Carboxylic acid salts
Apexbio Technology LLC Cefazolin (sodium salt) 27164-46-1 250mg
Cefazolin sodium salt (CAS 27164-46-1) is a semisynthetic antibiotic that inhibits bacterial cell wall synthesis by binding to specific penicillin-binding proteins thereby blocking transpeptidation reactions essential for peptidoglycan formation In in vitro studies cefazolin sodium salt suppresses the proliferation of cultured osteoblast-like MG-63 cells exhibiting substantial cytotoxicity at concentrations of 10 000 g/ml precise IC50 values depend on cell type and experimental conditions Cefazolin sodium salt is commonly used in microbiology pharmacokinetic investigations and infection models particularly within studies of antimicrobial susceptibility and renal dysfunction
Sigma Aldrich Fine Chemicals Biosciences Cefazolin sodium salt 891500MG
Chemical structure AY-lactam
TARGETMOL CHEMICALS INC GJ103 sodium salt 10MG
Also available in 1 mL, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes.GJ103 sodium salt is an active analog of GJ072, a read-through compound. It has been shown to reduce the surface tension of aqueous solutions, which makes it easier for molecules to move through the solution. It has also been shown to reduce the viscosity of aqueous solutions, which makes it easier for molecules to move through the solution. Additionally, it has been shown to reduce the pH of aqueous solutions, which can have a variety of effects on the biochemical and physiological processes of living organisms. Purity 99.72%
Sigma Aldrich Fine Chemicals Biosciences Potassium gluconate | 299-27-4 | MFCD00064211 | 500g
Potassium gluconate | Mol Wt: 234.25 | 299-27-4 | MFCD00064211 | 500g
Sigma Aldrich Fine Chemicals Biosciences Bumetanide >=98% | 28395-03-1 | MFCD00078949 | 250MG
Bumetanide >=98% | Purity: >=98% | Mol Wt: 364.42 | 28395-03-1 | MFCD00078949 | 250MG
TARGETMOL CHEMICALS INC SESAMOLIN 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Sesamolin and Sesamin has neuroprotective effect. 2. Sesamolin protects microglia against H2O2-induced cell injury by inhibiting of p38 MAPK and caspase-3 activation and ROS production. 3. Sesamolin and Sesamin can significantly attenuate the excess generation of nitric oxide in lipopolysaccharide-stimulated rat primary microglia cells. purity: 98%
Medchemexpress LLC Sp-cAMPS sodium salt | 142439-95-0 | 99.5% | 367.25 | C10H11N5NaO5PS | 1 ML
Sp-cAMPS sodium salt is a cyclic AMP analog used in biochemical research to activate cAMP-dependent protein kinase A (PKA) isoforms and to probe cyclic nucleotide signaling. It exhibits inhibitory activity against phosphodiesterases and is supplied in solution or solid form for laboratory assays.
- Activates cAMP-dependent protein kinase A (PKA I and PKA II).
- Acts as a competitive phosphodiesterase inhibitor useful for signaling studies.
- Available as a ready-to-use 10 mM solution in DMSO or as a solid form.
- High purity suitable for biochemical and enzymatic assays.
- Enables reproducible modulation of cyclic nucleotide pathways in vitro.
Cayman Chemical Fluvastatin sodium salt hydr
An HMG-CoA reductase inhibitor (Ki = 0.3 nM for the rat enzyme); inhibits CYP2C9 (IC50 = 100 nM); inhibits oxidized LDL-induced ferroptosis and reverses oxidized LDL-induced decreases in GPX4 and system Xc- levels in HUVECs; decreases serum cholesterol, triglyceride, and phospholipid levels, the formation of TBARS, and vascular ACE activity in rabbits fed a high-cholesterol diet at 2 mg/kg per day; increases survival in a mouse model of myocardial infarction at 10 mg/kg per day
Medchemexpress LLC Tasurgratinib succinate | 1879965-80-6 | 99.2% | 705.8 g/mol | C32H37N5O6.3/2C4H6O4 | 10 MG
Tasurgratinib succinate (E7090) is an orally available, selective inhibitor of fibroblast growth factor receptors FGFR1-3 used in preclinical oncology research. It potently inhibits FGFR signaling at low-nanomolar concentrations and has demonstrated antiproliferative activity in FGFR-driven cancer cell lines.
- Selective FGFR1-3 inhibition with low-nanomolar potency.
- Demonstrated antiproliferative activity in FGFR-driven cell lines.
- Supplied as the succinate salt for preclinical experiments.
- High purity suitable for biochemical and cellular assays.
- Provided in small-mass packages for research use.
TARGETMOL CHEMICALS INC Trimebutine CTB salt 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Trimebutine CTB salt (GIC-1001) is an opioid receptor agonist used in the study of pain. Purity 99.53%
Apexbio Technology LLC Moxalactam (sodium salt) 64953-12-4 10mM (in 1mL DMSO)
Moxalactam sodium salt (CAS 64953-12-4) is a small-molecule -lactam antibiotic belonging to the oxacephem subclass It is designed to inhibit bacterial cell wall biosynthesis by targeting penicillin-binding proteins (PBPs) Moxalactam sodium salt exerts its biological activity by interfering with PBPs thereby preventing cell wall synthesis In in vitro studies Moxalactam sodium salt demonstrates broad-spectrum inhibition of various Gram-positive Gram-negative and anaerobic bacteria including Klebsiella pneumoniae Escherichia coli Haemophilus influenzae and Neisseria gonorrhoeae Typical MIC values for susceptible organisms are generally in the low microgram-per-milliliter range Based on these pharmacological properties Moxalactam sodium salt holds research potential in antibacterial susceptibility assays studies on antibiotic resistance mechanisms and investigations of bacterial cell-wall synthesis pathways
eMolecules Tetrakis(decyl)ammonium bromide | 14937-42-9 | MFCD00043166 | 25g
Combi-Blocks | Tetrakis(decyl)ammonium bromide | 25g | 267196004 | QD-8053 | 97.000 | 14937-42-9 | MFCD00043166 | 659.023 | C40H84BrN
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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