Intense bitterness of molecules: Machine learning for expediting drug discovery
Conceptualization of BitterIntense contribution to optimizing drug development. Red dashed arrow represents the classical drug development process in which the palatability of the drug is assessed in or after clinical trials, with the risk of developing intensely bitter drugs. The green arrow repres...
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creator | Margulis, Eitan Dagan-Wiener, Ayana Ives, Robert S. Jaffari, Sara Siems, Karsten Niv, Masha Y. |
description | Conceptualization of BitterIntense contribution to optimizing drug development. Red dashed arrow represents the classical drug development process in which the palatability of the drug is assessed in or after clinical trials, with the risk of developing intensely bitter drugs. The green arrow represents the drug development process with BitterIntense, enabling easy assessment of aversive taste in early stages.
[Display omitted]
Drug development is a long, expensive and multistage process geared to achieving safe drugs with high efficacy. A crucial prerequisite for completing the medication regimen for oral drugs, particularly for pediatric and geriatric populations, is achieving taste that does not hinder compliance. Currently, the aversive taste of drugs is tested in late stages of clinical trials. This can result in the need to reformulate, potentially resulting in the use of more animals for additional toxicity trials, increased financial costs and a delay in release to the market. Here we present BitterIntense, a machine learning tool that classifies molecules into “very bitter” or “not very bitter”, based on their chemical structure. The model, trained on chemically diverse compounds, has above 80% accuracy on several test sets. Our results suggest that about 25% of drugs are predicted to be very bitter, with even higher prevalence (~40%) in COVID19 drug candidates and in microbial natural products. Only ~10% of toxic molecules are predicted to be intensely bitter, and it is also suggested that intense bitterness does not correlate with hepatotoxicity of drugs. However, very bitter compounds may be more cardiotoxic than not very bitter compounds, possessing significantly lower QPlogHERG values. BitterIntense allows quick and easy prediction of strong bitterness of compounds of interest for food, pharma and biotechnology industries. We estimate that implementation of BitterIntense or similar tools early in drug discovery process may lead to reduction in delays, in animal use and in overall financial burden. |
doi_str_mv | 10.1016/j.csbj.2020.12.030 |
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[Display omitted]
Drug development is a long, expensive and multistage process geared to achieving safe drugs with high efficacy. A crucial prerequisite for completing the medication regimen for oral drugs, particularly for pediatric and geriatric populations, is achieving taste that does not hinder compliance. Currently, the aversive taste of drugs is tested in late stages of clinical trials. This can result in the need to reformulate, potentially resulting in the use of more animals for additional toxicity trials, increased financial costs and a delay in release to the market. Here we present BitterIntense, a machine learning tool that classifies molecules into “very bitter” or “not very bitter”, based on their chemical structure. The model, trained on chemically diverse compounds, has above 80% accuracy on several test sets. Our results suggest that about 25% of drugs are predicted to be very bitter, with even higher prevalence (~40%) in COVID19 drug candidates and in microbial natural products. Only ~10% of toxic molecules are predicted to be intensely bitter, and it is also suggested that intense bitterness does not correlate with hepatotoxicity of drugs. However, very bitter compounds may be more cardiotoxic than not very bitter compounds, possessing significantly lower QPlogHERG values. BitterIntense allows quick and easy prediction of strong bitterness of compounds of interest for food, pharma and biotechnology industries. We estimate that implementation of BitterIntense or similar tools early in drug discovery process may lead to reduction in delays, in animal use and in overall financial burden.</description><identifier>ISSN: 2001-0370</identifier><identifier>EISSN: 2001-0370</identifier><identifier>DOI: 10.1016/j.csbj.2020.12.030</identifier><identifier>PMID: 33510862</identifier><language>eng</language><publisher>AMSTERDAM: Elsevier B.V</publisher><subject>Biochemistry & Molecular Biology ; Biotechnology & Applied Microbiology ; Bitter ; Drug discovery ; Drugs ; Life Sciences & Biomedicine ; Machine learning ; Science & Technology ; Taste ; Toxicity</subject><ispartof>Computational and structural biotechnology journal, 2021-01, Vol.19, p.568-576</ispartof><rights>2021 The Authors</rights><rights>2021 The Authors.</rights><rights>2021 The Authors 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>31</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000684852700008</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c521t-ed59d1723181f9c2bcbd99cae916ffcc991f41d4b997cd098b468a8ad8f7366f3</citedby><cites>FETCH-LOGICAL-c521t-ed59d1723181f9c2bcbd99cae916ffcc991f41d4b997cd098b468a8ad8f7366f3</cites><orcidid>0000-0002-5416-3337 ; 0000-0002-0644-8696 ; 0000-0001-8275-8795 ; 0000-0003-1920-2027</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807207/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807207/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2104,2116,27931,27932,39265,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33510862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Margulis, Eitan</creatorcontrib><creatorcontrib>Dagan-Wiener, Ayana</creatorcontrib><creatorcontrib>Ives, Robert S.</creatorcontrib><creatorcontrib>Jaffari, Sara</creatorcontrib><creatorcontrib>Siems, Karsten</creatorcontrib><creatorcontrib>Niv, Masha Y.</creatorcontrib><title>Intense bitterness of molecules: Machine learning for expediting drug discovery</title><title>Computational and structural biotechnology journal</title><addtitle>COMPUT STRUCT BIOTEC</addtitle><addtitle>Comput Struct Biotechnol J</addtitle><description>Conceptualization of BitterIntense contribution to optimizing drug development. Red dashed arrow represents the classical drug development process in which the palatability of the drug is assessed in or after clinical trials, with the risk of developing intensely bitter drugs. The green arrow represents the drug development process with BitterIntense, enabling easy assessment of aversive taste in early stages.
