Organic metal halides
Medchemexpress LLC Dicetyldimonium bromide | 70755-47-4 | 99.7% | 574.86 | 50 G
Dicetyldimonium bromide is a biochemical reagent utilized in life science research. It serves as a foundational material for various biological and organic applications.
- Functions as a biological material.
- Functions as an organic compound.
- Supports life science related research.
Medchemexpress LLC Atropine methyl bromide | 2870-71-5 | 99.8% | 384.31 | 25 MG
Atropine methyl bromide is a muscarinic receptor (mAChR) antagonist. It is a quaternary ammonium salt of atropine and acts as a mydriatic for pupil dilation during ophthalmic examinations. Due to its highly polar nature, it is used to relieve pyloric spasms in infants and penetrates the central nervous system less readily than atropine.
- Acts as a muscarinic receptor antagonist
- Used as a mydriatic for pupil dilation
- Relieves pyloric spasm in infants
- Less central nervous system penetration compared to atropine due to high polarity
eMolecules Sodium 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate | 15307-79-6 | 5G | Purity: 95%
Matrix Scientific | Sodium 2-(2-((2,6-dichlorophenyl)amino)phenyl)acetate | 5G | 15307-79-6 | MFCD00082251
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Medchemexpress LLC COB-187 | 1862177-86-3 | 95.0% | 302.41 | 50 MG
COB-187 is a potent, ATP-competitive, and selective inhibitor of GSK-3β. It inhibits GSK-3 through a reversible and Cysteine (Cys)-199-dependent mechanism. COB-187 inhibits LPS-induced cytokine production and SARS-CoV-2 spike protein-induced CXCL10 production.
- Potent, ATP-competitive, and selective inhibitor of GSK-3β.
- Inhibits GSK-3 through a reversible and Cysteine (Cys)-199-dependent mechanism.
- Inhibits LPS-induced cytokine production.
- Inhibits SARS-CoV-2 spike protein-induced CXCL10 production.
Medchemexpress LLC Dicetyldimonium bromide | 70755-47-4 | 99.7% | 574.86 | 5 G
Dicetyldimonium bromide (Synonyms: Dimethyldipalmitylammonium bromide) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is for research use only and not sold to patients.
- For research use only
- Not sold to patients
eMolecules AstaTech TETRABUTYLAMMONIUM BROMIDE 100g 718057353 D72482 98.000 1643-19-2 MFCD00011633 322.375 C16H36BrN
AstaTech TETRABUTYLAMMONIUM BROMIDE 100g 718057353 D72482 98.000 1643-19-2 MFCD00011633 322.375 C16H36BrN
Medchemexpress LLC Methscopolamine bromide | 155-41-9 | 99.8% | 100 MG
Methscopolamine Bromide is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is for research use only and not sold to patients.
- Molecular weight: 398.29
- Formula: C18H24BrNO4
- Appearance: Solid
- Color: White to off-white
- Solubility in DMSO: 50 mg/mL (125.54 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
- Solubility in H2O: 50 mg/mL (125.54 mM; need ultrasonic)
Medchemexpress LLC Anisotropine bromide | 80-50-2 | 98.0% | 5 MG
Anisotropine bromide, also known as Octatropine bromide, is an orally active anticholinergic muscarinic antagonist. It is capable of inhibiting gastric acid secretion and is employed as an adjunct in the treatment of peptic ulcers. This product is strictly for research use only.
- Anticholinergic muscarinic antagonist
- Inhibits gastric acid secretion
- Used as an adjunct to peptic ulcers
- Blocks acetylcholine-induced vocalization, intestinal spasm, and intestinal contractions
Medchemexpress LLC CVT-12012 | 1018675-35-8 | 99.58% | 434.41 | 25 MG
CVT-12012 is a potent and orally bioavailable stearoyl-coA desaturase (SCD) inhibitor, with IC50s of 38 nM for rat microsomal and 6.1 nM for human HEPG2.
- Potent and orally bioavailable stearoyl-coA desaturase (SCD) inhibitor.
- Demonstrates good oral bioavailability (78%) in a rat PK study.
- Oral absorption is not significantly affected by Pgp efflux.
Medchemexpress LLC BAY-677 | 2117404-84-7 | 98.0% | 400.35 | 10 MG
BAY-677 serves as an inactive control for BAY-678. BAY-678 is an orally bioavailable, highly potent, selective, and cell-permeable inhibitor of human neutrophil elastase (HNE), demonstrating an IC50 of 20 nM. This compound has also been nominated as a chemical probe to the public via the Structural Genomics Consortium (SGC).
- Inactive control for BAY-678.
- BAY-678 is an orally bioavailable inhibitor.
- Highly potent and selective inhibitor of human neutrophil elastase.
- Cell-permeable.
- IC50 of 20 nM against HNE.
- Nominated as a chemical probe by SGC.
Medchemexpress LLC Saroglitazar magnesium | 1639792-20-3 | 98.85% | 901.42 | 25 MG
Saroglitazar magnesium is a novel peroxisome proliferator-activated receptor (PPAR) agonist that exhibits predominant PPARα activity and moderate PPARγ activity, with EC50 values of 0.65 pM and 3 nM in HepG2 cells, respectively.
- Novel peroxisome proliferator-activated receptor (PPAR) agonist
- Predominant PPARα activity (EC50 of 0.65 pM in HepG2 cells)
- Moderate PPARγ activity (EC50 of 3 nM in HepG2 cells)
- Causes dose-dependent reductions in serum triglycerides (TG), free fatty acids (FFA), and glucose in db/db mice
- Shows lipid-lowering effects in preclinical models
- Indicated low risk of PPAR-associated side effects in humans
- Appears to have good potential as a novel therapeutic agent for the treatment of dyslipidemia and diabetes
TARGETMOL CHEMICALS INC FLECAINIDE ACETATE 50MG
Also available in 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Flecainide acetate (R-818) is a class Ic antiarrhythmic agent used to prevent and treat tachyarrhythmias (abnormal fast rhythms of the heart). purity: 99%