المؤلفون: Wanni Chia (11525311), Maria G. Gomez-Lorenzo (7832105), Isabel Castellote (2148934), Jie Xin Tong (8151210), Rajesh Chandramohanadas (217006), Trang Thi Thu Chu (11525314), Wanxiang Shen (11525317), Mei Lin Go (2855729), Cristina de Cozar (4354270), Benigno Crespo (181336), Maria J. Almela (7494524), Fernando Neria-Serrano (11525320), Virginia Franco (326417), Francisco-Javier Gamo (181360), Kevin S. W. Tan (8151216)

مصطلحات موضوعية: Biochemistry, Medicine, Cell Biology, Pharmacology, Cancer, Infectious Diseases, Virology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, tres cantos anti, throughput phenotypic screen, possible inhibitory effects, mitochondrial membrane potential, initiated lead inevitably, content phenotypic screen, computational methods identified, cause minimal toxicity, best fit assigned, low micromolar range, like features characterized, inducing calcium redistribution, tightly synchronized artemisinin, programmed cell death, parasite calcium distribution, action recently characterized, 50 , target specific mechanisms, identified three compounds, new antimalarial drugs, unexplored mechanisms

Relation: https://figshare.com/articles/journal_contribution/High-Content_Phenotypic_Screen_of_a_Focused_TCAMS_Drug_Library_Identifies_Novel_Disruptors_of_the_Malaria_Parasite_Calcium_Dynamics/16746145

الاتاحة: https://doi.org/10.1021/acschembio.1c00512.s001