Acrylic acids and derivatives
eMolecules Medchem Express / Inulicin / 1mg / 572597006 / HY-N0896 / / 33627-41-7 / MFCD30207877 / 308.374 / C17H24O5
Medchem Express / Inulicin / 1mg / 572597006 / HY-N0896 / / 33627-41-7 / MFCD30207877 / 308.374 / C17H24O5
Medchemexpress LLC Mivotilate (standard) | 130112-42-4 | 99.6% | 330.45 g/mol | C12H14N2O3S3 | 25 MG
Mivotilate is a research-grade small-molecule activator of the aryl hydrocarbon receptor (AhR) with reported hepatoprotective activity. It is supplied as a purified analytical standard for laboratory use and is intended for in vitro research and analytical applications.
- Potent, nontoxic activator of the aryl hydrocarbon receptor.
- Reported hepatoprotective activity in preclinical studies.
- High purity suitable for analytical and research use.
- Molecular weight 330.45 g/mol; formula C12H14N2O3S3.
- Available in small, research-oriented pack sizes.
Medchemexpress LLC Mivotilate | 130112-42-4 | MFCD02752797 | 99.6% | 330.45 g/mol | C12H14N2O3S3 | 100 MG
Mivotilate is a small-molecule activator of the aryl hydrocarbon receptor (AhR) with reported hepatoprotective activity. Provided as a research reagent and analytical standard, it is supplied as a solid and as a DMSO solution for biochemical and cell-based assays.
- Activates aryl hydrocarbon receptor (AhR).
- Described as nontoxic in supplier literature.
- High purity (99.6%).
- Molecular weight 330.45 g/mol.
- Available as solid and DMSO solution for flexibility in use.
- Suitable for biochemical and in vitro studies.
eMolecules Medchem Express / PD150606 / 5mg / 446255688 / HY-100529 / / 179528-45-1 / MFCD00949076 / 306.120 / C9H7IO2S
Medchem Express / PD150606 / 5mg / 446255688 / HY-100529 / / 179528-45-1 / MFCD00949076 / 306.120 / C9H7IO2S
Enzo Life Sciences Ro 48-8071 (50mg). CAS: 189197-69-1
Inhibits cholesterol biosynthesis at the level of 2,3-oxidosqualene cyclase (OSC). Blocks OSC and cholesterol synthesis in HepG2 cells in the nanomolar range. A novel lipid lowering agent. Purity: ≥95% (HPLC). Solubility: Soluble in water (25 mg/ml). Long Term Storage: Ambient.
![Strem, An Ascensus Company CAS 521272-85-5. 500mg. (2R3R)-(-)-23-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(15-cyclooctadiene)rhodium(I) tetrafluoroborate min. 97% (RR)-NORPHOS-Rh. MFCD09839137](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00009818-45-0184.JPG-250.jpg)
Strem, An Ascensus Company CAS 521272-85-5. 500mg. (2R3R)-(-)-23-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(15-cyclooctadiene)rhodium(I) tetrafluoroborate min. 97% (RR)-NORPHOS-Rh. MFCD09839137
CAS 521272-85-5. 500mg. (2R3R)-(-)-23-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(15-cyclooctadiene)rhodium(I) tetrafluoroborate min. 97% (RR)-NORPHOS-Rh. MFCD09839137. Molecular Weight 760.39. Molecular Formula [Rh(C8H12)(C31H28P2)]BF4ae. Color/form red-orange pwdr. Strem 45-0184. http//www.strem.com/catalog/v/45-0184/
Medchemexpress LLC MAX-40279 hemifumarate | 2388506-43-0 | 99.6% | C22H23FN6OS·1/2C4H4O4 | 10MG
MAX-40279 hemifumarate is a small-molecule research inhibitor that targets FLT3 and FGFR kinases. It is orally active and retains activity against clinically relevant FLT3 mutants (for example, D835Y), making it suitable for studies of kinase inhibitor resistance and acute myelogenous leukemia (AML) signaling. It also inhibits NDRG1 phosphorylation at Ser330 and suppresses endothelial-to-mesenchymal transition (EndMT).
- Dual FLT3 and FGFR kinase inhibition
- Orally active and effective against FLT3 mutants such as D835Y
- Useful for AML research and studies of inhibitor resistance
- Inhibits NDRG1 phosphorylation at Ser330 and suppresses EndMT
- High purity (~99.6%) and fully characterized chemical properties
eMolecules Medchem Express / Barnidipine (hydrochloride) / 10mg / 482203872 / HY-107322 / / 104757-53-1 / MFCD00915772 / 528.000 / C27H30ClN3O6
Medchem Express / Barnidipine (hydrochloride) / 10mg / 482203872 / HY-107322 / / 104757-53-1 / MFCD00915772 / 528.000 / C27H30ClN3O6
eMolecules Medchem Express / Manidipine (dihydrochloride) / 50mg / 446268343 / HY-17403 / / 89226-75-5 / MFCD00896434 / 683.630 / C35H40Cl2N4O6
Medchem Express / Manidipine (dihydrochloride) / 50mg / 446268343 / HY-17403 / / 89226-75-5 / MFCD00896434 / 683.630 / C35H40Cl2N4O6
eMolecules Medchem Express / ()-Praeruptorin A / 5mg / 495801769 / HY-N0081 / / 73069-25-7 / MFCD23105643 / 386.400 / C21H22O7
Medchem Express / ()-Praeruptorin A / 5mg / 495801769 / HY-N0081 / / 73069-25-7 / MFCD23105643 / 386.400 / C21H22O7
Medchemexpress LLC Rilmenidine (hemifumarate) | 207572-68-7 | 99.8% | 238.28 g/mol | C10H16N2O · 1/2 C4H4O4 | 10 MG
Rilmenidine hemifumarate is an orally active research compound that selectively agonizes I1 imidazoline receptors and α2-adrenoceptors. It is used in cellular studies to induce autophagy and modulate apoptotic pathways, and is supplied as a high-purity solid for laboratory research.
- Selective I1 imidazoline receptor and α2-adrenoceptor agonist.
- Reported to induce autophagy and affect mitochondrial apoptosis pathways in cell models.
- High-purity solid suitable for research applications.
- Stable when stored under recommended conditions (solid: -20°C; in solution: -80°C or -20°C as specified).
- Supplied in small research pack sizes for experimental use.
eMolecules AstaTech / 2-CHLOROETHYL ACRYLATE / 1g / 718059713 / F20423 / 95.000 / 2206-89-5 / MFCD00045292 / 134.560 / C5H7ClO2
AstaTech / 2-CHLOROETHYL ACRYLATE / 1g / 718059713 / F20423 / 95.000 / 2206-89-5 / MFCD00045292 / 134.560 / C5H7ClO2