
Buspirone
CAS No. 36505-84-7
Buspirone( Buspirone free base | Ansial )
Catalog No. M27358 CAS No. 36505-84-7
Buspirone free base is an agonist of serotonin receptor with anxiolytic activity. Buspirone free base has an efficacy comparable to diazepam.
Purity : >98% (HPLC)






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Biological Information
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Product NameBuspirone
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NoteResearch use only, not for human use.
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Brief DescriptionBuspirone free base is an agonist of serotonin receptor with anxiolytic activity. Buspirone free base has an efficacy comparable to diazepam.
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DescriptionBuspirone free base is an agonist of serotonin receptor with anxiolytic activity. Buspirone free base has an efficacy comparable to diazepam.
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In VitroBuspirone (0-400 μg/mL; 6 hours) has cytotoxic effect in Lymphocytes.Buspirone (0-180 μg/mL; 0-3 hours; Lymphocytes)induces ROS formation, mitochondrial membrane potential collapse(MMP), lipid peroxidation, lysosomal damage and elevation of glutathione disulfide (GSSG). Cell Viability Assay Cell Line:Lymphocytes Concentration:0, 4, 20, 40, 200 and 400 μg/mL Incubation Time:6 hours Result:Decreased cell viability in a dose-dependent manner.
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In VivoBuspirone (1-5 mg/kg; i.p. and i.g.; for 5 days; C57BL/6N mice) reduces anxiety/depression behaviors.Buspirone (1-5 mg/kg; i.p. and i.g.; for 5 days; C57BL/6N mice) restores IS-shifted β-diversity in the gut microbiota. Animal Model:Male C57BL/6N mice Dosage:1 and 5 mg/kg Administration:Oral gavage and intraperitoneal injection; for 5 days Result:Reduced TNF-α expression and NF-κB+/Iba1+ cell population in the hippocampus and myeloperoxidase activity and NF-κB+/CD11c+ cell population in the colon.Animal Model:Male C57BL/6N mice Dosage:1 and 5 mg/kg Administration:Oral gavage and intraperitoneal injection; for 5 days Result:Reduced the IS- or EC-induced gut Proteobacteria population.
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SynonymsBuspirone free base | Ansial
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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RecptorEGFR (T790M)|EGFR (L858R/T790M)|EGFR (del19/T790M)
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Research Area——
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Indication——
Chemical Information
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CAS Number36505-84-7
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Formula Weight385.512
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Molecular FormulaC21H31N5O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (259.40 mM)
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SMILESO=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Sullivan I, et al. Next-Generation EGFR Tyrosine Kinase Inhibitors for Treating EGFR-Mutant Lung Cancer beyond First Line. Front Med (Lausanne). 2017 Jan 18;3:76.
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