Application of Combination High‐Throughput Phenotypic Screening and Target Identification Methods for the Discovery of Natural Product‐Based Combination Drugs
Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge...
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Published in | Medicinal research reviews Vol. 38; no. 2; pp. 504 - 524 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.03.2018
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Subjects | |
Online Access | Get full text |
ISSN | 0198-6325 1098-1128 1098-1128 |
DOI | 10.1002/med.21444 |
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Abstract | Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge as a new paradigm in drug discovery, with a focus on multiple targets and drug combinations for treating disease. Studies on the benefits of drug combinations lay the groundwork for a renewed focus on natural products in drug discovery. Natural products consist of a multitude of constituents that can act on a variety of targets in the body to induce pharmacodynamic responses that may together culminate in an additive or synergistic therapeutic effect. Although natural products cannot be patented, they can be used as starting points in the discovery of potent combination therapeutics. The optimal mix of bioactive ingredients in natural products can be determined via phenotypic screening. The targets and molecular mechanisms of action of these active ingredients can then be determined using chemical proteomics, and by implementing a reverse pharmacokinetics approach. This review article provides evidence supporting the potential benefits of natural product‐based combination drugs, and summarizes drug discovery methods that can be applied to this class of drugs. |
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AbstractList | Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge as a new paradigm in drug discovery, with a focus on multiple targets and drug combinations for treating disease. Studies on the benefits of drug combinations lay the groundwork for a renewed focus on natural products in drug discovery. Natural products consist of a multitude of constituents that can act on a variety of targets in the body to induce pharmacodynamic responses that may together culminate in an additive or synergistic therapeutic effect. Although natural products cannot be patented, they can be used as starting points in the discovery of potent combination therapeutics. The optimal mix of bioactive ingredients in natural products can be determined via phenotypic screening. The targets and molecular mechanisms of action of these active ingredients can then be determined using chemical proteomics, and by implementing a reverse pharmacokinetics approach. This review article provides evidence supporting the potential benefits of natural product-based combination drugs, and summarizes drug discovery methods that can be applied to this class of drugs.Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge as a new paradigm in drug discovery, with a focus on multiple targets and drug combinations for treating disease. Studies on the benefits of drug combinations lay the groundwork for a renewed focus on natural products in drug discovery. Natural products consist of a multitude of constituents that can act on a variety of targets in the body to induce pharmacodynamic responses that may together culminate in an additive or synergistic therapeutic effect. Although natural products cannot be patented, they can be used as starting points in the discovery of potent combination therapeutics. The optimal mix of bioactive ingredients in natural products can be determined via phenotypic screening. The targets and molecular mechanisms of action of these active ingredients can then be determined using chemical proteomics, and by implementing a reverse pharmacokinetics approach. This review article provides evidence supporting the potential benefits of natural product-based combination drugs, and summarizes drug discovery methods that can be applied to this class of drugs. Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge as a new paradigm in drug discovery, with a focus on multiple targets and drug combinations for treating disease. Studies on the benefits of drug combinations lay the groundwork for a renewed focus on natural products in drug discovery. Natural products consist of a multitude of constituents that can act on a variety of targets in the body to induce pharmacodynamic responses that may together culminate in an additive or synergistic therapeutic effect. Although natural products cannot be patented, they can be used as starting points in the discovery of potent combination therapeutics. The optimal mix of bioactive ingredients in natural products can be determined via phenotypic screening. The targets and molecular mechanisms of action of these active ingredients can then be determined using chemical proteomics, and by implementing a reverse pharmacokinetics approach. This review article provides evidence supporting the potential benefits of natural product‐based combination drugs, and summarizes drug discovery methods that can be applied to this class of drugs. Modern drug discovery efforts have had mediocre success rates with increasing developmental costs, and this has encouraged pharmaceutical scientists to seek innovative approaches. Recently with the rise of the fields of systems biology and metabolomics, network pharmacology (NP) has begun to emerge as a new paradigm in drug discovery, with a focus on multiple targets and drug combinations for treating disease. Studies on the benefits of drug combinations lay the groundwork for a renewed focus on natural products in drug discovery. Natural products consist of a multitude of constituents that can act on a variety of targets in the body to induce pharmacodynamic responses that may together culminate in an additive or synergistic therapeutic effect. Although natural products cannot be patented, they can be used as starting points in the discovery of potent combination therapeutics. The optimal mix of bioactive ingredients in natural products can be determined via phenotypic screening. The targets and molecular mechanisms of action of these active ingredients can then be determined using chemical proteomics, and by implementing a reverse pharmacokinetics approach. This review article provides evidence supporting the potential benefits of natural product‐based combination drugs, and summarizes drug discovery methods that can be applied to this class of drugs. |
Author | Isgut, Monica Subrahmanyam, Vangala Aneja, Ritu Yang, Chunhua Rao, Mukkavilli Rida, Padmashree C. G. |
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Cites_doi | 10.1016/j.pharmthera.2016.01.010 10.1007/s00432-014-1899-5 10.1093/ajcn/79.5.727 10.1016/j.phymed.2015.03.011 10.1016/j.tips.2008.04.002 10.2174/1568009033333736 10.1038/nrd4539 10.1038/nbt1007-1110 10.1038/nrc3599 10.1038/nbt.2989 10.1021/np200906s 10.1023/A:1021210910821 10.1517/17425255.3.3.389 10.1016/j.fitote.2013.06.013 10.3390/ijms16010510 10.1186/1749-8546-9-17 10.1155/2013/137414 10.1002/mnfr.201500955 10.1038/nrd1984 10.3390/s151229848 10.1038/nchembio.118 10.1016/j.fitote.2013.10.010 10.1038/nrd3681 10.1016/j.lfs.2005.09.012 10.1201/b10787-8 10.1038/embor.2009.12 10.1016/j.drudis.2013.07.001 10.1093/jnci/89.24.1881 10.1126/science.1168243 10.1016/j.lfs.2005.12.006 10.3390/ijms150711245 10.1038/nrd1609 10.1016/j.tips.2014.02.001 10.1016/j.ejphar.2003.11.059 10.1002/ptr.5165 10.1016/j.drudis.2008.07.004 10.1038/srep07896 10.1093/carcin/bgu011 10.1038/nrd1657 10.1038/nrd2155 10.1158/1055-9965.EPI-07-2934 10.1080/01635581.2013.749925 10.1093/ajcn/78.3.517S 10.1073/pnas.1337088100 10.1093/carcin/8.3.487 10.1016/j.drudis.2008.07.002 10.1080/10408391003698669 10.1038/nrc723 |
