Hydrochlorides
Selleck Chemical LLC Nitrocaramiphen hydrochloride
Nitrocaramiphen hydrochloride is an antagonist of muscarinic acetylcholine receptor M1 (mAChR M1) which can completely remove the hyperpolarizing effect of muscarine
Medchemexpress LLC Ambroxol (hydrochloride) | 23828-92-4 | 99.9% | 25 MG
Ambroxol hydrochloride is an active metabolite of Bromhexine, known for its potent expectorant effects. It acts as a glucocerebrosidase (GCase) chaperone, enhancing GCase activity. It induces lung autophagy and is being researched for potential use in Parkinson's disease and neuronopathic Gaucher disease.
- Potent expectorant effects.
- Acts as a glucocerebrosidase (GCase) chaperone.
- Increases glucocerebrosidase activity.
- Induces lung autophagy.
- Potential for research in Parkinson's disease.
- Potential for research in neuronopathic Gaucher disease.
Apexbio Technology LLC Duloxetine HCl 136434-34-9 100mg
Duloxetine hydrochloride (CAS 136434-34-9) is a small molecule compound classified as a selective inhibitor of serotonin and norepinephrine reuptake By blocking the reabsorption of these neurotransmitters at the synaptic cleft duloxetine modulates serotonergic and noradrenergic signaling within the central nervous system This pharmacological action has rendered it a valuable tool in research models investigating neurochemical pathways involved in mood regulation pain perception and stress response Duloxetine HCl is commonly utilized in studies of depression anxiety and chronic pain to elucidate monoaminergic mechanisms and to evaluate therapeutic strategies targeting neurotransmitter reuptake
Medchemexpress LLC Cefotiam hydrochloride | 66309-69-1 | 98.0% | 100 MG
Cefotiam hydrochloride is a parenteral cephalosporin antibiotic that exhibits broad-spectrum activity against both Gram-positive and Gram-negative bacteria. It targets β-lactam and is suitable for various research applications.
- Exhibits antibacterial activity with a MIC value of 1.56 μg/mL for *P. mirabilis* IFO 3849.
- Highly active against *Staph. aureus* (MIC values of 0.5-1 μg/mL) and *Staph. albus* (MICs 0.25-0.5 μg/mL).
- Effective against haemolytic streptococci, pneumococci, and *Streptococcus viridans* with MIC values in the range of 0.06-4 μg/mL.
- Demonstrates in vivo efficacy in curing urinary tract infection with *P. mirabilis* in mice.
Indofine Chemical 4-Phenyl-1,2,3,6-Te, 98%, 1 Gm
4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE HYDROCHLORIDE 1 GM, Rare Organics & Biochemicals, C11H13N . HCl, MW: 195.69, >98%, 43064-12-6, MFCD00012752
TARGETMOL CHEMICALS INC Duloxetine hydrochloride 100MG
Also available in 1 mL, 10 mg, 50 mg, 200 mg and bulk. Please contact Fisher for quotes. Duloxetine hydrochloride ((S)-Duloxetine hydrochloride) is a thiophene derivative and selective neurotransmitter uptake inhibitor for serotonin and noradrenaline (SNRI). It is an antidepressant agent and anxiolytic, also used for treating pain in patients with diabetes mellitus and fibromyalgia. Purity 99.97%
Medchemexpress LLC Duloxetine | 116539-59-4 | 99.9% | 100 MG
Duloxetine | 116539-59-4 | 99.9% | 100 MG
Medchemexpress LLC KHK-IN-1 hydrochloride | 1303470-48-5 | 98.47% | 10 MG
KHK-IN-1 hydrochloride is a selective and cell membrane permeable ketohexokinase (KHK) inhibitor with an IC50 of 12 nM. It inhibits the production of F1P in HepG2 cell lysates with an IC50 of 400 nM and has potential for the study of diabetes and obesity.
- Selective and cell membrane permeable KHK inhibitor
- Inhibits F1P production in HepG2 cell lysates
- Potential for diabetes and obesity research
- Stable in human and rat liver microsome preparations
- Does not significantly inhibit cytochrome P450s
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 Queuine dihydrochloride | 86496-18-6 | 350.20 | 100 MG
Queuine dihydrochloride | 86496-18-6 | 350.20 | 100 MG
Medchemexpress LLC SB-743921 hydrochloride | 940929-33-9 | >98.0% | 50MG
SB-743921 hydrochloride | 940929-33-9 | >98.0% | 50MG
Medchemexpress LLC A 438079 hydrochloride | 899431-18-6 | C13H10Cl3N5 | 5 MG
A 438079 hydrochloride is a potent and selective P2X7 receptor antagonist with a pIC50 of 6.9. It is intended for research use only and not for patient administration.
- Potent and selective P2X7 receptor antagonist
- High purity of 99.99%
- Appearance as a solid, white to off-white
- For research use only
Medchemexpress LLC UAMC-3203 hydrochloride | 2271358-65-5 | 98.8% | 508.12 | 1 ML
UAMC-3203 hydrochloride is a potent and selective Ferroptosis inhibitor with an IC50 of 12 nM. No toxicity was observed in mice after repeated intraperitoneal injections (20 μmol/kg daily, over a period of 4 weeks).
- Potent and selective ferroptosis inhibitor.
- Has an IC50 of 12 nM for ferroptosis.
- No observed toxicity in mice at 20 μmol/kg daily for 4 weeks.
- Available in solid form (white to off-white).
- High purity: 98.82%.