Chemical constituents from Strychnos cathayensis

被引:38
作者
Cheng, MJ [1 ]
Tsai, IL [1 ]
Chen, IS [1 ]
机构
[1] Kaohsiung Med Univ, Grad Inst Nat Prod, Kaohsiung 807, Taiwan
关键词
Strychnos cathayensis; Loganiaceae; stem; secoiridoid; secostrychnosin; iridoid; alkaloid; indole alkaloid;
D O I
10.1002/jccs.200100038
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Secostrychnosin (1), a new secoiridoid, as well as seven compounds never before isolated from nature: 4-tert-butyl-2-oxazolidinone (2), 3-acetoxyindole (3), indole-2-carboxylic acid (4), benzocaine (5), 3-acetylindole (6), butylparaben (7) and 2-hydroxy-3-methoxybenzaldehyde (8), together with fifty other known compounds, have been isolated from the stem of Strychnos cathayensis. These compounds include twenty-three alkaloids, twelve benzenoids, four steroids, three flavonoids, three iridoids, two triterpenoids, two secoiridoids, two fatty acids, one lignan, one acetophenone, one coumarin, one chromane, one tetraterpenoid, one tannin, and one organic acid. The structures of these compounds were determined by means of spectral analyses.
引用
收藏
页码:235 / 239
页数:5
相关论文
共 55 条
[11]   4 AROMATIC DERIVATIVES FROM RUTA-ANGUSTIFOLIA [J].
DELCASTILLO, JB ;
SECUNDINO, M ;
LUIS, FR .
PHYTOCHEMISTRY, 1986, 25 (09) :2209-2210
[12]   Sterolic and triterpenoidic constituents of stem bark of Drypetes gossweileri [J].
Dupont, MP ;
Llabres, G ;
Delaude, C ;
Tchissambou, L ;
Gastmans, JP .
PLANTA MEDICA, 1997, 63 (03) :282-284
[13]   10′-hydroxyusambarensine, a new antimalarial bisindole alkaloid from the roots of Strychnos usambarensis [J].
Frédérich, M ;
Tits, M ;
Hayette, MP ;
Brandt, V ;
Penelle, J ;
DeMol, P ;
Llabrès, G ;
Angenot, L .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (04) :619-621
[14]  
Gaillard E., 1995, Annales Pharmaceutiques Francaises, V53, P75
[15]   A REGIOCONTROLLED SYNTHESIS OF N7-GUANINE AND N9-GUANINE NUCLEOSIDES [J].
GARNER, P ;
RAMAKANTH, S .
JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (06) :1294-1298
[16]   TERPENOIDS FROM HEMIDESMUS-INDICUS [J].
GUPTA, MM ;
VERMA, RK ;
MISRA, LN .
PHYTOCHEMISTRY, 1992, 31 (11) :4036-4037
[17]   STEREOCHEMISTRY AZIRIDINE RING EXPANSION SEQUENCES - NEW SYNTHESIS OF 2-OXAZOLIDONES [J].
HASSNER, A ;
BURKE, SS .
TETRAHEDRON, 1974, 30 (16) :2613-2621
[18]  
HINGORANI S, 1994, J INDIAN CHEM SOC, V71, P183
[19]   Glucopyranoside recognition by polypyridine-macrocyclic receptors possessing a wide cavity with a flexible linkage [J].
Inouye, M ;
Chiba, J ;
Nakazumi, H .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (22) :8170-8176
[20]   NOVEL BIS-IRIDOID GLUCOSIDES FROM DIPSACUS-SYLVESTRIS [J].
JENSEN, SR ;
LYSEPETERSEN, SE ;
NIELSEN, BJ .
PHYTOCHEMISTRY, 1979, 18 (02) :273-277