Quinolines and derivatives
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Filtered Search Results
Medchemexpress LLC Sulfur, [3-cyano-5-[[[2,4-dimethyl-5-[6-(3-pyridinyl)-1H-imidazo[1,2-b]pyrazol-1-yl]... | 1448316-08-2 | 99.9% | 558.53 g·mol⁻¹ | C26H19F5N6OS | 1 ML
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BAY-826 is a selective, potent small-molecule inhibitor of the TIE-2 kinase supplied for research use. It binds TIE-2 with high affinity (Kd ≈ 1.6 nM) and is provided as a 10 mM solution in DMSO (1 mL) or as solid quantities. Typical applications include biochemical kinase assays and cell-based studies of angiogenesis signaling pathways.
- Selective TIE-2 inhibition with Kd ≈ 1.6 nM.
- Available as 10 mM solution in DMSO (1 mL) and multiple solid sizes.
- High purity suitable for research applications.
- Molecular formula C26H19F5N6OS; molecular weight 558.53 g·mol⁻1.
- Soluble in DMSO for convenient assay preparation.
- Suitable for biochemical and cell-based assays targeting TIE-2 signaling.
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Medchemexpress LLC Veliparib | 912444-00-9 | MFCD16661059 | 244.29 g/mol | C13H16N4O | 200 MG
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Veliparib (ABT-888) is a small-molecule inhibitor of poly(ADP-ribose) polymerases used in research to probe DNA repair pathways and for chemosensitization studies. It is supplied as a solid for analytical and preclinical research and has documented storage recommendations for powder and solutions.
- Potent PARP1 and PARP2 inhibition (Ki 5.2 nM and 2.9 nM).
- Molecular formula C13H16N4O and molecular weight 244.29 g/mol.
- Identified by CAS number 912444-00-9.
- Supplied as a powder with recommended storage: -20°C (3 years) or 4°C (2 years).
- Stable in solvent when stored at -80°C (1 year) or -20°C (6 months).
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Selleck Chemical LLC Q-VD-Oph
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Q-VD-Oph (Quinoline-Val-Asp-Difluorophenoxymethylketone) is a potent pan-caspase inhibitor with IC50 ranged from 25 to 400 nM for caspases 1 3 8 and 9 Q-VD-OPh can inhibits HIV infection
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Apexbio Technology LLC Oxymatrine 16837-52-8 200mg
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Oxymatrine (CAS 16837-52-8) is a quinolizidine alkaloid extracted from Sophora flavescens It has been shown to modulate multiple cellular pathways associated with fibrosis and neurodegeneration including inhibition of TGF- 1-mediated signaling and reduction of pro-inflammatory cytokine expression Oxymatrine exhibits antifibrotic and neuroprotective properties in various experimental models It is also extensively studied for its antiviral activity against hepatitis B virus and has been applied in traditional Chinese medicine for hepatitis management This compound is valuable for investigating mechanisms of fibrosis neuroprotection and viral pathogenesis
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Apexbio Technology LLC Emodin 518-82-1 200mg
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Emodin (518-82-1) is a small-molecule inhibitor targeting casein kinase 2 (CK2) and the interaction between SARS coronavirus spike protein and angiotensin-converting enzyme 2 (ACE2) It is designed to block protein protein interactions and enzyme activity thereby modulating viral entry and kinase-mediated signaling Emodin exerts its biological activity primarily through inhibition of CK2 and disruption of spike ACE2 binding In hepatocellular carcinoma cell models (Hep3B HepG2 Huh7) emodin demonstrates antiproliferative activity with IC50 values of 66 9 M in Hep3B 74 36 M in HepG2 and 101 5 M in Huh7 cells Based on these pharmacological properties emodin holds research potential in cancer inflammation metabolic disorders and viral infection models
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Medchemexpress LLC 3,7,4'-Trihydroxyflavone | 2034-65-3 | 99.4% | 270.24 | 1 ML
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3,7,4'-Trihydroxyflavone, also known as 5-Deoxykampferol, is a flavonoid compound isolated from the stems of Rhus javanica var. roxburghiana. It exhibits anti-inflammatory and antioxidant properties by scavenging various reactive oxygen species (ROS) and reactive nitrogen species (RNS), and can also cleave DNA in the presence of copper ions.
- Isolated from natural sources like Rhus javanica var. roxburghiana.
- Functions as an anti-inflammatory agent.
- Possesses antioxidant activities.
- Capable of scavenging reactive oxygen and nitrogen species.
- Can cleave DNA when copper ions are present.
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Medchemexpress LLC Matrine | 519-02-8 | 98.0% | 248.37 | 200 MG
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Matrine (Matridin-15-one) is an alkaloid found in plants of the *Sophora* genus. It acts as an agonist for kappa opioid receptor and u-receptor, and exhibits a range of pharmacological properties, including anti-cancer, anti-oxidative stress, anti-inflammatory, and anti-apoptosis effects. It holds potential for research into diseases such as human non-small cell lung cancer, hepatoma, papillary thyroid cancer, and acute kidney injury (AKI).
