1,2,3,4-Tetrahydro-9H-pyrido[3,4-b]indole, 98%

Not available outside of the UK & Ireland.

Application

•Reactant for synthesis of the indolyl-β-carboline alkaloid eudistomin U via IBX mediated room temperature oxidative aromatization•Reactant for preparation of neuroprotective HDAC6 inhibitors•Reactant for preparation of aminofuranopyrimidines as EGFR and Aurora A kinase inhibitors•Reactant for preparation of inhibitors of CDK4•Reactant for preparation of tetrahydrocarboline derivatives of as human 5-HT5A receptor ligands•Reactant for preparation of 5-(diaminomethyl)-2,4-aminopyrimidines as dihydrofolate reductase inhibitors and antibacterial agents

1,2,3,4-Tetrahydro-9H-pyrido[3,4-b]indole was employed in alkaloid synthesis and in studies on neurodegenerative diseases.

General description

Ozonolysis of the enamine bond of 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole derivatives was studied.

Other Notes

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 300764.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Packaging

1, 5 g in glass bottle