Chemical synthesis and molecular docking study of new thiazole, thiophene, and thieno [2, 3-d] pyrimidine derivatives as potential antiproliferative and antimicrobial …

IMM Othman, ZM Alamshany, NY Tashkandi… - Journal of Molecular …, 2022 - Elsevier
This context deals with the design and synthesis of a new set of derivatives containing
thiazole, thiophene, and thieno [2, 3-d] pyrimidine motifs 3-13 starting with 2-((2 …

[HTML][HTML] Synthesis of novel mono-and bis-pyrazolylthiazole derivatives as anti-liver cancer agents through EGFR/HER2 target inhibition

ME Salem, EM Mahrous, EA Ragab, MS Nafie… - BMC chemistry, 2023 - Springer
Bromoacetyl-4-(2-naphthoyl)-1-phenyl-1H-pyrazole (6) was synthesized from 2-
acetylnaphthalene and was used as a new key building block for constructing the title …

[HTML][HTML] Design and synthesis of new bis (1, 2, 4-triazolo [3, 4-b][1, 3, 4] thiadiazines) and bis ((quinoxalin-2-yl) phenoxy) alkanes as anti-breast cancer agents through …

FM Thabet, KM Dawood, EA Ragab, MS Nafie… - RSC …, 2022 - pubs.rsc.org
A number of new 1, ω-bis ((acetylphenoxy) acetamide) alkanes 5a–f were prepared then
their bromination using NBS furnished the novel bis (2-bromoacetyl) phenoxy) acetamides …

[HTML][HTML] Synthesis of novel aminothiazole derivatives as promising antiviral, antioxidant and antibacterial candidates

R Minickaitė, B Grybaitė, R Vaickelionienė… - International Journal of …, 2022 - mdpi.com
It is well-known that thiazole derivatives are usually found in lead structures, which
demonstrate a wide range of pharmacological effects. The aim of this research was to …

[HTML][HTML] Synthesis of phthalazine-based derivatives as selective anti-breast cancer agents through EGFR-mediated apoptosis: in vitro and in silico studies

SM Emam, SME Rayes, IAI Ali, HA Soliman, MS Nafie - BMC chemistry, 2023 - Springer
Abstract The parent 2-(4-benzyl-1-oxophthalazin-2 (1 H)-yl)-acetohydrazide (4) has twenty-
nine compounds. The starting material for their corresponding mono, dipeptides and …

Novel bis-amide-based bis-thiazoles as anti-colorectal cancer agents through Bcl-2 inhibition: synthesis, in vitro, and in vivo studies

KM Dawood, MA Raslan, AA Abbas… - Anti-Cancer Agents …, 2023 - ingentaconnect.com
Background: Some heterocycles having bisamide linkage are receiving much interest due to
their remarkable biological potencies and they are naturally occurring. Some bisamides and …

Synthesis and Anti-Breast Cancer Potency of Mono- and Bis-(pyrazolyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine) Derivatives as EGFR/CDK-2 Target Inhibitors

ME Salem, EM Mahrous, EA Ragab, MS Nafie… - ACS …, 2023 - ACS Publications
The target mono-and bis-(6-pyrazolyltriazolo-thiadiazine) derivatives 4a-c and 6a-d were
synthesized using a straightforward protocol via reaction of 3-bromoacetylpyrazole 2 with 4 …

A review on advances in synthetic methodology and biological profile of spirothiazolidin‐4‐ones

J Yadav, RP Chaudhary - Journal of Heterocyclic Chemistry, 2022 - Wiley Online Library
Heterocycles are important structural components in pharmacophores that are currently
being used to treat several diseases. Among the various heterocyclic scaffolds, nitrogen and …

[HTML][HTML] Synthesis of 2-amino-9 H-chromeno [2, 3-d] thiazol-9-ones with anti-inflammatory activity via cascade reactions of 2-amino-3 iodochromones with amines and …

J Tan, Y He, Y Lin, Y Zhong, S He, J Zuo, C Yang - RSC advances, 2024 - pubs.rsc.org
A simple and efficient synthetic approach to 2-amino-9H-chromeno [2, 3-d] thiazol-9-ones
via copper-promoted cascade reactions was developed. The reaction employed easily …

New spiro-indeno[1,2-b]quinoxalines clubbed with benzimidazole scaffold as CDK2 inhibitors for halting non-small cell lung cancer; stereoselective synthesis …

A Barakat, S Alshahrani, AM Al-Majid… - Journal of Enzyme …, 2023 - Taylor & Francis
Despite the crucial role of CDK2 in tumorigenesis, few inhibitors reached clinical trials for
managing lung cancer, the leading cause of cancer death. Herein, we report combinatorial …