Abstract
New marine natural products, pulchranins B and C (2 and 3), were isolated from the marine sponge Monanchora pulchra and their structures were established using NMR and MS analysis. Compounds 2 and 3 were moderately active as inhibitors of TRPV1 (EC50 value of 95 and 183 μM, respectively) and less potent against TRPV3 and TRPA1 receptors.
Author supplied keywords
Cite
CITATION STYLE
Makarieva, T. N., Ogurtsova, E. K., Korolkova, Y. V., Andreev, Y. A., Mosharova, I. V., Tabakmakher, K. M., … Stonik, V. A. (2013). Pulchranins B and C, new acyclic guanidine alkaloids from the far-eastern marine sponge Monanchora pulchra. Natural Product Communications, 8(9), 1229–1232. https://doi.org/10.1177/1934578x1300800911
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.