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J Enzyme Inhib Med Chem ; 37(1): 2434-2451, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-36069240

RESUMO

In an effort to discover novel scaffolds of non-nucleotide-derived Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors to stimulate the Stimulator of Interferon Genes (STING) pathway, we designed and synthesised pyrrolopyrimidine and pyrrolopyridine derivatives and performed structure-activity relationship (SAR) study. We found 18p possessed high potency (IC50 = 25.0 nM) against ENPP1, and activated STING pathway in a concentration dependent manner. Also, in response to STING pathway activation, cytokines such as IFN-ß and IP-10 were induced by 18p in a concentration dependent manner. Finally, we discovered that 18p causes inhibition of tumour growth in 4T1 syngeneic mouse model. This study provides new insight into the designing of novel ENPP1 inhibitors and warrants further development of small molecule immune modulators for cancer immunotherapy.


Assuntos
Diester Fosfórico Hidrolases , Pirofosfatases , Animais , Camundongos , Diester Fosfórico Hidrolases/metabolismo , Pirimidinas , Pirofosfatases/genética , Pirofosfatases/metabolismo , Pirróis/farmacologia , Relação Estrutura-Atividade
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