos; Lizeth A Matías-Valdez; Francisco J Sayago; Carlos Cativiela; Mario Ordóñez
Journal:  Amino Acids       Date:  2021-03-01       Impact factor: 3.520

2.  Divergence of chemical function in the alkaline phosphatase superfamily: structure and mechanism of the P-C bond cleaving enzyme phosphonoacetate hydrolase.

Authors:  Alexander Kim; Matthew M Benning; Sang OkLee; John Quinn; Brian M Martin; Hazel M Holden; Debra Dunaway-Mariano
Journal:  Biochemistry       Date:  2011-04-08       Impact factor: 3.162

3.  Redox-neutral α-C-H bond functionalization of secondary amines with concurrent C-P bond formation/N-alkylation.

Authors:  Deepankar Das; Daniel Seidel
Journal:  Org Lett       Date:  2013-08-19       Impact factor: 6.005

4.  Functionalization of α-hydroxyphosphonates as a convenient route to N-tosyl-α-aminophosphonates.

Authors:  Tomasz Cytlak; Monika Skibińska; Patrycja Kaczmarek; Marcin Kaźmierczak; Magdalena Rapp; Maciej Kubicki; Henryk Koroniak
Journal:  RSC Adv       Date:  2018-03-27       Impact factor: 4.036

5.  Synthesis, cytotoxicity, DNA binding and apoptosis of rhein-phosphonate derivatives as antitumor agents.

Authors:  Man-Yi Ye; Gui-Yang Yao; Jing-Chen Wei; Ying-Ming Pan; Zhi-Xin Liao; Heng-Shan Wang
Journal:  Int J Mol Sci       Date:  2013-04-29       Impact factor: 5.923

6.  α,β-Aziridinylphosphonates by lithium amide-induced phosphonyl migration from nitrogen to carbon in terminal aziridines.

Authors:  David M Hodgson; Zhaoqing Xu
Journal:  Beilstein J Org Chem       Date:  2010-10-13       Impact factor: 2.883

7.  rac-Dimethyl [(9-anthr-yl)(4-methyl-anilino)meth-yl]phospho-nate.

Authors:  Ivanka Kraicheva; Ivelina Tsacheva; Elitsa Vodenicharova; Emil Tashev; Kolio Troev
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-07-16

8.  (R)-Methyl {[(2-carb-oxy-bicyclo-[2.2.2]octan-1-yl)-ammonio]-methyl}-phos-phon-ate dichloro-methane 0.25-solvate.

Authors:  Petar Todorov; Monique Calmes; Boris L Shivachev; Rosica P Nikolova
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-07-30

9.  Highly Diastereoselective Construction of Carbon- Heteroatom Quaternary Stereogenic Centers in the Synthesis of Analogs of Bioactive Compounds: From Monofluorinated Epoxyalkylphosphonates to α-Fluoro-, β-, or γ-Amino Alcohol Derivatives of Alkylphosphonates.

Authors:  Magdalena Rapp; Klaudia Margas-Musielak; Patrycja Kaczmarek; Agnieszka Witkowska; Tomasz Cytlak; Tomasz Siodła; Henryk Koroniak
Journal:  Front Chem       Date:  2021-06-02       Impact factor: 5.221

10.  Differentiation of diastereoisomers of protected 1,2-diaminoalkylphosphonic acids by EI mass spectrometry and density functional theory.

Authors:  Ewelina Drabik; Grzegorz Krasiński; Marek Cypryk; Roman Błaszczyk; Tadeusz Gajda; Marek Sochacki
Journal:  J Am Soc Mass Spectrom       Date:  2013-02-08       Impact factor: 3.109

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