Isothiocyanates
Medchemexpress LLC N-(4-Cyanophenyl)glycine | 42288-26-6 | 100.0% | C9H8N2O2 | 500 G
N-(4-Cyanophenyl)glycine is a Glycine derivative presented as a white to off-white solid, intended solely for research applications. This amino acid derivative is recognized for its commercial use as an ergogenic supplement. It influences the secretion of anabolic hormones, supports fuel supply during exercise, enhances mental performance during stress-related tasks, and aids in preventing exercise-induced muscle damage.
- Glycine derivative
- Used as an ergogenic supplement
- Influences secretion of anabolic hormones
- Supplies fuel during exercise
- Enhances mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
- Solid, white to off-white appearance
- For research use only
eMolecules 3326-32-7 | Fluorescein isothiocyanate isomer I | Ochem Incorporation | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 5g | 773137908
Fluorescein isothiocyanate isomer I | Ochem Incorporation | 3326-32-7 | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 5g | 773137908
eMolecules 3326-32-7 | Fluorescein isothiocyanate isomer I | Ochem Incorporation | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 0.25g | 773137906
Fluorescein isothiocyanate isomer I | Ochem Incorporation | 3326-32-7 | MFCD00005063 | 389.380 | C21H11NO5S | 96.000 | Oc1ccc2c(Oc3cc(O)ccc3C22OC(=O)c3cc(ccc23)N=C=S)c1 | 0.25g | 773137906
Apexbio Technology LLC Tempo 2564-83-2 100mg
Tempo (CAS 2564-83-2) is a stable nitroxide radical widely employed in biomedical research for its redox-active properties It facilitates the dismutation of superoxide radicals thereby modulating mitochondrial reactive oxygen species (ROS) levels and influencing cellular oxidative stress responses Tempo also serves as an oxidation catalyst particularly in the transformation of primary alcohols to aldehydes Studies indicate that Tempo exerts both antioxidant and mutagenic effects inducing DNA strand breaks and displaying cytotoxic and mutagenic activities in in vitro models such as murine lymphoma cells It is utilized for investigating oxidative stress redox regulation and chemical mutagenesis