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Phenylpropaniods are organic compounds characterized by having an aromatic ring and a three-carbon propene tail. Polyketides are compounds characterized by having two or more carbonyl functional groups connected with a single carbon atom.
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Tyrphostin 9 is a selective inhibitor targeting platelet-derived growth factor receptor (PDGFR) and epidermal growth factor receptor (EGFR) It inhibits PDGFR autophosphorylation with an IC50 of approximately 2 5 M and EGFR kinase activity (IC50 around 460 M) Additionally Tyrphostin 9 inhibits platelet-derived growth factor (PDGF)-stimulated smooth muscle cell proliferation (IC50 approximately 40 nM) as well as phosphorylation of phospholipase C gamma (PLC IC50 2 5 M) and induction of PDGF-dependent c-fos expression In research models Tyrphostin 9 has been utilized to study receptor-mediated signal transduction and vascular injury-related neointimal proliferation processes
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(4E)-7-(4-hydroxyphenyl)-1-phenylhept-4-en-3-one (CAS 100667-52-5) is a diarylheptanoid research chemical used as a biochemical reagent for laboratory studies. It appears as a white to off-white solid and is characterized by molecular formula C19H20O2 and a molecular weight of 280.4 g/mol. The compound is provided in small research-scale quantities for analytical, assay, and synthetic applications.
High purity (>98.0%).
Accurate molecular formula C19H20O2.
Suitable for assay and analytical use in research settings.
Supplied in small milligram package sizes for laboratory workflows.
Includes standard structural identifiers for cheminformatics (SMILES, InChIKey).
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool<|a>
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Tyrphostin AG-528 (Tyrphostin B66) is a potent inhibitor of epidermal growth factor receptors (EGFR) and ErbB2/HER2 with IC50 of 4 9 M and 2 1 M respectively Tyrphostin AG-528 exhibits anticancer activity
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Tyrphostin A1 (AG9) inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells. It is for research use only.
Inhibits CD40L-stimulated IL-12 production in macrophage cultures
Decreases IL-12 p40 production in a dose-dependent manner
Blocks CD40L-induced translocation of NF-κB to the nucleus
Reduces activation of IL-12 p40 gene
Leads to a decrease in the generation of myelin basic protein (MBP) specific encephalitogenic T cells in vivo therapy
Attenuates experimental allergic encephalomyelitis (EAE) in SJL/J mice
Weaker inhibitor of TK compared to other tyrphostins, useful for differentiating TK-mediated effects
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Tyrphostin A1 inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells. It causes a dose-dependent decrease of IL-12 p40 and blocks CD40L-induced translocation of NF-κB to the nucleus, reducing activation of the IL-12 p40 gene. This compound is a weaker inhibitor of TK, often used to differentiate TK-mediated effects from other non-specific effects.
Inhibits CD40L-stimulated IL-12 production
Reduces antigen-induced generation of Th1 cells
Blocks CD40L-induced translocation of NF-κB to the nucleus
Attenuates experimental allergic encephalomyelitis (EAE) in SJL/J mice
Useful for differentiating TK-mediated effects from non-specific effects
For research use only
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Curcumin 5-8 is a potent and orally active natural curcumin analog. It inhibits lipid droplet formation, increases autophagy, and inhibits apoptosis. It also improves insulin resistance and insulin sensitivity.
Inhibits lipid droplet formation.
Increases autophagy.
Inhibits apoptosis.
Improves insulin resistance.
Improves insulin sensitivity.
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Entacapone sodium salt (CAS 1047659-02-8) is a nitrocatechol small molecule that acts as a selective and reversible inhibitor of catechol-O-methyltransferase (COMT) a Mg2 -dependent enzyme involved in the metabolism of catecholamines and related compounds In biochemical assays entacapone exhibits an IC50 of 20 1 nM and a Ki of 10 7 nM for COMT inhibition The presence of a nitro group ortho to the hydroxyl group in its structure contributes to its inhibitory potency Entacapone has been widely used in research focused on Parkinson s disease particularly to study the modulation of levodopa bioavailability and pharmacokinetics
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Tyrphostin AG 528 is a small-molecule protein tyrosine kinase inhibitor used as a research reagent for biochemical and cellular studies targeting EGFR and ErbB2. It is supplied as a solid with high purity and defined storage recommendations for long-term stability.
Small-molecule inhibitor selective for EGFR and ErbB2.
Reported IC50: EGFR 4.9 μM, ErbB2 2.1 μM.
High purity (98.0%) suitable for preclinical research.
Solid, light yellow to yellow appearance for easy handling.
Molecular weight 306.32 and formula C18H14N2O3 for characterization.
Available in small pack sizes for screening and assay development.
Recommended storage: powder at -20°C (3 years) or 4°C (2 years).
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Also available in 1 mL, 1 mg, 2 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes.SAR405 (R enantiomer) is the less active form of SAR405, an inhibitor of PIK3C3/Vps34. Purity 98.04%
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Also available in 5 mg 10 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Polyinosinic-polycytidylic acid (Poly(IC)) is a synthetic double-stranded RNA (dsRNA) analog and is an immunostimulant that acts as the most potent interferon (IFN) inducer. It also is a Toll-like receptor- 3 (TLR3) agonist. purity: 98%
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Tyrphostin 9 is a selective inhibitor targeting platelet-derived growth factor receptor (PDGFR) and epidermal growth factor receptor (EGFR) It inhibits PDGFR autophosphorylation with an IC50 of approximately 2 5 M and EGFR kinase activity (IC50 around 460 M) Additionally Tyrphostin 9 inhibits platelet-derived growth factor (PDGF)-stimulated smooth muscle cell proliferation (IC50 approximately 40 nM) as well as phosphorylation of phospholipase C gamma (PLC IC50 2 5 M) and induction of PDGF-dependent c-fos expression In research models Tyrphostin 9 has been utilized to study receptor-mediated signal transduction and vascular injury-related neointimal proliferation processes
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3-Methylcinnamic acid is a drug intermediate for the synthesis of various active compounds. This product is intended for research use only and is not sold to patients. It typically appears as a white to off-white solid.
Drug intermediate for synthesis of various active compounds
For research use only
Appears as a white to off-white solid
Molecular weight of 162.19
Powder storage: -20°C for 3 years or 4°C for 2 years
In solvent storage: -80°C for 6 months or -20°C for 1 month
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