Organic cations
![eMolecules 1187446-93-0 | Ambeed | (3aR8aR)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine | 100mg | 633661881 | A257864 | MFCD23704801 | 797.073 | C53H65O4P](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502453277.PNG-250.jpg)
eMolecules 1187446-93-0 | Ambeed | (3aR8aR)-4488-Tetrakis(35-diethylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine | 100mg | 633661881 | A257864 | MFCD23704801 | 797.073 | C53H65O4P
ChemScene | 1-(5-Fluoropyridin-2-yl)piperidin-4-ol | 100mg | 441670379 | CS-0080287 | 1247792-84-2 | MFCD14621457 | 196.225 | C10H13FN2O
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Medchemexpress LLC BAY-6035 | 2247890-13-5 | 99.51% | 396.48 | 1 ML
BAY-6035 is a chemical probe and a potent, selective, and substrate-competitive inhibitor of SMYD3. It inhibits the methylation of MEKK2 peptide with an IC50 of 88 nM.
- Potent, selective, and substrate-competitive inhibitor of SMYD3.
- Inhibits methylation of MEKK2 peptide with an IC50 of 88 nM.
- Exhibits more than 100-fold selectivity over other histone methyltransferases.
- Inhibits the methylation of MEKK2 in cells with an IC50 of 70 nM.
![eMolecules 6242-98-4 | 4-Bromo-4'-nitrobiphenyl | Combi-Blocks | MFCD00024697 | 278.105 | C12H8BrNO2 | 95.000 | [O-][N+](=O)c1ccc(cc1)-c1ccc(Br)cc1 | 1g | 117519723](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502188003.JPG-250.jpg)
eMolecules 6242-98-4 | 4-Bromo-4'-nitrobiphenyl | Combi-Blocks | MFCD00024697 | 278.105 | C12H8BrNO2 | 95.000 | [O-][N+](=O)c1ccc(cc1)-c1ccc(Br)cc1 | 1g | 117519723
4-Bromo-4'-nitrobiphenyl | Combi-Blocks | 6242-98-4 | MFCD00024697 | 278.105 | C12H8BrNO2 | 95.000 | [O-][N+](=O)c1ccc(cc1)-c1ccc(Br)cc1 | 1g | 117519723
![eMolecules 35450-34-1 | 4'-Bromo-2-nitrobiphenyl | Combi-Blocks | MFCD00086504 | 278.105 | C12H8BrNO2 | 98.000 | [O-][N+](=O)c1ccccc1-c1ccc(Br)cc1 | 25g | 401038900](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502189371.JPG-250.jpg)
eMolecules 35450-34-1 | 4'-Bromo-2-nitrobiphenyl | Combi-Blocks | MFCD00086504 | 278.105 | C12H8BrNO2 | 98.000 | [O-][N+](=O)c1ccccc1-c1ccc(Br)cc1 | 25g | 401038900
4'-Bromo-2-nitrobiphenyl | Combi-Blocks | 35450-34-1 | MFCD00086504 | 278.105 | C12H8BrNO2 | 98.000 | [O-][N+](=O)c1ccccc1-c1ccc(Br)cc1 | 25g | 401038900
eMolecules Rongalite | 149-44-0 | MFCD00040426 | 5g
Combi-Blocks | Rongalite | 5g | 290695220 | QE-3508 | 96.000 | 149-44-0 | MFCD00040426 | 118.080 | CH3NaO3S
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![eMolecules 1361146-90-8 | Ambeed | (3aR8aR)-4488-Tetrakis(35-diisopropylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine | 100mg | 633662265 | A333711 | MFCD23704799 | 909.289 | C61H81O4P](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502450993.PNG-250.jpg)
eMolecules 1361146-90-8 | Ambeed | (3aR8aR)-4488-Tetrakis(35-diisopropylphenyl)-22-dimethyl-6-phenyltetrahydro-[13]dioxolo[45-e][132]dioxaphosphepine | 100mg | 633662265 | A333711 | MFCD23704799 | 909.289 | C61H81O4P
ChemScene | 6-Chloro-8-iodoquinolin-2(1H)-one | 100mg | 714104581 | CS-0201532 | 1693646-57-9 | 305.500 | C9H5ClINO
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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
eMolecules 1211-40-1 | 4-Amino-4'-nitrobiphenyl | MFCD00093527 | 1g
Ambeed | (3-Bromo-2-fluoro-6-methoxyphenyl)boronic acid | 250mg | 717677901 | A639543 | 1309980-91-3 | MFCD12026725 | 248.840 | C7H7BBrFO3
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Medchemexpress LLC Deferasirox (Fe3+ chelate) | 554435-83-5 | 98.0% | 426.18 | 50 MG
Deferasirox Fe3+ Chelate is an iron chelating agent. It is intended for research use only, extracted from patent WO2003053986.
- Iron chelating agent
- Intended for research use only
- Solid appearance with color ranging from light brown to black
- Soluble in DMSO: 50 mg/mL (117.32 mM)
- Store powder at -20°C for 3 years, 4°C for 2 years
- Store in solvent at -80°C for 2 years, -20°C for 1 year
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/
![Sigma Aldrich Fine Chemicals Biosciences [1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | 14647-23-5 | MFCD00013313 | 1G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/501804036.PNG-250.jpg)
Sigma Aldrich Fine Chemicals Biosciences [1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | 14647-23-5 | MFCD00013313 | 1G
[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | Mol Wt: 528.02 | 14647-23-5 | MFCD00013313 | 1G
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.
Medchemexpress LLC Gold sodium thiomalate | 12244-57-4 | MFCD00064304 | 98.0% | 390.08 g/mol | C4H6O4S·Au·xNa | 5 MG
Aurothiomalate sodium is a gold-containing research reagent reported as an anti-rheumatic agent that functions as a potent protein kinase C iota (PKCι) signaling inhibitor and a thioredoxin reductase (TrxR) inhibitor. It is supplied as a solid for biochemical and cellular research applications.
- Potent PKCι and thioredoxin reductase (TrxR) inhibitor.
- Reported anti-rheumatic agent with demonstrated anti-tumor activity.
- Supplied as a solid suitable for biochemical and cellular studies.
- High purity (98.0%) for research applications.
- Stored sealed at 4°C; in solvent: -80°C (6 months) or -20°C (1 month).
- Available in small milligram pack sizes for laboratory 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.
Thermo Scientific Production Chemicals and Services DOE AND INGALLS
NC3927944 DIBUTYL PHOSPHITE 14.5-16 P