Abstract: We have optimized previously discovered benzoic acids 1, which are active as inhibitors of PTP1B and LMW-PTP, two protein tyrosine phosphatases that have emerged as attractive targets for the development of novel therapeutic agents for the treatment of diabetes, obesity, and cancer. Our efforts led to the identification of new and more potent analogues with appreciable selectivity toward human PTP1B and the IF1 isoform of human LMW-PTP.

Structure-Based Optimization of Benzoic Acids as Inhibitors of Protein Tyrosine Phosphatase 1B and Low Molecular Weight Protein Tyrosine Phosphatase / R. Maccari; R. Ottanà; R. Ciurleo; P. Paoli; G. Manao; G. Camici; C. Laggner; T. Langer. - In: CHEMMEDCHEM. - ISSN 1860-7179. - STAMPA. - 4:(2009), pp. 957-962. [10.1002/cmdc.200800427]

Structure-Based Optimization of Benzoic Acids as Inhibitors of Protein Tyrosine Phosphatase 1B and Low Molecular Weight Protein Tyrosine Phosphatase

PAOLI, PAOLO;MANAO, GIAMPAOLO;CAMICI, GUIDO;
2009

Abstract

Abstract: We have optimized previously discovered benzoic acids 1, which are active as inhibitors of PTP1B and LMW-PTP, two protein tyrosine phosphatases that have emerged as attractive targets for the development of novel therapeutic agents for the treatment of diabetes, obesity, and cancer. Our efforts led to the identification of new and more potent analogues with appreciable selectivity toward human PTP1B and the IF1 isoform of human LMW-PTP.
2009
4
957
962
R. Maccari; R. Ottanà; R. Ciurleo; P. Paoli; G. Manao; G. Camici; C. Laggner; T. Langer
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