Pseudoguanolide sesquiterpene lactones from Vernoniopsis caudata and their in vitro antiplasmodial activities.J Nat Prod. 2005 May; 68(5):800-3.JN
Abstract
Two new helenanolide sesquiterpene lactones, 1 and 2, as well as one known related structure, 11alpha,13-dihydrohelenalin-[2-(1-hydroxyethyl)acrylate] (3), together with 4'-beta-d-O-glucopyranosyl-luteolin and ethyl 2,5-dihydroxycinnamate were isolated from an ethyl acetate extract of leaves of Vernoniopsis caudatawith potent antiplasmodial activity (IC50 1.6 microg/mL) in a preliminary biological screen. The structures of the new compounds were determined by spectroscopic techniques. The three sesquiterpene lactones 1-3 displayed strong in vitro antiplasmodial activity, with IC50 values of 1, 0.19, and 0.41 microM, respectively. However, these compounds also exhibited considerable cytotoxicity on KB cells (IC50 < 1 microM in each case).
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
15921436
Citation
Ramanandraibe, Voahangy, et al. "Pseudoguanolide Sesquiterpene Lactones From Vernoniopsis Caudata and Their in Vitro Antiplasmodial Activities." Journal of Natural Products, vol. 68, no. 5, 2005, pp. 800-3.
Ramanandraibe V, Martin MT, Rakotondramanana DL, et al. Pseudoguanolide sesquiterpene lactones from Vernoniopsis caudata and their in vitro antiplasmodial activities. J Nat Prod. 2005;68(5):800-3.
Ramanandraibe, V., Martin, M. T., Rakotondramanana, D. L., Mambu, L., Ramanitrahasimbola, D., Labaïed, M., Grellier, P., Rasoanaivo, P., & Frappier, F. (2005). Pseudoguanolide sesquiterpene lactones from Vernoniopsis caudata and their in vitro antiplasmodial activities. Journal of Natural Products, 68(5), 800-3.
Ramanandraibe V, et al. Pseudoguanolide Sesquiterpene Lactones From Vernoniopsis Caudata and Their in Vitro Antiplasmodial Activities. J Nat Prod. 2005;68(5):800-3. PubMed PMID: 15921436.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Pseudoguanolide sesquiterpene lactones from Vernoniopsis caudata and their in vitro antiplasmodial activities.
AU - Ramanandraibe,Voahangy,
AU - Martin,Marie-Thérèse,
AU - Rakotondramanana,Dina L,
AU - Mambu,Lengo,
AU - Ramanitrahasimbola,David,
AU - Labaïed,Medhi,
AU - Grellier,Philippe,
AU - Rasoanaivo,Philippe,
AU - Frappier,François,
PY - 2005/6/1/pubmed
PY - 2005/7/8/medline
PY - 2005/6/1/entrez
SP - 800
EP - 3
JF - Journal of natural products
JO - J Nat Prod
VL - 68
IS - 5
N2 - Two new helenanolide sesquiterpene lactones, 1 and 2, as well as one known related structure, 11alpha,13-dihydrohelenalin-[2-(1-hydroxyethyl)acrylate] (3), together with 4'-beta-d-O-glucopyranosyl-luteolin and ethyl 2,5-dihydroxycinnamate were isolated from an ethyl acetate extract of leaves of Vernoniopsis caudatawith potent antiplasmodial activity (IC50 1.6 microg/mL) in a preliminary biological screen. The structures of the new compounds were determined by spectroscopic techniques. The three sesquiterpene lactones 1-3 displayed strong in vitro antiplasmodial activity, with IC50 values of 1, 0.19, and 0.41 microM, respectively. However, these compounds also exhibited considerable cytotoxicity on KB cells (IC50 < 1 microM in each case).
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/15921436/Pseudoguanolide_sesquiterpene_lactones_from_Vernoniopsis_caudata_and_their_in_vitro_antiplasmodial_activities_
DB - PRIME
DP - Unbound Medicine
ER -