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Hesperadin
CAS No. : 422513-13-1
Biological Activity:Hesperadin is an ATP competitive indolinone inhibitor of Aurora A and B. Hesperadin inhibits Aurora B with an IC50 of 250 nM. Hesperadin inhibits the growth of Trypanosoma brucei by blocking nuclear division and cytokinesis. Hesperadin also is a broad-spectrum influenza antiviral[2][3].
Research Area:Cancer
Targets:Parasite|Autophagy|Influenza Virus|Aurora Kinase
Related Screening Libraries:Bioactive Compound Library Plus;Anti-Infection Compound Library;Cell Cycle/DNA Damage Compound Library;Epigenetics Compound Library;Kinase Inhibitor Library;Anti-Cancer Compound Library;Antiviral Compound Library;Autophagy Compound Library;Anti-Aging Compound Library;Anti-Blood Cancer Compound Library;Antiparasitic Compound library;
Related Small Molecules:(+)-Isopulegol;DB0614;SR9186;Antileishmanial agent-2;Azlocillin sodium salt;AT9283;Curcumin;SQ109;(R)-Camptothecin-d5;Trypanothione synthetase-IN-3;Pyrantel;α-Terpinene;Dehydrocorydaline;Glaucine;Hypericin;Neuraminidase-IN-3;Niclosamide monohydrate;Febrifugine dihydrochloride;Antimalarial agent 15;FGI-106 tetrahydrochloride;Molnupiravir;Cycloguanil hydrochloride
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