Aminophenols
Cayman Chemical N-formyl-2-AmInophenol 100mg
A bacterial secondary metabolite with antioxidant activity; scavenges DPPH radicals in a cell-free assay (IC50 = 3.23 UG/ml); has been used in the synthesis of compounds with antibacterial and antifungal activities
Medchemexpress LLC PF-8380 hydrochloride | 2070015-01-7 | 98.6% | 514.79 g/mol | C22H22ClN2O5S | 5 MG
PF-8380 hydrochloride is a small-molecule autotaxin (ATX) inhibitor supplied as a research reagent. It demonstrates potent inhibition in isolated enzyme assays and measurable activity in human whole blood, and is intended for laboratory research use only.
- Potent autotaxin inhibitor; IC50 2.8 nM in isolated enzyme assay.
- Active in human whole blood with IC50 ~101 nM.
- Molecular weight 514.79 g/mol and formula C22H22ClN2O5S.
- High purity (98.6%), suitable for biochemical and cellular assays.
- Available in small research pack sizes (1 mg, 5 mg, 10 mg).
- Intended for research use only; not for human or veterinary use.
Medchemexpress LLC LDC4297 hydrochloride | 2319747-14-1 | MFCD34676707 | 98.2% | 468.98 | C23H29ClN8O | 5 MG
LDC4297 hydrochloride is a small-molecule research reagent that selectively inhibits cyclin-dependent kinase 7 (CDK7). Supplied as the hydrochloride salt for laboratory use only, it is intended for cell-signaling and antiviral research and is available in both solid and solution formats.
- Selective CDK7 inhibition for target-specific studies.
- Suitable for in vitro cell-based assays and mechanistic studies.
- Available in multiple sizes including small solid quantities and DMSO solution.
- High purity suitable for research applications.
- Supplied as the hydrochloride salt for improved stability and solubility.
Medchemexpress LLC LDC4297 hydrochloride | 2319747-14-1 | 98.23% | 100 MG
LDC4297 hydrochloride is a selective inhibitor of CDK7 with an IC50 value of 0.13 nM. It inhibits human cytomegalovirus (HCMV) replication with an EC50 value of 24.5 nM. This compound demonstrates broad antiviral activities against various viruses, including Herpesviridae, Adenoviridae, Poxviridae, Retroviridae, and Orthomyxoviridae, with EC50 values ranging from 0.02-1.21 μM. LDC4297 hydrochloride is suitable for infection research.
- Selective CDK7 inhibitor (IC50: 0.13 nM)
- Inhibits human cytomegalovirus (HCMV) replication (EC50: 24.5 nM)
- Exhibits broad antiviral activities against various viruses (EC50: 0.02-1.21 μM)
- Useful for infection research
Medchemexpress LLC RS 67333 hydrochloride | 168986-60-5 | MFCD00938576 | 99.7% | 389.36 g/mol | C19H30Cl2N2O2 | 1 ML
RS 67333 hydrochloride is a research reagent that functions as a potent, selective partial agonist of the 5-HT4 (serotonin 4) receptor. It is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and in multiple solid pack sizes for use in pharmacology and neuroscience studies, including neuroprotection and Alzheimer's disease research. CAS: 168986-60-5; purity ~99.7%.
- Potent, selective 5-HT4 receptor partial agonist.
- Offered as 10 mM solution in DMSO (1 mL) and multiple solid sizes.
- High listed purity (~99.7%).
- Suitable for pharmacology and neuroscience research applications.
- Provided with datasheet, certificate of analysis, and safety data sheet.
Medchemexpress LLC Benzyltriethylammonium chloride | 56-37-1 | MFCD00011824 | ≥98.0% | 227.77 g·mol⁻¹ | C13H22ClN | 1000g
Benzyltriethylammonium chloride is a quaternary ammonium salt commonly used as a phase transfer catalyst surfactant and stabilizer in various chemical reactions especially in organic synthesis Benzyltriethylammonium chloride has unique chemical properties that facilitate the transfer of ions or molecules from one phase to another making it an important ingredient in a variety of industrial processes
Aobchem 2 4-Di-tert-butylphenol | ≥95% | CAS 96-76-4 | C14H22O | 500g
2 4-Di-tert-butylphenol | ≥95% | CAS 96-76-4 | C14H22O | 500g
TARGETMOL CHEMICALS INC TC-S 7005 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. TC-S 7005 is an effective inhibitor of Polo-like kinases (IC50s 214 nM 4 nM and 24 nM for Plk1 Plk2 and Plk3). purity: 99%
eMolecules 548-39-0 | Ambeed | Perinaphthenone | 250mg | 721954378 | A849159 | MFCD00004143 | 180.206 | C13H8O
Ambeed | Perinaphthenone | 250mg | 721954378 | A849159 | 548-39-0 | MFCD00004143 | 180.206 | C13H8O
TARGETMOL CHEMICALS INC ZM 226600 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ZM 226600 is an ATP-sensitive potassium channel opener with an EC50 value of 500 nM. ZM226600 has an inhibitory effect on spontaneous bladder activity. purity: 100%
Ambeed 2 1HImidazol4yl ethan1amine di
2-(1H-Imidazol-4-yl)ethan-1-amine dihydrochloride, 56-92-8, 98%