Pyridines and derivatives
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- (1)
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Filtered Search Results
Medchemexpress LLC ZSET1446 | 887603-94-3 | 98.01% | 236.27 | 1 MG
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ZSET1446 | 887603-94-3 | 98.01% | 236.27 | 1 MG
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Cayman Chemical 8iso Prostaglandin E2d4
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An internal standard for the quantification of 8-iso PGE2 by GC- or LC-MS
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Cayman Chemical AG879 Inhibitors
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A tyrphostin compound that inhibits nerve growth factor (NGF)-dependent TrkA tyrosine phosphorylation in PC-12 cells (IC50 = ~40μM), HER2-ErbB2 kinase in several breast and ovarian cancer cell lines (IC50 = ~0.5 μM), and the VEGF receptor FLK1 (IC50 = ~1 μM)
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Medchemexpress LLC JGB1741 | 1256375-38-8 | 99.4% | 440.56 | 10 MG
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JGB1741 is a potent and specific SIRT1 activity inhibitor with an IC50 of approximately 15 μM, demonstrating weaker inhibition against SIRT2 and SIRT3 with IC50 values greater than 100 μM. This compound increases acetylated p53 levels, leading to p53-mediated apoptosis through the modulation of Bax/Bcl2 ratio, cytochrome c release, and PARP cleavage. It shows potential for breast cancer research, inhibiting MDA-MB 231 cell proliferation more potently than K562 and HepG2 cells. JGB1741 induces apoptosis and cell cycle arrest at the G1 phase in MDA-MB 231 cells, causing a dose-dependent increase in global acetylation of H3K9, p53 expression, and acetylated p53K382 levels in these cells.
- Potent and specific SIRT1 activity inhibitor.
- Increases acetylated p53 levels.
- Induces apoptosis and cell cycle arrest.
- Causes a dose-dependent increase in global acetylation.
- Potential for breast cancer research.
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Medchemexpress LLC 5-(hydroxymethyl)furfural | 67-47-0 | MFCD00003234 | 126.11 g/mol | C6H6O3 | 10mg
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5-Hydroxymethylfurfural (Standard) is the analytical standard of 5-Hydroxymethylfurfural This product is intended for research and analytical applications 5-Hydroxymethylfurfural (2-Hydroxymethyl-5-furfural) derived from Cornus officinalis inhibits yeast growth and fermentation as stressors
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Medchemexpress LLC Exatecan intermediate 12 | 110351-93-4 | C15H17NO6 | 5 G
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Exatecan intermediate 12 is a chemical substance used in laboratory research and for the manufacture of other substances. This solid compound has a molecular weight of 307.30 and is classified with acute oral toxicity, skin and serious eye irritation, and may cause respiratory irritation. Proper handling and storage are crucial for safety and stability.
- Harmful if swallowed
- Causes skin irritation
- Causes serious eye irritation
- May cause respiratory irritation
- Stable under recommended storage conditions
- Recommended storage: -20°C for 3 years (powder), 4°C for 2 years (powder)
- Avoid inhalation, contact with eyes and skin
- Use in areas with appropriate exhaust ventilation
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Medchemexpress LLC Epi-inositol | 488-58-4 | MFCD00272608 | >=98.0% | 180.16 g/mol | C6H12O6 | 25 MG
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Epi-inositol (CAS 488-58-4) is an inositol isomer supplied as an analytical standard for research and analytical applications. It is offered in small pack sizes for laboratory use and is commonly used as a reference compound in biochemical and analytical assays.
- Analytical standard for research and analytical applications.
- High purity suitable for HPLC (≥98.0%).
- Available in small laboratory pack sizes (for example, 5-100 mg).
- Suitable as a reference standard in chromatographic and spectroscopic analyses.
- Provided as a solid for routine handling and storage.
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Medchemexpress LLC Padsevonil | 1294000-61-5 | 99.7% | 432.80 | 10 MG
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Padsevonil (UCB0942) is a potent antiepileptic agent that selectively acts on presynaptic and postsynaptic targets. It binds to synaptic vesicular protein 2 (SV2) with high affinity and is also a positive allosteric modulator and partial agonist of GABAAR, showing high potency against α1 and α5 receptors.
- Regulates GABAAR activity through allosteric sites on the receptor in CHO cells.
- Enhances natural GABAAR activity in primary rat neurons.
- Has protective effects on mouse models of acute epilepsy.
- Shows a protective effect in a rodent model of chronic epilepsy.
- Significantly decreased hippocampal paroxysmal discharges dose-dependently in kainate treated male mice.
- Produced dose-related suppression in the cumulative duration of spontaneous spike and wave discharges in platinum electrodes treated male Wistar rats.
