【摘 要】
:
AIM Mahkota Dewa (Phaleria macrocarpa [Seheff.] Boerl), with effects on antihistamine, anti-oxidation and anticancer, has been used to treat many diseases, including cancer, impotency, haemorrhoids an
【机 构】
:
School of Pharmaceutical Science,Zhengzhou University,Zhengzhou,China
【出 处】
:
第二届世界天然药物和传统药物药理学学术会议
论文部分内容阅读
AIM Mahkota Dewa (Phaleria macrocarpa [Seheff.] Boerl), with effects on antihistamine, anti-oxidation and anticancer, has been used to treat many diseases, including cancer, impotency, haemorrhoids and diabetes mellitus.The current study is designed to further understand and develop Mabkota Dewa for cancer treatment applications.METHODS AND RESULTS Two benzophenone glucopyranosides were isolated from the nut shell part of Mahkota Dewa.The structures were identified as 2,4 ,6-trihydroxy-4-methoxy-benzophenone-2-0-β-D-glucoside (Mahkoside A) and 2,4, 6-trihydroxy-4-methoxy-6"-acetyl-benzophenone-2-0-β-D-glucoside (Mahkoside B) NMR, HR-MS and UV.Mahkoside B was recognized as a novel compound.Furthermore, a series of benzophenone glucopyranoside derivatives (Compounds 3-18) were synthesized.In order to determine the relationship of structure and activity of the compounds above, several cancer cell lines, including esophageal cancer cell hnes : EC109 and EC9706, stomach cancer cell line: MGC-803 and prostate cancer cell line: PC-3, were randomly selected and cytotoxic activity was evaluated according to the standard SRB (sulforhodamine B) assay.Our results indicated that Compound 18 has significant cytotoxicity against EC109,EC9706, MGC-803 and PC-3, with IC50 ≤ 10 μmol· L-1, indicating its potential activity against cancer cells.CONCLUSION We found that a new derivative of Mahkoside A: Compound 18, demonstrated significant cytotoxicity against cancer cell growth.Future studies will be performed to generate and characterize more derivatives with azotic alkyl group and analyze their structure-effect relationships.
其他文献
AIM Urtica dentata hand (UDH) are traditionally used in the alpine region as a herbal medicine.Our goal was to elucidate the cellular and molecular pathway and explore a method to quantify the total c
AIM Previous pharmacological studies demonstrated that LW could ameliorate the decline of the learning and memory in senescence accelerated mouse/prone 8 (SAMP8), but the mechanism has not been well e
AIM Pseudoginsenoside-F11 (PF11), an ocotillol-type saponin, is one of the ingredients of Panax quinquefolium (American ginseng), previously isolated from leaves of Panax pseudoginseng subsp.himalaicu
AIM It has been reported that some polyphenols are able to up-regulate sirtuin 1 (SIRT1) activity, an NAD-dependent deacetylase.Salvianolic acid A(Sal A), an active compound extracted from Salvia mihi
AIM To investigate protect effect of Fufangdengzhanhua dripping pill (FDD)s oxidative stress induced by hydrogen peroxide on PC12 cell.METHODS PC12 cells were divided into six groups in culture: contr
AIM Qishenkeli (QSKL), a formula composed of six herbal medicines, has long been used for the routine treatment of coronary heart disease (CHD) or chronic heart failure (CHF) in China.However, how the
AIM Oridonin, a natural tetracycline diterpenoid isolated from Chinese herb Rabdosia rubescens, has been reported to be a potent cytotoxic agent against various cancers.However, the effect of oridonin
AIM Cryptotanshinone (CTN), one of the major constituents of tanshinones, was investigated for hepatoprotective effects in D-galactosamine (D-GalN)/lipopolysaccharide (LPS)-induced fulminant hepatic f
AIM To observe the therapeutic usefulness of Compound K (CK) in type 2 diabetes and its possible mechanisms.METHODS Type 2 diabetes was induced in male ICR mice by combining of streptozotocin (STZ, 10
AlM To study the inhibited effect of atractylon on HBsAg and HBeAg in the cultured hepatocarcinoma cell line 2215 (HepG2) which was genetransfered with hepatitis B virus(HBV) and its toxicity.MEHTODS