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International Journal for Parasitology. Drugs and Drug Resistance|September 29, 2019
Topoisomerase IB poisons induce histone H2A phosphorylation as a response to DNA damage in Leishmania infantumCamino Gutiérrez-Corbo, Raquel Álvarez-Velilla, Rosa M Reguera, et al.Molecular Pharmacology|November 9, 2004
Cellular topoisomerase I inhibition and antiproliferative activity by MJ-III-65 (NSC 706744), an indenoisoquinoline topoisomerase I poisonSmitha Antony, Glenda Kohlhagen, Keli Agama, et al.European Journal of Medicinal Chemistry|October 28, 2008
Synthesis of alkenyldiarylmethanes (ADAMs) containing benzo[d]isoxazole and oxazolidin-2-one rings, a new series of potent non-nucleoside HIV-1 reverse transcriptase inhibitorsBo-Liang Deng, Yujie Zhao, Tracy L Hartman, et al.Molecular Pharmacology|April 19, 2002
2-Methoxyestradiol and analogs as novel antiproliferative agents: analysis of three-dimensional quantitative structure-activity relationships for DNA synthesis inhibition and estrogen receptor bindingRichard A Hughes, Trudi Harris, Emile Altmann, et al.Bioorganic & Medicinal Chemistry|May 29, 2016
Systematic evaluation of methyl ester bioisosteres in the context of developing alkenyldiarylmethanes (ADAMs) as non-nucleoside reverse transcriptase inhibitors (NNRTIs) for anti-HIV-1 chemotherapyAyako Hoshi, Takeshi Sakamoto, Jun Takayama, et al.Bioorganic & Medicinal Chemistry Letters|March 4, 2017
Design, synthesis and structure-bactericidal activity relationships of novel 9-oxime ketolides and reductive epimers of acylidesJing-Chao Tian, Xu Han, Wei Lv, et al.Bioorganic & Medicinal Chemistry|September 21, 2016
A new Suzuki synthesis of triphenylethylenes that inhibit aromatase and bind to estrogen receptors α and βLi-Ming Zhao, Hai-Shan Jin, Jinzhong Liu, et al.Journal of Medicinal Chemistry|March 7, 2009
Synthesis of casimiroin and optimization of its quinone reductase 2 and aromatase inhibitory activitiesArup Maiti, P V Narasimha Reddy, Megan Sturdy, et al.Journal of Medicinal Chemistry|June 21, 2007
Synthesis and anti-HIV activity of new metabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1,2,4-oxadiazole systemsTakeshi Sakamoto, Matthew D Cullen, Tracy L Hartman, et al.Journal of Medicinal Chemistry|March 31, 2015
DUPA conjugation of a cytotoxic indenoisoquinoline topoisomerase I inhibitor for selective prostate cancer cell targetingJyoti Roy, Trung Xuan Nguyen, Ananda Kumar Kanduluru, et al.Pageof 18