共 12 条
Strongylophorines, meroditerpenoids from the marine sponge Petrosia corticata, function as proteasome inhibitors
被引:24
作者:
Noda, Ai
[1
]
Sakai, Eriko
[1
]
Kato, Hikaru
[1
]
Losung, Fitje
[2
]
Mangindaan, Remy E. P.
[2
]
de Voogd, Nicole J.
[3
]
Yokosawa, Hideyoshi
[4
]
Tsukamoto, Sachiko
[1
]
机构:
[1] Kumamoto Univ, Grad Sch Pharmaceut Sci, Dept Nat Med, Kumamoto 8620973, Japan
[2] Sam Ratulangi Univ, Fac Fisheries & Marine Sci, Manado 95115, Indonesia
[3] Nat Biodivers Ctr, NL-2300 RA Leiden, Netherlands
[4] Aichi Gakuin Univ, Sch Pharm, Chikusa Ku, Nagoya, Aichi 4648650, Japan
关键词:
Strongylophorine;
Meroditerpenoid;
Petrosia corticata;
Proteasome inhibitor;
ACANTHOSTRONGYLOPHORA-INGENS;
DRUG TARGETS;
DURISSIMA;
CANCER;
SYSTEM;
D O I:
10.1016/j.bmcl.2015.04.075
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Two new strongylophorine derivatives, along with six known strongylophorines, were isolated from the marine sponge Petrosia corticata as proteasome inhibitors. Of these, a hemiacetal mixture of strongylophorines-13/-14 was the strongest inhibitor of the proteasome with an IC50 of 2.1 mu M. (C) 2015 Elsevier Ltd. All rights reserved.
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页码:2650 / 2653
页数:4
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