Pyridazine as a privileged structure: An updated review on anticancer activity of pyridazine containing bioactive molecules

ZX He, YP Gong, X Zhang, LY Ma, W Zhao - European journal of medicinal …, 2021 - Elsevier
Identification of potent anticancer agents with high selectivity and low toxicity remains on the
way to human health. Pyridazine featuring advantageous physicochemical properties and …

Recent advances of LSD1/KDM1A inhibitors for disease therapy

C Zhang, Z Wang, Y Shi, B Yu, Y Song - Bioorganic Chemistry, 2023 - Elsevier
Abstract Lysine-specific demethylase 1 (LSD1/KDM1A) dysregulation is closely associated
with the pathological processes of various diseases, especially hematologic malignancies …

New pyrimidine-5-carbonitriles as COX-2 inhibitors: design, synthesis, anticancer screening, molecular docking, and in silico ADME profile studies

HA Al-Ghulikah, SA El-Sebaey, AKA Bass… - Molecules, 2022 - mdpi.com
Two series of cyanopyrimidine hybrids were synthesized bearing either benzo [d] imidazole,
benzo [d] oxazole, benzo [d] thiazole, and benzo [b] thiophene derivatives via methylene …

Design and synthesis of pyrazole–pyrazoline hybrids as cancer‐associated selective COX‐2 inhibitors

W Akhtar, A Marella, MM Alam, MF Khan… - Archiv der …, 2021 - Wiley Online Library
In continuation of our previous work on cancer and inflammation, 15 novel pyrazole–
pyrazoline hybrids (WSPP1–15) were synthesized and fully characterized. The formation of …

Synthesis, biological evaluation and docking studies of methylene bearing cyanopyrimidine derivatives possessing a hydrazone moiety as potent Lysine specific …

S Tasneem, KA Sheikh, M Naematullah, MM Alam… - Bioorganic …, 2022 - Elsevier
A series of novel cyanopyrimidine-hydrazone hybrids were synthesized and characterized
with various spectroscopic techniques. The synthesized compounds were tested at NCI …

Synthesis, COX-2 inhibition and metabolic stability studies of 6-(4-fluorophenyl)-pyrimidine-5-carbonitrile derivatives as anticancer and anti-inflammatory agents

W Akhtar, LM Nainwal, MF Khan, G Verma… - Journal of Fluorine …, 2020 - Elsevier
In continuation of previous work on cyanopyrimidine derivatives for cancer and
inflammation, eighteen novel amino containing cyanopyrimidine derivatives (4a-p) bearing …

A new series of pyridazinone derivatives as cholinesterases inhibitors: Synthesis, in vitro activity and molecular modeling studies

AB Özçelik, Z Özdemir, S Sari, S Utku, M Uysal - Pharmacological Reports, 2019 - Elsevier
Background The pyridazinone nucleus has been incorporated into a wide variety of
therapeutically interesting molecules to transform them into better drugs …

Synthesis, ADMET prediction and reverse screening study of 3, 4, 5-trimethoxy phenyl ring pendant sulfur‐containing cyanopyrimidine derivatives as promising …

LM Nainwal, M Shaququzzaman, M Akhter… - Bioorganic …, 2020 - Elsevier
Cancer remains considered as one of the leading global health problems either due to
meagre and suboptimal therapeutic response of chemotherapeutic agents or due to the …

Halogen‐based quinazolin‐4(3H)‐one derivatives as MCF‐7 breast cancer inhibitors: Current developments and structure–activity relationship

R Upadhyay, P Tandel, AB Patel - Archiv der Pharmazie, 2025 - Wiley Online Library
Currently, cancer is a serious health challenge with predominance beyond restrictions.
Breast cancer remains one of the major contributors to cancer‐related morbidity and …

An Overview of synthesis and biological activity of dihydropyrimidine derivatives

AC Dudhe, R Dudhe, O Porwal… - Mini Reviews in …, 2022 - benthamdirect.com
Dihydropyrimidine derivatives are the most important scaffolds due to structural similarities
with natural products; it is a heterocyclic compound. The chemistry of Dihydropyrimidine is a …