Synthesis and Pharmacological Evaluation of Novel Non-nucleotide Purine Derivatives as P2X7 Antagonists for the Treatment of Neuroinflammation.
第一作者:
Francesco,Calzaferri
第一单位:
Instituto-Fundación Teófilo Hernando and Departamento de Farmacología, Facultad de Medicina, Universidad Autónoma de Madrid, C/ Arzobispo Morcillo 4, 28029 Madrid, Spain.
作者:
主题词
腺苷三磷酸酶类(Adenosine Triphosphatases);动物(Animals);消炎药(Anti-Inflammatory Agents);HEK293细胞(HEK293 Cells);人类(Humans);白细胞介素1β(Interleukin-1beta);巨噬细胞, 腹膜(Macrophages, Peritoneal);男(雄)性(Male);小鼠, 近交C57BL(Mice, Inbred C57BL);卵母细胞(Oocytes);嘌呤能P2X受体拮抗剂(Purinergic P2X Receptor Antagonists);嘌呤类(Purines);受体, 嘌呤能P2X7(Receptors, Purinergic P2X7);光滑爪蟾(Xenopus laevis);小鼠(Mice)
DOI
10.1021/acs.jmedchem.0c02145
PMID
33560845
发布时间
2024-02-26
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Journal of medicinal chemistry
2272-2290页
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