Isoflavonoids
Cambridge Isotope Laboratories Daidzein (unlabeled) 60 ug/mL in acetonitrile 1 2 mL
Daidzein (unlabeled) 60 ug/mL in acetonitrile 1 2 mL
Medchemexpress LLC Genistein 7-β-d-glucuronide | 38482-81-4 | MFCD24849233 | 98.8% | 446.36 | C21H18O11 | 5 MG
Genistein 7-β-d-glucuronide is a natural isoflavone glucuronide reported to inhibit tubulogenesis and endothelial migration. It is provided as a research reagent and is characterized by formula C21H18O11 and molecular weight 446.36.
- High purity (98.8%) suitable for analytical and biological studies.
- Stable storage recommendations included for long-term and short-term preservation.
- Available in small milligram quantities for laboratory experiments.
- Suitable for studies of endothelial cell function and tubulogenesis.
- Provided with supplier characterization data for research reproducibility.
AdipoGen Formononetin
Chemical. CAS 485-72-3. Formula C16H12O4. MW 268.26. Formononetin is an isoflavonoid phytoestrogenic compound found in soy-based foods and is the precursor of daidzein. It acts as an agonist of the aryl hydrocarbon receptor and a selective inhibitor of ADH gamma the gamma-isoform of alcohol dehydrogenase. It displays potent antitumor, antiviral, anti-inflammatory inhibits NLRP3 inflammasome, antioxidant, neuroprotective and neuroinflammatory properties. Also shown to have vasorelaxant, antihypertensive and antihyperglycemic AMPK activator properties. Induces cell cycle arrest and apoptosis in several cancer cells in vitro and in vivo and shows anti-angiogenic FGFR2 inhibitor, anti-invasive and anti-migratory effects. Increases adipocyte thermogenesis by modulating PPARgamma activity.
Apexbio Technology LLC Flavone 525-82-6 25mg
Flavone (CAS 525-82-6) is a polyphenolic organic compound that serves as the structural prototype for the flavone subclass of flavonoids characterized by a 2-phenylchromen-4-one scaffold Flavone modulates diverse biological processes primarily through interactions with cellular signaling pathways and enzymes involved in oxidative stress and inflammation It is extensively utilized in biomedical research to investigate flavonoid metabolism antioxidant activity and anti-inflammatory mechanisms Flavone also functions as a reference standard in analytical assays and supports studies aiming to elucidate the pharmacological properties of related flavonoid derivatives
Sigma Aldrich Fine Chemicals Biosciences (+/-)-Equol >=99.0% (TLC) | 94105-90-5 | MFCD00016662 | 5MG
(+/-)-Equol >=99.0% (TLC) | Purity: >=99.0% (TLC) | Mol Wt: 242.27 | 94105-90-5 | MFCD00016662 | 5MG
Apexbio Technology LLC Daidzein 486-66-8 5g
Daidzein is an isoflavone compound derived from soybeans structurally classified as a phytoestrogen with structural similarity to endogenous estrogen It has been widely investigated for its potential in biomedical research particularly in oncology and cell biology studies Daidzein exhibits anticancer-related biological activity possibly via modulation of hormonal signaling pathways and interference with cell cycle progression as exemplified by inducing cell cycle arrest at the G1 phase in cultured mammalian cells Additionally it demonstrates antioxidant properties providing protective effects against oxidative stress-mediated cell injury such as hepatic cellular damage induced by chemical carcinogens Daidzein is thus employed in studies focused on hormone-dependent tumorigenesis cell-cycle regulation mechanisms and oxidative-stress-induced cellular responses
Medchemexpress LLC Genistein 7-sulfate sodium | 99.9% | 372.28 | 1 MG
Genistein 7-sulfate sodium is a metabolite of genistein. It has the ability to reduce the activity of estrogen agonists in MCF-7 cells and can also promote the growth of MCF-7 cells at concentrations of 10 μM and above.
- Metabolite of genistein
- Reduces activity of estrogen agonists in MCF-7 cells
- Promotes growth of MCF-7 cells at concentrations of 10 μM and above
- Used in research on effects on estrogen agonists and MCF-7 cell growth
Medchemexpress LLC Genistein 7-β-D-Glucuronide | 38482-81-4 | 98.8% | 446.36 | 1 MG
Genistein 7-β-D-Glucuronide is a natural product that functions as an inhibitor of tubulogenesis and endothelial migration. It is intended for research use only.
