Vinyl substituted radiohalogen conjugates for protein labeling
Vinyl radiohalogenated small molecules as shown in formulas I and II: I II wherein *X is a radiohalogen, C=C is a double bonded set of sp2 hybridized carbon atoms, and substituents R1, R2, and Y are as defined below. R1 and R2 are substituents independently selected from among hydrogen; alkyl or sub...
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creator | WILBUR DANIEL S HADLEY STEPHEN W |
description | Vinyl radiohalogenated small molecules as shown in formulas I and II: I II wherein *X is a radiohalogen, C=C is a double bonded set of sp2 hybridized carbon atoms, and substituents R1, R2, and Y are as defined below. R1 and R2 are substituents independently selected from among hydrogen; alkyl or substituted alkyl, provided that any sp2 or sp carbon atom substituted on the alkyl is separated from C=C by at least one fully substituted sp3 carbon atom; aryl or substituted aryl, provided that the aryl is bonded directly to C=C; heteroalkyl, provided, first, that no heteroatom of the heteroalkyl bonds directly to C=C and, second, that any sp2 or sp hybridized carbon bonded to a heteroatom of the heteroalkyl is not bonded directly to or otherwise conjugated with C=C and, third, that where a single sp3 carbon intervenes between C=C and an sp2 or sp carbon bonded to a heteroatom that intervening sp3 carbon must be fully substituted; heteroaryl, provided that a heteroatom of the heteroaryl is not bonded directly with C 50 C; mixed alkylaryl, provided first, that no heteroatom is bonded to C=C and, second that either an aryl moiety of the mixed alkylaryl is directly bonded to C=C or that any aryl moiety is separated from C=C by at least one sp3 carbon atom and, where only one sp3 hybridized carbon atom intervenes between C=C and an aryl moiety, that intervening sp3 carbon must be fully substituted. Y is substituent containing any of the groups described above for R1 and R2, except that Y cannot be hydrogen, and bearing a functional group suitable for binding to protein under conditions that preserve the biological activity of the protein. The compounds of formulas I and II can be coupled to proteins such as monoclonal antibodies ot provide reagents for diagnostic and therapeutic applications. Also metalated precursors of compounds I and II, as well as radiophormaceutical reagent kits containing any of the subject small molecules. |
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R1 and R2 are substituents independently selected from among hydrogen; alkyl or substituted alkyl, provided that any sp2 or sp carbon atom substituted on the alkyl is separated from C=C by at least one fully substituted sp3 carbon atom; aryl or substituted aryl, provided that the aryl is bonded directly to C=C; heteroalkyl, provided, first, that no heteroatom of the heteroalkyl bonds directly to C=C and, second, that any sp2 or sp hybridized carbon bonded to a heteroatom of the heteroalkyl is not bonded directly to or otherwise conjugated with C=C and, third, that where a single sp3 carbon intervenes between C=C and an sp2 or sp carbon bonded to a heteroatom that intervening sp3 carbon must be fully substituted; heteroaryl, provided that a heteroatom of the heteroaryl is not bonded directly with C 50 C; mixed alkylaryl, provided first, that no heteroatom is bonded to C=C and, second that either an aryl moiety of the mixed alkylaryl is directly bonded to C=C or that any aryl moiety is separated from C=C by at least one sp3 carbon atom and, where only one sp3 hybridized carbon atom intervenes between C=C and an aryl moiety, that intervening sp3 carbon must be fully substituted. Y is substituent containing any of the groups described above for R1 and R2, except that Y cannot be hydrogen, and bearing a functional group suitable for binding to protein under conditions that preserve the biological activity of the protein. The compounds of formulas I and II can be coupled to proteins such as monoclonal antibodies ot provide reagents for diagnostic and therapeutic applications. Also metalated precursors of compounds I and II, as well as radiophormaceutical reagent kits containing any of the subject small molecules.