Azobenzenes
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
Medchemexpress LLC 4-hydroxytolbutamide | 5719-85-7 | MFCD00144466 | 99.7% | 286.35 g/mol | C12H18N2O4S | 10 MG
4-Hydroxytolbutamide is a research-grade metabolite of the antidiabetic tolbutamide, provided as a solid powder for biochemical and pharmacological studies. It is commonly used as an analytical reference standard and in in vitro metabolism experiments involving CYP2C8 and CYP2C9.
- High purity (99.7%).
- CAS number 5719-85-7 for unambiguous identification.
- Molecular weight 286.35 g/mol, suitable for analytical calculations.
- Solid powder stable when stored at -20°C for long-term storage.
- Available in small pack sizes for analytical and research use.
Sigma Aldrich Fine Chemicals Biosciences Azobenzene 98% | 103-33-3 | MFCD00003022 | 5G
Azobenzene 98% | Purity: 98% | Mol Wt: 182.22 | 103-33-3 | MFCD00003022 | 5G
Sigma Aldrich Fine Chemicals Biosciences 4-(Phenylazo)diphenylamine 97% | 101-75-7 | MFCD00003023 | 25G
4-(Phenylazo)diphenylamine 97% | Purity: 97% | Mol Wt: 273.33 | 101-75-7 | MFCD00003023 | 25G
Medchemexpress LLC WR99210 50mg | 47326-86-3 | 394.7 g/mol | C14H18Cl3N5O2 | 50 MG
WR99210 is a potent dihydrofolate reductase (DHFR) inhibitor used in antiparasitic research and as a selection reagent for Plasmodium transfection. It is supplied as a research-grade free base and is used in laboratory studies that require selective inhibition of parasite DHFR.
- Potent dihydrofolate reductase (DHFR) inhibition with subnanomolar activity.
- Commonly used as a selection reagent for Plasmodium transfection experiments.
- Provided as the free base form suitable for research applications.
- Typical pack size: 50 mg.
- For research use only; not for human or clinical use.
eMolecules ChemScene / 1-(34-Difluorophenyl)cyclopropan-1-amine / 100mg / 572219114 / CS-B0485 / 0.000 / 474709-85-8 / MFCD09910057 / 169.175 / C9H9F2N
ChemScene / 1-(34-Difluorophenyl)cyclopropan-1-amine / 100mg / 572219114 / CS-B0485 / 0.000 / 474709-85-8 / MFCD09910057 / 169.175 / C9H9F2N
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.
Medchemexpress LLC EPQpYEEIPIYL | 147612-86-0 | 99.5% | 1473.52 | 5 MG
EPQpYEEIPIYL, a phosphopeptide, is a Src homology 2 (SH2) domain ligand. It activates Src family members (e.g. Lck, Hck, Fyn) by binding to SH2 domains.
- Phosphopeptide and Src homology 2 (SH2) domain ligand
- Activates Src family members (e.g., Lck, Hck, Fyn)
- Binds to SH2 domains
- Exhibits highest affinity binding to GST fusion proteins of Lck SH2 domain and Src SH2 domain
- Target: Src
- Pathway: Protein Tyrosine Kinase/RTK
Medchemexpress LLC Cp-409092 hydrochloride | 225240-86-8 | 99.8% | 333.81 g/mol | C17H20ClN3O2 | 10 MG
CP-409092 hydrochloride is a research-use small molecule described as a partial agonist of GABAA receptors with reported anti-anxiety activity. It is supplied as a solid for laboratory research and is not intended for human therapeutic use.
- Partial agonist of GABAA receptor, with anti-anxiety activity.
- High purity: 99.8% (reported).
- Solid, white to off-white appearance for handling and formulation.
- Recommended storage: 4°C sealed; in solvent, -80°C (up to 6 months) or -20°C (up to 1 month).
- Available in small research pack sizes; common pack: 10 MG.
- For research use only; not for clinical or human use.
![eMolecules 2170033-85-7 | Ambeed | (S)-2-(Benzo[b]thiophen-2-yl)-4-benzyl-45-dihydrooxazole | 50mg | 665578597 | A1493991 | 293.38 | C18H15NOS](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502452393.PNG-250.jpg)
eMolecules 2170033-85-7 | Ambeed | (S)-2-(Benzo[b]thiophen-2-yl)-4-benzyl-45-dihydrooxazole | 50mg | 665578597 | A1493991 | 293.38 | C18H15NOS
Ambeed | Methyl 4-amino-3-(trifluoromethoxy)benzoate | 1g | 525118326 | A202043 | 457097-93-7 | MFCD15527567 | 235.162 | C9H8F3NO3
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Medchemexpress LLC Vacuolin-1 | 351986-85-1 | MFCD00321410 | 98.5% | 577.42 | C26H24IN7O | 5 MG
Vacuolin-1 (CAS 351986-85-1) is a cell-permeable small molecule that inhibits PIKfyve and blocks Ca2+-dependent lysosomal exocytosis. It impairs lysosomal maturation, inhibits late-stage autophagy, and induces vacuole formation, making it useful for studying endosomal/lysosomal trafficking and membrane dynamics in cell biology research.
- Potent, cell-permeable PIKfyve inhibitor.
- Blocks Ca2+-dependent lysosomal exocytosis in cells.
- Impairs lysosomal maturation and inhibits late-stage autophagy.
- Induces vacuole formation and alters endosomal/lysosomal trafficking.
- Provided at high purity for research applications.
Medchemexpress LLC Guselkumab 5mg | 5mg
Guselkumab is a recombinant human IgG1 monoclonal antibody against the IL-23p19 subunit Guselkumab binds to human and cynomolgus monkey IL-23 with Kd values of 3 3 and 1 9 pmol/L respectively Guselkumab inhibits production of cytokines lying downstream of the IL-23 signaling pathway and can be used for psoriatic arthritis research[1] /br
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 | 100 MG
Sudoxicam is an enol-carboxamide non-steroidal anti-inflammatory compound that functions as a reversible cyclooxygenase (COX) antagonist. It is provided as a high-purity analytical reagent intended for in-vitro and preclinical research use only (not for human or clinical use).
- Purity: 99.96%.
- CAS number: 34042-85-8.
- Molecular weight: 337.37 g/mol.
- Molecular formula: C13H11N3O4S2.
- Typical pack size: 100 mg solid.
- Intended use: research reagent and analytical standard for COX inhibition studies.
eMolecules 877874-85-6 | Medchem Express | KG5 | 5mg | 713704945 | HY-15198 | MFCD27665470 | 459.45 | C20H16F3N7OS
Medchem Express | KG5 | 5mg | 713704945 | HY-15198 | 877874-85-6 | MFCD27665470 | 459.450 | C20H16F3N7OS
eMolecules 890819-86-0 | Medchem Express | ML349 | 5mg | 446255990 | HY-100737 | MFCD14808090 | 454.56 | C23H22N2O4S2
Medchem Express | ML349 | 5mg | 446255990 | HY-100737 | 890819-86-0 | MFCD14808090 | 454.560 | C23H22N2O4S2