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1.
Artigo em Inglês | MEDLINE | ID: mdl-37963000

RESUMO

Geographical entity representation learning (GERL) aims to embed geographical entities into a low-dimensional vector space, which provides a generalized approach for utilizing geographical entities to serve various geographical intelligence applications. In practice, the spatial distribution of geographical entities is highly unbalanced; thus, it is challenging to embed them accurately. Previous GERL models treated all geographical entities uniformly, resulting in insufficient entity representations. To address this issue, this article proposes an anchor-enhanced GERL (AE-GERL) model, which utilizes the key informative entities as anchors to improve the representations of geographical entities. Specifically, AE-GERL develops an anchor selection algorithm to identify anchors from large-scale geographical entities based on their spatial distribution and entity types. To utilize anchors to guide geographical entities, AE-GERL constructs an anchor-enhanced graph to establish explicit connections between anchors and nonanchor entities. Finally, a graph neural network (GNN) based anchor to nonanchor node learning model is designed to impute missing information of nonanchor entities. Extensive experiments are conducted on four datasets, and the experimental results demonstrate that AE-GERL outperforms the baseline models in both sparse and dense scenarios. This study provides a methodological reference for embedding geographical entities in various geographical applications and also provides an effective approach to improve the performance of message-passing-based GNN models.

2.
Bioorg Med Chem Lett ; 20(24): 7414-20, 2010 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-21055932

RESUMO

A novel series of quinolinone-based adenosine A(2B) receptor antagonists was identified via high throughput screening of an encoded combinatorial compound collection. Synthesis and assay of a series of analogs highlighted essential structural features of the initial hit. Optimization resulted in an A(2B) antagonist (2i) which exhibited potent activity in a cAMP accumulation assay (5.1 nM) and an IL-8 release assay (0.4 nM).


Assuntos
Antagonistas do Receptor A2 de Adenosina/química , Quinolonas/química , Receptor A2B de Adenosina/química , Antagonistas do Receptor A2 de Adenosina/síntese química , Antagonistas do Receptor A2 de Adenosina/farmacologia , Técnicas de Química Combinatória , Avaliação Pré-Clínica de Medicamentos , Humanos , Microssomos Hepáticos/metabolismo , Quinolonas/síntese química , Quinolonas/farmacologia , Receptor A2B de Adenosina/metabolismo , Relação Estrutura-Atividade
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