Hydrobromides
TARGETMOL CHEMICALS INC TC-E 5003 200MG
Also available in 1 mL, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. TC-E 5003 (NSC-30176) is a selective inhibitor of PRMT1 with IC50 of 1.5 uM. Purity 97.01%
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 Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 25 MG
Pyrithiamine hydrobromide is a thiamine metabolic inhibitor supplied as a high-purity solid for laboratory research. It is used to study thiamine-dependent biochemical pathways and nervous system disease models.
- Thiamine metabolic inhibitor for biochemical research.
- Acts as a substrate for thiamine pyrophosphokinase.
- Purity 96.6% (manufacturer reported).
- Molecular formula C14H20Br2N4O and molecular weight 420.14 g·mol⁻¹.
- CAS number 534-64-5.
- Supplied as a 25 MG solid for laboratory use; not for human consumption.
Medchemexpress LLC Halofuginone hydrobromide | 64924-67-0 | MFCD00946455 | 100.0% | 495.59 g·mol⁻¹ | C16H18Br2ClN3O3 | 10 MG
Halofuginone hydrobromide is a febrifugine derivative and a competitive prolyl-tRNA synthetase inhibitor used as a research standard for studies of collagen synthesis, TGF-β signaling, fibrosis, cancer biology, and anti-parasitic activity.
- Competitive prolyl-tRNA synthetase inhibitor with reported Ki ≈ 18.3 nM.
- Inhibits type-I collagen synthesis, useful for fibrosis and TGF-β studies.
- High reported purity (99.99%), suitable as a reference standard.
- Characterized molecular weight (495.59 g·mol⁻¹) and CAS number (64924-67-0).
- Available in small mg quantities for in vitro and pharmacological assays.
Apexbio Technology LLC Scopolamine hydrobromide 114-49-8 500mg
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