Sulfoxides
Medchemexpress LLC Sulforaphane | 4478-93-7 | MFCD00198068 | 98.9% | 177.29 g/mol | C6H11NOS2 | 5 MG
Sulforaphane is a research-grade isothiocyanate that activates the Keap1/Nrf2/ARE antioxidant pathway and inhibits histone deacetylases. Supplied as a high-purity powder, it is intended for use in in vitro and in vivo studies of antioxidant response, anticancer activity, and anti-inflammatory mechanisms.
- High purity: 98.9%.
- CAS number: 4478-93-7.
- Molecular formula: C6H11NOS2; MW: 177.29 g/mol.
- Suitable for in vitro and in vivo applications.
- Storage: powder -20°C; in solvent -80°C for long-term storage.
- Available in small research quantities, including 5 mg.
![Medchemexpress LLC Acetic acid, 2-[4-[[4-(2-chlorophenyl)-2-thiazolyl]methoxy]-2-methylphenoxy]- | 1050506-75-6 | 98.1% | C19H16ClNO4S | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC Acetic acid, 2-[4-[[4-(2-chlorophenyl)-2-thiazolyl]methoxy]-2-methylphenoxy]- | 1050506-75-6 | 98.1% | C19H16ClNO4S | 1 ML
GPR120 modulator 1 is a G protein coupled receptor 120 (GPR120) modulator. This compound, extracted from patent US8394841B2 (compound example F1), is suitable for research into diseases linked to abnormal or deregulated GPR120, including diabetes.
- Modulates G protein coupled receptor 120 (GPR120)
- Supports research on diseases linked to GPR120 deregulation, such as diabetes
- Purity of 98.1% (HPLC)
- White to off-white solid appearance
- Chemical formula C19H16ClNO4S
Aobchem 6-Bromo-2-(methylsulfinyl)benzo[d]thiazole | 97% | C8H6BrNOS2 | 25g
6-Bromo-2-(methylsulfinyl)benzo[d]thiazole | 97% | C8H6BrNOS2 | 25g
Medchemexpress LLC Sulforaphane | 4478-93-7 | 99.75% | 177.29 | 200 MG
Sulforaphane is an orally active inducer of the Keap1/Nrf2/ARE pathway. It promotes the transcription of tumor-suppressing proteins and effectively inhibits the activity of HDACs. It protects the heart through the activation of the Keap1/Nrf2/ARE pathway and further induction of HO-1 expression. Sulforaphane suppresses high glucose-induced pancreatic cancer through AMPK-dependent signal transmission and exhibits both anticancer and anti-inflammatory properties.
- Targets: HDAC, Keap1-Nrf2, Apoptosis, Bcl-2 family, Caspase, Reactive oxygen species (ROS)
- Research areas: Inflammation/Immunology, Cancer
Medchemexpress LLC Sodium decane-1-sulfonate | 13419-61-9 | MFCD00007526 | >98.0% | 244.33 | 10 G
Sodium decane-1-sulfonate is an anionic surfactant utilized for the analysis of organic small molecule compounds through HPLC and ion-pair liquid chromatography.
- Anionic surfactant
- Used for analysis of organic small molecule compounds
- Suitable for HPLC
- Suitable for ion-pair liquid chromatography
- Biochemical assay reagent
TARGETMOL CHEMICALS INC NR2F6 MODULATOR-1 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. NR2F6 modulator-1 is a potent modulator of nuclear receptor subfamily 2 group F member 6 (NR2F6). NR2F6 modulator-1 can be used to study immune regulation and modulation of tumour stem cell activity. purity: 97%
Medchemexpress LLC Cytochrome P450 1B1 Antibody (YA1836) | 100 UL
The Cytochrome P450 1B1 Antibody (YA1836) is a rabbit-derived, non-conjugated IgG monoclonal antibody specifically designed to target Cytochrome P450 1B1. This antibody is intended for research use only.
- Rabbit-derived recombinant monoclonal IgG antibody
- Targets Cytochrome P450 1B1
- Predicted and observed molecular weight: 61 kDa
- Species reactivity: Human, mouse, rat
- Applications include Western Blot (WB), Immunohistochemistry-Paraffin (IHC-P), and Flow Cytometry (FC)
- Purified by affinity chromatography
- Formulated in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA
- Stable for 1 year when stored at -20°C; avoid repeated freeze/thaw cycles
Cayman Chemical SulIndac-d3 500ug
An internal standard for the quantification of sulindac by GC- or LC-MS
Medchemexpress LLC CB2R/FAAH modulator-3 | 2876918-67-9 | C22H31NO2 | 5 MG
CB2R/FAAH modulator-3 (compound 27) is a dual-targeting modulator that acts as a CB2R agonist and FAAH inhibitor. It has Ki values of 20.1 nM for CB2R and 67.6 nM for CB1R, and an IC50 value of 3.4 μM for FAAH. This compound can be used in studies related to cancer, deleterious inflammatory cascades in neurodegenerative diseases, and COVID-19 infection.
- Dual-targeting modulator: acts as a CB2R agonist and FAAH inhibitor.
- Can be used in studies related to cancer, deleterious inflammatory cascades occurring in neurodegenerative diseases, and COVID-19 infection.
- At 10 μM, it reduces the production of the pro-inflammatory cytokines TNFα, IFN-γ, IL-1β, and IL6 in unstimulated monocytes and macrophages.
Medchemexpress LLC Nourseothricin (sulfate) | 96736-11-7 | 87.3% | 250 MG
Nourseothricin sulfate is a broad-spectrum antibiotic that inhibits protein biosynthesis in prokaryotic cells and strongly suppresses the growth of eukaryotes. It targets the outer membrane of Gram-negative bacteria and serves as a selective marker for various organisms, including bacteria, yeast, filamentous fungi, and plant cells.
- Broad-spectrum antibiotic
- Targets outer membrane of Gram-negative bacteria
- Serves as a selective marker for Fonsecaea pedrosoi
- Inhibits protein biosynthesis in prokaryotic cells
- Strongly suppresses growth of eukaryotes, such as fungi
- Sensitizes resistant Escherichia coli strains by eliminating outer membrane resistance
- Mixture of several Streptothricins (primarily D and F)
- Can create channels in the outer membrane
TARGETMOL CHEMICALS INC TETRABENAZINE METABOLITE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tetrabenazine Metabolite ((-)-(beta)-HTBZ) a vesicles monoamine transporter 2 (VMAT2) inhibitor is an active metabolite of Tetrabenazine. Tetrabenazine Metabolite has a high affinity for VMAT2 with a Ki of 13.4 nM. Tetrabenazine Metabolite is often used to study chorea associated with Huntington's disease and other hyperactivity disorders. purity: 95%