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.
eMolecules Aniline hydrobromide | 542-11-0 | MFCD00035465 | 1g
Oakwood Chemicals | Aniline hydrobromide | 1g | 480148775 | 098809 | | 542-11-0 | MFCD00035465 | 174.041 | C6H8BrN
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
Medchemexpress LLC Scopolamine hydrobromide trihydrate | 6533-68-2 | MFCD00150066 | 99.9% | 438.31 | 100 MG
Scopolamine hydrobromide trihydrate is a high-affinity muscarinic antagonist that can cross the blood-brain barrier. It acts as a competitive antagonist of 5-HT3 receptors. This compound can induce cognitive and memory deficits in animals and is used in research.
- High-affinity muscarinic antagonist
- Crosses the blood-brain barrier
- Competitive antagonist of 5-HT3 receptors
- Induces cognitive and memory deficits in animals
- Used in research for preventing postoperative nausea and vomiting
- Used in research for motion sickness
- Used in research for nervous system diseases
TARGETMOL CHEMICALS INC Galanthamine hydrobromide
Also available in 1 mL, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Galanthamine hydrobromide (Galantamine hydrobromide), a long-acting and centrally active AChE inhibitor (IC50410 nM), is an allosteric potentiator at neuronal nicotinic ACh receptors. Purity 99.19%
TARGETMOL CHEMICALS INC Immethridine dihydrobromide
Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Immethridine dihydrobromide is a novel, highly potent and selective histamine H3 receptor (H3R) agonist that inhibits dendritic cell function and alleviates experimental autoimmune encephalomyelitis.Immethridine dihydrobromide MesV induces depolarization of neurons and the MMN and prevents cardiorenal and renal injury. injury. Purity 98.16%
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
Accela Chembio Inc 3-(bromomethyl)pyridine Hydrobromide | 5g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
3-(bromomethyl)pyridine Hydrobromide | 5g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
Accela Chembio Inc 3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
Medchemexpress LLC 2-iminobiotin hydrobromide | 76985-52-9 | 98.0% | 324.24 g/mol | C10H18BrN3O2S | 25 MG
2-Iminobiotin hydrobromide (CAS 76985-52-9) is a synthetic biotin analog and a reversible inhibitor of nitric oxide synthases (iNOS and nNOS). Supplied as a solid or as ready-to-use DMSO solutions, it is used in biochemical and cellular assays to modulate nitric oxide production and investigate NOS-related pathways.
- Reversible inhibition of iNOS and nNOS for targeted enzyme studies.
- Suitable for biochemical assays and cellular research.
- Available in solid form and as DMSO solutions for flexible dosing.
- High purity (≈98.0%) to support reproducible results.
- Molecular weight 324.24 g/mol and well-defined chemical identity (C10H18BrN3O2S).
TARGETMOL CHEMICALS INC Halofuginone hydrobromide 10MG
Also available in 1 mL, 1 mg, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Halofuginone specifically inhibits collagen type I gene expression and matrix metalloproteinase 2 (MMP-2) gene expression, which may result in the suppression of angiogenesis, tumor stromal cell development, and tumor cell growth. Halofuginone Hydrobromide is the hydrobromide salt of halofuginone, a semisynthetic quinazolinone alkaloid anticoccidial derived from the plant Dichroa febrifuga, with antifibrotic and potential antineoplastic activities. These effects appear to be due to halofuginone-mediated inhibition of the collagen type I and MMP-2 promoters. Collagen type I and MMP-2 play important roles in fibroproliferative diseases. Purity 98.5%
Medchemexpress LLC Galanthamine hydrobromide | 1953-04-4 | MFCD00067672 | 99.9% | C17H22BrNO3 | 100 MG
Galanthamine hydrobromide is a selective, reversible, and competitive alkaloid acetylcholinesterase (AChE) inhibitor with an IC50 of 0.35 μM. It also acts as a potent allosteric potentiating ligand (APL) for human α3β4, α4β2, and α6β4 nicotinic receptors (nAChRs). This compound is developed for research related to Alzheimer's disease (AD).
- Selective, reversible, competitive AChE inhibitor
- Potent allosteric potentiating ligand for human nicotinic receptors
- Reduces cognitive deficits in APP23 mice
- Protects against Aβ toxicity in SH-SY5Y cells
Medchemexpress LLC Galanthamine hydrobromide | 1953-04-4 | 99.9% | C17H22BrNO3 | 1 ML
Galanthamine hydrobromide is a selective, reversible, competitive, alkaloid AChE inhibitor (IC50 0.35 μM) and a potent allosteric potentiating ligand (APL) for human α3β4, α4β2, α6β4 nicotinic receptors (nAChRs). It is developed for Alzheimer's disease (AD) research.
- Selective, reversible, competitive, alkaloid AChE inhibitor.
- Potent allosteric potentiating ligand (APL) of human nAChRs.
- Developed for Alzheimer's disease (AD) research.
- Demonstrates 53-fold selectivity for AChE over butyrylcholinesterase.
- Inhibits Aβ 1-40 and Aβ 1-42 aggregation (50 μM).
- Protects against Aβ(1-40) and Aβ(1-42) toxicity in SH-SY5Y cells.
- Reduces Aβ(1-40)-induced cellular apoptosis.
- Reduces cognitive deficits in APP23 mice.
Medchemexpress LLC Pifithrin-α hydrobromide | 63208-82-2 | C16H19BrN2OS | 25 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.
- Suppresses p53 protein transcription
- Prevents glucose oxidase (GOX)-induced p53 protein increase, Bcl-2 protein reduction, and Bax increase
- Inhibits p53-dependent apoptosis
- Acts as a potent AhR agonist, activating reporter activity, and up-regulating the AhR target gene CYP1A1
- Reduces the percentage of annexin V-positive Foxe3-/- SMCs
- Significantly reduces the incidence of aortic rupture and intramural hematomas
- Normalizes aortic diameter and TUNEL-positive cells in surviving Foxe3-/- animals