Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies
In this study, primarily, tetrachloro‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4 and 5) were prepared from the reactions of equimolar amounts of N‐alkyl‐N′‐2‐pyridylmethylethylenediamines, [PyCH2NH(CH2)2NHR (R:CH3, 2 and R:C2H5, 3)], and hexachlorocyclotriphosphazene [(HCCP, tr...
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creator | Bozkurt, Bilge Elmas, Gamze Yakut, Mehtap Okumuş, Aytuğ Çerçi, Nebahat Aytuna Zeyrek, Celal Tuğrul Kılıç, Zeynel Açık, Leyla Hökelek, Tuncer |
description | In this study, primarily, tetrachloro‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4 and 5) were prepared from the reactions of equimolar amounts of N‐alkyl‐N′‐2‐pyridylmethylethylenediamines, [PyCH2NH(CH2)2NHR (R:CH3, 2 and R:C2H5, 3)], and hexachlorocyclotriphosphazene [(HCCP, trimer), N3P3Cl6 (1)]. Compounds 4 and 5 react with secondary amines to yield the fully substituted tetraamino‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4a–5c) in dry THF, respectively. These derivatives were obtained by both conventional and microwave‐assisted reactions, and their yields were compared. In addition, it should also be noted that these cyclotriphosphazenes were obtained for use in the investigation of their spectral, crystallographic, antimicrobial, and anticancer properties. The structures of the compounds were elucidated by spectral data. The crystal structures of 4, 5a, and 5c were clarified by the single crystal X‐ray diffraction technique. Antibacterial activities and biofilm preventions of 4a–c and 5a–c against bacteria, and their antifungal activities against fungi were investigated. According to broth microdilution method, the results showed that all compounds were highly effective against C. albicans. The interactions of these compounds with DNA and their cytotoxic activities against L929 fibroblast and A549 lung cancer cell lines were investigated. In addition, Density Functional Theory (DFT) calculations of 4, 5a, and 5c were made, and molecular docking studies with DNA and cytochrome P450 enzyme were presented.
Syntheses, spectral and crystallographic characterizations, antimicrobial and cytotoxic activities and biofilm preventions, the interactions with plasmid DNA, Density Functional Theory (DFT) calculations, molecular docking studies of 2‐pyridylmethyl‐(N/N)ethylenediaminospiro cyclotriphosphazenes were investigated. |
doi_str_mv | 10.1002/jccs.202100475 |
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Syntheses, spectral and crystallographic characterizations, antimicrobial and cytotoxic activities and biofilm preventions, the interactions with plasmid DNA, Density Functional Theory (DFT) calculations, molecular docking studies of 2‐pyridylmethyl‐(N/N)ethylenediaminospiro cyclotriphosphazenes were investigated.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.202100475</identifier><language>eng</language><publisher>Weinheim: Wiley‐VCH Verlag GmbH & Co. KGaA</publisher><subject>2‐pyridylmethylspirocyclotriphosphazenes ; Amines ; Anticancer properties ; antimicrobial activity ; Crystal structure ; Crystallography ; Cytochromes P450 ; cytotoxicity ; Density functional theory ; DNA interaction ; Fungicides ; Investigations ; Molecular docking ; Nitrogen compounds ; Single crystals ; Structural analysis ; Trimers</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2022-02, Vol.69 (2), p.310-331</ispartof><rights>2021 Chemical Society Located in Taipei and Wiley‐VCH GmbH.</rights><rights>2022 The Chemical Society Located in Taipei & Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3175-71de04abf10ba331be6e45219c884dcf817ff04b90860ced4fbf4ca9de010cde3</citedby><cites>FETCH-LOGICAL-c3175-71de04abf10ba331be6e45219c884dcf817ff04b90860ced4fbf4ca9de010cde3</cites><orcidid>0000-0002-2169-5695</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjccs.202100475$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjccs.202100475$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids></links><search><creatorcontrib>Bozkurt, Bilge</creatorcontrib><creatorcontrib>Elmas, Gamze</creatorcontrib><creatorcontrib>Yakut, Mehtap</creatorcontrib><creatorcontrib>Okumuş, Aytuğ</creatorcontrib><creatorcontrib>Çerçi, Nebahat