DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF

Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the clas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: PALLADINO, MICHAEL, GRODBERG, JENNIFER, HAYASHI, YOSHIO
Format: Patent
Sprache:eng ; fre
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator PALLADINO, MICHAEL
GRODBERG, JENNIFER
HAYASHI, YOSHIO
description Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R1, R1', R1'', R2, R3, R4, R5, and R6, X1 and X2, Y, Z, Z1, Z2, Z3, and Z4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed. L'invention concerne des composés représentés par la structure (I), ainsi que des procédés permettant de préparer de tels composés. Ces procédés consistent à faire réagir une diacyldicétopipérazine avec un premier aldéhyde afin de produire un composé intermédiaire, et à faire réagir ce composé intermédiaire avec un second aldéhyde afin de produire une classe de composés présentant la structure générique, le premier aldéhyde et le second aldéhyde étant choisis dans le groupe constitué par un oxazolecarboxaldéhyde, un imidazolecarboxaldéhyde, un benzaldéhyde, des dérivés imidazolecarboxaldéhyde, et des dérivés de benzaldéhyde, de manière à former le composé décrit ci-dessus. R¿1?, R¿1? , R¿1? , R¿2?, R¿3?, R¿4?, R¿5?, et R¿6?, X¿1? et X¿2?, Y, Z, Z¿1?, Z¿2?, Z¿3?, et Z¿4? peuvent être définis chacun séparément d'une manière conforme au descriptif. L'invention concerne en outre des compositions et des méthodes de traitement du cancer et des infections fongiques.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CA2494049C</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CA2494049C</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CA2494049C3</originalsourceid><addsrcrecordid>eNrjZMhwcfWIdAnyD_Bw9Yv0cfTwDA7x9AtWcPRzAWJHH3_3YIUQD9cgV383sBiQrRAc6Qekgj2DFYCCRGvnYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxzo5GJpYmBiaWzsaEVQAAlhE1Ng</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF</title><source>esp@cenet</source><creator>PALLADINO, MICHAEL ; GRODBERG, JENNIFER ; HAYASHI, YOSHIO</creator><creatorcontrib>PALLADINO, MICHAEL ; GRODBERG, JENNIFER ; HAYASHI, YOSHIO</creatorcontrib><description>Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R1, R1', R1'', R2, R3, R4, R5, and R6, X1 and X2, Y, Z, Z1, Z2, Z3, and Z4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed. L'invention concerne des composés représentés par la structure (I), ainsi que des procédés permettant de préparer de tels composés. Ces procédés consistent à faire réagir une diacyldicétopipérazine avec un premier aldéhyde afin de produire un composé intermédiaire, et à faire réagir ce composé intermédiaire avec un second aldéhyde afin de produire une classe de composés présentant la structure générique, le premier aldéhyde et le second aldéhyde étant choisis dans le groupe constitué par un oxazolecarboxaldéhyde, un imidazolecarboxaldéhyde, un benzaldéhyde, des dérivés imidazolecarboxaldéhyde, et des dérivés de benzaldéhyde, de manière à former le composé décrit ci-dessus. R¿1?, R¿1? , R¿1? , R¿2?, R¿3?, R¿4?, R¿5?, et R¿6?, X¿1? et X¿2?, Y, Z, Z¿1?, Z¿2?, Z¿3?, et Z¿4? peuvent être définis chacun séparément d'une manière conforme au descriptif. L'invention concerne en outre des compositions et des méthodes de traitement du cancer et des infections fongiques.</description><language>eng ; fre</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>2011</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&amp;date=20111018&amp;DB=EPODOC&amp;CC=CA&amp;NR=2494049C$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20111018&amp;DB=EPODOC&amp;CC=CA&amp;NR=2494049C$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>PALLADINO, MICHAEL</creatorcontrib><creatorcontrib>GRODBERG, JENNIFER</creatorcontrib><creatorcontrib>HAYASHI, YOSHIO</creatorcontrib><title>DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF</title><description>Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R1, R1', R1'', R2, R3, R4, R5, and