Hydrobromides
Medchemexpress LLC 8-hydroxy-DPAT hydrobromide | 76135-31-4 | MFCD00055158 | 99.9% | 328.29 | C16H26BrNO | 10 MG
8-hydroxy-DPAT hydrobromide is the hydrobromide salt of 8-hydroxy-2-dipropylaminotetralin, a potent and selective agonist of the serotonin 5-HT1A receptor used in neuropharmacology research. Supplied as a high-purity solid, it is suitable for in vitro and in vivo studies and is provided with analytical documentation.
- Potent, selective 5-HT1A receptor agonist (pIC50 ~8.19).
- Hydrobromide salt for improved stability and handling.
- High purity (>99.8%) suitable for research applications.
- Available as a solid; common pack size 10 mg.
- Provided with COA, 1H NMR, and LC-MS documentation.
- Molecular formula C16H26BrNO; molecular weight 328.29.
Apexbio Technology LLC SR 95531 hydrobromide 104104-50-9 25mg
SR 95531 hydrobromide (CAS 104104-50-9) also known as Gabazine is a selective competitive antagonist of the GABAA receptor By binding to the GABA recognition site on the receptor it blocks the activation induced by -aminobutyric acid (GABA) Experimental studies report an inhibitory concentration (IC50) of approximately 0 2 M for GABAA receptor-mediated responses Widely utilized in neuroscience research Gabazine is applied to investigate the physiological and pathological roles of GABAA receptor-mediated synaptic transmission neural network modulation and neurotransmitter regulation
Medchemexpress LLC Eletriptan hydrobromide | 177834-92-3 | 99.8% | C22H27BrN2O2S | 25 MG
Eletriptan hydrobromide (Eletriptan HBr) is a 5-HT1B and 5-HT1D receptor agonist with antimigraine activity. It has Ki values of 0.92 nM for 5-HT1B receptors and 3.14 nM for 5-HT1D receptors.
- Dose-dependently reduces carotid blood flow in anesthetized dogs (1-1000 μg/kg; i.v.)
- Inhibits dural plasma protein extravasation in anesthetized rats (30-300 μg/kg; i.v.)
- Completely inhibits extravasation from the dura mater at 100 μg/kg
- Appears as an off-white to light brown solid
Apexbio Technology LLC Teneligliptin hydrobromide 906093-29-6 10mM (in 1mL DMSO)
Teneligliptin hydrobromide (CAS 906093-29-6) is a potent dipeptidyl peptidase-4 (DPP-4) inhibitor exhibiting competitive inhibition of human and rat plasma DPP-4 with an IC50 of approximately 1 nM DPP-4 also known as CD26 is a cell surface protease involved in immunoregulation signal transduction and apoptosis In vitro Teneligliptin hydrobromide reduces reactive oxygen species and modulates cell cycle and apoptotic gene expression in human endothelial cells exposed to high glucose In vivo it ameliorates hepatic steatosis and metabolic disturbances in murine models partly through activation of hepatic AMPK This compound supports studies of metabolic oxidative and inflammatory pathways
Medchemexpress LLC 1,4-PBIT (dihydrobromide) | 157254-60-9 | 98.0% | 444.25 g·mol⁻¹ | C12H20Br2N4S2 | 5 MG
1,4-PBIT (dihydrobromide) is a research-grade small-molecule inhibitor of nitric oxide synthases provided as the dihydrobromide salt (CAS 157254-60-9). Supplied in small-mass vials for biochemical and pharmacological studies, the compound is characterized by analytical documentation and high purity suitable for in vitro research.
- Potent inhibitor of iNOS, eNOS, and nNOS isoforms.
- High purity for reliable experimental results.
- Available in small-mass vials suitable for medicinal chemistry applications.
- Stable dihydrobromide salt form for consistent handling.
- Documented analytical data and certificate of analysis available.
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g/mol | C6H13Br2N3S | 10 MG
Amthamine dihydrobromide is the dihydrobromide salt of amthamine, a histamine receptor agonist active at H1-H4 subtypes. It is supplied for research use to investigate histamine receptor pharmacology, gastric acid secretion, and hepatotoxicity models. Follow standard laboratory safety and storage recommendations.
- High purity (99.6%) suitable for biochemical and pharmacological studies.
- Molecular weight 319.07 g/mol.
- Chemical formula C6H13Br2N3S.
- CAS number 142457-00-9 for unambiguous identification.
- Available in small research quantities, such as 10 MG, for laboratory use.
- Stable when stored sealed and kept away from moisture; refrigerated storage extends stability.
Medchemexpress LLC Adtn hydrobromide | 13575-86-5 | 98.0% | 10 MG
ADTN hydrobromide is the hydrobromide salt of ADTN, a long-acting dopamine receptor agonist used in research to probe dopaminergic signaling. It is supplied as a small, high-purity reagent for laboratory studies and has been reported to reduce behavioral visual threshold in DA-IPC-depleted zebrafish.
