Organic nitroso compounds
Cayman Chemical 5-NItroso-8-quInolInol 10mg
An HDAC inhibitor, antitumor agent that at 10 μM can induce oxidative stress contributing to apoptosis and differentiation in MCF-7 breast cancer cells; inhibits T. gondii tachyzoite propagation in human fibroblasts (EC50 = 80 nM) and inhibits P. falciparum growth in human red blood cells (EC50 = 1.3 μM)
Sigma Aldrich Fine Chemicals Biosciences N-Nitrosodiethylamine Phar1G
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards
Medchemexpress LLC (R)-PR-924 | 98.5% | 618.72 | 1 ML
(R)-PR-924 is an isomer of PR-924, which is a selective tripeptide epoxyketone immunoproteasome subunit LMP-7 inhibitor with an IC50 of 22 nM. It can be used as an experimental control. PR-924 covalently modifies proteasomal N-terminal threonine active sites, inhibits growth, and triggers apoptosis in multiple myeloma (MM) cells, also exhibiting antitumor activities.
- Used as an experimental control
- Selective tripeptide epoxyketone immunoproteasome subunit LMP-7 inhibitor
- Covalently modifies proteasomal N-terminal threonine active sites
- Inhibits growth and triggers apoptosis in multiple myeloma (MM) cells
- Exhibits antitumor activities
eMolecules 886766-60-5 | tert-Butyl 2-phenylpiperazine-1-carboxylate | Ambeed | MFCD07367734 | 262.353 | C15H22N2O2 | 98.000 | CC(C)(C)OC(=O)N1CCNCC1c1ccccc1 | 5g | 601097515
tert-Butyl 2-phenylpiperazine-1-carboxylate | Ambeed | 886766-60-5 | MFCD07367734 | 262.353 | C15H22N2O2 | 98.000 | CC(C)(C)OC(=O)N1CCNCC1c1ccccc1 | 5g | 601097515
Medchemexpress LLC N-Nitroso-N-methylurea | 684-93-5 | 103.08 | 5 G
N-Nitroso-N-methylurea is a potent carcinogen, mutagen, and teratogen. It functions as a direct-acting alkylating agent, interacting with DNA, and is known to target multiple animal organs, potentially leading to various cancers or degenerative diseases. This compound also serves as a precursor in the synthesis of diazomethane. It is a flammable solid intended for laboratory use in the manufacture of substances and is stable under recommended storage conditions.
- Functions as a direct-acting alkylating agent
- Interacts with DNA
- Targets multiple animal organs
- Leads to various cancers and/or degenerative diseases
- Precursor in the synthesis of diazomethane
- Used in animal modeling to construct tumor models
Medchemexpress LLC N-Nitroso-3-azabicyclo[3.3.0]octane-d4 | 1346604-35-0 | 95.0% | C7H8D4N2O | 100 MG
N-Nitroso-3-azabicyclo[3.3.0]octane-d4 is the deuterium labeled N-Nitroso-3-azabicyclo[3.3.0]octane. It is for research use only and not intended for human use. Deuterium labeled compounds can be used as tracers or internal standards for quantitative analysis by methods like NMR, GC-MS, or LC-MS. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Cayman Chemical N-NItroso SarcosIn 250mg
A carcinogen; induces the formation of metastatic liver carcinomas in mice at 225 mg/kg
Cayman Chemical 5-NItroso-8-quInolInol 50mg
An HDAC inhibitor, antitumor agent that at 10 μM can induce oxidative stress contributing to apoptosis and differentiation in MCF-7 breast cancer cells; inhibits T. gondii tachyzoite propagation in human fibroblasts (EC50 = 80 nM) and inhibits P. falciparum growth in human red blood cells (EC50 = 1.3 μM)
Medchemexpress LLC N-Nitroso-N-methylurea | 684-93-5 | 99.7% | 103.08 | 2 G
N-Nitroso-N-methylurea is a potent carcinogen, mutagen, and teratogen. It acts as a direct-acting alkylating agent that interacts with DNA, targeting multiple animal organs to cause various cancers and/or degenerative diseases. It is also a precursor in the synthesis of diazomethane.
- Potent carcinogen, mutagen, and teratogen
- Direct-acting alkylating agent that interacts with DNA
- Targets multiple animal organs to cause various cancers and/or degenerative diseases
- Precursor in the synthesis of diazomethane
- For research use only
Cayman Chemical N-NItroso FluoxetIn 10mg
A derivative of fluoxetine; genotoxic to S. typhimurium at 0.06-0.12 mg/ml
Medchemexpress LLC TANDSOPIRONE 50.0MG
Tandospirone /SM-3997/ is a potent and selective 5-HT1A receptor partial agonist with a Ki of 27 nM. Tandospirone has anxiolytic and antidepressant activities. Tandospirone can be used for the research of the central nervous system disorders and the underlying mechanisms.For research use only.
World Precision Instrument SNAP S-Nitroso-N-acetyl-D-penicillamine-SNAP50
SNAP is a stable green crystalline S-nitrosothiol compound that mimics the action of nitric oxide in vivo. It has vasodilatory properties and has been shown to relax isolated bovine coronary artery rings by activating soluble granulate cyclase. This reagent also actuates apoptosis in mouse thymocytes and has been accounted for reversible inactivation of protein Kinase C. SNAP can be used for calibration of all WPI NO sensors. Call for details. M.W. 220.2, Purity > 98% by NMR or TLC.