Hydrobromides
Cayman Chemical FenoterolhydrobromIde 10mg
An analytical reference standard categorized as a β2-adrenergic receptor agonist; has been used as a performance-enhancing drug in sports doping and is banned by WADA; intended for research and forensic applications
Medchemexpress LLC SCH-202676 hydrobromide | 265980-25-4 | 96.8% | 348.26 g·mol⁻¹ | C15H14BrN3S | 5 MG
SCH-202676 hydrobromide is a small-molecule allosteric modulator of G protein-coupled receptors and adenosine receptors with reported antiviral activity, including inhibition of 3CLpro. The compound is supplied for research use in solid and solution forms and is intended for biochemical and pharmacological studies.
- Allosteric modulator of GPCRs and adenosine receptors.
- Reported antiviral activity; inhibits 3CLpro with low-micromolar potency.
- Available as solid and 10 mM solution in DMSO.
- High purity (96.81%).
- Molecular formula C15H14BrN3S; molecular weight 348.26 g·mol⁻¹.
- Store at -20°C long term; in solvent store at -80°C for extended stability.
eMolecules 2403-33-0 | 2-BROMOPROPYLAMINE HBR | MFCD22055759 | 1g
AstaTech | 34-DIMETHOXY-2-METHYLBENZOIC ACID | 0.25g | 256638766 | 31432 | 95.000 | 5722-94-1 | MFCD09701444 | 196.202 | C10H12O4
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<|a>
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Synthonix - Stock | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 1g | 476497459
3-Bromopiperidine-2,6-dione | Synthonix - Stock | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 1g | 476497459
Medchemexpress LLC Guvacoline hydrobrom 10mg | 17210-51-4 | 222.08 g·mol⁻1 | C7H12BrNO2 | 10 MG
Guvacoline hydrobromide is the hydrobromide salt of guvacoline, a pyridine alkaloid that acts as a weak full agonist at atrial and ileal muscarinic acetylcholine receptors. This research-grade solid is provided for in vitro pharmacology and receptor-binding studies.
- High purity (96.09%) research-grade material.
- Molecular weight 222.08 g·mol⁻1; formula C7H12BrNO2.
- Suitable for muscarinic receptor pharmacology and neuropharmacology assays.
- Supplied as a 10 mg solid for small-scale experimental use.
Apexbio Technology LLC BD 1047 dihydrobromide 138356-21-5 50mg
BD 1047 dihydrobromide (CAS 138356-21-5) is a selective antagonist of the sigma-1 ( 1) receptor exhibiting Ki values of 0 93 nM for 1 and 47 nM for sigma-2 ( 2) receptors Sigma receptors distinct from opioid receptors include 1 and 2 subtypes and are implicated in modulating dopaminergic neurotransmission and drug-related behaviors In preclinical models BD 1047 dihydrobromide attenuates haloperidol- and DTG-induced dystonia and reverses cocaine-induced behavioral responses without affecting responses to natural rewards Additionally it alleviates mechanical allodynia in neuropathic pain models and modulates spinal 1 receptor and NR1 subunit expression This compound is utilized to investigate 1 receptor function in neuropharmacology and pain research
Medchemexpress LLC Sulfone, bis((4-chloroacetylamino)phenyl). | 17328-16-4 | MFCD00028183 | 98.0% | 401.26 g/mol | C16H14Cl2N2O4S | 1 ML
TC-E 5003 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor supplied as a ready-to-use 10 mM solution in DMSO for research use in biochemical and cell-based assays. Handle and store according to laboratory safety and storage guidelines.
- Selective PRMT1 inhibitor with reported IC50 ≈ 1.5 μM.
- Supplied as a 10 mM solution in DMSO, 1 mL vial.
- Purity 98.0% by HPLC.
- Molecular weight 401.26 g/mol.
- Store solution at -80°C for long-term stability; short-term storage at -20°C.
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Ambeed | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 250mg | 506392068
3-Bromopiperidine-2,6-dione | Ambeed | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 250mg | 506392068
Medchemexpress LLC Arecoline hydrobromide | 300-08-3 | 99.95% | 500 MG
Arecoline hydrobromide is a naturally occurring, brain-penetrant, and orally active psychoactive alkaloid. It functions as a partial agonist for both nicotinic and muscarinic acetylcholine receptors, influencing various neurological processes. This compound has been noted for its ability to induce stimulation, alertness, anxiolysis, and anti-parasitic effects, though it can also cause oxidative stress.
- Naturally occurring psychoactive alkaloid
- Brain-penetrant and orally active
- Acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors
- Can induce stimulation, alertness, anxiolysis, and anti-parasitic effects
- Induces reactive oxygen species and cell cycle arrest in HaCaT cells
- Alleviates anxiety and depression in CFA-induced mice
Medchemexpress LLC SCH-202676 (hydrobromide) | 265980-25-4 | 96.8% | 348.26 | 1 ML
SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). It demonstrates antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM.
- Purity: 96.81%
- Appearance: Solid
- Color: White to off-white
- Solubility: DMSO: 10 mg/mL
Medchemexpress LLC Remodelin (hydrobromide) | 1622921-15-6 | 99.6% | 363.28 | 500 MG
Remodelin hydrobromide is an orally active and selective inhibitor of acetyltransferase NAT10. It inhibits NAT10 activity, slows DNA replication, and suppresses the growth of prostate cancer cells. It also inhibits the growth of prostate cancer and hepatocellular carcinoma in xenograft models. Additionally, it enhances the healthspan in a Hutchinson-Gilford Progeria Syndrome (HGPS) mouse model.
- Orally active and selective inhibitor of acetyltransferase NAT10.
- Inhibits NAT10 activity.
- Slows DNA replication.
- Suppresses growth of prostate cancer cells.
- Inhibits the growth of prostate cancer and hepatocellular carcinoma in xenograft model.
- Enhances healthspan in Hutchinson-Gilford Progeria Syndrome (HGPS) mouse model.
AdipoGen 2 3-Diaminopropane-1-thiol HBr
Chemical. CAS 70548-07-1. Formula C3H10N2S . 2HBr. MW 106.2 . 161.8. Synthetic Building block for synthesis.
eMolecules 62595-74-8 | 3-bromopiperidine-2,6-dione | Pharmablock | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 250g | 812209008
3-bromopiperidine-2,6-dione | Pharmablock | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 250g | 812209008
Medchemexpress LLC Fenoterol hydrobromide | 1944-12-3 | 100.0% | 1 ML
Fenoterol hydrobromide (Th-1165a) is a sympathomimetic agent that acts as a selective and orally active β2-adrenoceptor agonist. It is an effective bronchodilator, making it suitable for research into bronchospasm associated with asthma, bronchitis, and other obstructive airway diseases.
- Selective and orally active β2-adrenoceptor agonist
- Functions as an effective bronchodilator
- Used in research for bronchospasm associated with asthma, bronchitis, and other obstructive airway diseases
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.