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1 Ergebnisse
1
Structure–Activity Relationships of Natural and Semisynthet..:
Morgan McCauley
;
Matthew Huston
;
Alanna R. Condren
...
doi:10.1021/acs.jmedchem.3c01574.s001. , 2024
Link:
https://doi.org/10.1021/acs.jmedchem.3c01574.s001
RT Journal T1
Structure–Activity Relationships of Natural and Semisynthetic Plecomacrolides Suggest Distinct Pathways for HIV‑1 Immune Evasion and Vacuolar ATPase-Dependent Lysosomal Acidification
UL https://suche.suub.uni-bremen.de/peid=base-ftgriffithunifig:oai:figshare.com:article_25365313&Exemplar=1&LAN=DE A1 Morgan McCauley A1 Matthew Huston A1 Alanna R. Condren A1 Filipa Pereira A1 Joel Cline A1 Marianne Yaple-Maresh A1 Mark M. Painter A1 Gretchen E. Zimmerman A1 Andrew W. Robertson A1 Nolan Carney A1 Christopher Goodall A1 Valeri Terry A1 Rolf Müller A1 David H. Sherman A1 Kathleen L. Collins YR 2024 K1 Biochemistry K1 Microbiology K1 Cell Biology K1 Genetics K1 Pharmacology K1 Immunology K1 Cancer K1 Infectious Diseases K1 Virology K1 Chemical Sciences not elsewhere classified K1 target cell viability K1 human immunodeficiency virus K1 cell surface expression K1 advanced lead anti K1 72 h viability K1 semisynthetic concanamycins revealed K1 assessed 76 compounds K1 dependent lysosomal acidification K1 lysosomal acidification K1 dependent downmodulation K1 lysosomal neutralization K1 vacuolar atpase K1 protecting hiv K1 potent compounds K1 natural concanamycins K1 known inhibitor K1 immune recognition K1 expressing primary K1 analysis demonstrated K1 (< b JF doi:10.1021/acs.jmedchem.3c01574.s001 LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.3c01574.s001 DO https://doi.org/10.1021/acs.jmedchem.3c01574.s001 SF ELIB - SuUB Bremen
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