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      One-Pot Multicomponent Synthesis of 3-Methyl-4-(Hetero)Arylmethylene Isoxazole-5(4H)-Ones Using Guanidine Hydrochloride as the Catalyst under Aqueous Conditions

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          Solvent-free organic synthesis.

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            4-[5-Methyl-3-phenylisoxazol-4-yl]- benzenesulfonamide, valdecoxib: a potent and selective inhibitor of COX-2.

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              Synthesis and antitumor activity of 2,5-bis(3'-indolyl)-furans and 3,5-bis(3'-indolyl)-isoxazoles, nortopsentin analogues.

              A series of novel 2,5-bis(3'-indolyl)furans and 3,5-bis(3'-indolyl)isoxazoles were synthesized as antitumor agents. The antiproliferative activity was evaluated in vitro toward diverse human tumor cell lines. Initially 5 isoxazoles and 3 furan derivatives were tested against a panel of 10 human tumor cell lines and the most active derivatives 3c and 4a were selected to be evaluated in an extended panel of 29 cell lines. By exhibiting mean IC(50) values of 17.4 microg/mL (3a) and 20.5 microg/mL (4c), in particular 4c showed a high level of tumor selectivity toward the 29 cell lines. Copyright 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                Polycyclic Aromatic Compounds
                Polycyclic Aromatic Compounds
                Informa UK Limited
                1040-6638
                1563-5333
                October 21 2022
                August 06 2021
                October 21 2022
                : 42
                : 9
                : 5870-5881
                Affiliations
                [1 ]Department of Pharmaceutical Sciences & Technology, Institute of Chemical Technology, Matunga, Mumbai, India
                Article
                10.1080/10406638.2021.1959353
                3dbc213a-af9b-4739-99c0-ee3430543476
                © 2022
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