Organic potassium salts
Alkali Scientific Potassium Acetate, 2.5 Kg
Potassium Acetate, Laboratory Grade, is offered in a 2.5 kg volume and is widely used in laboratory settings for buffering solutions, pH control, and chemical synthesis. This compound is essential for creating potassium-based buffers and for reactions requiring an acetate ion as a reactant. Potassium acetate serves in biological applications, such as the preparation of buffers for enzymatic reactions and the stabilization of various biochemical processes. The high purity of this reagent ensures consistency and reliability in experimental results. It is also used in the synthesis of various compounds and plays a key role in organic chemistry and biochemistry research.
Apexbio Technology LLC Acesulfame Potassium 55589-62-3 100mg
Acesulfame Potassium (CAS 55589-62-3) is a synthetic calorie-free sweetener belonging to the class of sulfonamide derivatives It is widely utilized in experimental studies to assess sweet taste receptor signaling and metabolic pathways involved in taste perception Acesulfame potassium serves as a reference compound in research evaluating the effects of artificial sweeteners on neuroendocrine responses and is used to distinguish responses to nutritive versus non-nutritive receptor agonists Based on these properties acesulfame potassium holds research potential in studies of taste signal transduction neuroendocrine regulation and metabolic effects in cell cultures and animal models
Medchemexpress LLC Acesulfame potassium | 55589-62-3 | 99.9% | 1 G
Acesulfame potassium is a synthetic sweetener that has been shown to affect cognitive function by altering neurometabolic functions in mice. It can also suppress autophagic degradation of PD-L1 in RIL-175 and SK-Hep1 cells. This product is useful for research in several areas.
- Used in research on neurological diseases, metabolic disorders, cancer, and immune evasion
- Targets include autophagy, biochemical assay reagents, ERK, isotope-labeled compounds, mTOR, PD-1/PD-L1, and reference standards
Aobchem Potassium Acetate | ≥95% | CAS 127-08-2 | C2H3KO2 | 1kg
Potassium Acetate | ≥95% | CAS 127-08-2 | C2H3KO2 | 1kg
Medchemexpress LLC Ethanedioic acid, disodium salt | 62-76-0 | MFCD00012465 | 99.7% | 134.00 g/mol | Na2C2O4 | 1g
Sodium oxalate is an orally active dispersant and coordination agent Sodium oxalate causes mitochondrial dysfunction Sodium oxalate has catalytic enhancing activity Sodium oxalate induces stable chronic kidney disease Sodium oxalate induces highly malignant and undifferentiated breast tumors[1][2][3][4][5][6][7][8]
Medchemexpress LLC GJ071 oxalate | 1216676-34-4 | 99.7% | 455.53 | 1 MG
GJ071 oxalate is a chemical that induces ATM kinase activity in ataxia telangiectasia (A-T) cells carrying homozygous TGA or TAG stop codons. It is intended for research use only and is not for patient use.
- Induces ATM kinase activity
- White to off-white solid appearance
- Shipping at room temperature (continental US)
- Storage at -20°C (sealed, away from moisture)
- For research use only
Medchemexpress LLC Naloxegol oxalate | 1354744-91-4 | 99.9% | C36H55NO15 | 5 MG
Naloxegol oxalate is an orally active, peripherally acting μ-opioid receptor antagonist (target Ki 7.42 nmol/L). It inhibits opioid binding to gastrointestinal μ-opioid receptors, alleviating opioid-induced gastrointestinal hypomotility, delayed transit, hypertonicity, and increased fluid reabsorption. It is applicable for research into opioid-induced constipation.
