【摘 要】
:
随着全球经济的快速发展,生活水平的日益提高,高热量高脂肪食物的过多摄入,以及体力劳动的减少,肥胖症的发病率与日俱增.据不完全统计,目前全世界肥胖症发病人数已近5亿,每年因肥胖症促成的直接或间接死亡人数达30万,并有可能成为21世纪的头号杀手.随着人类基因组测序的完成,寻找导致肥胖的遗传因素是目前科学界研究的热点问题.FTO (Fat Mass and Obesity Associated)基因是目
【机 构】
:
郑州大学化学与分子工程学院,郑州,450001
【出 处】
:
中国化学会第十届全国天然有机化学学术会议
论文部分内容阅读
随着全球经济的快速发展,生活水平的日益提高,高热量高脂肪食物的过多摄入,以及体力劳动的减少,肥胖症的发病率与日俱增.据不完全统计,目前全世界肥胖症发病人数已近5亿,每年因肥胖症促成的直接或间接死亡人数达30万,并有可能成为21世纪的头号杀手.随着人类基因组测序的完成,寻找导致肥胖的遗传因素是目前科学界研究的热点问题.FTO (Fat Mass and Obesity Associated)基因是目前科学界找到的第一个确切与广泛人群肥胖有关的基因1-4.在小鼠做的基因敲除实验、点突变以及过表达结果也显示了FTO可能是治疗与预防肥胖的非常重要的靶标5,6.
其他文献
Adenosine derivatives have significant sedative and hypnotic activity1,2.Five 2-deoxy-adenosine derivatives (4a-4e) and five adenosine derivatives (5a-5e) were synthesized, and accessed for their seda
Neutrophil gelatinase associated lipocalin (Ngal), was originally found from neutrophil granule as a complex to gelatinase B (matrix metalloproteinase 9, MMP9) and thus got its name.It can stabilize t
Screening of antimicrobial and antitumor agents from marine microorganisms is one of the hot spots for the research of marine drugs and screening models play important roles in this study.The authors
A novel SHP2 inhibitor-fumosorinone (Fumos) from entomogenous fungi was discovered;it possesses the selective inhibition for Shp2 over other PTPs (PTP1B, TCPTP, Shpl, HePTP, Lyp,STEP, PTPH1, PTPRA, Cd
微生物来源的天然产物是药物先导化合物的重要资源库1.基于"基因水平传递"2、"内共生理论"3和生物防御主导的"协同进化"3等理论,共生微生物能够产生与宿主相同或相似的活性化合物,成为获取结构和生物活性多样性天然产物的重要资源.,内生菌作为独特化学结构和良好生物活性的天然产物新来源,具有重要的研究潜力5,6.
Phytochemical study on the whole plant of Borreria latifolia led to the discovery of two new compounds, 3β,6β,23-trihydroxyursa-12,20(30)-dien-28-oic acid (1) and 3β,6β,30-trihydroxy-olean-12-en-28-oi
Marine fungi have developed their unique metabolic system to adapt the special marine environment.Their novel metabolites have enlarged the diversity of organic compounds and have shown exciting and u
25-OH-PPD1 (25-hydroxyprotopanaxadiol), a promising antitumor natural compound isolated from the fruits of Panax ginseng, could inhibit cancer cell proliferation, caused cell cycle arrest in vitro and
Gracilamine1 is a new member of the amaryllidaceae alkaloid family, and it can also be regarded as an aminal derivative of hydrofluorenone containing natural products (rings A-C).In this presentation,
异戊烯基酚性化合物是一类重要的植物次生代谢产物,具有广泛的生理活性,包括抗肿瘤、抗氧化、酪氨酸酶抑制、胰脂酶抑制、组织蛋白酶抑制等.桑科波罗蜜属(Artocarpus)植物是该类成分的一个重要来源.本课题组对两种波罗蜜属植物(A.styracifolius和A.heterophyllus)中的异戊烯基酚性成分进行了较系统的研究,目前获得了30多个异戊烯基酚性化合物,其中新化合物18个.新化合物种类