[Display omitted]
Drug development is a long, expensive and multistage process geared to achieving safe drugs with high efficacy. A crucial prerequisite for completing the medication regimen for oral drugs, particularly for pediatric and geriatric populations, is achieving taste that does not hinder compliance. Currently, the aversive taste of drugs is tested in late stages of clinical trials. This can result in the need to reformulate, potentially resulting in the use of more animals for additional toxicity trials, increased financial costs and a delay in release to the market. Here we present BitterIntense, a machine learning tool that classifies molecules into “very bitter” or “not very bitter”, based on their chemical structure. The model, trained on chemically diverse compounds, has above 80% accuracy on several test sets. Our results suggest that about 25% of drugs are predicted to be very bitter, with even higher prevalence (~40%) in COVID19 drug candidates and in microbial natural products. Only ~10% of toxic molecules are predicted to be intensely bitter, and it is also suggested that intense bitterness does not correlate with hepatotoxicity of drugs. However, very bitter compounds may be more cardiotoxic than not very bitter compounds, possessing significantly lower QPlogHERG values. BitterIntense allows quick and easy prediction of strong bitterness of compounds of interest for food, pharma and biotechnology industries. We estimate that implementation of BitterIntense or similar tools early in drug discovery process may lead to reduction in delays, in animal use and in overall financial burden.</description><subject>Biochemistry & Molecular Biology</subject><subject>Biotechnology & Applied Microbiology</subject><subject>Bitter</subject><subject>Drug discovery</subject><subject>Drugs</subject><subject>Life Sciences & Biomedicine</subject><subject>Machine learning</subject><subject>Science & Technology</subject><subject>Taste</subject><subject>Toxicity</subject><issn>2001-0370</issn><issn>2001-0370</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>DOA</sourceid><recordid>eNqNUstuEzEUHSEQrUp_gAWaJRJK6sfM2EYICUU8IhV1A2vLY1-njiZ2sD2B_j2eTojaTYUXflyfc-x7z62q1xgtMcLd1XapU79dEkRKgCwRRc-qc4IQXiDK0PMH-7PqMqUtKoPjTlD0sjqjtMWId-S8uln7DD5B3bucIXpIqQ623oUB9DhAel9_V_rWeagHUNE7v6ltiDX82YNxeTqaOJbJJR0OEO9eVS-sGhJcHteL6ueXzz9W3xbXN1_Xq0_XC90SnBdgWmEwIxRzbIUmve6NEFqBwJ21WguBbYNN0wvBtEGC903HFVeGW0a7ztKLaj3rmqC2ch_dTsU7GZST94EQN1LF7PQAkkKLWScss6JpSto9Y8oCb6lhVhM7aX2ctfZjvwOjweeohkeij2-8u5WbcJCMI0YQKwJvjwIx_BohZbkr9YBhUB7CmCRpOOW4bVpaoGSG6hhSimBPz2AkJ2PlVk7GyslYiYksxhbSm4cfPFH-2VgAfAb8hj7YpB14DSdYcb7jDW8Ju2-Clcsqu-BXYfS5UN_9P7WgP8xoKN4eHER5ZBgXQedSfPdUIn8B5dDWlg</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Margulis, Eitan</creator><creator>Dagan-Wiener, Ayana</creator><creator>Ives, Robert S.</creator><creator>Jaffari, Sara</creator><creator>Siems, Karsten</creator><creator>Niv, Masha Y.</creator><general>Elsevier B.V</general><general>Elsevier</general><general>Research Network of Computational and Structural Biotechnology</general><scope>6I.</scope><scope>AAFTH</scope><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5416-3337</orcidid><orcidid>https://orcid.org/0000-0002-0644-8696</orcidid><orcidid>https://orcid.org/0000-0001-8275-8795</orcidid><orcidid>https://orcid.org/0000-0003-1920-2027</orcidid></search><sort><creationdate>20210101</creationdate><title>Intense bitterness of molecules: Machine learning for expediting drug discovery</title><author>Margulis, Eitan ; Dagan-Wiener, Ayana ; Ives, Robert S. ; Jaffari, Sara ; Siems, Karsten ; Niv, Masha Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-ed59d1723181f9c2bcbd99cae916ffcc991f41d4b997cd098b468a8ad8f7366f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biochemistry & Molecular Biology</topic><topic>Biotechnology & Applied Microbiology</topic><topic>Bitter</topic><topic>Drug discovery</topic><topic>Drugs</topic><topic>Life Sciences & Biomedicine</topic><topic>Machine learning</topic><topic>Science & Technology</topic><topic>Taste</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Margulis, Eitan</creatorcontrib><creatorcontrib>Dagan-Wiener, Ayana</creatorcontrib><creatorcontrib>Ives, Robert S.