Suchergebnisse - "Allam, Heba Abdelrasheed"

PubPharm (20)

11

Nanomolar potency of imidazo[2,1-b]thiazole analogs as indoleamine 2,3-dioxygenase inhibitors

enthalten in: Archiv der Pharmazie | 2021

von Ewida, M. | Ewida, H. | Ahmed, M. | +5

12

3-Methyl-imidazo[2,1-b]thiazole derivatives as a new class of antifolates : Synthesis, in vitro/in vivo bio-evaluation and molecular modeling simulations

enthalten in: Bioorganic chemistry | 2021

von Ewida, M. | Ewida, H. | Ahmed, M. | +5

13

Nanomolar potency of imidazo[2,1‐ b]thiazole analogs as indoleamine 2,3‐dioxygenase inhibitors

enthalten in: Archiv der Pharmazie | 2021

von Ewida, M. | Ewida, H. | Ahmed, M. | +5

14

Design and Synthesis of some new 2,4,6-trisubstituted quinazoline EGFR inhibitors as targeted anticancer agents

enthalten in: Bioorganic chemistry | 2020

von Allam, H. | Aly, E. | Farouk, A. | +3

15

Synthesis and vasodilator activity of some pyridazin-3(2H)-one based compounds

enthalten in: Future medicinal chemistry | 2020

von Allam, H. | Kamel, A. | El-Daly, M. | +1

16

Design, synthesis and biological evaluation of some new 1,3,4-thiadiazine-thiourea derivatives as potential antitumor agents against non-small cell lung cancer cells

enthalten in: Bioorganic chemistry | 2019

von Ragab, F. | Abdel-Aziz, S. | Kamel, M. | +2

17

Application of hydrazino and hydrazido linkers to connect benzenesulfonamides with hydrophilic/phobic tails for targeting the middle region of human carbonic anhydrases active site : Selective inhibitors of hCA IX

enthalten in: European journal of medicinal chemistry | 2019

von Allam, H. | Fahim, S. | F Abo-Ashour, M. | +6

18

Synthesis and biological evaluation of some novel thiobenzimidazole derivatives as anti-renal cancer agents through inhibition of c-MET kinase

enthalten in: Bioorganic chemistry | 2019

von Ibrahim, H. | Albakri, M. | Mahmoud, W. | +3

19

Synthesis and vasodilator activity of some pyridazin-3(2H)-one based compounds

enthalten in: Future medicinal chemistry | 2019

von Allam, H. | Kamel, A. | El-Daly, M. | +1

20

Dual-tail arylsulfone-based benzenesulfonamides differently match the hydrophobic and hydrophilic halves of human carbonic anhydrases active sites : Selective inhibitors for the tumor-associated hCA IX isoform

enthalten in: European journal of medicinal chemistry | 2018

von Ibrahim, H. | Allam, H. | Mahmoud, W. | +6