Azobenzenes
Medchemexpress LLC Sudoxicam 50mg | 34042-85-8 | 50MG
Sudoxicam is a reversible and orally active COX antagonist and a non-steroidal anti-inflammatory drug (NSAID) from the enol-carboxamide class Sudoxicam has potent anti-inflammatory anti-edema and antipyretic activity[1 [2 [3
Medchemexpress LLC Cadrofloxacin 25mg | 153808-85-6 | 25 MG
Cadrofloxacin is an orally active fluoroquinolone antibiotic supplied for research use only. It exhibits activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria and is provided as a solid powder for laboratory research and assay development.
- Orally active fluoroquinolone antibacterial agent.
- Active against aerobic and anaerobic Gram-positive and Gram-negative bacteria.
- Supplied as a solid powder suitable for research use.
- Molecular formula C19H20F3N3O4; molecular weight 411.38 g·mol⁻¹.
- Typical purity approximately 98.2% as reported by the manufacturer.
Medchemexpress LLC Valategrast | 220847-86-9 | MFCD18782681 | 98.6% | C30H32Cl3N3O4 | 10MG
Valategrast (R-411 free base) is a potent, orally active dual antagonist of integrins α4β1 (VLA-4) and α4β7 provided for research use in inflammation and respiratory disease studies. It is supplied as a solid, characterized material for preclinical and in vitro investigations; not for human therapeutic use.
- Potent orally active dual integrin antagonist useful for mechanistic studies.
- Applicable to COPD and asthma research models.
- High purity solid suitable for analytical and biological assays.
- Available in multiple small pack sizes for research flexibility.
- Characterized with molecular weight, formula, and purity data for reproducibility.
- For research use only; not for human therapeutic use.
Medchemexpress LLC Catalposide | 6736-85-2 | MFCD28015867 | 1 MG
Catalposide is an iridoid glycoside isolated from Catalpa ovata G. Don (Bignoniaceae). It inhibits TNF-α, IL-1β, and IL-6 productions, and NF-κB (p65) activation in lipopolysaccharide-activated RAW 264.7 macrophages. This product is for research use only.
- Solid appearance
- White to yellow color
- Store at 4°C, protect from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protect from light
Medchemexpress LLC 2-Pyridinecarboxamide, 5-[[(6-chloro-2-pyridinyl)methyl](1-oxo-2-propen-1-yl)amino]-N-phenyl | 2305052-86-0 | 98.8% | C21H17ClN4O2 | 100 MG
BPK-25 is an active acrylamide that promotes the degradation of nucleosome remodeling and deacetylation (NuRD) complex proteins through a post-translational mechanism involving covalent protein engagement. It also inhibits TMEM173 activation by the cyclic dinucleotide ligand cGAMP.
- Promotes degradation of NuRD complex proteins.
- Inhibits TMEM173 activation.
- Active acrylamide.
- Intended for research and analytical applications.
Medchemexpress LLC N-cycloheptyl-6,7-dimethoxy-2-(4-piperidin-1-ylpiperidin-1-yl)quinazolin-4-amine | 864289-85-0 | 100.0% | 467.65 g/mol | C27H41N5O2 | 50 MG
C-021 is a small-molecule antagonist of CC chemokine receptor 4 (CCR4) developed for research applications; it blocks CCR4-mediated signaling and functional chemotaxis, with low-nanomolar activity in binding and cell-based assays.
- Potent CCR4 antagonist with low-nanomolar binding activity.
- Prevents CCL22-derived [35S]GTPγS binding to CCR4 (IC50 18 nM) and inhibits functional chemotaxis (human 140 nM, mouse 39 nM).
- Molecular formula C27H41N5O2; molecular weight 467.65 g/mol.
- High purity (~99.95%).
- Solid form with recommended storage: powder -20°C (long term) or 4°C (short term); in solvent store at -80°C.
- Intended for research use only; not for human use.
eMolecules 25109-86-8 | ChemScene | Methyl 2-(2-bromoethyl)benzoate | 250mg | 536865715 | CS-W022777 | MFCD21340317 | 243.1 | C10H11BrO2
Ambeed | 4-Nitrobenzo-15-crown-5 | 1g | 572962026 | A480372 | 60835-69-0 | MFCD00060713 | 313.306 | C14H19NO7
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Medchemexpress LLC Lupiwighteone | 104691-86-3 | 5 MG
Lupiwighteone is an isoflavone from wild-growing plants with antioxidant, antimicrobial, and anticancer properties. It induces apoptosis in human breast cancer cells by inhibiting the PI3K/Akt/mTOR pathway. For research use only.
