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Journal of natural products | Vol.51, Issue.5 | | Pages 884-92

Journal of natural products

Biosynthesis of staurosporine, 1. 1H- and 13C-NMR assignments.

D, Meksuriyen G A, Cordell  
Abstract

Complete and unambiguous assignments of the 1H- and 13C-nmr spectra of the potent antitumor antibiotic staurosporine have been accomplished using a combination of one- and two-dimensional nmr techniques, including one-bond and long-range heteronuclear multiple-quantum coherence spectroscopy (HMQC). Staurosporine was found to be highly cytotoxic in the KB and P-388 assays but was inactive in the microtubulin assembly assay.

Original Text (This is the original text for your reference.)

Biosynthesis of staurosporine, 1. 1H- and 13C-NMR assignments.

Complete and unambiguous assignments of the 1H- and 13C-nmr spectra of the potent antitumor antibiotic staurosporine have been accomplished using a combination of one- and two-dimensional nmr techniques, including one-bond and long-range heteronuclear multiple-quantum coherence spectroscopy (HMQC). Staurosporine was found to be highly cytotoxic in the KB and P-388 assays but was inactive in the microtubulin assembly assay.

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D, Meksuriyen G A, Cordell,.Biosynthesis of staurosporine, 1. 1H- and 13C-NMR assignments.. 51 (5),884-92.

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