Azobenzenes
![Medchemexpress LLC 2-([1,4'-bipiperidin]-1'-yl)-N-cycloheptyl-6,7-dimethoxyquinazolin-4-amine | 864289-85-0 | 100.0% | 467.65 g/mol | C27H41N5O2 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000244776.png-250.jpg)
Medchemexpress LLC 2-([1,4'-bipiperidin]-1'-yl)-N-cycloheptyl-6,7-dimethoxyquinazolin-4-amine | 864289-85-0 | 100.0% | 467.65 g/mol | C27H41N5O2 | 100 MG
C-021 is a small-molecule CCR4 antagonist developed for research applications in immunology and receptor pharmacology. It is provided as a solid powder with high purity and is used in biochemical assays and functional chemotaxis studies.
- Potent CCR4 antagonist with nanomolar activity.
- High purity suitable for biochemical and cellular assays.
- Supplied as a solid powder for flexible formulation.
- Stable when stored under recommended conditions.
- Appropriate for in vitro and in vivo pharmacology studies.
Medchemexpress LLC 4-hydroxy-2-methyl-1,1-dioxo-N-(1,3-thiazol-2-yl)-1λ6,2-benzothiazine-3-carboxamide | 34042-85-8 | MFCD00866053 | 100.0% | 337.37 g/mol | C13H11N3O4S2 | 25 MG
Sudoxicam is a reversible, orally active cyclooxygenase (COX) antagonist and a non-steroidal anti-inflammatory compound of the enol-carboxamide class supplied for research and analytical use only. It demonstrates anti-inflammatory, anti-edema, and antipyretic activity and is provided as a solid and in DMSO solution formulations for laboratory studies.
- Reversible, orally active COX antagonist.
- High reported purity suitable for analytical work.
- Chemical formula C13H11N3O4S2 and molecular weight 337.37 g/mol.
- Soluble in DMSO; ultrasonic warming may improve solubility.
- Stable as powder at -20°C for long-term storage; in solvent storage guidelines provided.
eMolecules 179693-85-7 | Ambeed | 23-Dimethoxyterephthalaldehyde | 100mg | 599119640 | A532477 | MFCD18072900 | 194.186 | C10H10O4
Furo[3,2-c]pyridin-4(5H)-one | Ambeed | 26956-43-4 | MFCD00183939 | 135.122 | C7H5NO2 | 95.000 | O=c1[nH]ccc2occc12 | 25g | 491620422
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Medchemexpress LLC Atuliflapon (AZD5718) | 2041075-86-7 | 99.0% | 100 MG
Atuliflapon (AZD5718) is a small-molecule, orally active inhibitor of 5-lipoxygenase activating protein (FLAP) investigated as a research compound for cardiovascular indications such as coronary artery disease. It potently suppresses leukotriene production and has documented preclinical and clinical pharmacology data.
- Oral FLAP inhibitor with potent activity (reported FLAP IC50 ≈ 2 nM).
- Reduces leukotriene production in human whole blood.
- Reported molecular weight 446.50 g·mol⁻¹ and formula C24H26N6O3.
- High purity (about 99.0%), white to off-white solid.
- Soluble in DMSO (≈125 mg/mL); sonication may be required for full dissolution.
- Powder storage: -20°C for long-term stability; in solvent, store at -80°C when possible.
Medchemexpress LLC Iclepertin | 1421936-85-7 | 512.42 | 50 MG
Iclepertin (BI-425809) is a potent, selective, and orally active glycine transporter 1 (GlyT1) inhibitor. It is inactive against GlyT2 and is used for research into Alzheimer's disease and schizophrenia. It inhibits GlyT1 in rat primary neurons and human SK-N-MC cells, and a single oral administration has shown to increase glycine CSF levels in rats.
- Potent, selective, and orally active glycine transporter 1 (GlyT1) inhibitor
- Inactive against GlyT2
- Used for Alzheimer's disease research
- Used for schizophrenia research
- Increases glycine cerebrospinal fluid (CSF) levels
eMolecules 544678-85-5 | Medchem Express | DB04760 | 1mg | 536984011 | HY-125166 | MFCD09878513 | 410.425 | C22H20F2N4O2
Medchem Express | DB04760 | 1mg | 536984011 | HY-125166 | 544678-85-5 | MFCD09878513 | 410.425 | C22H20F2N4O2
Medchemexpress LLC GSK1702934A | 924377-85-5 | 99.11% | 395.52 | 50 MG
GSK1702934A is a selective TRPC3 agonist that modulates cardiac contractility and arrhythmogenesis by activation of TRPC3.
- Selective TRPC3 agonist.
