Tyrosols and derivatives
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.
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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eMolecules Metoprolol tartrate | 56392-17-7 | MFCD00056257 | 1g
Combi-Blocks, Inc. | Metoprolol tartrate | 1g | 603140349 | QV-1764 | 95.000 | 56392-17-7 | MFCD00056257 | 684.824 | C34H56N2O12
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![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.
Medchemexpress LLC 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 500mg
(2 3-Dimethoxyphenyl)methanol is a drug impurity
TARGETMOL CHEMICALS INC VERBASCOSIDE 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Verbascoside (Kusaginin) is a protein kinase C inhibitor with antimicrobial anti-inflammatory activities. purity: 97%
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
Selleck Chemical LLC Verbascoside S5458-1mg
Verbascoside (Acteoside Kusaginin) a phenylpropanoid glycoside from lemon verbena has several biological properties such as anti-inflammatory antimicrobial antitumor and antioxidant
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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TARGETMOL CHEMICALS INC ABT-702 DIHYDROCHLORIDE 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor. purity: 98%
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.
Medchemexpress LLC 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 1mL
(2 3-Dimethoxyphenyl)methanol is a drug impurity
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
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