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Keywords | reverse pharmacokinetics phenotypic screening chemical proteomics combination drugs multicomponent drugs network pharmacology |
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References | 2015; 141 2004; 485 2015; 15 2015; 14 2014; 92 2015; 5 2006; 78 1987; 8 2013; 65 2011 2008; 17 1997; 89 2013; 90 2002; 2 2006; 5 2008; 13 2008; 4 2014; 28 2012; 11 2012; 75 2016; 162 2003; 78 2013; 18 2009; 14 2009; 10 2013; 2013 2013; 13 2008; 29 2015; 22 2011; 51 2002; 21 2004; 79 2014; 16 2005; 4 2003; 3 2014; 15 2007; 6 2014; 35 2016; 60 2007; 3 2014; 9 109 2012; 5 2003; 100 2007; 24 2005; 78 2009; 325 2014; 32 e_1_2_9_52_1 e_1_2_9_50_1 e_1_2_9_10_1 e_1_2_9_35_1 e_1_2_9_12_1 Fabricant DS (e_1_2_9_22_1); 109 e_1_2_9_33_1 Lan K (e_1_2_9_42_1) 2013; 2013 e_1_2_9_14_1 e_1_2_9_39_1 e_1_2_9_16_1 e_1_2_9_37_1 e_1_2_9_18_1 e_1_2_9_41_1 e_1_2_9_20_1 e_1_2_9_24_1 e_1_2_9_43_1 e_1_2_9_8_1 e_1_2_9_6_1 e_1_2_9_4_1 e_1_2_9_2_1 Kotz J (e_1_2_9_45_1) 2012; 5 Zhang GB (e_1_2_9_9_1) 2013; 2013 e_1_2_9_26_1 e_1_2_9_49_1 e_1_2_9_28_1 e_1_2_9_47_1 e_1_2_9_30_1 e_1_2_9_53_1 e_1_2_9_51_1 e_1_2_9_34_1 e_1_2_9_13_1 e_1_2_9_32_1 Yardley DA. (e_1_2_9_17_1) 2013; 2013 e_1_2_9_15_1 e_1_2_9_38_1 e_1_2_9_36_1 e_1_2_9_19_1 e_1_2_9_40_1 e_1_2_9_21_1 e_1_2_9_46_1 e_1_2_9_23_1 e_1_2_9_44_1 e_1_2_9_7_1 e_1_2_9_5_1 e_1_2_9_3_1 Wargovich MJ (e_1_2_9_31_1) 1987; 8 e_1_2_9_25_1 e_1_2_9_27_1 e_1_2_9_48_1 Hopkins AL (e_1_2_9_11_1) 2007; 24 e_1_2_9_29_1 |
References_xml | – volume: 4 start-page: 206 issue: 3 year: 2005 end-page: 220 article-title: The evolving role of natural products in drug discovery publication-title: Nat Rev Drug Discov – volume: 15 start-page: 31142 issue: 12 year: 2015 end-page: 31170 article-title: Microfluidic organ/body‐on‐a‐chip devices at the convergence of biology and microengineering publication-title: Sensors – volume: 485 start-page: 97 issue: 1–3 year: 2004 end-page: 103 article-title: Allicin (from garlic) induces caspase‐mediated apoptosis in cancer cells publication-title: Eur J Pharmacol – volume: 11 start-page: 191 issue: 3 year: 2012 end-page: 200 article-title: Diagnosing the decline in pharmaceutical R&D efficiency publication-title: Nat Rev Drug Discov – volume: 65 start-page: 263 issue: 2 year: 2013 end-page: 272 article-title: Ginger phytochemicals exhibit synergy to inhibit prostate cancer cell proliferation publication-title: Nutr Cancer – volume: 13 start-page: 714 issue: 10 year: 2013 end-page: 726 article-title: Cancer drug resistance: An evolving paradigm publication-title: Nat Rev Cancer – volume: 78 start-page: 2073 issue: 18 year: 2006 end-page: 2080 article-title: Green tea and its polyphenolic catechins: Medicinal uses in cancer and noncancer applications publication-title: Life Sci – volume: 2 start-page: 143 issue: 2 year: 2002 end-page: 148 article-title: Natural products in cancer chemotherapy: Past, present and future publication-title: Nat Rev Cancer – volume: 15 start-page: 11245 issue: 7 year: 2014 end-page: 11254 article-title: Elucidating polypharmacological mechanisms of polyphenols by gene module profile analysis publication-title: Int J Mol Sci – start-page: 131 year: 2011 end-page: 147 – volume: 75 start-page: 311 issue: 3 year: 2012 end-page: 335 article-title: Natural products as sources of new drugs over the 30 years from 1981 to 2010 publication-title: J Nat Prod – volume: 5 start-page: 7896 year: 2015 end-page: 7908 article-title: Mapping sites of aspirin‐induced acetylations in live cells by quantitative acid‐cleavable activity‐based protein profiling (QA‐ABPP) publication-title: Sci Rep – volume: 29 start-page: 331 issue: 7 year: 2008 end-page: 332 article-title: Synergy in natural medicines: Implications for drug discovery publication-title: Trends Pharmacol Sci – volume: 4 start-page: 682 issue: 11 year: 2008 end-page: 690 article-title: Network pharmacology: The next