Development and therapeutic potential of 2-aminothiazole derivatives in anticancer drug discovery
SR Alizadeh, SM Hashemi - Medicinal Chemistry Research, 2021 - Springer
Currently, the development of anticancer drug resistance is significantly restricted the clinical
efficacy of the most commonly prescribed anticancer drug. Malignant disease is widely …
efficacy of the most commonly prescribed anticancer drug. Malignant disease is widely …
[PDF][PDF] Recent Developments and Biological Activities of 2-Aminothiazole Derivatives.
ME Khalifa - Acta Chimica Slovenica, 2018 - researchgate.net
Aminothiazole nuclei and their various derivatives have been long used as precursors for
the synthesis of biologically active molecules. As a typical heterocyclic amine, 2 …
the synthesis of biologically active molecules. As a typical heterocyclic amine, 2 …
1-Piperazinylphthalazines as potential VEGFR-2 inhibitors and anticancer agents: synthesis and in vitro biological evaluation
In our endeavor towards the development of effective VEGFR-2 inhibitors, three novel series
of phthalazine derivatives based on 1-piperazinyl-4-arylphthalazine scaffold were …
of phthalazine derivatives based on 1-piperazinyl-4-arylphthalazine scaffold were …
2-(2-Hydrazinyl) thiazole derivatives: Design, synthesis and in vitro antimycobacterial studies
P Makam, R Kankanala, A Prakash… - European journal of …, 2013 - Elsevier
In an attempt to discover new potent inhibitors for Mycobacterium tuberculosis (Mtb), a series
of 2-(2-hydrazinyl) thiazole derivatives with a wide range of substitutions at 2-, 4-and 5 …
of 2-(2-hydrazinyl) thiazole derivatives with a wide range of substitutions at 2-, 4-and 5 …
A novel series of thiazolyl–pyrazoline derivatives: Synthesis and evaluation of antifungal activity, cytotoxicity and genotoxicity
In the current work, new thiazolyl–pyrazoline derivatives (1–22) were synthesized and
evaluated for their antifungal effects against pathogenic yeasts and molds using a broth …
evaluated for their antifungal effects against pathogenic yeasts and molds using a broth …
Synthesis, antitumor activity and mechanism of action of novel 1, 3-thiazole derivatives containing hydrazide–hydrazone and carboxamide moiety
H He, X Wang, L Shi, W Yin, Z Yang, H He… - Bioorganic & medicinal …, 2016 - Elsevier
Abstract A series of novel 2, 4, 5-trisubstituted 1, 3-thiazole derivatives containing hydrazide–
hydrazine, and carboxamide moiety including 46 compounds T were synthesized, and …
hydrazine, and carboxamide moiety including 46 compounds T were synthesized, and …
1, 3, 4-Trisubstituted pyrazole analogues as promising anti-inflammatory agents
SG Alegaon, KR Alagawadi, MK Garg, K Dushyant… - Bioorganic …, 2014 - Elsevier
Abstract Twenty-two 1, 3, 4-trisubstituted pyrazole (3a–d),(4a–d),(5a–d),(6a–l) derivatives
were synthesized and structure of newly synthesized compounds were characterized by IR …
were synthesized and structure of newly synthesized compounds were characterized by IR …
[HTML][HTML] Synthesis and anticancer activity of new quinazoline derivatives
HA Abuelizz, M Marzouk, H Ghabbour… - Saudi Pharmaceutical …, 2017 - Elsevier
In this study, a new series of quinazoline derivatives (3–26) was synthesized and
characterized via physicochemical and spectral means. Treatment of 2-amino-5 …
characterized via physicochemical and spectral means. Treatment of 2-amino-5 …
Design and synthesis of novel dithiazole carboxylic acid Derivatives: In vivo and in silico investigation of their Anti-Inflammatory and analgesic effects
Inflammation is a complex set of interactions that can occur in tissues as the body's
defensive response to infections, trauma, allergens, or toxic compounds. Therefore, in …
defensive response to infections, trauma, allergens, or toxic compounds. Therefore, in …
Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1, 3-thiazole analogs
A novel series of 2-acetamido-or 2-propanamido-4-(4-substituted phenyl)-1, 3-thiazoles (11–
34) was designed and synthesized. Compounds were subjected to National Cancer Institute …
34) was designed and synthesized. Compounds were subjected to National Cancer Institute …