TY - JOUR
T1 - Structure of constituents isolated from the bark of Cassipourea malosana and their cytotoxicity against a human ovarian cell line
AU - Nishiyama, Yumi
AU - Noda, Yuki
AU - Nakatani, Noriyoshi
AU - Shitan, Nobukazu
AU - Sudo, Tamotsu
AU - Kato, Atsushi
AU - Chalo Mutiso, Patrick B.
N1 - Publisher Copyright:
© 2018, The Japanese Society of Pharmacognosy and Springer Japan KK, part of Springer Nature.
PY - 2019/1/25
Y1 - 2019/1/25
N2 - Three aromatic compounds, 2α,3α-epoxyflavan-5,7,4′-triol-(4β → 8)-afzelechin (1), 2β,3β-epoxyflavan-5,7,4′-triol-(4α → 8)-epiafzelechin (2), and methyl 4-ethoxy-2-hydroxy-6-propylbenzoate (3), as well as eight known compounds (4–11) were isolated from the bark of Cassipourea malosana (Rhizophoraceae). Their structures were determined on the basis of an analysis of spectroscopic data. The in vitro cytotoxic activities of these compounds against human ovarian cancer cell line TOV21G were evaluated. Most compounds showed little activity; however, the methyl derivatives of flavan dimers (1a and 2a) showed higher activity (IC 50 value of 30.3 and 75.4 μM) than parent compounds 1 and 2.
AB - Three aromatic compounds, 2α,3α-epoxyflavan-5,7,4′-triol-(4β → 8)-afzelechin (1), 2β,3β-epoxyflavan-5,7,4′-triol-(4α → 8)-epiafzelechin (2), and methyl 4-ethoxy-2-hydroxy-6-propylbenzoate (3), as well as eight known compounds (4–11) were isolated from the bark of Cassipourea malosana (Rhizophoraceae). Their structures were determined on the basis of an analysis of spectroscopic data. The in vitro cytotoxic activities of these compounds against human ovarian cancer cell line TOV21G were evaluated. Most compounds showed little activity; however, the methyl derivatives of flavan dimers (1a and 2a) showed higher activity (IC 50 value of 30.3 and 75.4 μM) than parent compounds 1 and 2.
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U2 - 10.1007/s11418-018-1254-2
DO - 10.1007/s11418-018-1254-2
M3 - Article
C2 - 30353358
AN - SCOPUS:85055681244
SN - 1340-3443
VL - 73
SP - 289
EP - 296
JO - Journal of Natural Medicines
JF - Journal of Natural Medicines
IS - 1
ER -