Carboxylic acid salts
Cambridge Isotope Laboratories SUCCINIC ACID, DISODIUM SALT (2,3-13C2, 99%), 1 G, 83587-80-8
SUCCINIC ACID, DISODIUM SALT (2,3-13C2, 99%), 1 G, 83587-80-8
Sigma Aldrich Fine Chemicals Biosciences Cefazolin sodium salt 891500MG
Chemical structure AY-lactam
Research Products International Corp Timentin 10 Grams
Timentin contains two antibiotics: ticarcillin (a penicillin) and clavulanate potassium (a beta-lactamase inhibitor). The combination of ticarcillin and clavulanate enhances the spectrum of antibacterial activity by protecting ticarcillin from degradation by certain bacterial enzymes. Ticarcillin inhibits bacterial cell wall synthesis, disrupting the integrity of the bacterial cell wall and leading to bacterial cell lysis. Clavulanate potassium works by inhibiting beta-lactamases, enzymes produced by bacteria that can inactivate beta-lactam antibiotics, such as ticarcillin. This combination is effective against a broad spectrum of bacteria, including those producing beta-lactamases.
AdipoGen Ganglioside GD1b 2Na bovine
Chemical. CAS 19553-76-5. Formula C84H146N4O39 . 2Na. MW 1836.1 . 46.0 calculated on sphingosine C181 and stearic acid. Isolated from bovine brain. Gangliosides are acidic glycosphingolipids that form lipid rafts in the outer leaflet of the cell plasma membrane, especially in neuronal cells in the central nervous system. They participate in cellular proliferation, differentiation, adhesion, signal transduction, cell-to-cell interactions, tumorigenesis and metastasis. The accumulation of gangliosides has been linked to several diseases. Ganglioside GD1b may act as a bacterial toxin receptor tetanus, botulinus. High levels are found in gliomas and astrocytomas. It modulates protein kinase activities. In vivo and in vitro it is in equilibrium with the lactone structure.
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.
Selleck Chemical LLC Azlocillin sodium salt S3195-50mg
Azlocillin is an acylampicillin with a broad spectrum against bacteria
Medchemexpress LLC NADP sodium salt | 1184-16-3 | MFCD00150480 | 98.7% | 765.39 | C21H27N7NaO17P3 | 10 MG
NADP sodium salt is the sodium salt form of nicotinamide adenine dinucleotide phosphate supplied as an analytical standard for research and analytical applications. It participates in cellular redox reactions by cycling between oxidized (NADP+) and reduced (NADPH) states, and is used as a reference reagent in biochemical and analytical assays.
- Purity 98.7% (analytical)
- Molecular weight 765.39 g/mol
- Molecular formula C21H27N7NaO17P3
- Solid, white to off-white appearance
- Available in small research pack sizes, including 10 MG
- Intended for research and analytical applications; for research use only
![eMolecules Broadpharm / 44-bis(octyloxy)butanoic acid sodium salt / 250mg / 698443044 / BP-27928 / 95.000 / / [null] / 366.518 / C20H39NaO4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502475231.JPG-250.jpg)
eMolecules Broadpharm / 44-bis(octyloxy)butanoic acid sodium salt / 250mg / 698443044 / BP-27928 / 95.000 / / [null] / 366.518 / C20H39NaO4
Broadpharm / 44-bis(octyloxy)butanoic acid sodium salt / 250mg / 698443044 / BP-27928 / 95.000 / / [null] / 366.518 / C20H39NaO4
Medchemexpress LLC Tasurgratinib succinate | 1879965-80-6 | 99.2% | 764.82 g/mol | C32H37N5O6·3/2 C4H6O4 | 25 MG
Tasurgratinib succinate is an orally available, selective small-molecule inhibitor of fibroblast growth factor receptors FGFR1, FGFR2, and FGFR3. Supplied as the succinate salt for research use, the compound is characterized by a defined molecular formula and high purity for preclinical and translational studies probing FGFR-driven signaling and anticancer activity.
- Selective FGFR1-3 inhibition with low nanomolar potency.
- High reported purity suitable for research applications.
- Supplied as a succinate salt for improved stability and handling.
- Molecular weight and formula provided for analytical characterization.
- Soluble in common organic solvents for in vitro testing.
![eMolecules Ambeed / Tin(II) Acetate / 5g / 626256948 / A382331 / / 638-39-1 / [null] / 236.798 / C4H6O4Sn](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502426997.PNG-250.jpg)
eMolecules Ambeed / Tin(II) Acetate / 5g / 626256948 / A382331 / / 638-39-1 / [null] / 236.798 / C4H6O4Sn
Ambeed / Tin(II) Acetate / 5g / 626256948 / A382331 / / 638-39-1 / [null] / 236.798 / C4H6O4Sn