<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(6)</volume><submitter>Hung TQ</submitter><pubmed_abstract>A practical and efficient approach for the acid-catalysed synthesis of bis(1-imidazo[1,5-&lt;i>a&lt;/i>]pyridyl)arylmethane (BimPy) derivatives has been described. Interestingly, these BimPys showed potential cytotoxicity against various cancer cell lines (SK-LU-1, MCF-7, HepG2).</pubmed_abstract><journal>RSC advances</journal><pagination>4274-4280</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11808294</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>One-pot acid-catalysed synthesis of bis(1-imidazo[1,5-&lt;i>a&lt;/i>]pyridyl)arylmethanes and evaluation of cytotoxic activities.</pubmed_title><pmcid>PMC11808294</pmcid><pubmed_authors>Nguyen VT</pubmed_authors><pubmed_authors>Dang TT</pubmed_authors><pubmed_authors>Hung TQ</pubmed_authors><pubmed_authors>Nguyen HY</pubmed_authors><pubmed_authors>Nga TTT</pubmed_authors><pubmed_authors>Nguyen H</pubmed_authors><pubmed_authors>Tran TH</pubmed_authors><pubmed_authors>Truong Phuoc N</pubmed_authors><pubmed_authors>Phuc BV</pubmed_authors><pubmed_authors>Do DV</pubmed_authors><pubmed_authors>Do HN</pubmed_authors><pubmed_authors>Chi TM</pubmed_authors></additional><is_claimable>false</is_claimable><name>One-pot acid-catalysed synthesis of bis(1-imidazo[1,5-&lt;i>a&lt;/i>]pyridyl)arylmethanes and evaluation of cytotoxic activities.</name><description>A practical and efficient approach for the acid-catalysed synthesis of bis(1-imidazo[1,5-&lt;i>a&lt;/i>]pyridyl)arylmethane (BimPy) derivatives has been described. Interestingly, these BimPys showed potential cytotoxicity against various cancer cell lines (SK-LU-1, MCF-7, HepG2).</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-06-02T20:03:11.559Z</modification><creation>2025-04-07T07:53:45.881Z</creation></dates><accession>S-EPMC11808294</accession><cross_references><pubmed>39931403</pubmed><doi>10.1039/d4ra08868a</doi></cross_references></HashMap>