Asma A Ahmed

Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors.

K. Glaser, S. Davidsen, V. Stoll, 2005, Journal of medicinal chemistry.

Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor.

K. Glaser, S. Davidsen, V. Stoll, 2007, Journal of medicinal chemistry.

Two new sponge species (Demospongiae: Chalinidae and Suberitidae) isolated from hyperarid mangroves of Qatar with notes on their potential antibacterial bioactivity

A. Leitão, Asma A Ahmed, C. Goodwin, 2020, PloS one.

Thienopyridine urea inhibitors of KDR kinase.

K. Glaser, S. Davidsen, N. Soni, 2007, Bioorganic & medicinal chemistry letters.

Isothiazolopyrimidines and isoxazolopyrimidines as novel multi-targeted inhibitors of receptor tyrosine kinases.

K. Glaser, S. Davidsen, M. Michaelides, 2006, Bioorganic & medicinal chemistry letters.

Isoindolinone ureas: a novel class of KDR kinase inhibitors.

K. Glaser, S. Davidsen, M. Michaelides, 2004, Bioorganic & medicinal chemistry letters.

3-amino-benzo[d]isoxazoles as novel multitargeted inhibitors of receptor tyrosine kinases.

K. Glaser, S. Davidsen, N. Soni, 2008, Journal of medicinal chemistry.