paradigm in drug discovery publication-title: Nat Chem Biol – volume: 51 start-page: 499 issue: 6 year: 2011 end-page: 523 article-title: Update on the chemopreventive effects of ginger and its phytochemicals publication-title: Crit Rev Food Sci Nutr – volume: 28 start-page: 1423 issue: 10 year: 2014 end-page: 1446 article-title: Anticancer activities of essential oils constituents and synergy with conventional therapies: A review publication-title: Phytother Res – volume: 90 start-page: 1 year: 2013 end-page: 9 article-title: Comparative pharmacokinetics of paclitaxel after oral administration of extract and pure paclitaxel to rats publication-title: Fitoterapia – volume: 79 start-page: 727 issue: 5 year: 2004 end-page: 747 article-title: Polyphenols: Food sources and bioavailability publication-title: Am J Clin Nutr – volume: 109 start-page: 69 issue: Suppl 1) end-page: 75 article-title: The value of plants used in traditional medicine for drug discovery publication-title: Environ Health Perspect 2001 – volume: 3 start-page: 67 issue: 1 year: 2003 end-page: 81 article-title: Garlic [ ]: A review of its potential use as an anti‐cancer agent publication-title: Curr Cancer Drug Targets – volume: 78 start-page: 517S issue: 3 Suppl year: 2003 end-page: 520S article-title: Health benefits of fruit and vegetables are from additive and synergistic combinations of phytochemicals publication-title: Am J Clin Nutr – volume: 35 start-page: 168 issue: 4 year: 2014 end-page: 177 article-title: Insights into drug discovery from natural medicines using reverse pharmacokinetics publication-title: Trends Pharmacol Sci – volume: 2013 year: 2013 article-title: Drug resistance and the role of combination chemotherapy in improving patient outcomes publication-title: Int J Breast Cancer – volume: 5 start-page: 219 issue: 3 year: 2006 end-page: 234 article-title: Targeting multidrug resistance in cancer publication-title: Nat Rev Drug Discov – volume: 60 start-page: 1364 issue: 6 year: 2016 end-page: 1373 article-title: Ginger augmented chemotherapy: A novel multitarget nontoxic approach for cancer management publication-title: Mol Nutr Food Res – volume: 3 start-page: 389 issue: 3 year: 2007 end-page: 406 article-title: Natural polyphenol disposition via coupled metabolic pathways publication-title: Expert Opin Drug Metab Toxicol – volume: 6 start-page: 115 issue: 2 year: 2007 end-page: 120 article-title: Why is cancer drug discovery so difficult? publication-title: Nat Rev Drug Discov – volume: 10 start-page: 194 issue: 3 year: 2009 end-page: 200 article-title: Natural products and drug discovery. Can thousands of years of ancient medical knowledge lead us to new and powerful drug combinations in the fight against cancer and dementia? publication-title: EMBO Rep – volume: 162 start-page: 10 year: 2016 end-page: 22 article-title: Target identification of natural and traditional medicines with quantitative chemical proteomics approaches publication-title: Pharmacol Ther – volume: 92 start-page: 133 year: 2014 end-page: 147 article-title: Synergy effects of herb extracts: Pharmacokinetics and pharmacodynamic basis publication-title: Fitoterapia – volume: 24 start-page: 1110 year: 2007 end-page: 1111 article-title: Network pharmacology: Network biology illuminates our understanding of drug action publication-title: Nature Biotechnology – volume: 8 start-page: 487 issue: 3 year: 1987 end-page: 489 article-title: Diallyl sulfide, a flavor component of garlic (Allium sativum), inhibits dimethylhydrazine‐induced colon cancer publication-title: Carcinogenesis – volume: 2013 year: 2013 article-title: Towards polypharmacokinetics: Pharmacokinetics of multicomponent drugs and herbal medicines using a metabolomics approach publication-title: Evid Based Complement Alternat Med – volume: 14 start-page: 248 issue: 4 year: 2015 end-page: 260 article-title: Organs‐on‐chips at the frontiers of drug discovery