Aytuna</creatorcontrib><creatorcontrib>Zeyrek, Celal Tuğrul</creatorcontrib><creatorcontrib>Kılıç, Zeynel</creatorcontrib><creatorcontrib>Açık, Leyla</creatorcontrib><creatorcontrib>Hökelek, Tuncer</creatorcontrib><title>Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies</title><title>Journal of the Chinese Chemical Society (Taipei)</title><description>In this study, primarily, tetrachloro‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4 and 5) were prepared from the reactions of equimolar amounts of N‐alkyl‐N′‐2‐pyridylmethylethylenediamines, [PyCH2NH(CH2)2NHR (R:CH3, 2 and R:C2H5, 3)], and hexachlorocyclotriphosphazene [(HCCP, trimer), N3P3Cl6 (1)]. Compounds 4 and 5 react with secondary amines to yield the fully substituted tetraamino‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4a–5c) in dry THF, respectively. These derivatives were obtained by both conventional and microwave‐assisted reactions, and their yields were compared. In addition, it should also be noted that these cyclotriphosphazenes were obtained for use in the investigation of their spectral, crystallographic, antimicrobial, and anticancer properties. The structures of the compounds were elucidated by spectral data. The crystal structures of 4, 5a, and 5c were clarified by the single crystal X‐ray diffraction technique. Antibacterial activities and biofilm preventions of 4a–c and 5a–c against bacteria, and their antifungal activities against fungi were investigated. According to broth microdilution method, the results showed that all compounds were highly effective against C. albicans. The interactions of these compounds with DNA and their cytotoxic activities against L929 fibroblast and A549 lung cancer cell lines were investigated. In addition, Density Functional Theory (DFT) calculations of 4, 5a, and 5c were made, and molecular docking studies with DNA and cytochrome P450 enzyme were presented.
Syntheses, spectral and crystallographic characterizations, antimicrobial and cytotoxic activities and biofilm preventions, the interactions with plasmid DNA, Density Functional Theory (DFT) calculations, molecular docking studies of 2‐pyridylmethyl‐(N/N)ethylenediaminospiro cyclotriphosphazenes were investigated.</description><subject>2‐pyridylmethylspirocyclotriphosphazenes</subject><subject>Amines</subject><subject>Anticancer properties</subject><subject>antimicrobial activity</subject><subject>Crystal structure</subject><subject>Crystallography</subject><subject>Cytochromes P450</subject><subject>cytotoxicity</subject><subject>Density functional theory</subject><subject>DNA interaction</subject><subject>Fungicides</subject><subject>Investigations</subject><subject>Molecular docking</subject><subject>Nitrogen compounds</subject><subject>Single crystals</subject><subject>Structural analysis</subject><subject>Trimers</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhSMEEkNhy9oSG5Caqe04mZgdGpWfqipILevIsa8bD44dbAeUrngEnpAFT1J3pqJLFpZ17O_cY_kUxUuC1wRjerKTMq4pplmwTf2oWFHCadnUjD8uVhhjXrK6ap4Wz2LcZaSiNV8Vf74MPk6DD3P8--u3Myn4a3BI-nHys1MRTSIkVPM1uhoAxcWlASJE5DVKkIKQg_XBI-HUQYvROJ8n0bymJRi12BHSsNg4meBfX5xcvNlLcKDMHpaLtD4FM-0fIm7yTXyLLlOYZZqDsEgOIuckCOZGJOPdMeqNzwfmh0nL8T569BbkbEVAystvxl2jmGZlID4vnmhhI7y434-Kr-9Pr7Yfy_PPHz5t352XsiKbutwQBZiJXhPci6oiPTTA6vx_sm2ZkrolG60x6zluGyxBMd1rJgXPLoKlguqoeHWYOwX_fYaYup2fg8uRHW0qRtuWNDxT6wMlg48xgO6mYEYRlo7g7q7D7q7D7l-H2cAPhp_GwvIfujvbbi8fvLc_fKzg</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Bozkurt, Bilge</creator><creator>Elmas, Gamze</creator><creator>Yakut, Mehtap</creator><creator>Okumuş, Aytuğ</creator><creator>Çerçi, Nebahat Aytuna</creator><creator>Zeyrek, Celal Tuğrul</creator><creator>Kılıç, Zeynel</creator><creator>Açık, Leyla</creator><creator>Hökelek, Tuncer</creator><general>Wiley‐VCH Verlag GmbH & Co. KGaA</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2169-5695</orcidid></search><sort><creationdate>202202</creationdate><title>Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies</title><author>Bozkurt, Bilge ; Elmas, Gamze ; Yakut, Mehtap ; Okumuş, Aytuğ ; Çerçi, Nebahat Aytuna ; Zeyrek, Celal Tuğrul ; Kılıç, Zeynel ; Açık, Leyla ; Hökelek, Tuncer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3175-71de04abf10ba331be6e45219c884dcf817ff04b90860ced4fbf4ca9de010cde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>2‐pyridylmethylspirocyclotriphosphazenes</topic><topic>Amines</topic><topic>Anticancer properties</topic><topic>antimicrobial activity</topic><topic>Crystal structure</topic><topic>Crystallography</topic><topic>Cytochromes P450</topic><topic>cytotoxicity</topic><topic>Density functional theory</topic><topic>DNA interaction</topic><topic>Fungicides</topic><topic>Investigations</topic><topic>Molecular docking</topic><topic>Nitrogen compounds</topic><topic>Single crystals</topic><topic>Structural analysis</topic><topic>Trimers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bozkurt, Bilge</creatorcontrib><creatorcontrib>Elmas, Gamze</creatorcontrib><creatorcontrib>Yakut, Mehtap</creatorcontrib><creatorcontrib>Okumuş, Aytuğ</creatorcontrib><creatorcontrib>Çerçi, Nebahat Aytuna</creatorcontrib><creatorcontrib>Zeyrek, Celal Tuğrul</creatorcontrib><creatorcontrib>Kılıç, Zeynel</creatorcontrib><creatorcontrib>Açık, Leyla</creatorcontrib><creatorcontrib>Hökelek, Tuncer</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bozkurt, Bilge</au><au>Elmas, Gamze</au><au>Yakut, Mehtap</au><au>Okumuş, Aytuğ</au><au>Çerçi, Nebahat Aytuna</au><au>Zeyrek, Celal Tuğrul</au><au>Kılıç, Zeynel</au><au>Açık, Leyla</au><au>Hökelek, Tuncer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><date>2022-02</date><risdate>2022</risdate><volume>69</volume><issue>2</issue><spage>310</spage><epage>331</epage><pages>310-331</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>In this study, primarily, tetrachloro‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4 and 5) were prepared from the reactions of equimolar amounts of N‐alkyl‐N′‐2‐pyridylmethylethylenediamines, [PyCH2NH(CH2)2NHR (R:CH3, 2 and R:C2H5, 3)], and hexachlorocyclotriphosphazene [(HCCP, trimer), N3P3Cl6 (1)]. Compounds 4 and 5 react with secondary amines to yield the fully substituted tetraamino‐2‐pyridylmethylspiro‐N/N‐ethylenediamino‐cyclotriphosphazenes (4a–5c) in dry THF, respectively. These derivatives were obtained by both conventional and microwave‐assisted reactions, and their yields were compared. In addition, it should also be noted that these cyclotriphosphazenes were obtained for use in the investigation of their spectral, crystallographic, antimicrobial, and anticancer properties. The structures of the compounds were elucidated by spectral data. The crystal structures of 4, 5a, and 5c were clarified by the single crystal X‐ray diffraction technique. Antibacterial activities and biofilm preventions of 4a–c and 5a–c against bacteria, and their antifungal activities against fungi were investigated. According to broth microdilution method, the results showed that all compounds were highly effective against C. albicans. The interactions of these compounds with DNA and their cytotoxic activities against L929 fibroblast and A549 lung cancer cell lines were investigated. In addition, Density Functional Theory (DFT) calculations of 4, 5a, and 5c were made, and molecular docking studies with DNA and cytochrome P450 enzyme were presented.
Syntheses, spectral and crystallographic characterizations, antimicrobial and cytotoxic activities and biofilm preventions, the interactions with plasmid DNA, Density Functional Theory (DFT) calculations, molecular docking studies of 2‐pyridylmethyl‐(N/N)ethylenediaminospiro cyclotriphosphazenes were investigated.</abstract><cop>Weinheim</cop><pub>Wiley‐VCH Verlag GmbH & Co. KGaA</pub><doi>10.1002/jccs.202100475</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0002-2169-5695</orcidid></addata></record> |
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subjects | 2‐pyridylmethylspirocyclotriphosphazenes Amines Anticancer properties antimicrobial activity Crystal structure Crystallography Cytochromes P450 cytotoxicity Density functional theory DNA interaction Fungicides Investigations Molecular docking Nitrogen compounds Single crystals Structural analysis Trimers |
title | Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies |
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