Loading…

N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin

For the first time, N 6 -(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene when interacting with the cytoki...

Full description

Saved in:
Bibliographic Details
Published in:Doklady. Biochemistry and biophysics 2023-12, Vol.513 (Suppl 1), p.S23-S25
Main Authors: Zenchenko, A. A., Savelieva, E. M., Drenichev, M. S., Romanov, G. A., Oslovsky, V. E.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c231t-adafc0317e448f6d167c5285a20b964de81d6f7ec4344935472f0692dd46134f3
container_end_page S25
container_issue Suppl 1
container_start_page S23
container_title Doklady. Biochemistry and biophysics
container_volume 513
creator Zenchenko, A. A.
Savelieva, E. M.
Drenichev, M. S.
Romanov, G. A.
Oslovsky, V. E.
description For the first time, N 6 -(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene when interacting with the cytokinin receptor CRE1/AHK4 of the model plant Arabidopsis thaliana . This effect manifests itself much weaker with the related AHK2 receptor and is not observed at all with the AHK3 receptor. We showed that N 6 -(5-phenylpentan-1-yl)adenine does not bind to the ligand-binding sites of the Arabidopsis cytokinin receptors, which does not allow it to be classified as a true cytokinin antagonist. Despite the currently unknown mechanism of action, this compound may find its use as a component of plant growth regulators. Like true anticytokinins, it enhances root growth of Arabidopsis seedlings, apparently suppressing the action of endogenous cytokinins on the “root” receptor CRE1/AHK4.
doi_str_mv 10.1134/S1607672923700679
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2911846980</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2973655569</sourcerecordid><originalsourceid>FETCH-LOGICAL-c231t-adafc0317e448f6d167c5285a20b964de81d6f7ec4344935472f0692dd46134f3</originalsourceid><addsrcrecordid>eNp1kM9KAzEQxhdRsFYfwFvBSz1E82-TzbEU_0GpYhW8LWt2VlO3ybpJlb35ED6hT2JqBUHxNMPM7_uY-ZJkn-AjQhg_nhGBpZBUUSYxFlJtJL04yhDDimx-9RKt9tvJjvdzjCmmLO0ld1OBhim6egTb1Q3YUFhEUFcfFiVYY-Hj7X00mMLrYOos0m7RQDDBvMDgGjQ0wbVo1oA2ldGDkQ0G6S64JxOVu8lWVdQe9r5rP7k9PbkZn6PJ5dnFeDRBmjISUFEWlcaMSOA8q0RJhNQpzdKC4nsleAkZKUUlQXPGuWIpl7TCQtGy5CL-XbF-Mlz7Nq17XoIP-cJ4DXVdWHBLn1NFSMaFynBED36hc7dsbbwuUpKJNE2FihRZU7p13rdQ5U1rFkXb5QTnq6zzP1lHDV1rfGTtA7Q_zv-LPgEurX8x</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2973655569</pqid></control><display><type>article</type><title>N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin</title><source>Springer Nature</source><creator>Zenchenko, A. A. ; Savelieva, E. M. ; Drenichev, M. S. ; Romanov, G. A. ; Oslovsky, V. E.</creator><creatorcontrib>Zenchenko, A. A. ; Savelieva, E. M. ; Drenichev, M. S. ; Romanov, G. A. ; Oslovsky, V. E.</creatorcontrib><description>For the first time, N 6 -(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene when interacting with the cytokinin receptor CRE1/AHK4 of the model plant Arabidopsis thaliana . This effect manifests itself much weaker with the related AHK2 receptor and is not observed at all with the AHK3 receptor. We showed that N 6 -(5-phenylpentan-1-yl)adenine does not bind to the ligand-binding sites of the Arabidopsis cytokinin receptors, which does not allow it to be classified as a true cytokinin antagonist. Despite the currently unknown mechanism of action, this compound may find its use as a component of plant growth regulators. Like true anticytokinins, it enhances root growth of Arabidopsis seedlings, apparently suppressing the action of endogenous cytokinins on the “root” receptor CRE1/AHK4.