Organic potassium salts
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Potassium hydrogen phthalate, 877-24-7, MFCD00013070, 500 g
Linear Formula: HOOCC6H4COOK, Molecular Weight: 204.22, BioXtra, ≥99.95%, Synonym: KHP, Phthalic acid monopotassium salt, Potassium biphthalate, Potassium hydrogen phthalate, Potassium phthalate monobasic.
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U.S. Pharmacopeia U S PHARMACOPEIA
NC3996660 ACESULFAME POTASSIUM 200 MG
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eMolecules 13963-58-1 | Potassium hexacyanocobaltate(III) | MFCD00011391 | 5g
Medchem Express | T-3764518 | 5mg | 686240062 | HY-102045 | 1809151-56-1 | 473.379 | C20H17F6N5O2
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Medchemexpress LLC Acesulfame potassium | 55589-62-3 | MFCD00043833 | 99.38% | 100 G
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Acesulfame potassium | 55589-62-3 | MFCD00043833 | 99.38% | 100 G
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eMolecules 1111732-87-6 | Ambeed | Potassium 4-Pyridyltrifluoroborate | 1g | 525122433 | A206834 | MFCD09038543 | 185 | C5H4BF3KN
Ambeed | 3-Cyano-1H-pyrazole-5-carboxylic acid | 1g | 494129248 | A411525 | 1187361-13-2 | MFCD09036046 | 137.098 | C5H3N3O2
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Medchemexpress LLC Bleximenib oxalate | 2866179-95-3 | 98.0% | 689.82 | 1 MG
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Bleximenib oxalate is an orally active and selective menin-KMT2A inhibitor with IC50 values of 0.1 nM, 0.045 nM, and ≤0.066 nM for humans, mice, and dogs, respectively. It can inhibit the proliferation and induce apoptosis and differentiation of tumor cells, making it suitable for research into tumors such as leukemia.
- Orally active and selective menin-KMT2A inhibitor
- Inhibits proliferation and induces apoptosis and differentiation of tumor cells
- Reduces expression of MEIS1, PBX3, FLT3, and JMJD1C
- Exhibits anti-tumor activity in mouse models of leukemia
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Medchemexpress LLC Bleximenib (oxalate) | 2866179-95-3 | MFC32H50FN7O3.C2H2O4 | 98.0% | 689.82 | 100 MG
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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
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TARGETMOL CHEMICALS INC Naloxegol oxalate 50MG
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Also available in 1 mL, 5 mg, 10 mg, 25 mg and bulk. Please contact Fisher for quotes. Naloxegol oxalate (NKTR-118) is a peripherally-selective opioid antagonist for the treatment of opioid-induced constipation. Purity 99.82%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431520 OXALATE OXIDASE 5U
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Medchemexpress LLC L-703606 oxalate hydrate | 99.4% | 508.44 | 10 MG
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L-703606 oxalate hydrate is a potent and selective antagonist of the NK1 receptor. It is used for the study of gastric acid secretion.
- Potent, selective NK1 receptor antagonist
- Used for the study of gastric acid secretion
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eMolecules 84-73-1 | BIS(2-HYDROXYETHYL) PHTHALATE | MFCD27920521 | 1g
AstaTech | BIS(2-HYDROXYETHYL) PHTHALATE | 1g | 589954328 | C76700 | 95.000 | 84-73-1 | MFCD27920521 | 254.238 | C12H14O6
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Selleck Chemical LLC Phospho(enol)pyruvic acid monopotassium salt S3335-25mg
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Phospho(enol)pyruvic acid monopotassium salt (Potassium 1-carboxyvinyl hydrogenphosphate) is an endogenous metabolite
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GFS Chemicals Inc SODIUM OXALATE CERTIFIED 100GM
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NC3830855 SODIUM OXALATE CERTIFIED 100GM
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Medchemexpress LLC Naloxegol oxalate | 1354744-91-4 | 99.9% | C36H55NO15 | 5 MG
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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
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TARGETMOL CHEMICALS INC Naftidrofuryl oxalate 500MG
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Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Naftidrofuryl oxalate (Nafronyl oxalate) is a drug used in the management of peripheral and cerebral vascular disorders. It is claimed to enhance cellular oxidative capacity and to be a spasmolytic. It may also be an antagonist at 5HT-2 serotonin receptors. Purity 98.38%
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