TY - JOUR
T1 - New cytotoxic seco-type triterpene and labdane-type diterpenes from Nuxia oppositifolia
AU - Al-Massarani, Shaza M.
AU - El-Gamal, Ali A.
AU - Parvez, Mohammad K.
AU - Al-Dosari, Mohammed S.
AU - Al-Said, Mansour S.
AU - Abdel-Kader, Maged S.
AU - Basudan, Omer A.
N1 - Publisher Copyright:
© 2017 by the authors. Licensee MDPI.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Chromatographic purification of the n-hexane and dichloromethane extracts of Nuxia oppositifolia aerial parts, growing in Saudi Arabia, resulted in the isolation and characterization of three new labdane-type diterpene acids, 2β-acetoxy-labda-7-en-15-oic acid (1), 2β-acetoxy-7-oxolabda-8-en-15-oic acid (2), 2β-acetoxy-6-oxolabda-7-en-15-oic acid (3), and one new seco-triterpene, 3,4-seco olean-12-en-3,30 dioic acid (4), together with 10 known lupane, oleanane and ursane-type triterpenes, as well as the common phytosterols, β-sitosterol and stigmasterol (5-16). Their structures have been assigned on the basis of different spectroscopic techniques including 1D and 2D NMR. Moreover, 13 of the isolated compounds were tested on the human cancer cell lines HeLa (cervical), A549 (lung) and MDA (breast), and most of the compounds showed potent cytotoxic activities in vitro.
AB - Chromatographic purification of the n-hexane and dichloromethane extracts of Nuxia oppositifolia aerial parts, growing in Saudi Arabia, resulted in the isolation and characterization of three new labdane-type diterpene acids, 2β-acetoxy-labda-7-en-15-oic acid (1), 2β-acetoxy-7-oxolabda-8-en-15-oic acid (2), 2β-acetoxy-6-oxolabda-7-en-15-oic acid (3), and one new seco-triterpene, 3,4-seco olean-12-en-3,30 dioic acid (4), together with 10 known lupane, oleanane and ursane-type triterpenes, as well as the common phytosterols, β-sitosterol and stigmasterol (5-16). Their structures have been assigned on the basis of different spectroscopic techniques including 1D and 2D NMR. Moreover, 13 of the isolated compounds were tested on the human cancer cell lines HeLa (cervical), A549 (lung) and MDA (breast), and most of the compounds showed potent cytotoxic activities in vitro.
KW - Cytotoxicity
KW - Labdane-type diterpene
KW - Nuxia oppositifolia
KW - Seco-triterpene
KW - Triterpenes
UR - http://www.scopus.com/inward/record.url?scp=85014472175&partnerID=8YFLogxK
U2 - 10.3390/molecules22030389
DO - 10.3390/molecules22030389
M3 - Article
C2 - 28257105
AN - SCOPUS:85014472175
SN - 1420-3049
VL - 22
JO - Molecules
JF - Molecules
IS - 3
M1 - 389
ER -