Aminophenols
eMolecules 1965304-99-7 | 2-(3-Tolyl)-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | MFCD28166217 | 267.350 | C16H13NOS | 97.000 | Cc1cccc(c1)-c1nc(cs1)-c1ccccc1O | 1g | 537706226
2-(3-Tolyl)-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | 1965304-99-7 | MFCD28166217 | 267.350 | C16H13NOS | 97.000 | Cc1cccc(c1)-c1nc(cs1)-c1ccccc1O | 1g | 537706226
eMolecules 78546-66-4 | 2-Acetamido-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | MFCD00665950 | 234.270 | C11H10N2O2S | 97.000 | CC(=O)Nc1nc(cs1)-c1ccccc1O | 5g | 537706006
2-Acetamido-4-(2-hydroxyphenyl)thiazole | Oakwood Chemical | 78546-66-4 | MFCD00665950 | 234.270 | C11H10N2O2S | 97.000 | CC(=O)Nc1nc(cs1)-c1ccccc1O | 5g | 537706006
Medchemexpress LLC NNC 92-1687 10mM 1mL | 22903-37-3 | 300.33 g·mol⁻¹ | C15H12N2O3S | 1 ML
NNC 92-1687 is a non-peptide competitive antagonist of the human glucagon receptor (GCGR) used as a research tool for studies of glucose homeostasis and type 2 diabetes. It shows IC50 = 20 μM and Ki = 9.1 μM and is supplied as a 10 mM solution in DMSO (1 mL) or as a solid.
- Non-peptide competitive glucagon receptor antagonist
- Reported IC50 of 20 μM and Ki of 9.1 μM
- Molecular formula C15H12N2O3S and molecular weight 300.33 g·mol⁻¹
- Available as 10 mM solution in DMSO (1 mL) and in multiple solid sizes
- HPLC purity approximately 98.7%
- Storage: solid at room temperature (up to 3 years); in solvent at -80°C (2 years) or -20°C (1 year)
Medchemexpress LLC Verbenalin | 548-37-8 | 388.37 | 5 MG
Verbenalin is an orally active terpenoid glycoside extracted from the medicinal plant *Verbena officinalis*. It exhibits anti-inflammatory, antiviral, and neuroprotective effects. It binds strongly to the nsp-12 protein of the SARS-CoV-2 virus and is used in research for inflammatory and nervous system diseases such as hepatitis and Alzheimer's disease.
- Orally active terpenoid glycoside
- Exhibits anti-inflammatory effects
- Exhibits antiviral effects
- Exhibits neuroprotective effects
- Binds strongly to nsp-12 protein of SARS-CoV-2 virus
- Used in research for inflammatory diseases
- Used in research for nervous system diseases
- Purity: 99.90%
- Appearance: Solid
- Color: White to off-white
- For research use only
Medchemexpress LLC A-350619 hydrochloride | 1217201-17-6 | ≥99.0% | 425.41 g/mol | C21H25ClN2OS·HCl | 10 MG
A-350619 hydrochloride is a small-molecule soluble guanylate cyclase (sGC) activator used in preclinical research. It enhances cGMP production by activating basal sGC and synergizing with nitric oxide, producing vasodilatory effects such as cavernosum smooth muscle relaxation and increased blood flow in animal models. The material is supplied as a hydrochloride salt for improved solubility.
- High purity suitable for in vitro and in vivo studies.
- Soluble hydrochloride salt with good DMSO and aqueous solubility.
- Activates soluble guanylate cyclase and enhances NO-mediated signaling.
- Demonstrated vasodilatory and penile erection effects in rodent models.
- Store at 4°C to maintain stability.
Aobchem 2-Chloroethanamine hydrochloride | ≥95% | CAS 870-24-6 | C2H7Cl2N | 500g
2-Chloroethanamine hydrochloride | ≥95% | CAS 870-24-6 | C2H7Cl2N | 500g
Medchemexpress LLC Bepridil hydrochloride | 68099-86-5 | MFCD00065498 | 99.8% | 403.0 g/mol | C24H35ClN2O | 25 MG
Bepridil hydrochloride is a non-selective calcium channel blocker with antianginal activity, commonly used in cardiovascular and ion channel research to study calcium-mediated cardiac effects. The compound is provided as the hydrochloride salt (CAS 68099-86-5) with molecular formula C24H35ClN2O and molecular weight 403.0 g/mol.
- Non-selective calcium channel blocker used in cardiac and ion channel studies.
- Useful for investigating calcium-dependent electrophysiology and myocardial contractility.
- Hydrochloride salt form enhances solubility for assay preparation.
- Intended for in vitro and ex vivo research applications.
- Well-characterized chemical identifiers: CAS 68099-86-5; molecular formula C24H35ClN2O; molecular weight 403.0 g/mol.