- Inhibits tubulogenesis
- Inhibits endothelial migration
- Natural product
- Targets vascular endothelial growth factor receptor (VEGFR)
- Relevant to metabolic or endocrine disease research
Medchemexpress LLC Genistein (Standard) | 446-72-0 | MFCD00016952 | 98.7% | C₁₅H₁₀O₅ | 50 MG
Genistein (Standard) is an analytical standard and soy isoflavone. It acts as a multiple tyrosine kinases inhibitor, used in chemotherapeutic research to alter apoptosis, cell cycle, angiogenesis, and inhibit metastasis. This product is intended for research and analytical applications.
- Reference standard for assay
- Used in qualitative research
- Used in quantitative research
- Used in methodological research experiments
- Compatible with HPLC, GC, and MS
Medchemexpress LLC Genistein | 446-72-0 | MFCD00016952 | C15H10O5 | 10MG
Genistein analytical standard is a soy isoflavone reference material supplied for research and analytical use. The material has confirmed identity (CAS 446-72-0), formula C15H10O5, and molecular weight ~270.24 g/mol. It is supplied as a powder with documented stability guidelines and accompanying documentation to support analytical workflows.
- Analytical reference suitable for method validation and quality control.
- High purity: 99.3% as stated on supplier documentation.
- Documented chemical identity and properties (CAS 446-72-0, C15H10O5).
- Recommended cold storage for long-term stability.
- Provided with certificate of analysis and handling documentation.
Medchemexpress LLC Genistein 8-c-glucoside | 66026-80-0 | 1 ML
Genistein 8-c-glucoside (G8CG) is a glucoside for research use only that induces mitochondrial membrane depolarization and apoptosis.
- Induces mitochondrial membrane depolarization
- Induces apoptosis
- For research use only
Apexbio Technology LLC Genistein(Synonyms: 4',5,7-Trihydroxyisoflavone, Genisteol, Prunetol, Sophoricol, Differenol A), 100mg, CAS: 446-72-0.
Genistein (CAS 446-72-0) is an isoflavonoid compound that selectively inhibits protein tyrosine kinases enzymes implicated in signaling pathways associated with oncogenic activity and cellular proliferation Genistein inhibits tyrosine kinase activity with an IC50 of approximately 8 M In NIH-3T3 cell assays genistein suppresses epidermal growth factor (EGF)-mediated mitogenesis (IC50 12 M) and insulin-mediated effects (IC50 19 M) additionally inhibiting EGF-induced activation of S6 kinase at a concentration of 6 15 M In animal models oral administration of genistein demonstrates dose-dependent inhibition of prostate adenocarcinoma development highlighting its utility in cancer biology research and potential chemopreventive applications
Cayman Chemical SophorIcosIde 250mg
An isoflavone glycoside with diverse biological activities; inhibits oleic acid-induced lipid accumulation in HepG2 cells and stimulates glucose uptake in C2C12 mouse skeletal muscle myoblasts at 10 µM; inhibits compound 48/80- or histamine-induced scratching behavior in mice at 2 mg/kg; reduces serum levels of IgE in a mouse model of atopic dermatitis; increases serum levels of osteocalcin and ALP and restores mechanical bone hardness in an ovariectomized rat model of osteoporosis; decreases hepatic cholesterol and triglyceride levels, serum LDL and apolipoprotein B levels, and hepatic injury in a mouse model of fructose-induced liver injury at 80 and 160 mg/kg
7-Hydroxy-4'-nitroisoflavone, 98%, Thermo Scientific™
CAS: 15485-80-0 Molecular Formula: C15H9NO5 Molecular Weight (g/mol): 283.24 MDL Number: MFCD01546432 InChI Key: CEESSYSSRMOMDE-UHFFFAOYSA-N Synonym: 7-hydroxy-4'-nitroisoflavone,7-hydroxy-3-4-nitrophenyl-4h-chromen-4-one,7-hydroxy-3-4-nitrophenyl chromen-4-one,7-hydroxy-3-4-nitrophenyl-4h-1-benzopyran-4-one,7-hydroxy-4-nitroisoflavone,7-hydroxy-4/'-nitroisoflavone,7-hydroxy-4'-nitro-isoflavone 3c PubChem CID: 7454026 IUPAC Name: 7-hydroxy-3-(4-nitrophenyl)chromen-4-one SMILES: OC1=CC=C2C(=O)C(=COC2=C1)C1=CC=C(C=C1)[N+]([O-])=O