Carboxylic acid salts
Sigma Aldrich Fine Chemicals Biosciences BRL 54443 maleate salt solid | 1197333-54-2 | MFCD01860866 | 10MG
BRL 54443 maleate salt solid | Mol Wt: 346.38 | 1197333-54-2 | MFCD01860866 | 10MG
eMolecules Medchem Express / Trimethoprim (lactate) / 500mg / 602878487 / HY-B0510C / / 23256-42-0 / MFCD00171722 / 380.401 / C17H24N4O6
Medchem Express / Trimethoprim (lactate) / 500mg / 602878487 / HY-B0510C / / 23256-42-0 / MFCD00171722 / 380.401 / C17H24N4O6
Apexbio Technology LLC NADH (sodium salt)(Synonyms: Reduced β-Nicotinamide adenine dinucleotide disodium salt, NADH disodium salt), 500mg, 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
Cayman Chemical MK886 sodium salt
A potent FLAP antagonist that prevents 5-LO activation in vivo; inhibits LT biosynthesis in leukocytes with an IC50 value of 2.5 nM
Apexbio Technology LLC AVE 0991 sodium salt 306288-04-0 2mg
AVE 0991 sodium salt (CAS 306288-04-0) is a synthetic non-peptide agonist of the angiotensin-(1-7) receptor Mas Acting as a functional mimic of angiotensin-(1-7) AVE 0991 competitively binds to endothelial cell membranes with an IC50 of 21 35 nM in bovine aortic endothelial cells In vitro treatment with AVE 0991 promotes nitric oxide release to levels significantly greater than angiotensin-(1-7) In vivo AVE 0991 reduces urine volume and increases urine osmolality in mice effects reversed by angiotensin II antagonists indicating receptor specificity It also inhibits atherogenesis in ApoE knockout mice supporting its application in cardiovascular and renal research
TARGETMOL CHEMICALS INC BMT-124110 FORMATE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BMT-124110 Formate is a selective AAK1 inhibitor (IC50 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase BIKE with an IC50 17 nM.BMT-124110 Formate inhibits the cell-cycle protein G-related BMT-124110 Formate inhibits the cell cycle protein G-associated kinase GAK with an IC5099 nM.
Medchemexpress LLC Tasurgratinib succinate | 1879965-80-6 | 98.1% | 705.8 g/mol | C36H43N5O10 | 100 MG
Tasurgratinib succinate is the succinate salt of tasurgratinib, a potent, orally active inhibitor selective for fibroblast growth factor receptors FGFR1, FGFR2, and FGFR3. It is used in preclinical and clinical research of FGFR-driven cancers and is supplied as a research-grade compound with supporting analytical documentation.
Apexbio Technology LLC Taurochenodeoxycholic acid sodium salt 6009-98-9 100mg
Taurochenodeoxycholic acid sodium salt (CAS 6009-98-9) is an animal-derived bile acid derivative that modulates cell signaling pathways involved in apoptosis thereby influencing cellular growth and survival Research indicates that it also participates in the regulation of inflammatory responses and immune-related signaling mechanisms This compound is frequently utilized in cellular and animal models to investigate bile acid receptor-mediated physiological and pathological processes including its roles in metabolic disorders inflammatory diseases and immune-mediated conditions
Medchemexpress LLC POPG (sodium salt) | 268550-95-4 | 99.6% | C40H76NaO10P | 10MG
POPG (sodium salt) is a negatively charged phospholipid used to model anionic membrane environments and for liposome formation. It has molecular formula C40H76NaO10P, molecular weight 770.99, and CAS 268550-95-4, and is supplied as a solid suitable for laboratory membrane and biophysical studies.
- Negatively charged phospholipid for modeling anionic membranes.
- Suitable for liposome preparation and membrane reconstitution.
- High purity (>99% HPLC) for reproducible results.
- Molecular formula C40H76NaO10P, molecular weight 770.99.
- Available as a solid for formulation and experimental use.
Medchemexpress LLC Sodium formate | 141-53-7 | MFCD00013101 | 99.0% | 68.01 g/mol | CHNaO2 | 250 G
Sodium formate is the sodium salt of formic acid supplied as a solid biochemical reagent and reducing agent. It has a listed purity of 99.0% and is commonly used in catalytic oxidations and biochemical assays; storage recommendations include sealed storage at 4°C, away from moisture.
- High purity reagent: 99.0% purity suitable for analytical and assay use.
- Solid form: supplied as a dry powder for easy handling and storage.
- Reduces oxidation: provides reducing force in catalytic oxidation reactions.
- Surface chemistry: can react with zinc salts to form zinc oxide layers on supports.
- Multiple pack sizes: available in laboratory pack sizes, including 250 g.
- Stable storage: store sealed at 4°C and protect from moisture; in solvent, -80°C (6 months) or -20°C (1 month) for short-term.
Sigma Aldrich Fine Chemicals Biosciences dUTP PCR Grade sodium salt
dUTP PCR Grade is a 100 mM clear colorless SOLUTIONon of the sodium salt (pH 8.3).
Cayman Chemical Simvastatin sodium salt
An HMG-CoA reductase inhibitor (Ki = 0.12 nM); reduces plasma cholesterol levels in rats and dogs at 1.2 and 8 mg/kg, respectively; suppresses TNF-induced NF-κB activation (IC50 = ~13 µM) and potentiates apoptosis in human myeloid leukemia cells; inhibits GPX4, increases MDA levels, and induces ferroptosis in MDA-MB-231 and MCF-7 breast cancer cells
Cayman Chemical NADP sodium salt hydrate
The oxidized form of NADPH; serves as a cofactor in various biological reactions
Apexbio Technology LLC CL 316243 disodium salt 151126-84-0 5mg
CL 316243 disodium salt is a small-molecule agonist targeting the 3-adrenergic receptor It is designed to activate 3 receptors thereby modulating lipolytic and thermogenic pathways predominantly in adipose tissues CL 316243 disodium salt exerts its biological activity by selectively binding to 3-adrenergic receptors leading to enhanced adipocyte-mediated lipid metabolism In experimental rodent models administration of CL 316243 increases insulin sensitivity and reduces obesity-related hyperglycemia by promoting glucose uptake primarily in adipose tissue Based on these pharmacological properties CL 316243 disodium salt holds research potential in the study of 3 receptor-mediated metabolic mechanisms and the exploration of therapeutic strategies for metabolic disorders such as obesity and type 2 diabetes
Apexbio Technology LLC Cefoxitin (sodium salt) 33564-30-6 1g
Cefoxitin sodium salt (CAS 33564-30-6) is a small-molecule inhibitor targeting penicillin-binding proteins (PBPs) It is designed to inhibit PBPs thereby interfering with bacterial cell wall synthesis and peptidoglycan cross-linking Cefoxitin sodium salt exerts its biological activity primarily through inhibition of cell wall synthesis by binding to PBPs In in vitro enzymatic assays Cefoxitin sodium salt demonstrates inhibitory activity against various gram-positive and gram-negative bacteria with previously reported IC50 values in the low micromolar range due to its resistance to certain beta-lactamases including AmpC -lactamases Based on these pharmacological properties Cefoxitin sodium salt holds research potential in investigations of bacterial resistance mechanisms antimicrobial sensitivity profiling and beta-lactamase enzyme kinetics