Organic cations
![eMolecules Ambeed / (3aS8aS)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 250mg / 642080029 / A1480140 / / 2639939-72-1 / MFCD23705049 / 797.073 / C53H65O4P](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502452790.PNG-250.jpg)
eMolecules Ambeed / (3aS8aS)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 250mg / 642080029 / A1480140 / / 2639939-72-1 / MFCD23705049 / 797.073 / C53H65O4P
Ambeed / (3aS8aS)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 250mg / 642080029 / A1480140 / / 2639939-72-1 / MFCD23705049 / 797.073 / C53H65O4P
Chem-Impex International, Inc. (1,3-Bis(diphenylphosphino)propane)palladium(II) chloride Dichloromethane Adduct | MFCD28139116 | 5G
(1,3-Bis(diphenylphosphino)propane)palladium(II) chloride Dichloromethane Adduct, MFCD28139116, 5G
Thermo Scientific Production Chemicals and Services DOE AND INGALLS
NC3927944 DIBUTYL PHOSPHITE 14.5-16 P
Medchemexpress LLC HY-100530 1mg Medchemexpress, Rp-cAMPS (triethylammonium salt) CAS:151837-09-1 Purity:>98%
Medchemexpress, HY-100530 1mg Rp-cAMPS (triethylammonium salt) CAS:151837-09-1 Rp-cAMPS triethylammonium salt is an analog of cAMP which acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 6.05 µM and 9.75 µM, respectively). Rp-cAMPS triethylammonium salt is resistant to hydrolysis by phosphodiesterases[3][4][5]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
![eMolecules Ambeed / (3aR8aR)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 100mg / 633661881 / A257864 / / 1187446-93-0 / MFCD23704801 / 797.073 / C53H65O4P](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502453277.PNG-250.jpg)
eMolecules Ambeed / (3aR8aR)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 100mg / 633661881 / A257864 / / 1187446-93-0 / MFCD23704801 / 797.073 / C53H65O4P
Ambeed / (3aR8aR)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine / 100mg / 633661881 / A257864 / / 1187446-93-0 / MFCD23704801 / 797.073 / C53H65O4P
Sigma Aldrich Fine Chemicals Biosciences SIGMA ALDRICH FINE CHEMICALS BIOSCIENCES
NC3932371 TRIETHYLAMMONIUM ACETATE
Strem, An Ascensus Company CAS# 14523-22-9. 500mg. Chlorodicarbonylrhodium(I) dimer. MFCD00135610
CAS# 14523-22-9. 500mg. Chlorodicarbonylrhodium(I) dimer. MFCD00135610. Molecular Weight: 388.76. Molecular Formula: [RhCl(CO)2]2. Color/form: red xtl. Strem# 45-0450. http://www.strem.com/catalog/v/45-0450/
Medchemexpress LLC Sodium aurothiomalate | 12244-57-4 | MFCD00064304 | 98.0% | 371.11 g/mol | C4H6O4S.Au.xNa | 50 MG
Aurothiomalate sodium is a gold-containing compound used in research as a selective inhibitor of oncogenic PKCι signaling and as a thioredoxin reductase (TrxR) inhibitor. Historically used as an anti-rheumatic agent, it has reported anti-tumor activity and is applied in biochemical and cell-based studies.
- Potent inhibitor of PKCι signaling and thioredoxin reductase
- Shows anti-tumor and anti-inflammatory activity in studies
- Supplied as a solid, off-white to light yellow material
- Typical purity around 98.0%
- Stable under refrigerated, sealed storage away from moisture
- Available in small milligram quantities for research use
Medchemexpress LLC Sodium aurothiomalate | 12244-57-4 | MFCD00064304 | 98.0% | 390.08 g/mol | C4H3AuNa2O4S | 10 MG
Sodium aurothiomalate is a gold-containing small molecule supplied for research use. It functions as an inhibitor of oncogenic PKCι signaling and thioredoxin reductase, and has been used historically as an anti-rheumatic agent and in antitumor studies. Supplied as an off-white to light-yellow solid with high purity and available in mg-scale packages.
- Gold-containing thiomalate salt with defined biological activity.
- Potent inhibitor of PKCι signaling and thioredoxin reductase.
- High purity suitable for biochemical and cellular studies.
- Solid form, off-white to light yellow, for straightforward handling.
- Available in small mg-scale package sizes for research workflows.
Medchemexpress LLC Aurothiomalate sodium | 12244-57-4 | MFCD00064304 | 98.0% | 390.08 g/mol | C4H6O4S.Au.xNa | 100 MG
Aurothiomalate sodium is a gold-containing research compound used to study oncogenic signaling and redox biology. It functions as a PKCι signaling inhibitor and a thioredoxin reductase (TrxR) inhibitor, exhibiting anti-tumor and anti-rheumatic activity in preclinical studies. The material is supplied as a solid with 98.0% purity for laboratory use.
- Potent PKCι signaling inhibitor used in cancer signaling studies.
- Inhibits thioredoxin reductase and modulates NF-κB-related pathways.
- Demonstrates anti-tumor activity in preclinical lung cancer models.
- High purity formulation suitable for in vitro and in vivo research.
- Provided as a stable solid for convenient handling and storage.
Cayman Chemical DIethyl 1 4dIhydro2 4 6trI 25g
An inhibitor of heme production; inhibits ferrochelatase; induces Mallory-Denk body formation in mouse liver; reduces IL-12A methylation in mouse liver