Evidence map›Paper›PMID 40782141›Full record

ArticleMolecular diversity2026

Multicomponent reaction synthesis and evaluation of novel 3,4-dihydropyrazine[1,2-b]Indazole-1(2H)-one derivatives as inhibitors of pyroptosis and inflammation.

Zhen Dai, Donglin Yang, Ke Wang, Zhiping Chen, Jihong Tan, Yue Tian, DianYong Tang, Zhigang Xu, Zhongzhu Chen, Yong Li

Abstract read
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Article in Molecular diversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zhen DaiSchool of Pharmacy, Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu, 610106, Sichuan, China.
Donglin YangCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China. dlyang@cqwu.edu.cn.
Ke WangSchool of Pharmacy, Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu, 610106, Sichuan, China.
Zhiping ChenSchool of Pharmacy, Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu, 610106, Sichuan, China.
Jihong TanSchool of Pharmacy, Sichuan Industrial Institute of Antibiotics, Chengdu University, Chengdu, 610106, Sichuan, China.
Yue TianCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
DianYong TangCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Zhigang XuCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Zhongzhu ChenCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Yong LiCollege of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, Chongqing, 402160, China. 18708168370@163.com.

Funding

Sichuan Science and Technology Program 2023NSFSC1689the National Natural Science Foundation of China 82204220the Natural Science Foundation of Chongqing Science and Technology Bureau CSTB2024NSCQ-MSX0769the Natural Science Foundation of Chongqing Science and Technology Bureau cstc2022ycjh-bgzxm0170
6 · The paper itself

Abstract

Inflammation is a protective response by the body aimed at maintaining tissue homeostasis by eliminating pathogenic microbial infection, irritants, or tissue damage. However, dysregulated inflammation is pathological and involved in various diseases such as metabolic disorders, cancer, and neurodegenerative diseases. In this study, multicomponent reaction, an efficient tool for the synthesis of complex compounds with potential biological activities, was employed to synthesize twenty 3,4-dihydro-pyrazine[1,2-b]indazole-1(2H)-one derivatives and two 6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one analogues. We next identified compounds 6e and 6r as potential inhibitors for NLRP3 inflammasome-driven pyroptosis through activity-based screening and investigated their potential binding modes with the NLRP3 protein via molecular docking. Further studies on anti-inflammatory activity showed that compounds 6e and 6r also significantly inhibited LPS-induced NO release, among which compound 6e had better anti-inflammatory activity, with an IC

Indexed as

Anti-Inflammatory AgentsIndazolesInflammationPyrazinesPyroptosisAnimalsHumansMiceMolecular Docking SimulationNitric OxideNLR Family, Pyrin Domain-Containing 3 ProteinRAW 264.7 CellsStructure-Activity RelationshipAnti-Inflammatory AgentsIndazolesNitric OxideNLR Family, Pyrin Domain-Containing 3 ProteinPyrazinesInflammationMulticomponent reactionsPyroptosisUgi reaction

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.