Hydrochlorides
Medchemexpress LLC Pazopanib hydrochloride | 635702-64-6 | >95.0% | 500MG
Pazopanib hydrochloride | 635702-64-6 | >95.0% | 500MG
Medchemexpress LLC PXS-4787 hydrochloride | 2409964-40-3 | 99.7% | 265.73 g/mol | C10H13ClFNO2S | 10 MG
PXS-4787 hydrochloride is a research-use small-molecule pan-lysyl oxidase (LOX) inhibitor supplied as a solid. It inhibits LOX family enzymes with low micromolar potency, reduces collagen I deposition and crosslinking in fibroblasts, and is provided with analytical documentation for laboratory studies. Not for human or veterinary use.
- High purity (99.71%) suitable for research applications.
- Solid form for convenient handling and storage.
- Potent pan-LOX inhibitory activity with reported low micromolar IC50s.
- Reduces collagen I deposition and crosslinking in cell-based assays.
- Available in small research pack sizes for pilot and preclinical studies.
- Provided with COA, SDS, and handling documentation.
Medchemexpress LLC DAPI dihydrochloride | 28718-90-3 | 99.9% | 500 UG
DAPI dihydrochloride | 28718-90-3 | 99.9% | 500 UG
Medchemexpress LLC GSK-LSD1 dihydrochloride | 2102933-95-7 | 99.5% | 289.24 g·mol⁻1 | C14H22Cl2N2 | 50 MG
This dihydrochloride salt is a potent, selective, and irreversible inhibitor of lysine-specific demethylase 1 (LSD1), used as a research probe for epigenetic regulation and metabolic studies. It exhibits an IC50 of 16 nM and is supplied with high reported purity.
- Potent LSD1 inhibition with IC50 of 16 nM.
- High purity (≈99.5%).
- Supplied as a dihydrochloride salt in solid and DMSO solution formats.
- Suitable for epigenetic and metabolic research applications.
- Available in small research pack sizes including 50 MG.
Medchemexpress LLC Bepridil hydrochloride hydrate | 74764-40-2 | 99.9% | 421.02 | 1 ML
Bepridil hydrochloride hydrate is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor. It possesses antianginal and type I antiarrhythmic effects and functions as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. It can be used for the research of cardiovascular disorders.
- Blocks Ca2+-dependent action potentials in vascular smooth muscle.
- Inhibits Ca currents and Na currents in cultured ventricular cells.
- Decreases IKs under blockade of IKr.
- Suitable for research into cardiovascular disorders.
Medchemexpress LLC Vasicine (hydrochloride) | 7174-27-8 | 224.69 | 1 ML
Vasicine hydrochloride is a quinazoline alkaloid isolated from Justicia adhatoda. It activates the PI3K/Akt signaling pathway and exhibits antioxidant, anti-inflammatory, and antibacterial activities. This product is for research use only.
- Activates the PI3K/Akt signaling pathway.
- Exhibits antioxidant, anti-inflammatory, and antibacterial activities.
- Shows moderate inhibitory activity against H+/K+-ATPase.
- Scavenges DPPH free radicals.
- Reduces gastric acid secretion and has an anti-ulcer effect.
- Improves cardiac function and inhibits myocardial cell apoptosis.
- Alleviates myocardial necrosis, edema, and inflammatory cell infiltration.
Medchemexpress LLC Cefotiam (hydrochloride) | 66309-69-1 | 98.0% | 25 MG
Cefotiam hydrochloride is a parenteral cephalosporin antibiotic that exhibits broad-spectrum activity against both Gram-positive and Gram-negative bacteria. It is highly active against various bacterial strains.
- Parenteral cephalosporin antibiotic
- Broad-spectrum activity against Gram-positive and Gram-negative bacteria
- Exhibits antibacterial activity against P. mirabilis IFO 3849
- Highly active against Staph. aureus and Staph. albus
- Active against haemolytic streptococci, pneumococci, and Streptococcus viridans
- Can cure urinary tract infection with P. mirabilis in mice
Medchemexpress LLC Carteolol hydrochloride | 51781-21-6 | 99.96% | 328.83 | 500 MG
Carteolol hydrochloride (OPC-1085 hydrochloride) is a non-selective beta blocker used to treat glaucoma. It is a beta-adrenergic antagonist used as an anti-arrhythmia, anti-angina, antihypertensive, and antiglaucoma agent. It significantly inhibited H2O2-induced cell damage and was able to scavenge O2, showing protective action against UVB-induced HCEC damage.