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eMolecules 1121586-37-5 | 4-Bromo-2,6-dichloropyridin-3-amine | Combi-Blocks | MFCD12546348 | 241.900 | C5H3BrCl2N2 | 97.000 | Nc1c(Br)cc(Cl)nc1Cl | 1g | 401043174
4-Bromo-2,6-dichloropyridin-3-amine | Combi-Blocks | 1121586-37-5 | MFCD12546348 | 241.900 | C5H3BrCl2N2 | 97.000 | Nc1c(Br)cc(Cl)nc1Cl | 1g | 401043174
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Medchemexpress LLC Rhapontigenin | 500-65-2 | 1 ML
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Rhapontigenin, a natural analog of resveratrol, exhibits anticancer, antioxidant, antifungal, and antibacterial activities. It acts as a mechanism-based, potent, and selective cytochrome P450 1A1 inactivator with an IC50 of 400 nM, demonstrating high selectivity over P450 1A2 and P450 1B1.
- Anticancer, antioxidant, antifungal, and antibacterial properties
- Potent, selective cytochrome P450 1A1 inactivator (IC50 = 400 nM)
- 400-fold selectivity for P450 1A1 over P450 1A2, 23-fold over P450 1B1
- Molecular weight: 258.27; Formula: C15H14O4; Appearance: Solid, light yellow to yellow; Purity: 99.66%
- Source: Plants (Leguminosae, Trigonella foenum-graecum Linn.)
- Inhibits ADP- and collagen-induced platelet aggregation
- Demonstrates in vivo anti-thrombosis activity
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Medchemexpress LLC Leucine-rich repeat-containing protein 15, human recombinant (Fc tag) | >95.0% | 100 UG
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Recombinant human LRRC15 extracellular domain fused to a C-terminal human Fc tag, expressed in HEK293 cells and supplied as a purified protein for biochemical and cell-based assays. The construct corresponds to residues Y22-G538 and is provided with >95% purity; store frozen and aliquot to avoid freeze-thaw.
- Fc-tagged extracellular domain for detection and capture assays.
- Expressed in HEK293 cells for mammalian glycosylation.
- High purity (>95.0%) as determined by reducing SDS-PAGE.
- Construct corresponds to residues Y22-G538 (extracellular domain).
- Recommended storage: aliquot and freeze at -20°C or -80°C.
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Medchemexpress LLC Xanthotoxol | 2009-24-7 | 99.5% | 202.16 | 100 MG
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Xanthotoxol (8-Hydroxypsoralen) is a fragrant bean substance and a CYP450 inhibitor. It exhibits anti-inflammatory, and 5-HT antagonistic and protective effects. Xanthotoxol inhibits CYP3A4 and CYP1A2 with IC50s of 7.43 μM and 27.82 μM, respectively. It can pass through MAPK and NF-κB pathways, inhibiting inflammation.
- Fragrant bean substance
- CYP450 inhibitor
- Anti-inflammatory effects
- 5-HT antagonistic and protective effects
- Inhibits CYP3A4 and CYP1A2
- Acts through MAPK and NF-κB pathways to inhibit inflammation
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eMolecules 1185-53-1 | Tri(hydroxymethyl)aminomethane hydrochloride | AA Blocks LLC | MFCD00012590 | 157.590 | C4H12ClNO3 | 0.000 | Cl.NC(CO)(CO)CO | 25g | 410203698
Tri(hydroxymethyl)aminomethane hydrochloride | AA Blocks LLC | 1185-53-1 | MFCD00012590 | 157.590 | C4H12ClNO3 | 0.000 | Cl.NC(CO)(CO)CO | 25g | 410203698
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Alkali Scientific Methotrexate, 100 Milligrams
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Methotrexate, 100mg, is a laboratory-grade reagent used in research applications to study its effects on cancer, autoimmune diseases, and cellular processes. It is a folic acid antagonist that inhibits the enzyme dihydrofolate reductase, thereby blocking DNA and RNA synthesis, which leads to cell death. Methotrexate is frequently used in cell culture studies, drug testing, and cancer research. The 100mg quantity is ideal for smaller-scale research, providing sufficient material for experiments investigating its cytotoxic effects, as well as its role in targeting rapidly dividing cells in tumor tissues.
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Medchemexpress LLC Fludarabine | 21679-14-1 | 99.7% | C10H12FN5O4 | 25 MG
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Fludarabine is a DNA synthesis inhibitor and a fluorinated purine analogue, exhibiting antineoplastic activity in lymphoproliferative malignancies. It inhibits cytokine-induced activation of STAT1 and STAT1-dependent gene transcription in normal resting or activated lymphocytes.
- Acts as a DNA synthesis inhibitor
- Functions as a fluorinated purine analogue
- Exhibits antineoplastic activity in lymphoproliferative malignancies
- Inhibits cytokine-induced activation of STAT1 and STAT1-dependent gene transcription
- Induces a decrease in p27kip1 expression in vitro
- Decreases incidence of graft-versus-host disease in animal models
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