Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)

التفاصيل البيبلوغرافية
العنوان: Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)
المؤلفون: Helen Newman, Stephen E. Clarke, Steven Mark Bromidge, Halina T Serafinowska, Kerry Griffith, Peter J. Lovell, Tracey Gager, Douglas R Smith, Graham J. Riley, Carol Routledge, Andrew John Jennings, Stephen Moss, Phillip Jeffrey, Graham Francis Joiner, Derek C. Rogers, Frank D. King
المصدر: Bioorganicmedicinal chemistry letters. 11(1)
سنة النشر: 2001
مصطلحات موضوعية: Models, Molecular, Stereochemistry, Clinical Biochemistry, Molecular Conformation, Pharmaceutical Science, Biological Availability, Biochemistry, Chemical synthesis, Piperazines, Cns penetration, Substrate Specificity, chemistry.chemical_compound, Structure-Activity Relationship, Drug Discovery, Structure–activity relationship, Animals, Humans, Serotonin Antagonists, Molecular Biology, Sulfonamides, Molecular Structure, Organic Chemistry, SB-357134, In vitro, Bioavailability, Rats, chemistry, Blood-Brain Barrier, Receptors, Serotonin, Molecular Medicine, Selectivity
الوصف: Substituted N-phenyl-4-methoxy-3-piperazin-1-ylbenzenesulfonamides and conformationally restricted analogues have been identified as high affinity and selective 5-HT6 antagonists. Compounds from this series had a range of pharmacokinetic profiles in rat and in general there was a correlation between clearance and CNS penetration. Based on its overall biological profile 2 (SB-357134) was selected for further pre-clinical evaluation.
تدمد: 0960-894X
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d44523d73bdb36a9140fec64794b40f
https://pubmed.ncbi.nlm.nih.gov/11140733
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....3d44523d73bdb36a9140fec64794b40f
قاعدة البيانات: OpenAIRE