313394-46-6

Upstream product

• 22214-30-8 (E)-4-(4-hydroxyphenyl)-3-buten-2-one 
• 64-19-7 acetic acid 
• 22214-30-8 4-(4'-hydroxyphenyl)but-3-en-2-one 
• 200417-33-0 1H-4,5-dihydro-3-methyl-5-(4-hydroxyphenyl)pyrazole 

Downstream Products

• 1107065-17-7 4-(1-acetyl-3-methyl-4,5-dihydro-1H-pyrazol-5-yl)phenyl 2-chlorobenzoate 
• 421570-69-6 1-(5-(4-(benzyloxy)phenyl)-3-methyl-4,5-dihydropyrazol-1-yl)ethanone 
• 1239591-14-0 CCDC-762238 
• 1246890-39-0 C₂₂H₁₈Cl₂N₄O₂ 
• 1246890-38-9 C₂₃H₂₂N₄O₃ 
• 1246890-37-8 C₂₂H₂₀N₄O₂ 
• 1246890-40-3 C₂₃H₁₉F₃N₄O₂ 

Relevant academic research and scientific papers

Synthesis, characterization and microbial activity of N-substituted pyrazolines

Acetic acid and propanoic acid were treated with thionyl chloride to give respective acid chlorides, which were then reacted with synthesized pyrazolines using triethylamine as catalyst in dry dichloromethane to give N-acetylated pyrazolines (1b-7b) and N

Novel dihydropyrazole derivatives linked with 4H-chromene: Microwave-promoted synthesis and antibacterial activity

Seven novel 6-(1-acetyl-3-methyl-4,5-dihydro-1H-pyrazol-5-yl)-2-amino-4- substituted-phenyl-4H-chromene-3-carbonitrile derivatives were synthesized and characterized by ESI-MS, 1H NMR and 13C NMR. All of the compounds have been screened for their antibact

Synthesis and molecular docking studies of novel 2-chloro-pyridine derivatives containing flavone moieties as potential antitumor agents

A series of novel 2-chloro-pyridine derivatives containing flavone, chrome or dihydropyrazole moieties as potential telomerase inhibitors were synthesized. The bioassay tests showed that compounds 6e and 6f exhibited some effect against gastric cancer cell SGC-7901 with IC50 values of 22.28 ± 6.26 and 18.45 ± 2.79 μg/mL, respectively. All title compounds were assayed for telomerase inhibition by a modified TRAP assay, the results showed that compound 6e can strongly inhibit telomerase with IC50 value of 0.8 ± 0.07 μM. Docking simulation was performed to position compound 6e into the active site of telomerase (3DU6) to determine the probable binding model.

Synthesis, structure, and antibacterial activity of novel 5-arylpyrazole derivatives

A series of novel 1-(acetyl,carboxamide,carbothioamide)substituted-5- (substituted-phenyl)-3-methy-4,5-dihydropyrazole derivatives have been synthesized and characterized by 1H NMR, IR, ESI-MS, and elemental analysis. Compounds 6h and 6q were further characterized by single crystal X-ray structural analysis. All of the compounds have been screened for their antibacterial potential in vitro against Bacillus subtilis ATCC 6633, Escherichia coli ATCC 35218, Pseudomonas fluorescens ATCC 13525, and Staphylococcus aureus ATCC 6538. Among the tested compounds, some of them display significant activity against the tested strains, and compounds 5ac and 6h show potent activity with a minimum inhibitory concentration value of 1.562 ?g mL?1 against B. subtilis ATCC 6633, which is comparable to the positive control penicillin. Structure?effect relationships are also discussed based on the experimental data. CSIRO 2008.