<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mao J</submitter><funding>Natural Science Foundation of Chongqing</funding><pagination>9150324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9938769</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2023</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To explore the potential molecular mechanism of &lt;i>Pueraria Lobata Radix&lt;/i> (RP) and &lt;i>Salviae Miltiorrhizae Radix&lt;/i> (RS) in the treatment of type 2 diabetes mellitus (T2DM) based on network pharmacology and molecular docking.&lt;h4>Methods&lt;/h4>The chemical constituents and core targets of RP and RS were searched by Traditional Chinese Medicine System Pharmacology (TCMSP); target genes related to T2DM were obtained through GeneCards database, component target network diagram was constructed, intersection genes of active compounds and T2DM were synthesized, protein-protein interaction (PPI) relationship was obtained, and core targets were screened by using Cytoscape 3.7.2. Gene Ontology (GO) biological process and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway wer</pubmed_abstract><journal>Computational and mathematical methods in medicine</journal><pubmed_title>Combined Network Pharmacology and Molecular Docking to Verify the Treatment of Type 2 Diabetes with &lt;i>Pueraria Lobata Radix&lt;/i> and &lt;i>Salviae Miltiorrhizae Radix&lt;/i>.</pubmed_title><pmcid>PMC9938769</pmcid><funding_grant_id>cstc2021jcyjmsxmX0452</funding_grant_id><funding_grant_id>cmba2022kyym-zkxmQ0003</funding_grant_id><funding_grant_id>KJQN202002801</funding_grant_id><funding_grant_id>2020YYCXCQSJ050</funding_grant_id><funding_grant_id>ygz2022101</funding_grant_id><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Tang L</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Mu Z</pubmed_authors><pubmed_authors>Tian C</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Fang L</pubmed_authors><pubmed_authors>Mao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combined Network Pharmacology and Molecular Docking to Verify the Treatment of Type 2 Diabetes with &lt;i>Pueraria Lobata Radix&lt;/i> and &lt;i>Salviae Miltiorrhizae Radix&lt;/i>.</name><description>&lt;h4>Objective&lt;/h4>To explore the potential molecular mechanism of &lt;i>Pueraria Lobata Radix&lt;/i> (RP) and &lt;i>Salviae Miltiorrhizae Radix&lt;/i> (RS) in the treatment of type 2 diabetes mellitus (T2DM) based on network pharmacology and molecular docking.&lt;h4>Methods&lt;/h4>The chemical constituents and core targets of RP and RS were searched by Traditional Chinese Medicine System Pharmacology (TCMSP); target genes related to T2DM were obtained through GeneCards database, component target network diagram was constructed, intersection genes of active compounds and T2DM were synthesized, protein-protein interaction (PPI) relationship was obtained, and core targets were screened by using Cytoscape 3.7.2. Gene Ontology (GO) biological process and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway wer</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-22T10:10:03.832Z</modification><creation>2025-04-05T23:31:09.451Z</creation></dates><accession>S-EPMC9938769</accession><cross_references><pubmed>36820318</pubmed><doi>10.1155/2023/9150324</doi></cross_references></HashMap>