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Molecular Cancer Therapeutics|December 19, 2014
The use of dipeptide derivatives of 5-aminolaevulinic acid promotes their entry to tumor cells and improves tumor selectivity of photodynamic therapyGabriela Di Venosa, Pablo Vallecorsa, Francesca Giuntini, et al.Journal of Medicinal Chemistry|December 17, 2016
Highly Potent and Isoform Selective Dual Site Binding Tankyrase/Wnt Signaling Inhibitors That Increase Cellular Glucose Uptake and Have Antiproliferative ActivityAmit Nathubhai, Teemu Haikarainen, Jarkko Koivunen, et al.The Journal of Organic Chemistry|September 27, 2008
A pyrenyl-appended triazole-based calix[4]arene as a fluorescent sensor for Cd2+ and Zn2+Sun Young Park, Jung Hee Yoon, Chang Seop Hong, et al.Scientific Reports|April 14, 2021
A neoclerodane orthoester and other new neoclerodane diterpenoids from Teucrium yemense chemistry and effect on secretion of insulinMohammad Nur-E-Alam, Ifat Parveen, Barrie Wilkinson, et al.Scientific Reports|October 15, 2017
Conjugation with L,L-diphenylalanine Self-Assemblies Enhances In Vitro Antitumor Activity of Phthalocyanine PhotosensitizerMárcia I Souza, Tatiana Prieto, Tiago Rodrigues, et al.Journal of Natural Products|May 2, 2023
Compounds Related to Saudin and Three New Series of Diterpenoids from Clutia lanceolataSarfaraz Ahmed, Mohammad Nur-E-Alam, Ifat Parveen, et al.Nanoscale|August 12, 2015
Controlled intracellular generation of reactive oxygen species in human mesenchymal stem cells using porphyrin conjugated nanoparticlesAndrea S Lavado, Veeren M Chauhan, Amer Alhaj Zen, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|January 17, 2018
Fixing the Conformation of Calix[4]arenes: When Are Three Carbons Not Enough?Susan E Matthews, Samy Cecioni, John E O'Brien, et al.Organic & Biomolecular Chemistry|December 4, 2010
Synthesis of 4-alkyl-, 4-aryl- and 4-arylamino-5-aminoisoquinolin-1-ones and identification of a new PARP-2 selective inhibitorPeter T Sunderland, Archana Dhami, Mary F Mahon, et al.Bioorganic Chemistry|September 20, 2019
Novel 2-arylthiopropanoyl-CoA inhibitors of α-methylacyl-CoA racemase 1A (AMACR; P504S) as potential anti-prostate cancer agentsMaksims Yevglevskis, Amit Nathubhai, Katty Wadda, et al.Pageof 13