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New bisabolane sesquiterpenes from Ligularia songarica.
Pharmazie. 2000 Dec; 55(12):947-52.P

Abstract

Phytochemical investigation of Ligularia songarica (Compositae) afforded seven new bisabolane-type sesquiterpenes. Their structures were confirmed on the basis of spectroscopic methods, especially 2D-NMR techniques, and compound 7 showed stronger antibacterial activity against Escherichia coli, Pseudomonas acruginosa and Salmonella pullorum.

Authors+Show Affiliations

Fu B
National Laboratory of Applied Organic Chemistry, Department of Chemistry, Lanzhou University, Lanzhou, People's Republic of China.
Yang L
No affiliation info available
Yang XP
No affiliation info available
Li XP
No affiliation info available
Jia ZJ
No affiliation info available

MeSH

Anti-Bacterial AgentsAsteraceaeBacteriaChinaChromatography, Thin LayerMagnetic Resonance SpectroscopyMicrobial Sensitivity TestsPlant RootsPlants, MedicinalSesquiterpenesSpectrometry, Mass, Fast Atom Bombardment

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

11189875

Citation

Fu, B, et al. "New Bisabolane Sesquiterpenes From Ligularia Songarica." Die Pharmazie, vol. 55, no. 12, 2000, pp. 947-52.
Fu B, Yang L, Yang XP, et al. New bisabolane sesquiterpenes from Ligularia songarica. Pharmazie. 2000;55(12):947-52.
Fu, B., Yang, L., Yang, X. P., Li, X. P., & Jia, Z. J. (2000). New bisabolane sesquiterpenes from Ligularia songarica. Die Pharmazie, 55(12), 947-52.
Fu B, et al. New Bisabolane Sesquiterpenes From Ligularia Songarica. Pharmazie. 2000;55(12):947-52. PubMed PMID: 11189875.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - New bisabolane sesquiterpenes from Ligularia songarica. AU - Fu,B, AU - Yang,L, AU - Yang,X P, AU - Li,X P, AU - Jia,Z J, PY - 2001/2/24/pubmed PY - 2001/3/3/medline PY - 2001/2/24/entrez SP - 947 EP - 52 JF - Die Pharmazie JO - Pharmazie VL - 55 IS - 12 N2 - Phytochemical investigation of Ligularia songarica (Compositae) afforded seven new bisabolane-type sesquiterpenes. Their structures were confirmed on the basis of spectroscopic methods, especially 2D-NMR techniques, and compound 7 showed stronger antibacterial activity against Escherichia coli, Pseudomonas acruginosa and Salmonella pullorum. SN - 0031-7144 UR - https://www.unboundmedicine.com/medline/citation/11189875/New_bisabolane_sesquiterpenes_from_Ligularia_songarica_ DB - PRIME DP - Unbound Medicine ER -