- Modulates cardiac contractility and arrhythmogenesis.
- Induces TRPC3/6-currents in HEK293 cells.
- Induces a transient, non-selective conductance and prolonged action potentials in TRPC3-overexpressing myocytes.
- Promotes NCX currents in TRPC3-overexpressing myocytes.
- Transiently increases blood pressure in conscious Sprague Dawley rats.
- Useful for research applications.
- Available for research use only.
Medchemexpress LLC Cadrofloxacin 100mg | 153808-85-6 | 100 MG
Cadrofloxacin is an orally active fluoroquinolone antibiotic research chemical with activity against aerobic and anaerobic Gram-positive and Gram-negative bacteria. It is supplied as a powder for laboratory research and analytical applications.
- High purity: 98.2%.
- Molecular weight: 411.38 g/mol.
- Chemical formula: C19H20F3N3O4.
- CAS number: 153808-85-6.
- Supplied as a powder, stable at -20°C for long-term storage.
- Available in 100 MG quantity for research use.
eMolecules 19948-85-7 | Medchem Express | FAK-IN-7 | 5mg | 761041122 | HY-148109 | 295.36 | C16H13N3OS
Medchem Express | L-Valine-d8 | 5mg | 686240710 | HY-I1124 | 35045-72-8 | MFCD00144704 | 125.197 | C5H11NO2
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eMolecules 4254-85-7 | 1,5-DIHYDROXYPENTAN-3-ONE | AstaTech | MFCD06658431 | 118.132 | C5H10O3 | 95.000 | OCCC(=O)CCO | 0.25g | 297085484
1,5-DIHYDROXYPENTAN-3-ONE | AstaTech | 4254-85-7 | MFCD06658431 | 118.132 | C5H10O3 | 95.000 | OCCC(=O)CCO | 0.25g | 297085484
eMolecules 52-86-8 | HALOPERIDOL | AstaTech | MFCD00051423 | 375.870 | C21H23ClFNO2 | 95.000 | OC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c1ccc(Cl)cc1 | 1g | 696739973
HALOPERIDOL | AstaTech | 52-86-8 | MFCD00051423 | 375.870 | C21H23ClFNO2 | 95.000 | OC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c1ccc(Cl)cc1 | 1g | 696739973
Medchemexpress LLC Mind4-19 | 129544-85-0 | 99.93% | 373.47 | 50 MG
MIND4-19 is a potent SIRT2 inhibitor with an IC50 value of 7.0 μM. It can be used for researching Huntington's disease.
- Potent SIRT2 inhibitor.
- Exhibits an IC50 value of 7.0 μM for SIRT2.
- Applicable for research into Huntington's disease.
Sigma Aldrich Fine Chemicals Biosciences Chrysoidine G for microscopy (Bact., Bot., Vit.) | 532-82-1 | MFCD00012976 | 25G
Chrysoidine G for microscopy (Bact., Bot., Vit.) | Mol Wt: 248.71 | 532-82-1 | MFCD00012976 | 25G
Medchemexpress LLC 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenylethanone | 274925-86-9 | MFCD09954136 | 99.9% | 273.24 | C14H11NO5 | 50 MG
Nebicapone is a reversible catechol-O-methyltransferase (COMT) inhibitor provided as a solid research compound for in vitro and in vivo studies. It is used to study COMT-mediated metabolism of L-DOPA and related pharmacology, and is supplied with characterization data and storage recommendations for experimental stability.
- Reversible COMT inhibitor for research use.
- Reported purity 99.9%.
- Molecular weight 273.24 g/mol.
- Physical form solid powder.
- High solubility in DMSO (≥100 mg/mL) and formulated in vivo solubility ≥2.5 mg/mL in 10% DMSO/40% PEG300/5% Tween-80/45% saline.
- Recommended storage 4°C protected from light; in solution store at -80°C up to 6 months or -20°C up to 1 month.
Medchemexpress LLC KG5 | 877874-85-6 | C20H16F3N7OS | 50 MG
KG5 is an orally active dual PDGFRβ and B-Raf allosteric inhibitor, also inhibiting Flt3, KIT, and c-Raf. It demonstrates anticancer and antiangiogenic activities, preventing tumor growth and blocking angiogenesis in various models.
- Inhibits vascular smooth muscle cells (VSMCs) and endothelial cell viability
- Selectively blocks S338 phosphorylation
- Inhibits PDGFRα and β, Flt3, and KIT
- Inhibits phosphorylation of MEK and ERK in endothelial cells
- Prevents tumor growth in an orthotopic renal cell carcinoma model
- Completely blocks angiogenesis in mice