Synthetic analogues of irlbacholine: a novel antifungal plant metabolite isolated from Irlbachia alata.J Nat Prod. 1999 Jun; 62(6):824-8.JN
Abstract
Irlbacholine and a series of related analogues were synthesized and their antifungal activities against Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus were assessed. The natural bisphosphocholine, irlbacholine, was the most potent compound, its 22-carbon chain length appearing to be optimal.
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
10395496
Citation
Lu, Q, et al. "Synthetic Analogues of Irlbacholine: a Novel Antifungal Plant Metabolite Isolated From Irlbachia Alata." Journal of Natural Products, vol. 62, no. 6, 1999, pp. 824-8.
Lu Q, Ubillas RP, Zhou Y, et al. Synthetic analogues of irlbacholine: a novel antifungal plant metabolite isolated from Irlbachia alata. J Nat Prod. 1999;62(6):824-8.
Lu, Q., Ubillas, R. P., Zhou, Y., Dubenko, L. G., Dener, J. M., Litvak, J., Phuan, P. W., Flores, M., Ye, Z., Gerber, R. E., Truong, T., & Bierer, D. E. (1999). Synthetic analogues of irlbacholine: a novel antifungal plant metabolite isolated from Irlbachia alata. Journal of Natural Products, 62(6), 824-8.
Lu Q, et al. Synthetic Analogues of Irlbacholine: a Novel Antifungal Plant Metabolite Isolated From Irlbachia Alata. J Nat Prod. 1999;62(6):824-8. PubMed PMID: 10395496.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthetic analogues of irlbacholine: a novel antifungal plant metabolite isolated from Irlbachia alata.
AU - Lu,Q,
AU - Ubillas,R P,
AU - Zhou,Y,
AU - Dubenko,L G,
AU - Dener,J M,
AU - Litvak,J,
AU - Phuan,P W,
AU - Flores,M,
AU - Ye,Z,
AU - Gerber,R E,
AU - Truong,T,
AU - Bierer,D E,
PY - 1999/7/8/pubmed
PY - 1999/7/8/medline
PY - 1999/7/8/entrez
SP - 824
EP - 8
JF - Journal of natural products
JO - J Nat Prod
VL - 62
IS - 6
N2 - Irlbacholine and a series of related analogues were synthesized and their antifungal activities against Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus were assessed. The natural bisphosphocholine, irlbacholine, was the most potent compound, its 22-carbon chain length appearing to be optimal.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/10395496/Synthetic_analogues_of_irlbacholine:_a_novel_antifungal_plant_metabolite_isolated_from_Irlbachia_alata_
L2 - https://doi.org/10.1021/np980425n
DB - PRIME
DP - Unbound Medicine
ER -