</creatorcontrib><creatorcontrib>Jaffari, Sara</creatorcontrib><creatorcontrib>Siems, Karsten</creatorcontrib><creatorcontrib>Niv, Masha Y.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Computational and structural biotechnology journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Margulis, Eitan</au><au>Dagan-Wiener, Ayana</au><au>Ives, Robert S.</au><au>Jaffari, Sara</au><au>Siems, Karsten</au><au>Niv, Masha Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intense bitterness of molecules: Machine learning for expediting drug discovery</atitle><jtitle>Computational and structural biotechnology journal</jtitle><stitle>COMPUT STRUCT BIOTEC</stitle><addtitle>Comput Struct Biotechnol J</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>19</volume><spage>568</spage><epage>576</epage><pages>568-576</pages><issn>2001-0370</issn><eissn>2001-0370</eissn><abstract>Conceptualization of BitterIntense contribution to optimizing drug development. Red dashed arrow represents the classical drug development process in which the palatability of the drug is assessed in or after clinical trials, with the risk of developing intensely bitter drugs. The green arrow represents the drug development process with BitterIntense, enabling easy assessment of aversive taste in early stages.
[Display omitted]
Drug development is a long, expensive and multistage process geared to achieving safe drugs with high efficacy. A crucial prerequisite for completing the medication regimen for oral drugs, particularly for pediatric and geriatric populations, is achieving taste that does not hinder compliance. Currently, the aversive taste of drugs is tested in late stages of clinical trials. This can result in the need to reformulate, potentially resulting in the use of more animals for additional toxicity trials, increased financial costs and a delay in release to the market. Here we present BitterIntense, a machine learning tool that classifies molecules into “very bitter” or “not very bitter”, based on their chemical structure. The model, trained on chemically diverse compounds, has above 80% accuracy on several test sets. Our results suggest that about 25% of drugs are predicted to be very bitter, with even higher prevalence (~40%) in COVID19 drug candidates and in microbial natural products. Only ~10% of toxic molecules are predicted to be intensely bitter, and it is also suggested that intense bitterness does not correlate with hepatotoxicity of drugs. However, very bitter compounds may be more cardiotoxic than not very bitter compounds, possessing significantly lower QPlogHERG values. BitterIntense allows quick and easy prediction of strong bitterness of compounds of interest for food, pharma and biotechnology industries. We estimate that implementation of BitterIntense or similar tools early in drug discovery process may lead to reduction in delays, in animal use and in overall financial burden.</abstract><cop>AMSTERDAM</cop><pub>Elsevier B.V</pub><pmid>33510862</pmid><doi>10.1016/j.csbj.2020.12.030</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5416-3337</orcidid><orcidid>https://orcid.org/0000-0002-0644-8696</orcidid><orcidid>https://orcid.org/0000-0001-8275-8795</orcidid><orcidid>https://orcid.org/0000-0003-1920-2027</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biochemistry & Molecular Biology Biotechnology & Applied Microbiology Bitter Drug discovery Drugs Life Sciences & Biomedicine Machine learning Science & Technology Taste Toxicity |
title | Intense bitterness of molecules: Machine learning for expediting drug discovery |
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