</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>1989</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19890926&DB=EPODOC&CC=US&NR=4870188A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19890926&DB=EPODOC&CC=US&NR=4870188A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WILBUR; DANIEL S</creatorcontrib><creatorcontrib>HADLEY; STEPHEN W</creatorcontrib><title>Vinyl substituted radiohalogen conjugates for protein labeling</title><description>Vinyl radiohalogenated small molecules as shown in formulas I and II: I II wherein *X is a radiohalogen, C=C is a double bonded set of sp2 hybridized carbon atoms, and substituents R1, R2, and Y are as defined below. R1 and R2 are substituents independently selected from among hydrogen; alkyl or substituted alkyl, provided that any sp2 or sp carbon atom substituted on the alkyl is separated from C=C by at least one fully substituted sp3 carbon atom; aryl or substituted aryl, provided that the aryl is bonded directly to C=C; heteroalkyl, provided, first, that no heteroatom of the heteroalkyl bonds directly to C=C and, second, that any sp2 or sp hybridized carbon bonded to a heteroatom of the heteroalkyl is not bonded directly to or otherwise conjugated with C=C and, third, that where a single sp3 carbon intervenes between C=C and an sp2 or sp carbon bonded to a heteroatom that intervening sp3 carbon must be fully substituted; heteroaryl, provided that a heteroatom of the heteroaryl is not bonded directly with C 50 C; mixed alkylaryl, provided first, that no heteroatom is bonded to C=C and, second that either an aryl moiety of the mixed alkylaryl is directly bonded to C=C or that any aryl moiety is separated from C=C by at least one sp3 carbon atom and, where only one sp3 hybridized carbon atom intervenes between C=C and an aryl moiety, that intervening sp3 carbon must be fully substituted. Y is substituent containing any of the groups described above for R1 and R2, except that Y cannot be hydrogen, and bearing a functional group suitable for binding to protein under conditions that preserve the biological activity of the protein. The compounds of formulas I and II can be coupled to proteins such as monoclonal antibodies ot provide reagents for diagnostic and therapeutic applications. Also metalated precursors of compounds I and II, as well as radiophormaceutical reagent kits containing any of the subject small molecules.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1989</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLALy8yrzFEoLk0qLsksKS1JTVEoSkzJzM9IzMlPT81TSM7PyypNTyxJLVZIyy9SKCjKL0nNzFPISUxKzcnMS-dhYE1LzClO5YXS3Azybq4hzh66qQX58anFBYnJqXmpJfGhwSYW5gaGFhaOxoRVAAAJtzDP</recordid><startdate>19890926</startdate><enddate>19890926</enddate><creator>WILBUR; DANIEL S</creator><creator>HADLEY; STEPHEN W</creator><scope>EVB</scope></search><sort><creationdate>19890926</creationdate><title>Vinyl substituted radiohalogen conjugates for protein labeling</title><author>WILBUR; DANIEL S ; HADLEY; STEPHEN W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US4870188A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1989</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>WILBUR; DANIEL S</creatorcontrib><creatorcontrib>HADLEY; STEPHEN W</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WILBUR; DANIEL S</au><au>HADLEY; STEPHEN W</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Vinyl substituted radiohalogen conjugates for protein labeling</title><date>1989-09-26</date><risdate>1989</risdate><abstract>Vinyl radiohalogenated small molecules as shown in formulas I and II: I II wherein *X is a radiohalogen, C=C is a double bonded set of sp2 hybridized carbon atoms, and substituents R1, R2, and Y are as defined below. R1 and R2 are substituents independently selected from among hydrogen; alkyl or substituted alkyl, provided that any sp2 or sp carbon atom substituted on the alkyl is separated from C=C by at least one fully substituted sp3 carbon atom; aryl or substituted aryl, provided that the aryl is bonded directly to C=C; heteroalkyl, provided, first, that no heteroatom of the heteroalkyl bonds directly to C=C and, second, that any sp2 or sp hybridized carbon bonded to a heteroatom of the heteroalkyl is not bonded directly to or otherwise conjugated with C=C and, third, that where a single sp3 carbon intervenes between C=C and an sp2 or sp carbon bonded to a heteroatom that intervening sp3 carbon must be fully substituted; heteroaryl, provided that a heteroatom of the heteroaryl is not bonded directly with C 50 C; mixed alkylaryl, provided first, that no heteroatom is bonded to C=C and, second that either an aryl moiety of the mixed alkylaryl is directly bonded to C=C or that any aryl moiety is separated from C=C by at least one sp3 carbon atom and, where only one sp3 hybridized carbon atom intervenes between C=C and an aryl moiety, that intervening sp3 carbon must be fully substituted. Y is substituent containing any of the groups described above for R1 and R2, except that Y cannot be hydrogen, and bearing a functional group suitable for binding to protein under conditions that preserve the biological activity of the protein. The compounds of formulas I and II can be coupled to proteins such as monoclonal antibodies ot provide reagents for diagnostic and therapeutic applications. Also metalated precursors of compounds I and II, as well as radiophormaceutical reagent kits containing any of the subject small molecules.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES |
title | Vinyl substituted radiohalogen conjugates for protein labeling |
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