Glycosyl compounds
Medchemexpress LLC Isoconazole nitrate | 24168-96-5 | 98.0% | 100 MG
Isoconazole nitrate | 24168-96-5 | 98.0% | 100 MG
Cayman Chemical Sucrose hexasulfATpotasIu 10mg
A polysulfated disaccharide that is used as a reference standard for sucralfate
Medchemexpress LLC Azido-PEG4-alpha-D-mannose | 1632372-86-1 | 96.2% | C14H27N3O9 | 10MG
Azido-PEG4-alpha-D-mannose is a PEG4 linker with an azide functional group and an alpha-D-mannose residue, used for click-chemistry conjugation and glyco-conjugation in chemical biology and bioconjugation workflows.
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) for efficient bioconjugation.
- Provides a short, hydrophilic PEG4 spacer to improve solubility and reduce steric hindrance.
- Presents an alpha-D-mannose moiety for targeting mannose-binding lectins and receptors.
- Reported purity around 96.2% suitable for research applications.
- Available in small pack sizes for synthetic and analytical workflows.
Medchemexpress LLC D-Glucose, 4-O-β-D-galactopyranosyl- | 63-42-3 | 98.0% | 1 ML
Lactose is a β-galactoside composed of galactose and glucose residues, serving as the main carbohydrate in mammalian breast milk. This macronutrient acts as an inducer of host innate immune responses, possessing immune modulatory functions. In laboratory settings, it has been shown to inhibit regulatory T-cell-mediated suppression of effector T-cell interferon-γ and IL-17 production. Studies indicate that lactose can also improve acute pancreatitis by modulating early immune cell infiltration and cytokine production.
- White to light yellow solid appearance
- Molecular weight of 342.30 g/mol
- Inhibits regulatory T-cell-mediated suppression
- Modulates immune cell infiltration
- Suppresses ERK1/2 and NF-κB p65 signaling
- Suitable for in vitro and in vivo studies
Medchemexpress LLC Lactose octaacetate | 6291-42-5 | 98.0% | 678.59 | 25 G
Lactose octaacetate exhibits mild to moderate antifungal activity against certain fungi, but it shows low or no activity against bacteria and yeast. It also demonstrates low cytotoxicity to MDBK cells, Hep-2, and MDCK cells, and possesses antiviral activity against PV-1.
- Mild to moderate antifungal activity against some fungi.
- Low or no activity against bacteria and yeast.
- Low cytotoxicity to MDBK cells, Hep-2, and MDCK cells.
- Antiviral activity against PV-1.
Medchemexpress LLC VEGF-D Mouse HEK29 100ug
VEGF-D Protein a versatile growth factor orchestrates angiogenesis lymphangiogenesis and endothelial cell growth It stimulates proliferation migration and influences vessel permeability VEGF-D binds VEGFR-3 triggering crucial signaling for vascular development Structurally VEGF-D is a non-covalent homodimer emphasizing its intricate role in vascular processes VEGF-D Protein Mouse (HEK293 Fc) is the recombinant mouse-derived VEGF-D protein expressed by HEK293 with N-hFc labeled tag
Medchemexpress LLC D-KLVFFA | 342877-55-8 | 99.3% | 723.90 | 1 MG
D-KLVFFA is an inhibitor of Amyloid-β assembly, with an IC50 of 2.6 μM, that can be used in Alzheimer's disease study.
- Inhibitor of Amyloid-β assembly
- Has an IC50 of 2.6 μM
- Used in Alzheimer's disease study
- Appearance is solid, white to off-white
- Sequence: D-Lys-D-Leu-D-Val-D-Phe-D-Phe-D-Ala
- Sequence shortening: d-KLVFFA
Medchemexpress LLC 2,4(1H,3H)-pyrimidinedione, 1-β-D-arabinofuranosyl-5-methyl | 605-23-2 | MFCD00065474 | 98.0% | 258.23 g·mol⁻¹ | C10H14N2O6 | 5 MG
Thymine 1-β-D-arabinofuranoside is a thymine-derived nucleoside analogue used as a research reagent to study nucleoside metabolism and DNA synthesis inhibition. It is supplied as a characterized solid with high purity for in vitro biochemical and cell-based assays.
