posted on 2024-04-23, 21:32authored byWeihong Wang, JunI Lee, Eun Roh, Gauri Shetye, Jin Cao, James McAlpine, Guido PauliGuido Pauli, Scott FranzblauScott Franzblau, Thi Hanh Nguyen Vu, Ngoc Tung Quach, Eunseok Oh, Kyu-Hyung Park, Chanyoon Park, Youbin Cho, Hyeseon Jang, SongJoo Han, Hiyoung Kim, Sang Hyun ChoSang Hyun Cho, Quyet-Tien Phi, Heonjoong Kang
<p>Three unique linear oligomeric depsipeptides, designated as cavomycins A-C (1-3), were identified from Streptomyces cavourensis, a gut bacterium associated with the annelid Paraleonnates uschakovi. The structures of these depsipeptides were determined through a combination of spectroscopic methods and chemical derivatization techniques, including methanolysis, the modified Mosher's method, advanced Marfey's methods, and phenylglycine methyl ester derivatization. The unique dipeptidyl residue arrangements in compounds 1-3 indicate that they are not degradation products of valinomycin. Compound 2 and its methylation derivative 2a exhibited antiproliferative activity against PANC-1 pancreatic cancer cells with IC50 values of 1.2 and 1.7 μM, respectively.</p>
Wang, W., Lee, J., Roh, E., Shetye, G., Cao, J., McAlpine, J., Pauli, G., Franzblau, S., Vu, T. H. N., Quach, N. T., Oh, E., Park, K. -H., Park, C., Cho, Y., Jang, H., Han, S., Kim, H., Cho, S., Phi, Q. -T.Kang, H. (2024). Cavomycins A–C, Linear Oligomer Depsipeptides from an Annelid-Associated Streptomyces cavourensis. Journal of Natural Products. https://doi.org/10.1021/acs.jnatprod.3c01275