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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Veröffentlicht in:Journal of the Chinese Chemical Society (Taipei) 2022-02, Vol.69 (2), p.310-331
Hauptverfasser: Bozkurt, Bilge, Elmas, Gamze, Yakut, Mehtap, Okumuş, Aytuğ, Çerçi, Nebahat Aytuna, Zeyrek, Celal Tuğrul, Kılıç, Zeynel, Açık, Leyla, Hökelek, Tuncer
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container_title Journal of the Chinese Chemical Society (Taipei)
container_volume 69
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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The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies</title><source>Access via Wiley Online Library</source><creator>Bozkurt, Bilge ; Elmas, Gamze ; Yakut, Mehtap ; Okumuş, Aytuğ ; Çerçi, Nebahat Aytuna ; Zeyrek, Celal Tuğrul ; Kılıç, Zeynel ; Açık, Leyla ; Hökelek, Tuncer</creator><creatorcontrib>Bozkurt, Bilge ; Elmas, Gamze ; Yakut, Mehtap ; Okumuş, Aytuğ ; Çerçi, Nebahat Aytuna ; Zeyrek, Celal Tuğrul ; Kılıç, Zeynel ; Açık, Leyla ; Hökelek, Tuncer</creatorcontrib><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><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 &amp; Co. 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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 &amp; 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 &amp; 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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