Hydrobromides
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Filtered Search Results
Medchemexpress LLC Pyrithiamine (hydrobromide) | 534-64-5 | 96.6% | 5MG
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Pyrithiamine (hydrobromide) | 534-64-5 | 96.6% | 5MG
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eMolecules EMOLECULES INC
5000470566 3-BROMOPIPERIDINE-2 6-DION 10G
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eMolecules TERT-BUTYL 3 8-DIAZABICYCL 25G
5000280348 TERT-BUTYL 3 8-DIAZABICYCL 25G
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eMolecules EMOLECULES INC
5000483234 3-BROMOPIPERIDINE-2 6-DION 25G
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Abcam Arecoline hydrobromide, Muscarinic receptor agonist, 250MG
MW 236.11 Da, Purity >98%. Muscarinic receptor agonist (EC₅₀ values are 7 (M₁), 95 (M₂), 11 (M₃), 410 (M₄) and 69 nM (M₅)). Natural alkaloid. Induces decreased blood-brain barrier permeability.
The product is subject to the following: Abcam Restricted Use Statement
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Medchemexpress LLC Arecoline hydrobromide | 300-08-3 | 99.95% | 1 ML
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Arecoline hydrobromide is a naturally brain-penetrant and orally active psychoactive alkaloid. It acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors, exhibiting properties such as stimulation, alertness, anxiolysis, and anti-parasitic effects. It can also induce oxidative stress. This compound is 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
- Brain-penetrant and orally active
- Induces reactive oxygen species generation and G1/G0 phase cell cycle arrest in HaCaT cells
- Upregulates stress-responsive genes
- Alleviates anxiety and depression in CFA-induced mice
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Medchemexpress LLC Fatostatin hydrobromide | 298197-04-3 | MFCD00760867 | 99.5% | C18H19BrN2S | 10 MM 1 ML
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Fatostatin hydrobromide | 298197-04-3 | MFCD00760867 | 99.5% | C18H19BrN2S | 10 MM 1 ML
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Medchemexpress LLC Carbamimidothioic acid, C,C'-(1,4-phenylenedi-2,1-ethanediyl) ester, hydrobromide (1:2) | 157254-60-9 | 98.0% | C12H20Br2N4S2 | 10MG
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1,4-PBIT (dihydrobromide) is the dihydrobromide salt of the small-molecule 1,4-PBIT, supplied for research use. The compound is documented by manufacturer COA and SDS, and is provided as a white to off-white solid with molecular formula C12H20Br2N4S2, molecular weight 444.25, and reported purity 98.0%.
- 98.0% purity as reported on the certificate of analysis
- White to off-white solid form for solid-handling workflows
- Molecular formula C12H20Br2N4S2 and molecular weight 444.25
- Recommended storage: in solvent -80°C (6 months) or -20°C (1 month), sealed
- Used as a nitric oxide synthase inhibitor in research applications
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Medchemexpress LLC Nan-190 hydrobromide | 115338-32-4 | 99.1% | 474.39 | 200 MG
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NAN-190 hydrobromide is a serotonin receptor 5-HT antagonist that selectively targets the 5-HT1A receptor. This compound is intended for research use only. In vivo studies demonstrate its ability to reverse the catalepsy-improving effect of fluoxetine in 6-OHDA lesioned rats.
- Selective antagonist of 5-HT1A receptor
- Antagonist of 5-HT1 receptor
- Suitable for research applications
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Medchemexpress LLC Burixafor (hydrobromide) | 1191450-19-7 | 98.0% | 769.01 | 1 ML
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Burixafor hydrobromide is a potent CXCR4 antagonist that inhibits the binding of CXCL12 to CXCR4 and blocks downstream signaling. It mobilizes CD34+ hematopoietic stem/progenitor cells from bone marrow to peripheral blood. This compound is used for research on autologous hematopoietic stem cell transplantation (ASCT).
- Potent CXCR4 antagonist with a pIC50 of 7.4.
- Inhibits binding of CXCL12 to CXCR4.
- Mobilizes CD34+ hematopoietic stem/progenitor cells.
- Useful for research on autologous hematopoietic stem cell transplantation.
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Selleck Chemical LLC Arecoline HBr S2614-50mg
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Arecoline(NSC-31750) is a muscarinic acetylcholine receptor agonist
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000739202 ARECOLINE-D5 HYDROB 5MG
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Apexbio Technology LLC A 61603 hydrobromide 107756-30-9 5mg
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A 61603 hydrobromide (CAS 107756-30-9) is a potent and highly selective agonist of the 1A-adrenergic receptor one of the 1-adrenergic receptor subtypes involved in cellular growth and proliferation Compared to its activity at 1B- and 1D-adrenergic receptors A 61603 demonstrates approximately 35-fold higher potency for 1A-AR In cellular assays it robustly induces phosphoinositide hydrolysis in 1A-AR-expressing fibroblasts (pEC50 8 24) and in neonatal rat cardiomyocytes it increases calcium transient frequency in a dose-dependent manner (EC50 6 9 nM) In vascular models A 61603 markedly elevates perfusion pressure demonstrating significantly greater efficacy than noradrenaline This compound serves as a valuable tool for delineating 1A-AR-mediated signaling and vascular regulation
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eMolecules 1 8-DIAZABICYCLO 5.4.0 UN 100G
5000162048 1 8-DIAZABICYCLO 5.4.0 UN 100G
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Medchemexpress LLC Pyrithiamine hydrobromide | 534-64-5 | 96.6% | 50 MG
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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.
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