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Molecules (Basel, Switzerland)|August 10, 2024
Cheminformatics-Guided Exploration of Synthetic Marine Natural Product-Inspired Brominated Indole-3-Glyoxylamides and Their Potentials for Drug DiscoveryDarren C Holland, Dale W Prebble, Mark J Calcott, et al.Journal of Natural Products|April 22, 2009
Clavatadines C-E, guanidine alkaloids from the Australian sponge Suberea clavataMalcolm S Buchanan, Anthony R Carroll, Deborah Wessling, et al.Communications Biology|July 8, 2025
Identification of potent inhibitors of Leishmania donovani and Leishmania infantum chagasi, the causative agents of Old and New World visceral leishmaniasisBilal Zulfiqar, Fabio Antonio Colombo, Juliana Barbosa Nunes, et al.Journal of Inorganic Biochemistry|April 7, 2021
Bioactive half-sandwich Rh and Ir bipyridyl complexes containing artemisininPrinessa Chellan, Vicky M Avery, Sandra Duffy, et al.Journal of Natural Products|March 25, 2015
Design and Synthesis of a Screening Library Using the Natural Product Scaffold 3-Chloro-4-hydroxyphenylacetic AcidRohitesh Kumar, Martin C Sadowski, Claire Levrier, et al.European Journal of Medicinal Chemistry|September 20, 2019
Sulfide, sulfoxide and sulfone bridged acyclic nucleoside phosphonates as inhibitors of the Plasmodium falciparum and human 6-oxopurine phosphoribosyltransferases: Synthesis and evaluationTomáš Klejch, Dianne T Keough, Marina Chavchich, et al.Journal of Natural Products|August 28, 2020
Secoiridoids and Iridoids from Morinda asteroscepaLinda Zandi, Marco Makungu, Joan J E Munissi, et al.Journal of Medicinal Chemistry|October 10, 2014
Two-pronged attack: dual inhibition of Plasmodium falciparum M1 and M17 metalloaminopeptidases by a novel series of hydroxamic acid-based inhibitorsShailesh N Mistry, Nyssa Drinkwater, Chiara Ruggeri, et al.Inorganic Chemistry|November 25, 2011
Copper, nickel, and zinc cyclam-amino acid and cyclam-peptide complexes may be synthesized with "click" chemistry and are noncytotoxicMingfeng Yu, Jason R Price, Paul Jensen, et al.Chemmedchem|February 6, 2014
Synthesis, antimalarial properties, and SAR studies of alkoxyurea-based HDAC inhibitorsFinn K Hansen, Tina S Skinner-Adams, Sandra Duffy, et al.Pageof 42