Phenols
![Medchemexpress LLC 6-[[6-(1-methylpyrazol-4-yl)-triazolo[4,3-b]pyridazin-3-yl]sulfanyl]quinoline | 1022150-57-7 | ≥98.0% | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234303.png-250.jpg)
Medchemexpress LLC 6-[[6-(1-methylpyrazol-4-yl)-triazolo[4,3-b]pyridazin-3-yl]sulfanyl]quinoline | 1022150-57-7 | ≥98.0% | 1 ML
SGX-523 is a selective, ATP-competitive inhibitor of the MET (c-Met/HGFR) receptor tyrosine kinase used as a research tool to study MET signaling in vitro. It is commonly supplied as concentrated solutions (for example, 10 mM in 1 mL) or as a purified solid for biochemical and cell-based assays.
- Selective MET inhibitor with low-nanomolar potency.
- Potent ATP-competitive inhibition (IC50 ≈ 4 nM).
- Purity ≥98% by HPLC, suitable for research applications.
- Molecular weight 359.41 g/mol; formula C18H13N7S.
- Available as small-volume concentrated solutions for in vitro assays.
![eMolecules 1895-39-2 | Sodium chlorodifluoroacetate | Ambeed | MFCD00064771 | 152.460 | C2ClF2NaO2 | 97.000 | [Na+].[O-]C(=O)C(F)(F)Cl | 500g | 525169769](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000482821.jpg-250.jpg)
eMolecules 1895-39-2 | Sodium chlorodifluoroacetate | Ambeed | MFCD00064771 | 152.460 | C2ClF2NaO2 | 97.000 | [Na+].[O-]C(=O)C(F)(F)Cl | 500g | 525169769
Sodium chlorodifluoroacetate | Ambeed | 1895-39-2 | MFCD00064771 | 152.460 | C2ClF2NaO2 | 97.000 | [Na+].[O-]C(=O)C(F)(F)Cl | 500g | 525169769
eMolecules 754131-60-7 | 3-Bromo-2-(bromomethyl)pyridine | ChemScene | MFCD09999976 | 250.921 | C6H5Br2N | 97.000 | BrCc1ncccc1Br | 25g | 801476189
3-Bromo-2-(bromomethyl)pyridine | ChemScene | 754131-60-7 | MFCD09999976 | 250.921 | C6H5Br2N | 97.000 | BrCc1ncccc1Br | 25g | 801476189
eMolecules 116435-77-9 | 2-Amino-3-bromophenol | Ambeed | MFCD08445676 | 188.024 | C6H6BrNO | 97.000 | Nc1c(O)cccc1Br | 10g | 490493915
2-Amino-3-bromophenol | Ambeed | 116435-77-9 | MFCD08445676 | 188.024 | C6H6BrNO | 97.000 | Nc1c(O)cccc1Br | 10g | 490493915
Medchemexpress LLC Palmitoleoyl chlorid 100mg | 40426-22-0 | 272.85 | C16H29ClO | 100 MG
Palmitoleoyl chloride is an acyl chloride derivative of palmitoleic acid used as a reactive intermediate in organic synthesis. Supplied as a liquid reagent for research applications, it is employed to introduce the palmitoleoyl acyl group in acylation and coupling reactions.
- Reactive acyl chloride for acylation chemistry.
- Useful intermediate for synthesis of lipid-derived and small-molecule compounds.
- Available in lab-scale quantities, including 100 MG packaging.
- Typical purity around 95% as supplied.
- Requires low-temperature storage to preserve stability and shelf life.
eMolecules 950670-18-5 | 3-Bromo-5-fluoropicolinonitrile | Combi-Blocks | MFCD16988825 | 200.998 | C6H2BrFN2 | 97.000 | Fc1cnc(C#N)c(Br)c1 | 1g | 232322233
3-Bromo-5-fluoropicolinonitrile | Combi-Blocks | 950670-18-5 | MFCD16988825 | 200.998 | C6H2BrFN2 | 97.000 | Fc1cnc(C#N)c(Br)c1 | 1g | 232322233
Medchemexpress LLC Skatole (3-Methylindole) | 83-34-1 | MFCD00005627 | 131.17 | 100 G
Skatole (3-Methylindole) is a heterocyclic compound naturally occurring in vertebrate feces and some plants. Produced by intestinal bacteria, it can induce apoptosis in intestinal epithelial cells by activating aryl hydrocarbon receptors (AhR) and p38. This compound finds utility in the perfume industry and as a flavor additive in ice cream.
- Purity of 99.92%
- Molecular weight of 131.17
- Molecular formula: C9H9N
- Solid appearance
- White to light brown color
- Derived from endogenous metabolites, human gut microbiota metabolites, and microorganisms
- Used in the perfume industry
- Functions as a flavor additive in ice cream
- Induces apoptosis in intestinal epithelial cells by activating aryl hydrocarbon receptors (AhR) and p38
- Reverses suppression of Irisin on Ang II-evoked proliferation, migration, and phenotypic transformation in VSMCs
Medchemexpress LLC (-)-(E)-Guggulsterone | 39025-24-6 | 1 ML
(-)-(E)-Guggulsterone is an orally active natural stereoisomer that acts as an antagonist for the Farnesoid X Receptor (FXR). It exhibits potent hypolipidemic properties and suppresses dengue virus (DENV) replication by upregulating antiviral interferon responses. This compound also possesses antibacterial activities against Bacillus subtilis, Staphylococcus aureus, and Pseudomonas aeruginosa, and has cardiac protective and antioxidant activities.
- Acts as an antagonist for Farnesoid X Receptor (FXR)
- Exhibits potent hypolipidemic properties
- Suppresses dengue virus (DENV) replication
- Possesses antibacterial activities against Bacillus subtilis, Staphylococcus aureus, and Pseudomonas aeruginosa
- Has cardiac protective and antioxidant activities
