Carboxylic acid salts
eMolecules 22830-45-1 | Iron(II) Gluconate Hydrate | MFCD04037236 | 25g
ChemScene | 2-Ethynyl-11-biphenyl | 100mg | 599374619 | CS-0169597 | 52889-62-0 | MFCD28016698 | 178.234 | C14H10
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AdipoGen D-Luciferin potassium salt
Chemical. CAS 115144-35-9. Formula C11H7KN2O3S2. MW 318.41. D-Luciferin is the most popular and versatile bioluminescent substrate. Firefly luciferase produces light by the ATP-dependent oxidation Mg2 as cofactor of luciferin. It emits a characteristic yellow-green emission in the presence of oxygen, which shifts to red light in vivo. The 560nm chemiluminescence from this reaction peaks within seconds, with light output that is proportional to luciferase activity when luciferin and ATP are present in excess. Firefly luciferase has long been conjugated to antibodies and used as a label in immunoassays using luciferin as the substrate for detection. One particular advantage to the enzyme is that there is low endogenous luciferase activity in mammalian tissues besides its high sensitivity. Through the utilization of ATP, the reaction can be further used to indicate the presence of energy or life in order to function as a life-death stain.
Sigma Aldrich Fine Chemicals Biosciences Cibenzoline succinate >=98% (HPLC), solid | 100678-32-8 | MFCD00941423 | 10MG
Cibenzoline succinate >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 380.44 | 100678-32-8 | MFCD00941423 | 10MG
AdipoGen DL-3-Hydroxybutyric acid Na
Chemical. CAS 150-83-4. Formula C4H7NaO3. MW 126.1. Synthetic. Neuroprotective compound in experimental models of neurodegenerative diseases. Shown to be oxidized as an energetic substrate in the brain during starvation. May inhibit brain glucose oxidation, which may account for the suppression of hepatic glucose production observed after administration of ketone bodies in humans.
eMolecules 335299-59-7 | Tenatoprazole sodium salt | 25mg
Medchem Express | LP44 (hydrochloride) | 5mg | 779715339 | HY-103101 | 824958-12-5 | MFCD09971090 | 488.130 | C27H38ClN3OS
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Accela Chembio Inc Sodium Trimethylacetate Hydrate | 25g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
Sodium Trimethylacetate Hydrate | 25g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
Accela Chembio Inc Sodium Trimethylacetate Hydrate | 100g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
Sodium Trimethylacetate Hydrate | 100g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
![eMolecules 650-51-1 | Sodium trichloroacetate | Ambeed | MFCD00064198 | 185.360 | C2Cl3NaO2 | 98.000 | [Na+].[O-]C(=O)C(Cl)(Cl)Cl | 25g | 570995705](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502421485.JPG-250.jpg)
eMolecules 650-51-1 | Sodium trichloroacetate | Ambeed | MFCD00064198 | 185.360 | C2Cl3NaO2 | 98.000 | [Na+].[O-]C(=O)C(Cl)(Cl)Cl | 25g | 570995705
Sodium trichloroacetate | Ambeed | 650-51-1 | MFCD00064198 | 185.360 | C2Cl3NaO2 | 98.000 | [Na+].[O-]C(=O)C(Cl)(Cl)Cl | 25g | 570995705
Gold Biotechnology Inc Bialaphos Sodium Salt 500 mg
Bialaphos is a tripeptide antibiotic that is used in transformation experiments of many species of plants that make use of the bar gene for selection In corn it is more effective than glufosinate In wheat bialaphos was the most reliable selection criteria used to identify bar transformed plants
Sigma Aldrich Fine Chemicals Biosciences Etidronate disodium hydrate >=97% (NMR), solid | 7414-83-7 (anhydrous) | MFCD00152567 | 100MG
Etidronate disodium hydrate >=97% (NMR), solid | Purity: >=97% (NMR) | 7414-83-7 (anhydrous) | MFCD00152567 | 100MG
Gold Biotechnology Inc Bialaphos Sodium Salt 250 mg
Bialaphos is a tripeptide antibiotic that is used in transformation experiments of many species of plants that make use of the bar gene for selection In corn it is more effective than glufosinate In wheat bialaphos was the most reliable selection criteria used to identify bar transformed plants
Apexbio Technology LLC NADH (sodium salt)(Synonyms: Reduced β-Nicotinamide adenine dinucleotide disodium salt, NADH disodium salt), 5g, CAS: 606-68-8.
NADH (sodium salt) (CAS 606-68-8) is the reduced form of nicotinamide adenine dinucleotide functioning as an essential coenzyme involved in cellular bioenergetics Biologically NADH participates as an electron carrier in metabolic pathways including glycolysis -oxidation and the tricarboxylic acid (TCA) cycle facilitating ATP generation through electron transport In biomedical research NADH (sodium salt) is frequently applied to investigate cellular energy metabolism and elucidate mechanisms underpinning metabolic disorders
Apexbio Technology LLC Simvastatin (sodium salt)(Synonyms: Simvastatin sodium, Simvastatin sodium salt, Sodium simvastatin, Synvinolin sodium), 10mg, CAS: 101314-97-0.
Simvastatin (sodium salt) (CAS 101314-97-0) is an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase a critical enzyme controlling the rate-limiting step in cholesterol biosynthesis It binds with high affinity to HMG-CoA reductase exhibiting a Ki of approximately 0 12 nM In hepatocyte-derived Hep G2 cells simvastatin demonstrated potent suppression of cholesterol biosynthesis reducing the incorporation of radiolabeled acetate into sterols (IC50 15 nM) Animal studies with orally administered simvastatin indicated marked reduction in plasma cholesterol levels validating its utility in experimental models exploring cholesterol regulation and lipid metabolism
Apexbio Technology LLC Simvastatin (sodium salt)(Synonyms: Simvastatin sodium, Simvastatin sodium salt, Sodium simvastatin, Synvinolin sodium), 5mg, CAS: 101314-97-0.
Simvastatin (sodium salt) (CAS 101314-97-0) is an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase a critical enzyme controlling the rate-limiting step in cholesterol biosynthesis It binds with high affinity to HMG-CoA reductase exhibiting a Ki of approximately 0 12 nM In hepatocyte-derived Hep G2 cells simvastatin demonstrated potent suppression of cholesterol biosynthesis reducing the incorporation of radiolabeled acetate into sterols (IC50 15 nM) Animal studies with orally administered simvastatin indicated marked reduction in plasma cholesterol levels validating its utility in experimental models exploring cholesterol regulation and lipid metabolism