Material Feeders
Medchemexpress LLC ZD-0892 | 171964-73-1 | 95.0% | 499.52 | 100 MG
ZD-0892 is a selective and potent inhibitor of a neutrophil elastase with Kis of 6.7 and 200 nM for human neutrophil elastase and porcine pancreatic elastase, respectively. It is intended for research use only and not sold to patients.
- Reduces myocardial elastolytic activity and coronary microvascular perfusion injury in DBA/2 mice infected with EMC virus.
- Decreases pathologic severity of myocardial lesions associated with murine viral myocarditis.
- Can reverse advanced pulmonary vascular disease in rats.
Medchemexpress LLC ZD-4190 1mg | 1mg
ZD-4190 is a potent orally available inhibitor of the vascular endothelial cell growth factor receptor 2 (VEGFR2) and of epidermal growth factor receptor (EGFR) signalling used for the treatment of cancer
![Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000365551-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 1 MG
ZD 2138 is a selective 5-lipoxygenase inhibitor, suitable for research in areas such as asthma. This product is provided as an off-white to light yellow solid with a high purity.
- High purity: 99.9% (LCMS)
- Off-white to light yellow solid appearance
- Consistent with chemical structure (1H NMR, LCMS)
- Suitable for research use
Medchemexpress LLC N-(4-methoxybenzoyl)-L-valyl-N-(trifluoro-oxopentan-3-yl)pyrrolidine-2-carboxamide | 171964-73-1 | 95.0% | 499.5 g/mol | C24H32F3N3O5 | 10 MG
ZD-0892 is a small-molecule, selective inhibitor of neutrophil elastase with reported Ki values of 6.7 nM for human neutrophil elastase and 200 nM for porcine pancreatic elastase. It is supplied as a research-grade reagent (purity 95%) and is used in biochemical and enzymatic studies to probe elastase-dependent pathways.
- Selective inhibition of human neutrophil elastase (Ki ~6.7 nM).
- Also inhibits porcine pancreatic elastase (Ki ~200 nM).
- Suitable for biochemical and enzymatic assays.
- Provided at research-grade purity for reproducible results.
- Small-molecule compound with molecular weight approximately 499.5 g/mol.
Medchemexpress LLC ZD-4190 10mg | 10mg
ZD-4190 is a potent orally available inhibitor of the vascular endothelial cell growth factor receptor 2 (VEGFR2) and of epidermal growth factor receptor (EGFR) signalling used for the treatment of cancer
Apexbio Technology LLC ZD 7288(Synonyms: ZD7288, Zatebradine hydrochloride, HCN channel inhibitor ZD7288), 50mg, CAS: 133059-99-1.
ZD 7288 (CAS 133059-99-1) is a selective inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels These channels mediate Na and K currents notably the hyperpolarization-activated current (I h) contributing to neuronal excitability and rhythmic activity ZD 7288 reduces I h in a concentration-dependent voltage- and time-sensitive manner as demonstrated in rat facial motoneurons (IC 50 0 2 M) and hippocampal CA1 pyramidal neurons Additionally it inhibits T-type calcium currents in rat CA1 pyramidal cells ZD 7288 is utilized in research investigating neuronal excitability mechanisms pain signaling and chronic visceral pain models
Cayman Chemical ANTIBODY ZD 7288 50mg
A potent blocker of HCN channels that inhibits HCN4 more potently than HCN1 (IC50s = 32 and 158 nM, respectively); modulates the sinoatrial node and slows heart rate; reduces neuropathic pain in several animal models
Medchemexpress LLC ZD-0892 | 171964-73-1 | 95.0% | 499.52 | 25 MG
ZD-0892 is a selective and potent inhibitor of neutrophil elastase. It exhibits high affinity for human neutrophil elastase and porcine pancreatic elastase, making it suitable for targeted research.
- Selective and potent inhibitor of neutrophil elastase
- Suitable for in vitro and in vivo studies
- Available in solid form for various research needs
- Backed by scientific publications for its applications
Apexbio Technology LLC ZD 7288(Synonyms: ZD7288, Zatebradine hydrochloride, HCN channel inhibitor ZD7288), 25mg, CAS: 133059-99-1.
ZD 7288 (CAS 133059-99-1) is a selective inhibitor of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels These channels mediate Na and K currents notably the hyperpolarization-activated current (I h) contributing to neuronal excitability and rhythmic activity ZD 7288 reduces I h in a concentration-dependent voltage- and time-sensitive manner as demonstrated in rat facial motoneurons (IC 50 0 2 M) and hippocampal CA1 pyramidal neurons Additionally it inhibits T-type calcium currents in rat CA1 pyramidal cells ZD 7288 is utilized in research investigating neuronal excitability mechanisms pain signaling and chronic visceral pain models
Medchemexpress LLC ZD 7155 hydrochloride | 146709-78-6 | MFCD00921888 | 99.9% | 475.0 g/mol | C26H27ClN6O | 1 ML
ZD 7155 hydrochloride is a selective, nonpeptide antagonist of the angiotensin II type 1 (AT1) receptor supplied as a 10 mM solution in a 1 mL vial for research use. It blocks AT1-mediated signaling in pharmacology and physiological studies and is provided with batch-specific purity data (COA).
- Selective AT1 receptor antagonist useful for receptor pharmacology studies.
- Supplied as a 10 mM solution for direct use in assays.
- Provided with certificate of analysis and batch purity information.
- Available in multiple pack sizes for assay scale flexibility.
![Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000366030-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 25 MG
ZD 2138 is a chemical compound identified by CAS No. 140841-32-3. It has a molecular formula of C23H24FNO4 and a molecular weight of 397.44. This compound is typically an off-white to light yellow solid with a high purity of 99.9%.
- Chemical name: 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl-
- Molecular formula: C23H24FNO4
- Molecular weight: 397.44
- Purity: 99.9%
- Appearance: Off-white to light yellow solid
- Storage (powder): -20°C for 3 years; 4°C for 2 years
- Storage (in solvent): -80°C for 6 months; -20°C for 1 month
![Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000365616-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl- | 140841-32-3 | 99.9% | 397.44 | 10 MG
ZD 2138 is identified as 2(1H)-Quinolinone, 6-[[3-fluoro-5-(tetrahydro-4-methoxy-2H-pyran-4-yl)phenoxy]methyl]-1-methyl-. It has a molecular formula of C23H24FNO4 and a molecular weight of 397.44. This compound is typically an off-white to light yellow solid with a high purity of 99.9% confirmed by LCMS.
- High purity (99.9%) confirmed by LCMS.
- Consistent structure verified by 1H NMR spectrum.
- Available as an off-white to light yellow solid.
- Stable for extended periods under specified storage conditions.
- For research use only.
Medchemexpress LLC ZD-4190 10mM 1mL | 1mL
ZD-4190 is a potent orally available inhibitor of the vascular endothelial cell growth factor receptor 2 (VEGFR2) and of epidermal growth factor receptor (EGFR) signalling used for the treatment of cancer