| 501 |
Combining acetyl salicylic acid and rofecoxib into novel oral tablets normalize platelet function with potential higher tolerability in patients with cardiovascular disorders |
Department of Pharmaceutical Analytical Chemistry |
2020 |
| 502 |
Combining acetyl salicylic acid and rofecoxib into novel oral tablets normalize platelet function with potential higher tolerability in patients with cardiovascular disorders |
Department of Industrial Pharmacy |
2020 |
| 503 |
Combining acetyl salicylic acid and rofecoxib into novel oral tablets normalize platelet function with potential higher tolerability in patients with cardiovascular disorders |
Department of Industrial Pharmacy |
2020 |
| 504 |
Combining acetyl salicylic acid and rofecoxib into novel oral tablets normalize platelet function with potential higher tolerability in patients with cardiovascular disorders |
Department of Pharmaceutical Analytical Chemistry |
2020 |
| 505 |
Conjugation of 4-aminosalicylate with thiazolinones afforded non-cytotoxic potent in vitro and in vivo anti-inflammatory hybrids |
Department of Pharmaceutical Organic Chemistry |
2020 |
| 506 |
Cytotoxic Activity of Abietane-Type Diterpenes Isolated From Taxodium distichum Against Cancer Cells Adapted to Nutrient-Starved Conditions |
Department of Pharmacognosy |
2020 |
| 507 |
Design and synthesis of new 1,6-dihydropyrimidin-2-thio derivatives targeting VEGFR-2: Molecular docking and antiproliferative evaluation |
Department of Pharmaceutical Organic Chemistry |
2020 |
| 508 |
Design and synthesis of new pyranoquinolinone heteroannulated to triazolopyrimidine of potential apoptotic antiproliferative activity |
Department of Pharmaceutical Organic Chemistry |
2020 |
| 509 |
Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors |
Department of Pharmaceutical Organic Chemistry |
2020 |
| 510 |
Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAFV600E dual inhibitors |
Department of Pharmaceutical Organic Chemistry |
2020 |