43 results on '"Zaraei, Seyed-Omar"'
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2. The anti-amoebic potential of carboxamide derivatives containing sulfonyl or sulfamoyl moieties against brain-eating Naegleria fowleri
3. Design, synthesis, biological evaluation, and in silico studies of novel pyridopyridine derivatives as anticancer candidates targeting FMS kinase
4. Design and discovery of urease and Helicobacter pylori inhibitors based on benzofuran/benzothiophene-sulfonate and sulfamate scaffolds for the treatment of ureolytic bacterial infections
5. Anti-proliferative activity of RIHMS-Qi-23 against MCF-7 breast cancer cell line is through inhibition of cell proliferation and senescence but not inhibition of targeted kinases
6. Synthesis and biological evaluation of sulfamate derivatives as inhibitors of carbonic anhydrases II and IX
7. Synthesis, biological evaluation, and stability studies of raloxifene mono- and bis-sulfamates as dual-targeting agents
8. Potential anti-amoebic activity of sulfonate- and sulfamate-containing carboxamide derivatives against pathogenic Acanthamoeba castellanii belonging to the genotype T4
9. Synthesis, biological evaluation, and molecular modeling studies of a new series of imidazothiazole or imidazooxazole derivatives as inhibitors of ectonucleoside triphosphate diphosphohydrolases (NTPDases)
10. Evaluation of novel pyrazol-4-yl pyridine derivatives possessing arylsulfonamide tethers as c-Jun N-terminal kinase (JNK) inhibitors in leukemia cells
11. The latest perspectives of small molecules FMS kinase inhibitors
12. Design and synthesis of new adamantyl derivatives as promising antiproliferative agents
13. Design, synthesis, and biological evaluation of a new series of pyrazole derivatives: Discovery of potent and selective JNK3 kinase inhibitors
14. Evaluation of indole-picolinamide hybrid molecules as carbonic anhydrase-II inhibitors: Biological and computational studies
15. Design and synthesis of new quinoline derivatives as selective C-RAF kinase inhibitors with potent anticancer activity
16. Discovery of urease inhibitory effect of sulfamate derivatives: Biological and computational studies
17. Design, synthesis, in vitro determination and molecular docking studies of 4-(1-(tert-butyl)-3-phenyl-1H-pyrazol-4-yl) pyridine derivatives with terminal sulfonamide derivatives in LPS-induced RAW264.7 macrophage cells
18. Discovery of first-in-class imidazothiazole-based potent and selective ErbB4 (HER4) kinase inhibitors
19. Design, synthesis, biological evaluation, and docking studies of novel (imidazol-5-yl)pyrimidine-based derivatives as dual BRAFV600E/p38α inhibitors
20. Design, synthesis, biological evaluation, and modeling studies of novel conformationally-restricted analogues of sorafenib as selective kinase-inhibitory antiproliferative agents against hepatocellular carcinoma cells
21. Diarylamides in anticancer drug discovery: A review of pre-clinical and clinical investigations
22. Synthesis and Biological Activity of Sulfamate–Adamantane Derivatives as Glucosinolate Sulfatase Inhibitors
23. Evaluation of 2,3-dihydroimidazo[2,1-b]oxazole and imidazo[2,1–b]oxazole derivatives as chemotherapeutic agents
24. Synthesis, biological evaluation, and docking studies of new raloxifene sulfonate or sulfamate derivatives as inhibitors of nucleotide pyrophosphatase/phosphodiesterase
25. Sulfamates in drug design and discovery: Pre-clinical and clinical investigations
26. Novel anti-Acanthamoebic properties of Raloxifene sulfonate/sulfamate derivatives
27. Novel Anti-Acanthamoebic Activities of Irosustat and STX140 and Their Nanoformulations
28. Evaluation of Novel Pyrazol-4yl Pyridine Derivatives Possessing Arylsulfonamide Tethers as C-Jun N-Terminal Kinase (Jnk) Inhibitors in Leukemia Cells
29. Synthesis, biological evaluation, and molecular modeling studies of a new series of imidazothiazole or imidazooxazole derivatives as inhibitors of ectonucleoside triphosphate diphosphohydrolases (NTPDases)
30. Anti-amoebic activity of a series of benzofuran/benzothiophene derivatives against Acanthamoeba castellanii belonging to the T4 genotype
31. Anti-amoebic activity of a series of benzofuran/benzothiophene derivatives againstAcanthamoeba castellaniibelonging to the T4 genotype
32. Design and synthesis of novel anti-urease imidazothiazole derivatives with promising antibacterial activity against Helicobacter pylori.
33. Potent Imidazothiazole-based Inhibitor of BRAF V600E Overcomes Acquired Resistance via Inhibition of RAF Dimerization in PLX4032-resistant Melanoma
34. Structural optimization of 4-(imidazol-5-yl)pyridine derivatives affords broad-spectrum anticancer agents with selective B-RAFV600E/p38α kinase inhibitory activity: Synthesis, in vitro assays and in silico study
35. Anti-amoebic activity of a series of benzofuran/benzothiophene derivatives against Acanthamoeba castellanii belonging to the T4 genotype.
36. Evaluation of Substituted Pyrazole-Based Kinase Inhibitors in One Decade (2011–2020): Current Status and Future Prospects
37. A Review of HER4 (ErbB4) Kinase, Its Impact on Cancer, and Its Inhibitors
38. Evaluation of sulfonate and sulfamate derivatives possessing benzofuran or benzothiophene nucleus as inhibitors of nucleotide pyrophosphatases/phosphodiesterases and anticancer agents
39. Synthesis, biological evaluation, and docking studies of new pyrazole-based thiourea and sulfonamide derivatives as inhibitors of nucleotide pyrophosphatase/phosphodiesterase
40. A new series of aryl sulfamate derivatives: Design, synthesis, and biological evaluation
41. Sulfonate and sulfamate derivatives possessing benzofuran or benzothiophene nucleus as potent carbonic anhydrase II/IX/XII inhibitors
42. Evaluation of 2,3-dihydroimidazo[2,1- b ]oxazole and imidazo[2,1- b ]oxazole derivatives as chemotherapeutic agents.
43. Structural optimization of 4-(imidazol-5-yl)pyridine derivatives affords broad-spectrum anticancer agents with selective B-RAF V600E /p38α kinase inhibitory activity: Synthesis, in vitro assays and in silico study.
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