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Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum.
J Nat Prod. 1999 Nov; 62(11):1479-83.JN

Abstract

Five new highly oxygenated bisabolane sesquiterpenes (1-5) were isolated from Cremanthodium discoideum. Their structures were elucidated on the basis of spectroscopic analysis and chemical transformations. The structure and relative stereochemistry of 1 were determined by single-crystal X-ray crystallography on the acetate derivative, 1a. Compound 1 showed antibacterial activity against Bacillus acidilatici and Bacillus subtilis.

Authors+Show Affiliations

Department of Chemistry, National Laboratory of Applied Organic Chemistry, Chemistry and Chemical Engineering College, Lanzhou University, Lanzhou 730000, People's Republic of China.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

10579856

Citation

Zhu, Y, et al. "Novel Highly Oxygenated Bisabolane Sesquiterpenes From Cremanthodium Discoideum." Journal of Natural Products, vol. 62, no. 11, 1999, pp. 1479-83.
Zhu Y, Yang L, Jia ZJ. Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum. J Nat Prod. 1999;62(11):1479-83.
Zhu, Y., Yang, L., & Jia, Z. J. (1999). Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum. Journal of Natural Products, 62(11), 1479-83.
Zhu Y, Yang L, Jia ZJ. Novel Highly Oxygenated Bisabolane Sesquiterpenes From Cremanthodium Discoideum. J Nat Prod. 1999;62(11):1479-83. PubMed PMID: 10579856.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Novel highly oxygenated bisabolane sesquiterpenes from Cremanthodium discoideum. AU - Zhu,Y, AU - Yang,L, AU - Jia,Z J, PY - 1999/12/2/pubmed PY - 1999/12/2/medline PY - 1999/12/2/entrez SP - 1479 EP - 83 JF - Journal of natural products JO - J Nat Prod VL - 62 IS - 11 N2 - Five new highly oxygenated bisabolane sesquiterpenes (1-5) were isolated from Cremanthodium discoideum. Their structures were elucidated on the basis of spectroscopic analysis and chemical transformations. The structure and relative stereochemistry of 1 were determined by single-crystal X-ray crystallography on the acetate derivative, 1a. Compound 1 showed antibacterial activity against Bacillus acidilatici and Bacillus subtilis. SN - 0163-3864 UR - https://www.unboundmedicine.com/medline/citation/10579856/Novel_highly_oxygenated_bisabolane_sesquiterpenes_from_Cremanthodium_discoideum_ L2 - https://doi.org/10.1021/np990044p DB - PRIME DP - Unbound Medicine ER -