- Purity 98.0%.
- Molecular weight 258.23 g·mol⁻¹.
- Chemical formula C10H14N2O6.
- Supplied as a solid powder suitable for laboratory use.
- Available in small milligram packaging for research applications.
- Commonly used to investigate DNA synthesis and nucleoside metabolism.
Medchemexpress LLC [D-Ala2]-GIP (human) | 444073-04-5 | 99.0% | 4983.60 | 1 MG
[D-Ala2]-GIP (human) is a GIP receptor agonist (EC50 of 630 pM) that improves glucose tolerance and shows neuroprotective activity in Parkinson's disease models. It also enhances cognitive function and hippocampal synaptic plasticity in obese diabetic rats, making it suitable for research on type 2 diabetes and Parkinson's disease.
- GIP receptor agonist with an EC50 of 630 pM
- Improves glucose tolerance by stimulating insulin release
- Demonstrates neuroprotective activity in MPTP-induced Parkinson's disease models
- Enhances cognitive function and hippocampal synaptic plasticity in obese diabetic rats
- Suitable for research on type 2 diabetes and Parkinson's disease
Cambridge Isotope Laboratories Dodecyl-beta-D-maltopyranoside (DDM) (dodecyl-D25 97%) 0 1 g
Dodecyl-beta-D-maltopyranoside (DDM) (dodecyl-D25 97%) 0 1 g
Cambridge Isotope Laboratories Bromoxynil (ring-13C6 99%) 50 ug/mL in nonane 2 x 1 2 mL
Bromoxynil (ring-13C6 99%) 50 ug/mL in nonane 2 x 1 2 mL
Medchemexpress LLC Complement Factor D/ 50ug
Recombinant rat Complement Factor D (Adipsin) expressed in Pichia pastoris with an N-terminal 6xHis tag. Supplied as a lyophilized powder formulated in PBS with 6% trehalose, the protein is glycosylated, >95% pure by reducing SDS-PAGE, and has low endotoxin (<1 EU/μg). Intended for research on the alternative complement pathway; store at -20°C and follow reconstitution guidance (do not reconstitute below 100 μg/mL).
- Recombinant protein expressed in Pichia pastoris.
- N-terminal 6xHis tag for purification or detection.
- Lyophilized formulation in PBS with 6% trehalose for stability.
- High purity greater than 95% by reducing SDS-PAGE.
- Low endotoxin level below 1 EU/μg.
- Glycosylated; migrates ~43 kDa under reducing conditions.
- Stable when stored at -20°C; aliquot after reconstitution for long-term storage.
Medchemexpress LLC Thymine 1-beta-D-arabinofuranoside | 605-23-2 | 98.0% | 258.23 | 1 MG
Thymine 1-beta-D-arabinofuranoside is a purine nucleoside analogue recognized for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis.
- Suitable for research use only.
- Demonstrates cellular effects in various cell lines, including HL-60, KB, and OST cells.
- Shows inhibitory activity against herpes simplex virus type-1 (HSV-1) replication.
- Available as an off-white to light yellow solid.
- Related to oligonucleotides, nucleoside analogs, and thymidine.
- Relevant for research in cancer, blood diseases, and leukemia/lymphoma/myeloma.
Apexbio Technology LLC Bafilomycin D 98813-13-9 5mg
Bafilomycin D is an inhibitor targeting vacuolar-type H -ATPases (V-ATPases) displaying approximate IC of 2 nM in assays utilizing Neurospora crassa-derived enzymes V-ATPases function as proton pumps actively transporting protons across cellular membranes through ATP hydrolysis thus controlling pH homeostasis within intracellular compartments By selectively disrupting proton gradient formation mediated by V-ATPases Bafilomycin D serves as a useful investigative tool in studies of intracellular vesicular trafficking lysosome acidification endocytosis and related membrane transportation mechanisms in biomedical research contexts