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Synthesis, anti-inflammatory screening, molecular docking, and COX-1,2/-5-LOX inhibition profile of some novel quinoline derivatives.
Bioorg Chem. 2018 Aug;78:220-235. doi: 10.1016/j.bioorg.2018.03.023. Epub 2018 Mar 20.
Bioorg Chem. 2018.
PMID: 29602046
Synthesis, antibacterial evaluation, and DNA gyrase inhibition profile of some new quinoline hybrids.
Rizk OH, Bekhit MG, Hazzaa AAB, El-Khawass EM, Abdelwahab IA.
Rizk OH, et al. Among authors: el khawass em.
Arch Pharm (Weinheim). 2019 Oct;352(10):e1900086. doi: 10.1002/ardp.201900086. Epub 2019 Aug 7.
Arch Pharm (Weinheim). 2019.
PMID: 31389630
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Synthesis and biological evaluation of new oxadiazoline-substituted naphthalenyl acetates as anticancer agents.
Chaaban I, El Khawass el SM, Abd El Razik HA, El Salamouni NS, Redondo-Horcajo M, Barasoain I, Díaz JF, Yli-Kauhaluoma J, Moreira VM.
Chaaban I, et al.
Eur J Med Chem. 2014 Nov 24;87:805-13. doi: 10.1016/j.ejmech.2014.10.015. Epub 2014 Oct 13.
Eur J Med Chem. 2014.
PMID: 25440882
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Synthesis and Anti-Proliferative Activity of Sulfanyltriazolylnaphthalenols and Sulfanyltriazolylnaphthalene-1,4-diones.
Chaaban I, El Khawass el SM, Abd El Razik HA, El Salamouni NS, Redondo-Horcajo M, Barasoain I, Díaz JF, Yli-Kauhaluoma J, Moreira VM.
Chaaban I, et al.
Arch Pharm (Weinheim). 2016 Sep;349(9):749-61. doi: 10.1002/ardp.201600134. Epub 2016 Jul 12.
Arch Pharm (Weinheim). 2016.
PMID: 27404773
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Synthesis of some 2-(3,4-dimethoxy-phenyl)-1,3-propanediamines as potential dopaminergic agents.
Shafik RM, Ibrahim EA, el-Khawass EM, el-Hawash SA, el-Dardiry SA.
Shafik RM, et al. Among authors: el khawass em.
Pharmazie. 1989 Feb;44(2):115-8.
Pharmazie. 1989.
PMID: 2568640
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Residues at the indole-NH of LE300 modulate affinities and selectivities for dopamine receptors.
Robaa D, Kretschmer R, Siol O, Abulazm SE, Elkhawass E, Lehmann J, Enzensperger C.
Robaa D, et al.
Arch Pharm (Weinheim). 2011 Jan;344(1):28-36. doi: 10.1002/ardp.201000121. Epub 2010 Nov 11.
Arch Pharm (Weinheim). 2011.
PMID: 21213349
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Dopamine receptor ligands. Part 18: (1) modification of the structural skeleton of indolobenzazecine-type dopamine receptor antagonists.
Robaa D, Enzensperger C, Abul Azm Sel D, El Khawass el S, El Sayed O, Lehmann J.
Robaa D, et al.
J Med Chem. 2010 Mar 25;53(6):2646-50. doi: 10.1021/jm901291r.
J Med Chem. 2010.
PMID: 20180564
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