The synthesis of indolo[2,3-b]quinoline derivatives with a guanidine group: Highly selective cytotoxic agents

Synthesis and Structure-Activity Relationship of Methyl-Substituted Indolo[2,3-b]quinolines: Novel Cytotoxic, DNA Topoisomerase II Inhibitors

W Peczyńska-Czoch, François Pognan, Łukasz Kaczmarek et al. · Journal of Medicinal Chemistry · 1994 · 199 citations

Pharmacy, Medicinal Chemistry, Pharmacology +15

Utilization of Combined Chemical Modifications to Enhance the Blood-Brain Barrier Permeability and Pharmacological Activity of Endomorphin-1

Hongmei Liu, Jin-Long Yao, Changlin Wang et al. · Journal of Pharmacology and Experimental Therapeutics · 2006 · 70 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +17

Synthesis, and cytotoxic activity of some novel indolo[2,3-b]quinoline derivatives

Łukasz Kaczmarek, W Peczyńska-Czoch, Jarosław Osiadacz et al. · Bioorganic & Medicinal Chemistry · 1999 · 64 citations

Pharmacy, Medicinal Chemistry, Pharmacology +9

Vitamin D analogs enhance the anticancer activity of 5-fluorouracil in an in vivomouse colon cancer model

Magdalena Milczarek, Mateusz Psurski, Andrzej Kutner et al. · BMC Cancer · 2013 · 63 citations · Full text

Medicine, Oncology, Pharmacology +15

A Practical Entry to the Crambescidin Family of Guanidine Alkaloids. Enantioselective Total Syntheses of Ptilomycalin A, Crambescidin 657 and Its Methyl Ester (Neofolitispates 2), and Crambescidin 800

Donald S. Coffey, Andrew I. McDonald, Larry E. Overman et al. · Journal of the American Chemical Society · 2000 · 62 citations

Pharmacy, Medicinal Chemistry, Pharmacology +15