Phenols
Medchemexpress LLC Tetrahydro-β-carboline | 16502-01-5 | 99.4% | 172.23 | 10 MM * 1 ML
Tetrahydro-β-carboline (Tryptoline) is a metabolite of tryptamine and a competitive serotonin reuptake inhibitor. It is intended for research use only and not for patient use.
- Metabolite of tryptamine
- Competitive serotonin reuptake inhibitor with a Ki value of 6.1 μM
- Increases serotonin levels in the brain of rats in vivo studies
Medchemexpress LLC Daclatasvir dihydrochloride | 1009119-65-6 | MFCD25541736 | 99.8% | 811.80 | C40H52Cl2N8O6 | 1 G
Daclatasvir dihydrochloride is the dihydrochloride salt of daclatasvir, a potent hepatitis C virus (HCV) NS5A inhibitor supplied for laboratory research. The material is provided as a solid powder with documented analytical support for use in in vitro and biochemical studies targeting HCV replication pathways.
- High purity suitable for research applications.
- Provided as a solid dihydrochloride salt for stability.
- Supplied with datasheet, certificate of analysis, and safety data sheet for traceability.
- Available in multiple sizes and solution formats for assay flexibility.
- Molecular weight 811.80 and CAS 1009119-65-6 included for identification.
Medchemexpress LLC 1-((2-(2,4-difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate | 86386-77-8 | MFCD11111978 | 5g
1-((2-(2 4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1 2 4-triazole methanesulfonate (Efinaconazole Impurity) is a biological molecule
Medchemexpress LLC LysoFP-NO2 | 69408-75-9 | 98.2% | 1 MG
LysoFP-NO2 is a turn-on fluorescent probe for carbon monoxide (CO) that localizes to the lysosome. When lysosomal CO is present, LysoFP-NO2 transforms into lysoFP-NH2, which is highly fluorescent. It is selective for CO over various reactive nitrogen, oxygen, and sulfur species. It displays excitation/emission maxima of 440/528 nm and is not cytotoxic to HepG2 cells for up to five hours at a concentration of 30 μM.
- Turn-on fluorescent probe for carbon monoxide
- Localizes to the lysosome
- Highly fluorescent upon transformation in presence of lysosomal CO
- Selective for CO over reactive nitrogen, oxygen, and sulfur species
- Excitation/emission maxima of 440/528 nm
- Non-cytotoxic to HepG2 cells for up to five hours at 30 μM concentration
Medchemexpress LLC (+)-arabinogalactan | 9036-66-2 | MFCD00062638 | 80.0% | C20H36O14 | 500 G
(+)-Arabinogalactan is a larch-wood-derived polysaccharide supplied as a powdered reagent with approximately 80% polyarabinogalactan content. It is intended for research use in glycobiology, biochemical assays, formulation studies, and analytical applications. Consult the product datasheet for batch-specific details and handling instructions.
- Extracted from larch wood
- Approximately 80% polyarabinogalactan content
- Powdered form for reagent and formulation use
- Typical applications: glycobiology and biochemical assays
- CAS number 9036-66-2
- Store at -20°C as recommended on datasheet
Medchemexpress LLC ADAMTS13 Human CHO 10ug | 10ug
The ADAMTS13 protein a metalloproteinase has a metalloproteinase domain a disintegrin-like domain and a thrombospondin type 1 motif It cleaves von Willebrand Factor and defects in this gene cause thrombotic thrombocytopenic purpura Alternative splicing generates multiple transcript variants ADAMTS13 is broadly expressed in various tissues including the liver testis and 24 other tissues ADAMTS13 Protein Human (CHO His) is the recombinant human-derived ADAMTS13 expressed by CHO with C-10 His labeled tag The total length of ADAMTS13 Protein Human (CHO His) is 655 a a
Medchemexpress LLC Rhodium(II) triphenylacetate dimer | 142214-04-8 | MFCD15071082 | 1355.14 | C80H60O8Rh2 | 1 G
Rhodium(II) triphenylacetate dimer is a dirhodium(II) carboxylate complex used as a catalyst in organic synthesis and biochemical research. The complex contains two rhodium centers bridged by four triphenylacetate ligands and is commonly applied in carbene-transfer, C-H insertion, and related transformations. Handle under inert gas and protect from light.
Medchemexpress LLC Benzyltrimethylammonium tribromide | 111865-47-5 | MFCD00134423 | ≥98.0% | 389.95 g/mol | C10H16Br3N | 100 G
Benzyltrimethylammonium tribromide is a quaternary ammonium tribromide reagent used to supply controlled bromine for oxidation, cyclization, and other bromination reactions in organic synthesis. Supplied for research use, the compound is typically provided as a high-purity solid suitable for laboratory handling and storage.
- Provides controlled bromination for oxidation and cyclization reactions.
- High purity suitable for research applications.
- Solid form is stable and easy to weigh and handle.
- Dissolves readily in common polar solvents such as DMSO.
- Available in laboratory-scale package sizes for synthetic workflows.
