The biosynthetic pathways of amino acids are attractive targets for drug development against pathogens with an intracellular behavior like M. tuberculosis (Mtb). Indeed, while in the macrophages Mtb has restricted access to amino acids such as tryptophan (Trp). Auxotrophic Mtb strains, with mutations in the Trp biosynthetic pathway, showed reduced intracellular survival in cultured human and murine macrophages and failed to cause the disease in immunocompetent and immunocompromised mice. Herein we present recent efforts in the discovery of Trp biosynthesis inhibitors.

Mycobacterial tryptophan biosynthesis: a promising target for tuberculosis drug development? / Consalvi, Sara; Scarpecci, Cristina; Biava, Mariangela; Poce, Giovanna. - In: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - ISSN 0960-894X. - 29:23(2019), p. 126731. [10.1016/j.bmcl.2019.126731]

Mycobacterial tryptophan biosynthesis: a promising target for tuberculosis drug development?

Sara Consalvi
Primo
;
Cristina Scarpecci
Secondo
;
Mariangela Biava
Penultimo
;
Giovanna Poce
Ultimo
2019

Abstract

The biosynthetic pathways of amino acids are attractive targets for drug development against pathogens with an intracellular behavior like M. tuberculosis (Mtb). Indeed, while in the macrophages Mtb has restricted access to amino acids such as tryptophan (Trp). Auxotrophic Mtb strains, with mutations in the Trp biosynthetic pathway, showed reduced intracellular survival in cultured human and murine macrophages and failed to cause the disease in immunocompetent and immunocompromised mice. Herein we present recent efforts in the discovery of Trp biosynthesis inhibitors.
2019
tuberculosis; drug discovery; tryptophan; M. tuberculosis; inhibitors
01 Pubblicazione su rivista::01g Articolo di rassegna (Review)
Mycobacterial tryptophan biosynthesis: a promising target for tuberculosis drug development? / Consalvi, Sara; Scarpecci, Cristina; Biava, Mariangela; Poce, Giovanna. - In: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS. - ISSN 0960-894X. - 29:23(2019), p. 126731. [10.1016/j.bmcl.2019.126731]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1334361
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