Isoflavonoids

Biochanin A 98.0+%, TCI America™

CAS: 491-80-5 Molecular Formula: C16H12O5 Molecular Weight (g/mol): 284.27 MDL Number: MFCD00006839 InChI Key: WUADCCWRTIWANL-UHFFFAOYSA-N Synonym: biochanin a,biochanin,4'-methylgenistein,5,7-dihydroxy-4'-methoxyisoflavone,5,7-dihydroxy-3-4-methoxyphenyl-4h-chromen-4-one,genistein 4-methyl ether,pratensol,biochanine a,5,7-dihydrox-4'-methoxyisoflavone,4h-1-benzopyran-4-one, 5,7-dihydroxy-3-4-methoxyphenyl PubChem CID: 5280373 ChEBI: CHEBI:17574 IUPAC Name: 5,7-dihydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one SMILES: COC1=CC=C(C=C1)C1=COC2=CC(O)=CC(O)=C2C1=O

5,7-Dihydroxy-4'-methoxyisoflavone, 98%

CAS: 491-80-5 Molecular Formula: C16H12O5 Molecular Weight (g/mol): 284.27 MDL Number: MFCD00006839 InChI Key: WUADCCWRTIWANL-UHFFFAOYSA-N Synonym: biochanin a,biochanin,4'-methylgenistein,5,7-dihydroxy-4'-methoxyisoflavone,5,7-dihydroxy-3-4-methoxyphenyl-4h-chromen-4-one,genistein 4-methyl ether,pratensol,biochanine a,5,7-dihydrox-4'-methoxyisoflavone,4h-1-benzopyran-4-one, 5,7-dihydroxy-3-4-methoxyphenyl PubChem CID: 5280373 ChEBI: CHEBI:17574 IUPAC Name: 5,7-dihydroxy-3-(4-methoxyphenyl)chromen-4-one SMILES: COC1=CC=C(C=C1)C1=COC2=CC(O)=CC(O)=C2C1=O

Apexbio Technology LLC Biochanin A 491-80-5 10mM (in 1mL DMSO)

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Biochanin A (CAS number 491-80-5) is a naturally derived inhibitor of fatty acid amide hydrolase (FAAH) an enzyme responsible for metabolizing the endocannabinoid anandamide (AEA) In vitro studies show Biochanin A inhibits FAAH-mediated hydrolysis of AEA with IC50 values of 1 8 M (mouse) 1 4 M (rat) and 2 4 M (human) without affecting CB1 CB2 receptors or FAAH-2 In animal models Biochanin A attenuates formalin-induced phosphorylation of spinal extracellular signal-regulated kinase an effect reversible by CB1 receptor antagonist AM251 Biochanin A thus serves as a useful tool compound in pain regulation and endocannabinoid research

Medchemexpress LLC Biochanin A | 491-80-5 | C16H12O5 | 1 ML

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Biochanin A is a naturally occurring fatty acid amide hydrolase (FAAH) inhibitor. It inhibits FAAH with IC50s of 1.8 μM for mouse, 1.4 μM for rat, and 2.4 μM for human FAAH.

• Inhibits FAAH, autophagy, and endogenous metabolite pathways.
• Relevant for neurological disease and cancer research.
• Targets metabolic enzyme/protease and neuronal signaling pathways.
• Storage for powder: -20°C for 3 years, 4°C for 2 years.
• Storage in solvent: -80°C for 2 years, -20°C for 1 year.

Medchemexpress LLC PHGDH-inactive | 1914971-16-6 | 99.9% | 1 ML

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PHGDH-inactive is a chemically defined negative control compound used to validate PHGDH inhibitor assays. It is supplied in both ready-to-use solution and solid formats for in vitro research use only.

• Used as a negative control in PHGDH inhibitor assays.
• Available as a 10 mM solution in DMSO and as solid powders.
• High chemical purity (about 99.9%).
• Soluble in DMSO at approximately 83.33 mg/mL; ultrasonic assistance may be required.
• Store at 4°C protected from light; in solution, store long-term at -80°C.
• For research use only; not for human or clinical use.

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