Tyrosols and derivatives
![Medchemexpress LLC 6-[(aminocarbonyl)(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)-3-pyridinecarboxamide | 745833-23-2 | MFCD11616590 | 99.7% | 404.32 g/mol | C19H12F4N4O2 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000243608.png-250.jpg)
Medchemexpress LLC 6-[(aminocarbonyl)(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)-3-pyridinecarboxamide | 745833-23-2 | MFCD11616590 | 99.7% | 404.32 g/mol | C19H12F4N4O2 | 5 MG
VX-702 is a selective small-molecule inhibitor of p38α mitogen-activated protein kinase (MAPK) used in biochemical and cellular research to probe MAPK signaling and inflammatory pathways. It exhibits approximately 14-fold greater potency for p38α versus p38β and is provided as a high-purity research reagent.
- Selective inhibition of p38α with ~14-fold selectivity over p38β.
- High purity (≈99.7%), suitable for analytical and cellular studies.
- Solid form available in milligram quantities for research use.
- Compatible with common laboratory solvents (e.g., DMSO) for assay preparation.
- Recommended storage protocols support long-term stability of powder and solutions.
Sigma Aldrich Fine Chemicals Biosciences 4-ALLYL-2 6-DIMETHOXYPHENL 25G
NC3663646 4-ALLYL-2 6-DIMETHOXYPHENL 25G
Medchemexpress LLC Abt-702 dihydrochloride | 1188890-28-9 | 99.6% | 536.25 g/mol | C22H21BrCl2N6O | 50 MG
ABT-702 dihydrochloride is a potent, selective adenosine kinase (AK) inhibitor (IC50 = 1.7 nM) supplied as the dihydrochloride salt in solid form for laboratory research. The compound is reported with high purity and defined solubility and storage recommendations for in vitro and in vivo studies.
- Potent adenosine kinase inhibitor with IC50 of 1.7 nM.
- High purity reported at 99.64%.
- Solid dihydrochloride salt suitable for biochemical assays.
- Soluble in DMSO (≥ 33.33 mg/mL) and formulatable for in vivo dosing.
- Recommended sealed storage at 4°C; in solvent -80°C (6 months) or -20°C (1 month).
- Available in multiple pack sizes including 50 MG.
Apexbio Technology LLC VX-702 479543-46-9; 745833-23-2 200mg
VX-702 is a small-molecule inhibitor targeting p38 mitogen-activated protein kinase (MAPK) also known as MAPK14 It is designed to inhibit p38 MAPK thereby regulating cellular responses to cytokine signaling and various stressors VX-702 exerts its biological activity primarily through ATP-competitive inhibition In experimental models VX-702 demonstrates potent inhibition with reported IC50 values ranging from 4 to 20 nM Based on these pharmacological properties VX-702 holds research potential in the study of p38 MAPK-dependent pathways platelet storage lesions and renal excretion mechanisms
eMolecules Tetrahydrofurfuryl methacrylate | 2455-24-5 | MFCD00014515 | 25g
Combi-Blocks, Inc. | Tetrahydrofurfuryl methacrylate | 25g | 603138199 | QF-2521 | 95.000 | 2455-24-5 | MFCD00014515 | 170.208 | C9H14O3
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Cayman Chemical VerbascosIde 10mg
A natural phenylpropanoid glucoside; inhibits PKC (IC50 = 25 μM); inhibits the growth of Gram-positive and Gram-negative bacteria, including S. aureus and E. coli (MICs = 16 and 32 μg/ml, respectively); dose-dependently reduces extracellular hydrogen peroxide and increases cell viability of PC12 cells at 0.1-10 μg/ml following MPP+ administration to induce apoptosis and oxidative stress; dose-dependently inhibits the growth of MGC803 adenocarcinoma cells at 10-20 μM; reduces colon damage and the expression of TNF-α, IL-1β, and iNOS in a rat model of DNBS-induced colitis at 0.2-2 mg/kg
eMolecules (4-Ethoxyphenyl)hydrazine hydrochloride | 39943-51-6 | MFCD12403348 | 1g
Combi-Blocks, Inc. | (4-Ethoxyphenyl)hydrazine hydrochloride | 1g | 603148895 | QZ-2626 | 95.000 | 39943-51-6 | MFCD12403348 | 188.660 | C8H13ClN2O
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Medchemexpress LLC 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 500mg
(2 3-Dimethoxyphenyl)methanol is a drug impurity
Medchemexpress LLC 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 1mL
(2 3-Dimethoxyphenyl)methanol is a drug impurity
Sigma Aldrich Fine Chemicals Biosciences (±)-Metoprolol (+)-Tartrate Salt | 56392-17-7 | MFCD00056257 | 10g
(±)-Metoprolol (+)-Tartrate Salt | Purity: 98% | Mol Wt: 684.81 | 56392-17-7 | MFCD00056257 | 10g
Apexbio Technology LLC VX-702 479543-46-9; 745833-23-2 100mg
VX-702 is a small-molecule inhibitor targeting p38 mitogen-activated protein kinase (MAPK) also known as MAPK14 It is designed to inhibit p38 MAPK thereby regulating cellular responses to cytokine signaling and various stressors VX-702 exerts its biological activity primarily through ATP-competitive inhibition In experimental models VX-702 demonstrates potent inhibition with reported IC50 values ranging from 4 to 20 nM Based on these pharmacological properties VX-702 holds research potential in the study of p38 MAPK-dependent pathways platelet storage lesions and renal excretion mechanisms
Selleck Chemical LLC ABT 702 dihydrochloride
ABT-702 is a novel potent non-nucleoside Adenosine kinase inhibitor with an IC50 of 1 7 nM It has oral activity in animal models of pain and inflammation