- Antioxidant and antimicrobial effects.
- Anticancer properties: induces apoptosis in breast cancer cells by inhibiting PI3K/Akt/mTOR.
- Cytotoxicity against various cell lines (e.g., DU-145, SGC-7901).
- Induces cell cycle arrest and apoptosis in DU-145 cells.
- Dose-dependent reduction of cell cycle proteins (CDK1, 2, 4, 6, cyclinD1, B1) and increased ROS production.
- Activates mitochondria-based intrinsic apoptosis, up-regulating cytochrome c and caspase-3, and down-regulating p-Akt/Akt and VEGF.
![Medchemexpress LLC Ethyl 4'-((methyl(3-(pyridin-4-yl)benzyl)carbamoyl)oxy)-[1,1'-biphenyl]-4-carboxylate | 947669-86-5 | MFCD28160857 | 99.7% | 466.53 | C29H26N2O4 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000263530.png-250.jpg)
Medchemexpress LLC Ethyl 4'-((methyl(3-(pyridin-4-yl)benzyl)carbamoyl)oxy)-[1,1'-biphenyl]-4-carboxylate | 947669-86-5 | MFCD28160857 | 99.7% | 466.53 | C29H26N2O4 | 5 MG
WWL113 is a selective, orally active small-molecule inhibitor of carboxylesterases Ces3 and Ces1f used in biochemical and in vivo research to probe lipid metabolism and metabolic syndrome. It has shown efficacy in mouse models, improving lipid and glucose parameters after oral dosing.
- Selective Ces3 and Ces1f inhibitor with potent activity.
- Demonstrated in vivo efficacy in metabolic disease models.
- High purity suitable for research applications.
- Soluble in DMSO and formulatable for in vivo dosing protocols.
- Applicable to biochemical, cell-based, and animal studies.
eMolecules 1918125-85-5 | Ambeed | (4S5S)-2-(2-(Diphenylphosphanyl)phenyl)-45-diphenyl-45-dihydrooxazole | 100mg | 633660447 | A1352088 | 483.551 | C33H26NOP
Ambeed | (S)-2-Methylpiperidine | 1g | 552802083 | A714691 | 3197-42-0 | MFCD01862169 | 99.177 | C6H13N
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Medchemexpress LLC Chromeceptin 10mg | 331859-86-0 | 10 MG
Chromeceptin is a small-molecule IGF signaling pathway inhibitor for research use that suppresses IGF2 expression and reduces phosphorylation of AKT and mTOR. Supplied as a high-purity solid suitable for biochemical and cell-based studies.
- High purity suitable for biochemical assays and cell-based studies.
- Inhibits IGF signaling and suppresses IGF2 expression.
- Reduces phosphorylation of AKT and mTOR in target cells.
- Available as a 10 mg powder with recommended low-temperature storage.
- Soluble in common organic solvents for assay preparation.
Medchemexpress LLC Orismilast | 1353546-86-7 | 99.9% | 510.29 g/mol | C19H15Cl2F2NO7S | 100 MG
Orismilast (LEO-32731) is an orally active, selective phosphodiesterase 4 (PDE4) inhibitor used in research on inflammatory diseases. It exhibits potent inhibition of PDE4B and PDE4D splice variants and is supplied as a high-purity research compound for in vitro and preclinical studies.
- Selective PDE4 inhibitor with activity against PDE4B and PDE4D.
- Purity 99.9%.
- Molecular weight 510.29 g/mol; formula C19H15Cl2F2NO7S.
- Soluble in DMSO at 100 mg/mL; ultrasonic agitation recommended.
- Powder storage: -20°C for long-term stability; aliquot to avoid freeze-thaw.
- Intended for in vitro and preclinical research use only.
Medchemexpress LLC Kansuinine A | 57701-86-7 | 99.8% | 730.75 g·mol⁻1 | C37H46O15 | 5 MG
Kansuinine A is a natural diterpenoid research compound that inhibits IL-6-induced STAT3 activation and has reported antiviral and anticancer activity. It is supplied as a high-purity solid with documented solubility and storage profiles for in vitro experimentation and dosing accuracy.
- Inhibits IL-6-induced STAT3 activation
- Reported antiviral and anticancer activity
- High purity (≈99.8%) suitable for research applications
- Supplied as a white to off-white solid with high solubility in DMSO
- Stable when stored as powder at -20 °C and in solvent under recommended conditions
- Molecular weight 730.75 g·mol⁻1 and formula C37H46O15 for accurate dosing