<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(3)</volume><submitter>Djehiche C</submitter><pubmed_abstract>&lt;i>Ammodaucus leucotrichus&lt;/i> exhibits promising pharmacological activity, hinting at anti-inflammatory and anti-arthritic effects. This study investigated seed extracts from &lt;i>Ammodaucus leucotrichus&lt;/i> using methanol and n-hexane, focusing on anti-inflammatory and anti-arthritic properties. The methanol extract outperformed the n-hexane extract and diclofenac, a reference anti-inflammatory drug, in trypsin inhibition (85% vs. 30% and 64.67% at 125 μg/mL). For trypsin inhibition, the IC50 values were 82.97 μg/mL (methanol), 202.70 μg/mL (n-hexane), and 97.04 μg/mL (diclofenac). Additionally, the n-hexane extract surpassed the methanol extract and diclofenac in BSA (bovine serum albumin) denaturation inhibition (90.4% vs. 22.0% and 51.4% at 62.5 μg/mL). The BSA denaturation IC50 values were 14.30 μg/mL (n-hexane), 5408 μg/mL (methanol), and 42.30 μg/mL (diclofenac). Gas chromatography-mass spectrometry (GC-MS) revealed 59 and 58 secondary metabolites in the methanol and n-hexane extracts, respectively. The higher therapeutic activity of the methanol extract was attributed to hydroxyacetic acid hydrazide, absent in the n-hexane extract. In silico docking studies identified 28 compounds with negative binding energies, indicating potential trypsin inhibition. The 2-hydroxyacetohydrazide displayed superior inhibitory effects compared to diclofenac. Further mechanistic studies are crucial to validate 2-hydroxyacetohydrazide as a potential drug candidate for rheumatoid arthritis treatment.</pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pagination>385</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10974001</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exploring the Therapeutic Potential of &lt;i>Ammodaucus leucotrichus&lt;/i> Seed Extracts: A Multi-Faceted Analysis of Phytochemical Composition, Anti-Inflammatory Efficacy, Predictive Anti-Arthritic Properties, and Molecular Docking Insights.</pubmed_title><pmcid>PMC10974001</pmcid><pubmed_authors>Djeghim H</pubmed_authors><pubmed_authors>Mebrek S</pubmed_authors><pubmed_authors>Tebboub M</pubmed_authors><pubmed_authors>Djehiche C</pubmed_authors><pubmed_authors>Bechelany M</pubmed_authors><pubmed_authors>Bensouici C</pubmed_authors><pubmed_authors>Messaoudi M</pubmed_authors><pubmed_authors>Arrar L</pubmed_authors><pubmed_authors>Cornu D</pubmed_authors><pubmed_authors>Barhoum A</pubmed_authors><pubmed_authors>Benzidane N</pubmed_authors><pubmed_authors>Alsalme A</pubmed_authors><pubmed_authors>Mokrani EH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploring the Therapeutic Potential of &lt;i>Ammodaucus leucotrichus&lt;/i> Seed Extracts: A Multi-Faceted Analysis of Phytochemical Composition, Anti-Inflammatory Efficacy, Predictive Anti-Arthritic Properties, and Molecular Docking Insights.</name><description>&lt;i>Ammodaucus leucotrichus&lt;/i> exhibits promising pharmacological activity, hinting at anti-inflammatory and anti-arthritic effects. This study investigated seed extracts from &lt;i>Ammodaucus leucotrichus&lt;/i> using methanol and n-hexane, focusing on anti-inflammatory and anti-arthritic properties. The methanol extract outperformed the n-hexane extract and diclofenac, a reference anti-inflammatory drug, in trypsin inhibition (85% vs. 30% and 64.67% at 125 μg/mL). For trypsin inhibition, the IC50 values were 82.97 μg/mL (methanol), 202.70 μg/mL (n-hexane), and 97.04 μg/mL (diclofenac). Additionally, the n-hexane extract surpassed the methanol extract and diclofenac in BSA (bovine serum albumin) denaturation inhibition (90.4% vs. 22.0% and 51.4% at 62.5 μg/mL). The BSA denaturation IC50 values were 14.30 μg/mL (n-hexane), 5408 μg/mL (methanol), and 42.30 μg/mL (diclofenac). Gas chromatography-mass spectrometry (GC-MS) revealed 59 and 58 secondary metabolites in the methanol and n-hexane extracts, respectively. The higher therapeutic activity of the methanol extract was attributed to hydroxyacetic acid hydrazide, absent in the n-hexane extract. In silico docking studies identified 28 compounds with negative binding energies, indicating potential trypsin inhibition. The 2-hydroxyacetohydrazide displayed superior inhibitory effects compared to diclofenac. Further mechanistic studies are crucial to validate 2-hydroxyacetohydrazide as a potential drug candidate for rheumatoid arthritis treatment.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2024-11-13T16:28:14.514Z</modification><creation>2024-11-13T16:28:14.514Z</creation></dates><accession>S-EPMC10974001</accession><cross_references><pubmed>38543170</pubmed><doi>10.3390/ph17030385</doi></cross_references></HashMap>