Thiazoles
![Medchemexpress LLC 2,2'-[1,2-phenylenebis(oxy)]bis[N-phenyl-N-(phenylmethyl)acetamide] | 61595-77-5 | >98.0% | 556.65 | C36H32N2O4 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000222615.png-250.jpg)
Medchemexpress LLC 2,2'-[1,2-phenylenebis(oxy)]bis[N-phenyl-N-(phenylmethyl)acetamide] | 61595-77-5 | >98.0% | 556.65 | C36H32N2O4 | 5 MG
ETH 157 (Sodium ionophore II) is a neutral sodium (Na+) ionophore used in research to induce Na+/Ca2+ selectivity in membranes. It is employed in analytical chemistry and membrane electrode applications to selectively transport or detect sodium ions. Chemical formula C36H32N2O4; molecular weight 556.65; supplied as a solid.
Medchemexpress LLC 2,2'-(1,2-phenylenebis(oxy))bis(N-phenyl-N-(phenylmethyl)acetamide) | 61595-77-5 | MFCD00042979 | >98.0% | C36H32N2O4 | 10MG
ETH 157 (CAS 61595-77-5) is a sodium ionophore that induces Na+/Ca2+ selectivity in membranes. Supplied as a solid research chemical, it is intended for experimental modulation of sodium transport across lipid bilayers and other membrane studies. It exhibits high solubility in DMSO and has recommended cold storage for long-term stability.
- Sodium-selective ionophore for membrane transport studies.
- Induces Na+/Ca2+ selectivity in lipid membranes.
- High solubility in DMSO (100 mg/mL) with ultrasonic assistance.
- Stable as a powder when stored cold (powder: -20°C for long-term storage).
- Supplied in small research quantities suitable for laboratory use.
Medchemexpress LLC ETH 157 | 61595-77-5 | 556.65 | 50 MG
ETH 157 is a Na+ ionophore that induces a Na+/Ca2+ selectivity in membranes. It is intended for research use only.
- Na+ ionophore
- Induces Na+/Ca2+ selectivity in membranes
Medchemexpress LLC Carvacrol methyl ether | 6379-73-3 | 99.9% | 164.25 | C11H16O | 1 ML
Carvacrol methyl ether is a methyl ether derivative of carvacrol supplied as a research-grade reagent and analytical standard. It exhibits antibacterial activity and is available as a 10 mM solution in DMSO (1 mL) or as solids in multiple sizes for laboratory research purposes.
- Antibacterial activity observed in vitro.
- Available as 10 mM solution in DMSO (1 mL) and as solids (100 mg, 250 mg, 1 g, larger sizes on request).
- High purity (approximately 99.9%).
- Molecular formula C11H16O; molecular weight 164.25.
- Recommended storage: solids at -20°C (long term); solutions at -80°C for extended storage.
Medchemexpress LLC YTX-465 | 2225824-53-1 | 99.1% | 458.51 g·mol⁻1 | C25H26N6O3 | 10MG
YTX-465 is a small-molecule inhibitor of stearoyl-CoA desaturase (SCD) developed for research use in studies of lipid metabolism and neurodegenerative disease models. It shows activity against yeast Ole1 and human SCD1 and is supplied as a high-purity research chemical for biochemical and cell-based assays.
- Inhibits stearoyl-CoA desaturase (SCD) and yeast Ole1.
- Reported IC50: 0.039 μM (Ole1) and 30.4 μM (SCD1).
- High purity suitable for research applications.
- Molecular formula C25H26N6O3 and molecular weight 458.51 g·mol⁻1.
- Provided in milligram quantities for laboratory studies.
Medchemexpress LLC KL-11743 | 1369452-53-8 | 99.4% | C30H30N6O3 | 100 MG
KL-11743 is a potent, orally active, and glucose-competitive inhibitor of class I glucose transporters (GLUT1, GLUT2, GLUT3, and GLUT4), with IC50s of 115, 137, 90, and 68 nM respectively. It specifically blocks glucose metabolism and can synergize with electron transport inhibitors to induce cell death, additionally inducing cellular disulfidptosis by forming disulfide bonds in actin cytoskeletal proteins.
- Potent, orally active glucose-competitive inhibitor
- Inhibits class I glucose transporters (GLUT1, GLUT2, GLUT3, GLUT4)
- Blocks glucose metabolism
- Synergizes with electron transport inhibitors to induce cell death
- Induces cellular disulfidptosis
Aobchem (4-Chloro-2 6-difluorophenyl)methanol | ≥97% | CAS 252004-50-5 | C7H5ClF2O | 25g
(4-Chloro-2 6-difluorophenyl)methanol | ≥97% | CAS 252004-50-5 | C7H5ClF2O | 25g
Medchemexpress LLC 2,5-Dibromothiazole | 4175-78-4 | 99.9% | C3HBr2NS | 5 G
2,5-Dibromothiazole is a heterocyclic compound that serves as a key intermediate in organic synthesis. It is intended for research use only.
- Molecular weight of 242.92
- Appears as an off-white to yellow solid
- Store powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 6 months or -20°C for 1 month
- Soluble in DMSO at 100 mg/mL