Phenylpropanoids and polyketides
TARGETMOL CHEMICALS INC 3 4 -Dimethoxyflavone 25MG
Also available in 1 mL, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. 3',4'-Dimethoxyflavone is a standard flavonoid compound with numerous medicinal activities. Purity 98.05%
Medchemexpress LLC Hesperidin (Standard) | 520-26-3 | C28H34O15 | 1 ML
Hesperidin, also known as Hesperetin 7-rutinoside, is a flavanone glycoside naturally isolated from citrus fruits. This compound is recognized for its various biological properties, including significant antioxidant effects, the ability to decrease inflammatory mediators, and demonstrated antitumor and antiallergic activities.
- Decreases inflammatory mediators
- Significant antioxidant effects
- Exhibits antitumor activity
- Exhibits antiallergic activity
- Supports research in cancer
- Targets apoptosis
- Targets autophagy
- Targets reactive oxygen species (ROS)
- Functions as an endogenous metabolite
Selleck Chemical LLC Methyl-Hesperidin S2323-50mg
Methyl Hesperidin is a flavanone glycoside (flavonoid) (C28H34O15) found abundantly in citrus fruits Its aglycone form is called hesperetin
TARGETMOL CHEMICALS INC 5 7-DIMETHOXYFLAVONE 50MG
Also available in 1 mL, 10 mg, 25 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. 5,7-DIMETHOXYFLAVONE possessed remarkable leishmanicidal potential. Purity 99.41%
Medchemexpress LLC 3-Hydroxy-7-methoxyflavone | 7478-60-6 | 99.4% | 268.26 | 5 MG
3-Hydroxy-7-methoxyflavone is a flavonoid isolated from natural Salvia elegans, known for its anti-anxiety effects. This compound is for research use only.
- Isolated from natural Salvia elegans.
- Exhibits anti-anxiety effects.
- Cytotoxicity against human KB cells with an ED50 of 26 µg/mL.
- Recommended storage at room temperature for 3 years, or in solvent at -80°C for 2 years or -20°C for 1 year.
- Soluble in DMSO at 50 mg/mL.
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
Medchemexpress LLC 5,7-Dimethoxyflavone | 21392-57-4 | MFCD00016943 | 5 MG
5,7-Dimethoxyflavone is a major component of Kaempferia parviflora. It exhibits anti-obesity, anti-inflammatory, and antineoplastic effects. It is a potent Breast Cancer Resistance Protein (BCRP) inhibitor and inhibits cytochrome P450 (CYP) 3As.
- Exhibits anti-obesity properties
- Demonstrates anti-inflammatory effects
- Shows antineoplastic properties
- Inhibits cytochrome P450 (CYP) 3As
- Acts as a potent Breast Cancer Resistance Protein (BCRP) inhibitor
- Used in metabolic disease research
- Used in inflammation/immunology research
- Used in cancer research
Medchemexpress LLC 5,7-dimethoxyflavone | 21392-57-4 | MFCD00016943 | 282.29 g/mol | C17H14O4 | 10 MG
5,7-Dimethoxyflavone is a dimethoxylated flavone found in Kaempferia parviflora. It is supplied as a research and analytical reagent for laboratory use and serves as an analytical standard and reference material. Reported activities include inhibition of cytochrome P450 3A enzymes and breast cancer resistance protein (BCRP).
- CAS number: 21392-57-4.
- Molecular formula: C17H14O4.
- Molecular weight: 282.29 g/mol.
- Supplied as a small solid quantity suitable for analytical testing (10 MG).
- Intended for research and analytical use only; not for human use.
- Store protected from light; solid storage at 4°C; in solvent store at -80°C (up to 6 months) or -20°C (up to 1 month).
Medchemexpress LLC 6-Methoxyflavone 50mg
6-Methoxyflavone is an orally active methoxyflavone 6-Methoxyflavone suppresses neuroinflammation in microglia through the inhibition of TLR4/MyD88/p38 MAPK/NF- B dependent pathways and the activation of HO-1/NQO-1 signaling 6-Methoxyflavone induces S-phase arrest through the CCNA2/CDK2/p21CIP1 signaling pathway and activates the PERK/EIF2a/ATF4/CHOP pathway in HeLa cells 6-Methoxyflavone acts as a Flumazenil (HY-B0009)-insensitive positive allosteric modulator at human recombinant 1 2 2L and 2 2 2L GABA receptors 6-Methoxyflavone inhibits NFAT Translocation into the nucleus and suppresses T cell activation 6-Methoxyflavone partially restores chronic ethanol-induced behavioral deficits in mice 6-Methoxyflavone antagonizes chronic constriction injury and diabetes associated neuropathic nociception expression 6-Methoxyflavone can be used for the study of cancer inflammation and neurological diseases[1][2][3][4][5][6][7][8]
Medchemexpress LLC 7-Methoxyflavone | 22395-22-8 | MFCD00017462 | 100 MG
7-Methoxyflavone is a flavonoid compound isolated from Zornia brasiliensis. It binds to human serum albumin and acts as an aromatase inhibitor. It possesses peripheral analgesic and certain antitumor activities, being effective against chemical pain but not thermal pain.
- Isolated from Zornia brasiliensis
- Binds to human serum albumin
- Acts as an aromatase inhibitor
- Exhibits peripheral analgesic activity
- Exhibits antitumor activities
- Effective against chemical pain
Selleck Chemical LLC Myricetin 100mg 529-44-2 Cannabiscetin
Myricetin, a natural flavonoid with antioxidant and anti tumor properties, is a novel inhibitor of MEK1 activity and transformation of JB6 P+ mouse epidermal cells. It also inhibits PI3K? with Kd of 0.17 ?M. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC 4-Methoxycinnamaldehyde | 1963-36-6 | MFCD00017343 | 99.9% | 162.19 | 100 MG
4-Methoxycinnamaldehyde, an active constituent of *Agastache rugosa*, demonstrates cytoprotective activity against respiratory syncytial virus (RSV) in a human larynx carcinoma cell line. It effectively inhibits the cytopathic effect of RSV with an estimated IC50 of 0.055 μg/mL.
- Active constituent of *Agastache rugosa*.
- Exhibits cytoprotective activity against respiratory syncytial virus (RSV).
- Effectively inhibits cytopathic effect of RSV.
![eMolecules 3-Oxo-3H-benzo[f]chromene-2-carboxylic acid | 4361-00-6 | MFCD00445973 | 5mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502149563.JPG-250.jpg)
eMolecules 3-Oxo-3H-benzo[f]chromene-2-carboxylic acid | 4361-00-6 | MFCD00445973 | 5mg
Oakwood Chemical | 3-Oxo-3H-benzo[f]chromene-2-carboxylic acid | 5mg | 533803794 | 449053 | | 4361-00-6 | MFCD00445973 | 240.214 | C14H8O4
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Apexbio Technology LLC 2-Methoxycinnamaldehyde 1504-74-1 100mg
2-Methoxycinnamaldehyde (CAS 1504-74-1) is a natural compound derived from cinnamon investigated for its biomedical properties Studies indicate that it disrupts mitochondrial membrane potential leading to mitochondrial dysfunction This effect is associated with the activation of caspase-3 and caspase-9 resulting in the induction of apoptosis and reduced cellular proliferation Additionally 2-Methoxycinnamaldehyde has been shown to inhibit the migration of human aortic smooth muscle cells in response to platelet-derived growth factor (PDGF) These attributes support its application in research exploring cancer cell apoptosis and vascular smooth muscle cell biology