<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liang Y</submitter><funding>Natural Science Foundation of Tibet Autonomous Region</funding><funding>Central leading local project</funding><funding>The central government guided the local project &amp;quot;research and demonstration of high-efficiency double lamb vaccine and main supporting technologies&amp;quot;</funding><funding>Natural Science Foundation of Tibet Autonomous Region &amp;quot;Research on the preparation of double lambshin vaccine for sheep by heavy ion irradiation technology&amp;quot;</funding><pagination>2888</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9104299</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(9)</volume><pubmed_abstract>Dairy mastitis is a disease of dairy cattle caused by a variety of pathogenic microorganisms which has biought huge economic losses aused huge economic losses to the world. In this paper, Harmine derivatives and tetrahydro-β-carboline derivatives synthesized by the splice method are shown to have a good inhibitory effect on the pathogenic bacteria of dairy mastitis. The results of a bacteriostatic test on pathogenic bacteria of dairy cow mastitis (&lt;i>S. dysgalactiae&lt;/i>, &lt;i>S. pyogenes&lt;/i>, &lt;i>B. subtilis&lt;/i> and &lt;i>P. vulgaris&lt;/i>) showed that compound &lt;b>7l&lt;/b> had the best bacteriostatic effect on &lt;i>Streptococcus dysgalactiae&lt;/i>, with a mic value of 43.7 μ g/mL. When the concentration of &lt;b>7l&lt;/b> was 1 × MIC and 2 × MIC, it had a significant inhibitory effect on &lt;i>Streptococcus dysgalactiae&lt;/i>, and there was almost no growth of &lt;i>Streptococcus dysgalactiae&lt;/i> at 4 × MIC. The binding properties of target compound &lt;b>7l&lt;/b> to &lt;i>amine oxidase [flavin-containing] A&lt;/i> protein were simulated by the molecular docking technique. The ligand &lt;b>7l&lt;/b> achieved strong binding with the receptor through three hydrogen bonds. The hydrogen bonds were amino acid residues thr-52, arg-51 and ser-24, which are the main force for the compound to bind to active sites.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Synthesis and Antibacterial Study of Novel Harmine Derivatives and Tetrahydro-β-Carboline Derivatives In Vitro.</pubmed_title><pmcid>PMC9104299</pmcid><funding_grant_id>ZRKX2021000123</funding_grant_id><funding_grant_id>XZ202101YD0019C</funding_grant_id><funding_grant_id>XZ202101ZR0070G</funding_grant_id><pubmed_authors>Tang L</pubmed_authors><pubmed_authors>He D</pubmed_authors><pubmed_authors>Liang Y</pubmed_authors><pubmed_authors>Song T</pubmed_authors><pubmed_authors>Zhou D</pubmed_authors><pubmed_authors>He B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and Antibacterial Study of Novel Harmine Derivatives and Tetrahydro-β-Carboline Derivatives In Vitro.</name><description>Dairy mastitis is a disease of dairy cattle caused by a variety of pathogenic microorganisms which has biought huge economic losses aused huge economic losses to the world. In this paper, Harmine derivatives and tetrahydro-β-carboline derivatives synthesized by the splice method are shown to have a good inhibitory effect on the pathogenic bacteria of dairy mastitis. The results of a bacteriostatic test on pathogenic bacteria of dairy cow mastitis (&lt;i>S. dysgalactiae&lt;/i>, &lt;i>S. pyogenes&lt;/i>, &lt;i>B. subtilis&lt;/i> and &lt;i>P. vulgaris&lt;/i>) showed that compound &lt;b>7l&lt;/b> had the best bacteriostatic effect on &lt;i>Streptococcus dysgalactiae&lt;/i>, with a mic value of 43.7 μ g/mL. When the concentration of &lt;b>7l&lt;/b> was 1 × MIC and 2 × MIC, it had a significant inhibitory effect on &lt;i>Streptococcus dysgalactiae&lt;/i>, and there was almost no growth of &lt;i>Streptococcus dysgalactiae&lt;/i> at 4 × MIC. The binding properties of target compound &lt;b>7l&lt;/b> to &lt;i>amine oxidase [flavin-containing] A&lt;/i> protein were simulated by the molecular docking technique. The ligand &lt;b>7l&lt;/b> achieved strong binding with the receptor through three hydrogen bonds. The hydrogen bonds were amino acid residues thr-52, arg-51 and ser-24, which are the main force for the compound to bind to active sites.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-04-08T10:00:38.361Z</modification><creation>2025-02-19T00:56:54.18Z</creation></dates><accession>S-EPMC9104299</accession><cross_references><pubmed>35566239</pubmed><doi>10.3390/molecules27092888</doi></cross_references></HashMap>