Hydrobromides
Apexbio Technology LLC Imetit dihydrobromide 32385-58-3 10mg
Imetit dihydrobromide (CAS 32385-58-3) is a potent high-affinity agonist of histamine H3 and H4 receptors demonstrating Ki values of 0 3 nM and 2 7 nM respectively Functionally it replicates histaminergic effects by inducing morphological changes in eosinophils with an EC50 of 25 nM Owing to its selective receptor activity Imetit dihydrobromide is widely employed in studies investigating allergic inflammatory processes including asthma as well as in research focused on central nervous system physiology and histamine-related pathways
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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TARGETMOL CHEMICALS INC Clobenpropit dihydrobromide
Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Clobenpropit dihydrobromide is a potent antagonist and inverse agonist of histamine H3R (histamine H3LR,pEC50 of 8.07) Purity 99.48%
Cayman Chemical FenoterolhydrobromIde 10mg
An analytical reference standard categorized as a β2-adrenergic receptor agonist; has been used as a performance-enhancing drug in sports doping and is banned by WADA; intended for research and forensic applications
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.
![Medchemexpress LLC Piperidine, 4-[2-[(4-methylphenyl)thio]phenyl]-, hydrobromide | 960151-65-9 | 99.8% | 364.34 g/mol | C18H22BrNS | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000249020.png-250.jpg)
Medchemexpress LLC Piperidine, 4-[2-[(4-methylphenyl)thio]phenyl]-, hydrobromide | 960151-65-9 | 99.8% | 364.34 g/mol | C18H22BrNS | 1 ML
Tedatioxetine hydrobromide is the hydrobromide salt of tedatioxetine, a serotonin- and norepinephrine-preferring triple reuptake inhibitor that also antagonizes 5-HT2A, 5-HT2C, 5-HT3, and α1A-adrenergic receptors. It is supplied for research use as a solid and as a 10 mM solution in DMSO, intended for in vitro transporter and receptor pharmacology studies.
- High purity (99.83%) suitable for research applications.
- Supplied as solid and as a 10 mM solution in DMSO (1 mL).
- Suitable for transporter and receptor pharmacology assays.
- Molecular formula C18H22BrNS; molecular weight 364.34 g/mol.
- Store sealed, away from moisture; in solvent: -80°C (6 months) or -20°C (1 month).
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 Guvacoline hydrobrom 10mg | 17210-51-4 | 222.08 g·mol⁻1 | C7H12BrNO2 | 10 MG
Guvacoline hydrobromide is the hydrobromide salt of guvacoline, a pyridine alkaloid that acts as a weak full agonist at atrial and ileal muscarinic acetylcholine receptors. This research-grade solid is provided for in vitro pharmacology and receptor-binding studies.
- High purity (96.09%) research-grade material.
- Molecular weight 222.08 g·mol⁻1; formula C7H12BrNO2.
- Suitable for muscarinic receptor pharmacology and neuropharmacology assays.
- Supplied as a 10 mg solid for small-scale experimental use.