Hydrobromides
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 CPTH6 hydrobromide 5mg | 2321332-57-2 | 5 MG
CPTH6 hydrobromide is the hydrobromide salt of CPTH6, a thiazole-derived inhibitor of histone acetyltransferases selective for Gcn5 and pCAF. It reduces acetylation of histone H3/H4 and α-tubulin, impairs autophagy, and induces G0/G1 arrest and apoptosis in tumor cell lines; it is used as a research reagent for epigenetics and cancer biology studies.
- Research-grade compound for in vitro studies.
- Purity ≥98%.
- Molecular weight 386.7 g/mol.
- Molecular formula C15H16ClN3S · HBr.
- Soluble in DMSO, ethanol, and DMF.
- Available in 5 mg vials.
Apexbio Technology LLC Scopolamine hydrobromide 114-49-8 100mg
Scopolamine hydrobromide (114-49-8) is a small-molecule antagonist targeting muscarinic acetylcholine receptors and serotonin 5-HT3 receptors It is designed to reversibly block these receptors thereby modulating cholinergic and serotonergic signaling pathways Scopolamine hydrobromide exerts its biological activity primarily through reversible antagonism of muscarinic receptors and inhibition of serotonin 5-HT3 receptor responses In receptor binding studies Scopolamine hydrobromide demonstrates antagonistic activity with reported IC50 values generally ranging from nanomolar to micromolar concentrations depending on the receptor subtype and experimental conditions Based on these pharmacological properties Scopolamine hydrobromide holds research potential in studies of neurotransmission cholinergic signaling gastrointestinal motility assays cognitive impairment models and emesis reflex investigations
Chemscene ChemScene | 4-(Bromomethyl)pyridine hydrobromide | 10G | CS-W004084 | 0.98 | 73870-24-3| MFCD01863545 | 252.94
ChemScene | 4-(Bromomethyl)pyridine hydrobromide | 10G | CS-W004084 | 0.98 | 73870-24-3| MFCD01863545 | 252.94
Apexbio Technology LLC 6-Hydroxydopamine hydrobromide(Synonyms: Oxidopamine hydrobromide, 6-OHDA hydrobromide, 6-Hydroxydopamine HBr), 50mg, CAS: 636-00-0.
6-Hydroxydopamine hydrobromide (CAS 636-00-0) commonly referred to as 6-OHDA hydrobromide is a catecholamine-derived neurotoxin frequently used in neuroscience research to induce selective dopaminergic neuronal degeneration Upon administration it generates intracellular reactive oxygen species (ROS) activating apoptotic pathways via caspase-3 -8 and -9 as demonstrated in PC12 cell studies In rodent models targeted injection into substantia nigra striatum or medial forebrain bundle leads to loss of tyrosine hydroxylase-positive neurons and resultant locomotor dysfunction resembling symptoms observed in Parkinson s disease Consequently it serves as a valuable tool for elucidating dopaminergic dysfunction mechanisms and evaluating therapeutic candidates
Medchemexpress LLC 2-iminobiotin hydrobromide | 76985-52-9 | 98.0% | 324.24 g·mol⁻1 | C10H18BrN3O2S | 1 ML
2-Iminobiotin hydrobromide is a biotin analog and a reversible inhibitor of nitric oxide synthases used in research to probe NO signaling and neuroprotection. It is supplied as a 10 mM solution in DMSO (1 mL) and has reported Ki values of 21.8 μM for murine iNOS and 37.5 μM for rat n-cNOS. For research use only; not for human or therapeutic applications.
- Biotin analog that reversibly inhibits nitric oxide synthases (NOS).
- Reported Ki: 21.8 μM (murine iNOS) and 37.5 μM (rat n-cNOS).
- Supplied as 10 mM solution in DMSO, 1 mL vial.
- Molecular weight 324.24 g·mol⁻1; formula C10H18BrN3O2S.
- Purity: 98.0%.
- Suitable for research on NO signaling, immunology, and neuroprotection.
Apexbio Technology LLC Homatropine Bromide 51-56-9 1g
Homatropine Bromide (CAS 51-56-9) is a small molecule antagonist of muscarinic acetylcholine receptors (AChRs) It selectively inhibits muscarinic receptor-mediated responses in endothelial and smooth muscle cells with reported IC50 values of 162 5 nM and 170 3 nM for WKY-E and SHR-E cell models respectively This compound serves as a valuable tool for investigating the role of muscarinic signaling in vascular function and smooth muscle physiology within experimental research settings
Medchemexpress LLC Amthamine dihydrobromide | 142457-00-9 | MFCD00673891 | 99.6% | 319.07 g·mol⁻¹ | C6H13Br2N3S | 5 MG
Amthamine dihydrobromide is the dihydrobromide salt of amthamine, a selective histamine receptor agonist used in pharmacology and receptor research. It is supplied as a purified solid for use in in vitro and in vivo assays to probe histamine receptor function and signaling.
- High reported purity: 99.6%.
- Molecular weight 319.07 g·mol⁻¹.
- Supplied as a solid dihydrobromide salt.
- Suitable for histamine receptor pharmacology and assay work.
- Available in small milligram pack sizes for research use.
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