Azobenzenes
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⁻1 | C13H11N3O4S2 | 10 MG
Sudoxicam is a non-steroidal anti-inflammatory drug (NSAID) of the enol-carboxamide class that acts as a reversible, orally active cyclooxygenase (COX) antagonist. Provided as a research-grade chemical for in vitro and analytical use.
- Reversible COX antagonist for inflammation research.
- Analytical-grade solid with molecular formula C13H11N3O4S2 and molecular weight 337.37 g·mol⁻¹.
- High purity (99.96%), suitable for research and analytical applications.
- Available in small package sizes (1 mg, 5 mg, 10 mg) for assay and method development.
- Storage: powder - -20°C (3 years), 4°C (2 years); in solvent - -80°C (6 months), -20°C (1 month).
Medchemexpress LLC Oxypeucedanin hydrate | 2643-85-8 | 5 MG
Oxypeucedanin hydrate is a natural product isolated from D. anethifolia. It exhibits mild toxicity on fibroblasts and parental lymphoma cells. This product is for research use only.
- Isolated from D. anethifolia
- Exhibits mild toxicity on fibroblasts and parental lymphoma cells
- Molecular weight of 304.29
- Chemical formula is C16H16O6
- Appears as an off-white to light yellow solid
- Purity of 98.0%
- Soluble in DMSO at 100 mg/mL
eMolecules 881-86-7 | Dimethyl pyridine-2,5-dicarboxylate | Ambeed | MFCD00034767 | 195.174 | C9H9NO4 | 98.000 | COC(=O)c1ccc(nc1)C(=O)OC | 1g | 552704469
Dimethyl pyridine-2,5-dicarboxylate | Ambeed | 881-86-7 | MFCD00034767 | 195.174 | C9H9NO4 | 98.000 | COC(=O)c1ccc(nc1)C(=O)OC | 1g | 552704469
eMolecules 1215183-85-9 | ChemScene | 36-Dibromopicolinaldehyde | 100mg | 714110566 | CS-0146972 | MFCD16250664 | 264.904 | C6H3Br2NO
ChemScene | 2-Propylbenzene-13-diol | 250mg | 572195786 | CS-0128889 | 13331-19-6 | MFCD00100568 | 152.193 | C9H12O2
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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.
![Medchemexpress LLC 4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimidine-4,6-dicarboxamide | 544678-85-5 | MFCD09878513 | 99.2% | 410.42 g/mol | C22H20F2N4O2 | 1MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000238385.png-250.jpg)
Medchemexpress LLC 4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimidine-4,6-dicarboxamide | 544678-85-5 | MFCD09878513 | 99.2% | 410.42 g/mol | C22H20F2N4O2 | 1MG
DB04760 is a potent, highly selective, non-zinc-chelating inhibitor of matrix metalloproteinase-13 (MMP-13) with a reported biochemical IC50 of 8 nM. Preclinical studies show the compound reduces paclitaxel-induced neurotoxicity and exhibits anticancer activity. The material is supplied as a light yellow to yellow solid with high purity and recommended storage conditions for powder and solution forms.
Medchemexpress LLC FzM1.8 | 322.3 g/mol | C18H14N2O4 | 10MG
FzM1 8 derives from FzM1 is an allosteric agonist of FZD4 with pEC50 of 6 4 FzM1 8 binds to FZD4 and activates the WNT/ -catenin pathway by promoting TCF/LEF transcriptional activity in the absence of any WNT ligand FzM1 8 stabilizes FZD4 with an increased affinity for heterotrimeric G protein and stimulates the release of the G subunit that in turn activates PI3K[1]
Medchemexpress LLC Cdc7-IN-5 | 1402057-86-6 | 96.7% | 445.47 g/mol | C25H23N3O5 | 5 MG
Cdc7-IN-5 is a small-molecule inhibitor of the Cdc7 serine-threonine kinase supplied for research use. The compound is characterized by molecular formula C25H23N3O5, molecular weight 445.47 g/mol, and reported purity of about 96.7%. It is provided as a solid powder with documented solubility in DMSO and recommended storage conditions for powder and solutions.
- Potent inhibitor of Cdc7 kinase for cell cycle and DNA replication studies.
- Molecular formula C25H23N3O5; molecular weight 445.47 g/mol.
- High purity (about 96.7%).
- Soluble in DMSO; warming and sonication recommended to aid dissolution.
- Powder and solution storage conditions specified for long-term stability.
- Includes datasheet, SDS, COA, and analytical data for quality verification.
eMolecules 104691-86-3 | Medchem Express | Lupiwighteone | 5mg | 705861611 | HY-N3354 | MFCD06796683 | 338.359 | C20H18O5
Ambeed | 5-(Bromomethyl)-2-(trifluoromethyl)pyridine | 250mg | 602852497 | A793147 | 108274-33-5 | MFCD10697684 | 240.023 | C7H5BrF3N
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Medchemexpress LLC Beta-anhydroicaritin | 38226-86-7 | 99.7% | 368.38 g/mol | C21H20O6 | 10 MG
β-Anhydroicaritin is a prenylflavonoid natural product provided for laboratory research use. It is reported to exhibit biological activities such as anti-osteoporosis, estrogenic modulation, and anti-tumor effects, and is supplied as a small-scale research reagent suitable for biochemical and cellular studies.
- Prenylflavonoid natural product.
- Reported activities include anti-osteoporosis, estrogenic modulation, and anti-tumor effects.
- CAS number 38226-86-7 and molecular formula C21H20O6.
- High purity (99.7%).
- Available as a 10 mg research vial for biochemical assays.
eMolecules 78957-85-4 | Medchem Express | A-3 (hydrochloride) | 10mg | 533802412 | HY-125957 | MFCD00077311 | 321.22 | C12H14Cl2N2O2S
Medchem Express | A-3 (hydrochloride) | 10mg | 533802412 | HY-125957 | 78957-85-4 | MFCD00077311 | 321.220 | C12H14Cl2N2O2S
Medchemexpress LLC (-)-Corynoxidine | 57906-85-1 | 5 MG
(-)-Corynoxidine is an acetylcholinesterase inhibitor isolated from the aerial parts of Corydalis speciosa. It exhibits antibacterial activities against Staphylococcus aureus and methicillin-resistant S. aureus strains. With a molecular weight of 371.43 and a formula of C21H25NO5, it appears as an off-white to light yellow solid. It is primarily for research use only.
- Acetylcholinesterase inhibitor (IC50: 89.0 μM)
- Isolated from Corydalis speciosa
- Exhibits antibacterial activities
- Molecular weight: 371.43
- Formula: C21H25NO5
- Appearance: Off-white to light yellow solid
- Purity: 99.90%
- Classified as alkaloid and isoquinoline alkaloid
Medchemexpress LLC Cdc7-IN-5 (compound I-B) | 1402057-86-6 | 96.7% | C25H23N3O5 | 10MG
Cdc7-IN-5 is a small-molecule inhibitor of the CDC7 serine-threonine kinase used in research on DNA replication and cell cycle regulation. The compound is provided as a dry solid with molecular formula C25H23N3O5, molecular weight 445.47, and reported purity around 96.7%.
- Inhibits CDC7 kinase activity in biochemical and cellular assays.
- Useful for studies of DNA replication and cell cycle control.
- Supplied as a dry solid with high reported purity for research use.
- Soluble in DMSO for preparation of concentrated stock solutions.
- Available in research-scale quantities, including 10 mg and sample sizes.
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.