- Long-acting dopamine receptor agonist.
- Used to study dopaminergic signaling and zebrafish visual behavior.
- High purity: 98.0%.
- Supplied in a small research pack suitable for small-scale assays.
- Molecular formula C10H14BrNO2, molecular weight 260.13 g/mol.
Medchemexpress LLC CCT031374 hydrobromide | 1219184-91-4 | 98.1% | 434.33 | 10 MG
CCT031374 hydrobromide is a potent inhibitor of β-catenin/transcription factor (TCF) complex signaling. It inhibits TCF-dependent transcription of genes of the Wnt signaling pathway and exhibits antitumor activity.
- Potent inhibitor of β-catenin/TCF complex signaling
- Inhibits TCF-dependent transcription of Wnt signaling pathway genes
- Has antitumor activity
Medchemexpress LLC Halofuginone hydrobromide | 64924-67-0 | 495.59 | 1 MG
Halofuginone hydrobromide | 64924-67-0 | 495.59 | 1 MG
eMolecules Aniline hydrobromide | 542-11-0 | MFCD00035465 | 1g
Oakwood Chemicals | Aniline hydrobromide | 1g | 480148775 | 098809 | | 542-11-0 | MFCD00035465 | 174.041 | C6H8BrN
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Medchemexpress LLC Oxidopamine hydrobromide | 636-00-0 | 99.42% | 100 MG
Oxidopamine (6-OHDA) hydrobromide is an antagonist of the neurotransmitter dopamine. It is a widely used neurotoxin that selectively destroys dopaminergic neurons. It promotes COX-2 activation, leading to PGE2 synthesis and pro-inflammatory cytokine IL-1β secretion. Oxidopamine hydrobromide can be used for the research of Parkinson's disease (PD), attention-deficit hyperactivity disorder (ADHD), and Lesch-Nyhan syndrome.
- Antagonist of the neurotransmitter dopamine.
- Widely used neurotoxin.
- Selectively destroys dopaminergic neurons.
- Promotes COX-2 activation.
- Leads to PGE2 synthesis and pro-inflammatory cytokine IL-1β secretion.
- Used for research of Parkinson's disease (PD), attention-deficit hyperactivity disorder (ADHD), and Lesch-Nyhan syndrome.
Medchemexpress LLC Anisodamine hydrobromide | 55449-49-5 | 99.5% | 386.28 g/mol | C17H24BrNO4 | 10 MG
Anisodamine hydrobromide is the hydrobromide salt of anisodamine (6-hydroxyhyoscyamine), a belladonna alkaloid with muscarinic and nicotinic receptor activity. It is supplied as a high-purity research reagent for pharmacology and biochemical studies; not for clinical use.
- High purity (approximately 99.5%).
- Molecular weight 386.28 g/mol.
- Hydrobromide salt increases water solubility for aqueous assays.
- Supplied in small milligram quantities suitable for analytical and preclinical research.
- Commonly used in muscarinic receptor pharmacology and biochemical research applications.
Apexbio Technology LLC BD 1047 dihydrobromide 138356-21-5 10mg
BD 1047 dihydrobromide (CAS 138356-21-5) is a selective antagonist of the sigma-1 ( 1) receptor exhibiting Ki values of 0 93 nM for 1 and 47 nM for sigma-2 ( 2) receptors Sigma receptors distinct from opioid receptors include 1 and 2 subtypes and are implicated in modulating dopaminergic neurotransmission and drug-related behaviors In preclinical models BD 1047 dihydrobromide attenuates haloperidol- and DTG-induced dystonia and reverses cocaine-induced behavioral responses without affecting responses to natural rewards Additionally it alleviates mechanical allodynia in neuropathic pain models and modulates spinal 1 receptor and NR1 subunit expression This compound is utilized to investigate 1 receptor function in neuropharmacology and pain research
Medchemexpress LLC SCH-202676 hydrobromide | 265980-25-4 | 96.8% | 348.26 g·mol⁻¹ | C15H14BrN3S | 5 MG
SCH-202676 hydrobromide is a small-molecule allosteric modulator of G protein-coupled receptors and adenosine receptors with reported antiviral activity, including inhibition of 3CLpro. The compound is supplied for research use in solid and solution forms and is intended for biochemical and pharmacological studies.
- Allosteric modulator of GPCRs and adenosine receptors.
- Reported antiviral activity; inhibits 3CLpro with low-micromolar potency.
- Available as solid and 10 mM solution in DMSO.
- High purity (96.81%).
- Molecular formula C15H14BrN3S; molecular weight 348.26 g·mol⁻¹.
- Store at -20°C long term; in solvent store at -80°C for extended stability.
eMolecules 2403-33-0 | 2-BROMOPROPYLAMINE HBR | MFCD22055759 | 1g
AstaTech | 34-DIMETHOXY-2-METHYLBENZOIC ACID | 0.25g | 256638766 | 31432 | 95.000 | 5722-94-1 | MFCD09701444 | 196.202 | C10H12O4
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