Inhibition of Toxoplasma gondii by Indirubin and Tryptanthrin Analogs
Author:
Affiliation:
1. Stanley Laboratory, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland
2. Department of Chemistry and Biochemistry, University of Minnesota Duluth, Duluth, Minnesota
Abstract
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Link
https://journals.asm.org/doi/pdf/10.1128/AAC.00903-08
Reference12 articles.
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2. Bhattacharjee, A. K., M. G. Hartell, D. A. Nichols, R. P. Hicks, B. Stanton, J. E. van Hamont, and W. K. Milhous. 2004. Structure-activity relationship study of antimalarial indolo[2,1-b]quinazoline-6,12-diones (tryptanthrins). Three dimensional pharmacophore modeling and identification of new antimalarial candidates. Eur. J. Med. Chem.39:59-67.
3. Bhattacharjee, A. K., D. J. Skanchy, B. Jennings, T. H. Hudson, J. J. Brendle, and K. A. Werbovetz. 2002. Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1-b]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures. Bioorg. Med. Chem.10:1979-1989.
4. Inhibitors of Leishmania mexicana CRK3 Cyclin-Dependent Kinase: Chemical Library Screen and Antileishmanial Activity
5. Drugs used in the treatment of schizophrenia and bipolar disorder inhibit the replication of Toxoplasma gondii
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