Cinnamic acids and derivatives
![eMolecules N-(1-[4-(dimethylamino)phenyl]-3-{2-[(4-hydroxy-3-iodo-5-methoxyphenyl)methylidene]hydrazinyl}-3-oxoprop-1-en-2-yl)benzamide | ChemDiv SC |584.414 | C26H25IN4O4COc1cc(\C=N\NC(=O)C(\NC(=O)c2ccccc2)=C/c2ccc(cc2)N(C)C)cc(I)c1O | 2mg | 828451810](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC3733135.jpg-250.jpg)
eMolecules N-(1-[4-(dimethylamino)phenyl]-3-{2-[(4-hydroxy-3-iodo-5-methoxyphenyl)methylidene]hydrazinyl}-3-oxoprop-1-en-2-yl)benzamide | ChemDiv SC |584.414 | C26H25IN4O4COc1cc(\C=N\NC(=O)C(\NC(=O)c2ccccc2)=C/c2ccc(cc2)N(C)C)cc(I)c1O | 2mg | 828451810
N-(1-[4-(dimethylamino)phenyl]-3-{2-[(4-hydroxy-3-iodo-5-methoxyphenyl)methylidene]hydrazinyl}-3-oxoprop-1-en-2-yl)benzamide | ChemDiv SC |584.414 | C26H25IN4O4COc1cc(\C=N\NC(=O)C(\NC(=O)c2ccccc2)=C/c2ccc(cc2)N(C)C)cc(I)c1O | 2mg | 828451810
Selleck Chemical LLC AG 494
AG-494 a member of the tyrphostin family of tyrosine kinase inhibitors is a potent inhibitor of EGF receptor autophosphorylation (IC50 1 2 M) and EGF-dependent cell growth (IC50 6 M)
Medchemexpress LLC Tyrphostin AG 112 | 144978-82-5 | 98.3% | 236.23 | 25 MG
Tyrphostin AG 112 is an EGFR phosphorylation inhibitor intended for research use only. It inhibits EGFR in human A431 cells with an IC50 of 0.1 μM.
- EGFR phosphorylation inhibitor
- Inhibits EGFR in human A431 cells with an IC50 of 0.1 μM
- For research use only
- Appears as a light yellow to yellow solid
Medchemexpress LLC Entacapone | 130929-57-6 | MFCD00866580 | 99.2% | 305.29 g/mol | C14H15N3O5 | 5 MG
Entacapone (Standard) is an analytical reference standard of entacapone provided for research and analytical use. Supplied in small quantitative sizes suitable for assay development, method validation, and quality control, the product includes batch documentation and a Certificate of Analysis reporting high purity. It is used as a reference material in studies involving COMT inhibition and related biochemical assays.
- Analytical standard for assay development and method validation.
- Available in small sizes, including a 5 mg vial.
- Certified purity approximately 99.2% (COA available).
- Useful for quality control and reference material applications.
- Molecular formula C14H15N3O5; molecular weight 305.29 g/mol.
Medchemexpress LLC Tyrphostin AG1433 | 168835-90-3 | 99.1% | 1 ML
Tyrphostin AG1433 is a small-molecule tyrosine kinase inhibitor selective for PDGFRβ, supplied as a 10 mM solution in DMSO (1 mL) for research use. The compound has molecular formula C16H14N2O2 and molecular weight 266.29 g·mol⁻¹.
- Supplied as a 10 mM solution in DMSO, 1 mL.
- High purity (≈99.1%) suitable for biological research.
- Molecular formula C16H14N2O2; molecular weight 266.29 g·mol⁻¹.
- Also available as solid in multiple milligram quantities for custom preparations.
- For research use only; not for human or veterinary applications.
Apexbio Technology LLC Tyrphostin A1 2826-26-8 50mg
Tyrphostin A1 (CAS 2826-26-8) is a small molecule inhibitor targeting tyrosine kinase activity specifically involved in disrupting intracellular signaling pathways in immune cells It has been shown to interfere with CD40 ligand-induced signaling resulting in suppressed interleukin-12 (IL-12) secretion by macrophages and reduced differentiation of antigen-induced T helper 1 (Th1) cells Tyrphostin A1 is widely utilized in studies investigating cell-to-cell signaling immune response modulation and the mechanisms underlying inflammatory processes particularly in the context of autoimmune disease models
Medchemexpress LLC Tyrphostin AG 879 | 148741-30-4 | MFCD00236450 | 99.3% | 10 MG
Tyrphostin AG 879 is a small-molecule tyrosine kinase inhibitor widely used in laboratory research. It shows selectivity for ErbB2 (HER2) with a reported IC50 of about 1 μM and reduces TrkA phosphorylation at higher micromolar concentrations. The compound is supplied as a powder, is soluble in DMSO, and is intended for in vitro signaling and kinase pathway studies.
Apexbio Technology LLC Tyrphostin AG 1296 146535-11-7 10mM (in 1mL DMSO)
Tyrphostin AG 1296 (CAS 146535-11-7) is a selective inhibitor of platelet-derived growth factor receptor (PDGFR) kinase via ATP-competitive binding Its inhibitory activity (IC50 0 3 0 5 M) results from inducing conformational changes in the ATP-binding domain of PDGFR blocking receptor autophosphorylation induced by ligand binding In vitro studies demonstrate inhibition of PDGF-stimulated mitogenesis (IC50 1 5 M) and cell proliferation (IC50 3 2 M) using Swiss 3T3 cells without significant effects on EGF receptor signaling at concentrations up to 100 M Tyrphostin AG 1296 serves as a research tool for investigating PDGFR-mediated signaling pathways
Sigma Aldrich Fine Chemicals Biosciences Rivaroxaban R enantiomer U20MG
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Chem-Impex International, Inc. Curcumin | 458-37-7 | MFCD00008365 | 25G
Curcumin, 458-37-7, MFCD00008365, 25G
Medchemexpress LLC Cinnamamide | 621-79-4 | MFCD00008033 | 98.6% | 147.17 | C9H9NO | 1 ML
Cinnamamide (CAS 621-79-4) is an organic compound supplied as a 10 mM solution in a 1 mL vial for research use. It is used as a biochemical reagent in life-science studies, assay development, and synthetic chemistry applications.
- Ready-to-use 10 mM solution format.
- Convenient 1 mL vial for small-scale experiments.
- Suitable for biochemical and life-science research applications.
- Commonly used as a reference compound or substrate in assays.
- Reported high purity; verify exact specification on the SDS.