Tyrosols and derivatives
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
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.
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%
TARGETMOL CHEMICALS INC VX-702 10MG
Also available in 25mg 50mg and bulk. Please contact Fisher for quotes. VX-702 is a highly specific p38α MAPK inhibitor 14-fold higher selectivity for the p38α than p38β. VX-702 is a small molecule investigational oral anti-cytokine therapy for treatment of inflammatory diseases specifically rheumatoid arthritis (RA). purity: 99%
Apexbio Technology LLC Verbascoside 61276-17-3 10mg
Verbascoside (CAS 61276-17-3) is a small-molecule inhibitor targeting protein kinase C (PKC) and the NF- B signaling pathway It is designed to modulate these pathways thereby regulating signal transduction and transcriptional activity in cellular responses Verbascoside exerts its biological activity primarily through the inhibition of PKC and suppression of NF- B DNA-binding activation In cell-based studies Verbascoside demonstrates inhibitory activity with an IC50 value of approximately 4 8 M in RANKL-treated RAW264 7 cells and bone marrow macrophages (BMMs) Based on these pharmacological properties Verbascoside holds research potential in the investigation of PKC/NF- B-mediated signaling osteoclastogenesis and related cell signaling mechanisms
Sigma Aldrich Fine Chemicals Biosciences 4-ALLYL-2 6-DIMETHOXYPHENL 25G
NC3663646 4-ALLYL-2 6-DIMETHOXYPHENL 25G
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
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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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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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
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%
Medchemexpress LLC 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 1mL
(2 3-Dimethoxyphenyl)methanol is a drug impurity
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.
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