Hydrobromides
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
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Synthonix | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 25g | 831793877
3-Bromopiperidine-2,6-dione | Synthonix | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 25g | 831793877
Medchemexpress LLC SCH-202676 hydrobromide | 265980-25-4 | 96.81% | 348.26 | 100 MG
SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). It exhibits antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM.
- Allosteric modulator of G protein-coupled receptors and adenosine receptor.
- Exhibits antiviral activity.
- Inhibits 3CLpro in a time-dependent manner.
- IC50 value of 0.655 μM.
Medchemexpress LLC Homatropine Bromide | 51-56-9 | 99.9% | 1 ML
Homatropine Bromide is an orally active muscarinic acetylcholine receptor antagonist. It functions as an anticholinergic agent and is intended for research applications only. This product is provided as a 10 mM solution in DMSO.
- Orally active muscarinic acetylcholine receptor antagonist
- Functions as an anticholinergic agent
- Provided as a 10 mM solution in DMSO
- Purity of 99.9%
- Suitable for research applications
Medchemexpress LLC Halofuginone hydrobromide | 64924-67-0 | 495.59 | 500 MG
Halofuginone hydrobromide is a Febrifugine derivative and a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM. It is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibiting TGF-β activity. It also acts as a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated, and store-operated Ca2+ channels.
- Competitive prolyl-tRNA synthetase inhibitor (Ki of 18.3 nM).
- Specific inhibitor of type-I collagen synthesis.
- Attenuates osteoarthritis (OA) by inhibition of TGF-β activity.
- Potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated, and store-operated Ca2+ channels.
- Has anti-malaria, anti-inflammatory, anti-cancer, and anti-fibrosis effects.
Selleck Chemical LLC Homatropine Methylbromide S4024-50mg
Homatropine Methylbromide is muscarinic AChR antagonist inhibits endothelial and smooth muscle muscarinic receptors of WKY-E and SHR-E with IC50 of 162 5 nM and 170 3 nM respectively
Accela Chembio Inc 3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
Medchemexpress LLC Guvacoline hydrobrom 5mg | 17210-51-4 | 222.08 g/mol | C7H12BrNO2 | 5 MG
Guvacoline hydrobromide is the hydrobromide salt of guvacoline, a pyridine alkaloid that acts as a weak full agonist of atrial and ileal muscarinic acetylcholine receptors (mAChR). It is supplied as a solid reagent intended for biochemical and pharmacological research applications.
- Hydrobromide salt form suitable for laboratory handling
- CAS number 17210-51-4
- Molecular formula C7H12BrNO2; molecular weight 222.08 g/mol
- Purity 96.09% as verified by certificate of analysis
- Used as a pharmacological tool for muscarinic receptor studies
Selleck Chemical LLC Fenoterol hydrobromide
Fenoterol hydrobromide (Phenoterol) is the the hydrobromide salt of fenoterol a 2 adrenoreceptor agonist with bronchodilator activity
TARGETMOL CHEMICALS INC Tedatioxetine hydrobromide 1MG
Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) is a serotonin-norepinephrine-dopamine reuptake inhibitor and an antagonist of 5-HT2A, 5-HT2C, 5-HT3, and alpha1A-adrenergic receptors, which can be used to treat depression and anxiety. Purity 99.5%
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Ambeed | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 25g | 570570298
3-Bromopiperidine-2,6-dione | Ambeed | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 25g | 570570298
eMolecules 768-66-1 | 2,2,6,6-Tetramethylpiperidine | Ambeed | MFCD00005985 | 141.258 | C9H19N | 98.000 | CC1(C)CCCC(C)(C)N1 | 5g | 525234718
2,2,6,6-Tetramethylpiperidine | Ambeed | 768-66-1 | MFCD00005985 | 141.258 | C9H19N | 98.000 | CC1(C)CCCC(C)(C)N1 | 5g | 525234718
eMolecules 62595-74-8 | 3-bromopiperidine-2,6-dione | Abosyn Chemicals Inc. | MFCD11053059 | 192.012 | C5H6BrNO2 | 0.000 | BrC1CCC(=O)NC1=O | 5g | 812065078
3-bromopiperidine-2,6-dione | Abosyn Chemicals Inc. | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 0.000 | BrC1CCC(=O)NC1=O | 5g | 812065078
eMolecules 62595-74-8 | 3-Bromopiperidine-2,6-dione | Synthonix | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 100g | 831793878
3-Bromopiperidine-2,6-dione | Synthonix | 62595-74-8 | MFCD11053059 | 192.012 | C5H6BrNO2 | 97.000 | BrC1CCC(=O)NC1=O | 100g | 831793878