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Synthesis and Anticancer Activity Evaluation of Some Thienopyrimidine Derivatives
The current study focused on effective and straightforward routes for preparing a new series of thieno[2,3- d ]pyrimidine derivatives in addition to their acyclo nucleosides analogue. The chemical structures of the synthesized products have been elucidated through diverse spectroscopy analyses such...
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Published in: | Russian journal of bioorganic chemistry 2021-11, Vol.47 (6), p.1312-1323 |
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container_end_page | 1323 |
container_issue | 6 |
container_start_page | 1312 |
container_title | Russian journal of bioorganic chemistry |
container_volume | 47 |
creator | Mohamed, M. A. Khattab, R. R. Wasfy, A. A. F. Abo-Riya, M. A. El-Kalyoubi, S. Hassan, N. A. |
description | The current study focused on effective and straightforward routes for preparing a new series of thieno[2,3-
d
]pyrimidine derivatives in addition to their acyclo nucleosides analogue. The chemical structures of the synthesized products have been elucidated through diverse spectroscopy analyses such as (IR, NMR, MS, and elemental analyses). Some selected thienopyrimidine derivatives were investigated for their anticancer activity against two human cancer cell lines (HepG-2 and MCF-7). The results revealed that compounds 3-ethyl-2-hydrazineyl-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-oneand3-ethyl-2-(2-glucozylidenehydrazineyl)-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-one showed the most potent anticancer activity. |
doi_str_mv | 10.1134/S1068162021060194 |
format | article |
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d
]pyrimidine derivatives in addition to their acyclo nucleosides analogue. The chemical structures of the synthesized products have been elucidated through diverse spectroscopy analyses such as (IR, NMR, MS, and elemental analyses). Some selected thienopyrimidine derivatives were investigated for their anticancer activity against two human cancer cell lines (HepG-2 and MCF-7). The results revealed that compounds 3-ethyl-2-hydrazineyl-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-oneand3-ethyl-2-(2-glucozylidenehydrazineyl)-3,5,6,7-tetrahydro-4
H
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d
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d
]pyrimidine derivatives in addition to their acyclo nucleosides analogue. The chemical structures of the synthesized products have been elucidated through diverse spectroscopy analyses such as (IR, NMR, MS, and elemental analyses). Some selected thienopyrimidine derivatives were investigated for their anticancer activity against two human cancer cell lines (HepG-2 and MCF-7). The results revealed that compounds 3-ethyl-2-hydrazineyl-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-oneand3-ethyl-2-(2-glucozylidenehydrazineyl)-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-one showed the most potent anticancer activity.</description><subject>Anticancer properties</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>Cancer</subject><subject>Chemical synthesis</subject><subject>Infrared spectroscopy</subject><subject>Life Sciences</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Organic Chemistry</subject><issn>1068-1620</issn><issn>1608-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kFFLwzAQx4MoOKcfwLeAz9W7pk26xzHnFAYim-BbydKry9jSmXSFfnszJvgg3ssdd7___45j7BbhHlFkDwsEWaBMIY0F4Cg7YwOUUCRCwMd5rOM4Oc4v2VUIGwAEyIsBe1v0rl1TsIFrV_Gxa63RzpDnY9PazrY9n3Z6e9CtbRxvar5odsSXa0uu2ffe7mxlHfFH8raLTEfhml3Uehvo5icP2fvTdDl5Tuavs5fJeJ4YgbJNChnDoBKyRk0KR4KqFSoSZHSepgrzTNdFvBoqBZkyRmEW-4ZyvapyIcWQ3Z189775OlBoy01z8C6uLFOJMMog8pHCE2V8E4KnutzHo7XvS4Ty-Lnyz-eiJj1pQmTdJ_lf5_9F315Tb1I</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Mohamed, M. A.</creator><creator>Khattab, R. R.</creator><creator>Wasfy, A. A. F.</creator><creator>Abo-Riya, M. A.</creator><creator>El-Kalyoubi, S.</creator><creator>Hassan, N. A.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20211101</creationdate><title>Synthesis and Anticancer Activity Evaluation of Some Thienopyrimidine Derivatives</title><author>Mohamed, M. A. ; Khattab, R. R. ; Wasfy, A. A. F. ; Abo-Riya, M. A. ; El-Kalyoubi, S. ; Hassan, N. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-86666c1736f1ae7193edb17e3eca5227154af80680d7047cc714522ce5abd5363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anticancer properties</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bioorganic Chemistry</topic><topic>Cancer</topic><topic>Chemical synthesis</topic><topic>Infrared spectroscopy</topic><topic>Life Sciences</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Organic Chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohamed, M. A.</creatorcontrib><creatorcontrib>Khattab, R. R.</creatorcontrib><creatorcontrib>Wasfy, A. A. F.</creatorcontrib><creatorcontrib>Abo-Riya, M. A.</creatorcontrib><creatorcontrib>El-Kalyoubi, S.</creatorcontrib><creatorcontrib>Hassan, N. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohamed, M. A.</au><au>Khattab, R. R.</au><au>Wasfy, A. A. F.</au><au>Abo-Riya, M. A.</au><au>El-Kalyoubi, S.</au><au>Hassan, N. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Anticancer Activity Evaluation of Some Thienopyrimidine Derivatives</atitle><jtitle>Russian journal of bioorganic chemistry</jtitle><stitle>Russ J Bioorg Chem</stitle><date>2021-11-01</date><risdate>2021</risdate><volume>47</volume><issue>6</issue><spage>1312</spage><epage>1323</epage><pages>1312-1323</pages><issn>1068-1620</issn><eissn>1608-330X</eissn><abstract>The current study focused on effective and straightforward routes for preparing a new series of thieno[2,3-
d
]pyrimidine derivatives in addition to their acyclo nucleosides analogue. The chemical structures of the synthesized products have been elucidated through diverse spectroscopy analyses such as (IR, NMR, MS, and elemental analyses). Some selected thienopyrimidine derivatives were investigated for their anticancer activity against two human cancer cell lines (HepG-2 and MCF-7). The results revealed that compounds 3-ethyl-2-hydrazineyl-3,5,6,7-tetrahydro-4
H
-cyclopenta[4,5]thieno[2,3-
d
]pyrimidin-4-oneand3-ethyl-2-(2-glucozylidenehydrazineyl)-3,5,6,7-tetrahydro-4
H
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d
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language | eng |
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source | Springer Link |
subjects | Anticancer properties Biochemistry Biomedical and Life Sciences Biomedicine Bioorganic Chemistry Cancer Chemical synthesis Infrared spectroscopy Life Sciences NMR Nuclear magnetic resonance Organic Chemistry |
title | Synthesis and Anticancer Activity Evaluation of Some Thienopyrimidine Derivatives |
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