</description><identifier>ISSN: 1607-6729</identifier><identifier>EISSN: 1608-3091</identifier><identifier>DOI: 10.1134/S1607672923700679</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Adenine ; Arabidopsis ; Biochemistry ; Biological and Medical Physics ; Biomedical and Life Sciences ; Biophysics ; Cytokinins ; Growth regulators ; GUS gene ; Life Sciences ; Reporter gene</subject><ispartof>Doklady. Biochemistry and biophysics, 2023-12, Vol.513 (Suppl 1), p.S23-S25</ispartof><rights>Pleiades Publishing, Ltd. 2023. ISSN 1607-6729, Doklady Biochemistry and Biophysics, 2023, Vol. 513, Suppl. 1, pp. S23–S25. © Pleiades Publishing, Ltd., 2023. ISSN 1607-6729, Doklady Biochemistry and Biophysics, 2024. © Pleiades Publishing, Ltd., 2024.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c231t-adafc0317e448f6d167c5285a20b964de81d6f7ec4344935472f0692dd46134f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Zenchenko, A. A.</creatorcontrib><creatorcontrib>Savelieva, E. M.</creatorcontrib><creatorcontrib>Drenichev, M. S.</creatorcontrib><creatorcontrib>Romanov, G. A.</creatorcontrib><creatorcontrib>Oslovsky, V. E.</creatorcontrib><title>N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin</title><title>Doklady. Biochemistry and biophysics</title><addtitle>Dokl Biochem Biophys</addtitle><description>For the first time, N 6 -(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene when interacting with the cytokinin receptor CRE1/AHK4 of the model plant Arabidopsis thaliana . This effect manifests itself much weaker with the related AHK2 receptor and is not observed at all with the AHK3 receptor. We showed that N 6 -(5-phenylpentan-1-yl)adenine does not bind to the ligand-binding sites of the Arabidopsis cytokinin receptors, which does not allow it to be classified as a true cytokinin antagonist. Despite the currently unknown mechanism of action, this compound may find its use as a component of plant growth regulators. Like true anticytokinins, it enhances root growth of Arabidopsis seedlings, apparently suppressing the action of endogenous cytokinins on the “root” receptor CRE1/AHK4.</description><subject>Adenine</subject><subject>Arabidopsis</subject><subject>Biochemistry</subject><subject>Biological and Medical Physics</subject><subject>Biomedical and Life Sciences</subject><subject>Biophysics</subject><subject>Cytokinins</subject><subject>Growth regulators</subject><subject>GUS gene</subject><subject>Life Sciences</subject><subject>Reporter gene</subject><issn>1607-6729</issn><issn>1608-3091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kM9KAzEQxhdRsFYfwFvBSz1E82-TzbEU_0GpYhW8LWt2VlO3ybpJlb35ED6hT2JqBUHxNMPM7_uY-ZJkn-AjQhg_nhGBpZBUUSYxFlJtJL04yhDDimx-9RKt9tvJjvdzjCmmLO0ld1OBhim6egTb1Q3YUFhEUFcfFiVYY-Hj7X00mMLrYOos0m7RQDDBvMDgGjQ0wbVo1oA2ldGDkQ0G6S64JxOVu8lWVdQe9r5rP7k9PbkZn6PJ5dnFeDRBmjISUFEWlcaMSOA8q0RJhNQpzdKC4nsleAkZKUUlQXPGuWIpl7TCQtGy5CL-XbF-Mlz7Nq17XoIP-cJ4DXVdWHBLn1NFSMaFynBED36hc7dsbbwuUpKJNE2FihRZU7p13rdQ5U1rFkXb5QTnq6zzP1lHDV1rfGTtA7Q_zv-LPgEurX8x</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Zenchenko, A. A.</creator><creator>Savelieva, E. M.</creator><creator>Drenichev, M. S.</creator><creator>Romanov, G. A.</creator><creator>Oslovsky, V. E.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20231201</creationdate><title>N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin</title><author>Zenchenko, A. A. ; Savelieva, E. M. ; Drenichev, M. S. ; Romanov, G. A. ; Oslovsky, V. