Tyrosols and derivatives
Cayman Chemical VerbascosIde 25mg
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
Medchemexpress LLC Abt-702 dihydrochloride | 1188890-28-9 | MFCD03452809 | 99.6% | 536.25 g·mol-1 | C22H21BrCl2N6O | 10 MG
ABT-702 dihydrochloride is the dihydrochloride salt of ABT-702, a potent non-nucleoside adenosine kinase (AK) inhibitor (reported IC50 = 1.7 nM). It is provided as a solid research reagent for biochemical assays, pharmacological studies, and in vivo models involving adenosine metabolism and signaling.
- Potent adenosine kinase inhibitor with reported IC50 = 1.7 nM.
- Dihydrochloride salt form for improved handling and stability.
- Molecular weight 536.25 g·mol-1; formula C22H21BrCl2N6O.
- High purity (≈99.6%) suitable for research applications.
- Supplied in small-scale quantities for laboratory use (typical 10 mg).
- Commonly used in enzyme inhibition assays and in vivo pharmacology studies.
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 N-(4-Hydroxyphenyl)methacrylamide | 19243-95-9 | MFCD00080530 | 25g
Combi-Blocks | N-(4-Hydroxyphenyl)methacrylamide | 25g | 457917540 | QD-1907 | 98.000 | 19243-95-9 | MFCD00080530 | 177.203 | C10H11NO2
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Medchemexpress LLC (3,4-Dimethoxyphenyl)hydrazine (hydrochloride) | 40119-17-3 | 204.66 | 1 G
(3,4-Dimethoxyphenyl)hydrazine (hydrochloride) is a chemical compound primarily used as a drug intermediate for the synthesis of various active compounds. It is provided as a high-purity solid.
- Purity of 99.8%
- Appearance as a light brown to gray solid
- Molecular formula C8H13ClN2O2
- Molecular weight 204.66
- Store at 4°C under nitrogen
- When in solvent, store at -80°C for 6 months or -20°C for 1 month under nitrogen
Medchemexpress LLC VX-702 50mg | 745833-23-2 | 50MG
VX-702 is a highly selective inhibitor of p38 MAPK 14-fold higher potency against the p38 versus p38 [1