{"id":1776,"date":"2022-08-20T09:11:00","date_gmt":"2022-08-20T03:41:00","guid":{"rendered":"https:\/\/chiralpedia.com\/blog\/?p=1776"},"modified":"2024-07-05T10:49:23","modified_gmt":"2024-07-05T05:19:23","slug":"thalidomide","status":"publish","type":"post","link":"https:\/\/chiralpedia.com\/blog\/thalidomide\/","title":{"rendered":"Thalidomide"},"content":{"rendered":"\n<p><\/p>\n\n\n\n<figure class=\"wp-block-image alignright size-full is-style-rounded border\"><img loading=\"lazy\" decoding=\"async\" width=\"164\" height=\"262\" src=\"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Untitled-Phocomelia-1.png\" alt=\"\" class=\"wp-image-1851\"\/><\/figure>\n\n\n\n<p>Thalidomide was a racemic therapeutic and prescribed to pregnant women to control nausea and vomiting. The drug was withdrawn from world market when it became evident that the use in pregnancy causes phocomelia (clinical conditions where babies are born with deformed hand and limbs). Later in late 1970s, the thalidomide enantiomers were separated and enantioselective studies indicated that the (R)- enantiomer, the good partner, is an effective sedative, the (S)-enantiomer, the evil partner, harbors teratogenic effect and causes fetal abnormalities. The problem with thalidomide is one of the reasons that &nbsp;chiral separation&nbsp;and analysis  has become so important in drug design and development chemistry. [Read more on chiral separation and analysis @ <a href=\"https:\/\/en.wikipedia.org\/wiki\/Chiral_analysis\">https:\/\/en.wikipedia.org\/wiki\/Chiral_analysis<\/a>].<\/p>\n\n\n\n<p><\/p>\n\n\n\n<p><\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Events of thalidomide tragedy &#8211; an overview <\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"471\" height=\"254\" src=\"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide_780\u00d7300_3D_Conformer-4.png\" alt=\"\" class=\"wp-image-1861\" srcset=\"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide_780\u00d7300_3D_Conformer-4.png 471w, https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide_780\u00d7300_3D_Conformer-4-300x162.png 300w\" sizes=\"auto, (max-width: 471px) 100vw, 471px\" \/><\/figure>\n\n\n\n<p class=\"has-black-color has-text-color has-small-font-size\">1956:&nbsp; Introduced in world market  &nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"has-black-color has-text-color has-small-font-size\">1960: Teratogenic effect noticed<\/p>\n\n\n\n<p class=\"has-black-color has-text-color has-small-font-size\">1961:&nbsp; Withdrawn from world market&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"has-black-color has-text-color has-small-font-size\">1970:&nbsp; Resolved enantiomers<\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Chirality and drug toxicity<\/strong><\/p>\n\n\n\n<p>Thalidomide carries one stereogenic center at the C-3&nbsp;of the 2,6-piperidine-2,6-dione ring and hence the molecule exists as an enantiomeric pair. The (R)-enantiomer has the desired sedative effect while the (S)-enantiomer harbors embryo-toxic and teratogenic effect.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"625\" height=\"300\" src=\"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide-enantiomers.png\" alt=\"\" class=\"wp-image-1786\" srcset=\"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide-enantiomers.png 625w, https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2022\/08\/Thalidomide-enantiomers-300x144.png 300w\" sizes=\"auto, (max-width: 625px) 100vw, 625px\" \/><\/figure>\n\n\n\n<p>The hypothesis that the tragedy could be avoided in this case by using a single enantiomer is misleading and pointless, because it was later demonstrated that the \u201csafe\u201d&nbsp;<em>R<\/em>-thalidomide undergoes an <em>in vivo<\/em> chiral inversion to the \u201cteratogenic\u201d&nbsp;<em>S<\/em>-thalidomide. &nbsp;Under biological conditions, the enantiomers interconvert [<strong><em>bidirectional chiral inversion<\/em><\/strong> <em>&#8211; indicated by curved arrows<\/em>; (R)- to (S)- and vice versa]. <strong>Thalidomide tragedy<\/strong> (<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/21507989\/\">https:\/\/pubmed.ncbi.nlm.nih.gov\/21507989\/<\/a>) led to profound and sustainable change in toxicity testing, regulatory control and the ways we look at chiral molecules. Today enantiomers are treated as two different chemical entities at least with respect to chiral drugs, like a polypharmacy.<\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Return of thalidomide<\/strong><\/p>\n\n\n\n<p>However, there is renewed interest in restricted use of thalidomide because of its immunomodulatory, anti-angiogenic, and anti-inflammatory effects. <\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Therapeutic category<\/strong><\/p>\n\n\n\n<p>Immunomodulatory agent<\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Nomenclature<\/strong><\/p>\n\n\n\n<p>(RS)-2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione<\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>Exercise<\/strong><\/p>\n\n\n\n<p>Learn the numbering and nomenclature of the molecule<\/p>\n\n\n\n<p>Understand the terms employed &#8211; eutomer, distomer,  phocomelia, teratogen<\/p>\n\n\n\n<p>Will chiral switching of racemic thalidomide to (R)-thalidomide, the eutomer, work?