Electrophilic natural products and their biological targets

被引:241
作者
Gersch, Malte [1 ]
Kreuzer, Johannes [1 ]
Sieber, Stephan A. [1 ]
机构
[1] Tech Univ Munich, Ctr Integrated Prot Sci Munich, Inst Adv Study, Dept Chem, D-85747 Garching, Germany
基金
欧洲研究理事会;
关键词
NF-KAPPA-B; ACETYLGLUCOSAMINE ENOLPYRUVYL TRANSFERASE; CARBAMOYL-PHOSPHATE SYNTHETASE; TYROSINE KINASE INHIBITOR; ANTI-FUNGAL ANTIBIOTICS; ACTIVITY-BASED PROBES; DNA CROSS-LINKING; COVALENT MODIFICATION; LEPTOMYCIN-B; PHOSPHOINOSITIDE; 3-KINASE;
D O I
10.1039/c2np20012k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study of biologically active natural products has resulted in seminal contributions to our understanding of living systems. In the case of electrophilic natural products, the covalent nature of their interaction has largely facilitated the identification of their biological binding partners. In this review, we provide a comprehensive compilation of electrophilic natural products from all major chemical classes together with their biological targets. Covering Michael acceptor systems, ring-strained compounds and other electrophiles, such as esters or carbamates, we highlight representative and instructive examples for over 20 electrophilic moieties. The fruitful cooperation of natural product chemistry, medicinal chemistry and chemical biology has produced a collection of well-studied examples for how electrophilic natural products exert their biological functions that range from antibiotic to antitumor effects. Special emphasis is put on the elucidation of their respective biological targets via activity-based protein profiling, which together with the recent advancements in mass spectrometry has been crucial to the success of the field. The wealth of naturally occurring electrophilic moieties and their chemical complexity enables binding of a large variety of biological targets, such as enzymes of all classes, nonenzymatic proteins, DNA and other cellular compounds. With approximately 30 000 genes in the human genome but only 266 confirmed protein drug targets, the study of biologically active, electrophilic natural products has the potential to provide insights into fundamental biological processes and to greatly aid the discovery of new drug targets.
引用
收藏
页码:659 / 682
页数:24
相关论文
共 233 条
[1]   (-)-FR182877 is a potent and selective inhibitor of carboxylesterase-1 [J].
Adam, GC ;
Vanderwal, CD ;
Sorensen, EJ ;
Cravatt, BF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (44) :5480-5484
[2]   PHASE-II TRIAL OF ACIVICIN IN PATIENTS WITH ADVANCED COLORECTAL-CARCINOMA [J].
ADOLPHSON, CC ;
AJANI, JA ;
STROEHLEIN, JR ;
BARLOGIE, B ;
BODEY, GP ;
KORINEK, J ;
BEDIKIAN, AY .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1986, 9 (03) :189-191
[3]   A molecular model for DNA cross-linking by the antitumor agent azinomycin B [J].
Alcaro, S ;
Coleman, RS .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (15) :2783-2788
[4]  
ALLEN L, 1980, RES COMMUN CHEM PATH, V27, P175
[5]   NOVEL INTERSTRAND CROSS-LINKS INDUCED BY THE ANTITUMOR ANTIBIOTIC CARZINOPHILIN AZINOMYCIN-B [J].
ARMSTRONG, RW ;
SALVATI, ME ;
NGUYEN, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (08) :3144-3145
[6]   High antitrypanosomal activity of plant-derived sulphur-containing amides [J].
Astelbauer, Florian ;
Obwaller, Andreas ;
Raninger, Adriane ;
Brem, Brigitte ;
Greger, Harald ;
Duchene, Michael ;
Wernsdorfer, Walther ;
Walochnik, Julia .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2010, 36 (06) :570-572
[7]   Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions [J].
Barak, Dov ;
Ordentlich, Arie ;
Stein, Dana ;
Yu, Qian-sheng ;
Greig, Nigel H. ;
Shafferman, Avigdor .
BIOCHEMICAL JOURNAL, 2009, 417 :213-222
[8]   The tumor inhibitor and antiangiogenic agent withaferin A targets the intermediate filament protein vimentin [J].
Bargagna-Mohan, Paola ;
Hamza, Adel ;
Kim, Yang-eon ;
Ho, Yik Khuan ;
Mor-Valknin, Nirit ;
Wendschlag, Nicole ;
Li, Junjun ;
Evans, Robert M. ;
Markovitz, David M. ;
Zhan, Chang-Guo ;
Kim, Kyung Bo ;
Mohan, Royce .
CHEMISTRY & BIOLOGY, 2007, 14 (06) :623-634
[9]   Activity-based protein profiling for the functional annotation of enzymes [J].
Barglow, Katherine T. ;
Cravatt, Benjamin F. .
NATURE METHODS, 2007, 4 (10) :822-827
[10]   L-TRANS-EPOXYSUCCINYL-LEUCYLAMIDO(4-GUANIDINO)BUTANE (E-64) AND ITS ANALOGS AS INHIBITORS OF CYSTEINE PROTEINASES INCLUDING CATHEPSINS B, H AND L [J].
BARRETT, AJ ;
KEMBHAVI, AA ;
BROWN, MA ;
KIRSCHKE, H ;
KNIGHT, CG ;
TAMAI, M ;
HANADA, K .
BIOCHEMICAL JOURNAL, 1982, 201 (01) :189-198