Related Experiment Video
Updated: Aug 9, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Structure of thioviridamide, a novel apoptosis inducer from Streptomyces olivoviridis
Yoichi Hayakawa1, Kahori Sasaki, Koji Nagai
1Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan. hykw@rs.noda.tus.ac.jp
Abstract:
A novel apoptosis inducer, thioviridamide, was isolated from an actinomycete identified as Streptomyces olivoviridis. The molecular formula of thioviridamide was determined to be C56H93N14O10S7+ from high-resolution FAB-MS. The structure of thioviridamide was analyzed by NMR spectral analysis including a variety of two-dimensional techniques. COSY and HMBC experiments revealed the presence of a 2-hydroxy-2-methyl-4-oxopentanoyl group and eleven amino acid residues including two novel amino acids, beta-hydroxy-N1,N3-dimethylhistidinium and S-(2-aminovinyl)cysteine. 1H-13C long-range correlations observed in the HMBC, CT-HMBC and HMBC-HOHAHA spectra connected the partial structures with seven amide linkages and five thioamide linkages to establish the planar structure of thioviridamide as a unique cyclic peptide.
Related Concept Videos
Antiviral Nucleoside Inhibitors
Apoptosis
Inhibitors of Virion Maturation and Assembly
The Intrinsic Apoptotic Pathway
Inhibitors of Bacterial DNA Synthesis
Viral Structure

