Joachim Jose

Affiliations: 
Pharmacy University of Muenster, Germany, Münster, Nordrhein-Westfalen, Germany 
Website:
https://www.uni-muenster.de/Chemie.pz/forschen/ag/jose/curvitae.html
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"Joachim Jose"
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Parents

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Heinrich Kaltwasser grad student 1994 Universität des Saarlandes (Microtree)
 (Molekulargenetische und proteinbiochemische Untersuchungen zur Struktur und zum Reaktionsmechanismus der Urease aus Staphylococcus xylosus)
Thomas F. Meyer post-doc Max-Planck-Institut für Biologie (ID Tree)
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Publications

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Palei S, Jose J, Mootz HD. (2022) Preparation of Bacterial Cell-Surface Displayed Semisynthetic Cyclic Peptides. Methods in Molecular Biology (Clifton, N.J.). 2371: 193-213
Strätker K, Haidar S, Dubiel M, et al. (2021) Autodisplay of human PIP5K1α lipid kinase on Escherichia coli and inhibitor testing. Enzyme and Microbial Technology. 143: 109717
Strätker K, Haidar S, Dubiel M, et al. (2021) Autodisplay of human PIP5K1α lipid kinase on Escherichia coli and inhibitor testing. Enzyme and Microbial Technology. 143: 109717
Lindenblatt D, Nickelsen A, Applegate V, et al. (2020) Structural and mechanistic basis of the inhibitory potency of selected 2-aminothiazole compounds on protein kinase CK2. Journal of Medicinal Chemistry
Lengers I, Herrmann F, Le Borgne M, et al. (2020) Improved Surface Display of Human Hyal1 and Identification of Testosterone Propionate and Chicoric Acid as New Inhibitors. Pharmaceuticals (Basel, Switzerland). 13
Wünsch B, Kröger L, Daniliuc CG, et al. (2020) Synthesis and SAR of tetracyclic inhibitors of protein kinase CK2 derived from furocarbazole W16. Chemmedchem
Haidar S, Juergens F, Eichele D, et al. (2020) In silico and in vitro studies of natural compounds as human CK2 inhibitors. Current Computer-Aided Drug Design
Pietsch M, Viht K, Schnitzler A, et al. (2020) Unexpected CK2 beta-antagonistic functionality of bisubstrate inhibitors targeting protein kinase CK2. Bioorganic Chemistry. 96: 103608-103608
Haidar S, Marminon C, Aichele D, et al. (2019) QSAR Model of Indeno[1,2-]indole Derivatives and Identification of -isopentyl-2-methyl-4,9-dioxo-4,9-Dihydronaphtho[2,3-]furan-3-carboxamide as a Potent CK2 Inhibitor. Molecules (Basel, Switzerland). 25
Oramas-Royo S, Haidar S, Amesty Á, et al. (2019) Design, synthesis and biological evaluation of new embelin derivatives as CK2 inhibitors. Bioorganic Chemistry. 95: 103520
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