Hydrobromides
Medchemexpress LLC SCH-202676 hydrobromide | 265980-25-4 | 96.81% | 348.26 | 100 MG
SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). It exhibits antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM.
- Allosteric modulator of G protein-coupled receptors and adenosine receptor.
- Exhibits antiviral activity.
- Inhibits 3CLpro in a time-dependent manner.
- IC50 value of 0.655 μM.
Medchemexpress LLC Homatropine Bromide | 51-56-9 | 99.9% | 1 ML
Homatropine Bromide is an orally active muscarinic acetylcholine receptor antagonist. It functions as an anticholinergic agent and is intended for research applications only. This product is provided as a 10 mM solution in DMSO.
- Orally active muscarinic acetylcholine receptor antagonist
- Functions as an anticholinergic agent
- Provided as a 10 mM solution in DMSO
- Purity of 99.9%
- Suitable for research applications
Medchemexpress LLC Fenoterol hydrobromide | 1944-12-3 | 100.0% | 1 ML
Fenoterol hydrobromide (Th-1165a) is a sympathomimetic agent that acts as a selective and orally active β2-adrenoceptor agonist. It is an effective bronchodilator, making it suitable for research into bronchospasm associated with asthma, bronchitis, and other obstructive airway diseases.
- Selective and orally active β2-adrenoceptor agonist
- Functions as an effective bronchodilator
- Used in research for bronchospasm associated with asthma, bronchitis, and other obstructive airway diseases
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 BC-11 hydrobromide | 443776-49-6 | 99.0% | 290.97 | 25 MG
BC-11 hydrobromide is a selective TMPRSS2 inhibitor and a selective urokinase (uPA) inhibitor. It demonstrates cytotoxicity against triple-negative MDA-MB231 breast cancer cells.
- Selective TMPRSS2 inhibitor
- Selective urokinase (uPA) inhibitor
- Cytotoxic to triple-negative MDA-MB231 breast cancer cells
- Used in research on viral infections and cancer
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
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
Cayman Chemical Clobenpropit hydrobromide
A selective histamine H3 receptor antagonist (Ki = 0.17 nM in rat cortical membranes); reduces inhibition of electrically induced contractions in isolated guinea pig ileum longitudinal muscle by (R)-α-methylhistamine at 0.3, 0.1, and 3 nM; decreases the duration of the tonic, clonic, and convulsive coma phases of electrically induced convulsions in mice at 1 and 3 mg/kg, an effect that can be blocked by (R)-α-methylhistamine or imetit; increases GABA release and inhibits NMDA-induced neurotoxicity in primary rat cortical neurons at 0.1 μM
TARGETMOL CHEMICALS INC PIFITHRIN-ALPHA HYDROBRO 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-(alpha) hydrobromide (Pifithrin-(alpha) hydrobromide) is a p53 inhibitor inhibiting p53-dependent transactivation of p53-responsive genes. purity: 98%
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 Guvacoline hydrobrom 5mg | 17210-51-4 | 222.08 g/mol | C7H12BrNO2 | 5 MG
Guvacoline hydrobromide is the hydrobromide salt of guvacoline, a pyridine alkaloid that acts as a weak full agonist of atrial and ileal muscarinic acetylcholine receptors (mAChR). It is supplied as a solid reagent intended for biochemical and pharmacological research applications.
- Hydrobromide salt form suitable for laboratory handling
- CAS number 17210-51-4
- Molecular formula C7H12BrNO2; molecular weight 222.08 g/mol
- Purity 96.09% as verified by certificate of analysis
- Used as a pharmacological tool for muscarinic receptor studies
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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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