Flavonoids
Cayman Chemical HesperIdIn methylchalconC 50g
A C. aurantium extract that contains hesperidin methylchalcone, among other compounds
Medchemexpress LLC Acacetin, 5,7-dihydroxy-4'-methoxyflavone | 480-44-4 | 284.26 | 100 MG
Acacetin is an orally active flavonoid derived from *Dendranthema morifolium*. It acts by docking in the ATP binding pocket of PI3Kγ. Acacetin induces cell cycle arrest, apoptosis, and autophagy in cancer cells.
- Possesses potent anti-cancer and anti-inflammatory activity.
- Has potential for research into pain-related diseases.
- Decreases cancer cell viabilities in a dose-dependent manner.
- Induces apoptosis and autophagy.
Medchemexpress LLC Acacetin (5,7-dihydroxy-4'-methoxyflavone) | 480-44-4 | MFCD00016936 | 99.7% | 284.26 | C16H12O5 | 10 MG
Acacetin (5,7-dihydroxy-4'-methoxyflavone) is an O-methylated flavone used as a research reagent for studies of apoptosis, autophagy, and inflammatory signaling. It is supplied as a high-purity reference material for in vitro and preclinical experiments.
- CAS number: 480-44-4.
- Molecular formula: C16H12O5.
- Molecular weight: 284.26 g/mol.
- Purity: 99.7%.
- Available pack sizes: 1 mg-1 g for laboratory use.
- Documentation provided: data sheet, certificate of analysis, and safety data sheet.
Medchemexpress LLC Hesperidin | 520-26-3 | MFCD00075663 | 96.5% | 610.56 g/mol | C28H34O15 | 10 MG
Hesperidin (analytical standard) is a flavanone glycoside isolated from citrus fruits and supplied as a solid reference material for research and analytical applications. It is intended for method development, calibration, and quality control in chromatographic and mass spectrometric assays, and is characterized to support reliable identification and quantitation in analytical workflows.
- Intended for analytical and research use.
- Solid reference material for HPLC and LC-MS workflows.
- Reported purity 96.54%, supporting accurate quantitation.
- Includes standard chemical identifiers (CAS 520-26-3) for traceability.
- Available in small package sizes suitable for analytical laboratories.
Medchemexpress LLC 5,7-Dimethoxyflavone | 21392-57-4 | 100 MG
5,7-Dimethoxyflavone is a natural compound found in *Kaempferia parviflora* that exhibits diverse biological activities. It possesses anti-obesity, anti-inflammatory, and antineoplastic effects. This compound is known to inhibit cytochrome P450 (CYP) 3As and acts as a potent Breast Cancer Resistance Protein (BCRP) inhibitor.
- Inhibits cytochrome P450 (CYP) 3As
- Potent Breast Cancer Resistance Protein (BCRP) inhibitor
- Exhibits anti-obesity effects
- Demonstrates anti-inflammatory properties
- Shows antineoplastic activity
- Reduces liver CYP3A11 and CYP3A25 protein expression in mice
- Inhibits sarcopenia in aged mice
- Decreases body weight gain and inhibits fatty liver in HFD mice
![Medchemexpress LLC 2-(3,4-dimethoxyphenyl)benzo[h]chromen-4-one | 14756-24-2 | MFCD00143008 | 98.5% | 332.35 | C21H16O4 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000247015.png-250.jpg)
Medchemexpress LLC 2-(3,4-dimethoxyphenyl)benzo[h]chromen-4-one | 14756-24-2 | MFCD00143008 | 98.5% | 332.35 | C21H16O4 | 50 MG
DiMNF (3',4'-Dimethoxy-αNF) is a small-molecule aryl hydrocarbon receptor (AHR) modulator supplied as a light yellow to yellow solid for research use. It has molecular formula C21H16O4, molecular weight 332.35, and CAS 14756-24-2. Provided in small packaged quantities for in vitro and exploratory studies; not for clinical use.
- Used as an AHR modulator in biochemical and cell-based assays.
- High purity suitable for research applications.
- Available in small package sizes for laboratory studies.
- Solid, light yellow to yellow appearance for easy handling.
- Supplied for research use only; not for clinical or human use.
eMolecules 14756-24-2 | Medchem Express | DiMNF | 5mg | 724441992 | HY-103222 | MFCD00143008 | 332.355 | C21H16O4
Medchem Express | Oxibendazole | 50mg | 446272455 | HY-B0299 | 20559-55-1 | MFCD00847838 | 249.270 | C12H15N3O3
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Sigma Aldrich Fine Chemicals Biosciences 57-Dimethoxyflavone phypro25MG
This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity water residual solvents inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH Co. KG
Medchemexpress LLC 3',4'-Dimethoxy-alpha-naphthoflavone | 14756-24-2 | MFCD00143008 | 98.5% | 332.35 g·mol^-1 | C21H16O4 | 10 MG
DiMNF (3',4'-Dimethoxy-alpha-naphthoflavone) is a small-molecule aryl hydrocarbon receptor (AHR) modulator supplied for research use. It is offered as a solid and as concentrated DMSO solutions for in vitro biochemical and cell-based assays involving AHR signaling and CYP activity.
- Selective aryl hydrocarbon receptor (AHR) modulator for research applications.
- High purity (≈98.5%) to support reproducible experimental results.
- Molecular formula C21H16O4 and molecular weight 332.35 g·mol^-1.
- Available in multiple pack sizes, including small solid quantities and DMSO solutions.
- Supplied as a solid with optional preprepared DMSO solutions for convenient dosing.
Medchemexpress LLC Neohesperidin (Hesperetin 7-O-neohesperidoside) | 13241-33-3 | 98.7% | 610.56 | 500 MG
Neohesperidin is a flavonoid compound found in citrus plants, known for its antioxidant and anti-inflammatory properties. It has been shown to upregulate the Wnt/β-catenin signaling pathway and induce apoptosis in human breast adenocarcinoma MDA-MB-231 cells. In vivo, it significantly inhibits HCl/ethanol-induced gastric lesions and improves glucose tolerance and insulin sensitivity in diabetic mice.
- Possesses antioxidant and anti-inflammatory properties.
- Upregulates the Wnt/β-catenin signaling pathway.
- Induces apoptosis in human breast adenocarcinoma MDA-MB-231 cells.
- Inhibits HCl/ethanol-induced gastric lesions.
- Improves oral glucose tolerance and insulin sensitivity.
Cayman Chemical Hesperetin Natural Products Ex
A flavonoid with diverse biological activities; reduces ApoB protein levels, ACAT2 expression, and LDL degradation in HepG2 cells from 10-200 µM; inhibits IgG-induced β-hexosaminidase release from RBL-2H3 cells (IC50 = 0.099 mg/ml); inhibits LPS-induced NO production and reduces levels of iNOS, IL-6, and IL-1β in BV-2 microglial cells; inhibits passive cutaneous anaphylaxis in mice at 5 mg/kg; reduces body weight loss, colon shortening, and ulcer severity in a mouse model of TNBS-induced ulcerative colitis; reduces cortical and hippocampal neuronal apoptosis and increases time spent in the target quadrant in the Morris water maze in a mouse model of LPS-induced neuronal inflammation