Hydrobromides
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g·mol⁻¹ | C6H13Br2N3S | 5 MG
Amthamine dihydrobromide is the dihydrobromide salt of amthamine, a selective histamine receptor agonist used in pharmacology and receptor research. It is supplied as a purified solid for use in in vitro and in vivo assays to probe histamine receptor function and signaling.
- High reported purity: 99.6%.
- Molecular weight 319.07 g·mol⁻¹.
- Supplied as a solid dihydrobromide salt.
- Suitable for histamine receptor pharmacology and assay work.
- Available in small milligram pack sizes for research use.
Medchemexpress LLC Pifithrin-α hydrobromide | 63208-82-2 | C16H19BrN2OS | 500 MG
Pifithrin-α hydrobromide is a p53 inhibitor that blocks its transcriptional activity, preventing cells from apoptosis. It also acts as an aryl hydrocarbon receptor (AhR) agonist. This water-soluble compound can suppress p53 protein transcription and glucose oxidase (GOX)-induced p53 protein increase.
- Blocks p53 transcriptional activity
- Prevents cells from apoptosis
- Acts as an aryl hydrocarbon receptor (AhR) agonist
- Suppresses p53 protein transcription
- Blocks GOX-induced Bcl-2 protein reduction and prevents Bax increase
- Binds to AhR and activates reporter activity
- Up-regulates classic AhR target gene CYP1A1
Medchemexpress LLC Pifithrin-α hydrobromide | 63208-82-2 | C16H19BrN2OS | 100 MG
Pifithrin-α hydrobromide is a p53 inhibitor that blocks its transcriptional activity and prevents cells from apoptosis. It also acts as an aryl hydrocarbon receptor (AhR) agonist. It is a water-soluble compound that can suppress p53 protein transcription and block glucose oxidase (GOX)-induced Bcl-2 protein reduction and Bax increase.
- Blocks transcriptional activity of p53
- Prevents cells from apoptosis
- Acts as an aryl hydrocarbon receptor (AhR) agonist
- Suppresses p53 protein transcription
- Blocks GOX-induced Bcl-2 protein reduction and Bax increase
- Induces AhR DNA binding complex formation
- Activates reporter activity
- Up-regulates the classic AhR target gene CYP1A1
Apexbio Technology LLC Homatropine Bromide 51-56-9 1g
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 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.
Chemscene ChemScene | 4-(Bromomethyl)pyridine hydrobromide | 10G | CS-W004084 | 0.98 | 73870-24-3| MFCD01863545 | 252.94
ChemScene | 4-(Bromomethyl)pyridine hydrobromide | 10G | CS-W004084 | 0.98 | 73870-24-3| MFCD01863545 | 252.94
Medchemexpress LLC Arecoline | 63-75-2 | MFCD00005704 | 1 ML
Arecoline is a naturally occurring psychoactive alkaloid that is brain-penetrant and orally active. It acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors. This compound has been observed to exhibit stimulation, alertness, anxiolysis, and anti-parasitic effects, though it can also induce oxidative stress.
- Purity: 99.84%
- Molecular weight: 155.19
- Formula: C8H13NO2
- Appearance: liquid
- Color: light yellow to brown
- Structure classification: alkaloids, piperidine alkaloids
- Acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors
- Induces stimulation, alertness, anxiolysis, and anti-parasitic effects
- Can alleviate anxiety and depression in CFA-induced mice
Medchemexpress LLC (RS)-AMPA hydrobromide | 171259-81-7 | 99.5% | 267.08 g/mol | C7H11BrN2O4 | 10 MG
(RS)-AMPA hydrobromide is the hydrobromide salt of (RS)-AMPA, a glutamate analogue and selective agonist of AMPA-type glutamate receptors. Supplied as a white to off-white solid for research use in neuroscience and pharmacology studies where a water-soluble AMPA receptor agonist is required.
- Selective AMPA receptor agonist.
- CAS number 171259-81-7.
- Molecular weight 267.08 g/mol.
- Purity 99.5%.
- White to off-white solid.
- Solubility: DMSO 50 mg/mL; H2O 5 mg/mL (may require ultrasonic).
- Storage: sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 10MG
Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 10MG