Antiproliferative triterpene saponins from Entada africana.J Nat Prod. 2006 Sep; 69(9):1323-9.JN
Abstract
Nine new ester saponins (1-9) were isolated from the roots of Entada africana. Their structures were elucidated by 1D and 2D NMR experiments including 1D and 2D TOCSY, DQF-COSY, HSQC, and HMBC spectroscopy, as well as ESIMS analysis, and chemical methods. The aglycon moieties were found to be echinocystic acid for compounds 1, 2, 4-6, 8, and 9 and acacic acid for 3 and 7. All isolated compounds were tested for their antiproliferative activity against the J774.A1, HEK-293, and WEHI-164 cell lines. Moderate to high cytotoxic potency was found for almost all compounds tested.
MeSH
Pub Type(s)
Journal Article
Language
eng
PubMed ID
16989528
Citation
Cioffi, Giuseppina, et al. "Antiproliferative Triterpene Saponins From Entada Africana." Journal of Natural Products, vol. 69, no. 9, 2006, pp. 1323-9.
Cioffi G, Dal Piaz F, De Caprariis P, et al. Antiproliferative triterpene saponins from Entada africana. J Nat Prod. 2006;69(9):1323-9.
Cioffi, G., Dal Piaz, F., De Caprariis, P., Sanogo, R., Marzocco, S., Autore, G., & De Tommasi, N. (2006). Antiproliferative triterpene saponins from Entada africana. Journal of Natural Products, 69(9), 1323-9.
Cioffi G, et al. Antiproliferative Triterpene Saponins From Entada Africana. J Nat Prod. 2006;69(9):1323-9. PubMed PMID: 16989528.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Antiproliferative triterpene saponins from Entada africana.
AU - Cioffi,Giuseppina,
AU - Dal Piaz,Fabrizio,
AU - De Caprariis,Paolo,
AU - Sanogo,Rokia,
AU - Marzocco,Stefania,
AU - Autore,Giuseppina,
AU - De Tommasi,Nunziatina,
PY - 2006/9/23/pubmed
PY - 2006/10/31/medline
PY - 2006/9/23/entrez
SP - 1323
EP - 9
JF - Journal of natural products
JO - J Nat Prod
VL - 69
IS - 9
N2 - Nine new ester saponins (1-9) were isolated from the roots of Entada africana. Their structures were elucidated by 1D and 2D NMR experiments including 1D and 2D TOCSY, DQF-COSY, HSQC, and HMBC spectroscopy, as well as ESIMS analysis, and chemical methods. The aglycon moieties were found to be echinocystic acid for compounds 1, 2, 4-6, 8, and 9 and acacic acid for 3 and 7. All isolated compounds were tested for their antiproliferative activity against the J774.A1, HEK-293, and WEHI-164 cell lines. Moderate to high cytotoxic potency was found for almost all compounds tested.
SN - 0163-3864
UR - https://www.unboundmedicine.com/medline/citation/16989528/Antiproliferative_triterpene_saponins_from_Entada_africana_
L2 - https://doi.org/10.1021/np060257w
DB - PRIME
DP - Unbound Medicine
ER -