Can Invalid Bioactives Undermine Natural Product-Based Drug Discovery?

被引:188
作者
Bisson, Jonathan [1 ]
McAlpine, James B. [1 ,2 ]
Friesen, J. Brent [1 ,2 ,3 ]
Chen, Shao-Nong [1 ,2 ]
Graham, James [1 ]
Pauli, Guido F. [1 ,2 ]
机构
[1] Univ Illinois, Coll Pharm, Dept Med Chem & Pharmacognosy, Ctr Nat Prod Technol, 833 South Wood St, Chicago, IL 60612 USA
[2] Univ Illinois, Coll Pharm, Inst TB Res, 833 South Wood St, Chicago, IL 60612 USA
[3] Dominican Univ, Rosary Coll Arts & Sci, Dept Phys Sci, River Forest, IL 60305 USA
关键词
PURITY-ACTIVITY RELATIONSHIPS; COLLOIDAL AGGREGATION; FALSE POSITIVES; ASSAY INTERFERENCE; COMPOUND DISCOVERY; LINOLEIC-ACID; FATTY-ACIDS; FLUORESCENCE; INHIBITION; IDENTIFICATION;
D O I
10.1021/acs.jmedchem.5b01009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
High-throughput biology has contributed a wealth of data on chemicals, including natural products (NPs). Recently, attention was drawn to certain, predominantly synthetic, compounds that are responsible for disproportionate percentages of hits but are false actives. Spurious bioassay interference led to their designation as pan-assay interference compounds (PAINS). NPs lack comparable scrutiny, which this study aims to rectify. Systematic mining of 80+ years of the phytochemistry and biology literature, using the NAPRALERT database, revealed that only 39 compounds represent the NPs most reported by occurrence, activity, and distinct activity. Over 50% are not explained by phenomena known for synthetic libraries, and all had manifold ascribed bioactivities, designating them as invalid metabolic panaceas (IMPs). Cumulative distributions of similar to 200,000 NPs uncovered that NP research follows power-law characteristics typical for behavioral phenomena. Projection into occurrence-bioactivity-effort space produces the hyperbolic black hole of NPs, where IMPs populate the high-effort base.
引用
收藏
页码:1671 / 1690
页数:20
相关论文
共 122 条
  • [11] [Anonymous], 547370399341 CHEMBL
  • [12] [Anonymous], 514314366285 CHEMBL
  • [13] [Anonymous], 606761455703 CHEMBL
  • [14] [Anonymous], 514313366284 CHEMBL
  • [15] Flavonoids as dietary regulators of nuclear receptor activity
    Avior, Yishai
    Bomze, David
    Ramon, Ory
    Nahmias, Yaakov
    [J]. FOOD & FUNCTION, 2013, 4 (06) : 831 - 844
  • [16] PAINS: Relevance to Tool Compound Discovery and Fragment-Based Screening
    Baell, Jonathan B.
    Ferrins, Lori
    Falk, Hendrik
    Nikolakopoulos, George
    [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 2013, 66 (12) : 1483 - 1494
  • [17] New Substructure Filters for Removal of Pan Assay Interference Compounds (PAINS) from Screening Libraries and for Their Exclusion in Bioassays
    Baell, Jonathan B.
    Holloway, Georgina A.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (07) : 2719 - 2740
  • [18] Interference by naturally occurring fatty acids in a noncellular enzyme-based aromatase bioassay
    Balunas, MJ
    Su, B
    Landini, S
    Brueggemeier, RW
    Kinghorn, AD
    [J]. JOURNAL OF NATURAL PRODUCTS, 2006, 69 (04): : 700 - 703
  • [19] Impact of a red-shifted dye label for high throughput fluorescence polarization assays of G protein-coupled receptors
    Banks, P
    Gosselin, M
    Prystay, L
    [J]. JOURNAL OF BIOMOLECULAR SCREENING, 2000, 5 (05) : 329 - 334
  • [20] The ChEMBL bioactivity database: an update
    Bento, A. Patricia
    Gaulton, Anna
    Hersey, Anne
    Bellis, Louisa J.
    Chambers, Jon
    Davies, Mark
    Krueger, Felix A.
    Light, Yvonne
    Mak, Lora
    McGlinchey, Shaun
    Nowotka, Michal
    Papadatos, George
    Santos, Rita
    Overington, John P.
    [J]. NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) : D1083 - D1090