Organosulfur Compounds
Medchemexpress LLC Sodium butane-1-sulfonate | 2386-54-1 | MFCD00007540 | 98.0% | 160.17 g/mol | C4H9NaO3S | 500 MG
Sodium butane-1-sulfonate is the sodium salt of butane-1-sulfonic acid used as an ionic mobile-phase additive for chromatographic separation of arsenic, selenium, and related analytes. It appears as a white to off-white crystalline powder, supplied for research use, and is commonly used to improve ion-pairing and retention in aqueous chromatographic methods.
- Used as ionic mobile-phase additive for chromatographic separations.
- Improves separation and resolution of arsenic and selenium species.
- High purity suitable for analytical applications (manufacturer lists ~98% assay).
- White to off-white crystalline powder; stable and easy to weigh.
- Suits ion-pairing and retention control in aqueous methods.
TARGETMOL CHEMICALS INC SULINDAC SULFIDE 10MG
Also available in 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Sulindac sulfide (cis-Sulindac sulfide) is a non-steroidal anti-inflammatory compound that has a high affinity for COX-1 and acts as an inhibitor in Ras activation of Raf-1. Sulindac sulfide is a non-competitive inhibitor of gamma-secretase with an IC50 value of 20.2 uM. It is an active metabolite of sulinic acid. purity: 99%
Cayman Chemical Sulindac Inhibitors
An NSAID, a COX-2 inhibitor (IC50 = 0.79 µM), and a prodrug form of sulindac sulfide; selective for COX-2 over COX-1 (IC50 = >1,000 µM); inhibits acetic acid-induced writhing in mice and reduces carrageenan-induced paw edema in rats at 100 mg/kg; reduces tumor growth in a BxPC-3 mouse xenograft model at 60 mg/kg
Cayman Chemical GlycerophosphoNPalmitoyl Etha
Precursor of PEA, an endogenous CB found in brain, liver, and other mammalian tissues; PEA has potent anti-inflammatory activity in vivo
eMolecules Medchem Express / (R)-Sulforaphane / 5mg / 599150753 / HY-13755A / / 142825-10-3 / MFCD09039283 / 177.280 / C6H11NOS2
Medchem Express / (R)-Sulforaphane / 5mg / 599150753 / HY-13755A / / 142825-10-3 / MFCD09039283 / 177.280 / C6H11NOS2
Medchemexpress LLC Cb2r/faah modulator-2 | 2876918-68-0 | 367.52 g·mol⁻¹ | C24H33NO2 | 10 MG
CB2R/FAAH modulator-2 is a research-grade small-molecule dual-target modulator that acts as an agonist at the cannabinoid CB2 receptor and an inhibitor of fatty acid amide hydrolase (FAAH). It is supplied as a solid for in vitro and in vivo pharmacology studies involving cannabinoid signaling and endocannabinoid metabolism. The compound has CAS 2876918-68-0, molecular formula C24H33NO2, and molecular weight 367.52 g·mol⁻¹.
- Dual CB2R agonist and FAAH inhibitor.
- Suitable for in vitro and in vivo pharmacology studies.
- Provided as a solid, with an option as 10 mM in DMSO solution.
- Available in small research sizes, for example 10 mg.
- CAS number 2876918-68-0 for unambiguous identification.
- Recommended storage: powder at -20°C or 4°C; in solvent at -80°C or -20°C.
Cayman Chemical SulIndac sulfon 25mg
An oxidized metabolite of sulindac that is produced in many mammals but minimally in mice and rats; generally considered to be inactive against COX enzymes, although it can reduce azoxymethane-induced colon cancer in rats; inhibits aldose reductase (IC50 = 367 nM) in vitro
TARGETMOL CHEMICALS INC CB2R/FAAH MODULATOR-3 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-3 acts as a CB2R agonist and FAAH inhibitor the Ki values are 20.1 and 67.6 nM for CB2R and CB1R respectively and the IC50 value for FAAH is 3.4 uM. CB2R/FAAH modulator-3 has research value related to cancer deleterious inflammatory cascades occurring in neurodegenerative diseases and COVID-19 infection. purity: 99%
Medchemexpress LLC GLP-1R modulator C5 | 421578-93-0 | 99.8% | C24H21NO3 | 10MG
GLP-1R modulator C5 is a small-molecule allosteric modulator that enhances GLP-1 binding to the GLP-1 receptor via a transmembrane site. It is intended for research use and is characterized by an EC50 of 1.59 ± 0.53 μM, molecular formula C24H21NO3, and molecular weight 371.43 g·mol⁻1.
- Allosteric enhancer of GLP-1 binding to GLP-1R.
- Measured EC50 of 1.59 ± 0.53 μM.
- Available as solid (5-100 mg) and 10 mM solution in DMSO.
- High purity (99.81% by LCMS).
- Supplied with certificate of analysis for analytical verification.
![eMolecules [2-(Methylsulfinyl)ethyl]amine hydrobromide | 49773-19-5 | MFCD16036096 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502191370.JPG-250.jpg)
eMolecules [2-(Methylsulfinyl)ethyl]amine hydrobromide | 49773-19-5 | MFCD16036096 | 1g
Combi-Blocks | [2-(Methylsulfinyl)ethyl]amine hydrobromide | 1g | 448005944 | QZ-8070 | 95.000 | 49773-19-5 | MFCD16036096 | 188.080 | C3H10BrNOS
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Medchemexpress LLC 2H-Indol-2-one, 1,3-dihydro-3-hydroxy-3-(2-oxo-2-phenylethyl)-1-(2-phenylethyl)- | 421578-93-0 | 99.8% | 371.43 g·mol⁻¹ | C24H21NO3 | 5 MG
GLP-1R modulator C5 is a small-molecule allosteric modulator that enhances GLP-1 binding to the GLP-1 receptor via a transmembrane site. It shows in vitro activity (EC50 1.59 ± 0.53 μM) and is provided for research applications with supporting characterization and handling data.
- Allosteric enhancement of GLP-1 binding (EC50 1.59 ± 0.53 μM).
- High reported purity of 99.81%.
- Molecular formula C24H21NO3; molecular weight 371.43 g·mol⁻¹.
- Soluble in DMSO at 50 mg/mL; ultrasonic assistance recommended.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months).
- Available in multiple small package sizes suitable for laboratory testing.
Medchemexpress LLC Il-17 modulator 1 disodium | 2446803-91-2 | 98.4% | C28H35N6Na2O6P | 1 ML
IL-17 modulator 1 disodium is an orally active, highly efficacious small molecule IL-17 modulator. Extracted from patent WO 2020127685, this salt form offers enhanced water solubility and stability compared to its free form. It is suitable for research aimed at preventing or ameliorating diseases such as psoriasis, ankylosing spondylitis, and psoriatic arthritis. This product is for research use only.
- Orally active and highly efficacious
- Small molecule IL-17 modulator
- Enhanced water solubility and stability in disodium salt form
- Useful for research into psoriasis, ankylosing spondylitis, and psoriatic arthritis
- White to off-white solid appearance
