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European Journal of Medicinal Chemistry|February 21, 2019
Synthesis, in vitro and in vivo biological evaluation of substituted 3-(5-imidazo[2,1-b]thiazolylmethylene)-2-indolinones as new potent anticancer agentsRita Morigi, Alessandra Locatelli, Alberto Leoni, et al.
Bioorganic & Medicinal Chemistry Letters|April 10, 2010
Symmetrical alpha-bromoacryloylamido diaryldienone derivatives as a novel series of antiproliferative agents. Design, synthesis and biological evaluationRomeo Romagnoli, Pier Giovanni Baraldi, Olga Cruz-Lopez, et al.
Organic & Biomolecular Chemistry|October 16, 2015
Complementary isonitrile-based multicomponent reactions for the synthesis of diversified cytotoxic hemiasterlin analoguesGiordano Lesma, Ivan Bassanini, Roberta Bortolozzi, et al.
Journal of Medicinal Chemistry|September 13, 2013
Design, synthesis, and structure-activity relationships of azolylmethylpyrroloquinolines as nonsteroidal aromatase inhibitorsMaria Grazia Ferlin, Davide Carta, Roberta Bortolozzi, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|July 5, 2022
Identification of Homoharringtonine as a potent inhibitor of glioblastoma cell proliferation and migrationElena Porcù, Francesca Maule, Lorenzo Manfreda, et al.
Blood|November 5, 2017
Glucocorticoid resistance is reverted by LCK inhibition in pediatric T-cell acute lymphoblastic leukemiaValentina Serafin, Giorgia Capuzzo, Gloria Milani, et al.
European Journal of Medicinal Chemistry|May 18, 2020
Design, synthesis, in vitro and in vivo biological evaluation of 2-amino-3-aroylbenzo[b]furan derivatives as highly potent tubulin polymerization inhibitorsPaola Oliva, Romeo Romagnoli, Stefano Manfredini, et al.
European Journal of Medicinal Chemistry|February 3, 2022
Cinnamic acid derivatives linked to arylpiperazines as novel potent inhibitors of tyrosinase activity and melanin synthesisRomeo Romagnoli, Paola Oliva, Filippo Prencipe, et al.
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