Hydrobromides
Medchemexpress LLC Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 50 MG
Pyrithiamine hydrobromide is a thiamine analog and metabolic inhibitor used as a research reagent to study thiamine-dependent pathways and to model thiamine deficiency in cellular and animal studies.
- Thiamine metabolism inhibitor for experimental studies.
- Acts as a substrate for thiamine pyrophosphokinase.
- Suitable for biochemical and neuroscience research applications.
- Solid, white to light yellow powder with reported purity of 96.6%.
- Store at -20°C; follow recommended storage for solutions.
Medchemexpress LLC CCT031374 hydrobromide | 1219184-91-4 | 98.08% | 434.33 | 25 MG
CCT031374 hydrobromide is a potent inhibitor of β-catenin/transcription factor (TCF) complex signaling. It inhibits TCF-dependent transcription of genes in the Wnt signaling pathway and demonstrates antitumor activity.
- Potent inhibitor of β-catenin/TCF complex signaling
- Inhibits TCF-dependent transcription of Wnt signaling pathway genes
- Demonstrates antitumor activity
- For research use only
TARGETMOL CHEMICALS INC CCT 031374 HYDROBROMIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CCT 031374 hydrobromide is a TCF/(beta)-catenin inhibitor with antitumor activities. purity: 98%
Medchemexpress LLC NAN-190 hydrobromide | 115338-32-4 | 99.1% | 474.39 | 1 ML
NAN-190 hydrobromide is a serotonin receptor 5-HT antagonist and a selective antagonist of 5-HT1A. It is intended for research use only and can reverse the catalepsy-improving effect of fluoxetine in 6-OHDA lesioned rats.
- Appearance: solid
- Color: light yellow to yellow
- Shipping: room temperature in continental US; may vary elsewhere
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month (sealed storage, away from moisture)
- For research use only
Medchemexpress LLC SCH-202676 (hydrobromide) | 265980-25-4 | 96.8% | 348.26 | 25 MG
SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). It exhibits antiviral activity, inhibiting 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM.
- Allosteric modulator of G protein-coupled receptors (GPCRs)
- Allosteric modulator of adenosine receptor (AR)
- Antiviral activity
- Inhibits 3CLpro in a time-dependent manner
Medchemexpress LLC 3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-methyl-, methyl ester, hydrobromide | 300-08-3 | 99.95% | 1 G
Arecoline hydrobromide is a naturally occurring psychoactive alkaloid that is brain-penetrant and orally active. It acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors. It exhibits stimulation, alertness, anxiolysis, and anti-parasitic effects, and can also induce oxidative stress. It is intended for research use only.
- Acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors.
- Exhibits stimulation, alertness, anxiolysis, and anti-parasitic effects.
- Can induce oxidative stress.
- Induces reactive oxygen species generation and G1/G0 phase cell cycle arrest in HaCaT cells.
- Alleviates anxiety and depression in CFA-induced mice.
Medchemexpress LLC CPTH6 hydrobromide 1mg | 2321332-57-2 | 1 MG
CPTH6 hydrobromide is a thiazole-derived small molecule that modulates histone acetyltransferase activity and induces apoptotic and autophagic features in leukemia cell lines. It is provided as the hydrobromide salt for use in biochemical and cell-based cancer research applications.
- Thiazole-derived HAT inhibitor that reduces histone acetylation.
- Promotes apoptotic program and increases autophagic features in leukemia cells.
- Provided as a solid hydrobromide salt for improved handling and stability.
- Suitable for biochemical assays and cell-based studies of acetylation-dependent processes.
- Supplied in small research quantities for screening and mechanistic experiments.