Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase

被引:69
|
作者
Li, Baojian [1 ]
Zhou, Binhua [1 ]
Lu, Hailiang [1 ]
Ma, Lin [1 ]
Peng, Ai-Yun [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cholesterol esterase; Inhibitor; Isocoumarin; Phosphaisocoumarin; INTESTINAL-CELLS; HYDROLYSIS; LIPASE; SERINE; 2-(1-ALKYNYL)PHENYLPHOSPHONATES; 4-HALOPHOSPHAISOCOUMARINS; HALOCYCLIZATION; TRANSPORT; PROTEASES; ENZYMES;
D O I
10.1016/j.ejmech.2010.01.038
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Due to the importance of pancreatic cholesterol esterase (CEase) as a potential target in atherosclerosis and for the development of hypocholesterolemic agents, there are increasing interests in designing and synthesizing CEase inhibitors. In the present study, we prepared forty-five isocoumarin phosphorus analogues (i.e., phosphaisocoumarins) and investigated the inhibition of these compounds on the CEase. The results showed that some phosphaisocoumarins could act as potent inhibitors of CEase. The most potent inhibitors, compounds 9d, 10a and 12e give IC(50) values of 4.8 mu M, 2.3 mu M and 1.9 mu M, respectively. The inhibition mechanism and kinetic characterization studies indicate that they are reversible competitive inhibitors. (C) 2010 Published by Elsevier Masson SAS.
引用
收藏
页码:1955 / 1963
页数:9
相关论文
共 50 条
  • [21] Structure-reactivity probes for active site shapes of cholesterol esterase by carbamate inhibitors
    Lin, GL
    Shieh, CT
    Tsai, YC
    Hwang, CI
    Lu, CP
    Chen, GH
    BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1999, 1431 (02): : 500 - 511
  • [22] Hypocholesterolaemic mechanism of bitter melon aqueous extracts via inhibition of pancreatic cholesterol esterase and reduction of cholesterol micellar solubility
    Su, Jianhui
    Wang, Hongxin
    Ma, Chaoyang
    Liu, Chengxiang
    Gao, Chuanzhong
    Nie, Rongjing
    Rahman, Md Ramim Tanver
    INTERNATIONAL JOURNAL OF FOOD SCIENCES AND NUTRITION, 2016, 67 (01) : 20 - 28
  • [23] A novel class of potent NF-icB signaling inhibitors
    Leban, Johann
    Baierl, Marcel
    Mies, Jan
    Trentinaglia, Viola
    Rath, Sandra
    Kronthaler, Kerstin
    Wolf, Kristina
    Gotschlich, Astrid
    Seifert, Markus H. J.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (21) : 5858 - 5862
  • [24] Evaluation of indazole-based compounds as a new class of potent KDR/VEGFR-2 inhibitors
    Bauer, David
    Whittington, Douglas A.
    Coxon, Angela
    Bready, James
    Harriman, Shawn P.
    Patel, Vinod F.
    Polverino, Anthony
    Harmange, Jean-Christophe
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (17) : 4844 - 4848
  • [25] Purification and characterization of rat pancreatic fatty acid ethyl ester synthase and its structural and functional relationship to pancreatic cholesterol esterase
    Kaphalia, BS
    Ansari, GAS
    JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2003, 17 (06) : 338 - 345
  • [26] Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors
    Sellmer, Andreas
    Stangl, Hubert
    Beyer, Mandy
    Gruenstein, Elisabeth
    Leonhardt, Michel
    Pongratz, Herwig
    Eichhorn, Emerich
    Elz, Sigurd
    Striegl, Birgit
    Jenei-Lanzl, Zsuzsa
    Dove, Stefan
    Straub, Rainer H.
    Kraemer, Oliver H.
    Mahboobi, Siavosh
    JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (08) : 3454 - 3477
  • [27] Estradiol dimers as a new class of steroid sulfatase reversible inhibitors
    Fournier, Diane
    Poirier, Donald
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (03) : 693 - 696
  • [28] Stereochemically altered cephalosporins as potent inhibitors of New Delhi metallo-β-lactamases
    Hu, Liqiang
    Yang, Huixin
    Yu, Tao
    Chen, Fangfang
    Liu, Runqiu
    Xue, Shuyuan
    Zhang, Shuangzhan
    Mao, Wuyu
    Ji, Changge
    Wang, Hao
    Xie, Hexin
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2022, 232
  • [29] Design and synthesis of N-alkyl oxindolylidene acetic acids as a new class of potent Cdc25A inhibitors
    Shimazawa, Rumiko
    Kuriyama, Masami
    Shirai, Ryuichi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (11) : 3350 - 3353
  • [30] Imidazoles: SAR and development of a potent class of cyclin-dependent kinase inhibitors
    Anderson, Malcolm
    Andrews, David M.
    Barker, Andy J.
    Brassington, Claire A.
    Breed, Jason
    Byth, Kate F.
    Culshaw, Janet D.
    Finlay, M. Raymond V.
    Fisher, Eric
    McMiken, Helen H. J.
    Green, Clive P.
    Heaton, Dave W.
    Nash, Ian A.
    Newcombe, Nicholas J.
    Oakes, Sandra E.
    Pauptit, Richard A.
    Roberts, Andrew
    Stanway, Judith J.
    Thomas, Andrew P.
    Tucker, Julie A.
    Walker, Mike
    Weir, Hazel M.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (20) : 5487 - 5492