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Synthesis, modeling and biological evaluation of some pyrazolo[3,4-d]pyrimidinones and pyrazolo[4,3-e][1,2,4]triazolo[4,3-a]pyrimidinones as anti-inflammatory agents.
Bioorg Chem. 2019 Sep;90:102844. doi: 10.1016/j.bioorg.2019.03.018. Epub 2019 Mar 12.
Bioorg Chem. 2019.
PMID: 31229797
Design, synthesis and evaluation of some pyrazolo[3,4-d]pyrimidines as anti-inflammatory agents.
Tageldin GN, Fahmy SM, Ashour HM, Khalil MA, Nassra RA, Labouta IM.
Tageldin GN, et al.
Bioorg Chem. 2018 Aug;78:358-371. doi: 10.1016/j.bioorg.2018.03.030. Epub 2018 Apr 3.
Bioorg Chem. 2018.
PMID: 29627656
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Design, synthesis and evaluation of some pyrazolo[3,4-d]pyrimidine derivatives bearing thiazolidinone moiety as anti-inflammatory agents.
Tageldin GN, Fahmy SM, Ashour HM, Khalil MA, Nassra RA, Labouta IM.
Tageldin GN, et al.
Bioorg Chem. 2018 Oct;80:164-173. doi: 10.1016/j.bioorg.2018.06.013. Epub 2018 Jun 5.
Bioorg Chem. 2018.
PMID: 29929077
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Targeting the interplay between MMP-2, CA II and VEGFR-2 via new sulfonamide-tethered isomeric triazole hybrids; Microwave-assisted synthesis, computational studies and evaluation.
Reda Aouad M, Almehmadi MA, Faleh Albelwi F, Teleb M, Tageldin GN, Abu-Serie MM, Hagar M, Rezki N.
Reda Aouad M, et al. Among authors: tageldin gn.
Bioorg Chem. 2022 Jul;124:105816. doi: 10.1016/j.bioorg.2022.105816. Epub 2022 Apr 16.
Bioorg Chem. 2022.
PMID: 35489270
Review.
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Challenging the anticolorectal cancer capacity of quinoxaline-based scaffold via triazole ligation unveiled new efficient dual VEGFR-2/MAO-B inhibitors.
Ayoup MS, Ammar A, Abdel-Hamid H, Amer A, Abu-Serie MM, Nasr SA, Ghareeb DA, Teleb M, Tageldin GN.
Ayoup MS, et al. Among authors: tageldin gn.
Bioorg Chem. 2024 Feb;143:107102. doi: 10.1016/j.bioorg.2024.107102. Epub 2024 Jan 6.
Bioorg Chem. 2024.
PMID: 38211551
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