Paper
Synthesis and biological activity of 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives, novel pro-apoptotic mitochondrial targeted agents.
Published 2009 · L. Dalla Via, A. Marini, S. Salerno
Bioorganic & medicinal chemistry
Q2 SJR score
25
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
The synthesized 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives effectively inhibit cell growth by inducing mitochondrial permeability transition and triggering caspase activation.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Full text analysis coming soon...
References
Synthesis and in vitro Antiproliferative Activity of New Substituted Benzo[3′,2′:5,6]thiopyrano[4,3‐d]pyrimidines.
The 2-phenyl substituted derivative of benzo[3′,2′:5,6]thiopyrano[4,3-d]pyrimidine shows antiproliferative activity against human tumor cell lines HL-60 and HeLa, but does not form molecular complexes with DNA.
2008·13citations·A. Marini et al.·ChemInform
ChemInform
Mitochondrial permeability transition induced by novel pyridothiopyranopyrimidine derivatives: potential new antimitochondrial antitumour agents.
PTP1 and PTP2 show potential as new antimitochondrial antitumour agents by inducing mitochondrial permeability transition and affecting cell growth through oxidative stress-induced mitochondrial dysfunction.
2006·14citations·L. D. Via et al.·Biochemical pharmacology
Biochemical pharmacology
Inhibition of cellular respiration by doxorubicin.
Doxorubicin inhibits cellular respiration through caspase-mediated inhibition of oxidative phosphorylation, leading to a decline in cellular ATP levels.
2006·31citations·Zhimin Tao et al.·Chemical research in toxicology
Chemical research in toxicology
The course of etoposide‐induced apoptosis in Jurkat cells lacking p53 and Bax
Etoposide-induced apoptosis in Jurkat cells involves DNA damage, Bid translocation, mitochondrial permeability transition, and cell death.
2006·57citations·N. Karpinich et al.·Journal of Cellular Physiology
Journal of Cellular Physiology
Mitochondrial localization and activity of P-glycoprotein in doxorubicin-resistant K562 cells.
P-glycoprotein is present and functional in mitochondria of doxorubicin-resistant K562 cells, potentially protecting the nucleus from doxorubicin.
2006·76citations·E. Munteanu et al.·Biochemical pharmacology
Biochemical pharmacology
Citations
Diastereomeric pure pyrazolyl-indolyl dihydrofurans: Unveiling isomeric selectivity in antibacterial action via in vitro and in silico insights.
Diastereomeric pure pyrazolyl-dihydrofurans show high inhibition of bacterial growth, but less antifungal activity compared to Fluconazole, offering potential for antibacterial agents.
2024·1citation·Hari Prakash et al.·Bioorganic & medicinal chemistry letters
Bioorganic & medicinal chemistry letters
New antiproliferative agents derived from tricyclic 3,4‐dihydrobenzo[4,5]imidazo[1,2‐a][1,3,5]triazine scaffold: Synthesis and pharmacological effects
BIT derivatives show promising antiproliferative activity against human colorectal adenocarcinoma and dermal microvascular endothelial cells, targeting the microtubule cytoskeleton.
2022·3citations·Marco Robello et al.·Archiv der Pharmazie
Archiv der Pharmazie
The Novel Synthesis of Functionalized Indenopyrazolones Using Fe 3 O 4 nanoparticles stabilized on MMT: An Efficient Magnetically Recoverable Heterogeneous Nanocomposite Catalyst
This eco-friendly method for synthesizing indenopyrazolones using MMT@Fe3O4 catalyst allows for quick, easy, and reusable reactions without hazardous solvents.
2019·8citations·Narges Hosseini Nasab et al.·Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry
4-(1,2-diarylbut-1-en-1-yl)isobutyranilide derivatives as inhibitors of topoisomerase II.
The new 4-(1,2-diarylbut-1-en-1-yl)isobutyranilide library shows potential as cytotoxic agents for human tumor cells, with the most active compound 6g inducing apoptosis and suggesting topoisomerase II as a potential intracellular target
2016·27citations·M. Christodoulou et al.·European journal of medicinal chemistry
European journal of medicinal chemistry
One-pot synthesis, biological evaluation, and docking study of new chromeno-annulated thiopyrano[2,3-c]pyrazoles
New chromeno-annulated thiopyrano[2,3-c]pyrazoles show potential as antibacterial, antifungal, and anti-oxidant compounds with potential anti-hypertensive activity.
2016·6citations·Bhagyashri D. Parmar et al.·Molecular Diversity
Molecular Diversity
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII.
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX, and XII, but no highly isoform-selective inhibition profiles.
2016·19citations·E. Barresi et al.·Bioorganic & medicinal chemistry
Bioorganic & medicinal chemistry
Synthesis and biological evaluation of pyrazolo-triazole hybrids as cytotoxic and apoptosis inducing agents.
Compounds 17, 23, and 29 show promising cytotoxicity against various cancer cell lines and induce apoptosis in U87MG cancer cells through mitochondrial pathway.
2015·63citations·T. Srinivasa Reddy et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Pyrazole scaffold: a remarkable tool in the development of anticancer agents.
Pyrazole scaffolds show promise in designing novel anticancer agents by targeting various receptors, offering potential for future cancer treatment research.
2013·164citations·Harish Kumar et al.·European journal of medicinal chemistry
European journal of medicinal chemistry
Synthesis, antiproliferative and mitochondrial impairment activities of bis-alkyl-amino transplatinum complexes.
Bis-alkyl-amino transplatinum complexes show antiproliferative activity against human tumor cells, with the most active complex 4 affecting mitochondrial functions and inducing mitochondrial permeability transition and membrane damage depending on concentration.
2013·18citations·L. Dalla Via et al.·Bioorganic & medicinal chemistry
Bioorganic & medicinal chemistry