R6, X1 and X2, Y, Z, Z1, Z2, Z3, and Z4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed. L'invention concerne des composés représentés par la structure (I), ainsi que des procédés permettant de préparer de tels composés. Ces procédés consistent à faire réagir une diacyldicétopipérazine avec un premier aldéhyde afin de produire un composé intermédiaire, et à faire réagir ce composé intermédiaire avec un second aldéhyde afin de produire une classe de composés présentant la structure générique, le premier aldéhyde et le second aldéhyde étant choisis dans le groupe constitué par un oxazolecarboxaldéhyde, un imidazolecarboxaldéhyde, un benzaldéhyde, des dérivés imidazolecarboxaldéhyde, et des dérivés de benzaldéhyde, de manière à former le composé décrit ci-dessus. R¿1?, R¿1? , R¿1? , R¿2?, R¿3?, R¿4?, R¿5?, et R¿6?, X¿1? et X¿2?, Y, Z, Z¿1?, Z¿2?, Z¿3?, et Z¿4? peuvent être définis chacun séparément d'une manière conforme au descriptif. L'invention concerne en outre des compositions et des méthodes de traitement du cancer et des infections fongiques.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</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><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2011</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZMhwcfWIdAnyD_Bw9Yv0cfTwDA7x9AtWcPRzAWJHH3_3YIUQD9cgV383sBiQrRAc6Qekgj2DFYCCRGvnYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxzo5GJpYmBiaWzsaEVQAAlhE1Ng</recordid><startdate>20111018</startdate><enddate>20111018</enddate><creator>PALLADINO, MICHAEL</creator><creator>GRODBERG, JENNIFER</creator><creator>HAYASHI, YOSHIO</creator><scope>EVB</scope></search><sort><creationdate>20111018</creationdate><title>DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF</title><author>PALLADINO, MICHAEL ; GRODBERG, JENNIFER ; HAYASHI, YOSHIO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CA2494049C3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2011</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</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><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>PALLADINO, MICHAEL</creatorcontrib><creatorcontrib>GRODBERG, JENNIFER</creatorcontrib><creatorcontrib>HAYASHI, YOSHIO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>PALLADINO, MICHAEL</au><au>GRODBERG, JENNIFER</au><au>HAYASHI, YOSHIO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF</title><date>2011-10-18</date><risdate>2011</risdate><abstract>Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R1, R1', R1'', R2, R3, R4, R5, and R6, X1 and X2, Y, Z, Z1, Z2, Z3, and Z4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed. L'invention concerne des composés représentés par la structure (I), ainsi que des procédés permettant de préparer de tels composés. Ces procédés consistent à faire réagir une diacyldicétopipérazine avec un premier aldéhyde afin de produire un composé intermédiaire, et à faire réagir ce composé intermédiaire avec un second aldéhyde afin de produire une classe de composés présentant la structure générique, le premier aldéhyde et le second aldéhyde étant choisis dans le groupe constitué par un oxazolecarboxaldéhyde, un imidazolecarboxaldéhyde, un benzaldéhyde, des dérivés imidazolecarboxaldéhyde, et des dérivés de benzaldéhyde, de manière à former le composé décrit ci-dessus. R¿1?, R¿1? , R¿1? , R¿2?, R¿3?, R¿4?, R¿5?, et R¿6?, X¿1? et X¿2?, Y, Z, Z¿1?, Z¿2?, Z¿3?, et Z¿4? peuvent être définis chacun séparément d'une manière conforme au descriptif. L'invention concerne en outre des compositions et des méthodes de traitement du cancer et des infections fongiques.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng ; fre
recordid cdi_epo_espacenet_CA2494049C
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T21%3A25%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=PALLADINO,%20MICHAEL&rft.date=2011-10-18&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECA2494049C%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true