Abstract
Three new pyrrolobenzodiazepine derivatives, boseongazepines A-C (1-3), were isolated from a culture broth of Streptomyces sp. 11A057, together with the known compound usabamycin B (4). The structures of 1-4 were determined through the analysis of spectroscopic data including extensive 1D-, 2D-NMR, and MS techniques. Cell growth inhibition effects of these compounds were evaluated against Jurkat, K-562, HL-60, and HepG2 cell lines.
Keywords:
Boseongazepines; Cytotoxicity; Pyrrolobenzodiazepine; Streptomyces.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / isolation & purification
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Antineoplastic Agents / pharmacology*
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Benzodiazepines / chemistry
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Benzodiazepines / isolation & purification
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Benzodiazepines / pharmacology*
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Benzodiazepinones / chemistry
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Benzodiazepinones / isolation & purification
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Benzodiazepinones / pharmacology*
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Cell Proliferation / drug effects
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Dose-Response Relationship, Drug
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Drug Screening Assays, Antitumor
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HL-60 Cells
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Hep G2 Cells
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Humans
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Jurkat Cells
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K562 Cells
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Molecular Conformation
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Pyrroles / chemistry
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Pyrroles / isolation & purification
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Pyrroles / pharmacology*
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Streptomyces / chemistry*
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Benzodiazepinones
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Pyrroles
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boseongazepine C
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pyrrolo(2,1-c)(1,4)benzodiazepine
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Benzodiazepines