[HTML][HTML] Synthesis and biological activity screening of newly synthesized trimethoxyphenyl-based analogues as potential anticancer agents
T Al-Warhi, M Abualnaja, OA Abu Ali, F Althobaiti… - Molecules, 2022 - mdpi.com
A group of novel trimethoxyphenyl (TMP)-based analogues were synthesized by varying the
azalactone ring of 2-(3, 4-dimethoxyphenyl)-4-(3, 4, 5-trimethoxybenzylidene) oxazolone 1 …
azalactone ring of 2-(3, 4-dimethoxyphenyl)-4-(3, 4, 5-trimethoxybenzylidene) oxazolone 1 …
One-pot synthesis, anti-tumor evaluation and structure–activity relationships of novel 25-OCH 3-PPD derivatives
FZ Qu, C Zhao, JQ Cao, Y Zhang, YQ Zhao - MedChemComm, 2017 - pubs.rsc.org
Based on the fact that 25-OCH3-PPD, a natural ginsengenin isolated from the leaves of
Panax ginseng, is a promising lead compound, novel 25-OCH3-PPD derivatives were …
Panax ginseng, is a promising lead compound, novel 25-OCH3-PPD derivatives were …
Structure-based design, structure–activity relationship analysis, and antitumor activity of diaryl ether derivatives
SM Yang, ZN Huang, ZS Zhou, J Hou… - Archives of pharmacal …, 2015 - Springer
To identify novel therapeutic agents to treat cancer, we synthesized a series of diaryl ether
derivatives. Structure–activity relationship studies revealed that the presence of a chlorine or …
derivatives. Structure–activity relationship studies revealed that the presence of a chlorine or …
[HTML][HTML] New Derivatives of 1-(3-Methyl-1-Benzofuran-2-yl) Ethan-1-one: Synthesis and Preliminary Studies of Biological Activity
M Napiórkowska, P Kumaravel… - International Journal of …, 2024 - mdpi.com
A set of nine derivatives, including five brominated compounds, was synthesized and the
structures of these novel compounds were confirmed using 1H and 13C NMR as well as ESI …
structures of these novel compounds were confirmed using 1H and 13C NMR as well as ESI …
Design, synthesis and in vitro antitumor activity of novel N-substituted-4-phenyl/benzylphthalazin-1-ones
A novel series of N-substituted-4-phenylphthalazin-1-ones 14a–g bearing different anilines
at the N-2 of phthalazin-1-one scaffold via acetyl-flexible linker was designed and …
at the N-2 of phthalazin-1-one scaffold via acetyl-flexible linker was designed and …
Design, synthesis and preliminary antiproliferative activity studies of new diheteroaryl thioether derivatives
ZH Li, XQ Liu, TQ Zhao, PF Geng, Y Liu, B Zhao… - Bioorganic & Medicinal …, 2017 - Elsevier
A series of structurally new diheteroaryl thioether analogs was designed, prepared and
screened toward MGC-803, MKN-45, EC-109 and H1650. Most of the target compounds …
screened toward MGC-803, MKN-45, EC-109 and H1650. Most of the target compounds …
Synthesis and Biological evaluation of novel 4β-[(5-substituted)-1, 2, 3, 4-tetrazolyl] podophyllotoxins as anticancer compounds
I Hyder, D Yedlapudi, SV Kalivendi, J Khazir… - Bioorganic & Medicinal …, 2015 - Elsevier
A series of novel 4β-[(5-substituted)-1, 2, 3, 4-tetrazolyl] podophyllotoxin derivatives were
synthesized by employing azide-nitrile click chemistry approach. All the derivatives were …
synthesized by employing azide-nitrile click chemistry approach. All the derivatives were …
Design, synthesis and biological evaluation of novel benzimidazole-2-substituted phenyl or pyridine propyl ketene derivatives as antitumour agents
L Wu, Z Jiang, J Shen, H Yi, Y Zhan, M Sha… - European Journal of …, 2016 - Elsevier
A series of novel benzimidazole-2-subsituted phenyl or pyridine propyl ketene derivatives
were designed and synthesized. The biological activities of these derivatives were then …
were designed and synthesized. The biological activities of these derivatives were then …
4β-[(4-Alkyl)-1, 2, 3-triazol-1-yl] podophyllotoxins as anticancer compounds: Design, synthesis and biological evaluation
DM Reddy, J Srinivas, G Chashoo, AK Saxena… - European journal of …, 2011 - Elsevier
Abstract A series of 4β-[(4-alkyl)-1, 2, 3-triazol-1-yl] podophyllotoxin derivatives were
designed in silico, synthesised by employing click chemistry approach, and evaluated for …
designed in silico, synthesised by employing click chemistry approach, and evaluated for …
[HTML][HTML] Selected novel 5'-amino-2'-hydroxy-1, 3-diaryl-2-propen-1-ones arrest cell cycle of HCT-116 in G0/G1 phase
L Simon, KK Srinivasan, N Kumar, ND Reddy… - EXCLI …, 2016 - ncbi.nlm.nih.gov
Abstract A series of 5'-amino-2'-hydroxy-1, 3-diaryl-2-propen-1-ones (AC1-AC15) were
synthesized by Claisen-Schmidt condensation of 5'-acetamido-2'-hydroxy acetophenone …
synthesized by Claisen-Schmidt condensation of 5'-acetamido-2'-hydroxy acetophenone …