- Acts as a kappa opioid receptor and u-receptor agonist.
- Demonstrates anti-cancer effects.
- Possesses anti-oxidative stress properties.
- Exhibits anti-inflammatory effects.
- Has anti-apoptosis effects.
- Potential for research in human non-small cell lung cancer, hepatoma, papillary thyroid cancer, and acute kidney injury (AKI).
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eMolecules 383907-43-5 | Medchem Express | NSC 663284 | 2mg | 446254896 | HY-100034 | MFCD08276924 | 321.76 | C15H16ClN3O3
Ambeed | 4-Bromo-25-dichlorobenzoic acid | 250mg | 525031901 | A128739 | 885532-41-2 | MFCD08444534 | 269.900 | C7H3BrCl2O2
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Apexbio Technology LLC CP 339818 hydrochloride 50mg
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CP 339818 hydrochloride (CAS 478341-55-8) is a small-molecule antagonist targeting the Kv1 3 potassium channel It is designed to selectively inhibit Kv1 3-mediated ion conductance thereby modulating T-cell activation CP 339818 hydrochloride exerts its biological activity primarily through stabilization of the Kv1 3 channel s C-type inactivation state In in vitro studies CP 339818 hydrochloride demonstrates potent inhibition of Kv1 3 channels with an IC50 value of approximately 200 nM Based on these pharmacological properties CP 339818 hydrochloride holds research potential in the investigation of immune modulation mechanisms relevant to autoimmune and inflammatory disorders
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Apexbio Technology LLC CAY10505 1218777-13-9 200mg
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CAY10505 is a small-molecule inhibitor targeting phosphatidylinositol 3-kinase gamma (PI3K ) It is designed to selectively inhibit PI3K thereby modulating cellular processes governed by the PI3K/Akt/mTOR signaling pathway CAY10505 exerts its biological activity primarily through inhibition of PI3K In cultured neuron studies CAY10505 demonstrates inhibition of baicalein-induced Akt phosphorylation with an IC50 value of approximately 30 nM Based on these pharmacological properties CAY10505 holds research potential in neuroscience cardiovascular biology and cancer biology studies
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Medchemexpress LLC (1E)-CFI-400437 dihydrochloride | 1247000-76-5 | 98.0% | 565.49 | 5 MG
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(1E)-CFI-400437 dihydrochloride is a potent PLK4 inhibitor with high selectivity. It also inhibits Aurora A, Aurora B, KDR, and FLT-3, demonstrating antiproliferative activity. This compound has shown effectiveness in a mouse xenograft model of tumor growth.
- Potent PLK4 inhibitor with IC50 of 0.6 nM
- Selective against other PLK family members
- Inhibits Aurora A, Aurora B, KDR, and FLT-3
- Exhibits antiproliferative activity
- Effective in mouse xenograft models of tumor growth
- Plasma protein binding is 99%
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Medchemexpress LLC SRI 6409-94 | 127697-58-9 | 99.3% | 379.49 | 1 ML
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SRI 6409-94 is an orally active Ro 13-6298 analogue that is teratogenic. It serves as a molecular tool to study the effect of the three-dimensional configuration of retinol on teratogenic activity.
- Causes virgin female outbred Syrian golden hamsters to produce deformed offspring in a dose-dependent manner.
- Leads to significant reductions in mean fetal body weight and in the numbers of ossified skeletal districts.
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Medchemexpress LLC Scopoletin | 92-61-5 | MFCD00006872 | 99.9% | 192.17 | 200 MG
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Scopoletin is an inhibitor of acetylcholinesterase (AChE). This compound is used in research to study its effects on cellular processes, including proliferation and apoptosis in various cell lines, and its impact on cognitive functions in animal models.
- Enhances K+-stimulated release of ACh from rat frontal cortex synaptosomes.
- Inhibits PC3 proliferation by inducing apoptosis of PC3 cells.
- Increases T-maze alternation and ameliorates scopolamine-induced cholinergic deficit and age-associated deficits in object memory in mice.
- Available as solid or solution formulations in various quantities.
- For research use only.
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Selleck Chemical LLC FLI-06
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FLI-06 is a novel inhibitor of Notch signaling with EC50 of 2 3 M
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Apexbio Technology LLC TDZD-8 327036-89-5 200mg
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TDZD-8 (CAS 327036-89-5) is a selective non-ATP competitive inhibitor of glycogen synthase kinase 3 (GSK-3 ) exhibiting an IC50 of 1 4 M In addition to GSK-3 TDZD-8 also inhibits protein kinase C isoforms PKC I and PKC with IC50 values of 1 4 M and 1 1 M respectively Cellular studies have demonstrated that TDZD-8 suppresses both GSK-3 and PKC activity leading to reduced photodynamic therapy-induced neuronal necrosis and glial cell apoptosis Furthermore TDZD-8 has been shown to exert anti-leukemic effects in primary human leukemia cell models possibly through dual inhibition of PKC and FLT3 highlighting its utility in studies related to neuroprotection and leukemia
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