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天然产物作为通过筛选获得潜在衰老细胞裂解化合物候选物的主要来源。

Natural Products as a Major Source of Candidates for Potential Senolytic Compounds obtained by Screening.

作者信息

Barrera-Vázquez Oscar S, Magos-Guerrero Gil A, Escobar-Ramírez Juan L, Gomez-Verjan Juan C

机构信息

Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.

Dirección de Investigación, Instituto Nacional de Geriatría, Mexico City, Mexico.

出版信息

Med Chem. 2023;19(7):653-668. doi: 10.2174/1573406419666221019153537.

Abstract

BACKGROUND

Preclinical studies suggest that senolytic compounds such as quercetin (a natural product) and dasatinib (a synthetic product) decrease senescent cells, reduce inflammation, and alleviate human frailty. This evidence has opened a new field of research for studying the effect of these compounds on age-related dysfunction and diseases.

OBJECTIVE

The present study performed in silico and we identified new potential senolytic candidates from an extensive database that contains natural products (NPs) and semi-synthetic products (SMSs).

METHODS

Computer programs Chemminer and rcdk packages, which compared the fingerprints of numerous molecules (40,383) with reference senolytics, and the creation of a pharmacological network built with signaling pathways and targets involved in senescence processes were used to identify compounds with a potential activity.

RESULTS

Six drug-like candidates (3,4'-dihydroxypropiophenone, baicalein, α, β-dehydrocurvularin, lovastatin, luteolin, and phloretin) were identified.

CONCLUSION

To our knowledge, this is the first time that these six natural molecules have been proposed to have senolytic activity. To validate the methodology employed in the identification of new drug-like senolytics, experimental evidence is needed with models that evaluate senolytic activity.

摘要

背景

临床前研究表明,槲皮素(一种天然产物)和达沙替尼(一种合成产物)等衰老细胞裂解化合物可减少衰老细胞、减轻炎症并缓解人体虚弱。这一证据开启了一个新的研究领域,用于研究这些化合物对与年龄相关的功能障碍和疾病的影响。

目的

本研究通过计算机模拟进行,我们从一个包含天然产物(NPs)和半合成产物(SMSs)的广泛数据库中鉴定出了新的潜在衰老细胞裂解候选物。

方法

使用计算机程序Chemminer和rcdk软件包,将众多分子(40383个)的指纹与参考衰老细胞裂解剂进行比较,并构建一个由衰老过程中涉及的信号通路和靶点组成的药理网络,以识别具有潜在活性的化合物。

结果

鉴定出六种类药物候选物(3,4'-二羟基苯丙酮、黄芩素、α,β-脱氢弯孢霉菌素、洛伐他汀、木犀草素和根皮素)。

结论

据我们所知,这是首次提出这六种天然分子具有衰老细胞裂解活性。为验证鉴定新的类药物衰老细胞裂解剂所采用的方法,需要使用评估衰老细胞裂解活性的模型提供实验证据。

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