Hydrobromides
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 MTSEA hydrobromide | 16599-33-0 | 97.9% | 50 MG
MTSEA hydrobromide is a sulfhydryl-reactive reagent used to modify free cysteine residues in proteins, introducing a positively charged side chain approximately the size of lysine. The hydrobromide salt is supplied as a solid and is used in biochemical assays and site-directed cysteine modification to probe protein structure and function.
- Sulfhydryl-reactive reagent for cysteine modification.
- Introduces a positively charged side chain similar in size to lysine.
- Suitable for biochemical assays and site-directed mutagenesis studies.
- Soluble in water and common organic solvents such as DMSO.
- High purity suitable for research applications.
Medchemexpress LLC Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 100 MG
Pyrithiamine hydrobromide is the hydrobromide salt of pyrithiamine, a thiamine metabolic inhibitor used in biochemical research. It serves as a substrate for thiamine pyrophosphokinase and is applied in studies of thiamine metabolism and nervous system disorders.
- Thiamine metabolic inhibitor used in biochemical research.
- Acts as a substrate for thiamine pyrophosphokinase.
- Useful in research on nervous system diseases and vitamin B1 metabolism.
- Chemical formula C14H20Br2N4O, molecular weight 420.14 g/mol.
- Supplied with high purity (≈96.6%).
- Available in small research quantities, including 100 mg.
TARGETMOL CHEMICALS INC PIFITHRIN-BETA HYDROBROM 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-(beta) hydrobromide (Cyclic PFT-(alpha)) is an inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and apoptosis. Protects against neuronal death in models of stroke and neurodegenerative disorders. Active in vivo; protects mice from the side-effects of Y therapy associated with p53 induction. Supresses self-renewal of embryonic stem cells. Also aryl hydrocarbon receptor (AHR) agonist causes upregulation of AHR target gene CYP1A1 (EC50 = 1.1 uM). purity: 99%
Medchemexpress LLC (RS)-AMPA hydrobromide | 171259-81-7 | MFCD00055183 | 99.5% | 267.08 g·mol⁻¹ | C7H11BrN2O4 | 5 MG
(RS)-AMPA hydrobromide is a research-grade glutamate analogue that acts as a potent, selective agonist of AMPA-type ionotropic glutamate receptors. Supplied as a solid hydrobromide salt with high purity, it is intended for use in neuropharmacology, electrophysiology, and receptor pharmacology studies. The compound is soluble in DMSO and water (sonication recommended) and should be stored protected from moisture under refrigerated or low-temperature conditions as specified by the supplier.
- Potent, selective agonist of AMPA receptors.
- Hydrobromide salt increases aqueous solubility.
- High purity suitable for research and analytical applications.
- Soluble in DMSO and water; sonication recommended.
- Stable when stored sealed and protected from moisture.
- Provided in small milligram quantities for experimental use.
eMolecules Synthonix 3-Bromopiperidine-2 6-dione 250mg 534611341 B41113 0 000 62595-74-8 MFCD11053059 192 012 C5H6BrNO2
Synthonix 3-Bromopiperidine-2 6-dione 250mg 534611341 B41113 0 000 62595-74-8 MFCD11053059 192 012 C5H6BrNO2
Active Motif Arecoline hydrobromide
Active Motif's Arecoline hydrobromide is an inhibitor of acetyl-CoA acetyltransferase 1 (ACAT1). Tyrosine 407 phosphorylation activates mitochondrial acetyl-CoA ACAT1 by stabilizing its tetramer. This is believed to be the mechanisms by which ACAT1 is "hijacked" and contributes to the Warburg effect in cancer. Arecoline is a covalent inhibitor of ACAT1 which binds to and disrupts only ACAT1 tetramers (IC50 = 11.1 uM). ACAT2 and DLAT are not inhibited. Treatment of xenograft nude mice with Arecoline resulted in a dose-dependent reduction in tumor mass. It is an agonist at muscarinic acetylcholine receptors M1-M5 (EC50 in the range of 7-410 nM), and may be involved in dementia.
Medchemexpress LLC Halofuginone (hydrobromide) | 64924-67-0 | MFCD00946455 | 100.0% | 495.59 g/mol | C16H18Br2ClN3O3 | 10 MG
Halofuginone hydrobromide is the hydrobromide salt of halofuginone, a febrifugine-derived small molecule that competitively inhibits prolyl-tRNA synthetase and is supplied for research applications studying fibrosis, inflammation, malaria, and cancer. It is provided as a white to off-white solid with high purity and defined storage and solvent recommendations.
- Hydrobromide salt for improved handling and solubility.
- Competitive prolyl-tRNA synthetase inhibitor used in mechanistic research.
- High purity suitable for research applications.
- White to off-white solid, soluble in DMSO (≈50 mg/mL) and water (≈2.6 mg/mL).
- Store sealed and away from moisture; in solution keep at -80°C for long-term stability.
- Applicable for preclinical studies of fibrosis, inflammation, malaria, and cancer pathways.