TY - JOUR
T1 - New triterpenoid estersaponins from the root barks of Pittosporum verticillatum subsp. verticillatum and evaluation of cytotoxicities
AU - Manase, Mahenina Jaovita
AU - Mitaine-Offer, Anne Claire
AU - Miyamoto, Tomofumi
AU - Tanaka, Chiaki
AU - Delemasure, Stéphanie
AU - Dutartre, Patrick
AU - Lacaille-Dubois, Marie Aleth
PY - 2013
Y1 - 2013
N2 - The phytochemical investigation of the root barks of Pittosporum verticillatum Bojer subsp. verticillatum led to the isolation of three new triterpene saponins, 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l- arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-R1-barrigenol (1), 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l-arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d- glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-28-O-acetyl-R1-barrigenol (2), 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l-arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d- glucuronopyranosyl-21-O-β,β-dimethylacryloyl-22-O-angeloyl-R1- barrigenol (3), and one known saponin senaciapittoside B (4). Their structures were elucidated mainly by 1D- and 2D-NMR spectroscopy and HRESIMS. Compounds 1-4 were evaluated for their cytotoxicity against one human cancer cell line (SW480) and one rat cardiomyoblast cell line (H9c2).
AB - The phytochemical investigation of the root barks of Pittosporum verticillatum Bojer subsp. verticillatum led to the isolation of three new triterpene saponins, 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l- arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-R1-barrigenol (1), 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l-arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d- glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-28-O-acetyl-R1-barrigenol (2), 3-O-[β-d-glucopyranosyl-(1 → 2)]-[α-l-arabinopyranosyl-(1 → 3)]-[α-l-arabinofuranosyl-(1 → 4)]-β-d- glucuronopyranosyl-21-O-β,β-dimethylacryloyl-22-O-angeloyl-R1- barrigenol (3), and one known saponin senaciapittoside B (4). Their structures were elucidated mainly by 1D- and 2D-NMR spectroscopy and HRESIMS. Compounds 1-4 were evaluated for their cytotoxicity against one human cancer cell line (SW480) and one rat cardiomyoblast cell line (H9c2).
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U2 - 10.1016/j.fitote.2013.09.002
DO - 10.1016/j.fitote.2013.09.002
M3 - Article
C2 - 24042073
AN - SCOPUS:84885631514
SN - 0367-326X
VL - 91
SP - 231
EP - 235
JO - Fitoterapia
JF - Fitoterapia
ER -