Sugar acids and derivatives
TARGETMOL CHEMICALS INC Rehmannioside D 10MG
Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Rehmannioside D is a carotenoid glycoside that existed in the roots of Rehmannia glutinosa. Purity 98.67%
Medchemexpress LLC Aloeresin D | 105317-67-7 | MFCD32004290 | 99.5% | 556.56 | C29H32O11 | 10 MG
Aloeresin D is a chromone glycoside isolated from Aloe vera that inhibits β-secretase (BACE1) with a reported IC50 of 39 μM. It is supplied as a purified research compound with defined solubility and storage recommendations for biochemical and pharmacological studies.
- Chromone glycoside isolated from Aloe vera.
- Inhibits β-secretase (BACE1); IC50 = 39 μM.
- High purity (≈99.5%).
- Molecular formula C29H32O11; molecular weight 556.56 g/mol.
- Soluble in DMSO (250 mg/mL); reported in vivo solubility ≥2.08 mg/mL.
- Solid storage: 4°C, sealed, protected from moisture and light.
Medchemexpress LLC Integrin alpha V bet 50ug | 50ug
Integrin alpha V beta 6 Protein Human (HEK293 His-Avi) is a recombinant protein dimer complex containing human-derived Integrin alpha V beta 6 protein expressed by HEK293 with C-His C-Avi labeled tag Integrin alpha V beta 6 Protein Human (HEK293 His-Avi) has molecular weight of 90-150 kDa
Medchemexpress LLC Zen-3694 | 1643947-30-1 | 99.7% | 333.39 | C19H19N5O | 25MG
BET-IN-19 is a potent small-molecule BET bromodomain inhibitor for research use. It inhibits hIL-6 mRNA transcription and c-myc activity in AML MV4-11 cells (IC50 ≤ 0.3 μM). The compound has molecular formula C19H19N5O, molecular weight 333.39, and reported purity ≈99.7%; it is supplied as a powder and is typically stored at -20°C (powder) or at -80°C in solvent for longer term.
Medchemexpress LLC D-Nmappd | 35922-06-6 | MFCD08062172 | 99.7% | 422.6 g/mol | C23H38N2O5 | 25MG
D-NMAPPD ((1R,2R)-B13) is a research-grade small-molecule acid ceramidase inhibitor that modulates NMDA receptor properties by enhancing endogenous ceramide production. It is used in biochemical and neurological research and has been reported to show anticancer activity in experimental studies. The compound is supplied in milligram-scale quantities with high reported purity suitable for laboratory applications.
- Inhibits acid ceramidase activity.
- Modulates NMDA receptor properties by enhancing endogenous ceramide production.
- Reported anticancer activity in experimental studies.
- High purity (~99.7%) suitable for research use.
- Molecular formula C23H38N2O5; molecular weight 422.6 g/mol.
- Available in milligram-scale package sizes for laboratory experiments.
Medchemexpress LLC Sodium zirconium cyclosilicate | 17141-74-1 | 95.0% | 100 MG
Sodium zirconium cyclosilicate is an inorganic, microporous zirconium silicate compound used as a selective cation-exchange reagent that binds potassium ions for biomedical and kidney disease research.
- Selectively binds potassium ions for removal in vitro or preclinical studies.
- Inorganic, non-absorbed microporous structure suitable for research applications.
- Available in multiple small-scale sizes for laboratory use.
- Supplied as a solid reagent with specified purity for experimental reproducibility.
Medchemexpress LLC D-3263 hydrochloride | 1008763-54-9 | MFCD22665741 | 98.0% | 409.95 | C21H32ClN3O3 | 10 MG
D-3263 hydrochloride is an enteric-coated, orally bioavailable agonist of transient receptor potential melastatin member 8 (TRPM8). It binds and activates TRPM8, modulates calcium and sodium flux, and has been investigated for potential antineoplastic effects and modulation of androgen-related pathways.
- Orally bioavailable TRPM8 agonist suitable for in vivo studies.
- Enteric-coated formulation for improved gastrointestinal stability.
- High purity (98.0%) supports reproducible experimental results.
- Soluble in DMSO and formulatable for common in vivo vehicles.
- Stable when stored sealed at 4°C; solvent stability at -80°C for extended storage.