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Org Lett ; 22(19): 7439-7442, 2020 10 02.
Article in English | MEDLINE | ID: mdl-32886519

ABSTRACT

Baicalensines A (1) and B (2) were isolated from the roots of Thalictrum baicalense and structurally characterized using spectroscopic data, 13C NMR calculations, and the CASE algorithm. Compound 1, representing a new class of alkaloid dimers, contains berberine conjugated to a ring-opened isoquinoline. Compound 2 is the first reported natural benzylisoquinoline bearing a formyl group at C-3. Plausible biosynthetic pathways are proposed. Compound 1 exerted moderate cytotoxicity against the Caco-2 and HL-60 cell lines.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Berberine/pharmacology , Thalictrum/chemistry , Alkaloids/chemistry , Alkaloids/isolation & purification , Alkaloids/pharmacology , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Berberine/chemistry , Berberine/isolation & purification , Caco-2 Cells , HL-60 Cells , Humans , Isoquinolines/chemistry , Isoquinolines/isolation & purification , Isoquinolines/pharmacology , Molecular Structure , Plant Roots/chemistry
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