Tyrosols and derivatives
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
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
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%
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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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 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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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
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 2,3-dimethoxybenzyl alcohol | 5653-67-8 | MFCD00004612 | 500mg
(2 3-Dimethoxyphenyl)methanol is a drug impurity
Apexbio Technology LLC Verbascoside 61276-17-3 50mg
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
Medchemexpress LLC 6-(N-carbamoyl-2,6-difluoroanilino)-2-(2,4-difluorophenyl)pyridine-3-carboxamide | 745833-23-2 | MFCD11616590 | 99.7% | 404.32 g/mol | C19H12F4N4O2 | 100 MG
VX-702 is a small-molecule research inhibitor selective for the p38α isoform of mitogen-activated protein kinase (MAPK). It is used to probe MAPK signaling and inflammatory cytokine production in preclinical and cellular studies. The compound is supplied as a powder with high reported purity and documented potency against p38α.