Hepatoprotective Constituents from Cleome droserifolia

被引:23
作者
Abdel-Kader, Maged Saad [1 ]
Alqasoumi, Saleh Ibrahim [1 ]
Al-Taweel, Areej Mohammad [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacognosy, Riyadh 11451, Saudi Arabia
关键词
Cleome droserifolia; hepatoprotection; flavonoid; terpene; SESQUITERPENES; FLAVONOIDS;
D O I
10.1248/cpb.57.620
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The effect of ethanol extract from aerial parts of Cleome droserifolia was investigated against carbon tetrachloride induced liver injury. The hepatoprotective activity was evaluated through the quantification of biochemical parameters and confirmed using histopathology analysis. Efficient hepatoprotective effect was achieved by crude extract, fractions and some pure compounds. The phytochemical studies showed that the petroleum ether fraction afforded two known guaiane sesquiterpenes buchariol (1) and teucladiol (2) in addition to daucosterol (beta-sitosterol glucoside) (3). The CHCl3 fraction afforded three known flavonoid derivatives; 5,3'-dihydroxy-3,6,7,4',5'-pentamethoxyflavone (4), 5'-hydroxy-3,6,7,3',4',5'-hexamethoxyflavone (5) and luteolin (6) and a known dolabellane diterpene (1R,2R,3E,7E,11R,12S)-2-O-acetyl-16-O-(3-hydroxy-3-methylglutaryl)-dolabella-3,7-dien-2,16,18-triol (7). The active parts of the MeOH fraction afforded the previously unreported 3'-methoxy-3,5,4'-trihydroxy flavone-7-neohesperidoside (8) and a known megastigmane norterpene; (6S,9R)-roseoside (9).
引用
收藏
页码:620 / 624
页数:5
相关论文
共 17 条
[1]  
Abdel-Kader MS, 2008, ALEX J PHARM SCI, V22, P47
[2]  
Alqasoumi S. I., 2008, Natural Product Sciences, V14, P95
[3]   GUAIANE SESQUITERPENES FROM TEUCRIUM-LEUCOCLADUM [J].
BRUNO, M ;
DELATORRE, MC ;
RODRIGUEZ, B ;
OMAR, AA .
PHYTOCHEMISTRY, 1993, 34 (01) :245-247
[4]   Terpenoids from Cleome droserifolia (Forssk.) Del. [J].
El-Askary, HI .
MOLECULES, 2005, 10 (08) :971-977
[5]  
El-Shenawy Nahla S., 2006, Rev. Inst. Med. trop. S. Paulo, V48, P223, DOI 10.1590/S0036-46652006000400010
[6]   Flavonoids from Cleome droserifolia suppress NO production in activated macrophages in vitro [J].
Fushiya, S ;
Kishi, Y ;
Hattori, K ;
Batkhuu, J ;
Takano, F ;
Singab, ANB ;
Okuyama, T .
PLANTA MEDICA, 1999, 65 (05) :404-407
[7]  
HUSSEIN NS, 1994, PHARMAZIE, V49, P76
[8]   Phenolic and terpenoid compounds from Chione venosa (sw.) URBAN var. venosa (Bois Bande) [J].
Lendl, A ;
Werner, I ;
Glasl, S ;
Kletter, C ;
Mucaji, P ;
Presser, A ;
Reznicek, G ;
Jurenitsch, J ;
Taylor, DW .
PHYTOCHEMISTRY, 2005, 66 (19) :2381-2387
[9]   Radical-scavenging activities of new megastigmane glucosides from Macaranga tanarius (L.) MULL.-ARG. [J].
Matsunami, Katsuyoshi ;
Takamori, Ichiko ;
Shinzato, Takakazu ;
Aramoto, Mitsunori ;
Kondo, Kazunari ;
Otsuka, Hideaki ;
Takeda, Yoshio .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2006, 54 (10) :1403-1407
[10]   3-HYDROXY-3-METHYLGLUTARYL DOLABELLANE DITERPENES FROM CHROZOPHORA-OBLIQUA [J].
MOHAMED, KM ;
OHTANI, K ;
KASAI, R ;
YAMASAKI, K .
PHYTOCHEMISTRY, 1995, 39 (01) :151-161