Organic sulfuric acids and derivatives
TARGETMOL CHEMICALS INC Vindesine sulfate 20MG
Also available in 1 mL, 5 mg and bulk. Please contact Fisher for quotes. Vindesine sulfate (Desacetyl Vinblastine amide) is a vinca alkaloid which is a synthetic derivative of vinblastine, binds to the microtubular proteins of the mitotic spindle, leading to crystallization of the microtubule and mitotic arrest or cell death. Purity 99.93%
Apexbio Technology LLC Cystamine dihydrochloride 56-17-7 50mg
Cystamine dihydrochloride (CAS 56-17-7) is a disulfide-linked derivative of cysteamine that functions as an inhibitor of transglutaminase (Tgase) Additionally it exhibits inhibitory activity against the cysteine protease caspase-3 with a reported IC of approximately 23 6 M Cystamine dihydrochloride is orally bioactive and is commonly utilized in studies investigating the molecular mechanisms and therapeutic strategies for neurodegenerative diseases particularly Huntington s disease Its dual modulatory roles make it valuable for modeling cellular processes relevant to disease pathology
Selleck Chemical LLC Cefoselis Sulfate S1371-5mg
Cefoselis (FK 037 Sulfate) is a widely used beta-lactam antibiotic
Selleck Chemical LLC Sodium L-lactate
Sodium L-lactate is used as a food additive preservative acidity regulator and bulking agent
Apexbio Technology LLC Colistin Sulfate 1264-72-8 50mg
Colistin Sulfate (1264-72-8) is a cyclic antimicrobial peptide targeting the outer membrane of Gram-negative bacteria It is designed to interact electrostatically with negatively charged lipopolysaccharides thereby disrupting membrane integrity and permeability Colistin Sulfate exerts its biological activity primarily through disruption of the bacterial outer membrane In bacterial inhibition assays Colistin Sulfate demonstrates inhibitory activity with IC50 values typically ranging from 0 5 5 g/mL depending on the bacterial strain and experimental conditions Based on these pharmacological properties Colistin Sulfate holds research potential in antimicrobial applications particularly against multidrug-resistant Gram-negative organisms and as a selective agent in bacterial cell culture protocols
Selleck Chemical LLC H-151
H-151 is a highly potent and covalent inhibitor of STING that has noteworthy inhibitory activity both in human cells and in vivo
Selleck Chemical LLC Cefoselis Sulfate S1371-25mg
Cefoselis (FK 037 Sulfate) is a widely used beta-lactam antibiotic
Cayman Chemical S Clopidogreld3 sulfate
An internal standard for the quantification of (S)-(+)-clopidogrel by GC- or LC-MS
eMolecules 6640-23-9 | 4,5,6-Triaminopyrimidine sulfate hydrate | MFCD00150095 | 1g
Combi-Blocks, Inc. | 4,5,6-Triaminopyrimidine sulfate hydrate | 1g | 603154798 | QF-1867 | 95.000 | 6640-23-9 | MFCD00150095 | 241.220 | C4H11N5O5S
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Selleck Chemical LLC Heparan Sulfate
Heparan sulfate (HS Heparitin sulfate Alpha-idosane HHS 5 N-Acetylheparan Sulfate Suleparoid Tavidan) a constituent of HS proteoglycans (HSPGs) is a linear polysaccharide present on the cell surface Heparan sulfate influences the binding affinity of intestinal epithelium cells (IECs) to Wnt thereby promoting activation of canonical Wnt signaling and facilitating regeneration of small intestinal crypts after epithelial injury
Cayman Chemical S Clopidogreld3 sulfate
An internal standard for the quantification of (S)-(+)-clopidogrel by GC- or LC-MS
![eMolecules 7758-99-8 | Copper(II) Sulfate pentahydrate | Oakwood Chemicals | MFCD00149681 | 249.680 | CuH10O9S | 99.000 | O.O.O.O.O.[Cu++].[O-]S([O-])(=O)=O | 25g | 480131729](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000161184.jpg-250.jpg)
eMolecules 7758-99-8 | Copper(II) Sulfate pentahydrate | Oakwood Chemicals | MFCD00149681 | 249.680 | CuH10O9S | 99.000 | O.O.O.O.O.[Cu++].[O-]S([O-])(=O)=O | 25g | 480131729
Copper(II) Sulfate pentahydrate | Oakwood Chemicals | 7758-99-8 | MFCD00149681 | 249.680 | CuH10O9S | 99.000 | O.O.O.O.O.[Cu++].[O-]S([O-])(=O)=O | 25g | 480131729
Cayman Chemical Pioglitazone potassium salt
A PPARγ agonist (EC50 = ~500-600 nM for both human and murine PPARγ); selective for PPARγ over PPARα exhibiting low level activation of PPARα at 1 µM and 5.4-fold activation at a concentration of 10 µM; reduces hyperglycemia, hyperlipidemia, and hyperinsulinemia in a dose-dependent manner in male Wistar fatty rats from 0.3-3 mg/kg; reduces the number of lesions in a TRAP model; decreases production of neuroinflammatory cytokines and reduces immobility in the forced swim and tail suspension tests in a mouse model of chronic mild stress at 2.5 mg/kg
eMolecules 7758-98-7 | Copper(II) sulfate | Combi-Blocks159.600 | CuO4S | 95.000 | [Cu++].[O-]S([O-])(=O)=O | 25g | 290692207
Copper(II) sulfate | Combi-Blocks | 7758-98-7159.600 | CuO4S | 95.000 | [Cu++].[O-]S([O-])(=O)=O | 25g | 290692207