publication-title: Nat Rev Drug Discov – volume: 35 start-page: 1320 issue: 6 year: 2014 end-page: 1329 article-title: Enterohepatic recirculation of bioactive ginger phytochemicals is associated with enhanced tumor growth‐inhibitory activity of ginger extract publication-title: Carcinogenesis – volume: 100 start-page: 7977 issue: 13 year: 2003 end-page: 7982 article-title: Systematic discovery of multicomponent therapeutics publication-title: Proc Natl Acad Sci USA – volume: 13 start-page: 894 issue: 19–20 year: 2008 end-page: 901 article-title: Natural products in drug discovery publication-title: Drug Discov Today – volume: 4 start-page: 71 issue: 1 year: 2005 end-page: 78 article-title: Multicomponent therapeutics for networked systems publication-title: Nat Rev Drug Discov – volume: 22 start-page: 573 issue: 5 year: 2015 end-page: 578 article-title: Pharmacokinetic synergy from the taxane extract of improves the bioavailability of paclitaxel publication-title: Phytomedicine – volume: 32 start-page: 760 issue: 8 year: 2014 end-page: 772 article-title: Microfluidic organs‐on‐chips publication-title: Nat Biotechnol – volume: 2013 year: 2013 article-title: Network pharmacology: A new approach for Chinese herbal medicine research publication-title: Evid Based Complement Alternat Med – volume: 17 start-page: 1930 issue: 8 year: 2008 end-page: 1936 article-title: Pharmacokinetics of 6‐gingerol, 8‐gingerol, 10‐gingerol, and 6‐shogaol and conjugate metabolites in healthy human subjects publication-title: Cancer Epidemiol Biomarkers Prev – volume: 18 start-page: 1067 issue: 21–22 year: 2013 end-page: 1073 article-title: Phenotypic screens as a renewed approach for drug discovery publication-title: Drug Discov Today – volume: 141 start-page: 1511 issue: 9 year: 2015 end-page: 1522 article-title: Synergistic enhancement of anticancer effects on numerous human cancer cell lines treated with the combination of EGCG, other green tea catechins, and anticancer compounds publication-title: J Cancer Res Clin Oncol – volume: 325 start-page: 161 issue: 5937 year: 2009 end-page: 165 article-title: Drug discovery and natural products: End of an era or an endless frontier? publication-title: Science – volume: 78 start-page: 431 issue: 5 year: 2005 end-page: 441 article-title: Drug discovery from medicinal plants publication-title: Life Sci – volume: 89 start-page: 1881 issue: 24 year: 1997 end-page: 1886 article-title: Green tea constituent epigallocatechin‐3‐gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells publication-title: J Natl Cancer Inst – volume: 21 start-page: 265 issue: 3–4 year: 2002 end-page: 280 article-title: Mechanisms of cancer chemoprevention by soy isoflavone genistein publication-title: Cancer Metastasis Rev – volume: 5 start-page: 380 year: 2012 end-page: 383 article-title: Phenotypic screening, take two publication-title: SciBX – volume: 14 start-page: 115 issue: 3–4 year: 2009 end-page: 119 article-title: Where is the hope for drug discovery? Let history tell the future publication-title: Drug Discov Today – volume: 16 start-page: 510 issue: 1 year: 2014 end-page: 520 article-title: Elucidating pharmacological mechanisms of natural medicines by biclustering analysis of the gene expression profile: A case study on curcumin and Si‐Wu‐Tang publication-title: Int J Mol Sci – volume: 9 start-page: 17 year: 2014 end-page: 21 article-title: Myriad and its implications for patent protection of isolated natural products in the United States publication-title: Chin Med – ident: e_1_2_9_49_1 doi: 10.1016/j.pharmthera.2016.01.010 – ident: e_1_2_9_13_1 doi: 10.1007/s00432-014-1899-5 – ident: e_1_2_9_43_1 doi: 10.1093/ajcn/79.5.727 – ident: e_1_2_9_12_1 doi: 10.1016/j.phymed.2015.03.011 – ident: e_1_2_9_39_1 doi: 10.1016/j.tips.2008.04.002 – ident: e_1_2_9_26_1 doi: 10.2174/1568009033333736 – volume: 109 start-page: 69 issue: 1 ident: e_1_2_9_22_1 article-title: The