<\/p>\n\n\n\n<p class=\"has-ast-global-color-0-color has-text-color has-medium-font-size\"><strong>References<\/strong><\/p>\n\n\n\n<p>Tokunaga, E., Yamamoto, T., Ito, E.&nbsp;<em>et al.<\/em>&nbsp;Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers.&nbsp;<em>Sci Rep<\/em>&nbsp;<strong>8<\/strong>, 17131 (2018). https:\/\/doi.org\/10.1038\/s41598-018-35457-6; <strong><a href=\"https:\/\/rdcu.be\/cVeXt\">https:\/\/rdcu.be\/cVeXt<\/a><\/strong><\/p>\n\n\n\n<p>Chiral drugs. Wikipedia, Wikipedia Foundation, 18\/08\/2022. &nbsp;<a href=\"https:\/\/en.wikipedia.org\/wiki\/Chiral_drugs\">https:\/\/en.wikipedia.org\/wiki\/Chiral_drugs<\/a> and references therein<\/p>\n\n\n\n<p>Chiral analysis. Wikipedia, Wikipedia Foundation, 20\/08\/2022.<a href=\"https:\/\/en.wikipedia.org\/wiki\/Chiral_analysis\"> &nbsp;https:\/\/en.wikipedia.org\/wiki\/Chiral_analysis<\/a> and references therein<\/p>\n\n\n\n<p>Lien Ai Nguyen,&nbsp;Hua He,&nbsp;and&nbsp;Chuong Pham-Huy, Chiral drugs: An overview, Int J. Biomed. Sci.  1,2,85-100, 2006; <a rel=\"noreferrer noopener\" href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC3614593\/\" target=\"_blank\">https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC3614593<\/a>\/<\/p>\n\n\n\n<p>Mellin, Gilbert W.; Katzenstein, Michael (1962-12-06).&nbsp;<a href=\"https:\/\/doi.org\/10.1056\/nejm196212062672305\">&#8220;The Saga of Thalidomide&#8221;<\/a>.&nbsp;<em>New England Journal of Medicine<\/em>.&nbsp;<strong>267<\/strong>&nbsp;(23): 1184\u20131193.&nbsp;<\/p>\n\n\n\n<p>De Camp, Wilson H. (1989).&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/chir.530010202\">&#8220;Letter to the editor&#8221;<\/a>.&nbsp;<em>Chirality<\/em>.&nbsp;<strong>1<\/strong>&nbsp;(2): 97\u201398.&nbsp;<\/p>\n\n\n\n<p>James H Kim<sup>&nbsp;<\/sup>,&nbsp;Anthony R Scialli, Thalidomide: the tragedy of birth defects and the effective treatment of disease, Toxicol Sci.&nbsp;2011 Jul;122(1):1-6. DOI:&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1093\/toxsci\/kfr088\" target=\"_blank\">10.1093\/toxsci\/kfr088<\/a><\/p>\n\n\n\n<p><a href=\"https:\/\/www.understandinganimalresearch.org.uk\/news\/sixty-years-on-the-history-of-the-thalidomide-tragedy\">https:\/\/www.understandinganimalresearch.org.uk\/news\/sixty-years-on-the-history-of-the-thalidomide-tragedy<\/a><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Toxicol+Sci%22%5Bjour%5D&amp;sort=date&amp;sort_order=desc\"><\/a><\/p>\n\n\n\n<p>Hassan Y. Aboul-Enein, Irving W. Wainer, The Impact of Stereochemistry on Drug Development and Use, John Wiley &amp; Sons, New York, 1997. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.wiley.com\/en-in\/The+Impact+of+Stereochemistry+on+Drug+Development+and+Use-p-9780471596448\" target=\"_blank\">https:\/\/www.wiley.com\/en-<\/a><\/p>\n\n\n\n<p>Harkishan Singh and V.K. Kapoor.<em><strong>&nbsp;<\/strong>Medicinal chemistry and pharmaceutical chemistry,<\/em>&nbsp;Vallabh Prakashan, New Delhi, Page 689, 2012.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Thalidomide was a racemic therapeutic and prescribed to pregnant women to control nausea and vomiting. The drug was withdrawn from world market when it became evident that the use in pregnancy causes phocomelia (clinical conditions where babies are born with deformed hand and limbs). Later in late 1970s, the thalidomide enantiomers were separated and enantioselective studies indicated that the (R)- enantiomer, the good partner, is an effective sedative, the (S)-enantiomer, the evil partner, harbors teratogenic &hellip;<\/p>\n<p class=\"read-more\"> <a class=\"\" href=\"https:\/\/chiralpedia.com\/blog\/thalidomide\/\"> <span class=\"screen-reader-text\">Thalidomide<\/span> Read More &raquo;<\/a><\/p>\n","protected":false},"author":1,"featured_media":1879,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"site-sidebar-layout":"","site-content-layout":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","footnotes":""},"categories":[43],"tags":[23,22,67,82],"ppma_author":[93],"class_list":["post-1776","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-chirality","tag-chiral_drugs","tag-chirality","tag-chiralpedia","tag-drug_withdrawls"],"authors":[{"term_id":93,"user_id":1,"is_guest":0,"slug":"chiralusrblg","display_name":"Valliappan Kannappan","avatar_url":{"url":"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2024\/09\/vk.jpg","url2x":"https:\/\/chiralpedia.com\/blog\/wp-content\/uploads\/2024\/09\/vk.jpg"},"first_name":"","last_name":"","user_url":"https:\/\/chiralpedia.com\/blog\/","job_title":"Founder, chiralpedia.com","description":""}],"_links":{"self":[{"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/posts\/1776","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/comments?post=1776"}],"version-history":[{"count":62,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/posts\/1776\/revisions"}],"predecessor-version":[{"id":4096,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/posts\/1776\/revisions\/4096"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/media\/1879"}],"wp:attachment":[{"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/media?parent=1776"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/categories?post=1776"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/tags?post=1776"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/chiralpedia.com\/blog\/wp-json\/wp\/v2\/ppma_author?post=1776"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}