Carboxylic acid salts
![eMolecules 127-20-8 | 2,2-DICHLOROPROPIONIC ACID SODIUM SALT | AstaTech | MFCD00064199 | 164.940 | C3H3Cl2NaO2 | 95.000 | [Na+].CC(Cl)(Cl)C([O-])=O | 1g | 718058511](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502442217.PNG-250.jpg)
eMolecules 127-20-8 | 2,2-DICHLOROPROPIONIC ACID SODIUM SALT | AstaTech | MFCD00064199 | 164.940 | C3H3Cl2NaO2 | 95.000 | [Na+].CC(Cl)(Cl)C([O-])=O | 1g | 718058511
2,2-DICHLOROPROPIONIC ACID SODIUM SALT | AstaTech | 127-20-8 | MFCD00064199 | 164.940 | C3H3Cl2NaO2 | 95.000 | [Na+].CC(Cl)(Cl)C([O-])=O | 1g | 718058511
Selleck Chemical LLC Etomoxir sodium salt
Etomoxir sodium salt ((R)-( )-Etomoxir sodium salt) is an irreversible inhibitor of carnitine palmitoyltransferase-1 (CPT-1) on the outer face of the inner mitochondrial membrane Etomoxir enhances palmitate-induced cell apoptosis
Medchemexpress LLC Rp-cAMPS sodium salt | 142439-94-9 | 99.7% | 367.25 g/mol | C10H11N5NaO5PS | 100 MG
Rp-cAMPS sodium salt is a cyclic AMP analogue that acts as a competitive antagonist of cAMP-dependent protein kinase A (PKA) isoforms I and II. It is resistant to phosphodiesterase hydrolysis and supplied for research use in both solid and solution formats, suitable for biochemical and cell-based assays.
- Potent competitive antagonist of PKA I and II.
- Resistant to phosphodiesterase hydrolysis.
- High purity (≈99.7%) for reliable results.
- Soluble in water and DMSO with sonication and warming as needed.
- Available in multiple solid pack sizes and prepared solutions.
- Stable as a solid at -20°C; solutions stored frozen for limited time.
![eMolecules 22466-49-5 | Sodium hexafluoroacetylacetonate, 97% | Strem Chemicals | MFCD00156524 | 230.041 | C5HF6NaO2 | 97.000 | [Na+].[O-]\C(=C/C(=O)C(F)(F)F)C(F)(F)F | 25g | 321335355](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502168782.JPG-250.jpg)
eMolecules 22466-49-5 | Sodium hexafluoroacetylacetonate, 97% | Strem Chemicals | MFCD00156524 | 230.041 | C5HF6NaO2 | 97.000 | [Na+].[O-]\C(=C/C(=O)C(F)(F)F)C(F)(F)F | 25g | 321335355
Sodium hexafluoroacetylacetonate, 97% | Strem Chemicals | 22466-49-5 | MFCD00156524 | 230.041 | C5HF6NaO2 | 97.000 | [Na+].[O-]\C(=C/C(=O)C(F)(F)F)C(F)(F)F | 25g | 321335355
TARGETMOL CHEMICALS INC NAAD sodium salt 5MG
Also available in 1 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. NAAD sodium salt (NAAD Na salt) is a substrate of nicotinamide adenine dinucleotide synthase and can be used in studies about the specificity and kinetics of the substrate. Purity 98%
Cayman Chemical FR900098 sodium salt
A derivative of fosmidomycin that has antimalarial activity; inhibits DOXP reductoisomerase in vitro in a dose-dependent manner; exhibits in vitro antimalarial activity against three P. falciparum strains (IC50s = 170, 170, and 90 nM for HB3, A2, and Dd2 strains, respectively); FR900098 (>10 mg/kg, i.p.) eradicated P. vinckei parasites within four days in mice
Apexbio Technology LLC CX-4945 sodium salt 1309357-15-0 50mg
CX-4945 sodium salt (Silmitasertib sodium salt CAS 1309357-15-0) is a potent and selective inhibitor of casein kinase 2 (CK2) effectively targeting both the CK2 and CK2 catalytic subunits By inhibiting CK2 activity CX-4945 disrupts signaling pathways involved in cell cycle progression transcriptional regulation and cell survival The compound exhibits oral bioavailability and is widely utilized in research focused on tumor biology mechanistic studies of signaling cascades and the functional characterization of protein kinases
Apexbio Technology LLC Cefoxitin (sodium salt) 33564-30-6 500mg
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
Apexbio Technology LLC Concanavalin A (Con A)-HyperFluor 488 5x5mg(5 mg/mL)
Concanavalin A (Con A) derived from Canavalia ensiformis (jack bean) is a plant lectin protein with a molecular weight of approximately 104 kDa Each subunit can bind one Ca2 ion and one Mn2 ion and has one carbohydrate binding site Con A is capable of binding to various glycoproteins glycolipids and -D-glucose and -D-mannose residues HyperFluorTM 488 is a fluorescent dye that emits green fluorescence under UV light (Ex/Em 495 nm/519 nm) This combination grants Con A-HyperFluorTM 488 superior visualization capability when detecting carbohydrate molecules on cell surfaces This product is HyperFluorTM 488-labeled Con A in solution form It is applicable in glycobiology research serving as a probe to detect carbohydrate molecules on the cell surface and analyzed effectively using flow cytometry Applying IHC staining procedures with this product allows visualization of carbohydrate distribution in tissues or cells under a fluorescence microscope
Apexbio Technology LLC CL 316243 disodium salt 151126-84-0 10mg
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
Sigma Aldrich Fine Chemicals Biosciences PF-04634817 succinate >=98% (HPLC) | 1228111-63-4 (free base) | 25MG
PF-04634817 succinate >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 629.67 | 1228111-63-4 (free base) | 25MG
Apexbio Technology LLC 8-CPT-2Me-cAMP, sodium salt 634207-53-7 5mg
8-CPT-2Me-cAMP sodium salt (CAS 634207-53-7) is a selective agonist of exchange proteins directly activated by cAMP (EPACs) which are key intracellular cAMP sensors acting as guanine nucleotide exchange factors for Rap1 and Rap2 This compound effectively activates EPAC1 leading to increased Rap1 activity and enhanced cell adhesion particularly in the presence of MAP1A light chain 2 In Jurkat T cells 8-CPT-2Me-cAMP induces Rap1 activation independently of PKA inhibition In prostate cancer cell models it dose-dependently upregulates Epac1 phosphorylated Akt and stimulates mTORC1/mTORC2 signaling It is widely utilized to dissect EPAC-specific pathways in cell signaling adhesion and proliferation studies
TARGETMOL CHEMICALS INC Cloprostenol sodium salt 5MG
Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Cloprostenol sodium salt (ICI 80996 sodium salt) is a more water-soluble, crystalline form of cloprostenol compared to the free acid and is a synthetic analog of prostaglandin F2alpha. Purity 98%
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