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c231t-adafc0317e448f6d167c5285a20b964de81d6f7ec4344935472f0692dd46134f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adenine</topic><topic>Arabidopsis</topic><topic>Biochemistry</topic><topic>Biological and Medical Physics</topic><topic>Biomedical and Life Sciences</topic><topic>Biophysics</topic><topic>Cytokinins</topic><topic>Growth regulators</topic><topic>GUS gene</topic><topic>Life Sciences</topic><topic>Reporter gene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zenchenko, A. A.</creatorcontrib><creatorcontrib>Savelieva, E. M.</creatorcontrib><creatorcontrib>Drenichev, M. S.</creatorcontrib><creatorcontrib>Romanov, G. A.</creatorcontrib><creatorcontrib>Oslovsky, V. E.</creatorcontrib><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Doklady. Biochemistry and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zenchenko, A. A.</au><au>Savelieva, E. M.</au><au>Drenichev, M. S.</au><au>Romanov, G. A.</au><au>Oslovsky, V. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin</atitle><jtitle>Doklady. Biochemistry and biophysics</jtitle><stitle>Dokl Biochem Biophys</stitle><date>2023-12-01</date><risdate>2023</risdate><volume>513</volume><issue>Suppl 1</issue><spage>S23</spage><epage>S25</epage><pages>S23-S25</pages><issn>1607-6729</issn><eissn>1608-3091</eissn><abstract>For the first time, N 6 -(5-phenylpentan-1-yl)adenine, a synthetic adenine derivative with a receptor-specific anticytokinin effect, was obtained. This compound exhibits a pronounced anticytokinin effect, reducing cytokinin-induced expression of the GUS reporter gene when interacting with the cytokinin receptor CRE1/AHK4 of the model plant Arabidopsis thaliana . This effect manifests itself much weaker with the related AHK2 receptor and is not observed at all with the AHK3 receptor. We showed that N 6 -(5-phenylpentan-1-yl)adenine does not bind to the ligand-binding sites of the Arabidopsis cytokinin receptors, which does not allow it to be classified as a true cytokinin antagonist. Despite the currently unknown mechanism of action, this compound may find its use as a component of plant growth regulators. Like true anticytokinins, it enhances root growth of Arabidopsis seedlings, apparently suppressing the action of endogenous cytokinins on the “root” receptor CRE1/AHK4.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1607672923700679</doi></addata></record>
fulltext fulltext
identifier ISSN: 1607-6729
ispartof Doklady. Biochemistry and biophysics, 2023-12, Vol.513 (Suppl 1), p.S23-S25
issn 1607-6729
1608-3091
language eng
recordid cdi_proquest_miscellaneous_2911846980
source Springer Nature
subjects Adenine
Arabidopsis
Biochemistry
Biological and Medical Physics
Biomedical and Life Sciences
Biophysics
Cytokinins
Growth regulators
GUS gene
Life Sciences
Reporter gene
title N6-(5-Phenylpentan-1-yl)adenine—A New Non-competitive Receptor-Specific Anti-cytokinin
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T01%3A17%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=N6-(5-Phenylpentan-1-yl)adenine%E2%80%94A%20New%20Non-competitive%20Receptor-Specific%20Anti-cytokinin&rft.jtitle=Doklady.%20Biochemistry%20and%20biophysics&rft.au=Zenchenko,%20A.%20A.&rft.date=2023-12-01&rft.volume=513&rft.issue=Suppl%201&rft.spage=S23&rft.epage=S25&rft.pages=S23-S25&rft.issn=1607-6729&rft.eissn=1608-3091&rft_id=info:doi/10.1134/S1607672923700679&rft_dat=%3Cproquest_cross%3E2973655569%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c231t-adafc0317e448f6d167c5285a20b964de81d6f7ec4344935472f0692dd46134f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2973655569&rft_id=info:pmid/&rfr_iscdi=true