Organonitrogen Compounds
Medchemexpress LLC Allantoin | 97-59-6 | MFCD00005260 | 158.12 | 5 G
Allantoin is a widely recognized skin conditioning agent that supports healthy skin and stimulates new tissue growth. It exhibits anti-oxidative and anti-inflammatory properties, and has been observed to attenuate apoptosis and cytotoxicity, enhancing the viability of STZ-induced β-cells in a dose-dependent manner. Additionally, allantoin decreases caspase-3 levels, boosts phosphorylated B-cell lymphoma 2 (Bcl-2) expression, and activates imidazoline 3 (I3) receptors.
- Skin conditioning agent
- Promotes healthy skin and new tissue growth
- Exhibits anti-oxidative and anti-inflammatory activities
- Attenuates apoptosis and cytotoxicity
- Increases viability of STZ-induced β-cells
- Activates imidazoline 3 (I3) receptors
eMolecules 1280786-87-9 | 1-Bromo-3-chloro-5-piperidinobenzene | Combi-Blocks | MFCD18783174 | 274.590 | C11H13BrClN | 96.000 | Clc1cc(Br)cc(c1)N1CCCCC1 | 1g | 117543871
1-Bromo-3-chloro-5-piperidinobenzene | Combi-Blocks | 1280786-87-9 | MFCD18783174 | 274.590 | C11H13BrClN | 96.000 | Clc1cc(Br)cc(c1)N1CCCCC1 | 1g | 117543871
Medchemexpress LLC (S)-Nimodipine | 77940-93-3 | 418.44 | 5 MG
(S)-Nimodipine ((S)-BAY-e 9736) is an enantiomer of Nimodipine. Nimodipine (BAY-e 9736) is an orally active, well-tolerated, and light-sensitive dihydropyridine calcium antagonist. It can be used for the research of cerebrovascular disorders.
- Target: Calcium channel
- Pathway: Membrane transporter/ion channel; neuronal signaling
- 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
- Solubility in vitro: DMSO: 100 mg/mL (238.98 mM; requires ultrasonic)
eMolecules 106263-50-7 | Ambeed | 4-(2-Chlorophenyl)-4-oxobutanoic acid | 1g | 528955790 | A415168 | MFCD03844205 | 212.63 | C10H9ClO3
Ambeed | 4455-Tetramethyl-2-(3-(triphenylen-2-yl)phenyl)-132-dioxaborolane | 1g | 600848856 | A844373 | 1115639-92-3 | MFCD28130383 | 430.350 | C30H27BO2
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![Medchemexpress LLC Pyrrolo[3,4-b]pyrrole-5(1H)-carboxamide, N-[4-[(3-ethynylphenyl)amino]-7-methoxy-6-quinazolinyl] | 1353644-70-8 | 99.7% | 442.51 g/mol | C25H26N6O2 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000243817.png-250.jpg)
Medchemexpress LLC Pyrrolo[3,4-b]pyrrole-5(1H)-carboxamide, N-[4-[(3-ethynylphenyl)amino]-7-methoxy-6-quinazolinyl] | 1353644-70-8 | 99.7% | 442.51 g/mol | C25H26N6O2 | 50 MG
Theliatinib is a potent, ATP-competitive, orally active, and highly selective epidermal growth factor receptor (EGFR) inhibitor provided for research use in preclinical biochemical and cell-based studies.
- Potent ATP-competitive EGFR inhibitor with low-nanomolar activity.
- High chemical purity (99.72%).
- Molecular weight 442.51 g/mol; formula C25H26N6O2.
- Soluble in DMSO (~1 mg/mL) with recommended warming and pH adjustment.
- Stable when stored under recommended powder and solution conditions.
- Suitable for studies of wild-type and mutant EGFR signaling.
Medchemexpress LLC Bathocuproine disulfonate disodium | 52698-84-7 | MFCD00011679 | 99.5% | 564.54 g·mol⁻¹ | C26H18N2Na2O6S2 | 500 MG
Bathocuproine disulfonate disodium (BCS) is a water-soluble, sulfonated phenanthroline derivative that selectively chelates Cu(I) and is used as a colorimetric and spectrophotometric reagent to detect and quantify copper ions in biochemical and analytical assays. Supplied as a solid with high stated purity, it is intended for laboratory analytical applications.
- Selective chelator for copper(I) ions.
- Water-soluble sulfonated phenanthroline derivative.
- High purity suitable for analytical assays.
- Off-white to light brown solid form.
- Store at 4°C, protect from light, and under nitrogen for stability.
Medchemexpress LLC 3-pyridylamide oxime | 1594-58-7 | >98.0% | 137.14 g·mol⁻¹ | C6H7N3O | 50 G
3-Pyridylamide oxime is a pyridine-derived amidoxime used as a synthetic intermediate in pharmaceutical and organic chemistry. It is provided as a solid research reagent and is used for building heterocycles, introducing amidoxime functionality, and advancing medicinal chemistry workflows.
- Chemical identity: pyridine-based amidoxime (C6H7N3O), CAS 1594-58-7.
- Molecular weight 137.14 g·mol⁻¹.
- High purity suitable for synthesis (>98% typical).
- Useful for medicinal chemistry and pharmaceutical intermediate synthesis.
- Supplied as a solid, compatible with common organic solvents.
- Available in multiple pack sizes to support small-scale and scale-up work.
eMolecules 313655-45-7 | 2-(2-Hydroxyethoxy)-benzonitrile | Combi-Blocks | MFCD09743449 | 163.176 | C9H9NO2 | 98.000 | OCCOc1ccccc1C#N | 1g | 117556045
2-(2-Hydroxyethoxy)-benzonitrile | Combi-Blocks | 313655-45-7 | MFCD09743449 | 163.176 | C9H9NO2 | 98.000 | OCCOc1ccccc1C#N | 1g | 117556045
eMolecules 655239-64-8 | 5,6,7,8-Tetrahydroquinolin-3-ol | Combi-Blocks, Inc. | MFCD13178913 | 149.193 | C9H11NO | 95.000 | Oc1cnc2CCCCc2c1 | 1g | 586071513
5,6,7,8-Tetrahydroquinolin-3-ol | Combi-Blocks, Inc. | 655239-64-8 | MFCD13178913 | 149.193 | C9H11NO | 95.000 | Oc1cnc2CCCCc2c1 | 1g | 586071513
Medchemexpress LLC β-catenin-IN-2 | 1458664-10-2 | 99.6% | C15H14FN3 | 10MG
β-catenin-IN-2 (Compound H1B1) is a small-molecule inhibitor of β-catenin intended for preclinical research, particularly studies of colorectal cancer and Wnt/β-catenin signaling. The compound is characterized by CAS 1458664-10-2, molecular formula C15H14FN3, molecular weight 255.29, and is supplied with analytical documentation for research use.
- Potent β-catenin inhibitor suitable for cellular and biochemical assays.
- Reported applicability in colorectal cancer research.
- High purity (99.6%) for reliable experimental results.
- Characterized with COA, HNMR, and LCMS data available.
- Small-molecule properties: molecular weight 255.29, formula C15H14FN3.