Organic disulfides
Cambridge Isotope Laboratories Dicyclohexyl phthalate (unlabeled) 100 ug/mL in nonane 1 2 mL
Dicyclohexyl phthalate (unlabeled) 100 ug/mL in nonane 1 2 mL
Medchemexpress LLC Captopril disulfide | 64806-05-9 | MFCD08063643 | 99.3% | 432.55 g/mol | C18H28N2O6S2 | 25MG
Captopril disulfide is a metabolite and disulfide dimer of captopril that exhibits antihypertensive activity. It is supplied as a research-grade analytical standard for laboratory use, suitable for biochemical assays, metabolic studies, and analytical reference work. Store solid material at 4°C protected from light; in solution, store at -80°C (up to 6 months) or -20°C (up to 1 month).
- Research-grade analytical standard with documented antihypertensive activity.
- Purity 99.3%.
- Chemical formula C18H28N2O6S2.
- Molecular weight 432.55 g/mol.
- CAS number 64806-05-9.
- Storage: solid at 4°C, protected from light; in solution at -80°C (up to 6 months) or -20°C (up to 1 month).
Medchemexpress LLC NX-2127 | 2416131-46-7 | C39H45N9O5 | 200 MG
Zelebrudomide (NX-2127) is an orally active PROTAC degrader targeting Bruton's Tyrosine Kinase (Btk). It effectively inhibits proliferation of BTKC481S mutant TMD8 cells and catalyzes degradation of Ikaros (IKZF1) and Aiolos (IKZF3). It also stimulates T cell activation and increases IL-2 production.
- Orally active PROTAC degrader.
- Targets Bruton's tyrosine kinase (Btk).
- Inhibits BTKC481S mutant TMD8 cell proliferation (EC50 <30 nM).
- Catalyzes Ikaros (IKZF1) and Aiolos (IKZF3) degradation.
- Stimulates T cell activation; increases IL-2 production.
- Potent BTK degradation in cynomolgus monkeys in vivo.
- Superior tumor growth inhibition in WT TMD8 and C481S mutant xenograft models.
- Appearance: solid, light yellow to yellow.
- Purity: 99.72%.
Medchemexpress LLC Dibenzyl disulfide | 150-60-7 | MFCD00004783 | 99.9% | 246.39 | 500 G
Dibenzyl disulfide is an endogenous metabolite. It is a solid with a white to off-white appearance.
- Purity: 99.94%
- Molecular Weight: 246.39
- CAS number: 150-60-7
- Formula: C14H14S2
- Initial source: Plants Petiveriaceae Petiveria alliacea
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: Powder at -20°C for 3 years, 4°C for 2 years; In solvent at -80°C for 6 months, -20°C for 1 month
Medchemexpress LLC 2,6-Dichlorodiphenylamine | 15307-93-4 | 99.8% | 238.12 | 1 ML
2,6-Dichlorodiphenylamine is an analogue of Diclofenac Sodium and demonstrates anti-Candida albicans activity. Diclofenac Sodium is a potent and nonselective anti-inflammatory agent, functioning as a COX inhibitor with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells, respectively. This product is intended for research use only and is not sold to patients.
- Analogue of diclofenac sodium
- Demonstrates anti-Candida albicans activity
- Potent and nonselective anti-inflammatory agent
- Functions as a COX inhibitor
- High purity of 99.78%
- Causes skin irritation
- Causes serious eye irritation
- Very toxic to aquatic life with long lasting effects
- Store at 4°C, protected from light
- Avoid inhalation, contact with eyes and skin
- Avoid dust and aerosol formation
- Use in areas with appropriate exhaust ventilation
Chemscene ChemScene | SPDP | 250MG | CS-5649 | 0.98 | 68181-17-9| MFCD00009636 | 312.37
ChemScene | SPDP | 250MG | CS-5649 | 0.98 | 68181-17-9| MFCD00009636 | 312.37
Selleck Chemical LLC NX-2127-E1381-1G
NX-2127 is a unique potent inhibitor of BTK that prevents its functions by catalyzing the ubiquitylation and proteasomal degradation of BTK rather than via direct binding NX-2127 stimulates T cell activation and increases IL-2 production in primary human T Cells
eMolecules S ALPHA ALPHA BIS 4 METHOXYP1G
(S)-ALPHA,ALPHA-BIS(4-METHOXYPHENYL)-2-PYRROLIDINEMETHANOL, 1g, 131180-57-9