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Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters
[Display omitted] •26-Hydroxycholestan-22-one derivatives were synthesized from the steroidal sapogenin diosgenin.•The new cholestane derivatives act as phytohormones.•Plant growth promotion was measured in Mexican rice cultivars.•All the compounds show excellent activity compared to homobrassinolid...
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Published in: | Steroids 2017-09, Vol.125, p.20-26 |
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container_title | Steroids |
container_volume | 125 |
creator | Zeferino-Diaz, Reyna Hilario-Martinez, J. Ciciolil Rodriguez-Acosta, Maricela Carrasco-Carballo, Alan Hernandez-Linares, Maria Guadalupe Sandoval-Ramirez, Jesus Fernandez-Herrera, Maria A. |
description | [Display omitted]
•26-Hydroxycholestan-22-one derivatives were synthesized from the steroidal sapogenin diosgenin.•The new cholestane derivatives act as phytohormones.•Plant growth promotion was measured in Mexican rice cultivars.•All the compounds show excellent activity compared to homobrassinolide.
26-Hydroxycholestan-22-one derivatives with oxygenated functions in the rings A and/or B were successfully synthesized from diosgenin. After the modifications of rings A and B, the spiroketal side chain was selectively opened through a Lewis acid mediated acetolysis to afford the cholestane derivatives. These compounds incorporate pharmacophores, which mimic the activity of natural phytohormones and show high growth promoting activity in Mexican rice cultivars using the rice lamina inclination test. |
doi_str_mv | 10.1016/j.steroids.2017.06.004 |
format | article |
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•26-Hydroxycholestan-22-one derivatives were synthesized from the steroidal sapogenin diosgenin.•The new cholestane derivatives act as phytohormones.•Plant growth promotion was measured in Mexican rice cultivars.•All the compounds show excellent activity compared to homobrassinolide.
26-Hydroxycholestan-22-one derivatives with oxygenated functions in the rings A and/or B were successfully synthesized from diosgenin. After the modifications of rings A and B, the spiroketal side chain was selectively opened through a Lewis acid mediated acetolysis to afford the cholestane derivatives. These compounds incorporate pharmacophores, which mimic the activity of natural phytohormones and show high growth promoting activity in Mexican rice cultivars using the rice lamina inclination test.</description><identifier>ISSN: 0039-128X</identifier><identifier>EISSN: 1878-5867</identifier><identifier>DOI: 10.1016/j.steroids.2017.06.004</identifier><identifier>PMID: 28636873</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>26-Hydroxycholestan-22-one derivatives ; Biomimetic Materials - chemical synthesis ; Biomimetic Materials - chemistry ; Biomimetic Materials - pharmacology ; Cholestanols - chemistry ; Dose-Response Relationship, Drug ; Mimic phytohormones ; Oryza - drug effects ; Oryza - growth & development ; Plant growth promoting activity ; Plant Growth Regulators - chemical synthesis ; Plant Growth Regulators - chemistry ; Plant Growth Regulators - pharmacology ; Rice lamina inclination test</subject><ispartof>Steroids, 2017-09, Vol.125, p.20-26</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-d5e758242357f7f1c79d031ac602a9ae2cf4412dd5e1a175ceed51de4bc7e9413</citedby><cites>FETCH-LOGICAL-c368t-d5e758242357f7f1c79d031ac602a9ae2cf4412dd5e1a175ceed51de4bc7e9413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28636873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeferino-Diaz, Reyna</creatorcontrib><creatorcontrib>Hilario-Martinez, J. Ciciolil</creatorcontrib><creatorcontrib>Rodriguez-Acosta, Maricela</creatorcontrib><creatorcontrib>Carrasco-Carballo, Alan</creatorcontrib><creatorcontrib>Hernandez-Linares, Maria Guadalupe</creatorcontrib><creatorcontrib>Sandoval-Ramirez, Jesus</creatorcontrib><creatorcontrib>Fernandez-Herrera, Maria A.</creatorcontrib><title>Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters</title><title>Steroids</title><addtitle>Steroids</addtitle><description>[Display omitted]
•26-Hydroxycholestan-22-one derivatives were synthesized from the steroidal sapogenin diosgenin.•The new cholestane derivatives act as phytohormones.•Plant growth promotion was measured in Mexican rice cultivars.•All the compounds show excellent activity compared to homobrassinolide.
26-Hydroxycholestan-22-one derivatives with oxygenated functions in the rings A and/or B were successfully synthesized from diosgenin. After the modifications of rings A and B, the spiroketal side chain was selectively opened through a Lewis acid mediated acetolysis to afford the cholestane derivatives. 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Ciciolil</creatorcontrib><creatorcontrib>Rodriguez-Acosta, Maricela</creatorcontrib><creatorcontrib>Carrasco-Carballo, Alan</creatorcontrib><creatorcontrib>Hernandez-Linares, Maria Guadalupe</creatorcontrib><creatorcontrib>Sandoval-Ramirez, Jesus</creatorcontrib><creatorcontrib>Fernandez-Herrera, Maria A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Steroids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeferino-Diaz, Reyna</au><au>Hilario-Martinez, J. Ciciolil</au><au>Rodriguez-Acosta, Maricela</au><au>Carrasco-Carballo, Alan</au><au>Hernandez-Linares, Maria Guadalupe</au><au>Sandoval-Ramirez, Jesus</au><au>Fernandez-Herrera, Maria A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters</atitle><jtitle>Steroids</jtitle><addtitle>Steroids</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>125</volume><spage>20</spage><epage>26</epage><pages>20-26</pages><issn>0039-128X</issn><eissn>1878-5867</eissn><abstract>[Display omitted]
•26-Hydroxycholestan-22-one derivatives were synthesized from the steroidal sapogenin diosgenin.•The new cholestane derivatives act as phytohormones.•Plant growth promotion was measured in Mexican rice cultivars.•All the compounds show excellent activity compared to homobrassinolide.
26-Hydroxycholestan-22-one derivatives with oxygenated functions in the rings A and/or B were successfully synthesized from diosgenin. After the modifications of rings A and B, the spiroketal side chain was selectively opened through a Lewis acid mediated acetolysis to afford the cholestane derivatives. These compounds incorporate pharmacophores, which mimic the activity of natural phytohormones and show high growth promoting activity in Mexican rice cultivars using the rice lamina inclination test.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28636873</pmid><doi>10.1016/j.steroids.2017.06.004</doi><tpages>7</tpages></addata></record> |
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subjects | 26-Hydroxycholestan-22-one derivatives Biomimetic Materials - chemical synthesis Biomimetic Materials - chemistry Biomimetic Materials - pharmacology Cholestanols - chemistry Dose-Response Relationship, Drug Mimic phytohormones Oryza - drug effects Oryza - growth & development Plant growth promoting activity Plant Growth Regulators - chemical synthesis Plant Growth Regulators - chemistry Plant Growth Regulators - pharmacology Rice lamina inclination test |
title | Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters |
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