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AnLeadOp

Financiado

Cerrado

Antibiotic Lead Optimization

The bacterial sliding clamp (DnaN) is an innovative target for the development of novel antibiotics, which are urgently needed to overcome the alarming antimicrobial resistance crisis. In the previous ERC starting grant (NovAnI),... ver más

30/11/2024

HZI

150K€

Presupuesto del proyecto: 150K€

Líder del proyecto

HELMHOLTZZENTRUM FUR INFEKTIONSFORSCHUNG GMBH No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo HORIZON EUROPE notifico la concesión del proyecto el día 2024-11-30

ERC-2022-POC2: ERC PROOF OF CONCEPT GRANTS2 Objective:Objectives:

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Cerrada hace 2 años

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Información adicional privada

No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

HZI

150.00K€ | Lider

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Duración del proyecto: 18 meses Fecha Inicio: 2023-05-05
Fecha Fin: 2024-11-30

Líder del proyecto

HELMHOLTZZENTRUM FUR INFEKTIONSFORSCHUNG GMBH No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 150K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto The bacterial sliding clamp (DnaN) is an innovative target for the development of novel antibiotics, which are urgently needed to overcome the alarming antimicrobial resistance crisis. In the previous ERC starting grant (NovAnI), we discovered a novel DnaN inhibitor (WAM-N17) with promising broad-spectrum antibacterial activity including multidrug-resistant (MDR) pathogens. In this PoC project, we will optimize the antibacterial potency and spectrum and characterize the in vivo pharmacokinetic (PK) and pharmacodynamic (PD) properties of the WAM-N17 class so as to develop preclinical lead candidates for the treatment of bacterial infections, especially those caused by MDR germs. To achieve this goal, we will pursue three main activities. (i) Design and synthesis of 25–30 compounds (in two rounds) with modifications focusing on improving the anti-Gram-negative activity as well as target identification through chemical probes to further validate DnaN and identify other potential targets in bacteria. (ii) Evaluation of antibacterial activity, target binding/inhibition, and in vitro ADME-T (absorption, distribution, metabolism, excretion, toxicity) characterization for all new compounds. The frontrunners will be profiled for antibacterial activity against an extended panel of Gram-negative and MDR clinical isolates and subjected to mode of action (MoA) and target-identification studies. The most promising ten compounds will be submitted for in vivo PK studies and the best two lead candidates will be tested in a proof-of-concept in vivo efficacy study using relevant infection mouse models. (iii) Ultimately, we will file a patent to secure our intellectual property rights and continue to move this class of compounds forward into preclinical and then clinical studies in collaboration with a pharmaceutical industry partner. The knowledge that will be gained from this PoC project is essential to develop an urgently needed new antibiotic with an unprecedented mode of action.

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