value of plants used in traditional medicine for drug discovery publication-title: Environ Health Perspect 2001 – ident: e_1_2_9_47_1 doi: 10.1038/nrd4539 – volume: 24 start-page: 1110 year: 2007 ident: e_1_2_9_11_1 article-title: Network pharmacology: Network biology illuminates our understanding of drug action publication-title: Nature Biotechnology doi: 10.1038/nbt1007-1110 – ident: e_1_2_9_18_1 doi: 10.1038/nrc3599 – ident: e_1_2_9_48_1 doi: 10.1038/nbt.2989 – ident: e_1_2_9_21_1 doi: 10.1021/np200906s – ident: e_1_2_9_32_1 doi: 10.1023/A:1021210910821 – ident: e_1_2_9_15_1 doi: 10.1517/17425255.3.3.389 – ident: e_1_2_9_35_1 doi: 10.1016/j.fitote.2013.06.013 – ident: e_1_2_9_51_1 doi: 10.3390/ijms16010510 – volume: 2013 year: 2013 ident: e_1_2_9_9_1 article-title: Network pharmacology: A new approach for Chinese herbal medicine research publication-title: Evid Based Complement Alternat Med – ident: e_1_2_9_41_1 doi: 10.1186/1749-8546-9-17 – volume: 2013 year: 2013 ident: e_1_2_9_17_1 article-title: Drug resistance and the role of combination chemotherapy in improving patient outcomes publication-title: Int J Breast Cancer doi: 10.1155/2013/137414 – ident: e_1_2_9_38_1 doi: 10.1002/mnfr.201500955 – volume: 2013 year: 2013 ident: e_1_2_9_42_1 article-title: Towards polypharmacokinetics: Pharmacokinetics of multicomponent drugs and herbal medicines using a metabolomics approach publication-title: Evid Based Complement Alternat Med – ident: e_1_2_9_16_1 doi: 10.1038/nrd1984 – ident: e_1_2_9_5_1 doi: 10.3390/s151229848 – ident: e_1_2_9_3_1 doi: 10.1038/nchembio.118 – ident: e_1_2_9_8_1 doi: 10.1016/j.fitote.2013.10.010 – ident: e_1_2_9_2_1 doi: 10.1038/nrd3681 – ident: e_1_2_9_24_1 doi: 10.1016/j.lfs.2005.09.012 – ident: e_1_2_9_36_1 doi: 10.1201/b10787-8 – ident: e_1_2_9_40_1 doi: 10.1038/embor.2009.12 – ident: e_1_2_9_46_1 doi: 10.1016/j.drudis.2013.07.001 – ident: e_1_2_9_33_1 doi: 10.1093/jnci/89.24.1881 – ident: e_1_2_9_20_1 doi: 10.1126/science.1168243 – ident: e_1_2_9_27_1 doi: 10.1016/j.lfs.2005.12.006 – ident: e_1_2_9_52_1 doi: 10.3390/ijms150711245 – volume: 5 start-page: 380 year: 2012 ident: e_1_2_9_45_1 article-title: Phenotypic screening, take two publication-title: SciBX – ident: e_1_2_9_6_1 doi: 10.1038/nrd1609 – ident: e_1_2_9_53_1 doi: 10.1016/j.tips.2014.02.001 – ident: e_1_2_9_30_1 doi: 10.1016/j.ejphar.2003.11.059 – ident: e_1_2_9_37_1 doi: 10.1002/ptr.5165 – ident: e_1_2_9_23_1 doi: 10.1016/j.drudis.2008.07.004 – ident: e_1_2_9_50_1 doi: 10.1038/srep07896 – ident: e_1_2_9_34_1 doi: 10.1093/carcin/bgu011 – ident: e_1_2_9_7_1 doi: 10.1038/nrd1657 – ident: e_1_2_9_19_1 doi: 10.1038/nrd2155 – ident: e_1_2_9_29_1 doi: 10.1158/1055-9965.EPI-07-2934 – ident: e_1_2_9_14_1 doi: 10.1080/01635581.2013.749925 – ident: e_1_2_9_25_1 doi: 10.1093/ajcn/78.3.517S – ident: e_1_2_9_10_1 doi: 10.1073/pnas.1337088100 – volume: 8 start-page: 487 issue: 3 year: 1987 ident: e_1_2_9_31_1 article-title: Diallyl sulfide, a flavor component of garlic (Allium sativum), inhibits dimethylhydrazine‐induced colon cancer publication-title: Carcinogenesis doi: 10.1093/carcin/8.3.487 – ident: e_1_2_9_4_1 doi: 10.1016/j.drudis.2008.07.002 – ident: e_1_2_9_28_1 doi: 10.1080/10408391003698669 – ident: e_1_2_9_44_1 doi: 10.1038/nrc723 |
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SubjectTerms | Animals Biological Products - pharmacokinetics Biological Products - pharmacology chemical proteomics combination drugs Drug Delivery Systems - methods Drug Discovery - methods Drug Therapy, Combination High-Throughput Screening Assays - methods Humans multicomponent drugs Natural products network pharmacology Phenotype phenotypic screening reverse pharmacokinetics |
Title | Application of Combination High‐Throughput Phenotypic Screening and Target Identification Methods for the Discovery of Natural Product‐Based Combination Drugs |
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