- Non-selective beta blocker
- Treats glaucoma
- Anti-arrhythmia agent
- Anti-angina agent
- Antihypertensive agent
- Protective action against UVB-induced HCEC damage in vitro
- Radical scavenging ability (scavenges O2)
- Long-acting alginate formulation is as effective as standard for glaucoma treatment
Medchemexpress LLC TG 100572 hydrochloride | 867331-64-4 | 98.8% | 512.43 g/mol | C26H27Cl2N5O2 | 10 MG
TG 100572 Hydrochloride is a multi-targeted kinase inhibitor used in research to probe VEGFR, FGFR, PDGFR, and Src family kinase signaling. It is provided as a high-purity solid suitable for biochemical and cellular assays, with recommended sealed storage away from moisture.
Medchemexpress LLC Nisoxetine | 53179-07-0 | MFCD00865443 | 98.6% | 271.35 | C17H21NO2 | 10 MG
Nisoxetine is a selective norepinephrine transporter (NET) inhibitor intended for research use. It is supplied as a high-purity solid suitable for pharmacology, binding, and analytical studies.
- Selective norepinephrine transporter inhibitor for research use only.
- High purity (≈98.6%) suitable for analytical assays.
- Molecular weight 271.35 and formula C17H21NO2.
- Available in sizes from 5-500 mg to support assay scale-up.
- Supplied with analytical documentation (COA, LCMS, NMR, SDS).
Sigma Aldrich Fine Chemicals Biosciences Cysteamine hydrochloride >=98% (titration) | 156-57-0 | MFCD00012904 | 100G
Cysteamine hydrochloride >=98% (titration) | Purity: >=98% (titration) | Mol Wt: 113.61 | 156-57-0 | MFCD00012904 | 100G
Medchemexpress LLC Nisoxetine hydrochloride | 57754-86-6 | MFCD00078426 | 99.92% | 5 MG
Nisoxetine hydrochloride is a potent and selective inhibitor of the noradrenaline transporter (NET), with a Kd of 0.76 nM. It functions as an antidepressant and local anesthetic by blocking voltage-gated sodium channels.
- Potent and selective inhibitor of noradrenaline transporter (NET)
- Acts as an antidepressant
- Functions as a local anesthetic
- Blocks voltage-gated sodium channels
Medchemexpress LLC Idazoxan (hydrochloride) | 79944-56-2 | 99.3% | C11H13ClN2O2 | 25 MG
Idazoxan hydrochloride is an α2-adrenoceptor and imidazoline receptor antagonist that competitively blocks the hypotensive effect of imidazoline-like agents. It also shows potential in improving motor symptoms associated with Parkinson's disease, L-DOPA-induced dyskinesias, and experimental Parkinsonism.
- Acts as an alpha-2 adrenoceptor antagonist.
- Functions as an imidazoline receptor antagonist.
- Antagonizes centrally induced hypotensive effects.
- May improve motor symptoms in Parkinson's disease.
- May alleviate L-DOPA-induced dyskinesias.
- Applicable to experimental Parkinsonism research.
Medchemexpress LLC AZD-7762 (hydrochloride) | 1246094-78-9 | 98.0 % | 398.88 | 10 MG
AZD-7762 (hydrochloride) | 1246094-78-9 | 98.0 % | 398.88 | 10 MG
eMolecules 4-Pyridineacetic acid | Combi-Blocks | 28356-58-3 | MFCD03701446 | 137.138 | C7H7NO2 | 98.000 | OC(=O)Cc1ccncc1 | 1g | 357561050
4-Pyridineacetic acid | Combi-Blocks | 28356-58-3 | MFCD03701446 | 137.138 | C7H7NO2 | 98.000 | OC(=O)Cc1ccncc1 | 1g | 357561050