An overview on applications of SwissADME web tool in the design and development of anticancer, antitubercular and antimicrobial agents: A medicinal chemist's …
B Bakchi, AD Krishna, E Sreecharan… - Journal of Molecular …, 2022 - Elsevier
Recently, in silico techniques have gained tremendous popularity in the field of small
molecule drug discovery. The computational jobs include not only hit generation, lead …
molecule drug discovery. The computational jobs include not only hit generation, lead …
[HTML][HTML] Target-based anticancer indole derivatives and insight into structure‒activity relationship: A mechanistic review update (2018–2021)
A Dhiman, R Sharma, RK Singh - Acta Pharmaceutica Sinica B, 2022 - Elsevier
Cancer, which is the uncontrolled growth of cells, is the second leading cause of death after
heart disease. Targeting drugs, especially to specific genes and proteins involved in growth …
heart disease. Targeting drugs, especially to specific genes and proteins involved in growth …
Pyrazoline containing compounds as therapeutic targets for neurodegenerative disorders
Pyrazolines are a significant class of heterocyclic compounds with essential biological
activities. They are quite stable, which has inspired medicinal chemists to experiment with …
activities. They are quite stable, which has inspired medicinal chemists to experiment with …
[HTML][HTML] Synthesis, molecular docking, and in-vitro studies of pyrimidine-2-thione derivatives as antineoplastic agents via potential RAS/PI3K/Akt/JNK inhibition in …
In the present investigation, derivatives from (2–6) containing pyrimidine-2-thione moiety
incorporated with different heterocycles such as pyrazoline, phenyl pyrazoline, and …
incorporated with different heterocycles such as pyrazoline, phenyl pyrazoline, and …
The metal sensing applications of chalcones: The synthesis, characterization and theoretical calculations
H Karaca, S Kazancı - Journal of Molecular Structure, 2022 - Elsevier
In this study, three different chalcone compounds were synthesized by Aldol condensation
reaction. 4-hydroxybenzaldehyde and ketone compounds (acetophenone, acetofuran and …
reaction. 4-hydroxybenzaldehyde and ketone compounds (acetophenone, acetofuran and …
Synthesis, Antibacterial, and Antioxidant Activities of Thiazolyl‐Pyrazoline Schiff Base Hybrids: A Combined Experimental and Computational Study
D Zelelew, M Endale, Y Melaku, F Kedir… - Journal of …, 2022 - Wiley Online Library
Thiazole‐pyrazoline Schiff base hybrids have a broad range of pharmacological potential
with an ability to control the activity of numerous metabolic enzymes. In this work, a greener …
with an ability to control the activity of numerous metabolic enzymes. In this work, a greener …
Recent progresses in chalcone derivatives as potential anticancer agents
J Yang, J Lv, S Cheng, T Jing, T Meng… - Anti-Cancer Agents …, 2023 - ingentaconnect.com
Chalcones are members of the flavonoid family and act as intermediates in the biosynthesis
of flavonoids, which are widespread in plants. Meanwhile, chalcones are important …
of flavonoids, which are widespread in plants. Meanwhile, chalcones are important …
Anticancer effect of umbelliferone on MKN-45 and MIA PaCa-2 cell lines
ÖS Aslantürk, TA Çelik - Toxicology in Vitro, 2023 - Elsevier
In this study, the anticancer activity of umbelliferone (7-hydroxycoumarin-UMB) was
investigated in MKN-45 human gastric cancer and MIA PaCa-2 human pancreatic cancer …
investigated in MKN-45 human gastric cancer and MIA PaCa-2 human pancreatic cancer …
Synthesis, Biological Evaluation and in Silico Studies of New Pyrazoline Derivatives Bearing Benzo[d]thiazol‐2(3H)‐one Moiety as Potential Urease Inhibitors
Novel pyrazoline derivatives containing benzo [d] thiazol‐2 (3H)‐one moiety were
synthesized and screened for their inhibitory properties against urease, a clinically important …
synthesized and screened for their inhibitory properties against urease, a clinically important …