Hydrobromides
Apexbio Technology LLC AMTHAMINE-DIHYDROBROMIDE-50MG
Amthamine dihydrobromide (CAS No 142457-00-9) is a potent histamine H2 receptor agonist primarily used in biomedical research Originating from studies on histaminergic pathways this compound selectively targets H2 receptors facilitating the study of gastric acid secretion and immune response modulation In vitro its activity is typically observed in the nanomolar range making it highly effective in precise mechanism studies Amthamine dihydrobromide is commonly applied in cell models to dissect receptor signaling and in animal studies to explore physiological responses linked to H2 receptor activation It is also valuable in drug screening processes for developing new therapeutics targeting histamine pathways Experimental concentrations typically depend on the specific research design
TARGETMOL CHEMICALS INC PIFITHRIN-BETA HYDROBROM 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Pifithrin-(beta) hydrobromide (Cyclic PFT-(alpha)) is an inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and apoptosis. Protects against neuronal death in models of stroke and neurodegenerative disorders. Active in vivo; protects mice from the side-effects of Y therapy associated with p53 induction. Supresses self-renewal of embryonic stem cells. Also aryl hydrocarbon receptor (AHR) agonist causes upregulation of AHR target gene CYP1A1 (EC50 = 1.1 uM). purity: 99%
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g/mol | C6H13Br2N3S | 50 MG
Amthamine dihydrobromide is a research-grade histamine receptor agonist provided as the dihydrobromide salt. It is used in pharmacology and toxicology research to study histamine receptor activation and downstream physiological effects in vitro and in vivo.
- Selective histamine H2 receptor agonist.
- High chemical purity suitable for research applications.
- Available as a solid for flexible dosing and formulation.
- Includes molecular and CAS identifiers for unambiguous compound identification.
Selleck Chemical LLC Remodelin hydrobromide
Remodelin hydrobromide (HBr) is a potent acetyl-transferase NAT10 inhibitor
Medchemexpress LLC Scopolamine hydrobromide trihydrate | 6533-68-2 | 99.86% | 438.31 | 5 MG
Scopolamine (Hyoscine) hydrobromide trihydrate is a high-affinity muscarinic antagonist that can cross the blood-brain barrier. It competitively antagonizes 5-HT3 receptors with an IC50 of 2.09 μM. It can induce cognitive and memory deficits in animals and is used in research for preventing postoperative nausea and vomiting, motion sickness, and nervous system diseases. This product is for research use only and not sold to patients.
- High-affinity muscarinic antagonist
- Can cross the blood-brain barrier
- Competitively antagonizes 5-HT3 receptors
- Induces cognitive and memory deficits in animals, useful for research in these areas
- Used in research for preventing postoperative nausea and vomiting, motion sickness, nervous system diseases
TARGETMOL CHEMICALS INC Teneligliptin hydrobromide
Also available in 5 mg, 10 mg, 25 mg, 100 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Teneligliptin hydrobromide (MP-513 (hydrobromide)) is a novel, potent, and long-lasting dipeptidyl peptidase-4 inhibitor; competitively inhibited human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50 values of approximately 1 nM. Purity 100%
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Synthonix | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 5g | 532154821
3-Bromopiperidine-2,6-dione | Synthonix | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 5g | 532154821