2003
DOI: 10.1016/j.tetlet.2003.09.110
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A one-pot, efficient and facile synthesis of 4β-arylaminopodophyllotoxins: synthesis of NPF and GL-331 as DNA topoisomerase II inhibitors

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Cited by 33 publications
(21 citation statements)
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“…Docking results of these ligands are given in Table 1. Compounds 12,13,20,21,22 and 29 showed good interaction with TP-II and these results were matching with wet lab findings. Compound 20 was found to have a score of À4.08 with 3 strong Hbonds with Arg98 and 2 Hbonds with Ser149 with strengths of 2.14 Å and 1.83 Å.…”
Section: Docking Studiessupporting
confidence: 86%
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“…Docking results of these ligands are given in Table 1. Compounds 12,13,20,21,22 and 29 showed good interaction with TP-II and these results were matching with wet lab findings. Compound 20 was found to have a score of À4.08 with 3 strong Hbonds with Arg98 and 2 Hbonds with Ser149 with strengths of 2.14 Å and 1.83 Å.…”
Section: Docking Studiessupporting
confidence: 86%
“…Compounds 9 and 10 were synthesised according to literature procedures [21,22]. Compound 9 was obtained by the reaction of podophyllotoxin with CH 3 SO 3 H and NaI in acetonitrile followed by hydrolysis with H 2 O/Me 2 CO/BaCO 3 and reaction with NaN 3 in TFA.…”
Section: Chemistrymentioning
confidence: 99%
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“…etopophos which are more potent antitumor agents than 4'-o-demethylepipodophyllotoxin. These have been approved for many years for clinical use in the treatment of various types of cancers (breast, testicular, small cell lung cancer, lymphomas, Kaposi's sarcoma, nonlymphocytic leukemia) [10][11][12][13] .…”
Section: Research Articlementioning
confidence: 99%
“…Elemental analyses corresponded with those calculated. GL331 was prepared by the literature method [14].…”
Section: ′-O-demethyl-4β-(4″-nitroanilino)-4-desoxypodophyllotoxinmentioning
confidence: 99%