- Orally active
- Peripherally acting μ-opioid receptor antagonist
- Inhibits opioid binding to gastrointestinal μ-opioid receptors
- Alleviates opioid-induced gastrointestinal hypomotility and related issues
- Applicable to research on opioid-induced constipation
- High affinity binding to μ and κ-opioid receptors in vitro
- Low affinity to δ-opioid receptors in vitro
- No significant activity at non-opioid targets in vitro
- Available in solid and solution forms
![Medchemexpress LLC N-(2-chlorophenyl)-6-(piperidin-4-yl)imidazo[1,2-a]pyridine-3-carboxamide oxalate | 1198408-78-4 | MFCD28023573 | 99.0% | 444.87 g/mol | C21H21ClN4O5 | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240341.png-250.jpg)
Medchemexpress LLC N-(2-chlorophenyl)-6-(piperidin-4-yl)imidazo[1,2-a]pyridine-3-carboxamide oxalate | 1198408-78-4 | MFCD28023573 | 99.0% | 444.87 g/mol | C21H21ClN4O5 | 1 MG
LDN-211904 oxalate is the oxalate salt of a research small molecule described as a potent, reversible EphB3 inhibitor for biochemical and cellular studies. It is provided in milligram quantities for laboratory research, with a reported molecular weight of 444.87 g/mol and CAS 1198408-78-4. Not for clinical or human use.
- Potent, reversible EphB3 inhibitor (IC50 ≈ 79 nM).
- Reported molecular weight 444.87 g/mol and CAS 1198408-78-4.
- High purity suitable for research (>99.0%).
- Demonstrated metabolic stability in mouse liver microsomes.
- Supplied in research-scale quantities (for example, 1 mg).
Medchemexpress LLC Acesulfame (potassium) (Standard) | 55589-62-3 | 99.9% | 25 MG
Acesulfame (potassium) (Standard) is the analytical standard of Acesulfame (potassium). It is intended for research and analytical applications. Acesulfame potassium is an artificial sweetener that has been observed to affect cognitive functions in mice, potentially by altering neuro-metabolic functions.
- Analytical standard for Acesulfame (potassium)
- Used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
- Artificial sweetener
- Purity: 99.89%
Medchemexpress LLC Xanomeline (oxalate) | 141064-23-5 | MFCD12828778 | 99.9% | 371.45 | 50 MG
Xanomeline oxalate is a potent and selective muscarinic receptor agonist (SMRA) that stimulates phosphoinositide hydrolysis in vivo. This compound is used for the research of Alzheimer's disease. It stimulates phosphoinositide (PI) hydrolysis in A9 L m1 cells and inhibits [3H]-pirenzepine and [3H]-oxotremorine-M binding to rat brain. This product is for research use only.
- Potent and selective muscarinic receptor agonist
- Stimulates phosphoinositide hydrolysis in vivo
- Used for Alzheimer's disease research
- Stimulates PI hydrolysis in A9 L m1 cells
- Inhibits [3H]-pirenzepine and [3H]-oxotremorine-M binding to rat brain
- Robustly stimulates in vivo PI hydrolysis, an effect blocked by muscarinic antagonists
Medchemexpress LLC Bleximenib (oxalate) | 2866179-95-3 | MFC32H50FN7O3.C2H2O4 | 98.0% | 689.82 | 100 MG
Bleximenib oxalate (JNJ-75276617) is an orally active and selective menin-KMT2A inhibitor. It exhibits IC50 values of 0.1 nM, 0.045 nM, and ≤0.066 nM for humans, mice, and dogs, respectively. This compound can inhibit the proliferation and induce apoptosis and differentiation of tumor cells, making it valuable for research into tumors such as leukemia.
- Orally active and selective menin-KMT2A inhibitor
- Inhibits proliferation of tumor cells
- Induces apoptosis and differentiation of tumor cells
- Exhibits anti-tumor activity in mouse models of leukemia
- Reduces expression of MEIS1, PBX3, FLT3, and JMJD1C in MOLM-14 and OCI-AML3 cells
Sigma Aldrich Fine Chemicals Biosciences Sodium oxalate ACS reagent100G
Sodium oxalate is a water soluble inorganic salt mainly used for the standardization of permanganate SOLUTIONon during titration.
