Flavonoids
Selleck Chemical LLC Farrerol-5mg
Farrerol, an important bioactive constituent of rhododendron, exhibits broad activities such as anti-oxidative and anti-inflammatory effects.
Medchemexpress LLC Naringenin chalcone | 73692-50-9 | MFCD00016762 | 272.25 g/mol | C15H12O5 | 10 MG
Naringenin chalcone is a tetrahydroxychalcone flavonoid intermediate supplied for laboratory research and analytical applications. It is used in studies of flavonol biosynthesis and in biological assays where its reported activities (apoptosis induction, anti-inflammatory, anti-allergic, and anticancer effects) are relevant.
- Research reagent for studies of flavonol biosynthesis.
- Reported biological activities include apoptosis induction and anti-inflammatory effects.
- Suitable for analytical applications and small-scale laboratory assays.
- Molecular weight 272.25 g/mol; chemical formula C15H12O5.
- CAS number 73692-50-9; supplied in small package sizes for research use.
eMolecules 3,4'-Dihydroxyflavone | 14919-49-4 | MFCD00017690 | 1g
Combi-Blocks | 3,4'-Dihydroxyflavone | 1g | 267185521 | QC-6653 | 95.000 | 14919-49-4 | MFCD00017690 | 254.241 | C15H10O4
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
eMolecules 108238-41-1 | 3,6-Dihydroxyflavone | Combi-Blocks, Inc. | MFCD00143082 | 254.241 | C15H10O4 | 97.000 | Oc1ccc2oc(-c3ccccc3)c(O)c(=O)c2c1 | 1g | 603154804
3,6-Dihydroxyflavone | Combi-Blocks, Inc. | 108238-41-1 | MFCD00143082 | 254.241 | C15H10O4 | 97.000 | Oc1ccc2oc(-c3ccccc3)c(O)c(=O)c2c1 | 1g | 603154804
American Radiolabeled Chemicals Inc DIHYDROXYFLAVONE 10ME
7,8-Dihydroxyflavone 10mg as solid, M.W. 254.24, Solvent: Solid, CAS # 38183-03-8, Tyrosine kinase receptor B (TrkB) agonist
Apexbio Technology LLC (-)-epicatechin 490-46-0 5mg
(-)-Epicatechin (CAS 490-46-0) is a flavonoid compound known for inducing pancreatic -cell regeneration and modulating nitric oxide (NO) metabolism It inhibits nitric oxide-related nitrite formation induced by interferon- and lipopolysaccharide in mouse macrophages and reduces peroxynitrite-mediated tyrosine nitration in HL-60 human leukemia cells Additionally in human endothelial cells (HUVECs) it enhances NO production displaying vasodilatory properties In diabetic rat models (alloxan-induced) (-)-epicatechin administration promotes -cell recovery reduces hyperglycemia and prevents -cell necrosis This profile underscores its research relevance for diabetes and vascular biology investigations
TARGETMOL CHEMICALS INC LUTEOLIN 7-O-GLUCURONIDE 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Luteolin 7-O-glucuronide (Luteolin-7-glucuronide) possesses antioxidant activities. purity: 99%
Medchemexpress LLC Luteolin | 491-70-3 | 99.51% | 286.24 | 10 MG
Luteolin, also known as Luteoline or Luteolol, is a flavonoid compound and a potent Nrf2 inhibitor. It possesses anti-inflammatory and anti-cancer properties. This product is for research use only and is not sold to patients.
- Induces apoptosis and cell cycle arrest
- Inhibits metastasis and angiogenesis in various cancer cell lines
- Suitable for research applications
Medchemexpress LLC (-)-Epicatechin | 490-46-0 | 99.0% | 290.27 | 500 MG
(-)-Epicatechin | 490-46-0 | 99.0% | 290.27 | 500 MG
Medchemexpress LLC Apigenin-7-glucuronide | 29741-09-1 | 446.36 | 1 ML
Apigenin-7-glucuronide is a chemical compound that acts as an inhibitor of Matrix Metalloproteinases (MMP) activities, with specific IC50 values for MMP-3, MMP-8, MMP-9, and MMP-13. This product is intended for research use only.
- Inhibits Matrix Metalloproteinases (MMP) activities
- Purity of 99.74%
- Available as a solid
- Soluble in DMSO for in vitro studies
- Specific storage conditions for powder and in solvent
Medchemexpress LLC Luteolin 7-O-glucuronide | 29741-10-4 | 462.36 | 25 MG
Luteolin 7-O-glucuronide is an inhibitor of Matrix Metalloproteinases (MMP) activities. It is a solid, white to light yellow in color, and is intended for research use only. This compound inhibits NO production and mRNA expression of various inflammatory mediators in LPS-stimulated RAW 264.7 macrophages.
- Inhibits matrix metalloproteinases (MMP) activities
- Inhibits NO production and mRNA expression of inflammatory mediators
- Improves depression-like and stress coping behaviors in mouse models
- Available as a white to light yellow solid
- For research use only
Medchemexpress LLC Apigenin | 520-36-5 | 270.24 | 5 MG
Apigenin (4',5,7-Trihydroxyflavone) is a competitive CYP2C9 inhibitor with a Ki of 2 μM. It inhibits cell proliferation in SGC-7901 cells in a dose- and time-dependent manner and possesses a broad spectrum of biological properties including antioxidative, anti-inflammatory, anticancer, and neuroprotective effects.
- Inhibits cell proliferation
- Suppresses clone formation of SGC-7901 cells
- Alleviates adriamycin-induced myocardial injury
- Reduces serum aspartate amino transferase release
- Reduces serum lactate dehydrogenase release
- Reduces serum creatine kinase contents
Apexbio Technology LLC (-)-epicatechin 490-46-0 10mM (in 1mL DMSO)
(-)-Epicatechin (CAS 490-46-0) is a flavonoid compound known for inducing pancreatic -cell regeneration and modulating nitric oxide (NO) metabolism It inhibits nitric oxide-related nitrite formation induced by interferon- and lipopolysaccharide in mouse macrophages and reduces peroxynitrite-mediated tyrosine nitration in HL-60 human leukemia cells Additionally in human endothelial cells (HUVECs) it enhances NO production displaying vasodilatory properties In diabetic rat models (alloxan-induced) (-)-epicatechin administration promotes -cell recovery reduces hyperglycemia and prevents -cell necrosis This profile underscores its research relevance for diabetes and vascular biology investigations
Medchemexpress LLC 4H-1-benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)- | 520-36-5 | 270.24 | 200 MG
Apigenin (4',5,7-Trihydroxyflavone) is a competitive CYP2C9 inhibitor with a Ki of 2 μM. It inhibits cytochrome P450 2C9 (CYP2C9) with a Ki of 2 μM in the CYP2C9 RECO system, a purified, reconstituted enzyme system. This natural flavonoid possesses broad biological properties including antioxidative, anti-inflammatory, anticancer, and neuroprotective effects.
- Inhibits cell proliferation
- Suppresses clone formation of SGC-7901 cells
- Alleviates Adriamycin-induced myocardial injury
- Reduces serum aspartate amino transferase (AST) release
- Reduces serum lactate dehydrogenase (LDH) release
- Reduces serum creatine kinase (CK) contents