Alkali Scientific Benzamidine Hydrochloride, 100 G
Benzamidine Hydrochloride is a high-purity protease inhibitor provided in a 100g package, ideal for use in biochemical and molecular biology applications. As a potent inhibitor of serine proteases, it is frequently used to prevent enzymatic degradation in protein purification and enzyme activity assays. Benzamidine Hydrochloride is commonly employed in laboratory workflows to inhibit trypsin, thrombin, and other proteases during protein analysis, ensuring that protein samples remain intact and active. This reagent is widely used in cell culture, biochemical research, and the preparation of cell lysates and other protein-rich samples where protease activity must be suppressed.
Medchemexpress LLC Furamidine dihydrochloride | 55368-40-6 | 99.0% | 377.27 | 1 ML
Furamidine dihydrochloride | 55368-40-6 | 99.0% | 377.27 | 1 ML
Medchemexpress LLC Levacetylleucine | 1188-21-2 | 98.0% | C8H15NO3 | 25 G
Levacetylleucine is an orally bioavailable and brain-penetrant compound, derived from the amino acid Leucine. It is the active form of N-acetyl-leucine (NAL). This compound has been shown to attenuate neuronal death and neuroinflammation in mice, and may also improve lysosomal and metabolic dysfunction.
- Orally bioavailable and brain-penetrant
- Acetylated derivative of amino acid leucine
- Active form of N-acetyl-leucine (NAL)
- Attenuates neuronal death and neuroinflammation
- Ameliorates lysosomal and metabolic dysfunction
- Improves postural symptoms after unilateral chemical labyrinthectomy (UL) in rats
- Promising for research in Niemann-Pick disease type C, traumatic brain injury, and neurodegeneration prevention
Medchemexpress LLC Slingshot inhibitor D3 | 1715076-35-9 | 99.5% | 461.55 g·mol⁻¹ | C25H19NO4S2 | 10MM 1ML
Slingshot inhibitor D3 is a potent, selective, reversible, and competitive inhibitor of Slingshot phosphatases (SSH family) used in biochemical and cell-based assays to probe SSH function. It is supplied as a ready-to-use 10 mM solution in DMSO and is intended for inhibition studies, mechanistic assays, and compound screening.
- Potent inhibition of Slingshot 1 (IC50 = 3 μM) and activity against Slingshot 2 (Ki = 3.9 μM).
- Supplied as a 10 mM solution in DMSO, 1 mL vial ready for use.
- High purity (~99.5%) suitable for research applications.
- Molecular weight 461.55 g·mol⁻¹ and formula C25H19NO4S2.
- Useful for biochemical and cell-based assays to study Slingshot-mediated dephosphorylation pathways.
Medchemexpress LLC Phospho-p95/NBS1 (Ser343) Antibody (YA165) | 10 UL
This product is an antibody named Phospho-p95/NBS1 (Ser343) Antibody (YA165), identified by the catalog number HY-P80473. It is a Rabbit-derived, non-conjugated IgG monoclonal antibody that targets Phospho-p95/NBS1 (Ser343). The antibody is suitable for applications such as Western Blot (WB), Immunocytochemistry/Immunofluorescence (ICC/IF), Immunohistochemistry-Paraffin (IHC-P), and Immunoprecipitation (IP), and shows reactivity with Human and Mouse samples.
- Targets Phospho-p95/NBS1 (Ser343).
- Rabbit-derived, non-conjugated IgG monoclonal antibody.
- Suitable for WB, ICC/IF, IHC-P, and IP.
- Reacts with human and mouse samples.
Medchemexpress LLC AS 1411 (AGRO-100) | 301636-59-9 | 99.5% | 8272.31 | 1 MG
AS 1411 (AGRO-100) is an oligonucleotide aptamer that targets nucleoproteins. It inhibits tumor cell proliferation by affecting the activity of nucleoprotein-containing complexes. This aptamer can also serve as a carrier to precisely deliver nanoparticles, oligonucleotides, and small molecules to cancer cells.
- Inhibits tumor cell proliferation
- Reduces PRMT5 expression
- Blocks binding of nucleoproteins to bcl-2 mRNA
- Serves as a carrier for targeted delivery
- Crosses the blood-brain barrier with low tissue toxicity
Medchemexpress LLC IRAK4-IN-21 | 2170694-04-7 | C28H28FN7O2 | 10 MM 1 ML
IRAK4-IN-21 (compound 17) is an orally active, potent and selective IRAK4 inhibitor with IC50 values of 5 and 56 nM for IRAK4 and TAK1, respectively. It effectively inhibits IL-23 production (IC50=0.17 μM) and can be used in studies of autoimmune diseases such as plaque psoriasis and psoriatic arthritis.
- Decreases the levels of IL-23 (in THP-1 and DC cells), IL-6 (in HUVEC cells), and MIP-1β (in human whole blood).
- Inhibits IL-23 levels in THP-1 and DC cells with IC50 of 0.17 and 0.51 μM, respectively.
- Inhibits IL-6 level in HUVEC cells with an IC50 of 0.20 μM.
- Inhibits MIP-1β level in human whole blood with an IC50 of 0.47 μM.
- Shows moderate efficacy in acute animal model studies for the inhibition of IL-6 production (in vivo).
- Oral administration of 75 mg/kg showed 54% inhibition of IL-6 in BALB/c mice.