Hydrobromides
Medchemexpress LLC CPTH6 hydrobromide 5mg | 2321332-57-2 | 5 MG
CPTH6 hydrobromide is the hydrobromide salt of CPTH6, a thiazole-derived inhibitor of histone acetyltransferases selective for Gcn5 and pCAF. It reduces acetylation of histone H3/H4 and α-tubulin, impairs autophagy, and induces G0/G1 arrest and apoptosis in tumor cell lines; it is used as a research reagent for epigenetics and cancer biology studies.
- Research-grade compound for in vitro studies.
- Purity ≥98%.
- Molecular weight 386.7 g/mol.
- Molecular formula C15H16ClN3S · HBr.
- Soluble in DMSO, ethanol, and DMF.
- Available in 5 mg vials.
Apexbio Technology LLC Homatropine Bromide 51-56-9 5g
Homatropine Bromide (CAS 51-56-9) is a small molecule antagonist of muscarinic acetylcholine receptors (AChRs) It selectively inhibits muscarinic receptor-mediated responses in endothelial and smooth muscle cells with reported IC50 values of 162 5 nM and 170 3 nM for WKY-E and SHR-E cell models respectively This compound serves as a valuable tool for investigating the role of muscarinic signaling in vascular function and smooth muscle physiology within experimental research settings
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g/mol | C6H13Br2N3S | 1 ML
Amthamine dihydrobromide is a histamine receptor agonist supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and as solid material for laboratory use. It is used in receptor pharmacology and hepatotoxicity research to probe histamine-mediated biological responses.
- Ready-to-use 10 mM solution in DMSO, 1 mL.
- High purity (99.6%) suitable for biological assays.
- Also available as solid in multiple vial sizes for synthesis or formulation.
- CAS number 142457-00-9 for unambiguous identification.
- Useful for histamine receptor pharmacology and hepatotoxicity studies.
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g·mol⁻¹ | C6H13Br2N3S | 25 MG
Amthamine dihydrobromide is the dihydrobromide salt of amthamine, a histamine receptor agonist active at H1-H4 receptors. It is supplied as a solid and in ready-to-use DMSO solution formats for pharmacological research, and includes storage recommendations for both solids and stock solutions.
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.
Apexbio Technology LLC A 61603 hydrobromide 107756-30-9 1mg
A 61603 hydrobromide (CAS 107756-30-9) is a potent and highly selective agonist of the 1A-adrenergic receptor one of the 1-adrenergic receptor subtypes involved in cellular growth and proliferation Compared to its activity at 1B- and 1D-adrenergic receptors A 61603 demonstrates approximately 35-fold higher potency for 1A-AR In cellular assays it robustly induces phosphoinositide hydrolysis in 1A-AR-expressing fibroblasts (pEC50 8 24) and in neonatal rat cardiomyocytes it increases calcium transient frequency in a dose-dependent manner (EC50 6 9 nM) In vascular models A 61603 markedly elevates perfusion pressure demonstrating significantly greater efficacy than noradrenaline This compound serves as a valuable tool for delineating 1A-AR-mediated signaling and vascular regulation
Medchemexpress LLC Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 50 MG
Pyrithiamine hydrobromide is a thiamine analog and metabolic inhibitor used as a research reagent to study thiamine-dependent pathways and to model thiamine deficiency in cellular and animal studies.
- Thiamine metabolism inhibitor for experimental studies.
- Acts as a substrate for thiamine pyrophosphokinase.
- Suitable for biochemical and neuroscience research applications.
- Solid, white to light yellow powder with reported purity of 96.6%.
- Store at -20°C; follow recommended storage for solutions.
Medchemexpress LLC Halofuginone (hydrobromide) | 64924-67-0 | MFCD00946455 | 100.0% | 495.59 g/mol | C16H18Br2ClN3O3 | 10 MG
Halofuginone hydrobromide is the hydrobromide salt of halofuginone, a febrifugine-derived small molecule that competitively inhibits prolyl-tRNA synthetase and is supplied for research applications studying fibrosis, inflammation, malaria, and cancer. It is provided as a white to off-white solid with high purity and defined storage and solvent recommendations.
- Hydrobromide salt for improved handling and solubility.
- Competitive prolyl-tRNA synthetase inhibitor used in mechanistic research.
- High purity suitable for research applications.
- White to off-white solid, soluble in DMSO (≈50 mg/mL) and water (≈2.6 mg/mL).
- Store sealed and away from moisture; in solution keep at -80°C for long-term stability.
- Applicable for preclinical studies of fibrosis, inflammation, malaria, and cancer pathways.
Medchemexpress LLC CCT031374 hydrobromide | 1219184-91-4 | MFCD06737234 | 98.1% | 434.33 g·mol⁻¹ | C23H20BrN3O | 5 MG
CCT031374 hydrobromide is the hydrobromide salt of a small-molecule β-catenin/TCF signaling inhibitor supplied for research use only. It is provided as an off-white to light yellow solid with high chemical purity and is intended for pathway inhibition, cell signaling assays, and preclinical studies.
- β-catenin/TCF signaling inhibitor
- High purity (98.1%)
- Molecular weight 434.33 g·mol⁻¹
- Off-white to light yellow solid form
- Available in milligram-scale packages for research use
- Intended for in vitro and in vivo research applications